[{"file":[{"checksum":"bac881601e1f33c3cf8f51d50b958e68","file_id":"20910","date_created":"2025-12-30T09:39:44Z","file_name":"2025_NanoLetters_York.pdf","file_size":3144989,"success":1,"access_level":"open_access","creator":"dernst","date_updated":"2025-12-30T09:39:44Z","relation":"main_file","content_type":"application/pdf"}],"corr_author":"1","day":"25","oa":1,"language":[{"iso":"eng"}],"oa_version":"Published Version","date_updated":"2025-12-30T09:39:55Z","issue":"36","user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","pmid":1,"doi":"10.1021/acs.nanolett.5c03764","OA_type":"hybrid","month":"08","tmp":{"short":"CC BY (4.0)","image":"/images/cc_by.png","name":"Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)","legal_code_url":"https://creativecommons.org/licenses/by/4.0/legalcode"},"status":"public","date_published":"2025-08-25T00:00:00Z","ddc":["540"],"publication_status":"published","abstract":[{"lang":"eng","text":"Here, we present a foundational investigation of charge transport through three BODIPY-based molecules using the scanning tunneling microscope–break junction (STM-BJ) technique. We demonstrate that molecular conductance through the BODIPY core can be measured by introducing aurophilic linkers at the 2,6-positions. By varying these linkers, we systematically modulate the frontier molecular orbital energies and fine-tune transport behavior. Our experimental results are supported by DFT-based calculations, which feature a new computationally efficient correction to standard PBE-level transmission predictions. Together, these findings establish the viability of BODIPY-based systems for molecular junction applications and lay the groundwork for future studies of their single-molecule optoelectronic properties."}],"isi":1,"type":"journal_article","PlanS_conform":"1","publisher":"American Chemical Society","intvolume":"        25","file_date_updated":"2025-12-30T09:39:44Z","_id":"20331","author":[{"full_name":"York, Emma","id":"08dde91e-8e0a-11f0-9d7d-9e8d80864f16","last_name":"York","first_name":"Emma"},{"full_name":"Stone, Ilana","first_name":"Ilana","last_name":"Stone"},{"first_name":"Wanzhuo","id":"a3010425-87c8-11f0-8106-bec32bea74da","last_name":"Shi","full_name":"Shi, Wanzhuo"},{"last_name":"Roy","first_name":"Xavier","full_name":"Roy, Xavier"},{"full_name":"Venkataraman, Latha","orcid":"0000-0002-6957-6089","id":"9ebb78a5-cc0d-11ee-8322-fae086a32caf","last_name":"Venkataraman","first_name":"Latha"}],"citation":{"ama":"York E, Stone I, Shi W, Roy X, Venkataraman L. Tuning conductance in BODIPY-based single-molecule junctions. <i>Nano Letters</i>. 2025;25(36):13697-13702. doi:<a href=\"https://doi.org/10.1021/acs.nanolett.5c03764\">10.1021/acs.nanolett.5c03764</a>","ista":"York E, Stone I, Shi W, Roy X, Venkataraman L. 2025. Tuning conductance in BODIPY-based single-molecule junctions. Nano Letters. 25(36), 13697–13702.","mla":"York, Emma, et al. “Tuning Conductance in BODIPY-Based Single-Molecule Junctions.” <i>Nano Letters</i>, vol. 25, no. 36, American Chemical Society, 2025, pp. 13697–702, doi:<a href=\"https://doi.org/10.1021/acs.nanolett.5c03764\">10.1021/acs.nanolett.5c03764</a>.","ieee":"E. York, I. Stone, W. Shi, X. Roy, and L. Venkataraman, “Tuning conductance in BODIPY-based single-molecule junctions,” <i>Nano Letters</i>, vol. 25, no. 36. American Chemical Society, pp. 13697–13702, 2025.","chicago":"York, Emma, Ilana Stone, Wanzhuo Shi, Xavier Roy, and Latha Venkataraman. “Tuning Conductance in BODIPY-Based Single-Molecule Junctions.” <i>Nano Letters</i>. American Chemical Society, 2025. <a href=\"https://doi.org/10.1021/acs.nanolett.5c03764\">https://doi.org/10.1021/acs.nanolett.5c03764</a>.","apa":"York, E., Stone, I., Shi, W., Roy, X., &#38; Venkataraman, L. (2025). Tuning conductance in BODIPY-based single-molecule junctions. <i>Nano Letters</i>. American Chemical Society. <a href=\"https://doi.org/10.1021/acs.nanolett.5c03764\">https://doi.org/10.1021/acs.nanolett.5c03764</a>","short":"E. York, I. Stone, W. Shi, X. Roy, L. Venkataraman, Nano Letters 25 (2025) 13697–13702."},"scopus_import":"1","quality_controlled":"1","has_accepted_license":"1","department":[{"_id":"LaVe"}],"publication_identifier":{"eissn":["1530-6992"],"issn":["1530-6984"]},"acknowledged_ssus":[{"_id":"LifeSc"}],"article_processing_charge":"Yes (via OA deal)","date_created":"2025-09-10T05:48:29Z","acknowledgement":"We thank the National Science Foundation (No. NSF-DMR 2241180) for supporting this research. Synthetic work at Columbia was funded in part by the Air Force Office of Scientific Research (AFOSR), under Grant No. FA9550-22-1-0389. The cryoprobe on the 500 MHz NMR instrument used in this research at Columbia was purchased through the NIH Award No. S10OD026749. This work was supported in part by the Institute of Science and Technology Austria. HRMS sample preparation, analysis, and data evaluation were performed by Aikaterina Paraskevopoulou, Mass Spec Service, LSF, ISTA.","publication":"Nano Letters","year":"2025","volume":25,"title":"Tuning conductance in BODIPY-based single-molecule junctions","article_type":"letter_note","external_id":{"isi":["001557017200001"],"pmid":["40855728"]},"OA_place":"publisher","page":"13697-13702"},{"intvolume":"        25","publisher":"American Chemical Society","type":"journal_article","quality_controlled":"1","scopus_import":"1","citation":{"ieee":"W. Lee, C. R. Prindle, W. Shi, S. Louie, M. L. Steigerwald, and L. Venkataraman, “Formation of metallocene single-molecule junctions via metal–metal bonds,” <i>Nano Letters</i>, vol. 25, no. 8. American Chemical Society, pp. 3316–3322, 2025.","ista":"Lee W, Prindle CR, Shi W, Louie S, Steigerwald ML, Venkataraman L. 2025. Formation of metallocene single-molecule junctions via metal–metal bonds. Nano Letters. 25(8), 3316–3322.","mla":"Lee, Woojung, et al. “Formation of Metallocene Single-Molecule Junctions via Metal–Metal Bonds.” <i>Nano Letters</i>, vol. 25, no. 8, American Chemical Society, 2025, pp. 3316–22, doi:<a href=\"https://doi.org/10.1021/acs.nanolett.4c06450\">10.1021/acs.nanolett.4c06450</a>.","ama":"Lee W, Prindle CR, Shi W, Louie S, Steigerwald ML, Venkataraman L. Formation of metallocene single-molecule junctions via metal–metal bonds. <i>Nano Letters</i>. 2025;25(8):3316-3322. doi:<a href=\"https://doi.org/10.1021/acs.nanolett.4c06450\">10.1021/acs.nanolett.4c06450</a>","short":"W. Lee, C.R. Prindle, W. Shi, S. Louie, M.L. Steigerwald, L. Venkataraman, Nano Letters 25 (2025) 3316–3322.","apa":"Lee, W., Prindle, C. R., Shi, W., Louie, S., Steigerwald, M. L., &#38; Venkataraman, L. (2025). Formation of metallocene single-molecule junctions via metal–metal bonds. <i>Nano Letters</i>. American Chemical Society. <a href=\"https://doi.org/10.1021/acs.nanolett.4c06450\">https://doi.org/10.1021/acs.nanolett.4c06450</a>","chicago":"Lee, Woojung, Claudia R. Prindle, Wanzhuo Shi, Shayan Louie, Michael L. Steigerwald, and Latha Venkataraman. “Formation of Metallocene Single-Molecule Junctions via Metal–Metal Bonds.” <i>Nano Letters</i>. American Chemical Society, 2025. <a href=\"https://doi.org/10.1021/acs.nanolett.4c06450\">https://doi.org/10.1021/acs.nanolett.4c06450</a>."},"author":[{"first_name":"Woojung","last_name":"Lee","full_name":"Lee, Woojung"},{"first_name":"Claudia R.","last_name":"Prindle","full_name":"Prindle, Claudia R."},{"first_name":"Wanzhuo","last_name":"Shi","full_name":"Shi, Wanzhuo"},{"first_name":"Shayan","last_name":"Louie","full_name":"Louie, Shayan"},{"full_name":"Steigerwald, Michael L.","first_name":"Michael L.","last_name":"Steigerwald"},{"full_name":"Venkataraman, Latha","orcid":"0000-0002-6957-6089","id":"9ebb78a5-cc0d-11ee-8322-fae086a32caf","last_name":"Venkataraman","first_name":"Latha"}],"_id":"20528","date_created":"2025-10-23T12:18:56Z","article_processing_charge":"No","publication_identifier":{"issn":["1530-6984"],"eissn":["1530-6992"]},"page":"3316-3322","article_type":"letter_note","external_id":{"pmid":["39945435"]},"title":"Formation of metallocene single-molecule junctions via metal–metal bonds","volume":25,"year":"2025","publication":"Nano Letters","day":"13","issue":"8","oa_version":"None","date_updated":"2025-10-23T13:01:26Z","language":[{"iso":"eng"}],"OA_type":"closed access","month":"02","pmid":1,"doi":"10.1021/acs.nanolett.4c06450","user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","publication_status":"published","abstract":[{"lang":"eng","text":"We study single-molecule junction formation of group VIII metallocenes─ferrocene, ruthenocene, and osmocene─with gold (Au) electrodes using the scanning tunneling microscope-based break junction technique. Unlike ferrocene, both ruthenocene and osmocene can form molecular junctions under ambient conditions without chemical linkers. We propose that Au electrodes bind to the metal center and one of the cyclopentadienyl (Cp) rings via a ring-slippage process, forming a molecular junction. Control measurements demonstrate that the metal centers bind to uncoordinated Au exclusively in the +3 oxidation state. Ab initio quantum transport calculations corroborate this mechanism for metallocene junction formation. This work highlights the formation of metal–metal (Ru–Au and Os–Au) bonds in metallocene-based single-molecule devices, challenging the assumption that metallocenes bind exclusively through van der Waals interactions between the Cp ring and the Au electrode. Our findings introduce a method for creating organometallic single-molecule devices with metal–metal bonds, enabling more stable and versatile molecular electronics."}],"extern":"1","date_published":"2025-02-13T00:00:00Z","status":"public"},{"type":"journal_article","isi":1,"publisher":"American Chemical Society","intvolume":"        25","author":[{"full_name":"Puglia, Denise","first_name":"Denise","orcid":"0000-0003-1144-2763","last_name":"Puglia","id":"4D495994-AE37-11E9-AC72-31CAE5697425"},{"full_name":"Odessey, Rachel H","first_name":"Rachel H","last_name":"Odessey","id":"9a7a5123-8972-11ed-ae7b-dd1f2af457bd"},{"last_name":"Burns","first_name":"Peter","full_name":"Burns, Peter"},{"full_name":"Luhmann, Niklas","first_name":"Niklas","last_name":"Luhmann"},{"full_name":"Schmid, Silvan","first_name":"Silvan","last_name":"Schmid"},{"id":"4AD6785A-F248-11E8-B48F-1D18A9856A87","last_name":"Higginbotham","orcid":"0000-0003-2607-2363","first_name":"Andrew P","full_name":"Higginbotham, Andrew P"}],"_id":"19026","citation":{"chicago":"Puglia, Denise, Rachel H Odessey, Peter Burns, Niklas Luhmann, Silvan Schmid, and Andrew P Higginbotham. “Room Temperature, Cavity-Free Capacitive Strong Coupling to Mechanical Motion.” <i>Nano Letters</i>. American Chemical Society, 2025. <a href=\"https://doi.org/10.1021/acs.nanolett.4c05796\">https://doi.org/10.1021/acs.nanolett.4c05796</a>.","apa":"Puglia, D., Odessey, R. H., Burns, P., Luhmann, N., Schmid, S., &#38; Higginbotham, A. P. (2025). Room temperature, cavity-free capacitive strong coupling to mechanical motion. <i>Nano Letters</i>. American Chemical Society. <a href=\"https://doi.org/10.1021/acs.nanolett.4c05796\">https://doi.org/10.1021/acs.nanolett.4c05796</a>","short":"D. Puglia, R.H. Odessey, P. Burns, N. Luhmann, S. Schmid, A.P. Higginbotham, Nano Letters 25 (2025) 2749–2755.","ama":"Puglia D, Odessey RH, Burns P, Luhmann N, Schmid S, Higginbotham AP. Room temperature, cavity-free capacitive strong coupling to mechanical motion. <i>Nano Letters</i>. 2025;25(7):2749-2755. doi:<a href=\"https://doi.org/10.1021/acs.nanolett.4c05796\">10.1021/acs.nanolett.4c05796</a>","ista":"Puglia D, Odessey RH, Burns P, Luhmann N, Schmid S, Higginbotham AP. 2025. Room temperature, cavity-free capacitive strong coupling to mechanical motion. Nano Letters. 25(7), 2749–2755.","ieee":"D. Puglia, R. H. Odessey, P. Burns, N. Luhmann, S. Schmid, and A. P. Higginbotham, “Room temperature, cavity-free capacitive strong coupling to mechanical motion,” <i>Nano Letters</i>, vol. 25, no. 7. American Chemical Society, pp. 2749–2755, 2025.","mla":"Puglia, Denise, et al. “Room Temperature, Cavity-Free Capacitive Strong Coupling to Mechanical Motion.” <i>Nano Letters</i>, vol. 25, no. 7, American Chemical Society, 2025, pp. 2749–55, doi:<a href=\"https://doi.org/10.1021/acs.nanolett.4c05796\">10.1021/acs.nanolett.4c05796</a>."},"quality_controlled":"1","scopus_import":"1","department":[{"_id":"AnHi"}],"acknowledged_ssus":[{"_id":"M-Shop"},{"_id":"NanoFab"}],"publication_identifier":{"eissn":["1530-6992"],"issn":["1530-6984"]},"date_created":"2025-02-16T23:02:34Z","acknowledgement":"We thank Carissa Kumar and Vibha Padmanabhan for assistance in comparing performance with devices across the literature. We thank Andrew Cleland for helpful comments on this work. We are grateful for support from the Miba Machine Shop and Nanofabrication facility at IST Austria. This work was supported by the Austrian FWF grant P33692–N and includes a recipient of a DOC Fellowship of the Austrian Academy of Sciences (DOC – No. 26088) at the Institute of Science and Technology, Austria.","article_processing_charge":"No","year":"2025","publication":"Nano Letters","project":[{"grant_number":"P33692","name":"Cavity electromechanics across a quantum phase transition","_id":"0aa3608a-070f-11eb-9043-e9cd8a2bd931"},{"grant_number":"26088","_id":"62843413-2b32-11ec-9570-c4ec6eabfae7","name":"Surface Charge and Tunneling Multi-Mode Imaging"}],"external_id":{"isi":["001415246000001"],"arxiv":["2407.15314"]},"title":"Room temperature, cavity-free capacitive strong coupling to mechanical motion","article_type":"original","volume":25,"related_material":{"record":[{"id":"18143","status":"public","relation":"earlier_version"}]},"OA_place":"repository","page":"2749-2755","corr_author":"1","day":"06","oa":1,"language":[{"iso":"eng"}],"arxiv":1,"issue":"7","oa_version":"Preprint","date_updated":"2025-09-30T10:29:58Z","doi":"10.1021/acs.nanolett.4c05796","user_id":"317138e5-6ab7-11ef-aa6d-ffef3953e345","main_file_link":[{"open_access":"1","url":"https://doi.org/10.48550/arXiv.2407.15314"}],"month":"02","OA_type":"green","status":"public","date_published":"2025-02-06T00:00:00Z","abstract":[{"text":"The back-action damping of mechanical motion by electromagnetic radiation is typically overwhelmed by internal loss channels unless demanding experimental ingredients such as superconducting resonators, high-quality optical cavities, or large magnetic fields are employed. Here we demonstrate the first room temperature, cavity-free, all-electric device where back-action damping exceeds internal loss, enabled by a mechanically compliant parallel-plate capacitor with a nanoscale plate separation and an aspect ratio exceeding 1,000. The device has 4 orders of magnitude lower insertion loss than a comparable commercial quartz crystal and achieves a position imprecision rivaling optical interferometers. With the help of a back-action isolation scheme, we observe radiative cooling of mechanical motion by a remote cryogenic load. This work provides a technologically accessible route to high-precision sensing, transduction, and signal processing.","lang":"eng"}],"publication_status":"published"},{"user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","doi":"10.1021/acs.nanolett.4c05353","pmid":1,"month":"02","OA_type":"hybrid","tmp":{"short":"CC BY (4.0)","image":"/images/cc_by.png","name":"Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)","legal_code_url":"https://creativecommons.org/licenses/by/4.0/legalcode"},"main_file_link":[{"url":"https://doi.org/10.1021/acs.nanolett.4c05353","open_access":"1"}],"date_published":"2025-02-19T00:00:00Z","status":"public","extern":"1","ddc":["530"],"publication_status":"published","abstract":[{"text":"Fast-emitting scintillators are essential for advanced diagnostic techniques, yet many suffer from low radiation attenuation. This trade-off is particularly pronounced in polymer scintillators, which, despite their fast emission, exhibit low density and low atomic numbers, limiting the radiation attenuation factor, resulting in low detection efficiency. Here, we overcome this limitation by creating a heterostructure scintillator of alternating nanometric layers, combining fast light-emitting polymer scintillator layers and transparent stopping layers with a high radiation attenuation factor. The nanolayer thicknesses are tuned to optimize the penetration depth of recoil electrons in active emissive layers, maximizing the conversion of X-rays to visible light. This design increases light output by up to 1.5 times and enhances imaging resolution by a factor of 2 compared to homogeneous polymer scintillators due to the ability to use thinner samples. These results demonstrate the potential of heterostructure scintillators as next-generation detector materials, overcoming the limitations of homogeneous scintillators.","lang":"eng"}],"day":"19","language":[{"iso":"eng"}],"oa":1,"oa_version":"Published Version","date_updated":"2026-04-27T10:05:22Z","issue":"9","article_processing_charge":"No","date_created":"2026-03-30T12:22:47Z","publication_identifier":{"eissn":["1530-6992"],"issn":["1530-6984"]},"volume":25,"title":"Heterostructure nanoscintillator for matching radiation absorbing layers with fast light-emitting layers","article_type":"letter_note","external_id":{"pmid":["39969821"]},"publication":"Nano Letters","year":"2025","page":"3422-3429","OA_place":"publisher","type":"journal_article","intvolume":"        25","publisher":"American Chemical Society","_id":"21521","author":[{"full_name":"Be’er, Orr","first_name":"Orr","last_name":"Be’er"},{"full_name":"Shultzman, Avner","last_name":"Shultzman","first_name":"Avner"},{"full_name":"Strassberg, Rotem","first_name":"Rotem","last_name":"Strassberg"},{"full_name":"Dosovitskiy, Georgy","last_name":"Dosovitskiy","first_name":"Georgy"},{"full_name":"Veber, Noam","last_name":"Veber","first_name":"Noam"},{"full_name":"Schuetz, Roman","first_name":"Roman","last_name":"Schuetz"},{"id":"e2e68fc9-6505-11ef-a541-eb4e72cc3e82","last_name":"Roques-Carmes","first_name":"Charles","full_name":"Roques-Carmes, Charles"},{"first_name":"Ido","last_name":"Kaminer","full_name":"Kaminer, Ido"},{"full_name":"Bekenstein, Yehonadav","first_name":"Yehonadav","last_name":"Bekenstein"}],"scopus_import":"1","quality_controlled":"1","keyword":["Scintillator","Heterostructure","Thin film","X-ray imaging","X-ray detector"],"citation":{"ieee":"O. Be’er <i>et al.</i>, “Heterostructure nanoscintillator for matching radiation absorbing layers with fast light-emitting layers,” <i>Nano Letters</i>, vol. 25, no. 9. American Chemical Society, pp. 3422–3429, 2025.","ista":"Be’er O, Shultzman A, Strassberg R, Dosovitskiy G, Veber N, Schuetz R, Roques-Carmes C, Kaminer I, Bekenstein Y. 2025. Heterostructure nanoscintillator for matching radiation absorbing layers with fast light-emitting layers. Nano Letters. 25(9), 3422–3429.","mla":"Be’er, Orr, et al. “Heterostructure Nanoscintillator for Matching Radiation Absorbing Layers with Fast Light-Emitting Layers.” <i>Nano Letters</i>, vol. 25, no. 9, American Chemical Society, 2025, pp. 3422–29, doi:<a href=\"https://doi.org/10.1021/acs.nanolett.4c05353\">10.1021/acs.nanolett.4c05353</a>.","ama":"Be’er O, Shultzman A, Strassberg R, et al. Heterostructure nanoscintillator for matching radiation absorbing layers with fast light-emitting layers. <i>Nano Letters</i>. 2025;25(9):3422-3429. doi:<a href=\"https://doi.org/10.1021/acs.nanolett.4c05353\">10.1021/acs.nanolett.4c05353</a>","apa":"Be’er, O., Shultzman, A., Strassberg, R., Dosovitskiy, G., Veber, N., Schuetz, R., … Bekenstein, Y. (2025). Heterostructure nanoscintillator for matching radiation absorbing layers with fast light-emitting layers. <i>Nano Letters</i>. American Chemical Society. <a href=\"https://doi.org/10.1021/acs.nanolett.4c05353\">https://doi.org/10.1021/acs.nanolett.4c05353</a>","short":"O. Be’er, A. Shultzman, R. Strassberg, G. Dosovitskiy, N. Veber, R. Schuetz, C. Roques-Carmes, I. Kaminer, Y. Bekenstein, Nano Letters 25 (2025) 3422–3429.","chicago":"Be’er, Orr, Avner Shultzman, Rotem Strassberg, Georgy Dosovitskiy, Noam Veber, Roman Schuetz, Charles Roques-Carmes, Ido Kaminer, and Yehonadav Bekenstein. “Heterostructure Nanoscintillator for Matching Radiation Absorbing Layers with Fast Light-Emitting Layers.” <i>Nano Letters</i>. American Chemical Society, 2025. <a href=\"https://doi.org/10.1021/acs.nanolett.4c05353\">https://doi.org/10.1021/acs.nanolett.4c05353</a>."}},{"month":"02","user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","pmid":1,"doi":"10.1021/acs.nanolett.3c04207","extern":"1","abstract":[{"lang":"eng","text":"Biased metal–molecule–metal junctions emit light through electroluminescence, a phenomenon at the intersection of molecular electronics and nanoplasmonics. This can occur when the junction plasmon mode is excited by inelastic electron current fluctuations. Here, we simultaneously measure the conductance and electroluminescence intensity from single-molecule junctions with time resolution in a solution environment at room temperature. We use current versus bias data to determine the molecular junction transport parameters and then relate these to the expected current shot noise. We find that the electroluminescence signal accurately matches the theoretical prediction of shot-noise-driven emission in a large fraction of the molecular junctions studied. This introduces a novel experimental method for qualitatively estimating finite-frequency shot noise in single-molecule junctions under ambient conditions. We further demonstrate that electroluminescence can be used to obtain the level alignment of the frontier orbital dominating transport in the molecular junction."}],"publication_status":"published","date_published":"2024-02-05T00:00:00Z","status":"public","day":"05","oa_version":"None","date_updated":"2024-11-18T10:58:19Z","issue":"6","language":[{"iso":"eng"}],"article_processing_charge":"No","date_created":"2024-09-06T12:44:24Z","publication_identifier":{"issn":["1530-6984","1530-6992"]},"page":"1931-1935","volume":24,"title":"Determining transmission characteristics from shot-noise-driven electroluminescence in single-molecule junctions","article_type":"letter_note","external_id":{"pmid":["38315038"]},"publication":"Nano Letters","year":"2024","intvolume":"        24","publisher":"American Chemical Society","type":"journal_article","quality_controlled":"1","scopus_import":"1","citation":{"apa":"Paoletta, A. L., &#38; Venkataraman, L. (2024). Determining transmission characteristics from shot-noise-driven electroluminescence in single-molecule junctions. <i>Nano Letters</i>. American Chemical Society. <a href=\"https://doi.org/10.1021/acs.nanolett.3c04207\">https://doi.org/10.1021/acs.nanolett.3c04207</a>","short":"A.L. Paoletta, L. Venkataraman, Nano Letters 24 (2024) 1931–1935.","chicago":"Paoletta, Angela L., and Latha Venkataraman. “Determining Transmission Characteristics from Shot-Noise-Driven Electroluminescence in Single-Molecule Junctions.” <i>Nano Letters</i>. American Chemical Society, 2024. <a href=\"https://doi.org/10.1021/acs.nanolett.3c04207\">https://doi.org/10.1021/acs.nanolett.3c04207</a>.","ista":"Paoletta AL, Venkataraman L. 2024. Determining transmission characteristics from shot-noise-driven electroluminescence in single-molecule junctions. Nano Letters. 24(6), 1931–1935.","mla":"Paoletta, Angela L., and Latha Venkataraman. “Determining Transmission Characteristics from Shot-Noise-Driven Electroluminescence in Single-Molecule Junctions.” <i>Nano Letters</i>, vol. 24, no. 6, American Chemical Society, 2024, pp. 1931–35, doi:<a href=\"https://doi.org/10.1021/acs.nanolett.3c04207\">10.1021/acs.nanolett.3c04207</a>.","ieee":"A. L. Paoletta and L. Venkataraman, “Determining transmission characteristics from shot-noise-driven electroluminescence in single-molecule junctions,” <i>Nano Letters</i>, vol. 24, no. 6. American Chemical Society, pp. 1931–1935, 2024.","ama":"Paoletta AL, Venkataraman L. Determining transmission characteristics from shot-noise-driven electroluminescence in single-molecule junctions. <i>Nano Letters</i>. 2024;24(6):1931-1935. doi:<a href=\"https://doi.org/10.1021/acs.nanolett.3c04207\">10.1021/acs.nanolett.3c04207</a>"},"_id":"17855","author":[{"first_name":"Angela L.","last_name":"Paoletta","full_name":"Paoletta, Angela L."},{"full_name":"Venkataraman, Latha","first_name":"Latha","last_name":"Venkataraman","id":"9ebb78a5-cc0d-11ee-8322-fae086a32caf","orcid":"0000-0002-6957-6089"}]},{"quality_controlled":"1","scopus_import":"1","citation":{"chicago":"Dalmieda, Johnson, Wanzhuo Shi, Liang Li, and Latha Venkataraman. “Solvent-Mediated Modulation of the Au–S Bond in Dithiol Molecular Junctions.” <i>Nano Letters</i>. American Chemical Society, 2024. <a href=\"https://doi.org/10.1021/acs.nanolett.3c04058\">https://doi.org/10.1021/acs.nanolett.3c04058</a>.","short":"J. Dalmieda, W. Shi, L. Li, L. Venkataraman, Nano Letters 24 (2024) 703–707.","apa":"Dalmieda, J., Shi, W., Li, L., &#38; Venkataraman, L. (2024). Solvent-mediated modulation of the Au–S bond in dithiol molecular junctions. <i>Nano Letters</i>. American Chemical Society. <a href=\"https://doi.org/10.1021/acs.nanolett.3c04058\">https://doi.org/10.1021/acs.nanolett.3c04058</a>","ama":"Dalmieda J, Shi W, Li L, Venkataraman L. Solvent-mediated modulation of the Au–S bond in dithiol molecular junctions. <i>Nano Letters</i>. 2024;24(2):703-707. doi:<a href=\"https://doi.org/10.1021/acs.nanolett.3c04058\">10.1021/acs.nanolett.3c04058</a>","mla":"Dalmieda, Johnson, et al. “Solvent-Mediated Modulation of the Au–S Bond in Dithiol Molecular Junctions.” <i>Nano Letters</i>, vol. 24, no. 2, American Chemical Society, 2024, pp. 703–07, doi:<a href=\"https://doi.org/10.1021/acs.nanolett.3c04058\">10.1021/acs.nanolett.3c04058</a>.","ieee":"J. Dalmieda, W. Shi, L. Li, and L. Venkataraman, “Solvent-mediated modulation of the Au–S bond in dithiol molecular junctions,” <i>Nano Letters</i>, vol. 24, no. 2. American Chemical Society, pp. 703–707, 2024.","ista":"Dalmieda J, Shi W, Li L, Venkataraman L. 2024. Solvent-mediated modulation of the Au–S bond in dithiol molecular junctions. Nano Letters. 24(2), 703–707."},"author":[{"full_name":"Dalmieda, Johnson","first_name":"Johnson","last_name":"Dalmieda"},{"first_name":"Wanzhuo","last_name":"Shi","full_name":"Shi, Wanzhuo"},{"full_name":"Li, Liang","last_name":"Li","first_name":"Liang"},{"last_name":"Venkataraman","id":"9ebb78a5-cc0d-11ee-8322-fae086a32caf","orcid":"0000-0002-6957-6089","first_name":"Latha","full_name":"Venkataraman, Latha"}],"_id":"17857","intvolume":"        24","publisher":"American Chemical Society","type":"journal_article","page":"703-707","article_type":"letter_note","title":"Solvent-mediated modulation of the Au–S bond in dithiol molecular junctions","external_id":{"pmid":["38175934"]},"volume":24,"year":"2024","publication":"Nano Letters","date_created":"2024-09-06T12:46:39Z","article_processing_charge":"No","publication_identifier":{"eissn":["1530-6992"],"issn":["1530-6984"]},"issue":"2","date_updated":"2024-11-19T12:50:27Z","oa_version":"None","language":[{"iso":"eng"}],"day":"04","abstract":[{"text":"Gold–dithiol molecular junctions have been studied both experimentally and theoretically. However, the nature of the gold–thiolate bond as it relates to the solvent has seldom been investigated. It is known that solvents can impact the electronic structure of single-molecule junctions, but the correlation between the solvent and dithiol-linked single-molecule junction conductance is not well understood. We study molecular junctions formed with thiol-terminated phenylenes from both 1-chloronaphthalene and 1-bromonaphthalene solutions. We find that the most probable conductance and the distribution of conductances are both affected by the solvent. First-principles calculations show that junction conductance depends on the binding configurations (adatom, atop, and bridge) of the thiolate on the Au surface, as has been shown previously. More importantly, we find that brominated solvents can restrict the binding of thiols to specific Au sites. This mechanism offers new insight into the effects of the solvent environment on covalent bonding in molecular junctions.","lang":"eng"}],"publication_status":"published","extern":"1","date_published":"2024-01-04T00:00:00Z","status":"public","month":"01","OA_type":"closed access","doi":"10.1021/acs.nanolett.3c04058","pmid":1,"user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87"},{"type":"journal_article","publisher":"American Chemical Society","intvolume":"        24","author":[{"last_name":"Shi","first_name":"Wanzhuo","full_name":"Shi, Wanzhuo"},{"full_name":"Greenwald, Julia E.","first_name":"Julia E.","last_name":"Greenwald"},{"full_name":"Venkataraman, Latha","first_name":"Latha","orcid":"0000-0002-6957-6089","last_name":"Venkataraman","id":"9ebb78a5-cc0d-11ee-8322-fae086a32caf"}],"_id":"17859","citation":{"ama":"Shi W, Greenwald JE, Venkataraman L. Impact of solvent electrostatic environment on molecular junctions probed via electrochemical impedance spectroscopy. <i>Nano Letters</i>. 2024;24(30):9283-9288. doi:<a href=\"https://doi.org/10.1021/acs.nanolett.4c02103\">10.1021/acs.nanolett.4c02103</a>","ista":"Shi W, Greenwald JE, Venkataraman L. 2024. Impact of solvent electrostatic environment on molecular junctions probed via electrochemical impedance spectroscopy. Nano Letters. 24(30), 9283–9288.","ieee":"W. Shi, J. E. Greenwald, and L. Venkataraman, “Impact of solvent electrostatic environment on molecular junctions probed via electrochemical impedance spectroscopy,” <i>Nano Letters</i>, vol. 24, no. 30. American Chemical Society, pp. 9283–9288, 2024.","mla":"Shi, Wanzhuo, et al. “Impact of Solvent Electrostatic Environment on Molecular Junctions Probed via Electrochemical Impedance Spectroscopy.” <i>Nano Letters</i>, vol. 24, no. 30, American Chemical Society, 2024, pp. 9283–88, doi:<a href=\"https://doi.org/10.1021/acs.nanolett.4c02103\">10.1021/acs.nanolett.4c02103</a>.","chicago":"Shi, Wanzhuo, Julia E. Greenwald, and Latha Venkataraman. “Impact of Solvent Electrostatic Environment on Molecular Junctions Probed via Electrochemical Impedance Spectroscopy.” <i>Nano Letters</i>. American Chemical Society, 2024. <a href=\"https://doi.org/10.1021/acs.nanolett.4c02103\">https://doi.org/10.1021/acs.nanolett.4c02103</a>.","apa":"Shi, W., Greenwald, J. E., &#38; Venkataraman, L. (2024). Impact of solvent electrostatic environment on molecular junctions probed via electrochemical impedance spectroscopy. <i>Nano Letters</i>. American Chemical Society. <a href=\"https://doi.org/10.1021/acs.nanolett.4c02103\">https://doi.org/10.1021/acs.nanolett.4c02103</a>","short":"W. Shi, J.E. Greenwald, L. Venkataraman, Nano Letters 24 (2024) 9283–9288."},"quality_controlled":"1","scopus_import":"1","publication_identifier":{"issn":["1530-6984"],"eissn":["1530-6992"]},"date_created":"2024-09-06T12:48:34Z","article_processing_charge":"No","year":"2024","publication":"Nano Letters","title":"Impact of solvent electrostatic environment on molecular junctions probed via electrochemical impedance spectroscopy","article_type":"original","external_id":{"pmid":["39023006"]},"volume":24,"page":"9283-9288","day":"18","language":[{"iso":"eng"}],"issue":"30","date_updated":"2024-11-20T15:24:37Z","oa_version":"None","doi":"10.1021/acs.nanolett.4c02103","pmid":1,"user_id":"68b8ca59-c5b3-11ee-8790-cd641c68093d","month":"07","OA_type":"closed access","status":"public","date_published":"2024-07-18T00:00:00Z","abstract":[{"lang":"eng","text":"The electrostatic environment around nanoscale molecular junctions modulates charge transport; solvents alter this environment. Methods to directly probe solvent effects require correlating measurements of the local electrostatic environment with charge transport across the metal–molecule–metal junction. Here, we measure the conductance and current–voltage characteristics of molecular wires using a scanning tunneling microscope–break junction (STM-BJ) setup in two commonly used solvents. Our results show that the solvent environment induces shifts in molecular conductance, which we quantify, but more importantly we find that the solvent also impacts the magnitude of current rectification in molecular junctions. By incorporating electrochemical impedance spectroscopy into the STM-BJ setup, we measure the capacitance of the dipole layer formed at the metal–solvent interface and show that rectification can be correlated with solvent capacitance. These results provide a method of quantifying the impact of the solvent environment and a path toward improved environmental control of molecular devices."}],"publication_status":"published","extern":"1"},{"user_id":"68b8ca59-c5b3-11ee-8790-cd641c68093d","doi":"10.1021/acs.nanolett.2c04098","pmid":1,"month":"01","OA_type":"closed access","date_published":"2023-01-05T00:00:00Z","status":"public","extern":"1","publication_status":"published","abstract":[{"text":"Understanding how molecular geometry affects the electronic properties of single-molecule junctions experimentally has been challenging. Typically, metal–molecule–metal junctions are measured using a break-junction method where electrode separation is mechanically evolving during measurement. Here, to probe the impact of the junction geometry on conductance, we apply a sinusoidal modulation to the molecular junction electrode position. Simultaneously, we probe the nonlinearity of the current–voltage characteristics of each junction through a modulation in the applied bias at a different frequency. In turn, we show that junctions formed with molecules that have different molecule–electrode interfaces exhibit statistically distinguishable Fourier-transformed conductances. In particular, we find a marked bias dependence for the modulation of junctions where transmission is mediated thorough the van der Waals (vdW) interaction. We attribute our findings to voltage-modulated vdW interactions at the single-molecule level.","lang":"eng"}],"day":"05","language":[{"iso":"eng"}],"oa_version":"None","date_updated":"2024-11-25T14:49:19Z","issue":"2","article_processing_charge":"No","date_created":"2024-09-06T12:58:41Z","publication_identifier":{"issn":["1530-6984"],"eissn":["1530-6992"]},"volume":23,"external_id":{"pmid":["36602221"]},"title":"Voltage-modulated van der waals interaction in single-molecule junctions","article_type":"original","publication":"Nano Letters","year":"2023","page":"567-572","type":"journal_article","intvolume":"        23","publisher":"American Chemical Society","_id":"17865","author":[{"full_name":"Wei, Yujing","first_name":"Yujing","last_name":"Wei"},{"first_name":"Liang","last_name":"Li","full_name":"Li, Liang"},{"last_name":"Greenwald","first_name":"Julia E.","full_name":"Greenwald, Julia E."},{"full_name":"Venkataraman, Latha","first_name":"Latha","orcid":"0000-0002-6957-6089","id":"9ebb78a5-cc0d-11ee-8322-fae086a32caf","last_name":"Venkataraman"}],"quality_controlled":"1","citation":{"ista":"Wei Y, Li L, Greenwald JE, Venkataraman L. 2023. Voltage-modulated van der waals interaction in single-molecule junctions. Nano Letters. 23(2), 567–572.","ieee":"Y. Wei, L. Li, J. E. Greenwald, and L. Venkataraman, “Voltage-modulated van der waals interaction in single-molecule junctions,” <i>Nano Letters</i>, vol. 23, no. 2. American Chemical Society, pp. 567–572, 2023.","mla":"Wei, Yujing, et al. “Voltage-Modulated van Der Waals Interaction in Single-Molecule Junctions.” <i>Nano Letters</i>, vol. 23, no. 2, American Chemical Society, 2023, pp. 567–72, doi:<a href=\"https://doi.org/10.1021/acs.nanolett.2c04098\">10.1021/acs.nanolett.2c04098</a>.","ama":"Wei Y, Li L, Greenwald JE, Venkataraman L. Voltage-modulated van der waals interaction in single-molecule junctions. <i>Nano Letters</i>. 2023;23(2):567-572. doi:<a href=\"https://doi.org/10.1021/acs.nanolett.2c04098\">10.1021/acs.nanolett.2c04098</a>","short":"Y. Wei, L. Li, J.E. Greenwald, L. Venkataraman, Nano Letters 23 (2023) 567–572.","apa":"Wei, Y., Li, L., Greenwald, J. E., &#38; Venkataraman, L. (2023). Voltage-modulated van der waals interaction in single-molecule junctions. <i>Nano Letters</i>. American Chemical Society. <a href=\"https://doi.org/10.1021/acs.nanolett.2c04098\">https://doi.org/10.1021/acs.nanolett.2c04098</a>","chicago":"Wei, Yujing, Liang Li, Julia E. Greenwald, and Latha Venkataraman. “Voltage-Modulated van Der Waals Interaction in Single-Molecule Junctions.” <i>Nano Letters</i>. American Chemical Society, 2023. <a href=\"https://doi.org/10.1021/acs.nanolett.2c04098\">https://doi.org/10.1021/acs.nanolett.2c04098</a>."}},{"language":[{"iso":"eng"}],"ec_funded":1,"oa":1,"issue":"10","date_updated":"2025-04-14T07:59:30Z","oa_version":"Published Version","file":[{"checksum":"9734d4c617bab3578ef62916b764547a","file_id":"13100","date_created":"2023-05-30T07:55:31Z","file_name":"2023_NanoLetters_Azadbakht.pdf","file_size":3654910,"success":1,"access_level":"open_access","creator":"dernst","date_updated":"2023-05-30T07:55:31Z","relation":"main_file","content_type":"application/pdf"}],"day":"04","date_published":"2023-05-04T00:00:00Z","status":"public","abstract":[{"text":"Endocytosis is a key cellular process involved in the uptake of nutrients, pathogens, or the therapy of diseases. Most studies have focused on spherical objects, whereas biologically relevant shapes can be highly anisotropic. In this letter, we use an experimental model system based on Giant Unilamellar Vesicles (GUVs) and dumbbell-shaped colloidal particles to mimic and investigate the first stage of the passive endocytic process: engulfment of an anisotropic object by the membrane. Our model has specific ligand–receptor interactions realized by mobile receptors on the vesicles and immobile ligands on the particles. Through a series of experiments, theory, and molecular dynamics simulations, we quantify the wrapping process of anisotropic dumbbells by GUVs and identify distinct stages of the wrapping pathway. We find that the strong curvature variation in the neck of the dumbbell as well as membrane tension are crucial in determining both the speed of wrapping and the final states.","lang":"eng"}],"publication_status":"published","ddc":["540"],"doi":"10.1021/acs.nanolett.3c00375","pmid":1,"user_id":"4359f0d1-fa6c-11eb-b949-802e58b17ae8","tmp":{"short":"CC BY (4.0)","image":"/images/cc_by.png","name":"Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)","legal_code_url":"https://creativecommons.org/licenses/by/4.0/legalcode"},"month":"05","author":[{"full_name":"Azadbakht, Ali","last_name":"Azadbakht","first_name":"Ali"},{"full_name":"Meadowcroft, Billie","orcid":"0000-0003-3441-1337","id":"a4725fd6-932b-11ed-81e2-c098c7f37ae1","last_name":"Meadowcroft","first_name":"Billie"},{"full_name":"Varkevisser, Thijs","last_name":"Varkevisser","first_name":"Thijs"},{"orcid":"0000-0002-7854-2139","last_name":"Šarić","id":"bf63d406-f056-11eb-b41d-f263a6566d8b","first_name":"Anđela","full_name":"Šarić, Anđela"},{"full_name":"Kraft, Daniela J.","last_name":"Kraft","first_name":"Daniela J."}],"_id":"13094","file_date_updated":"2023-05-30T07:55:31Z","has_accepted_license":"1","scopus_import":"1","quality_controlled":"1","citation":{"short":"A. Azadbakht, B. Meadowcroft, T. Varkevisser, A. Šarić, D.J. Kraft, Nano Letters 23 (2023) 4267–4273.","apa":"Azadbakht, A., Meadowcroft, B., Varkevisser, T., Šarić, A., &#38; Kraft, D. J. (2023). Wrapping pathways of anisotropic dumbbell particles by Giant Unilamellar Vesicles. <i>Nano Letters</i>. American Chemical Society. <a href=\"https://doi.org/10.1021/acs.nanolett.3c00375\">https://doi.org/10.1021/acs.nanolett.3c00375</a>","chicago":"Azadbakht, Ali, Billie Meadowcroft, Thijs Varkevisser, Anđela Šarić, and Daniela J. Kraft. “Wrapping Pathways of Anisotropic Dumbbell Particles by Giant Unilamellar Vesicles.” <i>Nano Letters</i>. American Chemical Society, 2023. <a href=\"https://doi.org/10.1021/acs.nanolett.3c00375\">https://doi.org/10.1021/acs.nanolett.3c00375</a>.","ista":"Azadbakht A, Meadowcroft B, Varkevisser T, Šarić A, Kraft DJ. 2023. Wrapping pathways of anisotropic dumbbell particles by Giant Unilamellar Vesicles. Nano Letters. 23(10), 4267–4273.","ieee":"A. Azadbakht, B. Meadowcroft, T. Varkevisser, A. Šarić, and D. J. Kraft, “Wrapping pathways of anisotropic dumbbell particles by Giant Unilamellar Vesicles,” <i>Nano Letters</i>, vol. 23, no. 10. American Chemical Society, pp. 4267–4273, 2023.","mla":"Azadbakht, Ali, et al. “Wrapping Pathways of Anisotropic Dumbbell Particles by Giant Unilamellar Vesicles.” <i>Nano Letters</i>, vol. 23, no. 10, American Chemical Society, 2023, pp. 4267–4273, doi:<a href=\"https://doi.org/10.1021/acs.nanolett.3c00375\">10.1021/acs.nanolett.3c00375</a>.","ama":"Azadbakht A, Meadowcroft B, Varkevisser T, Šarić A, Kraft DJ. Wrapping pathways of anisotropic dumbbell particles by Giant Unilamellar Vesicles. <i>Nano Letters</i>. 2023;23(10):4267–4273. doi:<a href=\"https://doi.org/10.1021/acs.nanolett.3c00375\">10.1021/acs.nanolett.3c00375</a>"},"type":"journal_article","isi":1,"intvolume":"        23","publisher":"American Chemical Society","external_id":{"pmid":["37141427"],"isi":["000985481400001"]},"article_type":"letter_note","title":"Wrapping pathways of anisotropic dumbbell particles by Giant Unilamellar Vesicles","volume":23,"year":"2023","publication":"Nano Letters","project":[{"grant_number":"802960","call_identifier":"H2020","_id":"eba2549b-77a9-11ec-83b8-a81e493eae4e","name":"Non-Equilibrium Protein Assembly: from Building Blocks to Biological Machines"}],"page":"4267–4273","department":[{"_id":"AnSa"}],"acknowledgement":"We sincerely thank Casper van der Wel for providing open-source packages for tracking, as well as Yogesh Shelke for his assistance with PAA coverslip preparation and Rachel Doherty for her assistance with particle functionalization. We are grateful to Felix Frey for useful discussions on the theory of membrane wrapping. B.M. and A.Š. acknowledge funding by the European Union’s Horizon 2020 research and innovation programme (ERC Starting Grant No. 802960).","date_created":"2023-05-28T22:01:03Z","article_processing_charge":"No","publication_identifier":{"eissn":["1530-6992"],"issn":["1530-6984"]}},{"day":"31","issue":"12","oa_version":"None","date_updated":"2024-12-10T09:40:39Z","language":[{"iso":"eng"}],"month":"05","pmid":1,"doi":"10.1021/acs.nanolett.2c01549","user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","abstract":[{"text":"Coherent tunneling electron transport through molecular wires has been theoretically established as a temperature-independent process. Although several experimental studies have shown counter examples, robust models to describe this temperature dependence have not been thoroughly developed. Here, we demonstrate that dynamic molecular structures lead to temperature-dependent conductance within coherent tunneling regime. Using a custom-built variable-temperature scanning tunneling microscopy break-junction instrument, we find that oligo[n]phenylenes exhibit clear temperature-dependent conductance. Our calculations reveal that thermally activated dihedral rotations allow these molecular wires to have a higher probability of being in a planar conformation. As the tunneling occurs primarily through π-orbitals, enhanced coplanarization substantially increases the time-averaged tunneling probability. These calculations are consistent with the observation that more rotational pivot points in longer molecular wires leads to larger temperature-dependence on conductance. These findings reveal that molecular conductance within coherent and off-resonant electron transport regimes can be controlled by manipulating dynamic molecular structure.","lang":"eng"}],"publication_status":"published","extern":"1","date_published":"2022-05-31T00:00:00Z","status":"public","intvolume":"        22","publisher":"American Chemical Society","type":"journal_article","scopus_import":"1","quality_controlled":"1","citation":{"ista":"Lee W, Louie S, Evans AM, Orchanian NM, Stone IB, Zhang B, Wei Y, Roy X, Nuckolls C, Venkataraman L. 2022. Increased molecular conductance in Oligo[n]phenylene wires by thermally enhanced dihedral planarization. Nano Letters. 22(12), 4919–4924.","ieee":"W. Lee <i>et al.</i>, “Increased molecular conductance in Oligo[n]phenylene wires by thermally enhanced dihedral planarization,” <i>Nano Letters</i>, vol. 22, no. 12. American Chemical Society, pp. 4919–4924, 2022.","mla":"Lee, Woojung, et al. “Increased Molecular Conductance in Oligo[n]Phenylene Wires by Thermally Enhanced Dihedral Planarization.” <i>Nano Letters</i>, vol. 22, no. 12, American Chemical Society, 2022, pp. 4919–24, doi:<a href=\"https://doi.org/10.1021/acs.nanolett.2c01549\">10.1021/acs.nanolett.2c01549</a>.","ama":"Lee W, Louie S, Evans AM, et al. Increased molecular conductance in Oligo[n]phenylene wires by thermally enhanced dihedral planarization. <i>Nano Letters</i>. 2022;22(12):4919-4924. doi:<a href=\"https://doi.org/10.1021/acs.nanolett.2c01549\">10.1021/acs.nanolett.2c01549</a>","short":"W. Lee, S. Louie, A.M. Evans, N.M. Orchanian, I.B. Stone, B. Zhang, Y. Wei, X. Roy, C. Nuckolls, L. Venkataraman, Nano Letters 22 (2022) 4919–4924.","apa":"Lee, W., Louie, S., Evans, A. M., Orchanian, N. M., Stone, I. B., Zhang, B., … Venkataraman, L. (2022). Increased molecular conductance in Oligo[n]phenylene wires by thermally enhanced dihedral planarization. <i>Nano Letters</i>. American Chemical Society. <a href=\"https://doi.org/10.1021/acs.nanolett.2c01549\">https://doi.org/10.1021/acs.nanolett.2c01549</a>","chicago":"Lee, Woojung, Shayan Louie, Austin M. Evans, Nicholas M. Orchanian, Ilana B. Stone, Boyuan Zhang, Yujing Wei, Xavier Roy, Colin Nuckolls, and Latha Venkataraman. “Increased Molecular Conductance in Oligo[n]Phenylene Wires by Thermally Enhanced Dihedral Planarization.” <i>Nano Letters</i>. American Chemical Society, 2022. <a href=\"https://doi.org/10.1021/acs.nanolett.2c01549\">https://doi.org/10.1021/acs.nanolett.2c01549</a>."},"author":[{"first_name":"Woojung","last_name":"Lee","full_name":"Lee, Woojung"},{"first_name":"Shayan","last_name":"Louie","full_name":"Louie, Shayan"},{"first_name":"Austin M.","last_name":"Evans","full_name":"Evans, Austin M."},{"full_name":"Orchanian, Nicholas M.","last_name":"Orchanian","first_name":"Nicholas M."},{"full_name":"Stone, Ilana B.","first_name":"Ilana B.","last_name":"Stone"},{"first_name":"Boyuan","last_name":"Zhang","full_name":"Zhang, Boyuan"},{"first_name":"Yujing","last_name":"Wei","full_name":"Wei, Yujing"},{"full_name":"Roy, Xavier","first_name":"Xavier","last_name":"Roy"},{"first_name":"Colin","last_name":"Nuckolls","full_name":"Nuckolls, Colin"},{"id":"9ebb78a5-cc0d-11ee-8322-fae086a32caf","last_name":"Venkataraman","orcid":"0000-0002-6957-6089","first_name":"Latha","full_name":"Venkataraman, Latha"}],"_id":"17872","date_created":"2024-09-06T13:06:35Z","article_processing_charge":"No","publication_identifier":{"issn":["1530-6984"],"eissn":["1530-6992"]},"page":"4919-4924","article_type":"letter_note","external_id":{"pmid":["35640062"]},"title":"Increased molecular conductance in Oligo[n]phenylene wires by thermally enhanced dihedral planarization","volume":22,"year":"2022","publication":"Nano Letters"},{"day":"27","issue":"8","date_updated":"2025-06-11T13:47:08Z","oa_version":"Preprint","arxiv":1,"language":[{"iso":"eng"}],"oa":1,"month":"04","main_file_link":[{"open_access":"1","url":" https://doi.org/10.48550/arXiv.2109.00556"}],"pmid":1,"doi":"10.1021/acs.nanolett.2c00435","user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","abstract":[{"lang":"eng","text":"Bernal-stacked multilayer graphene is a versatile platform to explore quantum transport phenomena and interaction physics due to its exceptional tunability via electrostatic gating. For instance, upon applying a perpendicular electric field, its band structure exhibits several off-center Dirac points (so-called Dirac gullies) in each valley. Here, the formation of Dirac gullies and the interaction-induced breakdown of gully coherence is explored via magnetotransport measurements in high-quality Bernal-stacked (ABA) trilayer graphene. At zero magnetic field, multiple Lifshitz transitions indicating the formation of Dirac gullies are identified. In the quantum Hall regime, the emergence of Dirac gullies is evident as an increase in Landau level degeneracy. When tuning both electric and magnetic fields, electron–electron interactions can be controllably enhanced until, beyond critical electric and magnetic fields, the gully degeneracy is eventually lifted. The arising correlated ground state is consistent with a previously predicted nematic phase that spontaneously breaks the rotational gully symmetry."}],"publication_status":"published","date_published":"2022-04-27T00:00:00Z","status":"public","intvolume":"        22","publisher":"American Chemical Society","type":"journal_article","isi":1,"quality_controlled":"1","scopus_import":"1","citation":{"mla":"Winterer, Felix, et al. “Spontaneous Gully-Polarized Quantum Hall States in ABA Trilayer Graphene.” <i>Nano Letters</i>, vol. 22, no. 8, American Chemical Society, 2022, pp. 3317–22, doi:<a href=\"https://doi.org/10.1021/acs.nanolett.2c00435\">10.1021/acs.nanolett.2c00435</a>.","ista":"Winterer F, Seiler AM, Ghazaryan A, Geisenhof FR, Watanabe K, Taniguchi T, Serbyn M, Weitz RT. 2022. Spontaneous gully-polarized quantum hall states in ABA trilayer graphene. Nano Letters. 22(8), 3317–3322.","ieee":"F. Winterer <i>et al.</i>, “Spontaneous gully-polarized quantum hall states in ABA trilayer graphene,” <i>Nano Letters</i>, vol. 22, no. 8. American Chemical Society, pp. 3317–3322, 2022.","ama":"Winterer F, Seiler AM, Ghazaryan A, et al. Spontaneous gully-polarized quantum hall states in ABA trilayer graphene. <i>Nano Letters</i>. 2022;22(8):3317-3322. doi:<a href=\"https://doi.org/10.1021/acs.nanolett.2c00435\">10.1021/acs.nanolett.2c00435</a>","short":"F. Winterer, A.M. Seiler, A. Ghazaryan, F.R. Geisenhof, K. Watanabe, T. Taniguchi, M. Serbyn, R.T. Weitz, Nano Letters 22 (2022) 3317–3322.","apa":"Winterer, F., Seiler, A. M., Ghazaryan, A., Geisenhof, F. R., Watanabe, K., Taniguchi, T., … Weitz, R. T. (2022). Spontaneous gully-polarized quantum hall states in ABA trilayer graphene. <i>Nano Letters</i>. American Chemical Society. <a href=\"https://doi.org/10.1021/acs.nanolett.2c00435\">https://doi.org/10.1021/acs.nanolett.2c00435</a>","chicago":"Winterer, Felix, Anna M. Seiler, Areg Ghazaryan, Fabian R. Geisenhof, Kenji Watanabe, Takashi Taniguchi, Maksym Serbyn, and R. Thomas Weitz. “Spontaneous Gully-Polarized Quantum Hall States in ABA Trilayer Graphene.” <i>Nano Letters</i>. American Chemical Society, 2022. <a href=\"https://doi.org/10.1021/acs.nanolett.2c00435\">https://doi.org/10.1021/acs.nanolett.2c00435</a>."},"author":[{"first_name":"Felix","last_name":"Winterer","full_name":"Winterer, Felix"},{"last_name":"Seiler","first_name":"Anna M.","full_name":"Seiler, Anna M."},{"full_name":"Ghazaryan, Areg","first_name":"Areg","last_name":"Ghazaryan","id":"4AF46FD6-F248-11E8-B48F-1D18A9856A87","orcid":"0000-0001-9666-3543"},{"last_name":"Geisenhof","first_name":"Fabian R.","full_name":"Geisenhof, Fabian R."},{"first_name":"Kenji","last_name":"Watanabe","full_name":"Watanabe, Kenji"},{"full_name":"Taniguchi, Takashi","first_name":"Takashi","last_name":"Taniguchi"},{"full_name":"Serbyn, Maksym","orcid":"0000-0002-2399-5827","id":"47809E7E-F248-11E8-B48F-1D18A9856A87","last_name":"Serbyn","first_name":"Maksym"},{"full_name":"Weitz, R. Thomas","last_name":"Weitz","first_name":"R. Thomas"}],"_id":"11379","date_created":"2022-05-15T22:01:41Z","acknowledgement":"We acknowledge funding from the Center for Nanoscience (CeNS) and by the Deutsche\r\nForschungsgemeinschaft (DFG, German Research Foundation) under Germany’s Excellence Strategy-EXC-2111-390814868 (MCQST). K.W. and T.T. acknowledge support from the Elemental Strategy Initiative conducted by the MEXT, Japan (Grant Number PMXP0112101001) and JSPS KAKENHI (Grant Numbers 19H05790 and JP20H00354).","article_processing_charge":"No","publication_identifier":{"eissn":["1530-6992"],"issn":["1530-6984"]},"department":[{"_id":"MaSe"}],"page":"3317-3322","title":"Spontaneous gully-polarized quantum hall states in ABA trilayer graphene","article_type":"original","external_id":{"isi":["000809056900019"],"pmid":["35405074"],"arxiv":["2109.00556"]},"volume":22,"year":"2022","publication":"Nano Letters"},{"_id":"13996","author":[{"last_name":"Baykusheva","id":"71b4d059-2a03-11ee-914d-dfa3beed6530","first_name":"Denitsa Rangelova","full_name":"Baykusheva, Denitsa Rangelova"},{"full_name":"Chacón, Alexis","last_name":"Chacón","first_name":"Alexis"},{"full_name":"Lu, Jian","last_name":"Lu","first_name":"Jian"},{"full_name":"Bailey, Trevor P.","first_name":"Trevor P.","last_name":"Bailey"},{"full_name":"Sobota, Jonathan A.","first_name":"Jonathan A.","last_name":"Sobota"},{"last_name":"Soifer","first_name":"Hadas","full_name":"Soifer, Hadas"},{"first_name":"Patrick S.","last_name":"Kirchmann","full_name":"Kirchmann, Patrick S."},{"full_name":"Rotundu, Costel","last_name":"Rotundu","first_name":"Costel"},{"last_name":"Uher","first_name":"Ctirad","full_name":"Uher, Ctirad"},{"full_name":"Heinz, Tony F.","last_name":"Heinz","first_name":"Tony F."},{"last_name":"Reis","first_name":"David A.","full_name":"Reis, David A."},{"full_name":"Ghimire, Shambhu","first_name":"Shambhu","last_name":"Ghimire"}],"keyword":["Mechanical Engineering","Condensed Matter Physics","General Materials Science","General Chemistry","Bioengineering"],"citation":{"short":"D.R. Baykusheva, A. Chacón, J. Lu, T.P. Bailey, J.A. Sobota, H. Soifer, P.S. Kirchmann, C. Rotundu, C. Uher, T.F. Heinz, D.A. Reis, S. Ghimire, Nano Letters 21 (2021) 8970–8978.","apa":"Baykusheva, D. R., Chacón, A., Lu, J., Bailey, T. P., Sobota, J. A., Soifer, H., … Ghimire, S. (2021). All-optical probe of three-dimensional topological insulators based on high-harmonic generation by circularly polarized laser fields. <i>Nano Letters</i>. American Chemical Society. <a href=\"https://doi.org/10.1021/acs.nanolett.1c02145\">https://doi.org/10.1021/acs.nanolett.1c02145</a>","chicago":"Baykusheva, Denitsa Rangelova, Alexis Chacón, Jian Lu, Trevor P. Bailey, Jonathan A. Sobota, Hadas Soifer, Patrick S. Kirchmann, et al. “All-Optical Probe of Three-Dimensional Topological Insulators Based on High-Harmonic Generation by Circularly Polarized Laser Fields.” <i>Nano Letters</i>. American Chemical Society, 2021. <a href=\"https://doi.org/10.1021/acs.nanolett.1c02145\">https://doi.org/10.1021/acs.nanolett.1c02145</a>.","ista":"Baykusheva DR, Chacón A, Lu J, Bailey TP, Sobota JA, Soifer H, Kirchmann PS, Rotundu C, Uher C, Heinz TF, Reis DA, Ghimire S. 2021. All-optical probe of three-dimensional topological insulators based on high-harmonic generation by circularly polarized laser fields. Nano Letters. 21(21), 8970–8978.","ieee":"D. R. Baykusheva <i>et al.</i>, “All-optical probe of three-dimensional topological insulators based on high-harmonic generation by circularly polarized laser fields,” <i>Nano Letters</i>, vol. 21, no. 21. American Chemical Society, pp. 8970–8978, 2021.","mla":"Baykusheva, Denitsa Rangelova, et al. “All-Optical Probe of Three-Dimensional Topological Insulators Based on High-Harmonic Generation by Circularly Polarized Laser Fields.” <i>Nano Letters</i>, vol. 21, no. 21, American Chemical Society, 2021, pp. 8970–78, doi:<a href=\"https://doi.org/10.1021/acs.nanolett.1c02145\">10.1021/acs.nanolett.1c02145</a>.","ama":"Baykusheva DR, Chacón A, Lu J, et al. All-optical probe of three-dimensional topological insulators based on high-harmonic generation by circularly polarized laser fields. <i>Nano Letters</i>. 2021;21(21):8970-8978. doi:<a href=\"https://doi.org/10.1021/acs.nanolett.1c02145\">10.1021/acs.nanolett.1c02145</a>"},"scopus_import":"1","quality_controlled":"1","type":"journal_article","publisher":"American Chemical Society","intvolume":"        21","publication":"Nano Letters","year":"2021","volume":21,"title":"All-optical probe of three-dimensional topological insulators based on high-harmonic generation by circularly polarized laser fields","article_type":"original","external_id":{"arxiv":["2109.15291"],"pmid":["34676752"]},"page":"8970-8978","publication_identifier":{"eissn":["1530-6992"],"issn":["1530-6984"]},"article_processing_charge":"No","date_created":"2023-08-09T13:09:15Z","oa":1,"language":[{"iso":"eng"}],"arxiv":1,"oa_version":"Published Version","date_updated":"2024-10-14T12:26:13Z","issue":"21","day":"22","status":"public","date_published":"2021-10-22T00:00:00Z","extern":"1","publication_status":"published","abstract":[{"lang":"eng","text":"We report the observation of an anomalous nonlinear optical response of the prototypical three-dimensional topological insulator bismuth selenide through the process of high-order harmonic generation. We find that the generation efficiency increases as the laser polarization is changed from linear to elliptical, and it becomes maximum for circular polarization. With the aid of a microscopic theory and a detailed analysis of the measured spectra, we reveal that such anomalous enhancement encodes the characteristic topology of the band structure that originates from the interplay of strong spin–orbit coupling and time-reversal symmetry protection. The implications are in ultrafast probing of topological phase transitions, light-field driven dissipationless electronics, and quantum computation."}],"user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","pmid":1,"doi":"10.1021/acs.nanolett.1c02145","main_file_link":[{"open_access":"1","url":"https://doi.org/10.1021/acs.nanolett.1c02145"}],"month":"10"},{"language":[{"iso":"eng"}],"issue":"1","date_updated":"2024-12-10T10:26:22Z","oa_version":"None","day":"18","date_published":"2020-12-18T00:00:00Z","status":"public","abstract":[{"text":"Probing structural changes of a molecule induced by charge transfer is important for understanding the physicochemical properties of molecules and developing new electronic devices. Here, we interrogate the structural changes of a single diketopyrrolopyrrole (DPP) molecule induced by charge transport at a high bias using scanning tunneling microscope break junction (STM-BJ) techniques. Specifically, we demonstrate that application of a high bias increases the average nonresonant conductance of single Au–DPP–Au junctions. We infer from the increased conductance that resonant charge transport induces planarization of the molecular backbone. We further show that this conformational planarization is assisted by thermally activated junction reorganization. The planarization only occurs under specific electronic conditions, which we rationalize by ab initio calculations. These results emphasize the need for a comprehensive view of single-molecule junctions which includes both the electronic properties and structure of the molecules and the electrodes when designing electrically driven single-molecule motors.","lang":"eng"}],"publication_status":"published","extern":"1","doi":"10.1021/acs.nanolett.0c04260","pmid":1,"user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","month":"12","OA_type":"closed access","author":[{"full_name":"Zang, Yaping","last_name":"Zang","first_name":"Yaping"},{"full_name":"Fung, E-Dean","first_name":"E-Dean","last_name":"Fung"},{"last_name":"Fu","first_name":"Tianren","full_name":"Fu, Tianren"},{"full_name":"Ray, Suman","first_name":"Suman","last_name":"Ray"},{"full_name":"Garner, Marc H.","last_name":"Garner","first_name":"Marc H."},{"full_name":"Borges, Anders","last_name":"Borges","first_name":"Anders"},{"full_name":"Steigerwald, Michael L.","first_name":"Michael L.","last_name":"Steigerwald"},{"full_name":"Patil, Satish","last_name":"Patil","first_name":"Satish"},{"last_name":"Solomon","first_name":"Gemma","full_name":"Solomon, Gemma"},{"orcid":"0000-0002-6957-6089","id":"9ebb78a5-cc0d-11ee-8322-fae086a32caf","last_name":"Venkataraman","first_name":"Latha","full_name":"Venkataraman, Latha"}],"_id":"17902","scopus_import":"1","quality_controlled":"1","citation":{"apa":"Zang, Y., Fung, E.-D., Fu, T., Ray, S., Garner, M. H., Borges, A., … Venkataraman, L. (2020). Voltage-induced single-molecule junction planarization. <i>Nano Letters</i>. American Chemical Society. <a href=\"https://doi.org/10.1021/acs.nanolett.0c04260\">https://doi.org/10.1021/acs.nanolett.0c04260</a>","short":"Y. Zang, E.-D. Fung, T. Fu, S. Ray, M.H. Garner, A. Borges, M.L. Steigerwald, S. Patil, G. Solomon, L. Venkataraman, Nano Letters 21 (2020) 673–679.","chicago":"Zang, Yaping, E-Dean Fung, Tianren Fu, Suman Ray, Marc H. Garner, Anders Borges, Michael L. Steigerwald, Satish Patil, Gemma Solomon, and Latha Venkataraman. “Voltage-Induced Single-Molecule Junction Planarization.” <i>Nano Letters</i>. American Chemical Society, 2020. <a href=\"https://doi.org/10.1021/acs.nanolett.0c04260\">https://doi.org/10.1021/acs.nanolett.0c04260</a>.","ieee":"Y. Zang <i>et al.</i>, “Voltage-induced single-molecule junction planarization,” <i>Nano Letters</i>, vol. 21, no. 1. American Chemical Society, pp. 673–679, 2020.","ista":"Zang Y, Fung E-D, Fu T, Ray S, Garner MH, Borges A, Steigerwald ML, Patil S, Solomon G, Venkataraman L. 2020. Voltage-induced single-molecule junction planarization. Nano Letters. 21(1), 673–679.","mla":"Zang, Yaping, et al. “Voltage-Induced Single-Molecule Junction Planarization.” <i>Nano Letters</i>, vol. 21, no. 1, American Chemical Society, 2020, pp. 673–79, doi:<a href=\"https://doi.org/10.1021/acs.nanolett.0c04260\">10.1021/acs.nanolett.0c04260</a>.","ama":"Zang Y, Fung E-D, Fu T, et al. Voltage-induced single-molecule junction planarization. <i>Nano Letters</i>. 2020;21(1):673-679. doi:<a href=\"https://doi.org/10.1021/acs.nanolett.0c04260\">10.1021/acs.nanolett.0c04260</a>"},"type":"journal_article","intvolume":"        21","publisher":"American Chemical Society","title":"Voltage-induced single-molecule junction planarization","article_type":"letter_note","external_id":{"pmid":["33337876"]},"volume":21,"year":"2020","publication":"Nano Letters","page":"673-679","date_created":"2024-09-09T06:48:30Z","article_processing_charge":"No","publication_identifier":{"issn":["1530-6984"],"eissn":["1530-6992"]}},{"day":"18","issue":"12","date_updated":"2024-12-10T10:28:52Z","oa_version":"None","language":[{"iso":"eng"}],"month":"11","OA_type":"closed access","doi":"10.1021/acs.nanolett.0c03994","pmid":1,"user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","publication_status":"published","abstract":[{"text":"Light emission from tunnel junctions are a potential photon source for nanophotonic applications. Surprisingly, the photons emitted can have energies exceeding the energy supplied to the electrons by the bias. Three mechanisms for generating these so-called overbias photons have been proposed, but the relationship between these mechanisms has not been clarified. In this work, we argue that multielectron processes provide the best framework for understanding overbias light emission in tunnel junctions. Experimentally, we demonstrate for the first time that the superlinear dependence of emission on conductance predicted by this theory is robust to the temperature of the tunnel junction, indicating that tunnel junctions are a promising candidate for electrically driven broadband photon sources.","lang":"eng"}],"extern":"1","status":"public","date_published":"2020-11-18T00:00:00Z","publisher":"American Chemical Society","intvolume":"        20","type":"journal_article","citation":{"ama":"Fung E-D, Venkataraman L. Too cool for blackbody radiation: Overbias photon emission in ambient STM due to multielectron processes. <i>Nano Letters</i>. 2020;20(12):8912-8918. doi:<a href=\"https://doi.org/10.1021/acs.nanolett.0c03994\">10.1021/acs.nanolett.0c03994</a>","mla":"Fung, E. Dean, and Latha Venkataraman. “Too Cool for Blackbody Radiation: Overbias Photon Emission in Ambient STM Due to Multielectron Processes.” <i>Nano Letters</i>, vol. 20, no. 12, American Chemical Society, 2020, pp. 8912–18, doi:<a href=\"https://doi.org/10.1021/acs.nanolett.0c03994\">10.1021/acs.nanolett.0c03994</a>.","ista":"Fung E-D, Venkataraman L. 2020. Too cool for blackbody radiation: Overbias photon emission in ambient STM due to multielectron processes. Nano Letters. 20(12), 8912–8918.","ieee":"E.-D. Fung and L. Venkataraman, “Too cool for blackbody radiation: Overbias photon emission in ambient STM due to multielectron processes,” <i>Nano Letters</i>, vol. 20, no. 12. American Chemical Society, pp. 8912–8918, 2020.","chicago":"Fung, E-Dean, and Latha Venkataraman. “Too Cool for Blackbody Radiation: Overbias Photon Emission in Ambient STM Due to Multielectron Processes.” <i>Nano Letters</i>. American Chemical Society, 2020. <a href=\"https://doi.org/10.1021/acs.nanolett.0c03994\">https://doi.org/10.1021/acs.nanolett.0c03994</a>.","short":"E.-D. Fung, L. Venkataraman, Nano Letters 20 (2020) 8912–8918.","apa":"Fung, E.-D., &#38; Venkataraman, L. (2020). Too cool for blackbody radiation: Overbias photon emission in ambient STM due to multielectron processes. <i>Nano Letters</i>. American Chemical Society. <a href=\"https://doi.org/10.1021/acs.nanolett.0c03994\">https://doi.org/10.1021/acs.nanolett.0c03994</a>"},"quality_controlled":"1","scopus_import":"1","author":[{"last_name":"Fung","first_name":"E-Dean","full_name":"Fung, E-Dean"},{"full_name":"Venkataraman, Latha","last_name":"Venkataraman","id":"9ebb78a5-cc0d-11ee-8322-fae086a32caf","orcid":"0000-0002-6957-6089","first_name":"Latha"}],"_id":"17903","publication_identifier":{"eissn":["1530-6992"],"issn":["1530-6984"]},"date_created":"2024-09-09T07:12:19Z","article_processing_charge":"No","page":"8912-8918","year":"2020","publication":"Nano Letters","external_id":{"pmid":["33206534"]},"article_type":"letter_note","title":"Too cool for blackbody radiation: Overbias photon emission in ambient STM due to multielectron processes","volume":20},{"author":[{"full_name":"Zang, Yaping","last_name":"Zang","first_name":"Yaping"},{"last_name":"Fu","first_name":"Tianren","full_name":"Fu, Tianren"},{"full_name":"Zou, Qi","last_name":"Zou","first_name":"Qi"},{"last_name":"Ng","first_name":"Fay","full_name":"Ng, Fay"},{"full_name":"Li, Hexing","last_name":"Li","first_name":"Hexing"},{"last_name":"Steigerwald","first_name":"Michael L.","full_name":"Steigerwald, Michael L."},{"full_name":"Nuckolls, Colin","last_name":"Nuckolls","first_name":"Colin"},{"first_name":"Latha","last_name":"Venkataraman","id":"9ebb78a5-cc0d-11ee-8322-fae086a32caf","orcid":"0000-0002-6957-6089","full_name":"Venkataraman, Latha"}],"_id":"17906","citation":{"ieee":"Y. Zang <i>et al.</i>, “Cumulene wires display increasing conductance with increasing length,” <i>Nano Letters</i>, vol. 20, no. 11. American Chemical Society, pp. 8415–8419, 2020.","mla":"Zang, Yaping, et al. “Cumulene Wires Display Increasing Conductance with Increasing Length.” <i>Nano Letters</i>, vol. 20, no. 11, American Chemical Society, 2020, pp. 8415–19, doi:<a href=\"https://doi.org/10.1021/acs.nanolett.0c03794\">10.1021/acs.nanolett.0c03794</a>.","ista":"Zang Y, Fu T, Zou Q, Ng F, Li H, Steigerwald ML, Nuckolls C, Venkataraman L. 2020. Cumulene wires display increasing conductance with increasing length. Nano Letters. 20(11), 8415–8419.","ama":"Zang Y, Fu T, Zou Q, et al. Cumulene wires display increasing conductance with increasing length. <i>Nano Letters</i>. 2020;20(11):8415-8419. doi:<a href=\"https://doi.org/10.1021/acs.nanolett.0c03794\">10.1021/acs.nanolett.0c03794</a>","apa":"Zang, Y., Fu, T., Zou, Q., Ng, F., Li, H., Steigerwald, M. L., … Venkataraman, L. (2020). Cumulene wires display increasing conductance with increasing length. <i>Nano Letters</i>. American Chemical Society. <a href=\"https://doi.org/10.1021/acs.nanolett.0c03794\">https://doi.org/10.1021/acs.nanolett.0c03794</a>","short":"Y. Zang, T. Fu, Q. Zou, F. Ng, H. Li, M.L. Steigerwald, C. Nuckolls, L. Venkataraman, Nano Letters 20 (2020) 8415–8419.","chicago":"Zang, Yaping, Tianren Fu, Qi Zou, Fay Ng, Hexing Li, Michael L. Steigerwald, Colin Nuckolls, and Latha Venkataraman. “Cumulene Wires Display Increasing Conductance with Increasing Length.” <i>Nano Letters</i>. American Chemical Society, 2020. <a href=\"https://doi.org/10.1021/acs.nanolett.0c03794\">https://doi.org/10.1021/acs.nanolett.0c03794</a>."},"quality_controlled":"1","scopus_import":"1","type":"journal_article","publisher":"American Chemical Society","intvolume":"        20","year":"2020","publication":"Nano Letters","title":"Cumulene wires display increasing conductance with increasing length","article_type":"letter_note","external_id":{"pmid":["33095021"]},"volume":20,"page":"8415-8419","publication_identifier":{"issn":["1530-6984"],"eissn":["1530-6992"]},"date_created":"2024-09-09T07:16:20Z","article_processing_charge":"No","language":[{"iso":"eng"}],"issue":"11","date_updated":"2024-12-10T10:41:40Z","oa_version":"None","day":"23","status":"public","date_published":"2020-10-23T00:00:00Z","publication_status":"published","abstract":[{"text":"One-dimensional sp-hybridized carbon wires, including cumulenes and polyynes, can be regarded as finite versions of carbynes. They are likely to be good candidates for molecular-scale conducting wires as they are predicted to have a high-conductance. In this study, we first characterize the single-molecule conductance of a series of cumulenes and polyynes with a backbone ranging in length from 4 to 8 carbon atoms, including [7]cumulene, the longest cumulenic carbon wire studied to date for molecular electronics. We observe different length dependence of conductance when comparing these two forms of carbon wires. Polyynes exhibit conductance decays with increasing molecular length, while cumulenes show a conductance increase with increasing molecular length. Their distinct conducting behaviors are attributed to their different bond length alternation, which is supported by theoretical calculations. This study confirms the long-standing theoretical predictions on sp-hybridized carbon wires and demonstrates that cumulenes can form highly conducting molecular wires.","lang":"eng"}],"extern":"1","pmid":1,"doi":"10.1021/acs.nanolett.0c03794","user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","month":"10","OA_type":"closed access"},{"publisher":"American Chemical Society","intvolume":"        20","type":"journal_article","citation":{"short":"M. Camarasa-Gómez, D. Hernangómez-Pérez, M.S. Inkpen, G. Lovat, E.-D. Fung, X. Roy, L. Venkataraman, F. Evers, Nano Letters 20 (2020) 6381–6386.","apa":"Camarasa-Gómez, M., Hernangómez-Pérez, D., Inkpen, M. S., Lovat, G., Fung, E.-D., Roy, X., … Evers, F. (2020). Mechanically tunable quantum interference in ferrocene-based single-molecule junctions. <i>Nano Letters</i>. American Chemical Society. <a href=\"https://doi.org/10.1021/acs.nanolett.0c01956\">https://doi.org/10.1021/acs.nanolett.0c01956</a>","chicago":"Camarasa-Gómez, María, Daniel Hernangómez-Pérez, Michael S. Inkpen, Giacomo Lovat, E-Dean Fung, Xavier Roy, Latha Venkataraman, and Ferdinand Evers. “Mechanically Tunable Quantum Interference in Ferrocene-Based Single-Molecule Junctions.” <i>Nano Letters</i>. American Chemical Society, 2020. <a href=\"https://doi.org/10.1021/acs.nanolett.0c01956\">https://doi.org/10.1021/acs.nanolett.0c01956</a>.","ista":"Camarasa-Gómez M, Hernangómez-Pérez D, Inkpen MS, Lovat G, Fung E-D, Roy X, Venkataraman L, Evers F. 2020. Mechanically tunable quantum interference in ferrocene-based single-molecule junctions. Nano Letters. 20(9), 6381–6386.","ieee":"M. Camarasa-Gómez <i>et al.</i>, “Mechanically tunable quantum interference in ferrocene-based single-molecule junctions,” <i>Nano Letters</i>, vol. 20, no. 9. American Chemical Society, pp. 6381–6386, 2020.","mla":"Camarasa-Gómez, María, et al. “Mechanically Tunable Quantum Interference in Ferrocene-Based Single-Molecule Junctions.” <i>Nano Letters</i>, vol. 20, no. 9, American Chemical Society, 2020, pp. 6381–86, doi:<a href=\"https://doi.org/10.1021/acs.nanolett.0c01956\">10.1021/acs.nanolett.0c01956</a>.","ama":"Camarasa-Gómez M, Hernangómez-Pérez D, Inkpen MS, et al. Mechanically tunable quantum interference in ferrocene-based single-molecule junctions. <i>Nano Letters</i>. 2020;20(9):6381-6386. doi:<a href=\"https://doi.org/10.1021/acs.nanolett.0c01956\">10.1021/acs.nanolett.0c01956</a>"},"quality_controlled":"1","scopus_import":"1","_id":"17908","author":[{"full_name":"Camarasa-Gómez, María","first_name":"María","last_name":"Camarasa-Gómez"},{"full_name":"Hernangómez-Pérez, Daniel","last_name":"Hernangómez-Pérez","first_name":"Daniel"},{"last_name":"Inkpen","first_name":"Michael S.","full_name":"Inkpen, Michael S."},{"last_name":"Lovat","first_name":"Giacomo","full_name":"Lovat, Giacomo"},{"last_name":"Fung","first_name":"E-Dean","full_name":"Fung, E-Dean"},{"first_name":"Xavier","last_name":"Roy","full_name":"Roy, Xavier"},{"orcid":"0000-0002-6957-6089","id":"9ebb78a5-cc0d-11ee-8322-fae086a32caf","last_name":"Venkataraman","first_name":"Latha","full_name":"Venkataraman, Latha"},{"last_name":"Evers","first_name":"Ferdinand","full_name":"Evers, Ferdinand"}],"publication_identifier":{"issn":["1530-6984"],"eissn":["1530-6992"]},"article_processing_charge":"No","date_created":"2024-09-09T07:18:19Z","page":"6381-6386","OA_place":"repository","publication":"Nano Letters","year":"2020","volume":20,"title":"Mechanically tunable quantum interference in ferrocene-based single-molecule junctions","external_id":{"pmid":["32787164"]},"article_type":"letter_note","day":"03","date_updated":"2024-12-10T10:49:18Z","oa_version":"Preprint","issue":"9","oa":1,"language":[{"iso":"eng"}],"main_file_link":[{"url":"https://doi.org/10.26434/chemrxiv.12252059.v1","open_access":"1"}],"month":"08","OA_type":"green","user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","pmid":1,"doi":"10.1021/acs.nanolett.0c01956","extern":"1","publication_status":"published","abstract":[{"lang":"eng","text":"Ferrocenes are ubiquitous organometallic building blocks that comprise a Fe atom sandwiched between two cyclopentadienyl (Cp) rings that rotate freely at room temperature. Of widespread interest in fundamental studies and real-world applications, they have also attracted some interest as functional elements of molecular-scale devices. Here we investigate the impact of the configurational degrees of freedom of a ferrocene derivative on its single-molecule junction conductance. Measurements indicate that the conductance of the ferrocene derivative, which is suppressed by 2 orders of magnitude as compared to a fully conjugated analogue, can be modulated by altering the junction configuration. Ab initio transport calculations show that the low conductance is a consequence of destructive quantum interference effects of the Fano type that arise from the hybridization of localized metal-based d-orbitals and the delocalized ligand-based π-system. By rotation of the Cp rings, the hybridization, and thus the quantum interference, can be mechanically controlled, resulting in a conductance modulation that is seen experimentally."}],"status":"public","date_published":"2020-08-03T00:00:00Z"},{"day":"03","oa_version":"None","date_updated":"2024-12-10T12:08:53Z","issue":"5","language":[{"iso":"eng"}],"month":"04","user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","pmid":1,"doi":"10.1021/acs.nanolett.0c00198","extern":"1","publication_status":"published","abstract":[{"lang":"eng","text":"The scanning tunneling microscope-based break junction (STM-BJ) is used widely to create and characterize single metal-molecule-metal junctions. In this technique, conductance is continuously recorded as a metal point contact is broken in a solution of molecules. Conductance plateaus are seen when stable molecular junctions are formed. Typically, thousands of junctions are created and measured, yielding thousands of distinct conductance versus extension traces. However, such traces are rarely analyzed individually to recognize the types of junctions formed. Here, we present a deep learning-based method to identify molecular junctions and show that it performs better than several commonly used and recently reported techniques. We demonstrate molecular junction identification from mixed solution measurements with accuracies as high as 97%. We also apply this model to an in situ electric field-driven isomerization reaction of a [3]cumulene to follow the reaction over time. Furthermore, we demonstrate that our model can remain accurate even when a key parameter, the average junction conductance, is eliminated from the analysis, showing that our model goes beyond conventional analysis in existing methods."}],"status":"public","date_published":"2020-04-03T00:00:00Z","publisher":"American Chemical Society","intvolume":"        20","type":"journal_article","citation":{"chicago":"Fu, Tianren, Yaping Zang, Qi Zou, Colin Nuckolls, and Latha Venkataraman. “Using Deep Learning to Identify Molecular Junction Characteristics.” <i>Nano Letters</i>. American Chemical Society, 2020. <a href=\"https://doi.org/10.1021/acs.nanolett.0c00198\">https://doi.org/10.1021/acs.nanolett.0c00198</a>.","short":"T. Fu, Y. Zang, Q. Zou, C. Nuckolls, L. Venkataraman, Nano Letters 20 (2020) 3320–3325.","apa":"Fu, T., Zang, Y., Zou, Q., Nuckolls, C., &#38; Venkataraman, L. (2020). Using deep learning to identify molecular junction characteristics. <i>Nano Letters</i>. American Chemical Society. <a href=\"https://doi.org/10.1021/acs.nanolett.0c00198\">https://doi.org/10.1021/acs.nanolett.0c00198</a>","ama":"Fu T, Zang Y, Zou Q, Nuckolls C, Venkataraman L. Using deep learning to identify molecular junction characteristics. <i>Nano Letters</i>. 2020;20(5):3320-3325. doi:<a href=\"https://doi.org/10.1021/acs.nanolett.0c00198\">10.1021/acs.nanolett.0c00198</a>","mla":"Fu, Tianren, et al. “Using Deep Learning to Identify Molecular Junction Characteristics.” <i>Nano Letters</i>, vol. 20, no. 5, American Chemical Society, 2020, pp. 3320–25, doi:<a href=\"https://doi.org/10.1021/acs.nanolett.0c00198\">10.1021/acs.nanolett.0c00198</a>.","ista":"Fu T, Zang Y, Zou Q, Nuckolls C, Venkataraman L. 2020. Using deep learning to identify molecular junction characteristics. Nano Letters. 20(5), 3320–3325.","ieee":"T. Fu, Y. Zang, Q. Zou, C. Nuckolls, and L. Venkataraman, “Using deep learning to identify molecular junction characteristics,” <i>Nano Letters</i>, vol. 20, no. 5. American Chemical Society, pp. 3320–3325, 2020."},"quality_controlled":"1","scopus_import":"1","_id":"17910","author":[{"last_name":"Fu","first_name":"Tianren","full_name":"Fu, Tianren"},{"full_name":"Zang, Yaping","last_name":"Zang","first_name":"Yaping"},{"full_name":"Zou, Qi","first_name":"Qi","last_name":"Zou"},{"last_name":"Nuckolls","first_name":"Colin","full_name":"Nuckolls, Colin"},{"full_name":"Venkataraman, Latha","orcid":"0000-0002-6957-6089","id":"9ebb78a5-cc0d-11ee-8322-fae086a32caf","last_name":"Venkataraman","first_name":"Latha"}],"publication_identifier":{"eissn":["1530-6992"],"issn":["1530-6984"]},"article_processing_charge":"No","date_created":"2024-09-09T07:20:52Z","page":"3320-3325","publication":"Nano Letters","year":"2020","volume":20,"title":"Using deep learning to identify molecular junction characteristics","external_id":{"pmid":["32242671"]},"article_type":"letter_note"},{"type":"journal_article","publisher":"American Chemical Society","intvolume":"        20","_id":"17913","author":[{"full_name":"Gunasekaran, Suman","first_name":"Suman","last_name":"Gunasekaran"},{"last_name":"Greenwald","first_name":"Julia E.","full_name":"Greenwald, Julia E."},{"first_name":"Latha","id":"9ebb78a5-cc0d-11ee-8322-fae086a32caf","last_name":"Venkataraman","orcid":"0000-0002-6957-6089","full_name":"Venkataraman, Latha"}],"citation":{"ama":"Gunasekaran S, Greenwald JE, Venkataraman L. Visualizing quantum interference in molecular junctions. <i>Nano Letters</i>. 2020;20(4):2843-2848. doi:<a href=\"https://doi.org/10.1021/acs.nanolett.0c00605\">10.1021/acs.nanolett.0c00605</a>","ista":"Gunasekaran S, Greenwald JE, Venkataraman L. 2020. Visualizing quantum interference in molecular junctions. Nano Letters. 20(4), 2843–2848.","mla":"Gunasekaran, Suman, et al. “Visualizing Quantum Interference in Molecular Junctions.” <i>Nano Letters</i>, vol. 20, no. 4, American Chemical Society, 2020, pp. 2843–48, doi:<a href=\"https://doi.org/10.1021/acs.nanolett.0c00605\">10.1021/acs.nanolett.0c00605</a>.","ieee":"S. Gunasekaran, J. E. Greenwald, and L. Venkataraman, “Visualizing quantum interference in molecular junctions,” <i>Nano Letters</i>, vol. 20, no. 4. American Chemical Society, pp. 2843–2848, 2020.","chicago":"Gunasekaran, Suman, Julia E. Greenwald, and Latha Venkataraman. “Visualizing Quantum Interference in Molecular Junctions.” <i>Nano Letters</i>. American Chemical Society, 2020. <a href=\"https://doi.org/10.1021/acs.nanolett.0c00605\">https://doi.org/10.1021/acs.nanolett.0c00605</a>.","short":"S. Gunasekaran, J.E. Greenwald, L. Venkataraman, Nano Letters 20 (2020) 2843–2848.","apa":"Gunasekaran, S., Greenwald, J. E., &#38; Venkataraman, L. (2020). Visualizing quantum interference in molecular junctions. <i>Nano Letters</i>. American Chemical Society. <a href=\"https://doi.org/10.1021/acs.nanolett.0c00605\">https://doi.org/10.1021/acs.nanolett.0c00605</a>"},"quality_controlled":"1","scopus_import":"1","publication_identifier":{"issn":["1530-6984"],"eissn":["1530-6992"]},"article_processing_charge":"No","date_created":"2024-09-09T07:36:41Z","publication":"Nano Letters","year":"2020","volume":20,"external_id":{"pmid":["32142291"]},"article_type":"letter_note","title":"Visualizing quantum interference in molecular junctions","page":"2843-2848","day":"06","language":[{"iso":"eng"}],"oa_version":"None","date_updated":"2024-12-10T12:24:13Z","issue":"4","user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","doi":"10.1021/acs.nanolett.0c00605","pmid":1,"month":"03","OA_type":"closed access","status":"public","date_published":"2020-03-06T00:00:00Z","extern":"1","abstract":[{"lang":"eng","text":"Electron transport across a molecular junction is characterized by an energy-dependent transmission function. The transmission function accounts for electrons tunneling through multiple molecular orbitals (MOs) with different phases, which gives rise to quantum interference (QI) effects. Because the transmission function comprises both interfering and noninterfering effects, individual interferences between MOs cannot be deduced from the transmission function directly. Herein, we demonstrate how the transmission function can be deconstructed into its constituent interfering and noninterfering contributions for any model molecular junction. These contributions are arranged in a matrix and displayed pictorially as a QI map, which allows one to easily identify individual QI effects. Importantly, we show that exponential conductance decay with increasing oligomer length is primarily due to an increase in destructive QI. With an ability to “see” QI effects using the QI map, we find that QI is vital to all molecular-scale electron transport."}],"publication_status":"published"},{"_id":"17914","author":[{"full_name":"Hernangómez-Pérez, Daniel","first_name":"Daniel","last_name":"Hernangómez-Pérez"},{"full_name":"Gunasekaran, Suman","last_name":"Gunasekaran","first_name":"Suman"},{"orcid":"0000-0002-6957-6089","last_name":"Venkataraman","id":"9ebb78a5-cc0d-11ee-8322-fae086a32caf","first_name":"Latha","full_name":"Venkataraman, Latha"},{"first_name":"Ferdinand","last_name":"Evers","full_name":"Evers, Ferdinand"}],"citation":{"ama":"Hernangómez-Pérez D, Gunasekaran S, Venkataraman L, Evers F. Solitonics with polyacetylenes. <i>Nano Letters</i>. 2020;20(4):2615-2619. doi:<a href=\"https://doi.org/10.1021/acs.nanolett.0c00136\">10.1021/acs.nanolett.0c00136</a>","mla":"Hernangómez-Pérez, Daniel, et al. “Solitonics with Polyacetylenes.” <i>Nano Letters</i>, vol. 20, no. 4, American Chemical Society, 2020, pp. 2615–19, doi:<a href=\"https://doi.org/10.1021/acs.nanolett.0c00136\">10.1021/acs.nanolett.0c00136</a>.","ieee":"D. Hernangómez-Pérez, S. Gunasekaran, L. Venkataraman, and F. Evers, “Solitonics with polyacetylenes,” <i>Nano Letters</i>, vol. 20, no. 4. American Chemical Society, pp. 2615–2619, 2020.","ista":"Hernangómez-Pérez D, Gunasekaran S, Venkataraman L, Evers F. 2020. Solitonics with polyacetylenes. Nano Letters. 20(4), 2615–2619.","chicago":"Hernangómez-Pérez, Daniel, Suman Gunasekaran, Latha Venkataraman, and Ferdinand Evers. “Solitonics with Polyacetylenes.” <i>Nano Letters</i>. American Chemical Society, 2020. <a href=\"https://doi.org/10.1021/acs.nanolett.0c00136\">https://doi.org/10.1021/acs.nanolett.0c00136</a>.","short":"D. Hernangómez-Pérez, S. Gunasekaran, L. Venkataraman, F. Evers, Nano Letters 20 (2020) 2615–2619.","apa":"Hernangómez-Pérez, D., Gunasekaran, S., Venkataraman, L., &#38; Evers, F. (2020). Solitonics with polyacetylenes. <i>Nano Letters</i>. American Chemical Society. <a href=\"https://doi.org/10.1021/acs.nanolett.0c00136\">https://doi.org/10.1021/acs.nanolett.0c00136</a>"},"quality_controlled":"1","scopus_import":"1","type":"journal_article","publisher":"American Chemical Society","intvolume":"        20","publication":"Nano Letters","year":"2020","volume":20,"article_type":"letter_note","title":"Solitonics with polyacetylenes","external_id":{"pmid":["32125870"]},"page":"2615-2619","publication_identifier":{"issn":["1530-6984"],"eissn":["1530-6992"]},"article_processing_charge":"No","date_created":"2024-09-09T07:38:36Z","language":[{"iso":"eng"}],"oa_version":"None","date_updated":"2024-12-10T12:26:43Z","issue":"4","day":"03","status":"public","date_published":"2020-03-03T00:00:00Z","extern":"1","publication_status":"published","abstract":[{"text":"Polyacetylene molecular wires have attracted a long-standing interest for the past 40 years. From a fundamental perspective, there are two main reasons for the interest. First, polyacetylenes are a prime realization of a one-dimensional topological insulator. Second, long molecules support freely propagating topological domain-wall states, so-called “solitons,” which provide an early paradigm for spin-charge separation. Because of recent experimental developments, individual polyacetylene chains can now be synthesized on substrates. Motivated by this breakthrough, we here propose a novel way for chemically supported soliton design in these systems. We demonstrate how to control the soliton position and how to read it out via external means. Also, we show how extra soliton–antisoliton pairs arise when applying a moderate static electric field. We thus make a step toward functionality of electronic devices based on soliton manipulation, that is, “solitonics”.","lang":"eng"}],"user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","doi":"10.1021/acs.nanolett.0c00136","pmid":1,"month":"03","OA_type":"closed access"},{"day":"01","language":[{"iso":"eng"}],"oa":1,"oa_version":"Preprint","date_updated":"2023-09-05T12:05:58Z","issue":"7","arxiv":1,"user_id":"c635000d-4b10-11ee-a964-aac5a93f6ac1","pmid":1,"doi":"10.1021/acs.nanolett.0c01673","month":"07","main_file_link":[{"url":"https://arxiv.org/abs/2004.14599","open_access":"1"}],"date_published":"2020-07-01T00:00:00Z","status":"public","abstract":[{"text":"Recent discoveries have shown that, when two layers of van der Waals (vdW) materials are superimposed with a relative twist angle between them, the electronic properties of the coupled system can be dramatically altered. Here, we demonstrate that a similar concept can be extended to the optics realm, particularly to propagating phonon polaritons–hybrid light-matter interactions. To do this, we fabricate stacks composed of two twisted slabs of a vdW crystal (α-MoO3) supporting anisotropic phonon polaritons (PhPs), and image the propagation of the latter when launched by localized sources. Our images reveal that, under a critical angle, the PhPs isofrequency curve undergoes a topological transition, in which the propagation of PhPs is strongly guided (canalization regime) along predetermined directions without geometric spreading. These results demonstrate a new degree of freedom (twist angle) for controlling the propagation of polaritons at the nanoscale with potential for nanoimaging, (bio)-sensing, or heat management.","lang":"eng"}],"publication_status":"published","isi":1,"type":"journal_article","intvolume":"        20","publisher":"American Chemical Society","_id":"10866","author":[{"full_name":"Duan, Jiahua","first_name":"Jiahua","last_name":"Duan"},{"full_name":"Capote-Robayna, Nathaniel","last_name":"Capote-Robayna","first_name":"Nathaniel"},{"full_name":"Taboada-Gutiérrez, Javier","first_name":"Javier","last_name":"Taboada-Gutiérrez"},{"first_name":"Gonzalo","last_name":"Álvarez-Pérez","full_name":"Álvarez-Pérez, Gonzalo"},{"full_name":"Prieto Gonzalez, Ivan","orcid":"0000-0002-7370-5357","last_name":"Prieto Gonzalez","id":"2A307FE2-F248-11E8-B48F-1D18A9856A87","first_name":"Ivan"},{"last_name":"Martín-Sánchez","first_name":"Javier","full_name":"Martín-Sánchez, Javier"},{"last_name":"Nikitin","first_name":"Alexey Y.","full_name":"Nikitin, Alexey Y."},{"full_name":"Alonso-González, Pablo","last_name":"Alonso-González","first_name":"Pablo"}],"scopus_import":"1","quality_controlled":"1","keyword":["Mechanical Engineering","Condensed Matter Physics","General Materials Science","General Chemistry","Bioengineering"],"citation":{"ama":"Duan J, Capote-Robayna N, Taboada-Gutiérrez J, et al. Twisted nano-optics: Manipulating light at the nanoscale with twisted phonon polaritonic slabs. <i>Nano Letters</i>. 2020;20(7):5323-5329. doi:<a href=\"https://doi.org/10.1021/acs.nanolett.0c01673\">10.1021/acs.nanolett.0c01673</a>","ieee":"J. Duan <i>et al.</i>, “Twisted nano-optics: Manipulating light at the nanoscale with twisted phonon polaritonic slabs,” <i>Nano Letters</i>, vol. 20, no. 7. American Chemical Society, pp. 5323–5329, 2020.","mla":"Duan, Jiahua, et al. “Twisted Nano-Optics: Manipulating Light at the Nanoscale with Twisted Phonon Polaritonic Slabs.” <i>Nano Letters</i>, vol. 20, no. 7, American Chemical Society, 2020, pp. 5323–29, doi:<a href=\"https://doi.org/10.1021/acs.nanolett.0c01673\">10.1021/acs.nanolett.0c01673</a>.","ista":"Duan J, Capote-Robayna N, Taboada-Gutiérrez J, Álvarez-Pérez G, Prieto Gonzalez I, Martín-Sánchez J, Nikitin AY, Alonso-González P. 2020. Twisted nano-optics: Manipulating light at the nanoscale with twisted phonon polaritonic slabs. Nano Letters. 20(7), 5323–5329.","chicago":"Duan, Jiahua, Nathaniel Capote-Robayna, Javier Taboada-Gutiérrez, Gonzalo Álvarez-Pérez, Ivan Prieto Gonzalez, Javier Martín-Sánchez, Alexey Y. Nikitin, and Pablo Alonso-González. “Twisted Nano-Optics: Manipulating Light at the Nanoscale with Twisted Phonon Polaritonic Slabs.” <i>Nano Letters</i>. American Chemical Society, 2020. <a href=\"https://doi.org/10.1021/acs.nanolett.0c01673\">https://doi.org/10.1021/acs.nanolett.0c01673</a>.","apa":"Duan, J., Capote-Robayna, N., Taboada-Gutiérrez, J., Álvarez-Pérez, G., Prieto Gonzalez, I., Martín-Sánchez, J., … Alonso-González, P. (2020). Twisted nano-optics: Manipulating light at the nanoscale with twisted phonon polaritonic slabs. <i>Nano Letters</i>. American Chemical Society. <a href=\"https://doi.org/10.1021/acs.nanolett.0c01673\">https://doi.org/10.1021/acs.nanolett.0c01673</a>","short":"J. Duan, N. Capote-Robayna, J. Taboada-Gutiérrez, G. Álvarez-Pérez, I. Prieto Gonzalez, J. Martín-Sánchez, A.Y. Nikitin, P. Alonso-González, Nano Letters 20 (2020) 5323–5329."},"department":[{"_id":"NanoFab"}],"article_processing_charge":"No","date_created":"2022-03-18T11:37:38Z","acknowledgement":"J.T.-G. and G.Á.-P. acknowledge support through the Severo Ochoa Program from the\r\nGovernment of the Principality of Asturias (nos. PA-18-PF-BP17-126 and PA20-PF-BP19-053,\r\nrespectively). J. M-S acknowledges financial support through the Ramón y Cajal Program from\r\nthe Government of Spain (RYC2018-026196-I). A.Y.N. acknowledges the Spanish Ministry of\r\nScience, Innovation and Universities (national project no. MAT201788358-C3-3-R). P.A.-G.\r\nacknowledges support from the European Research Council under starting grant no. 715496,\r\n2DNANOPTICA.","publication_identifier":{"issn":["1530-6984"],"eissn":["1530-6992"]},"volume":20,"title":"Twisted nano-optics: Manipulating light at the nanoscale with twisted phonon polaritonic slabs","external_id":{"pmid":["32530634"],"isi":["000548893200082"],"arxiv":["2004.14599"]},"article_type":"original","publication":"Nano Letters","year":"2020","page":"5323-5329"}]