@article{21001, abstract = {Copper chalcogenides offer high charge mobility and low lattice thermal conductivity but suffer from structural instability due to dynamic Cu+ migration. Here, we report a colloidal hot-injection synthesis of ternary cesium copper selenide (CsCu5Se3) nanocrystals (NCs), achieving precise control over phase, size, and morphology through tailored precursor-ligand modulation. This strategy enabled systematic exploration of stable and metastable Cs–Cu–Se phases and mechanistic investigation of nucleation and growth, providing insight into phase modulation and dimensional control at the nanoscale. CsCu5Se3 NCs exhibit low lattice thermal conductivity (∼0.5 Wm–1K–1) and an experimental zT of 0.27 at 718 K. Complementary first-principles calculations, consistent with experimental electronic and optical responses, predict a zT of 1.05 at 1000 K. These findings elucidate the formation dynamics of CsCu5Se3 and establish ABZ (A = alkali, B = metal, Z = chalcogen) NCs as tunable platforms for advanced functional applications.}, author = {Patil, Niraj Nitish and Wu, Ruiqi and Fiedler, Christine and Kapuria, Nilotpal and Nan, Bingfei and Navita, Navita and Cabot, Andreu and Ibáñez, Maria and Ryan, Kevin M. and Ganose, Alex M. and Singh, Shalini}, issn = {2380-8195}, journal = {ACS Energy Letters}, number = {1}, pages = {481--488}, publisher = {American Chemical Society}, title = {{Layered alkali-copper selenides: Deciphering thermoelectric properties and reaction pathways for nanostructuring β-CsCu5Se3}}, doi = {10.1021/acsenergylett.5c02909}, volume = {11}, year = {2026}, } @article{20593, abstract = {“Quasi-solid-state” conversion mechanisms using sparingly solvating electrolytes (SPSEs) bridge the gap between traditional solid–liquid–solid and solid-state sulfur conversion in lithium–sulfur (Li–S) batteries. Although these terms are commonly used, their precise distinctions and impacts on key performance metrics, such as rate capability, energy density, and capacity fading, remain poorly understood. In this work, we employ operando small- and wide-angle X-ray scattering alongside cryogenic transmission electron microscopy (cryo-TEM) to compare Li–S batteries in sparingly solvating and solvating ether-based electrolytes. We find that, unlike solvating electrolytes, SPSEs lead to an extended presence of lithium sulfide during cycling, coexisting with sulfur at a 50% state of charge and beyond. In the charged state, solid sulfur is present in its amorphous form inside the carbon black nanopores. These findings indicate that the limited solubility confines polysulfides in regions near the carbon surface, where these polysulfides enable conversion between the coexisting solid discharge and charge product.}, author = {Dutta, Pronoy and Von Mentlen, Jean Marc and Mondal, Soumyadip and Kostoglou, Nikolaos and Wilts, Bodo D. and Freunberger, Stefan Alexander and Zickler, Gregor A. and Prehal, Christian}, issn = {2380-8195}, journal = {ACS Energy Letters}, pages = {5722--5732}, publisher = {American Chemical Society}, title = {{Bridging solution and solid-state mechanism: Confined quasi-solid-state conversion in Li–S batteries}}, doi = {10.1021/acsenergylett.5c02093}, volume = {10}, year = {2025}, } @article{12065, abstract = {Capacity, rate performance, and cycle life of aprotic Li–O2 batteries critically depend on reversible electrodeposition of Li2O2. Current understanding states surface-adsorbed versus solvated LiO2 controls Li2O2 growth as surface film or as large particles. Herein, we show that Li2O2 forms across a wide range of electrolytes, carbons, and current densities as particles via solution-mediated LiO2 disproportionation, bringing into question the prevalence of any surface growth under practical conditions. We describe a unified O2 reduction mechanism, which can explain all found capacity relations and Li2O2 morphologies with exclusive solution discharge. Determining particle morphology and achievable capacities are species mobilities, true areal rate, and the degree of LiO2 association in solution. Capacity is conclusively limited by mass transport through the tortuous Li2O2 rather than electron transport through a passivating Li2O2 film. Provided that species mobilities and surface growth are high, high capacities are also achieved with weakly solvating electrolytes, which were previously considered prototypical for low capacity via surface growth.}, author = {Prehal, Christian and Mondal, Soumyadip and Lovicar, Ludek and Freunberger, Stefan Alexander}, issn = {2380-8195}, journal = {ACS Energy Letters}, number = {9}, pages = {3112--3119}, publisher = {American Chemical Society}, title = {{Exclusive solution discharge in Li-O₂ batteries?}}, doi = {10.1021/acsenergylett.2c01711}, volume = {7}, year = {2022}, } @article{9118, abstract = {Cesium lead halides have intrinsically unstable crystal lattices and easily transform within perovskite and nonperovskite structures. In this work, we explore the conversion of the perovskite CsPbBr3 into Cs4PbBr6 in the presence of PbS at 450 °C to produce doped nanocrystal-based composites with embedded Cs4PbBr6 nanoprecipitates. We show that PbBr2 is extracted from CsPbBr3 and diffuses into the PbS lattice with a consequent increase in the concentration of free charge carriers. This new doping strategy enables the adjustment of the density of charge carriers between 1019 and 1020 cm–3, and it may serve as a general strategy for doping other nanocrystal-based semiconductors.}, author = {Calcabrini, Mariano and Genc, Aziz and Liu, Yu and Kleinhanns, Tobias and Lee, Seungho and Dirin, Dmitry N. and Akkerman, Quinten A. and Kovalenko, Maksym V. and Arbiol, Jordi and Ibáñez, Maria}, issn = {2380-8195}, journal = {ACS Energy Letters}, number = {2}, pages = {581--587}, publisher = {American Chemical Society}, title = {{Exploiting the lability of metal halide perovskites for doping semiconductor nanocomposites}}, doi = {10.1021/acsenergylett.0c02448}, volume = {6}, year = {2021}, }