---
_id: '9737'
article_processing_charge: No
author:
- first_name: Olga
full_name: Symonova, Olga
id: 3C0C7BC6-F248-11E8-B48F-1D18A9856A87
last_name: Symonova
orcid: 0000-0003-2012-9947
- first_name: Christopher
full_name: Topp, Christopher
last_name: Topp
- first_name: Herbert
full_name: Edelsbrunner, Herbert
id: 3FB178DA-F248-11E8-B48F-1D18A9856A87
last_name: Edelsbrunner
orcid: 0000-0002-9823-6833
citation:
ama: Symonova O, Topp C, Edelsbrunner H. Root traits computed by DynamicRoots for
the maize root shown in fig 2. 2015. doi:10.1371/journal.pone.0127657.s001
apa: Symonova, O., Topp, C., & Edelsbrunner, H. (2015). Root traits computed
by DynamicRoots for the maize root shown in fig 2. Public Library of Science.
https://doi.org/10.1371/journal.pone.0127657.s001
chicago: Symonova, Olga, Christopher Topp, and Herbert Edelsbrunner. “Root Traits
Computed by DynamicRoots for the Maize Root Shown in Fig 2.” Public Library of
Science, 2015. https://doi.org/10.1371/journal.pone.0127657.s001.
ieee: O. Symonova, C. Topp, and H. Edelsbrunner, “Root traits computed by DynamicRoots
for the maize root shown in fig 2.” Public Library of Science, 2015.
ista: Symonova O, Topp C, Edelsbrunner H. 2015. Root traits computed by DynamicRoots
for the maize root shown in fig 2, Public Library of Science, 10.1371/journal.pone.0127657.s001.
mla: Symonova, Olga, et al. Root Traits Computed by DynamicRoots for the Maize
Root Shown in Fig 2. Public Library of Science, 2015, doi:10.1371/journal.pone.0127657.s001.
short: O. Symonova, C. Topp, H. Edelsbrunner, (2015).
date_created: 2021-07-28T06:20:13Z
date_published: 2015-06-01T00:00:00Z
date_updated: 2025-09-23T08:30:43Z
day: '01'
department:
- _id: MaJö
- _id: HeEd
doi: 10.1371/journal.pone.0127657.s001
month: '06'
oa_version: Published Version
publisher: Public Library of Science
related_material:
record:
- id: '1793'
relation: used_in_publication
status: public
status: public
title: Root traits computed by DynamicRoots for the maize root shown in fig 2
type: research_data_reference
user_id: 6785fbc1-c503-11eb-8a32-93094b40e1cf
year: '2015'
...
---
_id: '9742'
abstract:
- lang: eng
text: 'Repeated pathogen exposure is a common threat in colonies of social insects,
posing selection pressures on colony members to respond with improved disease-defense
performance. We here tested whether experience gained by repeated tending of low-level
fungus-exposed (Metarhizium robertsii) larvae may alter the performance of sanitary
brood care in the clonal ant, Platythyrea punctata. We trained ants individually
over nine consecutive trials to either sham-treated or fungus-exposed larvae.
We then compared the larval grooming behavior of naive and trained ants and measured
how effectively they removed infectious fungal conidiospores from the fungus-exposed
larvae. We found that the ants changed the duration of larval grooming in response
to both, larval treatment and their level of experience: (1) sham-treated larvae
received longer grooming than the fungus-exposed larvae and (2) trained ants performed
less self-grooming but longer larval grooming than naive ants, which was true
for both, ants trained to fungus-exposed and also to sham-treated larvae. Ants
that groomed the fungus-exposed larvae for longer periods removed a higher number
of fungal conidiospores from the surface of the fungus-exposed larvae. As experienced
ants performed longer larval grooming, they were more effective in fungal removal,
thus making them better caretakers under pathogen attack of the colony. By studying
this clonal ant, we can thus conclude that even in the absence of genetic variation
between colony members, differences in experience levels of brood care may affect
performance of sanitary brood care in social insects.'
article_processing_charge: No
author:
- first_name: Claudia
full_name: Westhus, Claudia
last_name: Westhus
- first_name: Line V
full_name: Ugelvig, Line V
id: 3DC97C8E-F248-11E8-B48F-1D18A9856A87
last_name: Ugelvig
orcid: 0000-0003-1832-8883
- first_name: Edouard
full_name: Tourdot, Edouard
last_name: Tourdot
- first_name: Jürgen
full_name: Heinze, Jürgen
last_name: Heinze
- first_name: Claudie
full_name: Doums, Claudie
last_name: Doums
- first_name: Sylvia
full_name: Cremer, Sylvia
id: 2F64EC8C-F248-11E8-B48F-1D18A9856A87
last_name: Cremer
orcid: 0000-0002-2193-3868
citation:
ama: 'Westhus C, Ugelvig LV, Tourdot E, Heinze J, Doums C, Cremer S. Data from:
Increased grooming after repeated brood care provides sanitary benefits in a clonal
ant. 2015. doi:10.5061/dryad.7kc79'
apa: 'Westhus, C., Ugelvig, L. V., Tourdot, E., Heinze, J., Doums, C., & Cremer,
S. (2015). Data from: Increased grooming after repeated brood care provides sanitary
benefits in a clonal ant. Dryad. https://doi.org/10.5061/dryad.7kc79'
chicago: 'Westhus, Claudia, Line V Ugelvig, Edouard Tourdot, Jürgen Heinze, Claudie
Doums, and Sylvia Cremer. “Data from: Increased Grooming after Repeated Brood
Care Provides Sanitary Benefits in a Clonal Ant.” Dryad, 2015. https://doi.org/10.5061/dryad.7kc79.'
ieee: 'C. Westhus, L. V. Ugelvig, E. Tourdot, J. Heinze, C. Doums, and S. Cremer,
“Data from: Increased grooming after repeated brood care provides sanitary benefits
in a clonal ant.” Dryad, 2015.'
ista: 'Westhus C, Ugelvig LV, Tourdot E, Heinze J, Doums C, Cremer S. 2015. Data
from: Increased grooming after repeated brood care provides sanitary benefits
in a clonal ant, Dryad, 10.5061/dryad.7kc79.'
mla: 'Westhus, Claudia, et al. Data from: Increased Grooming after Repeated Brood
Care Provides Sanitary Benefits in a Clonal Ant. Dryad, 2015, doi:10.5061/dryad.7kc79.'
short: C. Westhus, L.V. Ugelvig, E. Tourdot, J. Heinze, C. Doums, S. Cremer, (2015).
date_created: 2021-07-28T08:52:53Z
date_published: 2015-07-09T00:00:00Z
date_updated: 2025-09-29T11:42:25Z
day: '09'
department:
- _id: SyCr
doi: 10.5061/dryad.7kc79
main_file_link:
- open_access: '1'
url: https://doi.org/10.5061/dryad.7kc79
month: '07'
oa: 1
oa_version: Published Version
publisher: Dryad
related_material:
record:
- id: '2161'
relation: used_in_publication
status: public
status: public
title: 'Data from: Increased grooming after repeated brood care provides sanitary
benefits in a clonal ant'
type: research_data_reference
user_id: 6785fbc1-c503-11eb-8a32-93094b40e1cf
year: '2015'
...
---
_id: '9765'
article_processing_charge: No
author:
- first_name: Guillaume
full_name: Chevereau, Guillaume
id: 424D78A0-F248-11E8-B48F-1D18A9856A87
last_name: Chevereau
- first_name: Marta
full_name: Lukacisinova, Marta
id: 4342E402-F248-11E8-B48F-1D18A9856A87
last_name: Lukacisinova
orcid: 0000-0002-2519-8004
- first_name: Tugce
full_name: Batur, Tugce
last_name: Batur
- first_name: Aysegul
full_name: Guvenek, Aysegul
last_name: Guvenek
- first_name: Dilay Hazal
full_name: Ayhan, Dilay Hazal
last_name: Ayhan
- first_name: Erdal
full_name: Toprak, Erdal
last_name: Toprak
- first_name: Mark Tobias
full_name: Bollenbach, Mark Tobias
id: 3E6DB97A-F248-11E8-B48F-1D18A9856A87
last_name: Bollenbach
orcid: 0000-0003-4398-476X
citation:
ama: Chevereau G, Lukacisinova M, Batur T, et al. Gene ontology enrichment analysis
for the most sensitive gene deletion strains for all drugs. 2015. doi:10.1371/journal.pbio.1002299.s008
apa: Chevereau, G., Lukacisinova, M., Batur, T., Guvenek, A., Ayhan, D. H., Toprak,
E., & Bollenbach, M. T. (2015). Gene ontology enrichment analysis for the
most sensitive gene deletion strains for all drugs. Public Library of Science.
https://doi.org/10.1371/journal.pbio.1002299.s008
chicago: Chevereau, Guillaume, Marta Lukacisinova, Tugce Batur, Aysegul Guvenek,
Dilay Hazal Ayhan, Erdal Toprak, and Mark Tobias Bollenbach. “Gene Ontology Enrichment
Analysis for the Most Sensitive Gene Deletion Strains for All Drugs.” Public Library
of Science, 2015. https://doi.org/10.1371/journal.pbio.1002299.s008.
ieee: G. Chevereau et al., “Gene ontology enrichment analysis for the most
sensitive gene deletion strains for all drugs.” Public Library of Science, 2015.
ista: Chevereau G, Lukacisinova M, Batur T, Guvenek A, Ayhan DH, Toprak E, Bollenbach
MT. 2015. Gene ontology enrichment analysis for the most sensitive gene deletion
strains for all drugs, Public Library of Science, 10.1371/journal.pbio.1002299.s008.
mla: Chevereau, Guillaume, et al. Gene Ontology Enrichment Analysis for the Most
Sensitive Gene Deletion Strains for All Drugs. Public Library of Science,
2015, doi:10.1371/journal.pbio.1002299.s008.
short: G. Chevereau, M. Lukacisinova, T. Batur, A. Guvenek, D.H. Ayhan, E. Toprak,
M.T. Bollenbach, (2015).
date_created: 2021-08-03T07:05:16Z
date_published: 2015-11-18T00:00:00Z
date_updated: 2025-09-23T09:58:54Z
day: '18'
department:
- _id: ToBo
doi: 10.1371/journal.pbio.1002299.s008
month: '11'
oa_version: Published Version
publisher: Public Library of Science
related_material:
record:
- id: '1619'
relation: used_in_publication
status: public
status: public
title: Gene ontology enrichment analysis for the most sensitive gene deletion strains
for all drugs
type: research_data_reference
user_id: 6785fbc1-c503-11eb-8a32-93094b40e1cf
year: '2015'
...
---
_id: '9772'
article_processing_charge: No
author:
- first_name: Barbora
full_name: Trubenova, Barbora
id: 42302D54-F248-11E8-B48F-1D18A9856A87
last_name: Trubenova
orcid: 0000-0002-6873-2967
- first_name: Sebastian
full_name: Novak, Sebastian
id: 461468AE-F248-11E8-B48F-1D18A9856A87
last_name: Novak
orcid: 0000-0002-2519-824X
- first_name: Reinmar
full_name: Hager, Reinmar
last_name: Hager
citation:
ama: Trubenova B, Novak S, Hager R. Description of the agent based simulations.
2015. doi:10.1371/journal.pone.0126907.s003
apa: Trubenova, B., Novak, S., & Hager, R. (2015). Description of the agent
based simulations. Public Library of Science. https://doi.org/10.1371/journal.pone.0126907.s003
chicago: Trubenova, Barbora, Sebastian Novak, and Reinmar Hager. “Description of
the Agent Based Simulations.” Public Library of Science, 2015. https://doi.org/10.1371/journal.pone.0126907.s003.
ieee: B. Trubenova, S. Novak, and R. Hager, “Description of the agent based simulations.”
Public Library of Science, 2015.
ista: Trubenova B, Novak S, Hager R. 2015. Description of the agent based simulations,
Public Library of Science, 10.1371/journal.pone.0126907.s003.
mla: Trubenova, Barbora, et al. Description of the Agent Based Simulations.
Public Library of Science, 2015, doi:10.1371/journal.pone.0126907.s003.
short: B. Trubenova, S. Novak, R. Hager, (2015).
date_created: 2021-08-05T12:55:20Z
date_published: 2015-05-18T00:00:00Z
date_updated: 2025-09-23T09:21:54Z
day: '18'
department:
- _id: NiBa
doi: 10.1371/journal.pone.0126907.s003
month: '05'
oa_version: Published Version
publisher: Public Library of Science
related_material:
record:
- id: '1809'
relation: used_in_publication
status: public
status: public
title: Description of the agent based simulations
type: research_data_reference
user_id: 6785fbc1-c503-11eb-8a32-93094b40e1cf
year: '2015'
...
---
_id: '9773'
article_processing_charge: No
author:
- first_name: Tamar
full_name: Friedlander, Tamar
id: 36A5845C-F248-11E8-B48F-1D18A9856A87
last_name: Friedlander
- first_name: Avraham E.
full_name: Mayo, Avraham E.
last_name: Mayo
- first_name: Tsvi
full_name: Tlusty, Tsvi
last_name: Tlusty
- first_name: Uri
full_name: Alon, Uri
last_name: Alon
citation:
ama: Friedlander T, Mayo AE, Tlusty T, Alon U. Evolutionary simulation code. 2015.
doi:10.1371/journal.pcbi.1004055.s002
apa: Friedlander, T., Mayo, A. E., Tlusty, T., & Alon, U. (2015). Evolutionary
simulation code. Public Library of Science. https://doi.org/10.1371/journal.pcbi.1004055.s002
chicago: Friedlander, Tamar, Avraham E. Mayo, Tsvi Tlusty, and Uri Alon. “Evolutionary
Simulation Code.” Public Library of Science, 2015. https://doi.org/10.1371/journal.pcbi.1004055.s002.
ieee: T. Friedlander, A. E. Mayo, T. Tlusty, and U. Alon, “Evolutionary simulation
code.” Public Library of Science, 2015.
ista: Friedlander T, Mayo AE, Tlusty T, Alon U. 2015. Evolutionary simulation code,
Public Library of Science, 10.1371/journal.pcbi.1004055.s002.
mla: Friedlander, Tamar, et al. Evolutionary Simulation Code. Public Library
of Science, 2015, doi:10.1371/journal.pcbi.1004055.s002.
short: T. Friedlander, A.E. Mayo, T. Tlusty, U. Alon, (2015).
date_created: 2021-08-05T12:58:07Z
date_published: 2015-03-23T00:00:00Z
date_updated: 2025-09-23T08:43:16Z
day: '23'
department:
- _id: GaTk
doi: 10.1371/journal.pcbi.1004055.s002
month: '03'
oa_version: Published Version
publisher: Public Library of Science
related_material:
record:
- id: '1827'
relation: used_in_publication
status: public
status: public
title: Evolutionary simulation code
type: research_data_reference
user_id: 6785fbc1-c503-11eb-8a32-93094b40e1cf
year: '2015'
...
---
_id: '981'
abstract:
- lang: eng
text: The tunability of topological surface states and controllable opening of the
Dirac gap are of fundamental and practical interest in the field of topological
materials. In the newly discovered topological crystalline insulators (TCIs),
theory predicts that the Dirac node is protected by a crystalline symmetry and
that the surface state electrons can acquire a mass if this symmetry is broken.
Recent studies have detected signatures of a spontaneously generated Dirac gap
in TCIs; however, the mechanism of mass formation remains elusive. In this work,
we present scanning tunnelling microscopy (STM) measurements of the TCI Pb 1â'x
Sn x Se for a wide range of alloy compositions spanning the topological and non-topological
regimes. The STM topographies reveal a symmetry-breaking distortion on the surface,
which imparts mass to the otherwise massless Dirac electrons-a mechanism analogous
to the long sought-after Higgs mechanism in particle physics. Interestingly, the
measured Dirac gap decreases on approaching the trivial phase, whereas the magnitude
of the distortion remains nearly constant. Our data and calculations reveal that
the penetration depth of Dirac surface states controls the magnitude of the Dirac
mass. At the limit of the critical composition, the penetration depth is predicted
to go to infinity, resulting in zero mass, consistent with our measurements. Finally,
we discover the existence of surface states in the non-topological regime, which
have the characteristics of gapped, double-branched Dirac fermions and could be
exploited in realizing superconductivity in these materials.
acknowledgement: We thank R. Buczko, C. Chamon, J. C. Seamus Davis, M. El-Batanouny,
A. Mesaros, Y. Ran and A. Soumyanarayanan for useful conversations and G. McMahon
for help with EDS measurements. V.M. gratefully acknowledges funding from the US
Department of Energy, Scanned Probe Division under Award Number DE-FG02-12ER46880
for the support of I.Z., Y.O., W.Z. and D.W. for this project. Work at Massachusetts
Institute of Technology is supported by US Department of Energy, Office of Basic
Energy Sciences, Division of Materials Sciences and Engineering under Award DE-SC0010526
(L.F.), and NSF-DMR-1104498 (M.S.). H.L. acknowledges the Singapore National Research
Foundation for support under NRF Award No. NRF-NRFF2013-03. Y.O. was partly supported
by JSPS KAKENHI Grant Numbers 26707016 and 00707656. The work at Northeastern University
is supported by the US Department of Energy grant number DE-FG02-07ER46352, and
benefited from Northeastern University’s Advanced Scientific Computation Center
(ASCC), theory support at the Advanced Light Source, Berkeley and the allocation
of supercomputer time at the NERSC through DOE grant number DE-AC02-05CH11231. Work
at Princeton University is supported by the US National Science Foundation Grant,
NSF-DMR-1006492. F.C. acknowledges the support provided by MOST-Taiwan under project
number NSC-102-2119-M-002-004.
author:
- first_name: Ilija
full_name: Zeljkovic, Ilija
last_name: Zeljkovic
- first_name: Yoshinori
full_name: Okada, Yoshinori
last_name: Okada
- first_name: Maksym
full_name: Maksym Serbyn
id: 47809E7E-F248-11E8-B48F-1D18A9856A87
last_name: Serbyn
orcid: 0000-0002-2399-5827
- first_name: Raman
full_name: Sankar, Raman
last_name: Sankar
- first_name: Daniel
full_name: Walkup, Daniel
last_name: Walkup
- first_name: Wenwen
full_name: Zhou, Wenwen
last_name: Zhou
- first_name: Junwei
full_name: Liu, Junwei
last_name: Liu
- first_name: Guoqing
full_name: Chang, Guoqing
last_name: Chang
- first_name: Yungjui
full_name: Wang, Yungjui
last_name: Wang
- first_name: Md
full_name: Hasan, Md Z
last_name: Hasan
- first_name: Fangcheng
full_name: Chou, Fangcheng
last_name: Chou
- first_name: Hsin
full_name: Lin, Hsin
last_name: Lin
- first_name: Arun
full_name: Bansil, Arun
last_name: Bansil
- first_name: Liang
full_name: Fu, Liang
last_name: Fu
- first_name: Vidya
full_name: Madhavan, Vidya
last_name: Madhavan
citation:
ama: Zeljkovic I, Okada Y, Serbyn M, et al. Dirac mass generation from crystal symmetry
breaking on the surfaces of topological crystalline insulators. Nature Materials.
2015;14(3):318-324. doi:10.1038/nmat4215
apa: Zeljkovic, I., Okada, Y., Serbyn, M., Sankar, R., Walkup, D., Zhou, W., … Madhavan,
V. (2015). Dirac mass generation from crystal symmetry breaking on the surfaces
of topological crystalline insulators. Nature Materials. Nature Publishing
Group. https://doi.org/10.1038/nmat4215
chicago: Zeljkovic, Ilija, Yoshinori Okada, Maksym Serbyn, Raman Sankar, Daniel
Walkup, Wenwen Zhou, Junwei Liu, et al. “Dirac Mass Generation from Crystal Symmetry
Breaking on the Surfaces of Topological Crystalline Insulators.” Nature Materials.
Nature Publishing Group, 2015. https://doi.org/10.1038/nmat4215.
ieee: I. Zeljkovic et al., “Dirac mass generation from crystal symmetry breaking
on the surfaces of topological crystalline insulators,” Nature Materials,
vol. 14, no. 3. Nature Publishing Group, pp. 318–324, 2015.
ista: Zeljkovic I, Okada Y, Serbyn M, Sankar R, Walkup D, Zhou W, Liu J, Chang G,
Wang Y, Hasan M, Chou F, Lin H, Bansil A, Fu L, Madhavan V. 2015. Dirac mass generation
from crystal symmetry breaking on the surfaces of topological crystalline insulators.
Nature Materials. 14(3), 318–324.
mla: Zeljkovic, Ilija, et al. “Dirac Mass Generation from Crystal Symmetry Breaking
on the Surfaces of Topological Crystalline Insulators.” Nature Materials,
vol. 14, no. 3, Nature Publishing Group, 2015, pp. 318–24, doi:10.1038/nmat4215.
short: I. Zeljkovic, Y. Okada, M. Serbyn, R. Sankar, D. Walkup, W. Zhou, J. Liu,
G. Chang, Y. Wang, M. Hasan, F. Chou, H. Lin, A. Bansil, L. Fu, V. Madhavan, Nature
Materials 14 (2015) 318–324.
date_created: 2018-12-11T11:49:31Z
date_published: 2015-03-01T00:00:00Z
date_updated: 2021-01-12T08:22:24Z
day: '01'
doi: 10.1038/nmat4215
extern: 1
intvolume: ' 14'
issue: '3'
main_file_link:
- open_access: '1'
url: https://arxiv.org/abs/1403.4906
month: '03'
oa: 1
page: 318 - 324
publication: Nature Materials
publication_status: published
publisher: Nature Publishing Group
publist_id: '6419'
quality_controlled: 0
status: public
title: Dirac mass generation from crystal symmetry breaking on the surfaces of topological
crystalline insulators
type: journal_article
volume: 14
year: '2015'
...
---
_id: '982'
abstract:
- lang: eng
text: We propose a new approach to probing ergodicity and its breakdown in one-dimensional
quantum manybody systems based on their response to a local perturbation. We study
the distribution of matrix elements of a local operator between the system's eigenstates,
finding a qualitatively different behavior in the manybody localized (MBL) and
ergodic phases. To characterize how strongly a local perturbation modifies the
eigenstates, we introduce the parameter g(L) = (In (Vnm/δ)) which represents the
disorder-averaged ratio of a typical matrix element of a local operator V to energy
level spacing δ this parameter is reminiscent of the Thouless conductance in the
single-particle localization. We show that the parameter g(L) decreases with system
size L in the MBL phase and grows in the ergodic phase. We surmise that the delocalization
transition occurs when g(L) is independent of system size, g(L)=gc ~ 1. We illustrate
our approach by studying the many-body localization transition and resolving the
many-body mobility edge in a disordered one-dimensional XXZ spin-1=2 chain using
exact diagonalization and time-evolving block-decimation methods. Our criterion
for the MBL transition gives insights into microscopic details of transition.
Its direct physical consequences, in particular, logarithmically slow transport
at the transition and extensive entanglement entropy of the eigenstates, are consistent
with recent renormalization-group predictions.
acknowledgement: We acknowledge helpful discussions with Sid Parameswaran, Andrew
Potter, Antonello Scardicchio, Romain Vasseur, and especially with Ehud Altman and
David Huse. We would like to thank Miles Stoudenmire for the assistance with ITensor
library. Research at Perimeter Institute is supported by the Government of Canada
through Industry Canada and by the Province of Ontario through the Ministry of Economic
Development & Innovation. This research was supported by Gordon and Betty Moore
Foundation EPiQS Initiative through Grant No. GBMF4307 (M. S.), Sloan Foundation,
NSERC, and Early Researcher Award of Ontario (D. A.). This work made use of the
facilities of N8 HPC Centre of Excellence, provided and funded by the N8 consortium
and EPSRC (Grant No. EP/K000225/1). The Centre is coordinated by the Universities
of Leeds and Manchester.
author:
- first_name: Maksym
full_name: Maksym Serbyn
id: 47809E7E-F248-11E8-B48F-1D18A9856A87
last_name: Serbyn
orcid: 0000-0002-2399-5827
- first_name: Zlatko
full_name: Papić, Zlatko
last_name: Papić
- first_name: Dmitry
full_name: Abanin, Dmitry A
last_name: Abanin
citation:
ama: Serbyn M, Papić Z, Abanin D. Criterion for many-body localization-delocalization
phase transition. Physical Review X. 2015;5(4). doi:10.1103/PhysRevX.5.041047
apa: Serbyn, M., Papić, Z., & Abanin, D. (2015). Criterion for many-body localization-delocalization
phase transition. Physical Review X. American Physical Society. https://doi.org/10.1103/PhysRevX.5.041047
chicago: Serbyn, Maksym, Zlatko Papić, and Dmitry Abanin. “Criterion for Many-Body
Localization-Delocalization Phase Transition.” Physical Review X. American
Physical Society, 2015. https://doi.org/10.1103/PhysRevX.5.041047.
ieee: M. Serbyn, Z. Papić, and D. Abanin, “Criterion for many-body localization-delocalization
phase transition,” Physical Review X, vol. 5, no. 4. American Physical
Society, 2015.
ista: Serbyn M, Papić Z, Abanin D. 2015. Criterion for many-body localization-delocalization
phase transition. Physical Review X. 5(4).
mla: Serbyn, Maksym, et al. “Criterion for Many-Body Localization-Delocalization
Phase Transition.” Physical Review X, vol. 5, no. 4, American Physical
Society, 2015, doi:10.1103/PhysRevX.5.041047.
short: M. Serbyn, Z. Papić, D. Abanin, Physical Review X 5 (2015).
date_created: 2018-12-11T11:49:32Z
date_published: 2015-01-01T00:00:00Z
date_updated: 2021-01-12T08:22:25Z
day: '01'
doi: 10.1103/PhysRevX.5.041047
extern: 1
intvolume: ' 5'
issue: '4'
main_file_link:
- open_access: '1'
url: https://arxiv.org/abs/1507.01635
month: '01'
oa: 1
publication: Physical Review X
publication_status: published
publisher: American Physical Society
publist_id: '6418'
quality_controlled: 0
status: public
title: Criterion for many-body localization-delocalization phase transition
type: journal_article
volume: 5
year: '2015'
...
---
_id: '6507'
abstract:
- lang: eng
text: The osteoclast-associated receptor (OSCAR) is a collagen-binding immune receptor
with important roles in dendritic cell maturation and activation of inflammatory
monocytes as well as in osteoclastogenesis. The crystal structure of the OSCAR
ectodomain is presented, both free and in complex with a consensus triple-helical
peptide (THP). The structures revealed a collagen-binding site in each immunoglobulin-like
domain (D1 and D2). The THP binds near a predicted collagen-binding groove in
D1, but a more extensive interaction with D2 is facilitated by the unusually wide
D1-D2 interdomain angle in OSCAR. Direct binding assays, combined with site-directed
mutagenesis, confirm that the primary collagen-binding site in OSCAR resides in
D2, in marked contrast to the related collagen receptors, glycoprotein VI (GPVI)
and leukocyte-associated immunoglobulin-like receptor-1 (LAIR-1). Monomeric OSCAR
D1D2 binds to the consensus THP with a KD of 28 µM measured in solution, but shows
a higher affinity (KD 1.5 μM) when binding to a solid-phase THP, most likely due
to an avidity effect. These data suggest a 2-stage model for the interaction of
OSCAR with a collagen fibril, with transient, low-affinity interactions initiated
by the membrane-distal D1, followed by firm adhesion to the primary binding site
in D2.
author:
- first_name: Long
full_name: Zhou, Long
id: 3E751364-F248-11E8-B48F-1D18A9856A87
last_name: Zhou
orcid: 0000-0002-1864-8951
- first_name: J. M.
full_name: Hinerman, J. M.
last_name: Hinerman
- first_name: M.
full_name: Blaszczyk, M.
last_name: Blaszczyk
- first_name: J. L. C.
full_name: Miller, J. L. C.
last_name: Miller
- first_name: D. G.
full_name: Conrady, D. G.
last_name: Conrady
- first_name: A. D.
full_name: Barrow, A. D.
last_name: Barrow
- first_name: D. Y.
full_name: Chirgadze, D. Y.
last_name: Chirgadze
- first_name: D.
full_name: Bihan, D.
last_name: Bihan
- first_name: R. W.
full_name: Farndale, R. W.
last_name: Farndale
- first_name: A. B.
full_name: Herr, A. B.
last_name: Herr
citation:
ama: Zhou L, Hinerman JM, Blaszczyk M, et al. Structural basis for collagen recognition
by the immune receptor OSCAR. Blood. 2015;127(5):529-537. doi:10.1182/blood-2015-08-667055
apa: Zhou, L., Hinerman, J. M., Blaszczyk, M., Miller, J. L. C., Conrady, D. G.,
Barrow, A. D., … Herr, A. B. (2015). Structural basis for collagen recognition
by the immune receptor OSCAR. Blood. American Society of Hematology. https://doi.org/10.1182/blood-2015-08-667055
chicago: Zhou, Long, J. M. Hinerman, M. Blaszczyk, J. L. C. Miller, D. G. Conrady,
A. D. Barrow, D. Y. Chirgadze, D. Bihan, R. W. Farndale, and A. B. Herr. “Structural
Basis for Collagen Recognition by the Immune Receptor OSCAR.” Blood. American
Society of Hematology, 2015. https://doi.org/10.1182/blood-2015-08-667055.
ieee: L. Zhou et al., “Structural basis for collagen recognition by the immune
receptor OSCAR,” Blood, vol. 127, no. 5. American Society of Hematology,
pp. 529–537, 2015.
ista: Zhou L, Hinerman JM, Blaszczyk M, Miller JLC, Conrady DG, Barrow AD, Chirgadze
DY, Bihan D, Farndale RW, Herr AB. 2015. Structural basis for collagen recognition
by the immune receptor OSCAR. Blood. 127(5), 529–537.
mla: Zhou, Long, et al. “Structural Basis for Collagen Recognition by the Immune
Receptor OSCAR.” Blood, vol. 127, no. 5, American Society of Hematology,
2015, pp. 529–37, doi:10.1182/blood-2015-08-667055.
short: L. Zhou, J.M. Hinerman, M. Blaszczyk, J.L.C. Miller, D.G. Conrady, A.D. Barrow,
D.Y. Chirgadze, D. Bihan, R.W. Farndale, A.B. Herr, Blood 127 (2015) 529–537.
date_created: 2019-05-31T09:38:50Z
date_published: 2015-11-02T00:00:00Z
date_updated: 2021-01-12T08:07:47Z
day: '02'
doi: 10.1182/blood-2015-08-667055
extern: '1'
external_id:
pmid:
- '26552697'
intvolume: ' 127'
issue: '5'
language:
- iso: eng
month: '11'
oa_version: None
page: 529-537
pmid: 1
publication: Blood
publication_identifier:
issn:
- 0006-4971
- 1528-0020
publication_status: published
publisher: American Society of Hematology
quality_controlled: '1'
status: public
title: Structural basis for collagen recognition by the immune receptor OSCAR
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 127
year: '2015'
...
---
_id: '6736'
abstract:
- lang: eng
text: Motivated by the significant performance gains which polar codes experience
under successive cancellation list decoding, their scaling exponent is studied
as a function of the list size. In particular, the error probability is fixed,
and the tradeoff between the block length and back-off from capacity is analyzed.
A lower bound is provided on the error probability under MAP decoding with list
size L for any binary-input memoryless output-symmetric channel and for any class
of linear codes such that their minimum distance is unbounded as the block length
grows large. Then, it is shown that under MAP decoding, although the introduction
of a list can significantly improve the involved constants, the scaling exponent
itself, i.e., the speed at which capacity is approached, stays unaffected for
any finite list size. In particular, this result applies to polar codes, since
their minimum distance tends to infinity as the block length increases. A similar
result is proved for genie-aided successive cancellation decoding when transmission
takes place over the binary erasure channel, namely, the scaling exponent remains
constant for any fixed number of helps from the genie. Note that since genie-aided
successive cancellation decoding might be strictly worse than successive cancellation
list decoding, the problem of establishing the scaling exponent of the latter
remains open.
arxiv: 1
author:
- first_name: Marco
full_name: Mondelli, Marco
id: 27EB676C-8706-11E9-9510-7717E6697425
last_name: Mondelli
orcid: 0000-0002-3242-7020
- first_name: Hamed
full_name: Hassani, Hamed
last_name: Hassani
- first_name: Rudiger
full_name: Urbanke, Rudiger
last_name: Urbanke
citation:
ama: Mondelli M, Hassani H, Urbanke R. Scaling exponent of list decoders with applications
to polar codes. IEEE Transactions on Information Theory. 2015;61(9):4838-4851.
doi:10.1109/tit.2015.2453315
apa: Mondelli, M., Hassani, H., & Urbanke, R. (2015). Scaling exponent of list
decoders with applications to polar codes. IEEE Transactions on Information
Theory. IEEE. https://doi.org/10.1109/tit.2015.2453315
chicago: Mondelli, Marco, Hamed Hassani, and Rudiger Urbanke. “Scaling Exponent
of List Decoders with Applications to Polar Codes.” IEEE Transactions on Information
Theory. IEEE, 2015. https://doi.org/10.1109/tit.2015.2453315.
ieee: M. Mondelli, H. Hassani, and R. Urbanke, “Scaling exponent of list decoders
with applications to polar codes,” IEEE Transactions on Information Theory,
vol. 61, no. 9. IEEE, pp. 4838–4851, 2015.
ista: Mondelli M, Hassani H, Urbanke R. 2015. Scaling exponent of list decoders
with applications to polar codes. IEEE Transactions on Information Theory. 61(9),
4838–4851.
mla: Mondelli, Marco, et al. “Scaling Exponent of List Decoders with Applications
to Polar Codes.” IEEE Transactions on Information Theory, vol. 61, no.
9, IEEE, 2015, pp. 4838–51, doi:10.1109/tit.2015.2453315.
short: M. Mondelli, H. Hassani, R. Urbanke, IEEE Transactions on Information Theory
61 (2015) 4838–4851.
date_created: 2019-07-31T06:50:34Z
date_published: 2015-09-01T00:00:00Z
date_updated: 2021-01-12T08:08:45Z
day: '01'
doi: 10.1109/tit.2015.2453315
extern: '1'
external_id:
arxiv:
- '1304.5220'
intvolume: ' 61'
issue: '9'
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://arxiv.org/abs/1304.5220
month: '09'
oa: 1
oa_version: Preprint
page: 4838-4851
publication: IEEE Transactions on Information Theory
publication_status: published
publisher: IEEE
quality_controlled: '1'
status: public
title: Scaling exponent of list decoders with applications to polar codes
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 61
year: '2015'
...
---
_id: '6737'
abstract:
- lang: eng
text: This paper presents polar coding schemes for the two-user discrete memoryless
broadcast channel (DM-BC) which achieve Marton's region with both common and private
messages. This is the best achievable rate region known to date, and it is tight
for all classes of two-user DM-BCs whose capacity regions are known. To accomplish
this task, we first construct polar codes for both the superposition as well as
binning strategy. By combining these two schemes, we obtain Marton's region with
private messages only. Finally, we show how to handle the case of common information.
The proposed coding schemes possess the usual advantages of polar codes, i.e.,
they have low encoding and decoding complexity and a superpolynomial decay rate
of the error probability. We follow the lead of Goela, Abbe, and Gastpar, who
recently introduced polar codes emulating the superposition and binning schemes.
To align the polar indices, for both schemes, their solution involves some degradedness
constraints that are assumed to hold between the auxiliary random variables and
channel outputs. To remove these constraints, we consider the transmission of
k blocks and employ a chaining construction that guarantees the proper alignment
of the polarized indices. The techniques described in this paper are quite general,
and they can be adopted to many other multiterminal scenarios whenever there polar
indices need to be aligned.
arxiv: 1
author:
- first_name: Marco
full_name: Mondelli, Marco
id: 27EB676C-8706-11E9-9510-7717E6697425
last_name: Mondelli
orcid: 0000-0002-3242-7020
- first_name: Hamed
full_name: Hassani, Hamed
last_name: Hassani
- first_name: Igal
full_name: Sason, Igal
last_name: Sason
- first_name: Rudiger
full_name: Urbanke, Rudiger
last_name: Urbanke
citation:
ama: Mondelli M, Hassani H, Sason I, Urbanke R. Achieving Marton’s region for broadcast
channels using polar codes. IEEE Transactions on Information Theory. 2015;61(2):783-800.
doi:10.1109/tit.2014.2368555
apa: Mondelli, M., Hassani, H., Sason, I., & Urbanke, R. (2015). Achieving Marton’s
region for broadcast channels using polar codes. IEEE Transactions on Information
Theory. IEEE. https://doi.org/10.1109/tit.2014.2368555
chicago: Mondelli, Marco, Hamed Hassani, Igal Sason, and Rudiger Urbanke. “Achieving
Marton’s Region for Broadcast Channels Using Polar Codes.” IEEE Transactions
on Information Theory. IEEE, 2015. https://doi.org/10.1109/tit.2014.2368555.
ieee: M. Mondelli, H. Hassani, I. Sason, and R. Urbanke, “Achieving Marton’s region
for broadcast channels using polar codes,” IEEE Transactions on Information
Theory, vol. 61, no. 2. IEEE, pp. 783–800, 2015.
ista: Mondelli M, Hassani H, Sason I, Urbanke R. 2015. Achieving Marton’s region
for broadcast channels using polar codes. IEEE Transactions on Information Theory.
61(2), 783–800.
mla: Mondelli, Marco, et al. “Achieving Marton’s Region for Broadcast Channels Using
Polar Codes.” IEEE Transactions on Information Theory, vol. 61, no. 2,
IEEE, 2015, pp. 783–800, doi:10.1109/tit.2014.2368555.
short: M. Mondelli, H. Hassani, I. Sason, R. Urbanke, IEEE Transactions on Information
Theory 61 (2015) 783–800.
date_created: 2019-07-31T07:03:38Z
date_published: 2015-02-01T00:00:00Z
date_updated: 2021-01-12T08:08:46Z
day: '01'
doi: 10.1109/tit.2014.2368555
extern: '1'
external_id:
arxiv:
- '1401.6060'
intvolume: ' 61'
issue: '2'
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://arxiv.org/abs/1401.6060
month: '02'
oa: 1
oa_version: Preprint
page: 783-800
publication: IEEE Transactions on Information Theory
publication_status: published
publisher: IEEE
quality_controlled: '1'
status: public
title: Achieving Marton’s region for broadcast channels using polar codes
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 61
year: '2015'
...
---
_id: '7070'
abstract:
- lang: eng
text: 'Torque magnetization measurements on YBa2Cu3Oy (YBCO) at doping y=6.67 (p=0.12),
in dc fields (B) up to 33 T and temperatures down to 4.5 K, show that weak diamagnetism
persists above the extrapolated irreversibility field Hirr(T=0)≈24 T. The differential
susceptibility dM/dB, however, is more rapidly suppressed for B≳16 T than expected
from the properties of the low field superconducting state, and saturates at a
low value for fields B≳24 T. In addition, torque measurements on a p=0.11 YBCO
crystal in pulsed field up to 65 T and temperatures down to 8 K show similar behavior,
with no additional features at higher fields. We offer two candidate scenarios
to explain these observations: (a) superconductivity survives but is heavily suppressed
at high field by competition with charge-density-wave (CDW) order; (b) static
superconductivity disappears near 24 T and is followed by a region of fluctuating
superconductivity, which causes dM/dB to saturate at high field. The diamagnetic
signal observed above 50 T for the p=0.11 crystal at 40 K and below may be caused
by changes in the normal state susceptibility rather than bulk or fluctuating
superconductivity. There will be orbital (Landau) diamagnetism from electron pockets
and possibly a reduction in spin susceptibility caused by the stronger three-dimensional
ordered CDW.'
article_number: '180509'
article_processing_charge: No
article_type: original
author:
- first_name: Jing Fei
full_name: Yu, Jing Fei
last_name: Yu
- first_name: B. J.
full_name: Ramshaw, B. J.
last_name: Ramshaw
- first_name: I.
full_name: Kokanović, I.
last_name: Kokanović
- first_name: Kimberly A
full_name: Modic, Kimberly A
id: 13C26AC0-EB69-11E9-87C6-5F3BE6697425
last_name: Modic
orcid: 0000-0001-9760-3147
- first_name: N.
full_name: Harrison, N.
last_name: Harrison
- first_name: James
full_name: Day, James
last_name: Day
- first_name: Ruixing
full_name: Liang, Ruixing
last_name: Liang
- first_name: W. N.
full_name: Hardy, W. N.
last_name: Hardy
- first_name: D. A.
full_name: Bonn, D. A.
last_name: Bonn
- first_name: A.
full_name: McCollam, A.
last_name: McCollam
- first_name: S. R.
full_name: Julian, S. R.
last_name: Julian
- first_name: J. R.
full_name: Cooper, J. R.
last_name: Cooper
citation:
ama: Yu JF, Ramshaw BJ, Kokanović I, et al. Magnetization of underdoped YBa2Cu3Oy
above the irreversibility field. Physical Review B. 2015;92(18). doi:10.1103/physrevb.92.180509
apa: Yu, J. F., Ramshaw, B. J., Kokanović, I., Modic, K. A., Harrison, N., Day,
J., … Cooper, J. R. (2015). Magnetization of underdoped YBa2Cu3Oy above the irreversibility
field. Physical Review B. APS. https://doi.org/10.1103/physrevb.92.180509
chicago: Yu, Jing Fei, B. J. Ramshaw, I. Kokanović, Kimberly A Modic, N. Harrison,
James Day, Ruixing Liang, et al. “Magnetization of Underdoped YBa2Cu3Oy above
the Irreversibility Field.” Physical Review B. APS, 2015. https://doi.org/10.1103/physrevb.92.180509.
ieee: J. F. Yu et al., “Magnetization of underdoped YBa2Cu3Oy above the irreversibility
field,” Physical Review B, vol. 92, no. 18. APS, 2015.
ista: Yu JF, Ramshaw BJ, Kokanović I, Modic KA, Harrison N, Day J, Liang R, Hardy
WN, Bonn DA, McCollam A, Julian SR, Cooper JR. 2015. Magnetization of underdoped
YBa2Cu3Oy above the irreversibility field. Physical Review B. 92(18), 180509.
mla: Yu, Jing Fei, et al. “Magnetization of Underdoped YBa2Cu3Oy above the Irreversibility
Field.” Physical Review B, vol. 92, no. 18, 180509, APS, 2015, doi:10.1103/physrevb.92.180509.
short: J.F. Yu, B.J. Ramshaw, I. Kokanović, K.A. Modic, N. Harrison, J. Day, R.
Liang, W.N. Hardy, D.A. Bonn, A. McCollam, S.R. Julian, J.R. Cooper, Physical
Review B 92 (2015).
date_created: 2019-11-19T13:22:06Z
date_published: 2015-11-23T00:00:00Z
date_updated: 2021-01-12T08:11:42Z
day: '23'
doi: 10.1103/physrevb.92.180509
extern: '1'
intvolume: ' 92'
issue: '18'
language:
- iso: eng
month: '11'
oa_version: None
publication: Physical Review B
publication_identifier:
issn:
- 1098-0121
- 1550-235X
publication_status: published
publisher: APS
quality_controlled: '1'
status: public
title: Magnetization of underdoped YBa2Cu3Oy above the irreversibility field
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 92
year: '2015'
...
---
_id: '7456'
abstract:
- lang: eng
text: The rational design of monodisperse ferroelectric nanocrystals with controlled
size and shape and their organization into hierarchical structures has been a
critical step for understanding the polar ordering in nanoscale ferroelectrics,
as well as the design of nanocrystal-based functional materials which harness
the properties of individual nanoparticles and the collective interactions between
them. We report here on the synthesis and self-assembly of aggregate-free, single-crystalline
titanium-based perovskite nanoparticles with controlled morphology and surface
composition by using a simple, easily scalable and highly versatile colloidal
route. Single-crystalline, non-aggregated BaTiO3 colloidal nanocrystals, used
as a model system, have been prepared under solvothermal conditions at temperatures
as low as 180 °C. The shape of the nanocrystals was tuned from spheroidal to cubic
upon changing the polarity of the solvent, whereas their size was varied from
16 to 30 nm for spheres and 5 to 78 nm for cubes by changing the concentration
of the precursors and the reaction time, respectively. The hydrophobic, oleic
acid-passivated nanoparticles exhibit very good solubility in non-polar solvents
and can be rendered dispersible in polar solvents by a simple process involving
the oxidative cleavage of the double bond upon treating the nanopowders with the
Lemieux–von Rudloff reagent. Lattice dynamic analysis indicated that regardless
of their size, BaTiO3 nanocrystals present local disorder within the perovskite
unit cell, associated with the existence of polar ordering. We also demonstrate
for the first time that, in addition to being used for fabricating large area,
crack-free, highly uniform films, BaTiO3 nanocubes can serve as building blocks
for the design of 2D and 3D mesoscale structures, such as superlattices and superparticles.
Interestingly, the type of superlattice structure (simple cubic or face centered
cubic) appears to be determined by the type of solvent in which the nanocrystals
were dispersed. This approach provides an excellent platform for the synthesis
of other titanium-based perovskite colloidal nanocrystals with controlled chemical
composition, surface structure and morphology and for their assembly into complex
architectures, therefore opening the door for the design of novel mesoscale functional
materials/nanocomposites with potential applications in energy conversion, data
storage and the biomedical field.
article_processing_charge: No
article_type: original
author:
- first_name: Daniela
full_name: Caruntu, Daniela
last_name: Caruntu
- first_name: Taha
full_name: Rostamzadeh, Taha
last_name: Rostamzadeh
- first_name: Tommaso
full_name: Costanzo, Tommaso
id: D93824F4-D9BA-11E9-BB12-F207E6697425
last_name: Costanzo
orcid: 0000-0001-9732-3815
- first_name: Saman
full_name: Salemizadeh Parizi, Saman
last_name: Salemizadeh Parizi
- first_name: Gabriel
full_name: Caruntu, Gabriel
last_name: Caruntu
citation:
ama: Caruntu D, Rostamzadeh T, Costanzo T, Salemizadeh Parizi S, Caruntu G. Solvothermal
synthesis and controlled self-assembly of monodisperse titanium-based perovskite
colloidal nanocrystals. Nanoscale. 2015;7(30):12955-12969. doi:10.1039/c5nr00737b
apa: Caruntu, D., Rostamzadeh, T., Costanzo, T., Salemizadeh Parizi, S., & Caruntu,
G. (2015). Solvothermal synthesis and controlled self-assembly of monodisperse
titanium-based perovskite colloidal nanocrystals. Nanoscale. RSC. https://doi.org/10.1039/c5nr00737b
chicago: Caruntu, Daniela, Taha Rostamzadeh, Tommaso Costanzo, Saman Salemizadeh
Parizi, and Gabriel Caruntu. “Solvothermal Synthesis and Controlled Self-Assembly
of Monodisperse Titanium-Based Perovskite Colloidal Nanocrystals.” Nanoscale.
RSC, 2015. https://doi.org/10.1039/c5nr00737b.
ieee: D. Caruntu, T. Rostamzadeh, T. Costanzo, S. Salemizadeh Parizi, and G. Caruntu,
“Solvothermal synthesis and controlled self-assembly of monodisperse titanium-based
perovskite colloidal nanocrystals,” Nanoscale, vol. 7, no. 30. RSC, pp.
12955–12969, 2015.
ista: Caruntu D, Rostamzadeh T, Costanzo T, Salemizadeh Parizi S, Caruntu G. 2015.
Solvothermal synthesis and controlled self-assembly of monodisperse titanium-based
perovskite colloidal nanocrystals. Nanoscale. 7(30), 12955–12969.
mla: Caruntu, Daniela, et al. “Solvothermal Synthesis and Controlled Self-Assembly
of Monodisperse Titanium-Based Perovskite Colloidal Nanocrystals.” Nanoscale,
vol. 7, no. 30, RSC, 2015, pp. 12955–69, doi:10.1039/c5nr00737b.
short: D. Caruntu, T. Rostamzadeh, T. Costanzo, S. Salemizadeh Parizi, G. Caruntu,
Nanoscale 7 (2015) 12955–12969.
date_created: 2020-02-05T14:16:37Z
date_published: 2015-08-14T00:00:00Z
date_updated: 2023-02-23T13:08:24Z
day: '14'
doi: 10.1039/c5nr00737b
extern: '1'
external_id:
pmid:
- '26168304'
intvolume: ' 7'
issue: '30'
language:
- iso: eng
month: '08'
oa_version: None
page: 12955-12969
pmid: 1
publication: Nanoscale
publication_identifier:
issn:
- 2040-3364
- 2040-3372
publication_status: published
publisher: RSC
quality_controlled: '1'
status: public
title: Solvothermal synthesis and controlled self-assembly of monodisperse titanium-based
perovskite colloidal nanocrystals
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 7
year: '2015'
...
---
_id: '7457'
abstract:
- lang: eng
text: A new organic–inorganic ferroelectric hybrid capacitor designed by uniformly
incorporating surface modified monodisperse 15 nm ferroelectric BaTiO3 nanocubes
into non-polar polymer blends of poly(methyl methacrylate) (PMMA) polymer and
acrylonitrile-butadiene-styrene (ABS) terpolymer is described. The investigation
of spatial distribution of nanofillers via a non-distractive thermal pulse method
illustrates that the surface functionalization of nanocubes plays a key role in
the uniform distribution of charge polarization within the polymer matrix. The
discharged energy density of the nanocomposite with 30 vol% BaTiO3 nanocubes is
∼44 × 10−3 J cm−3, which is almost six times higher than that of the neat polymer.
The facile processing, along with the superior mechanical and electrical properties
of the BaTiO3/PMMA–ABS nanocomposites make them suitable for implementation into
capacitive electrical energy storage devices.
article_processing_charge: No
article_type: original
author:
- first_name: Saman Salemizadeh
full_name: Parizi, Saman Salemizadeh
last_name: Parizi
- first_name: Gavin
full_name: Conley, Gavin
last_name: Conley
- first_name: Tommaso
full_name: Costanzo, Tommaso
id: D93824F4-D9BA-11E9-BB12-F207E6697425
last_name: Costanzo
orcid: 0000-0001-9732-3815
- first_name: Bob
full_name: Howell, Bob
last_name: Howell
- first_name: Axel
full_name: Mellinger, Axel
last_name: Mellinger
- first_name: Gabriel
full_name: Caruntu, Gabriel
last_name: Caruntu
citation:
ama: Parizi SS, Conley G, Costanzo T, Howell B, Mellinger A, Caruntu G. Fabrication
of barium titanate/acrylonitrile-butadiene styrene/poly(methyl methacrylate) nanocomposite
films for hybrid ferroelectric capacitors. RSC Advances. 2015;5(93):76356-76362.
doi:10.1039/c5ra11347d
apa: Parizi, S. S., Conley, G., Costanzo, T., Howell, B., Mellinger, A., & Caruntu,
G. (2015). Fabrication of barium titanate/acrylonitrile-butadiene styrene/poly(methyl
methacrylate) nanocomposite films for hybrid ferroelectric capacitors. RSC
Advances. RSC. https://doi.org/10.1039/c5ra11347d
chicago: Parizi, Saman Salemizadeh, Gavin Conley, Tommaso Costanzo, Bob Howell,
Axel Mellinger, and Gabriel Caruntu. “Fabrication of Barium Titanate/Acrylonitrile-Butadiene
Styrene/Poly(Methyl Methacrylate) Nanocomposite Films for Hybrid Ferroelectric
Capacitors.” RSC Advances. RSC, 2015. https://doi.org/10.1039/c5ra11347d.
ieee: S. S. Parizi, G. Conley, T. Costanzo, B. Howell, A. Mellinger, and G. Caruntu,
“Fabrication of barium titanate/acrylonitrile-butadiene styrene/poly(methyl methacrylate)
nanocomposite films for hybrid ferroelectric capacitors,” RSC Advances,
vol. 5, no. 93. RSC, pp. 76356–76362, 2015.
ista: Parizi SS, Conley G, Costanzo T, Howell B, Mellinger A, Caruntu G. 2015. Fabrication
of barium titanate/acrylonitrile-butadiene styrene/poly(methyl methacrylate) nanocomposite
films for hybrid ferroelectric capacitors. RSC Advances. 5(93), 76356–76362.
mla: Parizi, Saman Salemizadeh, et al. “Fabrication of Barium Titanate/Acrylonitrile-Butadiene
Styrene/Poly(Methyl Methacrylate) Nanocomposite Films for Hybrid Ferroelectric
Capacitors.” RSC Advances, vol. 5, no. 93, RSC, 2015, pp. 76356–62, doi:10.1039/c5ra11347d.
short: S.S. Parizi, G. Conley, T. Costanzo, B. Howell, A. Mellinger, G. Caruntu,
RSC Advances 5 (2015) 76356–76362.
date_created: 2020-02-05T14:17:26Z
date_published: 2015-09-01T00:00:00Z
date_updated: 2023-02-23T13:08:26Z
day: '01'
doi: 10.1039/c5ra11347d
extern: '1'
intvolume: ' 5'
issue: '93'
language:
- iso: eng
month: '09'
oa_version: Submitted Version
page: 76356-76362
publication: RSC Advances
publication_identifier:
issn:
- 2046-2069
publication_status: published
publisher: RSC
quality_controlled: '1'
status: public
title: Fabrication of barium titanate/acrylonitrile-butadiene styrene/poly(methyl
methacrylate) nanocomposite films for hybrid ferroelectric capacitors
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 5
year: '2015'
...
---
_id: '99'
abstract:
- lang: eng
text: Quasiparticle excitations can compromise the performance of superconducting
devices, causing high-frequency dissipation, decoherence in Josephson qubits,
and braiding errors in proposed Majorana-based topological quantum computers.
Quasiparticle dynamics have been studied in detail in metallic superconductors
but remain relatively unexplored in semiconductor-superconductor structures, which
are now being intensely pursued in the context of topological superconductivity.
To this end, we use a system comprising a gate-confined semiconductor nanowire
with an epitaxially grown superconductor layer, yielding an isolated, proximitized
nanowire segment. We identify bound states in the semiconductor by means of bias
spectroscopy, determine the characteristic temperatures and magnetic fields for
quasiparticle excitations, and extract a parity lifetime (poisoning time) of the
bound state in the semiconductor exceeding 10 ms.
acknowledgement: Research support by Microsoft Project Q, the Danish National Research
Foundation, the Lundbeck Foundation, the Carlsberg Foundation, and the European
Commission. A.P.H. acknowledges support from the US Department of Energy, C.M.M.
acknowledges support from the Villum Foundation.
arxiv: 1
author:
- first_name: Andrew P
full_name: Higginbotham, Andrew P
id: 4AD6785A-F248-11E8-B48F-1D18A9856A87
last_name: Higginbotham
orcid: 0000-0003-2607-2363
- first_name: S M
full_name: Albrecht, S M
last_name: Albrecht
- first_name: Gediminas
full_name: Kiršanskas, Gediminas
last_name: Kiršanskas
- first_name: W
full_name: Chang, W
last_name: Chang
- first_name: Ferdinand
full_name: Kuemmeth, Ferdinand
last_name: Kuemmeth
- first_name: Peter
full_name: Krogstrup, Peter
last_name: Krogstrup
- first_name: Thomas
full_name: Jespersen, Thomas
last_name: Jespersen
- first_name: Jesper
full_name: Nygård, Jesper
last_name: Nygård
- first_name: Karsten
full_name: Flensberg, Karsten
last_name: Flensberg
- first_name: Charles
full_name: Marcus, Charles
last_name: Marcus
citation:
ama: Higginbotham AP, Albrecht SM, Kiršanskas G, et al. Parity lifetime of bound
states in a proximitized semiconductor nanowire. Nature Physics. 2015;11(12):1017-1021.
doi:10.1038/nphys3461
apa: Higginbotham, A. P., Albrecht, S. M., Kiršanskas, G., Chang, W., Kuemmeth,
F., Krogstrup, P., … Marcus, C. (2015). Parity lifetime of bound states in a proximitized
semiconductor nanowire. Nature Physics. Nature Publishing Group. https://doi.org/10.1038/nphys3461
chicago: Higginbotham, Andrew P, S M Albrecht, Gediminas Kiršanskas, W Chang, Ferdinand
Kuemmeth, Peter Krogstrup, Thomas Jespersen, Jesper Nygård, Karsten Flensberg,
and Charles Marcus. “Parity Lifetime of Bound States in a Proximitized Semiconductor
Nanowire.” Nature Physics. Nature Publishing Group, 2015. https://doi.org/10.1038/nphys3461.
ieee: A. P. Higginbotham et al., “Parity lifetime of bound states in a proximitized
semiconductor nanowire,” Nature Physics, vol. 11, no. 12. Nature Publishing
Group, pp. 1017–1021, 2015.
ista: Higginbotham AP, Albrecht SM, Kiršanskas G, Chang W, Kuemmeth F, Krogstrup
P, Jespersen T, Nygård J, Flensberg K, Marcus C. 2015. Parity lifetime of bound
states in a proximitized semiconductor nanowire. Nature Physics. 11(12), 1017–1021.
mla: Higginbotham, Andrew P., et al. “Parity Lifetime of Bound States in a Proximitized
Semiconductor Nanowire.” Nature Physics, vol. 11, no. 12, Nature Publishing
Group, 2015, pp. 1017–21, doi:10.1038/nphys3461.
short: A.P. Higginbotham, S.M. Albrecht, G. Kiršanskas, W. Chang, F. Kuemmeth, P.
Krogstrup, T. Jespersen, J. Nygård, K. Flensberg, C. Marcus, Nature Physics 11
(2015) 1017–1021.
date_created: 2018-12-11T11:44:37Z
date_published: 2015-09-14T00:00:00Z
date_updated: 2021-01-12T08:22:28Z
day: '14'
doi: 10.1038/nphys3461
extern: '1'
external_id:
arxiv:
- '1501.05155'
intvolume: ' 11'
issue: '12'
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://arxiv.org/abs/1501.05155
month: '09'
oa: 1
oa_version: Preprint
page: 1017 - 1021
publication: Nature Physics
publication_status: published
publisher: Nature Publishing Group
publist_id: '7955'
quality_controlled: '1'
status: public
title: Parity lifetime of bound states in a proximitized semiconductor nanowire
type: journal_article
user_id: 3E5EF7F0-F248-11E8-B48F-1D18A9856A87
volume: 11
year: '2015'
...
---
_id: '333'
abstract:
- lang: eng
text: 'We present a hybrid intercalation battery based on a sodium/magnesium (Na/Mg)
dual salt electrolyte, metallic magnesium anode, and a cathode based on FeS2 nanocrystals
(NCs). Compared to lithium or sodium, metallic magnesium anode is safer due to
dendrite-free electroplating and offers extremely high volumetric (3833 mAh cm-3)
and gravimetric capacities (2205 mAh g-1). Na-ion cathodes, FeS2 NCs in the present
study, may serve as attractive alternatives to Mg-ion cathodes due to the higher
voltage of operation and fast, highly reversible insertion of Na-ions. In this
proof-of-concept study, electrochemical cycling of the Na/Mg hybrid battery was
characterized by high rate capability, high Coulombic efficiency of 99.8%, and
high energy density. In particular, with an average discharge voltage of ∼1.1
V and a cathodic capacity of 189 mAh g-1 at a current of 200 mA g-1, the presented
Mg/FeS2 hybrid battery delivers energy densities of up to 210 Wh kg-1, comparable
to commercial Li-ion batteries and approximately twice as high as state-of-the-art
Mg-ion batteries based on Mo6S8 cathodes. Further significant gains in the energy
density are expected from the development of Na/Mg electrolytes with a broader
electrochemical stability window. Fully based on Earth-abundant elements, hybrid
Na-Mg batteries are highly promising for large-scale stationary energy storage. '
article_processing_charge: No
article_type: original
author:
- first_name: Marc
full_name: Walter, Marc
last_name: Walter
- first_name: Kostiantyn
full_name: Kravchyk, Kostiantyn
last_name: Kravchyk
- first_name: Maria
full_name: Ibáñez, Maria
id: 43C61214-F248-11E8-B48F-1D18A9856A87
last_name: Ibáñez
orcid: 0000-0001-5013-2843
- first_name: Maksym
full_name: Kovalenko, Maksym
last_name: Kovalenko
citation:
ama: Walter M, Kravchyk K, Ibáñez M, Kovalenko M. Efficient and inexpensive sodium
magnesium hybrid battery. Chemistry of Materials. 2015;27(21):7452-7458.
doi:10.1021/acs.chemmater.5b03531
apa: Walter, M., Kravchyk, K., Ibáñez, M., & Kovalenko, M. (2015). Efficient
and inexpensive sodium magnesium hybrid battery. Chemistry of Materials.
ACS. https://doi.org/10.1021/acs.chemmater.5b03531
chicago: Walter, Marc, Kostiantyn Kravchyk, Maria Ibáñez, and Maksym Kovalenko.
“Efficient and Inexpensive Sodium Magnesium Hybrid Battery.” Chemistry of Materials.
ACS, 2015. https://doi.org/10.1021/acs.chemmater.5b03531.
ieee: M. Walter, K. Kravchyk, M. Ibáñez, and M. Kovalenko, “Efficient and inexpensive
sodium magnesium hybrid battery,” Chemistry of Materials, vol. 27, no.
21. ACS, pp. 7452–7458, 2015.
ista: Walter M, Kravchyk K, Ibáñez M, Kovalenko M. 2015. Efficient and inexpensive
sodium magnesium hybrid battery. Chemistry of Materials. 27(21), 7452–7458.
mla: Walter, Marc, et al. “Efficient and Inexpensive Sodium Magnesium Hybrid Battery.”
Chemistry of Materials, vol. 27, no. 21, ACS, 2015, pp. 7452–58, doi:10.1021/acs.chemmater.5b03531.
short: M. Walter, K. Kravchyk, M. Ibáñez, M. Kovalenko, Chemistry of Materials 27
(2015) 7452–7458.
date_created: 2018-12-11T11:45:52Z
date_published: 2015-10-16T00:00:00Z
date_updated: 2021-01-12T07:42:42Z
day: '16'
doi: 10.1021/acs.chemmater.5b03531
extern: '1'
intvolume: ' 27'
issue: '21'
language:
- iso: eng
month: '10'
oa_version: None
page: 7452 - 7458
publication: Chemistry of Materials
publication_status: published
publisher: ACS
publist_id: '7507'
quality_controlled: '1'
status: public
title: Efficient and inexpensive sodium magnesium hybrid battery
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 27
year: '2015'
...
---
_id: '334'
abstract:
- lang: eng
text: A cation exchange-based route was used to produce Cu2ZnSnS4 (CZTS)-Ag2S nanoparticles
with controlled composition. We report a detailed study of the formation of such
CZTS-Ag2S nanoheterostructures and of their photocatalytic properties. When compared
to pure CZTS, the use of nanoscale p-n heterostructures as light absorbers for
photocatalytic water splitting provides superior photocurrents. We associate this
experimental fact to a higher separation efficiency of the photogenerated electron-hole
pairs. We believe this and other type-II nanoheterostructures will open the door
to the use of CZTS, with excellent light absorption properties and made of abundant
and environmental friendly elements, to the field of photocatalysis.
acknowledgement: This work was supported by the European Regional Development Funds,
the Framework 7 program under project SCALENANO (FP7-NMP-ENERGY-2011-284486), the
Spanish MINECO under Contract ENE2013-46624-C4-3-R and Fundamental Research Funds
for the Central Universities (2652015086). Authors acknowledge the funding from
Generalitat de Catalunya 2014 SGR 1638.
article_processing_charge: No
article_type: original
author:
- first_name: Xuelian
full_name: Yu, Xuelian
last_name: Yu
- first_name: Jingjing
full_name: Liu, Jingjing
last_name: Liu
- first_name: Aziz
full_name: Genç, Aziz
last_name: Genç
- first_name: Maria
full_name: Ibáñez, Maria
id: 43C61214-F248-11E8-B48F-1D18A9856A87
last_name: Ibáñez
orcid: 0000-0001-5013-2843
- first_name: Zhishan
full_name: Luo, Zhishan
last_name: Luo
- first_name: Alexey
full_name: Shavel, Alexey
last_name: Shavel
- first_name: Jordi
full_name: Arbiol, Jordi
last_name: Arbiol
- first_name: Guangjin
full_name: Zhang, Guangjin
last_name: Zhang
- first_name: Yihe
full_name: Zhang, Yihe
last_name: Zhang
- first_name: Andreu
full_name: Cabot, Andreu
last_name: Cabot
citation:
ama: Yu X, Liu J, Genç A, et al. Cu2ZnSnS4–Ag2S Nanoscale p–n heterostructures as
sensitizers for photoelectrochemical water splitting. Langmuir. 2015;31(38):10555-10561.
doi:10.1021/acs.langmuir.5b02490
apa: Yu, X., Liu, J., Genç, A., Ibáñez, M., Luo, Z., Shavel, A., … Cabot, A. (2015).
Cu2ZnSnS4–Ag2S Nanoscale p–n heterostructures as sensitizers for photoelectrochemical
water splitting. Langmuir. American Chemical Society. https://doi.org/10.1021/acs.langmuir.5b02490
chicago: Yu, Xuelian, Jingjing Liu, Aziz Genç, Maria Ibáñez, Zhishan Luo, Alexey
Shavel, Jordi Arbiol, Guangjin Zhang, Yihe Zhang, and Andreu Cabot. “Cu2ZnSnS4–Ag2S
Nanoscale p–n Heterostructures as Sensitizers for Photoelectrochemical Water Splitting.”
Langmuir. American Chemical Society, 2015. https://doi.org/10.1021/acs.langmuir.5b02490.
ieee: X. Yu et al., “Cu2ZnSnS4–Ag2S Nanoscale p–n heterostructures as sensitizers
for photoelectrochemical water splitting,” Langmuir, vol. 31, no. 38. American
Chemical Society, pp. 10555–10561, 2015.
ista: Yu X, Liu J, Genç A, Ibáñez M, Luo Z, Shavel A, Arbiol J, Zhang G, Zhang Y,
Cabot A. 2015. Cu2ZnSnS4–Ag2S Nanoscale p–n heterostructures as sensitizers for
photoelectrochemical water splitting. Langmuir. 31(38), 10555–10561.
mla: Yu, Xuelian, et al. “Cu2ZnSnS4–Ag2S Nanoscale p–n Heterostructures as Sensitizers
for Photoelectrochemical Water Splitting.” Langmuir, vol. 31, no. 38, American
Chemical Society, 2015, pp. 10555–61, doi:10.1021/acs.langmuir.5b02490.
short: X. Yu, J. Liu, A. Genç, M. Ibáñez, Z. Luo, A. Shavel, J. Arbiol, G. Zhang,
Y. Zhang, A. Cabot, Langmuir 31 (2015) 10555–10561.
date_created: 2018-12-11T11:45:52Z
date_published: 2015-09-07T00:00:00Z
date_updated: 2021-01-12T07:42:46Z
day: '07'
doi: 10.1021/acs.langmuir.5b02490
extern: '1'
intvolume: ' 31'
issue: '38'
language:
- iso: eng
month: '09'
oa_version: None
page: 10555 - 10561
publication: Langmuir
publication_status: published
publisher: American Chemical Society
publist_id: '7508'
quality_controlled: '1'
status: public
title: Cu2ZnSnS4–Ag2S Nanoscale p–n heterostructures as sensitizers for photoelectrochemical
water splitting
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 31
year: '2015'
...
---
_id: '354'
abstract:
- lang: eng
text: 'A simple and effective method to introduce precise amounts of doping in nanomaterials
produced from the bottom-up assembly of colloidal nanoparticles (NPs) is described.
The procedure takes advantage of a ligand displacement step to incorporate controlled
concentrations of halide ions while removing carboxylic acids from the NP surface.
Upon consolidation of the NPs into dense pellets, halide ions diffuse within the
crystal structure, doping the anion sublattice and achieving n-type electrical
doping. Through the characterization of the thermoelectric properties of nanocrystalline
PbS, we demonstrate this strategy to be effective to control charge transport
properties on thermoelectric nanomaterials assembled from NP building blocks.
This approach is subsequently extended to PbTexSe1-x@PbS core-shell NPs, where
a significant enhancement of the thermoelectric figure of merit is achieved. '
acknowledgement: At IREC, work was supported by European Regional Development Funds
and the Framework 7 program under project UNION (FP7-NMP 310250). M.I. and S.O.
thank AGAUR for their Beatriu i Pinós postdoctoral grant and the PhD grant, respectively.
At Northwestern, work was supported by the Revolutionary Materials for Solid State
Energy Conversion, an Energy Frontier Research Center funded by the U.S. Department
of Energy, Office of Science, and Office of Basic Energy Sciences under Award Number
DE-SC0001054.
article_processing_charge: No
article_type: original
author:
- first_name: Maria
full_name: Ibáñez, Maria
id: 43C61214-F248-11E8-B48F-1D18A9856A87
last_name: Ibáñez
orcid: 0000-0001-5013-2843
- first_name: Rachel
full_name: Korkosz, Rachel
last_name: Korkosz
- first_name: Zhishan
full_name: Luo, Zhishan
last_name: Luo
- first_name: Pau
full_name: Riba, Pau
last_name: Riba
- first_name: Doris
full_name: Cadavid, Doris
last_name: Cadavid
- first_name: Silvia
full_name: Ortega, Silvia
last_name: Ortega
- first_name: Andreu
full_name: Cabot, Andreu
last_name: Cabot
- first_name: Mercouri
full_name: Kanatzidis, Mercouri
last_name: Kanatzidis
citation:
ama: Ibáñez M, Korkosz R, Luo Z, et al. Electron doping in bottom up engineered
thermoelectric nanomaterials through HCl mediated ligand displacement. Journal
of the American Chemical Society. 2015;137(12):4046-4049. doi:10.1021/jacs.5b00091
apa: Ibáñez, M., Korkosz, R., Luo, Z., Riba, P., Cadavid, D., Ortega, S., … Kanatzidis,
M. (2015). Electron doping in bottom up engineered thermoelectric nanomaterials
through HCl mediated ligand displacement. Journal of the American Chemical
Society. American Chemical Society. https://doi.org/10.1021/jacs.5b00091
chicago: Ibáñez, Maria, Rachel Korkosz, Zhishan Luo, Pau Riba, Doris Cadavid, Silvia
Ortega, Andreu Cabot, and Mercouri Kanatzidis. “Electron Doping in Bottom up Engineered
Thermoelectric Nanomaterials through HCl Mediated Ligand Displacement.” Journal
of the American Chemical Society. American Chemical Society, 2015. https://doi.org/10.1021/jacs.5b00091.
ieee: M. Ibáñez et al., “Electron doping in bottom up engineered thermoelectric
nanomaterials through HCl mediated ligand displacement,” Journal of the American
Chemical Society, vol. 137, no. 12. American Chemical Society, pp. 4046–4049,
2015.
ista: Ibáñez M, Korkosz R, Luo Z, Riba P, Cadavid D, Ortega S, Cabot A, Kanatzidis
M. 2015. Electron doping in bottom up engineered thermoelectric nanomaterials
through HCl mediated ligand displacement. Journal of the American Chemical Society.
137(12), 4046–4049.
mla: Ibáñez, Maria, et al. “Electron Doping in Bottom up Engineered Thermoelectric
Nanomaterials through HCl Mediated Ligand Displacement.” Journal of the American
Chemical Society, vol. 137, no. 12, American Chemical Society, 2015, pp. 4046–49,
doi:10.1021/jacs.5b00091.
short: M. Ibáñez, R. Korkosz, Z. Luo, P. Riba, D. Cadavid, S. Ortega, A. Cabot,
M. Kanatzidis, Journal of the American Chemical Society 137 (2015) 4046–4049.
date_created: 2018-12-11T11:45:59Z
date_published: 2015-03-11T00:00:00Z
date_updated: 2021-01-12T07:44:10Z
day: '11'
doi: 10.1021/jacs.5b00091
extern: '1'
intvolume: ' 137'
issue: '12'
language:
- iso: eng
month: '03'
oa_version: None
page: 4046 - 4049
publication: Journal of the American Chemical Society
publication_status: published
publisher: American Chemical Society
publist_id: '7470'
quality_controlled: '1'
status: public
title: Electron doping in bottom up engineered thermoelectric nanomaterials through
HCl mediated ligand displacement
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 137
year: '2015'
...
---
_id: '361'
abstract:
- lang: eng
text: We report the synthesis and photocatalytic and magnetic characterization of
colloidal nanoheterostructures formed by combining a Pt-based magnetic metal alloy
(PtCo, PtNi) with Cu2ZnSnS4 (CZTS). While CZTS is one of the main candidate materials
for solar energy conversion, the introduction of a Pt-based alloy on its surface
strongly influences its chemical and electronic properties, ultimately determining
its functionality. In this regard, up to a 15-fold increase of the photocatalytic
hydrogen evolution activity was obtained with CZTS–PtCo when compared with CZTS.
Furthermore, two times higher hydrogen evolution rates were obtained for CZTS–PtCo
when compared with CZTS–Pt, in spite of the lower precious metal loading of the
former. Besides, the magnetic properties of the PtCo nanoparticles attached to
the CZTS nanocrystals were retained in the heterostructures, which could facilitate
catalyst purification and recovery for its posterior recycling and/or reutilization.
acknowledgement: This work was supported by the National Natural Science Foundation
of China (Grant 21401212), Fundamental Research Funds for the Central Universities
(2652015086), the Framework 7 program under project SCALENANO (FP7-NMP-ENERGY-2011-284486),
and the MICINN project ENE2013-46624-C4-3-R. Authors acknowledge the funding from
Generalitat de Catalunya 2014 SGR 1638.
article_processing_charge: No
author:
- first_name: Xuelian
full_name: Yu, Xuelian
last_name: Yu
- first_name: Xiaoqiang
full_name: An, Xiaoqiang
last_name: An
- first_name: Aziz
full_name: Genç, Aziz
last_name: Genç
- first_name: Maria
full_name: Ibáñez, Maria
id: 43C61214-F248-11E8-B48F-1D18A9856A87
last_name: Ibáñez
orcid: 0000-0001-5013-2843
- first_name: Jordi
full_name: Arbiol, Jordi
last_name: Arbiol
- first_name: Yihe
full_name: Zhang, Yihe
last_name: Zhang
- first_name: Andreu
full_name: Cabot, Andreu
last_name: Cabot
citation:
ama: Yu X, An X, Genç A, et al. Cu2ZnSnS4–PtM (M = Co, Ni) nanoheterostructures
for photocatalytic hydrogen evolution. Journal of Physical Chemistry C.
2015;119(38):21882-21888. doi:10.1021/acs.jpcc.5b06199
apa: Yu, X., An, X., Genç, A., Ibáñez, M., Arbiol, J., Zhang, Y., & Cabot, A.
(2015). Cu2ZnSnS4–PtM (M = Co, Ni) nanoheterostructures for photocatalytic hydrogen
evolution. Journal of Physical Chemistry C. American Chemical Society.
https://doi.org/10.1021/acs.jpcc.5b06199
chicago: Yu, Xuelian, Xiaoqiang An, Aziz Genç, Maria Ibáñez, Jordi Arbiol, Yihe
Zhang, and Andreu Cabot. “Cu2ZnSnS4–PtM (M = Co, Ni) Nanoheterostructures for
Photocatalytic Hydrogen Evolution.” Journal of Physical Chemistry C. American
Chemical Society, 2015. https://doi.org/10.1021/acs.jpcc.5b06199.
ieee: X. Yu et al., “Cu2ZnSnS4–PtM (M = Co, Ni) nanoheterostructures for
photocatalytic hydrogen evolution,” Journal of Physical Chemistry C, vol.
119, no. 38. American Chemical Society, pp. 21882–21888, 2015.
ista: Yu X, An X, Genç A, Ibáñez M, Arbiol J, Zhang Y, Cabot A. 2015. Cu2ZnSnS4–PtM
(M = Co, Ni) nanoheterostructures for photocatalytic hydrogen evolution. Journal
of Physical Chemistry C. 119(38), 21882–21888.
mla: Yu, Xuelian, et al. “Cu2ZnSnS4–PtM (M = Co, Ni) Nanoheterostructures for Photocatalytic
Hydrogen Evolution.” Journal of Physical Chemistry C, vol. 119, no. 38,
American Chemical Society, 2015, pp. 21882–88, doi:10.1021/acs.jpcc.5b06199.
short: X. Yu, X. An, A. Genç, M. Ibáñez, J. Arbiol, Y. Zhang, A. Cabot, Journal
of Physical Chemistry C 119 (2015) 21882–21888.
date_created: 2018-12-11T11:46:01Z
date_published: 2015-08-26T00:00:00Z
date_updated: 2021-01-12T07:44:38Z
day: '26'
doi: 10.1021/acs.jpcc.5b06199
extern: '1'
intvolume: ' 119'
issue: '38'
language:
- iso: eng
month: '08'
oa_version: None
page: 21882 - 21888
publication: Journal of Physical Chemistry C
publication_status: published
publisher: American Chemical Society
publist_id: '7468'
status: public
title: Cu2ZnSnS4–PtM (M = Co, Ni) nanoheterostructures for photocatalytic hydrogen
evolution
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 119
year: '2015'
...
---
OA_type: closed access
_id: '362'
abstract:
- lang: eng
text: 'Monodisperse Pd2Sn nanorods with tuned size and aspect ratio were prepared
by co-reduction of metal salts in the presence of trioctylphosphine, amine, and
chloride ions. Asymmetric Pd2Sn nanostructures were achieved by the selective
desorption of a surfactant mediated by chlorine ions. A preliminary evaluation
of the geometry influence on catalytic properties evidenced Pd2Sn nanorods to
have improved catalytic performance. In view of these results, Pd2Sn nanorods
were also evaluated for water denitration. '
article_processing_charge: No
article_type: original
author:
- first_name: Zhishan
full_name: Lu, Zhishan
last_name: Lu
- first_name: Maria
full_name: Ibáñez, Maria
id: 43C61214-F248-11E8-B48F-1D18A9856A87
last_name: Ibáñez
orcid: 0000-0001-5013-2843
- first_name: Ana
full_name: Antolín, Ana
last_name: Antolín
- first_name: Aziz
full_name: Genç, Aziz
last_name: Genç
- first_name: Alexey
full_name: Shavel, Alexey
last_name: Shavel
- first_name: Sandra
full_name: Contreras, Sandra
last_name: Contreras
- first_name: Francesc
full_name: Medina, Francesc
last_name: Medina
- first_name: Jordi
full_name: Arbiol, Jordi
last_name: Arbiol
- first_name: Andreu
full_name: Cabot, Andreu
last_name: Cabot
citation:
ama: Lu Z, Ibáñez M, Antolín A, et al. Size and aspect ratio control of Pd inf 2
inf Sn nanorods and their water denitration properties. Langmuir. 2015;31(13):3952-3957.
doi:10.1021/la504906q
apa: Lu, Z., Ibáñez, M., Antolín, A., Genç, A., Shavel, A., Contreras, S., … Cabot,
A. (2015). Size and aspect ratio control of Pd inf 2 inf Sn nanorods and their
water denitration properties. Langmuir. American Chemical Society. https://doi.org/10.1021/la504906q
chicago: Lu, Zhishan, Maria Ibáñez, Ana Antolín, Aziz Genç, Alexey Shavel, Sandra
Contreras, Francesc Medina, Jordi Arbiol, and Andreu Cabot. “Size and Aspect Ratio
Control of Pd Inf 2 Inf Sn Nanorods and Their Water Denitration Properties.” Langmuir.
American Chemical Society, 2015. https://doi.org/10.1021/la504906q.
ieee: Z. Lu et al., “Size and aspect ratio control of Pd inf 2 inf Sn nanorods
and their water denitration properties,” Langmuir, vol. 31, no. 13. American
Chemical Society, pp. 3952–3957, 2015.
ista: Lu Z, Ibáñez M, Antolín A, Genç A, Shavel A, Contreras S, Medina F, Arbiol
J, Cabot A. 2015. Size and aspect ratio control of Pd inf 2 inf Sn nanorods and
their water denitration properties. Langmuir. 31(13), 3952–3957.
mla: Lu, Zhishan, et al. “Size and Aspect Ratio Control of Pd Inf 2 Inf Sn Nanorods
and Their Water Denitration Properties.” Langmuir, vol. 31, no. 13, American
Chemical Society, 2015, pp. 3952–57, doi:10.1021/la504906q.
short: Z. Lu, M. Ibáñez, A. Antolín, A. Genç, A. Shavel, S. Contreras, F. Medina,
J. Arbiol, A. Cabot, Langmuir 31 (2015) 3952–3957.
date_created: 2018-12-11T11:46:02Z
date_published: 2015-04-07T00:00:00Z
date_updated: 2026-05-19T08:52:57Z
day: '07'
doi: 10.1021/la504906q
extern: '1'
external_id:
pmid:
- '25751745'
intvolume: ' 31'
issue: '13'
language:
- iso: eng
month: '04'
oa_version: None
page: 3952 - 3957
pmid: 1
publication: Langmuir
publication_identifier:
eissn:
- 1520-5827
issn:
- 0743-7463
publication_status: published
publisher: American Chemical Society
publist_id: '7469'
quality_controlled: '1'
scopus_import: '1'
status: public
title: Size and aspect ratio control of Pd inf 2 inf Sn nanorods and their water denitration
properties
type: journal_article
user_id: ba8df636-2132-11f1-aed0-ed93e2281fdd
volume: 31
year: '2015'
...
---
_id: '388'
abstract:
- lang: eng
text: We use ultrafast optical spectroscopy to observe binding of charged single-particle
excitations (SE) in the magnetically frustrated Mott insulator Na2IrO3. Above
the antiferromagnetic ordering temperature (TN) the system response is due to
both Hubbard excitons (HE) and their constituent unpaired SE. The SE response
becomes strongly suppressed immediately below TN. We argue that this increase
in binding energy is due to a unique interplay between the frustrated Kitaev and
the weak Heisenberg-type ordering term in the Hamiltonian, mediating an effective
interaction between the spin-singlet SE. This interaction grows with distance
causing the SE to become trapped in the HE, similar to quark confinement inside
hadrons. This binding of charged particles, induced by magnetic ordering, is a
result of a confinement-deconfinement transition of spin excitations. This observation
provides evidence for spin liquid type behavior which is expected in Na2IrO3.
article_processing_charge: No
article_type: original
author:
- first_name: Zhanybek
full_name: Alpichshev, Zhanybek
id: 45E67A2A-F248-11E8-B48F-1D18A9856A87
last_name: Alpichshev
orcid: 0000-0002-7183-5203
- first_name: Fahad
full_name: Mahmood, Fahad
last_name: Mahmood
- first_name: Gang
full_name: Cao, Gang
last_name: Cao
- first_name: Nuh
full_name: Gedik, Nuh
last_name: Gedik
citation:
ama: Alpichshev Z, Mahmood F, Cao G, Gedik N. Confinement deconfinement transition
as an indication of spin liquid type behavior in Na2IrO3. Physical Review Letters.
2015;114(1). doi:10.1103/PhysRevLett.114.017203
apa: Alpichshev, Z., Mahmood, F., Cao, G., & Gedik, N. (2015). Confinement deconfinement
transition as an indication of spin liquid type behavior in Na2IrO3. Physical
Review Letters. American Physical Society. https://doi.org/10.1103/PhysRevLett.114.017203
chicago: Alpichshev, Zhanybek, Fahad Mahmood, Gang Cao, and Nuh Gedik. “Confinement
Deconfinement Transition as an Indication of Spin Liquid Type Behavior in Na2IrO3.”
Physical Review Letters. American Physical Society, 2015. https://doi.org/10.1103/PhysRevLett.114.017203.
ieee: Z. Alpichshev, F. Mahmood, G. Cao, and N. Gedik, “Confinement deconfinement
transition as an indication of spin liquid type behavior in Na2IrO3,” Physical
Review Letters, vol. 114, no. 1. American Physical Society, 2015.
ista: Alpichshev Z, Mahmood F, Cao G, Gedik N. 2015. Confinement deconfinement transition
as an indication of spin liquid type behavior in Na2IrO3. Physical Review Letters.
114(1).
mla: Alpichshev, Zhanybek, et al. “Confinement Deconfinement Transition as an Indication
of Spin Liquid Type Behavior in Na2IrO3.” Physical Review Letters, vol.
114, no. 1, American Physical Society, 2015, doi:10.1103/PhysRevLett.114.017203.
short: Z. Alpichshev, F. Mahmood, G. Cao, N. Gedik, Physical Review Letters 114
(2015).
date_created: 2018-12-11T11:46:11Z
date_published: 2015-07-07T00:00:00Z
date_updated: 2021-01-12T07:52:54Z
day: '07'
doi: 10.1103/PhysRevLett.114.017203
extern: '1'
intvolume: ' 114'
issue: '1'
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://dspace.mit.edu/handle/1721.1/92979
month: '07'
oa: 1
oa_version: Published Version
publication: Physical Review Letters
publication_status: published
publisher: American Physical Society
publist_id: '7441'
quality_controlled: '1'
status: public
title: Confinement deconfinement transition as an indication of spin liquid type behavior
in Na2IrO3
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 114
year: '2015'
...