---
_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: '1619'
abstract:
- lang: eng
text: The emergence of drug resistant pathogens is a serious public health problem.
It is a long-standing goal to predict rates of resistance evolution and design
optimal treatment strategies accordingly. To this end, it is crucial to reveal
the underlying causes of drug-specific differences in the evolutionary dynamics
leading to resistance. However, it remains largely unknown why the rates of resistance
evolution via spontaneous mutations and the diversity of mutational paths vary
substantially between drugs. Here we comprehensively quantify the distribution
of fitness effects (DFE) of mutations, a key determinant of evolutionary dynamics,
in the presence of eight antibiotics representing the main modes of action. Using
precise high-throughput fitness measurements for genome-wide Escherichia coli
gene deletion strains, we find that the width of the DFE varies dramatically between
antibiotics and, contrary to conventional wisdom, for some drugs the DFE width
is lower than in the absence of stress. We show that this previously underappreciated
divergence in DFE width among antibiotics is largely caused by their distinct
drug-specific dose-response characteristics. Unlike the DFE, the magnitude of
the changes in tolerated drug concentration resulting from genome-wide mutations
is similar for most drugs but exceptionally small for the antibiotic nitrofurantoin,
i.e., mutations generally have considerably smaller resistance effects for nitrofurantoin
than for other drugs. A population genetics model predicts that resistance evolution
for drugs with this property is severely limited and confined to reproducible
mutational paths. We tested this prediction in laboratory evolution experiments
using the “morbidostat”, a device for evolving bacteria in well-controlled drug
environments. Nitrofurantoin resistance indeed evolved extremely slowly via reproducible
mutations—an almost paradoxical behavior since this drug causes DNA damage and
increases the mutation rate. Overall, we identified novel quantitative characteristics
of the evolutionary landscape that provide the conceptual foundation for predicting
the dynamics of drug resistance evolution.
article_number: e1002299
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: Dravecka, Marta
id: 4342E402-F248-11E8-B48F-1D18A9856A87
last_name: Dravecka
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
full_name: Ayhan, Dilay
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. Quantifying the determinants of
evolutionary dynamics leading to drug resistance. PLoS Biology. 2015;13(11).
doi:10.1371/journal.pbio.1002299
apa: Chevereau, G., Lukacisinova, M., Batur, T., Guvenek, A., Ayhan, D., Toprak,
E., & Bollenbach, M. T. (2015). Quantifying the determinants of evolutionary
dynamics leading to drug resistance. PLoS Biology. Public Library of Science.
https://doi.org/10.1371/journal.pbio.1002299
chicago: Chevereau, Guillaume, Marta Lukacisinova, Tugce Batur, Aysegul Guvenek,
Dilay Ayhan, Erdal Toprak, and Mark Tobias Bollenbach. “Quantifying the Determinants
of Evolutionary Dynamics Leading to Drug Resistance.” PLoS Biology. Public
Library of Science, 2015. https://doi.org/10.1371/journal.pbio.1002299.
ieee: G. Chevereau et al., “Quantifying the determinants of evolutionary
dynamics leading to drug resistance,” PLoS Biology, vol. 13, no. 11. Public
Library of Science, 2015.
ista: Chevereau G, Lukacisinova M, Batur T, Guvenek A, Ayhan D, Toprak E, Bollenbach
MT. 2015. Quantifying the determinants of evolutionary dynamics leading to drug
resistance. PLoS Biology. 13(11), e1002299.
mla: Chevereau, Guillaume, et al. “Quantifying the Determinants of Evolutionary
Dynamics Leading to Drug Resistance.” PLoS Biology, vol. 13, no. 11, e1002299,
Public Library of Science, 2015, doi:10.1371/journal.pbio.1002299.
short: G. Chevereau, M. Lukacisinova, T. Batur, A. Guvenek, D. Ayhan, E. Toprak,
M.T. Bollenbach, PLoS Biology 13 (2015).
corr_author: '1'
date_created: 2018-12-11T11:53:04Z
date_published: 2015-11-18T00:00:00Z
date_updated: 2026-07-01T22:30:39Z
day: '18'
ddc:
- '570'
department:
- _id: ToBo
doi: 10.1371/journal.pbio.1002299
ec_funded: 1
external_id:
isi:
- '000365898900011'
file:
- access_level: open_access
checksum: 0e82e3279f50b15c6c170c042627802b
content_type: application/pdf
creator: system
date_created: 2018-12-12T10:09:00Z
date_updated: 2020-07-14T12:45:07Z
file_id: '4723'
file_name: IST-2016-468-v1+1_journal.pbio.1002299.pdf
file_size: 1387760
relation: main_file
file_date_updated: 2020-07-14T12:45:07Z
has_accepted_license: '1'
intvolume: ' 13'
isi: 1
issue: '11'
language:
- iso: eng
month: '11'
oa: 1
oa_version: Published Version
project:
- _id: 25EB3A80-B435-11E9-9278-68D0E5697425
grant_number: RGP0042/2013
name: Revealing the fundamental limits of cell growth
- _id: 25E9AF9E-B435-11E9-9278-68D0E5697425
call_identifier: FWF
grant_number: P27201-B22
name: Revealing the mechanisms underlying drug interactions
- _id: 25E83C2C-B435-11E9-9278-68D0E5697425
call_identifier: FP7
grant_number: '303507'
name: Optimality principles in responses to antibiotics
publication: PLoS Biology
publication_status: published
publisher: Public Library of Science
publist_id: '5547'
pubrep_id: '468'
quality_controlled: '1'
related_material:
record:
- id: '9711'
relation: research_data
status: public
- id: '9765'
relation: research_data
status: public
- id: '6263'
relation: dissertation_contains
status: public
scopus_import: '1'
status: public
title: Quantifying the determinants of evolutionary dynamics leading to drug resistance
tmp:
image: /images/cc_by.png
legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
short: CC BY (4.0)
type: journal_article
user_id: 317138e5-6ab7-11ef-aa6d-ffef3953e345
volume: 13
year: '2015'
...