---
_id: '9749'
abstract:
- lang: eng
text: Cooperative behavior, where one individual incurs a cost to help another,
is a wide spread phenomenon. Here we study direct reciprocity in the context of
the alternating Prisoner's Dilemma. We consider all strategies that can be implemented
by one and two-state automata. We calculate the payoff matrix of all pairwise
encounters in the presence of noise. We explore deterministic selection dynamics
with and without mutation. Using different error rates and payoff values, we observe
convergence to a small number of distinct equilibria. Two of them are uncooperative
strict Nash equilibria representing always-defect (ALLD) and Grim. The third equilibrium
is mixed and represents a cooperative alliance of several strategies, dominated
by a strategy which we call Forgiver. Forgiver cooperates whenever the opponent
has cooperated; it defects once when the opponent has defected, but subsequently
Forgiver attempts to re-establish cooperation even if the opponent has defected
again. Forgiver is not an evolutionarily stable strategy, but the alliance, which
it rules, is asymptotically stable. For a wide range of parameter values the most
commonly observed outcome is convergence to the mixed equilibrium, dominated by
Forgiver. Our results show that although forgiving might incur a short-term loss
it can lead to a long-term gain. Forgiveness facilitates stable cooperation in
the presence of exploitation and noise.
article_processing_charge: No
author:
- first_name: Benjamin
full_name: Zagorsky, Benjamin
last_name: Zagorsky
- first_name: Johannes
full_name: Reiter, Johannes
id: 4A918E98-F248-11E8-B48F-1D18A9856A87
last_name: Reiter
orcid: 0000-0002-0170-7353
- first_name: Krishnendu
full_name: Chatterjee, Krishnendu
id: 2E5DCA20-F248-11E8-B48F-1D18A9856A87
last_name: Chatterjee
orcid: 0000-0002-4561-241X
- first_name: Martin
full_name: Nowak, Martin
last_name: Nowak
citation:
ama: Zagorsky B, Reiter J, Chatterjee K, Nowak M. Forgiver triumphs in alternating
prisoner’s dilemma . 2013. doi:10.1371/journal.pone.0080814.s001
apa: Zagorsky, B., Reiter, J., Chatterjee, K., & Nowak, M. (2013). Forgiver
triumphs in alternating prisoner’s dilemma . Public Library of Science. https://doi.org/10.1371/journal.pone.0080814.s001
chicago: Zagorsky, Benjamin, Johannes Reiter, Krishnendu Chatterjee, and Martin
Nowak. “Forgiver Triumphs in Alternating Prisoner’s Dilemma .” Public Library
of Science, 2013. https://doi.org/10.1371/journal.pone.0080814.s001.
ieee: B. Zagorsky, J. Reiter, K. Chatterjee, and M. Nowak, “Forgiver triumphs in
alternating prisoner’s dilemma .” Public Library of Science, 2013.
ista: Zagorsky B, Reiter J, Chatterjee K, Nowak M. 2013. Forgiver triumphs in alternating
prisoner’s dilemma , Public Library of Science, 10.1371/journal.pone.0080814.s001.
mla: Zagorsky, Benjamin, et al. Forgiver Triumphs in Alternating Prisoner’s Dilemma
. Public Library of Science, 2013, doi:10.1371/journal.pone.0080814.s001.
short: B. Zagorsky, J. Reiter, K. Chatterjee, M. Nowak, (2013).
date_created: 2021-07-28T15:45:07Z
date_published: 2013-12-12T00:00:00Z
date_updated: 2025-09-29T14:30:03Z
day: '12'
department:
- _id: KrCh
doi: 10.1371/journal.pone.0080814.s001
fulldoi: https://doi.org/10.1371/journal.pone.0080814.s001
month: '12'
oa_version: Published Version
publisher: Public Library of Science
related_material:
record:
- id: '2247'
relation: used_in_publication
status: public
status: public
title: 'Forgiver triumphs in alternating prisoner''s dilemma '
type: research_data_reference
user_id: 6785fbc1-c503-11eb-8a32-93094b40e1cf
year: '2013'
...
---
_id: '975'
abstract:
- lang: eng
text: Recent numerical work by Bardarson, Pollmann, and Moore revealed a slow, logarithmic
in time, growth of the entanglement entropy for initial product states in a putative
many-body localized phase. We show that this surprising phenomenon results from
the dephasing due to exponentially small interaction-induced corrections to the
eigenenergies of different states. For weak interactions, we find that the entanglement
entropy grows as ξln (Vt/), where V is the interaction strength, and ξ is the
single-particle localization length. The saturated value of the entanglement entropy
at long times is determined by the participation ratios of the initial state over
the eigenstates of the subsystem. Our work shows that the logarithmic entanglement
growth is a universal phenomenon characteristic of the many-body localized phase
in any number of spatial dimensions, and reveals a broad hierarchy of dephasing
time scales present in such a phase.
acknowledgement: We would like to thank E. Altman and J. Moore for useful comments
on the manuscript. This research was supported in part by Perimeter Institute for
Theoretical Physics. 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. Z. P. was supported by DOE Grant No. DE-SC0002140.
The simulations presented in this article were performed on computational resources
supported by the High Performance Computing Center (PICSciE) at Princeton University.
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. Universal slow growth of entanglement in interacting
strongly disordered systems. Physical Review Letters. 2013;110(26). doi:10.1103/PhysRevLett.110.260601
apa: Serbyn, M., Papić, Z., & Abanin, D. (2013). Universal slow growth of entanglement
in interacting strongly disordered systems. Physical Review Letters. American
Physical Society. https://doi.org/10.1103/PhysRevLett.110.260601
chicago: Serbyn, Maksym, Zlatko Papić, and Dmitry Abanin. “Universal Slow Growth
of Entanglement in Interacting Strongly Disordered Systems.” Physical Review
Letters. American Physical Society, 2013. https://doi.org/10.1103/PhysRevLett.110.260601.
ieee: M. Serbyn, Z. Papić, and D. Abanin, “Universal slow growth of entanglement
in interacting strongly disordered systems,” Physical Review Letters, vol.
110, no. 26. American Physical Society, 2013.
ista: Serbyn M, Papić Z, Abanin D. 2013. Universal slow growth of entanglement in
interacting strongly disordered systems. Physical Review Letters. 110(26).
mla: Serbyn, Maksym, et al. “Universal Slow Growth of Entanglement in Interacting
Strongly Disordered Systems.” Physical Review Letters, vol. 110, no. 26,
American Physical Society, 2013, doi:10.1103/PhysRevLett.110.260601.
short: M. Serbyn, Z. Papić, D. Abanin, Physical Review Letters 110 (2013).
date_created: 2018-12-11T11:49:29Z
date_published: 2013-06-28T00:00:00Z
date_updated: 2021-01-12T08:22:22Z
day: '28'
doi: 10.1103/PhysRevLett.110.260601
extern: 1
fulldoi: https://doi.org/10.1103/PhysRevLett.110.260601
intvolume: ' 110'
issue: '26'
main_file_link:
- open_access: '1'
url: https://arxiv.org/abs/1304.4605
month: '06'
oa: 1
publication: Physical Review Letters
publication_status: published
publisher: American Physical Society
publist_id: '6426'
quality_controlled: 0
status: public
title: Universal slow growth of entanglement in interacting strongly disordered systems
type: journal_article
volume: 110
year: '2013'
...
---
_id: '9751'
abstract:
- lang: eng
text: High relatedness among interacting individuals has generally been considered
a precondition for the evolution of altruism. However, kin-selection theory also
predicts the evolution of altruism when relatedness is low, as long as the cost
of the altruistic act is minor compared to its benefit. Here, we demonstrate evidence
for a low-cost altruistic act in bacteria. We investigated Escherichia coli responding
to the attack of an obligately lytic phage by committing suicide in order to prevent
parasite transmission to nearby relatives. We found that bacterial suicide provides
large benefits to survivors at marginal costs to committers. The cost of suicide
was low because infected cells are moribund, rapidly dying upon phage infection,
such that no more opportunity for reproduction remains. As a consequence of its
marginal cost, host suicide was selectively favoured even when relatedness between
committers and survivors approached zero. Altogether, our findings demonstrate
that low-cost suicide can evolve with ease, represents an effective host-defence
strategy, and seems to be widespread among microbes. Moreover, low-cost suicide
might also occur in higher organisms as exemplified by infected social insect
workers leaving the colony to die in isolation.
article_processing_charge: No
author:
- first_name: Dominik
full_name: Refardt, Dominik
last_name: Refardt
- first_name: Tobias
full_name: Bergmiller, Tobias
id: 2C471CFA-F248-11E8-B48F-1D18A9856A87
last_name: Bergmiller
orcid: 0000-0001-5396-4346
- first_name: Rolf
full_name: Kümmerli, Rolf
last_name: Kümmerli
citation:
ama: 'Refardt D, Bergmiller T, Kümmerli R. Data from: Altruism can evolve when relatedness
is low: evidence from bacteria committing suicide upon phage infection. 2013.
doi:10.5061/dryad.b1q2n'
apa: 'Refardt, D., Bergmiller, T., & Kümmerli, R. (2013). Data from: Altruism
can evolve when relatedness is low: evidence from bacteria committing suicide
upon phage infection. Dryad. https://doi.org/10.5061/dryad.b1q2n'
chicago: 'Refardt, Dominik, Tobias Bergmiller, and Rolf Kümmerli. “Data from: Altruism
Can Evolve When Relatedness Is Low: Evidence from Bacteria Committing Suicide
upon Phage Infection.” Dryad, 2013. https://doi.org/10.5061/dryad.b1q2n.'
ieee: 'D. Refardt, T. Bergmiller, and R. Kümmerli, “Data from: Altruism can evolve
when relatedness is low: evidence from bacteria committing suicide upon phage
infection.” Dryad, 2013.'
ista: 'Refardt D, Bergmiller T, Kümmerli R. 2013. Data from: Altruism can evolve
when relatedness is low: evidence from bacteria committing suicide upon phage
infection, Dryad, 10.5061/dryad.b1q2n.'
mla: 'Refardt, Dominik, et al. Data from: Altruism Can Evolve When Relatedness
Is Low: Evidence from Bacteria Committing Suicide upon Phage Infection. Dryad,
2013, doi:10.5061/dryad.b1q2n.'
short: D. Refardt, T. Bergmiller, R. Kümmerli, (2013).
date_created: 2021-07-30T08:08:09Z
date_published: 2013-03-21T00:00:00Z
date_updated: 2025-09-29T13:41:12Z
day: '21'
department:
- _id: CaGu
doi: 10.5061/dryad.b1q2n
fulldoi: https://doi.org/10.5061/dryad.b1q2n
main_file_link:
- open_access: '1'
url: https://doi.org/10.5061/dryad.b1q2n
month: '03'
oa: 1
oa_version: Published Version
publisher: Dryad
related_material:
record:
- id: '2853'
relation: used_in_publication
status: public
status: public
title: 'Data from: Altruism can evolve when relatedness is low: evidence from bacteria
committing suicide upon phage infection'
type: research_data_reference
user_id: 6785fbc1-c503-11eb-8a32-93094b40e1cf
year: '2013'
...
---
_id: '9754'
abstract:
- lang: eng
text: Short-read sequencing technologies have in principle made it feasible to draw
detailed inferences about the recent history of any organism. In practice, however,
this remains challenging due to the difficulty of genome assembly in most organisms
and the lack of statistical methods powerful enough to discriminate among recent,
non-equilibrium histories. We address both the assembly and inference challenges.
We develop a bioinformatic pipeline for generating outgroup-rooted alignments
of orthologous sequence blocks from de novo low-coverage short-read data for a
small number of genomes, and show how such sequence blocks can be used to fit
explicit models of population divergence and admixture in a likelihood framework.
To illustrate our approach, we reconstruct the Pleistocene history of an oak-feeding
insect (the oak gallwasp Biorhiza pallida) which, in common with many other taxa,
was restricted during Pleistocene ice ages to a longitudinal series of southern
refugia spanning theWestern Palaearctic. Our analysis of sequence blocks sampled
from a single genome from each of three major glacial refugia reveals support
for an unexpected history dominated by recent admixture. Despite the fact that
80% of the genome is affected by admixture during the last glacial cycle, we are
able to infer the deeper divergence history of these populations. These inferences
are robust to variation in block length, mutation model, and the sampling location
of individual genomes within refugia. This combination of de novo assembly and
numerical likelihood calculation provides a powerful framework for estimating
recent population history that can be applied to any organism without the need
for prior genetic resources.
article_processing_charge: No
author:
- first_name: Jack
full_name: Hearn, Jack
last_name: Hearn
- first_name: Graham
full_name: Stone, Graham
last_name: Stone
- first_name: Nicholas H
full_name: Barton, Nicholas H
id: 4880FE40-F248-11E8-B48F-1D18A9856A87
last_name: Barton
orcid: 0000-0002-8548-5240
- first_name: Konrad
full_name: Lohse, Konrad
last_name: Lohse
- first_name: Lynsey
full_name: Bunnefeld, Lynsey
last_name: Bunnefeld
citation:
ama: 'Hearn J, Stone G, Barton NH, Lohse K, Bunnefeld L. Data from: Likelihood-based
inference of population history from low coverage de novo genome assemblies. 2013.
doi:10.5061/dryad.r3r60'
apa: 'Hearn, J., Stone, G., Barton, N. H., Lohse, K., & Bunnefeld, L. (2013).
Data from: Likelihood-based inference of population history from low coverage
de novo genome assemblies. Dryad. https://doi.org/10.5061/dryad.r3r60'
chicago: 'Hearn, Jack, Graham Stone, Nicholas H Barton, Konrad Lohse, and Lynsey
Bunnefeld. “Data from: Likelihood-Based Inference of Population History from Low
Coverage de Novo Genome Assemblies.” Dryad, 2013. https://doi.org/10.5061/dryad.r3r60.'
ieee: 'J. Hearn, G. Stone, N. H. Barton, K. Lohse, and L. Bunnefeld, “Data from:
Likelihood-based inference of population history from low coverage de novo genome
assemblies.” Dryad, 2013.'
ista: 'Hearn J, Stone G, Barton NH, Lohse K, Bunnefeld L. 2013. Data from: Likelihood-based
inference of population history from low coverage de novo genome assemblies, Dryad,
10.5061/dryad.r3r60.'
mla: 'Hearn, Jack, et al. Data from: Likelihood-Based Inference of Population
History from Low Coverage de Novo Genome Assemblies. Dryad, 2013, doi:10.5061/dryad.r3r60.'
short: J. Hearn, G. Stone, N.H. Barton, K. Lohse, L. Bunnefeld, (2013).
date_created: 2021-07-30T08:31:22Z
date_published: 2013-10-01T00:00:00Z
date_updated: 2025-09-29T11:38:51Z
day: '01'
department:
- _id: NiBa
doi: 10.5061/dryad.r3r60
fulldoi: https://doi.org/10.5061/dryad.r3r60
main_file_link:
- open_access: '1'
url: https://doi.org/10.5061/dryad.r3r60
month: '10'
oa: 1
oa_version: Published Version
publisher: Dryad
related_material:
record:
- id: '2170'
relation: used_in_publication
status: public
status: public
title: 'Data from: Likelihood-based inference of population history from low coverage
de novo genome assemblies'
type: research_data_reference
user_id: 6785fbc1-c503-11eb-8a32-93094b40e1cf
year: '2013'
...
---
_id: '976'
abstract:
- lang: eng
text: 'Motivated by a search for experimental probes to access the physics of fractionalized
excitations called spinons in spin liquids, we study the interaction of spinons
with lattice vibrations. We consider the case of algebraic spin liquid, when spinons
have fermionic statistics and a Dirac-like dispersion. We establish the general
procedure for deriving spinon-phonon interactions, which is based on symmetry
considerations. The procedure is illustrated for four different algebraic spin
liquids: π-flux and staggered-flux phases on a square lattice, π-flux phase on
a kagome lattice, and zero-flux phase on a honeycomb lattice. Although the low-energy
description is similar for all these phases, different underlying symmetry groups
lead to a distinct form of spinon-phonon interaction Hamiltonian. The explicit
form of the spinon-phonon interaction is used to estimate the attenuation of ultrasound
in an algebraic spin liquid. The prospects of the sound attenuation as a probe
of spinons are discussed.'
acknowledgement: M. S. is grateful to X.-G. Wen, L. Levitov, M. Metlitski, K. Michaeli,
K.-T. Chen, and A. Potter for many useful discussions. We acknowledge support by
Grant No. NSF DMR 1104498. We acknowledge the hospitality of KITP, where final stages
of this project were completed.
author:
- first_name: Maksym
full_name: Maksym Serbyn
id: 47809E7E-F248-11E8-B48F-1D18A9856A87
last_name: Serbyn
orcid: 0000-0002-2399-5827
- first_name: Patrick
full_name: Lee, Patrick
last_name: Lee
citation:
ama: Serbyn M, Lee P. Spinon-phonon interaction in algebraic spin liquids. Physical
Review B - Condensed Matter and Materials Physics. 2013;87(17). doi:10.1103/PhysRevB.87.174424
apa: Serbyn, M., & Lee, P. (2013). Spinon-phonon interaction in algebraic spin
liquids. Physical Review B - Condensed Matter and Materials Physics. American
Physical Society. https://doi.org/10.1103/PhysRevB.87.174424
chicago: Serbyn, Maksym, and Patrick Lee. “Spinon-Phonon Interaction in Algebraic
Spin Liquids.” Physical Review B - Condensed Matter and Materials Physics.
American Physical Society, 2013. https://doi.org/10.1103/PhysRevB.87.174424.
ieee: M. Serbyn and P. Lee, “Spinon-phonon interaction in algebraic spin liquids,”
Physical Review B - Condensed Matter and Materials Physics, vol. 87, no.
17. American Physical Society, 2013.
ista: Serbyn M, Lee P. 2013. Spinon-phonon interaction in algebraic spin liquids.
Physical Review B - Condensed Matter and Materials Physics. 87(17).
mla: Serbyn, Maksym, and Patrick Lee. “Spinon-Phonon Interaction in Algebraic Spin
Liquids.” Physical Review B - Condensed Matter and Materials Physics, vol.
87, no. 17, American Physical Society, 2013, doi:10.1103/PhysRevB.87.174424.
short: M. Serbyn, P. Lee, Physical Review B - Condensed Matter and Materials Physics
87 (2013).
date_created: 2018-12-11T11:49:30Z
date_published: 2013-05-22T00:00:00Z
date_updated: 2021-01-12T08:22:22Z
day: '22'
doi: 10.1103/PhysRevB.87.174424
extern: 1
fulldoi: https://doi.org/10.1103/PhysRevB.87.174424
intvolume: ' 87'
issue: '17'
main_file_link:
- open_access: '1'
url: https://arxiv.org/abs/1303.0772
month: '05'
oa: 1
publication: Physical Review B - Condensed Matter and Materials Physics
publication_status: published
publisher: American Physical Society
publist_id: '6427'
quality_controlled: 0
status: public
title: Spinon-phonon interaction in algebraic spin liquids
type: journal_article
volume: 87
year: '2013'
...
---
_id: '6440'
abstract:
- lang: eng
text: In order to guarantee that each method of a data structure updates the logical
state exactly once, al-most all non-blocking implementations employ Compare-And-Swap
(CAS) based synchronization. For FIFO queue implementations this translates into concurrent enqueue or dequeue methods
competing among themselves to update the same variable, the tail or the head,
respectively, leading to high contention and poor scalability. Recent non-blocking
queue implementations try to alleviate high contentionby increasing the number
of contention points, all the while using CAS-based synchronization. Furthermore,
obtaining a wait-free implementation with competition is achieved by additional
synchronization which leads to further degradation of performance.In this paper
we formalize the notion of competitiveness of a synchronizing statement which
can beused as a measure for the scalability of concurrent implementations. We
present a new queue implementation, the Speculative Pairing (SP) queue, which,
as we show, decreases competitiveness by using Fetch-And-Increment (FAI) instead
of CAS. We prove that the SP queue is linearizable and lock-free.We also show
that replacing CAS with FAI leads to wait-freedom for dequeue methods without
an adverse effect on performance. In fact, our experiments suggest that the SP
queue can perform and scale better than the state-of-the-art queue implementations.
alternative_title:
- IST Austria Technical Report
author:
- first_name: Thomas A
full_name: Henzinger, Thomas A
id: 40876CD8-F248-11E8-B48F-1D18A9856A87
last_name: Henzinger
orcid: 0000−0002−2985−7724
- first_name: Hannes
full_name: Payer, Hannes
last_name: Payer
- first_name: Ali
full_name: Sezgin, Ali
id: 4C7638DA-F248-11E8-B48F-1D18A9856A87
last_name: Sezgin
citation:
ama: Henzinger TA, Payer H, Sezgin A. Replacing Competition with Cooperation
to Achieve Scalable Lock-Free FIFO Queues . IST Austria; 2013. doi:10.15479/AT:IST-2013-124-v1-1
apa: Henzinger, T. A., Payer, H., & Sezgin, A. (2013). Replacing competition
with cooperation to achieve scalable lock-free FIFO queues . IST Austria.
https://doi.org/10.15479/AT:IST-2013-124-v1-1
chicago: Henzinger, Thomas A, Hannes Payer, and Ali Sezgin. Replacing Competition
with Cooperation to Achieve Scalable Lock-Free FIFO Queues . IST Austria,
2013. https://doi.org/10.15479/AT:IST-2013-124-v1-1.
ieee: T. A. Henzinger, H. Payer, and A. Sezgin, Replacing competition with cooperation
to achieve scalable lock-free FIFO queues . IST Austria, 2013.
ista: Henzinger TA, Payer H, Sezgin A. 2013. Replacing competition with cooperation
to achieve scalable lock-free FIFO queues , IST Austria, 23p.
mla: Henzinger, Thomas A., et al. Replacing Competition with Cooperation to Achieve
Scalable Lock-Free FIFO Queues . IST Austria, 2013, doi:10.15479/AT:IST-2013-124-v1-1.
short: T.A. Henzinger, H. Payer, A. Sezgin, Replacing Competition with Cooperation
to Achieve Scalable Lock-Free FIFO Queues , IST Austria, 2013.
date_created: 2019-05-13T14:13:27Z
date_published: 2013-06-13T00:00:00Z
date_updated: 2020-07-14T23:06:19Z
day: '13'
ddc:
- '000'
- '005'
department:
- _id: ToHe
doi: 10.15479/AT:IST-2013-124-v1-1
file:
- access_level: open_access
checksum: a219ba4eada6cd62befed52262ee15d4
content_type: application/pdf
creator: dernst
date_created: 2019-05-13T14:11:39Z
date_updated: 2020-07-14T12:47:30Z
file_id: '6441'
file_name: 2013_TechRep_Henzinger.pdf
file_size: 549684
relation: main_file
file_date_updated: 2020-07-14T12:47:30Z
fulldoi: https://doi.org/10.15479/AT:IST-2013-124-v1-1
has_accepted_license: '1'
language:
- iso: eng
month: '06'
oa: 1
oa_version: Published Version
page: '23'
publication_identifier:
issn:
- 2664-1690
publication_status: published
publisher: IST Austria
pubrep_id: '124'
status: public
title: 'Replacing competition with cooperation to achieve scalable lock-free FIFO
queues '
type: technical_report
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
year: '2013'
...
---
_id: '6768'
abstract:
- lang: eng
text: The paper presents an algorithm that applies a stack filter simulating the
Mean Curvature Motion equation via a finite difference scheme.
article_type: original
author:
- first_name: Marco
full_name: Mondelli, Marco
id: 27EB676C-8706-11E9-9510-7717E6697425
last_name: Mondelli
orcid: 0000-0002-3242-7020
citation:
ama: Mondelli M. A finite difference scheme for the stack filter simulating the
MCM. Image Processing On Line. 2013;3:68-111. doi:10.5201/ipol.2013.53
apa: Mondelli, M. (2013). A finite difference scheme for the stack filter simulating
the MCM. Image Processing On Line. Image Processing On Line. https://doi.org/10.5201/ipol.2013.53
chicago: Mondelli, Marco. “A Finite Difference Scheme for the Stack Filter Simulating
the MCM.” Image Processing On Line. Image Processing On Line, 2013. https://doi.org/10.5201/ipol.2013.53.
ieee: M. Mondelli, “A finite difference scheme for the stack filter simulating the
MCM,” Image Processing On Line, vol. 3. Image Processing On Line, pp. 68–111,
2013.
ista: Mondelli M. 2013. A finite difference scheme for the stack filter simulating
the MCM. Image Processing On Line. 3, 68–111.
mla: Mondelli, Marco. “A Finite Difference Scheme for the Stack Filter Simulating
the MCM.” Image Processing On Line, vol. 3, Image Processing On Line, 2013,
pp. 68–111, doi:10.5201/ipol.2013.53.
short: M. Mondelli, Image Processing On Line 3 (2013) 68–111.
date_created: 2019-08-05T12:30:38Z
date_published: 2013-07-11T00:00:00Z
date_updated: 2021-01-12T08:08:56Z
day: '11'
ddc:
- '510'
doi: 10.5201/ipol.2013.53
extern: '1'
file:
- access_level: open_access
checksum: 83b7d429bc248c6c461229d3504fb139
content_type: application/pdf
creator: dernst
date_created: 2019-08-05T12:33:40Z
date_updated: 2020-07-14T12:47:40Z
file_id: '6769'
file_name: 2013_IPOL_Mondelli.pdf
file_size: 4306158
relation: main_file
file_date_updated: 2020-07-14T12:47:40Z
fulldoi: https://doi.org/10.5201/ipol.2013.53
has_accepted_license: '1'
intvolume: ' 3'
language:
- iso: eng
license: https://creativecommons.org/licenses/by-nc-sa/4.0/
month: '07'
oa: 1
oa_version: Published Version
page: 68-111
publication: Image Processing On Line
publication_identifier:
issn:
- 2105-1232
publication_status: published
publisher: Image Processing On Line
quality_controlled: '1'
status: public
title: A finite difference scheme for the stack filter simulating the MCM
tmp:
image: /images/cc_by_nc_sa.png
legal_code_url: https://creativecommons.org/licenses/by-nc-sa/4.0/legalcode
name: Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC
BY-NC-SA 4.0)
short: CC BY-NC-SA (4.0)
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 3
year: '2013'
...
---
_id: '7306'
abstract:
- lang: eng
text: Rechargeable lithium–air (O2) batteries are receiving intense interest because
their high theoretical specific energy exceeds that of lithium-ion batteries.
If the Li–O2 battery is ever to succeed, highly reversible formation/decomposition
of Li2O2 must take place at the cathode on cycling. However, carbon, used ubiquitously
as the basis of the cathode, decomposes during Li2O2 oxidation on charge and actively
promotes electrolyte decomposition on cycling. Replacing carbon with a nanoporous
gold cathode, when in contact with a dimethyl sulphoxide-based electrolyte, does
seem to demonstrate better stability. However, nanoporous gold is not a suitable
cathode; its high mass destroys the key advantage of Li–O2 over Li ion (specific
energy), it is too expensive and too difficult to fabricate. Identifying a suitable
cathode material for the Li–O2 cell is one of the greatest challenges at present.
Here we show that a TiC-based cathode reduces greatly side reactions (arising
from the electrolyte and electrode degradation) compared with carbon and exhibits
better reversible formation/decomposition of Li2O2 even than nanoporous gold (>98%
capacity retention after 100 cycles, compared with 95% for nanoporous gold); it
is also four times lighter, of lower cost and easier to fabricate. The stability
may originate from the presence of TiO2 (along with some TiOC) on the surface
of TiC. In contrast to carbon or nanoporous gold, TiC seems to represent a more
viable, stable, cathode for aprotic Li–O2 cells.
article_processing_charge: No
article_type: original
author:
- first_name: Muhammed M.
full_name: Ottakam Thotiyl, Muhammed M.
last_name: Ottakam Thotiyl
- first_name: Stefan Alexander
full_name: Freunberger, Stefan Alexander
id: A8CA28E6-CE23-11E9-AD2D-EC27E6697425
last_name: Freunberger
orcid: 0000-0003-2902-5319
- first_name: Zhangquan
full_name: Peng, Zhangquan
last_name: Peng
- first_name: Yuhui
full_name: Chen, Yuhui
last_name: Chen
- first_name: Zheng
full_name: Liu, Zheng
last_name: Liu
- first_name: Peter G.
full_name: Bruce, Peter G.
last_name: Bruce
citation:
ama: Ottakam Thotiyl MM, Freunberger SA, Peng Z, Chen Y, Liu Z, Bruce PG. A stable
cathode for the aprotic Li–O2 battery. Nature Materials. 2013;12(11):1050-1056.
doi:10.1038/nmat3737
apa: Ottakam Thotiyl, M. M., Freunberger, S. A., Peng, Z., Chen, Y., Liu, Z., &
Bruce, P. G. (2013). A stable cathode for the aprotic Li–O2 battery. Nature
Materials. Springer Nature. https://doi.org/10.1038/nmat3737
chicago: Ottakam Thotiyl, Muhammed M., Stefan Alexander Freunberger, Zhangquan Peng,
Yuhui Chen, Zheng Liu, and Peter G. Bruce. “A Stable Cathode for the Aprotic Li–O2 Battery.”
Nature Materials. Springer Nature, 2013. https://doi.org/10.1038/nmat3737.
ieee: M. M. Ottakam Thotiyl, S. A. Freunberger, Z. Peng, Y. Chen, Z. Liu, and P.
G. Bruce, “A stable cathode for the aprotic Li–O2 battery,” Nature Materials,
vol. 12, no. 11. Springer Nature, pp. 1050–1056, 2013.
ista: Ottakam Thotiyl MM, Freunberger SA, Peng Z, Chen Y, Liu Z, Bruce PG. 2013.
A stable cathode for the aprotic Li–O2 battery. Nature Materials. 12(11), 1050–1056.
mla: Ottakam Thotiyl, Muhammed M., et al. “A Stable Cathode for the Aprotic Li–O2 Battery.”
Nature Materials, vol. 12, no. 11, Springer Nature, 2013, pp. 1050–56,
doi:10.1038/nmat3737.
short: M.M. Ottakam Thotiyl, S.A. Freunberger, Z. Peng, Y. Chen, Z. Liu, P.G. Bruce,
Nature Materials 12 (2013) 1050–1056.
date_created: 2020-01-15T12:18:29Z
date_published: 2013-09-01T00:00:00Z
date_updated: 2021-01-12T08:12:55Z
day: '01'
doi: 10.1038/nmat3737
extern: '1'
fulldoi: https://doi.org/10.1038/nmat3737
intvolume: ' 12'
issue: '11'
language:
- iso: eng
month: '09'
oa_version: None
page: 1050-1056
publication: Nature Materials
publication_identifier:
issn:
- 1476-1122
- 1476-4660
publication_status: published
publisher: Springer Nature
quality_controlled: '1'
status: public
title: A stable cathode for the aprotic Li–O2 battery
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 12
year: '2013'
...
---
_id: '7307'
abstract:
- lang: eng
text: The non-aqueous Li–air (O2) battery is receiving intense interest because
its theoretical specific energy exceeds that of Li-ion batteries. Recharging the
Li–O2 battery depends on oxidizing solid lithium peroxide (Li2O2), which is formed
on discharge within the porous cathode. However, transporting charge between Li2O2
particles and the solid electrode surface is at best very difficult and leads
to voltage polarization on charging, even at modest rates. This is a significant
problem facing the non-aqueous Li–O2 battery. Here we show that incorporation
of a redox mediator, tetrathiafulvalene (TTF), enables recharging at rates that
are impossible for the cell in the absence of the mediator. On charging, TTF is
oxidized to TTF+ at the cathode surface; TTF+ in turn oxidizes the solid Li2O2,
which results in the regeneration of TTF. The mediator acts as an electron–hole
transfer agent that permits efficient oxidation of solid Li2O2. The cell with
the mediator demonstrated 100 charge/discharge cycles.
article_processing_charge: No
article_type: original
author:
- first_name: Yuhui
full_name: Chen, Yuhui
last_name: Chen
- first_name: Stefan Alexander
full_name: Freunberger, Stefan Alexander
id: A8CA28E6-CE23-11E9-AD2D-EC27E6697425
last_name: Freunberger
orcid: 0000-0003-2902-5319
- first_name: Zhangquan
full_name: Peng, Zhangquan
last_name: Peng
- first_name: Olivier
full_name: Fontaine, Olivier
last_name: Fontaine
- first_name: Peter G.
full_name: Bruce, Peter G.
last_name: Bruce
citation:
ama: Chen Y, Freunberger SA, Peng Z, Fontaine O, Bruce PG. Charging a Li–O2 battery
using a redox mediator. Nature Chemistry. 2013;5(6):489-494. doi:10.1038/nchem.1646
apa: Chen, Y., Freunberger, S. A., Peng, Z., Fontaine, O., & Bruce, P. G. (2013).
Charging a Li–O2 battery using a redox mediator. Nature Chemistry. Springer
Nature. https://doi.org/10.1038/nchem.1646
chicago: Chen, Yuhui, Stefan Alexander Freunberger, Zhangquan Peng, Olivier Fontaine,
and Peter G. Bruce. “Charging a Li–O2 Battery Using a Redox Mediator.” Nature
Chemistry. Springer Nature, 2013. https://doi.org/10.1038/nchem.1646.
ieee: Y. Chen, S. A. Freunberger, Z. Peng, O. Fontaine, and P. G. Bruce, “Charging
a Li–O2 battery using a redox mediator,” Nature Chemistry, vol. 5, no.
6. Springer Nature, pp. 489–494, 2013.
ista: Chen Y, Freunberger SA, Peng Z, Fontaine O, Bruce PG. 2013. Charging a Li–O2
battery using a redox mediator. Nature Chemistry. 5(6), 489–494.
mla: Chen, Yuhui, et al. “Charging a Li–O2 Battery Using a Redox Mediator.” Nature
Chemistry, vol. 5, no. 6, Springer Nature, 2013, pp. 489–94, doi:10.1038/nchem.1646.
short: Y. Chen, S.A. Freunberger, Z. Peng, O. Fontaine, P.G. Bruce, Nature Chemistry
5 (2013) 489–494.
date_created: 2020-01-15T12:18:43Z
date_published: 2013-05-12T00:00:00Z
date_updated: 2021-01-12T08:12:56Z
day: '12'
doi: 10.1038/nchem.1646
extern: '1'
fulldoi: https://doi.org/10.1038/nchem.1646
intvolume: ' 5'
issue: '6'
language:
- iso: eng
month: '05'
oa_version: None
page: 489-494
publication: Nature Chemistry
publication_identifier:
issn:
- 1755-4330
- 1755-4349
publication_status: published
publisher: Springer Nature
quality_controlled: '1'
status: public
title: Charging a Li–O2 battery using a redox mediator
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 5
year: '2013'
...
---
_id: '3116'
abstract:
- lang: eng
text: Multithreaded programs coordinate their interaction through synchronization
primitives like mutexes and semaphores, which are managed by an OS-provided resource
manager. We propose algorithms for the automatic construction of code-aware resource
managers for multithreaded embedded applications. Such managers use knowledge
about the structure and resource usage (mutex and semaphore usage) of the threads
to guarantee deadlock freedom and progress while managing resources in an efficient
way. Our algorithms compute managers as winning strategies in certain infinite
games, and produce a compact code description of these strategies. We have implemented
the algorithms in the tool Cynthesis. Given a multithreaded program in C, the
tool produces C code implementing a code-aware resource manager. We show in experiments
that Cynthesis produces compact resource managers within a few minutes on a set
of embedded benchmarks with up to 6 threads. © 2012 Springer Science+Business
Media, LLC.
acknowledgement: This research was supported in part by the National Science Foundation
CAREER award CCR-0132780, by the ONR grant N00014-02-1-0671, by the National Science
Foundation grants CCR-0427202 and CCR-0234690, and by the ARP award TO.030.MM.D.
article_processing_charge: No
author:
- first_name: Krishnendu
full_name: Chatterjee, Krishnendu
id: 2E5DCA20-F248-11E8-B48F-1D18A9856A87
last_name: Chatterjee
orcid: 0000-0002-4561-241X
- first_name: Luca
full_name: De Alfaro, Luca
last_name: De Alfaro
- first_name: Marco
full_name: Faella, Marco
last_name: Faella
- first_name: Ritankar
full_name: Majumdar, Ritankar
last_name: Majumdar
- first_name: Vishwanath
full_name: Raman, Vishwanath
last_name: Raman
citation:
ama: Chatterjee K, De Alfaro L, Faella M, Majumdar R, Raman V. Code aware resource
management. Formal Methods in System Design. 2013;42(2):142-174. doi:10.1007/s10703-012-0170-4
apa: Chatterjee, K., De Alfaro, L., Faella, M., Majumdar, R., & Raman, V. (2013).
Code aware resource management. Formal Methods in System Design. Springer.
https://doi.org/10.1007/s10703-012-0170-4
chicago: Chatterjee, Krishnendu, Luca De Alfaro, Marco Faella, Ritankar Majumdar,
and Vishwanath Raman. “Code Aware Resource Management.” Formal Methods in System
Design. Springer, 2013. https://doi.org/10.1007/s10703-012-0170-4.
ieee: K. Chatterjee, L. De Alfaro, M. Faella, R. Majumdar, and V. Raman, “Code aware
resource management,” Formal Methods in System Design, vol. 42, no. 2.
Springer, pp. 142–174, 2013.
ista: Chatterjee K, De Alfaro L, Faella M, Majumdar R, Raman V. 2013. Code aware
resource management. Formal Methods in System Design. 42(2), 142–174.
mla: Chatterjee, Krishnendu, et al. “Code Aware Resource Management.” Formal
Methods in System Design, vol. 42, no. 2, Springer, 2013, pp. 142–74, doi:10.1007/s10703-012-0170-4.
short: K. Chatterjee, L. De Alfaro, M. Faella, R. Majumdar, V. Raman, Formal Methods
in System Design 42 (2013) 142–174.
date_created: 2018-12-11T12:01:29Z
date_published: 2013-04-01T00:00:00Z
date_updated: 2025-09-29T13:24:54Z
day: '01'
department:
- _id: KrCh
doi: 10.1007/s10703-012-0170-4
external_id:
isi:
- '000316677500002'
fulldoi: https://doi.org/10.1007/s10703-012-0170-4
intvolume: ' 42'
isi: 1
issue: '2'
language:
- iso: eng
month: '04'
oa_version: None
page: 142 - 174
publication: Formal Methods in System Design
publication_status: published
publisher: Springer
publist_id: '3583'
quality_controlled: '1'
scopus_import: '1'
status: public
title: Code aware resource management
type: journal_article
user_id: 317138e5-6ab7-11ef-aa6d-ffef3953e345
volume: 42
year: '2013'
...
---
_id: '3261'
abstract:
- lang: eng
text: Cells in a developing embryo have no direct way of "measuring" their
physical position. Through a variety of processes, however, the expression levels
of multiple genes come to be correlated with position, and these expression levels
thus form a code for "positional information." We show how to measure
this information, in bits, using the gap genes in the Drosophila embryo as an
example. Individual genes carry nearly two bits of information, twice as much
as expected if the expression patterns consisted only of on/off domains separated
by sharp boundaries. Taken together, four gap genes carry enough information to
define a cell's location with an error bar of ~1% along the anterior-posterior
axis of the embryo. This precision is nearly enough for each cell to have a unique
identity, which is the maximum information the system can use, and is nearly constant
along the length of the embryo. We argue that this constancy is a signature of
optimality in the transmission of information from primary morphogen inputs to
the output of the gap gene network.
article_processing_charge: No
author:
- first_name: Julien
full_name: Dubuis, Julien
last_name: Dubuis
- first_name: Gasper
full_name: Tkacik, Gasper
id: 3D494DCA-F248-11E8-B48F-1D18A9856A87
last_name: Tkacik
orcid: 0000-0002-6699-1455
- first_name: Eric
full_name: Wieschaus, Eric
last_name: Wieschaus
- first_name: Thomas
full_name: Gregor, Thomas
last_name: Gregor
- first_name: William
full_name: Bialek, William
last_name: Bialek
citation:
ama: Dubuis J, Tkačik G, Wieschaus E, Gregor T, Bialek W. Positional information,
in bits. PNAS. 2013;110(41):16301-16308. doi:10.1073/pnas.1315642110
apa: Dubuis, J., Tkačik, G., Wieschaus, E., Gregor, T., & Bialek, W. (2013).
Positional information, in bits. PNAS. National Academy of Sciences. https://doi.org/10.1073/pnas.1315642110
chicago: Dubuis, Julien, Gašper Tkačik, Eric Wieschaus, Thomas Gregor, and William
Bialek. “Positional Information, in Bits.” PNAS. National Academy of Sciences,
2013. https://doi.org/10.1073/pnas.1315642110.
ieee: J. Dubuis, G. Tkačik, E. Wieschaus, T. Gregor, and W. Bialek, “Positional
information, in bits,” PNAS, vol. 110, no. 41. National Academy of Sciences,
pp. 16301–16308, 2013.
ista: Dubuis J, Tkačik G, Wieschaus E, Gregor T, Bialek W. 2013. Positional information,
in bits. PNAS. 110(41), 16301–16308.
mla: Dubuis, Julien, et al. “Positional Information, in Bits.” PNAS, vol.
110, no. 41, National Academy of Sciences, 2013, pp. 16301–08, doi:10.1073/pnas.1315642110.
short: J. Dubuis, G. Tkačik, E. Wieschaus, T. Gregor, W. Bialek, PNAS 110 (2013)
16301–16308.
date_created: 2018-12-11T12:02:19Z
date_published: 2013-10-08T00:00:00Z
date_updated: 2025-09-29T13:24:21Z
day: '08'
ddc:
- '570'
department:
- _id: GaTk
doi: 10.1073/pnas.1315642110
external_id:
isi:
- '000325395600021'
pmid:
- '24089448'
file:
- access_level: open_access
checksum: ecd859fe52a562193027d428b5524a8d
content_type: application/pdf
creator: dernst
date_created: 2019-01-22T13:53:23Z
date_updated: 2020-07-14T12:46:06Z
file_id: '5873'
file_name: 2013_PNAS_Dubuis.pdf
file_size: 1670548
relation: main_file
file_date_updated: 2020-07-14T12:46:06Z
fulldoi: https://doi.org/10.1073/pnas.1315642110
has_accepted_license: '1'
intvolume: ' 110'
isi: 1
issue: '41'
language:
- iso: eng
month: '10'
oa: 1
oa_version: Published Version
page: 16301 - 16308
pmid: 1
publication: PNAS
publication_status: published
publisher: National Academy of Sciences
publist_id: '3387'
quality_controlled: '1'
scopus_import: '1'
status: public
title: Positional information, in bits
type: journal_article
user_id: 317138e5-6ab7-11ef-aa6d-ffef3953e345
volume: 110
year: '2013'
...
---
_id: '331'
abstract:
- lang: eng
text: We report a procedure to prepare highly monodisperse copper telluride nanocubes,
nanoplates, and nanorods. The procedure is based on the reaction of a copper salt
with trioctylphosphine telluride in the presence of lithium bis(trimethylsilyl)amide
and oleylamine. CuTe nanocrystals display a strong near-infrared optical absorption
associated with localized surface plasmon resonances. We exploit this plasmon
resonance for the design of surface-enhanced Raman scattering sensors for unconventional
optical probes. Furthermore, we also report here our preliminary analysis of the
use of CuTe nanocrystals as cytotoxic and photothermal agents.
article_processing_charge: No
article_type: original
author:
- first_name: Wenhua
full_name: Li, Wenhua
last_name: Li
- first_name: Reza
full_name: Zamani, Reza
last_name: Zamani
- first_name: Pilar
full_name: Rivera Gil, Pilar
last_name: Rivera Gil
- first_name: Beatriz
full_name: Pelaz, Beatriz
last_name: Pelaz
- first_name: Maria
full_name: Ibáñez, Maria
id: 43C61214-F248-11E8-B48F-1D18A9856A87
last_name: Ibáñez
orcid: 0000-0001-5013-2843
- first_name: Doris
full_name: Cadavid, Doris
last_name: Cadavid
- first_name: Alexey
full_name: Shavel, Alexey
last_name: Shavel
- first_name: Ramon
full_name: Alvarez Puebla, Ramon
last_name: Alvarez Puebla
- first_name: Wolfgang
full_name: Parak, Wolfgang
last_name: Parak
- first_name: Jordi
full_name: Arbiol, Jordi
last_name: Arbiol
- first_name: Andreu
full_name: Cabot, Andreu
last_name: Cabot
citation:
ama: 'Li W, Zamani R, Rivera Gil P, et al. CuTe nanocrystals: Shape and size control,
plasmonic properties, and use as SERS probes and photothermal agents. Journal
of the American Chemical Society. 2013;135(19):7098-7101. doi:10.1021/ja401428e'
apa: 'Li, W., Zamani, R., Rivera Gil, P., Pelaz, B., Ibáñez, M., Cadavid, D., …
Cabot, A. (2013). CuTe nanocrystals: Shape and size control, plasmonic properties,
and use as SERS probes and photothermal agents. Journal of the American Chemical
Society. ACS. https://doi.org/10.1021/ja401428e'
chicago: 'Li, Wenhua, Reza Zamani, Pilar Rivera Gil, Beatriz Pelaz, Maria Ibáñez,
Doris Cadavid, Alexey Shavel, et al. “CuTe Nanocrystals: Shape and Size Control,
Plasmonic Properties, and Use as SERS Probes and Photothermal Agents.” Journal
of the American Chemical Society. ACS, 2013. https://doi.org/10.1021/ja401428e.'
ieee: 'W. Li et al., “CuTe nanocrystals: Shape and size control, plasmonic
properties, and use as SERS probes and photothermal agents,” Journal of the
American Chemical Society, vol. 135, no. 19. ACS, pp. 7098–7101, 2013.'
ista: 'Li W, Zamani R, Rivera Gil P, Pelaz B, Ibáñez M, Cadavid D, Shavel A, Alvarez
Puebla R, Parak W, Arbiol J, Cabot A. 2013. CuTe nanocrystals: Shape and size
control, plasmonic properties, and use as SERS probes and photothermal agents.
Journal of the American Chemical Society. 135(19), 7098–7101.'
mla: 'Li, Wenhua, et al. “CuTe Nanocrystals: Shape and Size Control, Plasmonic Properties,
and Use as SERS Probes and Photothermal Agents.” Journal of the American Chemical
Society, vol. 135, no. 19, ACS, 2013, pp. 7098–101, doi:10.1021/ja401428e.'
short: W. Li, R. Zamani, P. Rivera Gil, B. Pelaz, M. Ibáñez, D. Cadavid, A. Shavel,
R. Alvarez Puebla, W. Parak, J. Arbiol, A. Cabot, Journal of the American Chemical
Society 135 (2013) 7098–7101.
date_created: 2018-12-11T11:45:51Z
date_published: 2013-04-30T00:00:00Z
date_updated: 2021-01-12T07:42:33Z
day: '30'
doi: 10.1021/ja401428e
extern: '1'
fulldoi: https://doi.org/10.1021/ja401428e
intvolume: ' 135'
issue: '19'
language:
- iso: eng
month: '04'
oa_version: None
page: 7098 - 7101
publication: Journal of the American Chemical Society
publication_status: published
publisher: ACS
publist_id: '7521'
quality_controlled: '1'
status: public
title: 'CuTe nanocrystals: Shape and size control, plasmonic properties, and use as
SERS probes and photothermal agents'
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 135
year: '2013'
...
---
_id: '3321'
author:
- first_name: Novi
full_name: Quadrianto, Novi
last_name: Quadrianto
- first_name: Christoph
full_name: Lampert, Christoph
id: 40C20FD2-F248-11E8-B48F-1D18A9856A87
last_name: Lampert
orcid: 0000-0001-8622-7887
citation:
ama: 'Quadrianto N, Lampert C. Kernel based learning. In: Dubitzky W, Wolkenhauer
O, Cho K, Yokota H, eds. Encyclopedia of Systems Biology. Vol 3. Springer;
2013:1069-1069. doi:10.1007/978-1-4419-9863-7_604'
apa: Quadrianto, N., & Lampert, C. (2013). Kernel based learning. In W. Dubitzky,
O. Wolkenhauer, K. Cho, & H. Yokota (Eds.), Encyclopedia of Systems Biology
(Vol. 3, pp. 1069–1069). Springer. https://doi.org/10.1007/978-1-4419-9863-7_604
chicago: Quadrianto, Novi, and Christoph Lampert. “Kernel Based Learning.” In Encyclopedia
of Systems Biology, edited by Werner Dubitzky, Olaf Wolkenhauer, Kwang Cho,
and Hiroki Yokota, 3:1069–1069. Springer, 2013. https://doi.org/10.1007/978-1-4419-9863-7_604.
ieee: N. Quadrianto and C. Lampert, “Kernel based learning,” in Encyclopedia
of Systems Biology, vol. 3, W. Dubitzky, O. Wolkenhauer, K. Cho, and H. Yokota,
Eds. Springer, 2013, pp. 1069–1069.
ista: 'Quadrianto N, Lampert C. 2013.Kernel based learning. In: Encyclopedia of
Systems Biology. vol. 3, 1069–1069.'
mla: Quadrianto, Novi, and Christoph Lampert. “Kernel Based Learning.” Encyclopedia
of Systems Biology, edited by Werner Dubitzky et al., vol. 3, Springer, 2013,
pp. 1069–1069, doi:10.1007/978-1-4419-9863-7_604.
short: N. Quadrianto, C. Lampert, in:, W. Dubitzky, O. Wolkenhauer, K. Cho, H. Yokota
(Eds.), Encyclopedia of Systems Biology, Springer, 2013, pp. 1069–1069.
date_created: 2018-12-11T12:02:39Z
date_published: 2013-01-01T00:00:00Z
date_updated: 2021-01-12T07:42:38Z
day: '01'
department:
- _id: ChLa
doi: 10.1007/978-1-4419-9863-7_604
editor:
- first_name: Werner
full_name: Dubitzky, Werner
last_name: Dubitzky
- first_name: Olaf
full_name: Wolkenhauer, Olaf
last_name: Wolkenhauer
- first_name: Kwang
full_name: Cho, Kwang
last_name: Cho
- first_name: Hiroki
full_name: Yokota, Hiroki
last_name: Yokota
fulldoi: https://doi.org/10.1007/978-1-4419-9863-7_604
intvolume: ' 3'
language:
- iso: eng
month: '01'
oa_version: None
page: 1069 - 1069
publication: Encyclopedia of Systems Biology
publication_status: published
publisher: Springer
publist_id: '3314'
quality_controlled: '1'
status: public
title: Kernel based learning
type: encyclopedia_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 3
year: '2013'
...
---
_id: '342'
abstract:
- lang: eng
text: Morphology is a key parameter in the design of novel nanocrystals and nanomaterials
with controlled functional properties. Here, we demonstrate the potential of foreign
metal ions to tune the morphology of colloidal semiconductor nanoparticles. We
illustrate the underlying mechanism by preparing copper selenide nanocubes in
the presence of Al ions. We further characterize the plasmonic properties of the
obtained nanocrystals and demonstrate their potential as a platform to produce
cubic nanoparticles with different composition by cation exchange. © 2013 American
Chemical Society.
acknowledgement: The research was supported by the European Regional Development Funds.
M.I. thanks the Spanish MICINN for her Ph.D. grant. J.A. and R.Z. also acknowledge
MAT2010-15138.
article_processing_charge: No
article_type: original
author:
- first_name: Wenhua
full_name: Li, Wenhua
last_name: Li
- first_name: Reza
full_name: Zamani, Reza
last_name: Zamani
- first_name: Maria
full_name: Ibáñez, Maria
id: 43C61214-F248-11E8-B48F-1D18A9856A87
last_name: Ibáñez
orcid: 0000-0001-5013-2843
- first_name: Doris
full_name: Cadavid, Doris
last_name: Cadavid
- first_name: Alexey
full_name: Shavel, Alexey
last_name: Shavel
- first_name: Joan
full_name: Morante, Joan
last_name: Morante
- first_name: Jordi
full_name: Arbiol, Jordi
last_name: Arbiol
- first_name: Andreu
full_name: Cabot, Andreu
last_name: Cabot
citation:
ama: 'Li W, Zamani R, Ibáñez M, et al. Metal ions to control the morphology of semiconductor
nanoparticles: Copper selenide nanocubes. Journal of the American Chemical
Society. 2013;135(12):4664-4667. doi:10.1021/ja400472m'
apa: 'Li, W., Zamani, R., Ibáñez, M., Cadavid, D., Shavel, A., Morante, J., … Cabot,
A. (2013). Metal ions to control the morphology of semiconductor nanoparticles:
Copper selenide nanocubes. Journal of the American Chemical Society. American
Chemical Society. https://doi.org/10.1021/ja400472m'
chicago: 'Li, Wenhua, Reza Zamani, Maria Ibáñez, Doris Cadavid, Alexey Shavel, Joan
Morante, Jordi Arbiol, and Andreu Cabot. “Metal Ions to Control the Morphology
of Semiconductor Nanoparticles: Copper Selenide Nanocubes.” Journal of the
American Chemical Society. American Chemical Society, 2013. https://doi.org/10.1021/ja400472m.'
ieee: 'W. Li et al., “Metal ions to control the morphology of semiconductor
nanoparticles: Copper selenide nanocubes,” Journal of the American Chemical
Society, vol. 135, no. 12. American Chemical Society, pp. 4664–4667, 2013.'
ista: 'Li W, Zamani R, Ibáñez M, Cadavid D, Shavel A, Morante J, Arbiol J, Cabot
A. 2013. Metal ions to control the morphology of semiconductor nanoparticles:
Copper selenide nanocubes. Journal of the American Chemical Society. 135(12),
4664–4667.'
mla: 'Li, Wenhua, et al. “Metal Ions to Control the Morphology of Semiconductor
Nanoparticles: Copper Selenide Nanocubes.” Journal of the American Chemical
Society, vol. 135, no. 12, American Chemical Society, 2013, pp. 4664–67, doi:10.1021/ja400472m.'
short: W. Li, R. Zamani, M. Ibáñez, D. Cadavid, A. Shavel, J. Morante, J. Arbiol,
A. Cabot, Journal of the American Chemical Society 135 (2013) 4664–4667.
date_created: 2018-12-11T11:45:55Z
date_published: 2013-03-07T00:00:00Z
date_updated: 2021-01-12T07:43:21Z
day: '07'
doi: 10.1021/ja400472m
extern: '1'
fulldoi: https://doi.org/10.1021/ja400472m
intvolume: ' 135'
issue: '12'
language:
- iso: eng
month: '03'
oa_version: None
page: 4664 - 4667
publication: Journal of the American Chemical Society
publication_status: published
publisher: American Chemical Society
publist_id: '7482'
quality_controlled: '1'
status: public
title: 'Metal ions to control the morphology of semiconductor nanoparticles: Copper
selenide nanocubes'
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 135
year: '2013'
...
---
_id: '343'
abstract:
- lang: eng
text: The bottom-up assembly of nanocrystals provides access to a three-dimensional
composition control at the nanoscale not attainable by any other technology. In
particular, colloidal nanoheterostructures, with intrinsic multiphase organization,
are especially appealing building blocks for the bottom-up production of nanocomposites.
In the present work, we use PbTe-PbS as the model material system and thermoelectricity
as the paradigmatic application to investigate the potential of the bottom-up
assembly of core-shell nanoparticles to produce functional nanocomposites. With
this goal in mind, a rapid, high-yield and scalable colloidal synthetic route
to prepare grams of PbTe@PbS core-shell nanoparticles with unprecedented narrow
size distributions and exceptional composition control is detailed. PbTe@PbS nanoparticles
were used as building blocks for the bottom-up production of PbTe-PbS nanocomposites
with tuned composition. In such PbTe-PbS nanocomposites, synergistic nanocrystal
doping effects result in up to 10-fold higher electrical conductivities than in
pure PbTe and PbS nanomaterials. At the same time, the acoustic impedance mismatch
between PbTe and PbS phases and a partial phase alloying provide PbTe-PbS nanocomposites
with strongly reduced thermal conductivities. As a result, record thermoelectric
figures of merit (ZT) of ∼1.1 were obtained from undoped PbTe and PbS phases at
710 K. These high ZT values prove the potential of the proposed processes to produce
efficient functional nanomaterials with programmable properties. © 2013 American
Chemical Society.
acknowledgement: "The research was supported by the European Regional Development
Funds (ERDF, “FEDER Programa Competitivitat de Catalunya 2007-2013”) and the Spanish
MICINN Projects MAT2008-05779, MAT2010-15138, CSD2009-00050, and CSD2009-00013.
M.I. thanks the Spanish MICINN for her Ph.D. grant. J.A. and R.Z. also acknowledge
Generalitat de Catalunya 2009-SGR-770 and XaRMAE.\r\n\r\nThe authors declare no
competing financial interest."
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: Reza
full_name: Zamani, Reza
last_name: Zamani
- first_name: Stéphane
full_name: Gorsse, Stéphane
last_name: Gorsse
- first_name: Jiandong
full_name: Fan, Jiandong
last_name: Fan
- first_name: Silvia
full_name: Ortega, Silvia
last_name: Ortega
- first_name: Doris
full_name: Cadavid, Doris
last_name: Cadavid
- first_name: Joan
full_name: Morante, Joan
last_name: Morante
- first_name: Jordi
full_name: Arbiol, Jordi
last_name: Arbiol
- first_name: Andreu
full_name: Cabot, Andreu
last_name: Cabot
citation:
ama: 'Ibáñez M, Zamani R, Gorsse S, et al. Core shell nanoparticles as building
blocks for the bottom-up production of functional nanocomposites: PbTe PbS thermoelectric
properties. ACS Nano. 2013;7(3):2573-2586. doi:10.1021/nn305971v'
apa: 'Ibáñez, M., Zamani, R., Gorsse, S., Fan, J., Ortega, S., Cadavid, D., … Cabot,
A. (2013). Core shell nanoparticles as building blocks for the bottom-up production
of functional nanocomposites: PbTe PbS thermoelectric properties. ACS Nano.
American Chemical Society. https://doi.org/10.1021/nn305971v'
chicago: 'Ibáñez, Maria, Reza Zamani, Stéphane Gorsse, Jiandong Fan, Silvia Ortega,
Doris Cadavid, Joan Morante, Jordi Arbiol, and Andreu Cabot. “Core Shell Nanoparticles
as Building Blocks for the Bottom-up Production of Functional Nanocomposites:
PbTe PbS Thermoelectric Properties.” ACS Nano. American Chemical Society,
2013. https://doi.org/10.1021/nn305971v.'
ieee: 'M. Ibáñez et al., “Core shell nanoparticles as building blocks for
the bottom-up production of functional nanocomposites: PbTe PbS thermoelectric
properties,” ACS Nano, vol. 7, no. 3. American Chemical Society, pp. 2573–2586,
2013.'
ista: 'Ibáñez M, Zamani R, Gorsse S, Fan J, Ortega S, Cadavid D, Morante J, Arbiol
J, Cabot A. 2013. Core shell nanoparticles as building blocks for the bottom-up
production of functional nanocomposites: PbTe PbS thermoelectric properties. ACS
Nano. 7(3), 2573–2586.'
mla: 'Ibáñez, Maria, et al. “Core Shell Nanoparticles as Building Blocks for the
Bottom-up Production of Functional Nanocomposites: PbTe PbS Thermoelectric Properties.”
ACS Nano, vol. 7, no. 3, American Chemical Society, 2013, pp. 2573–86,
doi:10.1021/nn305971v.'
short: M. Ibáñez, R. Zamani, S. Gorsse, J. Fan, S. Ortega, D. Cadavid, J. Morante,
J. Arbiol, A. Cabot, ACS Nano 7 (2013) 2573–2586.
date_created: 2018-12-11T11:45:55Z
date_published: 2013-02-28T00:00:00Z
date_updated: 2021-01-12T07:43:25Z
day: '28'
doi: 10.1021/nn305971v
extern: '1'
fulldoi: https://doi.org/10.1021/nn305971v
intvolume: ' 7'
issue: '3'
language:
- iso: eng
month: '02'
oa_version: None
page: 2573 - 2586
publication: ACS Nano
publication_status: published
publisher: American Chemical Society
publist_id: '7483'
quality_controlled: '1'
status: public
title: 'Core shell nanoparticles as building blocks for the bottom-up production of
functional nanocomposites: PbTe PbS thermoelectric properties'
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 7
year: '2013'
...
---
_id: '344'
abstract:
- lang: eng
text: Copper-based selenides are attracting increasing interest due to their outstanding
optoelectronic and thermoelectric properties. Herein a novel colloidal synthetic
route to prepare Cu2SnSe3 nanocrystals with controlled size, shape and composition
is presented. The high yield of the developed procedure allowed its up-scaling
to the production of grams of colloidal Cu2SnSe3 nanocrystals. These nanocrystals
were used as building blocks for the production of Cu2SnSe3 bulk nanostructured
materials by spark plasma sintering. The thermoelectric properties of the prepared
nanocrystalline Cu2SnSe3 pellets were characterized in the temperature range from
300 to 720 K. The obtained results show the bottom-up production of nanocrystalline
materials from solution-processed nanocrystals to be a potentially advantageous
alternative to conventional methods of production of efficient thermoelectric
materials.
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: Doris
full_name: Cadavid, Doris
last_name: Cadavid
- first_name: Umberto
full_name: Anselmi Tamburini, Umberto
last_name: Anselmi Tamburini
- first_name: Reza
full_name: Zamani, Reza
last_name: Zamani
- first_name: Stéphane
full_name: Gorsse, Stéphane
last_name: Gorsse
- first_name: Wenhua
full_name: Li, Wenhua
last_name: Li
- first_name: Antonio
full_name: López, Antonio
last_name: López
- first_name: Joan
full_name: Morante, Joan
last_name: Morante
- first_name: Jordi
full_name: Arbiol, Jordi
last_name: Arbiol
- first_name: Andreu
full_name: Cabot, Andreu
last_name: Cabot
citation:
ama: Ibáñez M, Cadavid D, Anselmi Tamburini U, et al. Colloidal synthesis and thermoelectric
properties of Cu 2SnSe3 nanocrystals. Journal of Materials Chemistry A.
2013;1(4):1421-1426. doi:10.1039/C2TA00419D
apa: Ibáñez, M., Cadavid, D., Anselmi Tamburini, U., Zamani, R., Gorsse, S., Li,
W., … Cabot, A. (2013). Colloidal synthesis and thermoelectric properties of Cu
2SnSe3 nanocrystals. Journal of Materials Chemistry A. Royal Society of
Chemistry. https://doi.org/10.1039/C2TA00419D
chicago: Ibáñez, Maria, Doris Cadavid, Umberto Anselmi Tamburini, Reza Zamani, Stéphane
Gorsse, Wenhua Li, Antonio López, Joan Morante, Jordi Arbiol, and Andreu Cabot.
“Colloidal Synthesis and Thermoelectric Properties of Cu 2SnSe3 Nanocrystals.”
Journal of Materials Chemistry A. Royal Society of Chemistry, 2013. https://doi.org/10.1039/C2TA00419D.
ieee: M. Ibáñez et al., “Colloidal synthesis and thermoelectric properties
of Cu 2SnSe3 nanocrystals,” Journal of Materials Chemistry A, vol. 1, no.
4. Royal Society of Chemistry, pp. 1421–1426, 2013.
ista: Ibáñez M, Cadavid D, Anselmi Tamburini U, Zamani R, Gorsse S, Li W, López
A, Morante J, Arbiol J, Cabot A. 2013. Colloidal synthesis and thermoelectric
properties of Cu 2SnSe3 nanocrystals. Journal of Materials Chemistry A. 1(4),
1421–1426.
mla: Ibáñez, Maria, et al. “Colloidal Synthesis and Thermoelectric Properties of
Cu 2SnSe3 Nanocrystals.” Journal of Materials Chemistry A, vol. 1, no.
4, Royal Society of Chemistry, 2013, pp. 1421–26, doi:10.1039/C2TA00419D.
short: M. Ibáñez, D. Cadavid, U. Anselmi Tamburini, R. Zamani, S. Gorsse, W. Li,
A. López, J. Morante, J. Arbiol, A. Cabot, Journal of Materials Chemistry A 1
(2013) 1421–1426.
date_created: 2018-12-11T11:45:56Z
date_published: 2013-01-28T00:00:00Z
date_updated: 2021-01-12T07:43:28Z
day: '28'
doi: 10.1039/C2TA00419D
extern: '1'
fulldoi: https://doi.org/10.1039/C2TA00419D
intvolume: ' 1'
issue: '4'
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://hal.archives-ouvertes.fr/hal-00917429/
month: '01'
oa: 1
oa_version: Submitted Version
page: 1421 - 1426
publication: Journal of Materials Chemistry A
publication_status: published
publisher: Royal Society of Chemistry
publist_id: '7484'
quality_controlled: '1'
status: public
title: Colloidal synthesis and thermoelectric properties of Cu 2SnSe3 nanocrystals
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 1
year: '2013'
...
---
_id: '351'
abstract:
- lang: eng
text: 'A multistrategy approach to overcome the main challenges of nanoparticle-based
solution-processed Cu2ZnSnSe4 thin film solar cells is presented. We developed
an efficient ligand exchange strategy, using an antimony salt, to displace organic
ligands from the surface of Cu 2ZnSnS4 nanoparticles. An automated pulsed spray-deposition
system was used to deposit the nanoparticles into homogeneous and crack-free films
with controlled thickness. After annealing the film in a Se-rich atmosphere, carbon-free
and crystalline Cu2ZnSnSe4 absorber layers were obtained. Not only was crystallization
promoted by the complete removal of organics, but also Sb itself played a critical
role. The Sb-assisted crystal growth is associated with the formation of a Sb-based
compound at the grain boundaries, which locally reduces the melting point, thus
promoting the film diffusion-limited crystallization. '
acknowledgement: This work was supported by the European Regional Development Funds
and the Framework 7 program under project SCALENANO (FP7-NMP-ENERGY-2011-284486).
E.S. thanks the Spanish government for the “Ramon y Cajal” fellowship (RYC-2011-09212).
article_processing_charge: No
article_type: original
author:
- first_name: Alex
full_name: Carrete, Alex
last_name: Carrete
- first_name: Alexey
full_name: Shavel, Alexey
last_name: Shavel
- first_name: Xavier
full_name: Fontané, Xavier
last_name: Fontané
- first_name: Joana
full_name: Montserrat, Joana
last_name: Montserrat
- first_name: Jiandong
full_name: Fan, Jiandong
last_name: Fan
- first_name: Maria
full_name: Ibáñez, Maria
id: 43C61214-F248-11E8-B48F-1D18A9856A87
last_name: Ibáñez
orcid: 0000-0001-5013-2843
- first_name: Edgardo
full_name: Saucedo, Edgardo
last_name: Saucedo
- first_name: Alejandro
full_name: Pérez Rodríguez, Alejandro
last_name: Pérez Rodríguez
- first_name: Andreu
full_name: Cabot, Andreu
last_name: Cabot
citation:
ama: Carrete A, Shavel A, Fontané X, et al. Antimony-based ligand exchange to promote
crystallization in spray-deposited Cu2ZnSnSe4 solar cells. Journal of the American
Chemical Society. 2013;135(43):15982-15985. doi:10.1021/ja4068639
apa: Carrete, A., Shavel, A., Fontané, X., Montserrat, J., Fan, J., Ibáñez, M.,
… Cabot, A. (2013). Antimony-based ligand exchange to promote crystallization
in spray-deposited Cu2ZnSnSe4 solar cells. Journal of the American Chemical
Society. American Chemical Society. https://doi.org/10.1021/ja4068639
chicago: Carrete, Alex, Alexey Shavel, Xavier Fontané, Joana Montserrat, Jiandong
Fan, Maria Ibáñez, Edgardo Saucedo, Alejandro Pérez Rodríguez, and Andreu Cabot.
“Antimony-Based Ligand Exchange to Promote Crystallization in Spray-Deposited
Cu2ZnSnSe4 Solar Cells.” Journal of the American Chemical Society. American
Chemical Society, 2013. https://doi.org/10.1021/ja4068639.
ieee: A. Carrete et al., “Antimony-based ligand exchange to promote crystallization
in spray-deposited Cu2ZnSnSe4 solar cells,” Journal of the American Chemical
Society, vol. 135, no. 43. American Chemical Society, pp. 15982–15985, 2013.
ista: Carrete A, Shavel A, Fontané X, Montserrat J, Fan J, Ibáñez M, Saucedo E,
Pérez Rodríguez A, Cabot A. 2013. Antimony-based ligand exchange to promote crystallization
in spray-deposited Cu2ZnSnSe4 solar cells. Journal of the American Chemical Society.
135(43), 15982–15985.
mla: Carrete, Alex, et al. “Antimony-Based Ligand Exchange to Promote Crystallization
in Spray-Deposited Cu2ZnSnSe4 Solar Cells.” Journal of the American Chemical
Society, vol. 135, no. 43, American Chemical Society, 2013, pp. 15982–85,
doi:10.1021/ja4068639.
short: A. Carrete, A. Shavel, X. Fontané, J. Montserrat, J. Fan, M. Ibáñez, E. Saucedo,
A. Pérez Rodríguez, A. Cabot, Journal of the American Chemical Society 135 (2013)
15982–15985.
date_created: 2018-12-11T11:45:58Z
date_published: 2013-10-30T00:00:00Z
date_updated: 2021-01-12T07:43:57Z
day: '30'
doi: 10.1021/ja4068639
extern: '1'
fulldoi: https://doi.org/10.1021/ja4068639
intvolume: ' 135'
issue: '43'
language:
- iso: eng
month: '10'
oa_version: None
page: 15982 - 15985
publication: Journal of the American Chemical Society
publication_status: published
publisher: American Chemical Society
publist_id: '7479'
quality_controlled: '1'
status: public
title: Antimony-based ligand exchange to promote crystallization in spray-deposited
Cu2ZnSnSe4 solar cells
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 135
year: '2013'
...
---
_id: '352'
abstract:
- lang: eng
text: The presence of organic ligands on the surface of colloidal nanoparticles
strongly limits their performance in technological applications where charge carrier
transfer/transport plays an important role. We use metal salts, matched with the
nanoparticle composition, to eliminate the surface organic ligands without introducing
extrinsic impurities in the final nanomaterial. The potential of the simple, general
and scalable processes presented here is demonstrated by characterizing the thermoelectric
properties of nanostructured Ag2Te produced by the bottom up assembly of Ag2Te
nanocrystals. A 6-fold increase of the thermoelectric figure of merit of Ag2Te
was obtained when organic ligands were displaced by AgNO3. The same procedure
can enhance the performance of nanocrystals and nanocrystal-based devices in a
broad range of applications, from photovoltaics and thermoelectrics to catalysis.
article_processing_charge: No
article_type: original
author:
- first_name: Doris
full_name: Cadavid, Doris
last_name: Cadavid
- first_name: Maria
full_name: Ibáñez, Maria
id: 43C61214-F248-11E8-B48F-1D18A9856A87
last_name: Ibáñez
orcid: 0000-0001-5013-2843
- first_name: Alexey
full_name: Shavel, Alexey
last_name: Shavel
- first_name: Oscar
full_name: Durá, Oscar
last_name: Durá
- first_name: Marco
full_name: López De La Torre, Marco
last_name: López De La Torre
- first_name: Andreu
full_name: Cabot, Andreu
last_name: Cabot
citation:
ama: 'Cadavid D, Ibáñez M, Shavel A, Durá O, López De La Torre M, Cabot A. Organic
ligand displacement by metal salts to enhance nanoparticle functionality: Thermoelectric
properties of Ag inf 2 inf Te. Journal of Materials Chemistry A. 2013;1(15):4864-4870.
doi:10.1039/C3TA01455J'
apa: 'Cadavid, D., Ibáñez, M., Shavel, A., Durá, O., López De La Torre, M., &
Cabot, A. (2013). Organic ligand displacement by metal salts to enhance nanoparticle
functionality: Thermoelectric properties of Ag inf 2 inf Te. Journal of Materials
Chemistry A. Royal Society of Chemistry. https://doi.org/10.1039/C3TA01455J'
chicago: 'Cadavid, Doris, Maria Ibáñez, Alexey Shavel, Oscar Durá, Marco López De
La Torre, and Andreu Cabot. “Organic Ligand Displacement by Metal Salts to Enhance
Nanoparticle Functionality: Thermoelectric Properties of Ag Inf 2 Inf Te.” Journal
of Materials Chemistry A. Royal Society of Chemistry, 2013. https://doi.org/10.1039/C3TA01455J.'
ieee: 'D. Cadavid, M. Ibáñez, A. Shavel, O. Durá, M. López De La Torre, and A. Cabot,
“Organic ligand displacement by metal salts to enhance nanoparticle functionality:
Thermoelectric properties of Ag inf 2 inf Te,” Journal of Materials Chemistry
A, vol. 1, no. 15. Royal Society of Chemistry, pp. 4864–4870, 2013.'
ista: 'Cadavid D, Ibáñez M, Shavel A, Durá O, López De La Torre M, Cabot A. 2013.
Organic ligand displacement by metal salts to enhance nanoparticle functionality:
Thermoelectric properties of Ag inf 2 inf Te. Journal of Materials Chemistry A.
1(15), 4864–4870.'
mla: 'Cadavid, Doris, et al. “Organic Ligand Displacement by Metal Salts to Enhance
Nanoparticle Functionality: Thermoelectric Properties of Ag Inf 2 Inf Te.” Journal
of Materials Chemistry A, vol. 1, no. 15, Royal Society of Chemistry, 2013,
pp. 4864–70, doi:10.1039/C3TA01455J.'
short: D. Cadavid, M. Ibáñez, A. Shavel, O. Durá, M. López De La Torre, A. Cabot,
Journal of Materials Chemistry A 1 (2013) 4864–4870.
date_created: 2018-12-11T11:45:58Z
date_published: 2013-02-13T00:00:00Z
date_updated: 2021-01-12T07:44:02Z
day: '13'
doi: 10.1039/C3TA01455J
extern: '1'
fulldoi: https://doi.org/10.1039/C3TA01455J
intvolume: ' 1'
issue: '15'
language:
- iso: eng
month: '02'
oa_version: None
page: 4864 - 4870
publication: Journal of Materials Chemistry A
publication_status: published
publisher: Royal Society of Chemistry
publist_id: '7481'
quality_controlled: '1'
status: public
title: 'Organic ligand displacement by metal salts to enhance nanoparticle functionality:
Thermoelectric properties of Ag inf 2 inf Te'
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 1
year: '2013'
...
---
_id: '376'
abstract:
- lang: eng
text: The compositional versatility of I2–II–IV–VI4 tetrahedrally-coordinated compounds
allows for accommodating their functional properties to numerous technological
applications. Among them, Cu2ZnSnSe4 is an emerging photovoltaic material and
Cu2CdSnSe4 displays excellent thermoelectric properties. The third compound of
this family, Cu2HgSnSe4, remains relatively unexplored. Herein, a synthetic route
to produce Cu2HgSnSe4 nanoparticles with narrow size distribution and controlled
composition is presented. Cu2HgSnSe4 nanoparticles were subsequently used as building
blocks to produce bulk nanocrystalline materials, whose thermoelectric properties
were analyzed. A very preliminary adjustment of the material composition yielded
Seebeck coefficients up to 160 μV K−1, electrical conductivities close to 104
S m−1 and thermal conductivities down to 0.5 W m−1 K−1.
author:
- first_name: Wenhua
full_name: Li, Wenhua
last_name: Li
- first_name: Maria
full_name: Ibáñez, Maria
id: 43C61214-F248-11E8-B48F-1D18A9856A87
last_name: Ibáñez
orcid: 0000-0001-5013-2843
- first_name: Reza
full_name: Zamani, Reza
last_name: Zamani
- first_name: Nuria
full_name: García Castelló, Nuria
last_name: García Castelló
- first_name: Grosse
full_name: Stéphane, Grosse
last_name: Stéphane
- first_name: Doris
full_name: Cadavid, Doris
last_name: Cadavid
- first_name: Joan
full_name: Prades, Joan
last_name: Prades
- first_name: Jordi
full_name: Arbiol, Jordi
last_name: Arbiol
- first_name: Andreu
full_name: Cabot, Andreu
last_name: Cabot
citation:
ama: 'Li W, Ibáñez M, Zamani R, et al. Cu2HgSnSe4 nanoparticles: synthesis and thermoelectric
properties. CrystEngComm. 2013;44:8966-8971. doi:10.1039/C3CE41583J'
apa: 'Li, W., Ibáñez, M., Zamani, R., García Castelló, N., Stéphane, G., Cadavid,
D., … Cabot, A. (2013). Cu2HgSnSe4 nanoparticles: synthesis and thermoelectric
properties. CrystEngComm. Royal Society of Chemistry. https://doi.org/10.1039/C3CE41583J'
chicago: 'Li, Wenhua, Maria Ibáñez, Reza Zamani, Nuria García Castelló, Grosse Stéphane,
Doris Cadavid, Joan Prades, Jordi Arbiol, and Andreu Cabot. “Cu2HgSnSe4 Nanoparticles:
Synthesis and Thermoelectric Properties.” CrystEngComm. Royal Society of
Chemistry, 2013. https://doi.org/10.1039/C3CE41583J.'
ieee: 'W. Li et al., “Cu2HgSnSe4 nanoparticles: synthesis and thermoelectric
properties,” CrystEngComm, vol. 44. Royal Society of Chemistry, pp. 8966–8971,
2013.'
ista: 'Li W, Ibáñez M, Zamani R, García Castelló N, Stéphane G, Cadavid D, Prades
J, Arbiol J, Cabot A. 2013. Cu2HgSnSe4 nanoparticles: synthesis and thermoelectric
properties. CrystEngComm. 44, 8966–8971.'
mla: 'Li, Wenhua, et al. “Cu2HgSnSe4 Nanoparticles: Synthesis and Thermoelectric
Properties.” CrystEngComm, vol. 44, Royal Society of Chemistry, 2013, pp.
8966–71, doi:10.1039/C3CE41583J.'
short: W. Li, M. Ibáñez, R. Zamani, N. García Castelló, G. Stéphane, D. Cadavid,
J. Prades, J. Arbiol, A. Cabot, CrystEngComm 44 (2013) 8966–8971.
date_created: 2018-12-11T11:46:07Z
date_published: 2013-09-23T00:00:00Z
date_updated: 2021-01-12T07:52:00Z
day: '23'
doi: 10.1039/C3CE41583J
extern: '1'
fulldoi: https://doi.org/10.1039/C3CE41583J
intvolume: ' 44'
language:
- iso: eng
month: '09'
oa_version: None
page: 8966 - 8971
publication: CrystEngComm
publication_status: published
publisher: Royal Society of Chemistry
publist_id: '7453'
quality_controlled: '1'
status: public
title: 'Cu2HgSnSe4 nanoparticles: synthesis and thermoelectric properties'
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 44
year: '2013'
...
---
_id: '378'
abstract:
- lang: eng
text: Until recently, to prepare nanocrystals of a new material, scientists searched
their shelves for the appropriate molecular precursors, surfactants, and solvents.
They then optimized the reaction conditions for the atoms to self-assemble into
monodisperse nanocrystals (1). This approach is being replaced by a simpler strategy,
in which preformed nanocrystals serve as templates to produce nanoparticles with
a different composition through chemical transformation. On page 964 of this issue,
Oh et al. (2) report a powerful mechanism that allows the composition of oxide
nanoparticles to be transformed in solution and at low temperatures.
article_processing_charge: No
author:
- first_name: Maria
full_name: Ibáñez, Maria
id: 43C61214-F248-11E8-B48F-1D18A9856A87
last_name: Ibáñez
orcid: 0000-0001-5013-2843
- first_name: Andreu
full_name: Cabot, Andreu
last_name: Cabot
citation:
ama: Ibáñez M, Cabot A. All change for nanocrystals. Science. 2013;340(6135):935-936.
doi:10.1126/science.1239221
apa: Ibáñez, M., & Cabot, A. (2013). All change for nanocrystals. Science.
American Association for the Advancement of Science. https://doi.org/10.1126/science.1239221
chicago: Ibáñez, Maria, and Andreu Cabot. “All Change for Nanocrystals.” Science.
American Association for the Advancement of Science, 2013. https://doi.org/10.1126/science.1239221.
ieee: M. Ibáñez and A. Cabot, “All change for nanocrystals,” Science, vol.
340, no. 6135. American Association for the Advancement of Science, pp. 935–936,
2013.
ista: Ibáñez M, Cabot A. 2013. All change for nanocrystals. Science. 340(6135),
935–936.
mla: Ibáñez, Maria, and Andreu Cabot. “All Change for Nanocrystals.” Science,
vol. 340, no. 6135, American Association for the Advancement of Science, 2013,
pp. 935–36, doi:10.1126/science.1239221.
short: M. Ibáñez, A. Cabot, Science 340 (2013) 935–936.
date_created: 2018-12-11T11:46:08Z
date_published: 2013-05-24T00:00:00Z
date_updated: 2021-01-12T07:52:09Z
day: '24'
doi: 10.1126/science.1239221
extern: '1'
fulldoi: https://doi.org/10.1126/science.1239221
intvolume: ' 340'
issue: '6135'
language:
- iso: eng
month: '05'
oa_version: None
page: 935 - 936
publication: Science
publication_status: published
publisher: American Association for the Advancement of Science
publist_id: '7451'
status: public
title: All change for nanocrystals
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 340
year: '2013'
...