---
OA_type: closed access
_id: '22965'
abstract:
- lang: eng
text: Manganese-based aqueous zinc-ion batteries (AZIBs) have emerged as promising
candidates for large-scale energy storage owing to their low cost, intrinsic safety,
and the abundance of constituent elements. However, their practical deployment
is still restricted by severe capacity fading caused by Jahn–Teller-induced structural
instability and sluggish Zn2+ transport in the cathode. Although surface coating,
heteroatom doping, and structural regulation have been widely explored to improve
Mn-based cathodes, these approaches may suffer from increased interfacial resistance,
compositional complexity, or limited control over the intrinsic electronic structure.
In this context, oxygen-vacancy engineering offers a more direct route to modulate
local coordination environments and accelerate Zn2+/H+ storage kinetics. Herein,
lattice-level defect engineering of a dense Mn2O3 host is achieved through a metal–organic
framework-derived synthesis followed by mild secondary annealing. The introduced
oxygen vacancies regulate the local electronic structure and coordination environment,
thereby facilitating Zn2+ diffusion, accelerating charge-transfer kinetics, and
improving electrochemical reversibility. Combined experimental and theoretical
investigations further show that oxygen-vacancy engineering enhances electronic
conductivity, reduces the Zn2+ migration barrier, and enables a reversible dual-ion
storage mechanism involving both H+ and Zn2+. Benefiting from these effects, the
Zn‖Vo-Mn2O3 battery delivers a high specific capacity of 359 mAh g−1 at 0.3 A
g−1, maintains 210 mAh g−1 at 6 A g−1, and retains 74.3% of its capacity after
10 000 cycles at 12 A g−1 after only 150 s of initial preconditioning. This work
highlights oxygen-vacancy engineering as an effective route to enhancing the kinetic
and structural stability of Mn-based cathodes for advanced AZIBs.
acknowledgement: 'Ao Y. acknowledges financial support from the China Scholarship
Council (No. 202208320041), the National Natural Science Foundation of China (No.
22475231), and the Shenzhen Science and Technology Planning Project (No. KJZD20230923115227054).
The XAS experiments were performed in collaboration with ALBA staff at the NOTOS
beamline of ALBA Synchrotron (experiment ID: 2024028418), Barcelona, Spain. JL is
a Serra Húnter Fellow and is grateful to the Academia Excellence program (Generalitat
de Catalunya) and to the project PID2024-156765OB-C21 funded by MICIU/AEI/10.13039/501100011033
and the European Regional Development Fund (FEDER), and to the María de Maeztu Units
of Excellence Programme CEX2023-001300 M, funded by MCIN/AEI/10.13039/501100011033.'
article_processing_charge: No
article_type: original
author:
- first_name: Ao
full_name: Yu, Ao
last_name: Yu
- first_name: Xingqi
full_name: Chang, Xingqi
last_name: Chang
- first_name: Xuan
full_name: Lu, Xuan
last_name: Lu
- first_name: Ren
full_name: He, Ren
id: 366c4efa-f61c-11f0-808b-d12a4547ac69
last_name: He
- first_name: Linlin
full_name: Yang, Linlin
last_name: Yang
- first_name: Jiali
full_name: Chai, Jiali
last_name: Chai
- first_name: Xiaoyu
full_name: Bi, Xiaoyu
last_name: Bi
- first_name: Jesús
full_name: Chacón-Borrero, Jesús
last_name: Chacón-Borrero
- first_name: Karol V.
full_name: Mejia-Centeno, Karol V.
last_name: Mejia-Centeno
- first_name: Jordi
full_name: Llorca, Jordi
last_name: Llorca
- first_name: Eduardo
full_name: Villalobos-Portillo, Eduardo
last_name: Villalobos-Portillo
- first_name: Qirong
full_name: Liu, Qirong
last_name: Liu
- first_name: Jian
full_name: Shang, Jian
last_name: Shang
- first_name: Andreu
full_name: Cabot, Andreu
last_name: Cabot
citation:
ama: Yu A, Chang X, Lu X, et al. Lattice-level defect engineering of dense Mn2O3
hosts unlocks fast H+/Zn2+ storage and long-life aqueous zinc-ion batteries. Journal
of Materials Chemistry A. 2026. doi:10.1039/d6ta05844b
apa: Yu, A., Chang, X., Lu, X., He, R., Yang, L., Chai, J., … Cabot, A. (2026).
Lattice-level defect engineering of dense Mn2O3 hosts unlocks fast H+/Zn2+ storage
and long-life aqueous zinc-ion batteries. Journal of Materials Chemistry A.
Royal Society of Chemistry. https://doi.org/10.1039/d6ta05844b
chicago: Yu, Ao, Xingqi Chang, Xuan Lu, Ren He, Linlin Yang, Jiali Chai, Xiaoyu
Bi, et al. “Lattice-Level Defect Engineering of Dense Mn2O3 Hosts Unlocks Fast
H+/Zn2+ Storage and Long-Life Aqueous Zinc-Ion Batteries.” Journal of Materials
Chemistry A. Royal Society of Chemistry, 2026. https://doi.org/10.1039/d6ta05844b.
ieee: A. Yu et al., “Lattice-level defect engineering of dense Mn2O3 hosts
unlocks fast H+/Zn2+ storage and long-life aqueous zinc-ion batteries,” Journal
of Materials Chemistry A. Royal Society of Chemistry, 2026.
ista: Yu A, Chang X, Lu X, He R, Yang L, Chai J, Bi X, Chacón-Borrero J, Mejia-Centeno
KV, Llorca J, Villalobos-Portillo E, Liu Q, Shang J, Cabot A. 2026. Lattice-level
defect engineering of dense Mn2O3 hosts unlocks fast H+/Zn2+ storage and long-life
aqueous zinc-ion batteries. Journal of Materials Chemistry A.
mla: Yu, Ao, et al. “Lattice-Level Defect Engineering of Dense Mn2O3 Hosts Unlocks
Fast H+/Zn2+ Storage and Long-Life Aqueous Zinc-Ion Batteries.” Journal of
Materials Chemistry A, Royal Society of Chemistry, 2026, doi:10.1039/d6ta05844b.
short: A. Yu, X. Chang, X. Lu, R. He, L. Yang, J. Chai, X. Bi, J. Chacón-Borrero,
K.V. Mejia-Centeno, J. Llorca, E. Villalobos-Portillo, Q. Liu, J. Shang, A. Cabot,
Journal of Materials Chemistry A (2026).
das_tickbox: '1'
dataavailabilitystatement: 'The data that support the findings of this study are available
within the manuscript and the corresponding supplementary information (SI). Data
are available upon request from the authors. Supplementary information is available.
See DOI: https://doi.org/10.1039/d6ta05844b.'
date_created: 2026-09-20T22:01:48Z
date_published: 2026-08-31T00:00:00Z
date_updated: 2026-10-06T10:34:27Z
day: '31'
department:
- _id: MaIb
doi: 10.1039/d6ta05844b
fulldoi: https://doi.org/10.1039/d6ta05844b
language:
- iso: eng
month: '08'
oa_version: None
publication: Journal of Materials Chemistry A
publication_identifier:
eissn:
- 2050-7496
issn:
- 2050-7488
publication_status: epub_ahead
publisher: Royal Society of Chemistry
quality_controlled: '1'
researchdata_availability: no
scopus_import: '1'
status: public
supplementarymaterial: yes
title: Lattice-level defect engineering of dense Mn2O3 hosts unlocks fast H+/Zn2+
storage and long-life aqueous zinc-ion batteries
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
year: '2026'
...
---
OA_type: closed access
_id: '364'
abstract:
- lang: eng
text: The development of highly active, low cost and stable electrocatalysts for
direct alcohol fuel cells remains a critical challenge. While Pd2Sn has been reported
as an excellent catalyst for the ethanol oxidation reaction (EOR), here we present
DFT analysis results showing the (100) and (001) facets of orthorhombic Pd2Sn
to be more favourable for the EOR than (010). Accordingly, using tri-n-octylphosphine,
oleylamine (OLA) and methylamine hydrochloride as size and shape directing agents,
we produced colloidal Pd2Sn nanorods (NRs) grown in the [010] direction. Such
Pd2Sn NRs, supported on graphitic carbon, showed excellent performance and stability
as an anode electrocatalyst for the EOR in alkaline media, exhibiting 3 times
and 10 times higher EOR current densities than that of Pd2Sn and Pd nanospheres,
respectively. We associate this improved performance with the favourable faceting
of the NRs.
article_processing_charge: No
article_type: original
author:
- first_name: Zhishan
full_name: Luo, Zhishan
last_name: Luo
- first_name: Jianmin
full_name: Lu, Jianmin
last_name: Lu
- first_name: Cristina
full_name: Flox, Cristina
last_name: Flox
- first_name: Raquel
full_name: Nafria, Raquel
last_name: Nafria
- first_name: Aziz
full_name: Genç, Aziz
last_name: Genç
- first_name: Jordi
full_name: Arbiol, Jordi
last_name: Arbiol
- first_name: Jordi
full_name: Llorca, Jordi
last_name: Llorca
- first_name: Maria
full_name: Ibanez Sabate, Maria
id: 43C61214-F248-11E8-B48F-1D18A9856A87
last_name: Ibanez Sabate
orcid: 0000-0001-5013-2843
- first_name: Joan
full_name: Morante, Joan
last_name: Morante
- first_name: Andreu
full_name: Cabot, Andreu
last_name: Cabot
citation:
ama: Luo Z, Lu J, Flox C, et al. Pd2Sn [010] nanorods as a highly active and stable
ethanol oxidation catalyst. Journal of Materials Chemistry A. 2016;4(42):16706-16713.
doi:10.1039/c6ta06430b
apa: Luo, Z., Lu, J., Flox, C., Nafria, R., Genç, A., Arbiol, J., … Cabot, A. (2016).
Pd2Sn [010] nanorods as a highly active and stable ethanol oxidation catalyst.
Journal of Materials Chemistry A. Royal Society of Chemistry. https://doi.org/10.1039/c6ta06430b
chicago: Luo, Zhishan, Jianmin Lu, Cristina Flox, Raquel Nafria, Aziz Genç, Jordi
Arbiol, Jordi Llorca, Maria Ibáñez, Joan Morante, and Andreu Cabot. “Pd2Sn [010]
Nanorods as a Highly Active and Stable Ethanol Oxidation Catalyst.” Journal
of Materials Chemistry A. Royal Society of Chemistry, 2016. https://doi.org/10.1039/c6ta06430b.
ieee: Z. Luo et al., “Pd2Sn [010] nanorods as a highly active and stable
ethanol oxidation catalyst,” Journal of Materials Chemistry A, vol. 4,
no. 42. Royal Society of Chemistry, pp. 16706–16713, 2016.
ista: Luo Z, Lu J, Flox C, Nafria R, Genç A, Arbiol J, Llorca J, Ibáñez M, Morante
J, Cabot A. 2016. Pd2Sn [010] nanorods as a highly active and stable ethanol oxidation
catalyst. Journal of Materials Chemistry A. 4(42), 16706–16713.
mla: Luo, Zhishan, et al. “Pd2Sn [010] Nanorods as a Highly Active and Stable Ethanol
Oxidation Catalyst.” Journal of Materials Chemistry A, vol. 4, no. 42,
Royal Society of Chemistry, 2016, pp. 16706–13, doi:10.1039/c6ta06430b.
short: Z. Luo, J. Lu, C. Flox, R. Nafria, A. Genç, J. Arbiol, J. Llorca, M. Ibáñez,
J. Morante, A. Cabot, Journal of Materials Chemistry A 4 (2016) 16706–16713.
date_created: 2018-12-11T11:46:02Z
date_published: 2016-10-05T00:00:00Z
date_updated: 2026-05-13T14:52:40Z
day: '05'
doi: 10.1039/c6ta06430b
extern: '1'
fulldoi: https://doi.org/10.1039/c6ta06430b
intvolume: ' 4'
issue: '42'
language:
- iso: eng
month: '10'
oa_version: None
page: 16706 - 16713
publication: Journal of Materials Chemistry A
publication_identifier:
eissn:
- ' 2050-7496'
issn:
- 2050-7488
publication_status: published
publisher: Royal Society of Chemistry
publist_id: '7465'
quality_controlled: '1'
scopus_import: '1'
status: public
title: Pd2Sn [010] nanorods as a highly active and stable ethanol oxidation catalyst
type: journal_article
user_id: ba8df636-2132-11f1-aed0-ed93e2281fdd
volume: 4
year: '2016'
...
---
OA_type: closed access
_id: '370'
abstract:
- lang: eng
text: Copper-based chalcogenides that comprise abundant, low-cost, and environmental
friendly elements are excellent materials for a number of energy conversion applications,
including photovoltaics, photocatalysis, and thermoelectrics (TE). In such applications,
the use of solution-processed nanocrystals (NCs) to produce thin films or bulk
nanomaterials has associated several potential advantages, such as high material
yield and throughput, and composition control with unmatched spatial resolution
and cost. Here we report on the production of Cu3SbSe4 (CASe) NCs with tuned amounts
of Sn and Bi dopants. After proper ligand removal, as monitored by nuclear magnetic
resonance and infrared spectroscopy, these NCs were used to produce dense CASe
bulk nanomaterials for solid state TE energy conversion. By adjusting the amount
of extrinsic dopants, dimensionless TE figures of merit (ZT) up to 1.26 at 673
K were reached. Such high ZT values are related to an optimized carrier concentration
by Sn doping, a minimized lattice thermal conductivity due to efficient phonon
scattering at point defects and grain boundaries, and to an increase of the Seebeck
coefficient obtained by a modification of the electronic band structure with Bi
doping. Nanomaterials were further employed to fabricate ring-shaped TE generators
to be coupled to hot pipes, which provided 20 mV and 1 mW per TE element when
exposed to a 160 °C temperature gradient. The simple design and good thermal contact
associated with the ring geometry and the potential low cost of the material solution
processing may allow the fabrication of TE generators with short payback times.
article_processing_charge: No
article_type: original
author:
- first_name: Yu
full_name: Liu, Yu
id: 2A70014E-F248-11E8-B48F-1D18A9856A87
last_name: Liu
orcid: 0000-0001-7313-6740
- first_name: Gregorio
full_name: García, Gregorio
last_name: García
- first_name: Silvia
full_name: Ortega, Silvia
last_name: Ortega
- first_name: Doris
full_name: Cadavid, Doris
last_name: Cadavid
- first_name: Pablo
full_name: Palacios, Pablo
last_name: Palacios
- first_name: Jinyu
full_name: Lu, Jinyu
last_name: Lu
- first_name: Maria
full_name: Ibanez, Maria
last_name: Ibanez
- first_name: Lili
full_name: Xi, Lili
last_name: Xi
- first_name: Jonathan
full_name: De Roo, Jonathan
last_name: De Roo
- first_name: Antonio
full_name: López, Antonio
last_name: López
- first_name: Sara
full_name: Márti Sánchez, Sara
last_name: Márti Sánchez
- first_name: Ignasi
full_name: Cabezas, Ignasi
last_name: Cabezas
- first_name: Maria
full_name: De La Mata, Maria
last_name: De La Mata
- first_name: Zhishan
full_name: Luo, Zhishan
last_name: Luo
- first_name: Chaocha
full_name: Dun, Chaocha
last_name: Dun
- first_name: Oleksandr
full_name: Dobrozhan, Oleksandr
last_name: Dobrozhan
- first_name: David
full_name: Carroll, David
last_name: Carroll
- first_name: Wenging
full_name: Zhang, Wenging
last_name: Zhang
- first_name: José
full_name: Martins, José
last_name: Martins
- first_name: Mksym
full_name: Kovalenko, Mksym
last_name: Kovalenko
- first_name: Jordi
full_name: Arbiol, Jordi
last_name: Arbiol
- first_name: German
full_name: Noriega, German
last_name: Noriega
- first_name: Jiming
full_name: Song, Jiming
last_name: Song
- first_name: Perla
full_name: Wahnón, Perla
last_name: Wahnón
- first_name: Andreu
full_name: Cabot, Andreu
last_name: Cabot
citation:
ama: Liu Y, García G, Ortega S, et al. Solution based synthesis and processing of
Sn and Bi doped Cu inf 3 inf SbSe inf 4 inf nanocrystals nanomaterials and ring
shaped thermoelectric generators. Journal of Materials Chemistry A. 2016;5(6):2592-2602.
doi:10.1039/C6TA08467B
apa: Liu, Y., García, G., Ortega, S., Cadavid, D., Palacios, P., Lu, J., … Cabot,
A. (2016). Solution based synthesis and processing of Sn and Bi doped Cu inf 3
inf SbSe inf 4 inf nanocrystals nanomaterials and ring shaped thermoelectric generators.
Journal of Materials Chemistry A. Royal Society of Chemistry. https://doi.org/10.1039/C6TA08467B
chicago: Liu, Yu, Gregorio García, Silvia Ortega, Doris Cadavid, Pablo Palacios,
Jinyu Lu, Maria Ibanez, et al. “Solution Based Synthesis and Processing of Sn
and Bi Doped Cu Inf 3 Inf SbSe Inf 4 Inf Nanocrystals Nanomaterials and Ring Shaped
Thermoelectric Generators.” Journal of Materials Chemistry A. Royal Society
of Chemistry, 2016. https://doi.org/10.1039/C6TA08467B.
ieee: Y. Liu et al., “Solution based synthesis and processing of Sn and Bi
doped Cu inf 3 inf SbSe inf 4 inf nanocrystals nanomaterials and ring shaped thermoelectric
generators,” Journal of Materials Chemistry A, vol. 5, no. 6. Royal Society
of Chemistry, pp. 2592–2602, 2016.
ista: Liu Y, García G, Ortega S, Cadavid D, Palacios P, Lu J, Ibanez M, Xi L, De
Roo J, López A, Márti Sánchez S, Cabezas I, De La Mata M, Luo Z, Dun C, Dobrozhan
O, Carroll D, Zhang W, Martins J, Kovalenko M, Arbiol J, Noriega G, Song J, Wahnón
P, Cabot A. 2016. Solution based synthesis and processing of Sn and Bi doped Cu
inf 3 inf SbSe inf 4 inf nanocrystals nanomaterials and ring shaped thermoelectric
generators. Journal of Materials Chemistry A. 5(6), 2592–2602.
mla: Liu, Yu, et al. “Solution Based Synthesis and Processing of Sn and Bi Doped
Cu Inf 3 Inf SbSe Inf 4 Inf Nanocrystals Nanomaterials and Ring Shaped Thermoelectric
Generators.” Journal of Materials Chemistry A, vol. 5, no. 6, Royal Society
of Chemistry, 2016, pp. 2592–602, doi:10.1039/C6TA08467B.
short: Y. Liu, G. García, S. Ortega, D. Cadavid, P. Palacios, J. Lu, M. Ibanez,
L. Xi, J. De Roo, A. López, S. Márti Sánchez, I. Cabezas, M. De La Mata, Z. Luo,
C. Dun, O. Dobrozhan, D. Carroll, W. Zhang, J. Martins, M. Kovalenko, J. Arbiol,
G. Noriega, J. Song, P. Wahnón, A. Cabot, Journal of Materials Chemistry A 5 (2016)
2592–2602.
date_created: 2018-12-11T11:46:05Z
date_published: 2016-12-19T00:00:00Z
date_updated: 2026-05-13T13:12:04Z
day: '19'
doi: 10.1039/C6TA08467B
extern: '1'
fulldoi: https://doi.org/10.1039/C6TA08467B
intvolume: ' 5'
issue: '6'
language:
- iso: eng
month: '12'
oa_version: None
page: 2592 - 2602
publication: Journal of Materials Chemistry A
publication_identifier:
eissn:
- 2050-7496
issn:
- 2050-7488
publication_status: published
publisher: Royal Society of Chemistry
publist_id: '7457'
quality_controlled: '1'
scopus_import: '1'
status: public
title: Solution based synthesis and processing of Sn and Bi doped Cu inf 3 inf SbSe
inf 4 inf nanocrystals nanomaterials and ring shaped thermoelectric generators
type: journal_article
user_id: ba8df636-2132-11f1-aed0-ed93e2281fdd
volume: 5
year: '2016'
...
---
_id: '355'
abstract:
- lang: eng
text: 'We report on the photocatalytic hydrogen evolution under full-arc light irradiation
of CuIn1-xGaxS2 wurtzite nanocrystals in the presence of SO3 2- and S2- as sacrificial
reagents. We analyzed the hydrogen generation rate as a function of the Ga content
and associated it with the energy band positions. For photocatalytic water splitting,
the CuInS2 bandgap is slightly too low to efficiently overcome the reaction over-potential.
The presence of Ga shifts up the CuInS2 conduction band edge providing a larger
driving force for photogenerated carriers to activate the water splitting reduction
reaction. The larger the Ga content, the more energetically favorable the electron
injection, and thus a more efficient use of the photogenerated carriers is reached.
However, the band gap increase associated with the Ga incorporation reduces the
concentration of photogenerated carriers available for water splitting, and consequently
a lower hydrogen conversion rate is obtained for very high Ga contents. The optimum
Ga concentration was experimentally found at CuIn0.3Ga0.7S2. '
acknowledgement: "The research was supported by the European Regional Development\r\nFunds
(ERDF, “FEDER Programa Competitivitat de\r\nCatalunya 2007-2013”) and the Framework
7 program under\r\nproject SCALENANO (FP7-NMP-ENERGY-2011-284486)."
article_processing_charge: No
article_type: original
author:
- first_name: Xuelian
full_name: Yu, Xuelian
last_name: Yu
- first_name: Xiaoqiang
full_name: An, Xiaoqiang
last_name: An
- first_name: Alexey
full_name: Shavel, Alexey
last_name: Shavel
- 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: Yu X, An X, Shavel A, Ibáñez M, Cabot A. The effect of the Ga content on the
photocatalytic hydrogen evolution of CuIn1-xGaxS2 nanocrystals. Journal of
Materials Chemistry A. 2014;2(31):12317-12322. doi:10.1039/c4ta01315h
apa: Yu, X., An, X., Shavel, A., Ibáñez, M., & Cabot, A. (2014). The effect
of the Ga content on the photocatalytic hydrogen evolution of CuIn1-xGaxS2 nanocrystals.
Journal of Materials Chemistry A. Royal Society of Chemistry. https://doi.org/10.1039/c4ta01315h
chicago: Yu, Xuelian, Xiaoqiang An, Alexey Shavel, Maria Ibáñez, and Andreu Cabot.
“The Effect of the Ga Content on the Photocatalytic Hydrogen Evolution of CuIn1-XGaxS2
Nanocrystals.” Journal of Materials Chemistry A. Royal Society of Chemistry,
2014. https://doi.org/10.1039/c4ta01315h.
ieee: X. Yu, X. An, A. Shavel, M. Ibáñez, and A. Cabot, “The effect of the Ga content
on the photocatalytic hydrogen evolution of CuIn1-xGaxS2 nanocrystals,” Journal
of Materials Chemistry A, vol. 2, no. 31. Royal Society of Chemistry, pp.
12317–12322, 2014.
ista: Yu X, An X, Shavel A, Ibáñez M, Cabot A. 2014. The effect of the Ga content
on the photocatalytic hydrogen evolution of CuIn1-xGaxS2 nanocrystals. Journal
of Materials Chemistry A. 2(31), 12317–12322.
mla: Yu, Xuelian, et al. “The Effect of the Ga Content on the Photocatalytic Hydrogen
Evolution of CuIn1-XGaxS2 Nanocrystals.” Journal of Materials Chemistry A,
vol. 2, no. 31, Royal Society of Chemistry, 2014, pp. 12317–22, doi:10.1039/c4ta01315h.
short: X. Yu, X. An, A. Shavel, M. Ibáñez, A. Cabot, Journal of Materials Chemistry
A 2 (2014) 12317–12322.
date_created: 2018-12-11T11:45:59Z
date_published: 2014-08-21T00:00:00Z
date_updated: 2026-09-09T13:18:50Z
day: '21'
doi: 10.1039/c4ta01315h
extern: '1'
fulldoi: https://doi.org/10.1039/c4ta01315h
intvolume: ' 2'
issue: '31'
language:
- iso: eng
month: '08'
oa_version: None
page: 12317 - 12322
publication: Journal of Materials Chemistry A
publication_identifier:
eissn:
- 2050-7496
issn:
- 2050-7488
publication_status: published
publisher: Royal Society of Chemistry
publist_id: '7471'
quality_controlled: '1'
status: public
title: The effect of the Ga content on the photocatalytic hydrogen evolution of CuIn1-xGaxS2
nanocrystals
type: journal_article
user_id: 317138e5-6ab7-11ef-aa6d-ffef3953e345
volume: 2
year: '2014'
...