том 46 издание 8 страницы 1740-1748

Single-atom catalysts: a new frontier in heterogeneous catalysis.

Тип публикацииJournal Article
Дата публикации2013-07-01
SCImago Q1
Tоп 10% SCImago
WOS Q1
БС1
SJR5.472
CiteScore31.2
Impact factor17.7
ISSN00014842, 15204898
General Chemistry
General Medicine
Краткое описание
Supported metal nanostructures are the most widely used type of heterogeneous catalyst in industrial processes. The size of metal particles is a key factor in determining the performance of such catalysts. In particular, because low-coordinated metal atoms often function as the catalytically active sites, the specific activity per metal atom usually increases with decreasing size of the metal particles. However, the surface free energy of metals increases significantly with decreasing particle size, promoting aggregation of small clusters. Using an appropriate support material that strongly interacts with the metal species prevents this aggregation, creating stable, finely dispersed metal clusters with a high catalytic activity, an approach industry has used for a long time. Nevertheless, practical supported metal catalysts are inhomogeneous and usually consist of a mixture of sizes from nanoparticles to subnanometer clusters. Such heterogeneity not only reduces the metal atom efficiency but also frequently leads to undesired side reactions. It also makes it extremely difficult, if not impossible, to uniquely identify and control the active sites of interest. The ultimate small-size limit for metal particles is the single-atom catalyst (SAC), which contains isolated metal atoms singly dispersed on supports. SACs maximize the efficiency of metal atom use, which is particularly important for supported noble metal catalysts. Moreover, with well-defined and uniform single-atom dispersion, SACs offer great potential for achieving high activity and selectivity. In this Account, we highlight recent advances in preparation, characterization, and catalytic performance of SACs, with a focus on single atoms anchored to metal oxides, metal surfaces, and graphene. We discuss experimental and theoretical studies for a variety of reactions, including oxidation, water gas shift, and hydrogenation. We describe advances in understanding the spatial arrangements and electronic properties of single atoms, as well as their interactions with the support. Single metal atoms on support surfaces provide a unique opportunity to tune active sites and optimize the activity, selectivity, and stability of heterogeneous catalysts, offering the potential for applications in a variety of industrial chemical reactions.
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ГОСТ |
Цитировать
Yang X. et al. Single-atom catalysts: a new frontier in heterogeneous catalysis. // Accounts of Chemical Research. 2013. Vol. 46. No. 8. pp. 1740-1748.
ГОСТ со всеми авторами (до 50) Скопировать
Yang X., Wang A., Qiao B., Li J., Liu J., Zhang T. Single-atom catalysts: a new frontier in heterogeneous catalysis. // Accounts of Chemical Research. 2013. Vol. 46. No. 8. pp. 1740-1748.
RIS |
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TY - JOUR
DO - 10.1021/ar300361m
UR - https://doi.org/10.1021/ar300361m
TI - Single-atom catalysts: a new frontier in heterogeneous catalysis.
T2 - Accounts of Chemical Research
AU - Yang, Xiaofeng
AU - Wang, Aiqin
AU - Qiao, Botao
AU - Li, Jun
AU - Liu, J.
AU - Zhang, Tao
PY - 2013
DA - 2013/07/01
PB - American Chemical Society (ACS)
SP - 1740-1748
IS - 8
VL - 46
PMID - 23815772
SN - 0001-4842
SN - 1520-4898
ER -
BibTex |
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BibTex (до 50 авторов) Скопировать
@article{2013_Yang,
author = {Xiaofeng Yang and Aiqin Wang and Botao Qiao and Jun Li and J. Liu and Tao Zhang},
title = {Single-atom catalysts: a new frontier in heterogeneous catalysis.},
journal = {Accounts of Chemical Research},
year = {2013},
volume = {46},
publisher = {American Chemical Society (ACS)},
month = {jul},
url = {https://doi.org/10.1021/ar300361m},
number = {8},
pages = {1740--1748},
doi = {10.1021/ar300361m}
}
MLA
Цитировать
Yang, Xiaofeng, et al. “Single-atom catalysts: a new frontier in heterogeneous catalysis..” Accounts of Chemical Research, vol. 46, no. 8, Jul. 2013, pp. 1740-1748. https://doi.org/10.1021/ar300361m.
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