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Boosting the performance of single-atom catalysts via external electric field polarization

Single-atom catalysts represent a unique catalytic system with high atomic utilization and tunable reaction pathway. Despite current successes in their optimization and tailoring through structural and synthetic innovations, there is a lack of dynamic modulation approach for the single-atom catalysi...

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Autores principales: Pan, Yanghang, Wang, Xinzhu, Zhang, Weiyang, Tang, Lingyu, Mu, Zhangyan, Liu, Cheng, Tian, Bailin, Fei, Muchun, Sun, Yamei, Su, Huanhuan, Gao, Libo, Wang, Peng, Duan, Xiangfeng, Ma, Jing, Ding, Mengning
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9163078/
https://www.ncbi.nlm.nih.gov/pubmed/35654804
http://dx.doi.org/10.1038/s41467-022-30766-x
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author Pan, Yanghang
Wang, Xinzhu
Zhang, Weiyang
Tang, Lingyu
Mu, Zhangyan
Liu, Cheng
Tian, Bailin
Fei, Muchun
Sun, Yamei
Su, Huanhuan
Gao, Libo
Wang, Peng
Duan, Xiangfeng
Ma, Jing
Ding, Mengning
author_facet Pan, Yanghang
Wang, Xinzhu
Zhang, Weiyang
Tang, Lingyu
Mu, Zhangyan
Liu, Cheng
Tian, Bailin
Fei, Muchun
Sun, Yamei
Su, Huanhuan
Gao, Libo
Wang, Peng
Duan, Xiangfeng
Ma, Jing
Ding, Mengning
author_sort Pan, Yanghang
collection PubMed
description Single-atom catalysts represent a unique catalytic system with high atomic utilization and tunable reaction pathway. Despite current successes in their optimization and tailoring through structural and synthetic innovations, there is a lack of dynamic modulation approach for the single-atom catalysis. Inspired by the electrostatic interaction within specific natural enzymes, here we show the performance of model single-atom catalysts anchored on two-dimensional atomic crystals can be systematically and efficiently tuned by oriented external electric fields. Superior electrocatalytic performance have been achieved in single-atom catalysts under electrostatic modulations. Theoretical investigations suggest a universal “onsite electrostatic polarization” mechanism, in which electrostatic fields significantly polarize charge distributions at the single-atom sites and alter the kinetics of the rate determining steps, leading to boosted reaction performances. Such field-induced on-site polarization offers a unique strategy for simulating the catalytic processes in natural enzyme systems with quantitative, precise and dynamic external electric fields.
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spelling pubmed-91630782022-06-05 Boosting the performance of single-atom catalysts via external electric field polarization Pan, Yanghang Wang, Xinzhu Zhang, Weiyang Tang, Lingyu Mu, Zhangyan Liu, Cheng Tian, Bailin Fei, Muchun Sun, Yamei Su, Huanhuan Gao, Libo Wang, Peng Duan, Xiangfeng Ma, Jing Ding, Mengning Nat Commun Article Single-atom catalysts represent a unique catalytic system with high atomic utilization and tunable reaction pathway. Despite current successes in their optimization and tailoring through structural and synthetic innovations, there is a lack of dynamic modulation approach for the single-atom catalysis. Inspired by the electrostatic interaction within specific natural enzymes, here we show the performance of model single-atom catalysts anchored on two-dimensional atomic crystals can be systematically and efficiently tuned by oriented external electric fields. Superior electrocatalytic performance have been achieved in single-atom catalysts under electrostatic modulations. Theoretical investigations suggest a universal “onsite electrostatic polarization” mechanism, in which electrostatic fields significantly polarize charge distributions at the single-atom sites and alter the kinetics of the rate determining steps, leading to boosted reaction performances. Such field-induced on-site polarization offers a unique strategy for simulating the catalytic processes in natural enzyme systems with quantitative, precise and dynamic external electric fields. Nature Publishing Group UK 2022-06-02 /pmc/articles/PMC9163078/ /pubmed/35654804 http://dx.doi.org/10.1038/s41467-022-30766-x Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Pan, Yanghang
Wang, Xinzhu
Zhang, Weiyang
Tang, Lingyu
Mu, Zhangyan
Liu, Cheng
Tian, Bailin
Fei, Muchun
Sun, Yamei
Su, Huanhuan
Gao, Libo
Wang, Peng
Duan, Xiangfeng
Ma, Jing
Ding, Mengning
Boosting the performance of single-atom catalysts via external electric field polarization
title Boosting the performance of single-atom catalysts via external electric field polarization
title_full Boosting the performance of single-atom catalysts via external electric field polarization
title_fullStr Boosting the performance of single-atom catalysts via external electric field polarization
title_full_unstemmed Boosting the performance of single-atom catalysts via external electric field polarization
title_short Boosting the performance of single-atom catalysts via external electric field polarization
title_sort boosting the performance of single-atom catalysts via external electric field polarization
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9163078/
https://www.ncbi.nlm.nih.gov/pubmed/35654804
http://dx.doi.org/10.1038/s41467-022-30766-x
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