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e(g) occupancy as an effective descriptor for the catalytic activity of perovskite oxide-based peroxidase mimics
A peroxidase catalyzes the oxidation of a substrate with a peroxide. The search for peroxidase-like and other enzyme-like nanomaterials (called nanozymes) mainly relies on trial-and-error strategies, due to the lack of predictive descriptors. To fill this gap, here we investigate the occupancy of e(...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6370761/ https://www.ncbi.nlm.nih.gov/pubmed/30741958 http://dx.doi.org/10.1038/s41467-019-08657-5 |
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author | Wang, Xiaoyu Gao, Xuejiao J. Qin, Li Wang, Changda Song, Li Zhou, Yong-Ning Zhu, Guoyin Cao, Wen Lin, Shichao Zhou, Liqi Wang, Kang Zhang, Huigang Jin, Zhong Wang, Peng Gao, Xingfa Wei, Hui |
author_facet | Wang, Xiaoyu Gao, Xuejiao J. Qin, Li Wang, Changda Song, Li Zhou, Yong-Ning Zhu, Guoyin Cao, Wen Lin, Shichao Zhou, Liqi Wang, Kang Zhang, Huigang Jin, Zhong Wang, Peng Gao, Xingfa Wei, Hui |
author_sort | Wang, Xiaoyu |
collection | PubMed |
description | A peroxidase catalyzes the oxidation of a substrate with a peroxide. The search for peroxidase-like and other enzyme-like nanomaterials (called nanozymes) mainly relies on trial-and-error strategies, due to the lack of predictive descriptors. To fill this gap, here we investigate the occupancy of e(g) orbitals as a possible descriptor for the peroxidase-like activity of transition metal oxide (including perovskite oxide) nanozymes. Both experimental measurements and density functional theory calculations reveal a volcano relationship between the e(g) occupancy and nanozymes’ activity, with the highest peroxidase-like activities corresponding to e(g) occupancies of ~1.2. LaNiO(3-δ), optimized based on the e(g) occupancy, exhibits an activity one to two orders of magnitude higher than that of other representative peroxidase-like nanozymes. This study shows that the e(g) occupancy is a predictive descriptor to guide the design of peroxidase-like nanozymes; in addition, it provides detailed insight into the catalytic mechanism of peroxidase-like nanozymes. |
format | Online Article Text |
id | pubmed-6370761 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-63707612019-02-13 e(g) occupancy as an effective descriptor for the catalytic activity of perovskite oxide-based peroxidase mimics Wang, Xiaoyu Gao, Xuejiao J. Qin, Li Wang, Changda Song, Li Zhou, Yong-Ning Zhu, Guoyin Cao, Wen Lin, Shichao Zhou, Liqi Wang, Kang Zhang, Huigang Jin, Zhong Wang, Peng Gao, Xingfa Wei, Hui Nat Commun Article A peroxidase catalyzes the oxidation of a substrate with a peroxide. The search for peroxidase-like and other enzyme-like nanomaterials (called nanozymes) mainly relies on trial-and-error strategies, due to the lack of predictive descriptors. To fill this gap, here we investigate the occupancy of e(g) orbitals as a possible descriptor for the peroxidase-like activity of transition metal oxide (including perovskite oxide) nanozymes. Both experimental measurements and density functional theory calculations reveal a volcano relationship between the e(g) occupancy and nanozymes’ activity, with the highest peroxidase-like activities corresponding to e(g) occupancies of ~1.2. LaNiO(3-δ), optimized based on the e(g) occupancy, exhibits an activity one to two orders of magnitude higher than that of other representative peroxidase-like nanozymes. This study shows that the e(g) occupancy is a predictive descriptor to guide the design of peroxidase-like nanozymes; in addition, it provides detailed insight into the catalytic mechanism of peroxidase-like nanozymes. Nature Publishing Group UK 2019-02-11 /pmc/articles/PMC6370761/ /pubmed/30741958 http://dx.doi.org/10.1038/s41467-019-08657-5 Text en © The Author(s) 2019 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/. |
spellingShingle | Article Wang, Xiaoyu Gao, Xuejiao J. Qin, Li Wang, Changda Song, Li Zhou, Yong-Ning Zhu, Guoyin Cao, Wen Lin, Shichao Zhou, Liqi Wang, Kang Zhang, Huigang Jin, Zhong Wang, Peng Gao, Xingfa Wei, Hui e(g) occupancy as an effective descriptor for the catalytic activity of perovskite oxide-based peroxidase mimics |
title | e(g) occupancy as an effective descriptor for the catalytic activity of perovskite oxide-based peroxidase mimics |
title_full | e(g) occupancy as an effective descriptor for the catalytic activity of perovskite oxide-based peroxidase mimics |
title_fullStr | e(g) occupancy as an effective descriptor for the catalytic activity of perovskite oxide-based peroxidase mimics |
title_full_unstemmed | e(g) occupancy as an effective descriptor for the catalytic activity of perovskite oxide-based peroxidase mimics |
title_short | e(g) occupancy as an effective descriptor for the catalytic activity of perovskite oxide-based peroxidase mimics |
title_sort | e(g) occupancy as an effective descriptor for the catalytic activity of perovskite oxide-based peroxidase mimics |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6370761/ https://www.ncbi.nlm.nih.gov/pubmed/30741958 http://dx.doi.org/10.1038/s41467-019-08657-5 |
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