Photoexcited Ru single-atomic sites for efficient biomimetic redox catalysis

The unsatisfactory catalytic activity of nanozymes owing to their inefficient electron transfer (ET) is the major challenge in biomimetic catalysis-related biomedical applications. Inspired by the photoelectron transfers in natural photoenzymes, we herein report a photonanozyme of single-atom Ru anc...

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Veröffentlicht in:Proceedings of the National Academy of Sciences - PNAS 2023-05, Vol.120 (21), p.e2220315120-e2220315120
Hauptverfasser: Xu, Weiqing, Zhong, Hong, Wu, Yu, Qin, Ying, Jiao, Lei, Sha, Meng, Su, Rina, Tang, Yinjun, Zheng, Lirong, Hu, Liuyong, Zhang, Shipeng, Beckman, Scott P, Gu, Wenling, Yang, Yong, Guo, Shaojun, Zhu, Chengzhou
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Sprache:eng
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Zusammenfassung:The unsatisfactory catalytic activity of nanozymes owing to their inefficient electron transfer (ET) is the major challenge in biomimetic catalysis-related biomedical applications. Inspired by the photoelectron transfers in natural photoenzymes, we herein report a photonanozyme of single-atom Ru anchored on metal-organic frameworks (UiO-67-Ru) for achieving photoenhanced peroxidase (POD)-like activity. We demonstrate that the atomically dispersed Ru sites can realize high photoelectric conversion efficiency, superior POD-like activity (7.0-fold photoactivity enhancement relative to that of UiO-67), and good catalytic specificity. Both in situ experiments and theoretical calculations reveal that photoelectrons follow the cofactor-mediated ET process of enzymes to promote the production of active intermediates and the release of products, demonstrating more favorable thermodynamics and kinetics in H O reduction. Taking advantage of the unique interaction of the Zr-O-P bond, we establish a UiO-67-Ru-based immunoassay platform for the photoenhanced detection of organophosphorus pesticides.
ISSN:0027-8424
1091-6490
DOI:10.1073/pnas.2220315120