Universal Metal‐Exchange Strategy for Room Temperature Synthesis of Single‐Atom Nanozymes

The high-temperature limitations of single-atom catalysts (SACs) synthesis, primarily thermal aggregation and low metal loadings, are overcome by a novel room-temperature metal-exchange strategy. We leverage the weak Zn─N coordination in high-loading Zn SACs (12.10 wt%, synthesized via controlled ZIF-8 pyrolysis) as a platform for the facile exchange with a broad range of metals (Mn, Fe, Co, Ni, Cu, Ru, Pt, up to 12.67 wt%) and the creation of multi-metallic species. This ambient-temperature approach significantly reduces aggregation, enhancing the exposure of catalytic active sites and delivering superior multi-enzyme-like activities (catalase, peroxidase, oxidase). Our work not only provides a scalable, low-temperature route to high-performance SACs but also reveals crucial insights into the stability of SACs under metal-ion conditions.

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Publication Details

Journal
Angewandte Chemie International Edition
Published
2025-05-23
DOI
https://doi.org/10.1002/anie.202505123
Citations
5
Primary Topic
Advanced Nanomaterials in Catalysis
Type
article
Field-Weighted Citation Impact
2.59

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article

Universal Metal‐Exchange Strategy for Room Temperature Synthesis of Single‐Atom Nanozymes

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5 citations
Angewandte Chemie International Edition
Advanced Nanomaterials in Catalysis
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article

Universal Metal‐Exchange Strategy for Room Temperature Synthesis of Single‐Atom Nanozymes

Zezhong Huang, Jie Zhang, Zhijun Huang, Bolong Xu, Qingyuan Wu, Huiyu Liu
article en
5 citations

Abstract

The high-temperature limitations of single-atom catalysts (SACs) synthesis, primarily thermal aggregation and low metal loadings, are overcome by a novel room-temperature metal-exchange strategy. We leverage the weak Zn─N coordination in high-loading Zn SACs (12.10 wt%, synthesized via controlled ZIF-8 pyrolysis) as a platform for the facile exchange with a broad range of metals (Mn, Fe, Co, Ni, Cu, Ru, Pt, up to 12.67 wt%) and the creation of multi-metallic species. This ambient-temperature approach significantly reduces aggregation, enhancing the exposure of catalytic active sites and delivering superior multi-enzyme-like activities (catalase, peroxidase, oxidase). Our work not only provides a scalable, low-temperature route to high-performance SACs but also reveals crucial insights into the stability of SACs under metal-ion conditions.

Angewandte Chemie International EditionVol. 64(31)
Chinese Academy of Sciences (CN), Ningbo Institute of Industrial Technology (CN), Beijing University of Chemical Technology (CN)
National Natural Science Foundation of China, Beijing University of Chemical Technology, Beijing Nova Program, National Key Research and Development Program of China, Fundamental Research Funds for the Central Universities, National Science Fund for Distinguished Young Scholars
Life in Land
Openalex Percentile: Top 10%
Advanced Nanomaterials in Catalysis
2.59
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