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Heterojunction-Mediated Co-Adjustment of Band Structure and Valence State for Achieving Selective Regulation of Semiconductor Nanozymes.
Huang, Jiahao; Jia, Xiaodan; Wang, Yue; Qiao, Yue; Jiang, Xiue.
Afiliação
  • Huang J; Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun, Jilin, 130022, China.
  • Jia X; School of Applied Chemistry and Engineering, University of Science and Technology of China, Hefei, Anhui, 230026, China.
  • Wang Y; Research Center for Analytical Science, College of Chemistry, Nankai University, Tianjin, 300071, China.
  • Qiao Y; Research Center for Analytical Science, College of Chemistry, Nankai University, Tianjin, 300071, China.
  • Jiang X; Department of Radiology, China-Japan Union Hospital of Jilin University, Changchun, Jilin, 130000, China.
Adv Healthc Mater ; : e2400401, 2024 Apr 12.
Article em En | MEDLINE | ID: mdl-38609000
ABSTRACT
Improving reaction selectivity is the next target for nanozymes to mimic natural enzymes. Currently, the majority of strategies in this field are exclusively applicable to metal-organic-based or organic-based nanozymes, while limited in regulating metal oxide-based semiconductor nanozymes. Herein, taking semiconductor Co3O4 as an example, a heterojunction strategy to precisely regulate nanozyme selectivity by simultaneously regulating three vital factors including band structure, metal valence state, and oxygen vacancy content is proposed. After introducing MnO2 to form Z-scheme heterojunctions with Co3O4 nanoparticles, the catalase (CAT)-like and peroxidase (POD)-like activities of Co3O4 can be precisely regulated since the introduction of MnO2 affects the position of the conduction bands, preserves Co in a higher oxidation state (Co3+), and increases oxygen vacancy content, enabling Co3O4-MnO2 exhibit improved CAT-like activity and reduced POD-like activity. This study proposes a strategy for improving reaction selectivity of Co3O4, which contributes to the development of metal oxide-based semiconductor nanozymes.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article