活性氧
电子转移
清除
化学
锚固
氧气
纳米技术
光化学
材料科学
生物化学
有机化学
抗氧化剂
结构工程
工程类
作者
Juan Zhang,Sheng Wang,Xingen Lin,Xiaoping Gao,Qiuping Wang,Rui Huang,Yaner Ruan,Haonan Xu,Lin Tian,Ling Chen,Ran Shi,Suowen Xu,Kong Y. Chen,Yuen Wu
标识
DOI:10.1002/ange.202416686
摘要
Regulating appropriate valence states of metal active centers, such as Ce3+/Ce4+ and Mn3+/Mn2+, as well as surface vacancy defects, is crucial for enhancing the catalytic activity of cerium‐based and manganese‐based nanozymes. Drawing inspiration from the efficient substance exchange in rhizobia‐colonized root cells of legumes, we developed a symbiosis nanozyme system with rhizobia‐like nano CeOx clusters robustly anchored onto root‐like Mn3O4 nanosupports (CeOx/Mn3O4). The process of "substance exchange" between Ce and Mn atoms—reminiscent of electron transfer—not only fine‐tunes the metal active sites to achieve optimal Ce3+/Ce4+ and Mn3+/Mn2+ ratios but also enhances the vacancy ratio through interface defect engineering. Additionally, the confinement anchoring of CeOx on Mn3O4 ensures efficient electron transfer in catalytic reactions. The final CeOx/Mn3O4 nanozyme demonstrates potent catalase‐like (CAT‐ like) and superoxide dismutase‐like (SOD‐like) activities, excelling in both chemical settings and cellular environments with high reactive oxygen species (ROS) levels. This research not only unveils a novel material adept at effectively eliminating ROS but also presents an innovative approach for amplifying nanozyme efficacy.
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