材料科学
级联
过氧化物酶
铜
光热治疗
竞赛(生物学)
纳米技术
Atom(片上系统)
财产(哲学)
化学物理
化学工程
冶金
酶
有机化学
化学
计算机科学
生态学
哲学
认识论
嵌入式系统
工程类
生物
作者
Qiushuang Wu,Guoan Zheng,Lihua Li,Li Wang
标识
DOI:10.1002/adfm.202422588
摘要
Abstract Single‐atom nanozymes (SANs) are promising enzyme‐active catalysts due to their maximum atomic utilization. However, it is still a challenge to precisely regulate the single‐atom structure, especially in multimetallic MOFs. Based on the Cu‐N 4 structure of Zn 4 Cu 1 , a cascade competition strategy mediated by a buffer (polydopamine) is proposed for the first time, which induces a one‐step nonthermal reaction to precisely remove the inactive Zn site and adjust the Cu coordination environment. Experimental results and theoretical calculations show that the Cu single‐atom nanozyme with Cu‐N 2 O 2 structure (Cu‐N/O) breaks the strong steric restriction, and the exposed Cu active site can better adsorb H 2 O 2 , making it have peroxidase‐like activity. Compared with traditional bimetallic (Cu 4 Zn 1 ) and monometallic (Cu‐MoF) nanozymes, it has stronger peroxidase‐like catalytic activity and photothermal properties, as well as good photocatalytic activity and extremely strong stability. It is successfully applied to Lateral flow immunoassay to achieve three‐mode ultrasensitive detection of Escherichia coli O157:H7, and the test strips after detection are subjected to broad‐spectrum sterilization treatment.
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