合理设计
磷酸二酯键
纳米技术
基质(水族馆)
纳米结构
化学
催化作用
工作(物理)
钥匙(锁)
材料科学
设计要素和原则
底物特异性
分子构象
计算机科学
密度泛函理论
作者
Yidan Wang,Feifan Zhang,Zexiang Wang,Ruijie Fu,Jinjie Hou,Mengliu Zhao,Hao Bai,Yunlei Xianyu
出处
期刊:ACS Nano
[American Chemical Society]
日期:2026-04-28
卷期号:20 (18): 13913-13926
被引量:2
标识
DOI:10.1021/acsnano.6c04164
摘要
Nanozymes with multienzyme-like capabilities can function as self-catalytic reactors, exhibiting significant advantages over natural enzymes. However, it is still challenging to develop a general strategy to regulate the multienzyme-like activities of nanozymes and clarify their intricate catalytic mechanisms. Herein, we establish a seed-mediated strategy to modulate the multienzyme-like activities of gold@cerium oxide (Au@CeO 2 ) by altering the morphology of gold seeds. The end-coated nanostructure exhibits superior phosphatase-like (POP-like) activity compared to the core@shell nanostructure. Through structure–activity correlation, we reveal that Lewis acidity (LA) and oxygen-vacancy density serve as key descriptors governing the POP-like activity, synergistically activating the phosphoester substrate and water nucleophile. This work elucidates the mechanisms underlying morphology-dependent catalytic regulation, offering a rational design strategy for developing hydrolase-mimicking nanozymes.
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