化学
双金属片
合理设计
吸附
基质(水族馆)
甲酰胺
纳米技术
密度泛函理论
催化作用
组合化学
杀虫剂
金属有机骨架
碳纤维
设计要素和原则
鉴定(生物学)
人工酶
生物传感器
作者
Yanyue Chen,Peng Wei,Lin-Ru Bai,Huan Cheng,Hongling Tao,Yuan Wu,Jian Tang,Yunhui Yang,Rong Hu
标识
DOI:10.1021/acs.analchem.6c00883
摘要
Herein, by formamide self-condensation, an innovative Fe-Cu dual-atom nanozyme (FeCu-N-C) is presented, engineered with adjacent metal sites within a nitrogen-doped carbon scaffold, that exhibits synergistically enhanced peroxidase-, oxidase-, and laccase-like activities. This multienzymatic performance far exceeds that of single-atom Fe-N-C and Cu-N-C controls. Density functional theory (DFT) calculations reveal that the proximity of Cu sites induces an upshift in the Fe d-band center from -1.52 eV to -0.88 eV, optimizing substrate adsorption and providing a mechanistic rationale for the observed catalytic synergy. Leveraging this multienzymatic platform, we developed a single-material colorimetric sensor array capable of discriminating five distinct pesticides in complex matrices. These pesticides differentially modulate the triple-mimetic activities through compound-specific interaction mechanisms, as validated by DFT analysis. Integrated with an artificial neural network (ANN), the system achieved 100% identification accuracy. This work establishes a pioneering paradigm for the rational design of multienzyme mimics and underscores their potential for high-precision environmental monitoring.
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