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Breaking the Selectivity Barrier of Single-Atom Nanozymes Through Out-of-Plane Ligand Coordination.


ABSTRACT: Peroxidase (POD)-like nanozymes have emerged as effective alternatives to natural enzymes owing to their stability and cost-effectiveness in biosensors. In particular, single-atom nanozymes (SAzymes) featuring Fe-N4 active sites have attracted significant attention for their high catalytic performance. However, their 2D exposed active sites result in limited reaction selectivity and strong pH dependence, restricting their functionality under neutral conditions. This study introduces Ru-centered SAzymes coordinated out-of-plane with chlorine ligands (RuNC_Cl), achieving monofunctional POD-like activity. RuNC_Cl exhibited remarkable POD-like activity, which is 38-fold greater than its catalase (CAT)-like activity, indicating strong suppression of the competing CAT-like reaction. Density functional theory calculations and Bader charge analysis of RuNC_Cl reveal that repulsive forces preventing secondary H2O2 adsorption contribute to an increased energy barrier for the CAT-like reaction. This selective POD-like activity enables the precise detection of multiple biomarkers through a one-pot cascade reaction under near-neutral conditions. This advancement paves the way for the precise regulation of reaction pathways, enhancing the practicality of nanozymes for biosensing and related applications.

SUBMITTER: Park S 

PROVIDER: S-EPMC12464650 | biostudies-literature | 2025 Sep

REPOSITORIES: biostudies-literature

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Breaking the Selectivity Barrier of Single-Atom Nanozymes Through Out-of-Plane Ligand Coordination.

Park Seonhye S   Shim Kyu In KI   Nguyen Phuong Thy PT   Choi Daeeun D   Kim Seongbeen S   Yi Seung Yeop SY   Kim Moon Il MI   Han Jeong Woo JW   Lee Jinwoo J  

Advanced materials (Deerfield Beach, Fla.) 20250706 38


Peroxidase (POD)-like nanozymes have emerged as effective alternatives to natural enzymes owing to their stability and cost-effectiveness in biosensors. In particular, single-atom nanozymes (SAzymes) featuring Fe-N<sub>4</sub> active sites have attracted significant attention for their high catalytic performance. However, their 2D exposed active sites result in limited reaction selectivity and strong pH dependence, restricting their functionality under neutral conditions. This study introduces R  ...[more]

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