化学
催化作用
解聚
氯
辣根过氧化物酶
基质(水族馆)
木质素
单体
密度泛函理论
反应性(心理学)
血红素
无机化学
人工酶
香兰素
催化效率
组合化学
氧化磷酸化
活动站点
木质纤维素生物量
过氧化氢
绿色化学
过氧化物酶
有机化学
氧气
作者
Qifeng Li (585722),Wenzhi Jiang (1923145),Xiaoling Wu (547509),Hongming Lou (1881187),Xueqing Qiu (1465870),Zhixian Li (436532)
出处
期刊:
[Figshare (United Kingdom)]
日期:2025-07-16
标识
DOI:10.1021/acsami.5c06333.s001
摘要
Single-atom nanozymes (SAzymes) precisely emulate enzyme catalytic centers at the atomic level, offering exceptional catalytic efficiency and selectivity. Inspired by the heme structure of natural enzymes, this study introduces chlorine axial coordination into the Fe–N3O single-atom nanozyme, constructing a unique Fe–N3O–Cl catalytic site (Fe–N/O/Cl–C SA). As a result, the Fe–N/O/Cl–C SA demonstrates remarkable peroxidase-like activity toward the substrate 3,3′,5,5′-tetramethylbenzidine (TMB), achieving a catalytic efficiency 1.96-fold greater than horseradish peroxidase (HRP). Density functional theory (DFT) calculations further reveal that axial chlorine coordination significantly reduces the reaction energy barrier, complementing the planar oxygen coordination, which shortens the activation pathway for H2O2. Moreover, the Fe–N/O/Cl–C SA efficiently catalyzes the oxidative depolymerization of birch lignin under mild conditions, producing high-value aromatic monomers such as vanillin and cinnamaldehyde. These findings underscore the critical role of chlorine axial coordination in enhancing catalytic performance and highlight the great potential of single-atom nanozymes in biomass conversion and renewable energy applications.
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