催化作用
杂原子
过氧化物酶
活动站点
交货地点
磷
基质(水族馆)
材料科学
碳纤维
活动中心
兴奋剂
Atom(片上系统)
选择性
组合化学
纳米技术
酶
化学
有机化学
生物
光电子学
冶金
戒指(化学)
生态学
复合数
计算机科学
嵌入式系统
农学
复合材料
作者
Shichao Ding,Jordan A. Barr,Zhaoyuan Lyu,Fangyu Zhang,Maoyu Wang,Peter Tieu,Xin Li,Mark Engelhard,Zhenxing Feng,Scott P. Beckman,Xiaoqing Pan,Jincheng Li,Dan Du,Yuehe Lin
标识
DOI:10.1002/adma.202209633
摘要
Abstract Fe–N–C single‐atom catalysts (SACs) exhibit excellent peroxidase (POD)‐like catalytic activity, owing to their well‐defined isolated iron active sites on the carbon substrate, which effectively mimic the structure of natural peroxidase's active center. To further meet the requirements of diverse biosensing applications, SAC POD‐like activity still needs to be continuously enhanced. Herein, a phosphorus (P) heteroatom is introduced to boost the POD‐like activity of Fe–N–C SACs. A 1D carbon nanowire (FeNCP/NW) catalyst with enriched Fe–N 4 active sites is designed and synthesized, and P atoms are doped in the carbon matrix to affect the Fe center through long‐range interaction. The experimental results show that the P‐doping process can boost the POD‐like activity more than the non‐P‐doped one, with excellent selectivity and stability. The mechanism analysis results show that the introduction of P into SAC can greatly enhance POD‐like activity initially, but its effect becomes insignificant with increasing amount of P. As a proof of concept, FeNCP/NW is employed in an enzyme cascade platform for highly sensitive colorimetric detection of the neurotransmitter acetylcholine.
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