化学
电催化剂
NAD+激酶
辅因子
电子转移
电化学
组合化学
烟酰胺腺嘌呤二核苷酸
产量(工程)
普鲁士蓝
阴极
无机化学
膜
氧化还原
配位复合体
氰化物
氢化物
电极
活动站点
动力学
仿生合成
螺旋(腹足类)
人工光合作用
催化作用
阳离子聚合
烟酰胺
人工酶
纳米技术
法拉第效率
反应机理
分子内力
作者
Huali Wang,Yu Zhang,Liang Zhao,Chong Wang,Cheng He,Chunying Duan
标识
DOI:10.1002/anie.202519123
摘要
Abstract Sustainable conversion of NO offers a promising technology for artificial nitrogen cycle, but faces challenges in integrating electrocatalysis with NO capture. Herein, a biomimetic NO capture‐activation‐conversion strategy was firstly formulated by encapsulating N‐acetylcysteine ( NAC ) within a nicotinamide adenine dinucleotide (NADH) mimic‐containing coordination capsule, enabling efficiently NH 3 electrosynthesis. The installed NADH mimics onto the capsule interacted with the highly reactive NO‐adduct generated from NAC within the microenvironment akin to the pocket of enzyme, facilitating intramolecular hydride transfer of the substrate‐involving clathrate, accompanied by the formation of oxidated NAD + mimics. Subsequently, the cobalt‐based coordination capsule consecutively reserved e − from cathode while donating 2 e − to the NAD + mimic simultaneously for active cofactor recovered and recycle. This coordination capsule‐mediated biomimetic system exhibited enzymatic kinetics following the Michaelis–Menten mechanism in the electrochemical NO reduction and realized almost 100% Faraday efficiency at potentials below −0.2 V RHE with a substantial NH 3 yield rate of 121.6 µmol·h −1 ·cm −2 at −0.3 V RHE , ranking among the optimal electrocatalytic NO performance ever achieved, offering an attractive avenue toward renewable electricity‐driven nitrogen fixation exploiting bioinspired artificial catalyst.
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