电合成
材料科学
纳米技术
电化学
化学
化学工程
物理化学
电极
工程类
作者
Pingyi Feng,Buqi Ke,Shao Wang,Yanxu Chen,Mingyu Cheng,Zechuan Dai,Bocheng Zhang,Yifan Li,Genqiang Zhang
标识
DOI:10.1002/ange.202509834
摘要
Abstract Electrocatalytic urea synthesis from CO 2 and NO 3 − offers a sustainable strategy to address environmental challenges and growing urea demand. However, current systems suffer inefficient C‐N coupling due to poor selectivity toward critical C/N‐intermediates. Herein, we engineered atomic‐scale Mott–Schottky analogy in SnCu nanoalloy to create electron‐enriched Cu sites, enabling remarkable urea production through quadruple synergy. Sn 2 Cu delivered exceptional urea yield (28.9 mmol h −1 g cat. −1 ) with 46.7% Faradaic efficiency (FE) in H‐cell, while demonstrating practical potential with superior catalytic performance (yield: 72.6 mmol h −1 g cat. −1 , FE: 41.3%, stability: 60 h) at −0.52 V in flow cell. In‐situ synchrotron radiation‐Fourier transform infrared spectroscopy and theoretical calculations revealed electron‐enriched Cu active sites enhanced CO 2 /NO 3 − co‐adsorption and *CO coverage, while steering reaction pathway toward *CO‐*NHO coupling and suppressing hydrogen evolution, thereby reducing rate‐determining step energy barrier and prioritizing C‐N coupling. This work develops a structure–adsorption‐reactivity framework, providing fundamental guidance for advanced urea electrocatalyst design.
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