材料科学
合金
电合成
催化作用
缩放比例
氨
氨生产
化学工程
纳米技术
无机化学
冶金
电化学
物理化学
有机化学
电极
化学
几何学
工程类
数学
作者
Di Yin,Bowen Li,Boxiang Gao,Mengxue Chen,Dong Chen,You Meng,Shuai Zhang,Chenxu Zhang,Quan Quan,L Chen,Yang Cheng,Chun‐Yuen Wong,Johnny C. Ho
标识
DOI:10.1002/adma.202415739
摘要
Electrochemically converting nitrate (NO3 -) to value-added ammonia (NH3) is a complex process involving an eight-electron transfer and numerous intermediates, presenting a significant challenge for optimization. A multi-elemental synergy strategy to regulate the local electronic structure at the atomic level is proposed, creating a broad adsorption energy landscape in high-entropy alloy (HEA) catalysts. This approach enables optimal adsorption and desorption of various intermediates, effectively overcoming energy-scaling limitations for efficient NH3 electrosynthesis. The HEA catalyst achieved a high Faradaic efficiency of 94.5 ± 4.3% and a yield rate of 10.2 ± 0.5 mg h-1 mgcat -1. It also demonstrated remarkable stability over 250 h in an integrated three-chamber device, coupling electrocatalysis with an ammonia recovery unit for continuous NH3 collection. This work elucidates the catalytic mechanisms of multi-functional HEA systems and offers new perspectives for optimizing multi-step reactions by circumventing adsorption-energy scaling limitations.
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