电催化剂
电解
氮化物
材料科学
析氧
无机化学
化学工程
吸附
铜
电解水
碱性水电解
离子交换
分解水
钴
解吸
聚合物电解质膜电解
催化作用
氢
氮化铁
制氢
化学
异质结
交换电流密度
法拉第效率
电化学
作者
Nibedita Sinha,Chandni Das,Chen‐Chen Er,Rajashri Urkude,Santanu Pal,Biplab Ghosh,Siang‐Piao Chai,Poulomi Roy
出处
期刊:Small
[Wiley]
日期:2026-04-07
卷期号:: e00012-e00012
标识
DOI:10.1002/smll.202600012
摘要
ABSTRACT Urea oxidation reaction (UOR) is recognized for energy‐efficient hydrogen production, which nonetheless requires a meticulously designed electrocatalyst with active sites for intermediates adsorption and gaseous products desorption to fully exploit its advantages. Herein, we design the heterostructure consisting of cobalt copper nitride and iron nitride (Co 3 CuN/Fe x N y ) as an efficient and trifunctional electrocatalyst, which requires 1.35 V RHE , 1.55 V RHE, and 0.23 V RHE potentials to reach 100 mA cm −2 current density for UOR, oxygen evolution reaction (OER), and hydrogen evolution reaction (HER), respectively. Unlike the conventional UOR selective electrocatalyst, Co 3 CuN/Fe x N y not only facilitates the UOR → OER switching but also shows self‐regulatory ability in UOR ↔ OER. The Density Functional Theory (DFT) study explained that while Co 3 CuN promoted the adsorption of CO(NH 2 ) 2 and H 2 O, Fe x N y facilitated CO 2 and N 2 desorption, resulting in accelerated UOR and HER kinetics. The electrocatalyst also demonstrated outstanding performance in a urea‐coupled AEM electrolyzer with about 20% of power saving and great electrolyzer efficiency, further highlighting its potential for industry‐relevant applications.
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