过电位
材料科学
析氧
电场
化学物理
密度泛函理论
分解水
电子
电解水
X射线光电子能谱
异质结
氢
工作职能
拉曼光谱
吸附
电子转移
电解
可逆氢电极
吸收光谱法
离子
表面工程
分析化学(期刊)
X射线吸收光谱法
化学工程
吸收(声学)
再分配(选举)
开路电压
电荷密度
氢燃料
纳米技术
催化作用
作者
Siyu Wang,Laiyu Luo,Yu Fu,Yuying Fan,Li Sun,Dongxu Wang,Aiping Wu,Chungui Tian
标识
DOI:10.1002/adfm.202519088
摘要
Abstract Rational modulating spatial electron density through interfacial charge engineering presents a promising approach to enhance water electrolysis. Herein, a porous Co/Co 6 Mo 6 C 2 heterostructure is reported, featuring an ordered built‐in electric field (BIEF) directed from internal Co core to external Co 6 Mo 6 C 2 shell, engineered by the work function difference. This BIEF generates spatially separated electron‐deficient and electron‐rich regions, synergistically facilitating oxygen evolution reaction (OER) and hydrogen evolution reaction (HER). The porous structure ensures a large surface area and abundant active sites. X‐ray absorption spectroscopy, potential‐dependent X‐ray photoelectron spectroscopy, and in situ Raman spectroscopy reveal that the high‐valent Mo promotes Co conversion to CoOOH, accelerating OER kinetics and enabling a low overpotential of 170 mV at 10 mA cm −2 in 1 m KOH. A slight increase in Mo content yields an optimized HER catalyst (Co/Co 6 Mo 6 C 2 ‐H) with an overpotential of 39 mV at 10 mA cm −2 . Theoretical calculations combined with experiments corroborate that the ordered BIEF optimizes the adsorption of OER and HER intermediates through electronic redistribution and d‐band center regulation. The corresponding anion exchange membrane water electrolyzer (AEMWE) device demonstrates a voltage of 1.77 V at 500 mA cm −2 with 500 h durability in 1 m KOH, showing potential for industrial‐scale green hydrogen production.
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