材料科学
电解
析氧
制氢
分解水
阳极
氢
双金属片
碱性水电解
阴极
化学工程
聚合物电解质膜电解
碳化物
碳化钨
电解水
再分配(选举)
无机化学
交换电流密度
离子交换
解吸
氢燃料
吸附
钨
电化学
电流密度
高压电解
催化作用
膜
氧化还原
电催化剂
可逆氢电极
法拉第效率
离子
电极
作者
T.-I. Lin,Yu‐Chieh Ting,Chiung‐Wen Chang,Shang‐Hung Chang,Kai‐An Lee,Ting‐Jen Hsueh,Kun‐Han Lin,Shih‐Yuan Lu
出处
期刊:Small
[Wiley]
日期:2025-09-27
卷期号:21 (50): e11280-e11280
被引量:1
标识
DOI:10.1002/smll.202511280
摘要
Cost-effective, highly efficient, and robust electrocatalysts are critical for prevailing of anion exchange membrane water electrolysis technology for green hydrogen production. Here, Ni and Fe are incorporated into tungsten carbides to form bimetallic η-phase carbides Ni6W6C and Fe6W6C, respectively, achieving remarkably low overpotentials of 37/204 and 203/296 mV at current densities of 10/500 mA cm-2 for hydrogen evolution reaction (HER) and oxygen evolution reaction (OER), respectively, in 1 m KOH. With Ni6W6C and Fe6W6C serving as the cathode and anode catalysts, respectively, the anion exchange membrane water electrolyzer exhibits outstanding water electrolysis performances, achieving an ultrahigh current density of 2.8 A cm-2 at 2 V and exhibiting ultra-stability of a continuous operation at a commercially relevant high current density of 0.5 A cm-2 for 100 h without appreciable decay. Incorporation of Ni in Ni6W6C induces charge redistribution between Ni and W, leading to an upshift in hydrogen adsorption energy to near-ideal value of zero and a downshift in hydrogen desorption energy for fast release of hydrogen, both contributing to the high HER activities of Ni6W6C. In situ surface reconstruction of Fe6W6C to highly OER-active (Fe,W)OOH during OER operations gives rise to high OER activities of Fe6W6C.
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