电催化剂
材料科学
电解
阳极
阴极
法拉第效率
离子交换
碳纤维
催化作用
电解水
膜
堆积
化学工程
无机化学
分解水
氢氧化物
碱性水电解
电极
氢
制氢
聚合物电解质膜电解
膜电极组件
氢燃料
钒
高压电解
过电位
能量转换
可逆氢电极
作者
Thi Yen Nguyen,Thi Xuyen Nguyen,Hsuan‐Ya Huang,Chun‐Kuo Peng,Yu‐Ru Lin,Yan‐Gu Lin,Yen‐Hsun Su,Kao‐Shu Chuang,Chia‐Ying Su,Jyh Ming Wu,Jeng‐Kuei Chang,Jyh‐Ming Ting
标识
DOI:10.1002/adfm.202524180
摘要
Abstract Developing efficient and durable non‐precious metal electrocatalysts for hydrogen evolution reaction (HER) in an alkaline condition is essential for advancing green hydrogen production. Herein, the study reports a defect‐rich NiMoFe/MoO 2 heterostructure encapsulated in a carbon layer (designated as NiMoFe@C‐e) as a highly active and durable HER catalyst. The combined effect of Fe doping, stacking faults defect, and carbon encapsulation endows the catalyst with outstanding HER performance, showing ultralow overpotentials of 27 and 175 mV at 10 and 500 mA cm −2 , respectively, and exceptional stability that sustains operation for 2000 h at 500 mA cm −2 . An anion exchange membrane water electrolysis (AEMWE) single cell (25 cm 2 active area) having an NiMoFe@C‐e cathode and a high‐entropy FeNiCoMnCr layered double hydroxide anode achieves 1 A cm −2 at 1.89 V, and maintains stability for over 1000 h at 500 mA cm −2 with a degradation rate of only 190 µV h −1 . The system delivers a high energy conversion ≈82%, nearly 100% Faradaic efficiency, and low energy consumption (45.5 kWh per kg H 2 ). A two‐stack AEMWE cell further demonstrates the practical viability of the system, sustaining for 800 h at 1 A cm −2 . This work presents a promising pathway toward scalable, cost‐effective alkaline electrolysis using earth‐abundant catalysts.
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