材料科学
膜
电解质
阳极
阴极
电解
碱金属
氢氧化物
离子交换
化学工程
电解水
双功能
法拉第效率
离子
无机化学
催化作用
电极
有机化学
化学
物理化学
工程类
生物化学
作者
Pei-Syuan Jhu,Chiung-Wen Chang,Chih‐Chieh Cheng,Yu-Chieh Ting,Ting‐Yu Lin,Feng‐Wen Yen,Po‐Wei Chen,Shih‐Yuan Lu
出处
期刊:Nano Energy
[Elsevier]
日期:2024-07-01
卷期号:126: 109703-109703
标识
DOI:10.1016/j.nanoen.2024.109703
摘要
Cost-effective highly efficient and stable catalysts and alkali-resistant anion exchange membranes (AEMs) are critical for practical applications of anion exchange membrane water electrolyzers (AEMWEs). Here, bifunctional non-precious FeCoNiCuMo high entropy alloys (HEAs), electrochemically deposited on nickel mesh as an anode (FeCoNiCuMo/NM) and on carbon paper as a cathode (FeCoNiCuMo/CP), together with a NiFe layered double hydroxide (LDH) loaded AEM (AEM/LDH), were developed for high performance AEMWEs. The AEMWE thus fabricated delivered an ultrahigh current density of 1777 mA cm-2 at 2 V and exhibited remarkable stability with a less than 0.1% cell voltage increase after a 100-hour operation at 100 mA cm-2 at 50 oC, largely outperforming those of the precious metal based AEMWE, composed of IrO2/NM as the anode and Pt/C/CP as the cathode, 1231 mA cm-2@2 V and 4.57% increase in cell voltages. Composition of the alkali-resistant, hydrophilic, and water electrolysis active NiFe LDH into the AEM improved not only the electrolyte uptake and operational stability, but also the efficiency of the AEMWE, with a 10% boost in current density achieved at 2 V and a reduction in cell voltage increases from 2.94% to 0.0951%. The present development demonstrates the practicality of AEMWEs toward green hydrogen production.
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