化学
催化作用
膜
离子交换
化学工程
离子液体
离子电导率
电导率
阳离子聚合
析氧
限制电流
分解水
无机化学
离子键合
纳米技术
离子
高分子化学
电化学
电极
有机化学
材料科学
物理化学
工程类
电解质
生物化学
光催化
作者
Naiying Du,Claudie Roy,Retha Peach,Matthew J. Turnbull,Simon Thiele,Christina Bock
出处
期刊:Chemical Reviews
[American Chemical Society]
日期:2022-04-20
卷期号:122 (13): 11830-11895
被引量:444
标识
DOI:10.1021/acs.chemrev.1c00854
摘要
This Review provides an overview of the emerging concepts of catalysts, membranes, and membrane electrode assemblies (MEAs) for water electrolyzers with anion-exchange membranes (AEMs), also known as zero-gap alkaline water electrolyzers. Much of the recent progress is due to improvements in materials chemistry, MEA designs, and optimized operation conditions. Research on anion-exchange polymers (AEPs) has focused on the cationic head/backbone/side-chain structures and key properties such as ionic conductivity and alkaline stability. Several approaches, such as cross-linking, microphase, and organic/inorganic composites, have been proposed to improve the anion-exchange performance and the chemical and mechanical stability of AEMs. Numerous AEMs now exceed values of 0.1 S/cm (at 60-80 °C), although the stability specifically at temperatures exceeding 60 °C needs further enhancement. The oxygen evolution reaction (OER) is still a limiting factor. An analysis of thin-layer OER data suggests that NiFe-type catalysts have the highest activity. There is debate on the active-site mechanism of the NiFe catalysts, and their long-term stability needs to be understood. Addition of Co to NiFe increases the conductivity of these catalysts. The same analysis for the hydrogen evolution reaction (HER) shows carbon-supported Pt to be dominating, although PtNi alloys and clusters of Ni(OH)
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