催化作用
耐久性
溶解
电解水
化学工程
电解
离子交换
膜
化学
材料科学
无机化学
离子
电极
复合材料
电解质
有机化学
物理化学
工程类
生物化学
作者
Chong Lei,Kaicong Yang,Guangzhe Wang,Gongwei Wang,Juntao Lu,Li Xiao,Lin Zhuang
出处
期刊:ACS Sustainable Chemistry & Engineering
[American Chemical Society]
日期:2022-12-05
卷期号:10 (50): 16725-16733
被引量:28
标识
DOI:10.1021/acssuschemeng.2c04855
摘要
Anion exchange membrane water electrolysis (AEMWE) offers an opportunity to use inexpensive nonprecious metal catalysts. However, pure water-fed AEMWE still faces issues of durability. Herein, we compared the stability of AEMWE under different anolytes, including KOH, pure water, and a phosphate buffer (PB) using a NiFeCo oxygen evolution reaction catalyst. Upon thoroughly characterizing several changes before/after 100 h durability tests, such as the cell performance, catalyst dissolution, catalyst morphologies, impedance of the anion exchange membrane, and catalytic layer, we speculate that the change of the local pH is the main factor causing catalyst reconstruction, which further leads to the loss of cell performance in the pure water-fed mode. By using PB to control the local pH, the morphology of the catalyst will no longer change after the durability test, and the cell performance can recover to the initial performance in pure water. These results not only indicate that the catalyst structural transformation is the main reason for the deactivation of pure water-fed AEMWE but also help find a way to achieve highly durable pure water-fed AEMWE.
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