碱性水电解
材料科学
电解
电极
转化(遗传学)
碱性电池
无机化学
化学工程
电解质
物理化学
化学
生物化学
工程类
基因
作者
Guanzhi Wang,Haoyi Li,Finn Babbe,Andrew W. Tricker,Ethan J. Crumlin,Junko Yano,Rangachary Mukundan,Xiong Peng
标识
DOI:10.1002/aenm.202500886
摘要
Abstract Alkaline water electrolyzers (AWEs) play a pivotal role in the realm of large‐scale hydrogen production. However, AWEs face significant challenges in electrode degradation particularly under dynamic operating conditions, induced by reverse current phenomenon during frequent startup/shutdown. Herein, this study aims to rationalize the degradation mechanisms of AWEs under these conditions. A three‐electrode membrane electrode assembly (MEA) setup is first utilized to decouple polarization behaviors of anode and cathode in AWEs. Following a proposed accelerated stress testing protocol, the setup allows for tracking individual electrode performance transformations during frequent reverse current operation. Integrating operando cell studies with in situ and post‐mortem characterizations, it is showed that continuous formation of highly active species, nickel (oxy)hydroxides, improves the anode performance for oxygen evolution reaction. On the contrary, irreversible oxidation of nickel to β‐nickel hydroxide results in a severe degradation of cathode, leading to material dissolution, poor electrical conductivity and loss of catalytic activity for hydrogen evolution reaction. These results provide insights in nickel‐based electrode transformation mechanisms for alkaline water electrolysis and indicate that cathode with higher redox reversibility can potentially improve durability of AWEs under dynamic conditions.
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