Durability of NiFe-based oxygen evolution electrocatalysts in AEM water electrolyzer under fluctuating power supply

被引:0
|
作者
Wan, Zhihang [1 ]
Rui, Dongxue [1 ]
Wu, Lanlan [1 ]
Liu, Guihua [1 ]
Li, Jingde [1 ]
Du, Xiaohang [1 ]
机构
[1] Hebei Univ Technol, Sch Chem Engn & Technol, Hebei Prov Key Lab Green Chem Technol & High Effic, Tianjin 300130, Peoples R China
基金
中国国家自然科学基金;
关键词
NiFe-based catalysts; AEM water electrolyzer; Fluctuating power supply; Degradation mechanisms; Accelerated durability testing;
D O I
10.1016/j.jcis.2025.02.135
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
NiFe-based materials are widely utilized as anode electrocatalysts for the oxygen evolution reaction (OER) in anion exchange membrane water electrolyzers (AEMWE). However, their performance under actual fluctuating power supply remains poorly understood. In this study, the OER performance and degradation mechanisms of various NiFe-based OER catalysts are investigated in AEMWE under both constant and fluctuating voltage conditions. Among the tested materials, NixFe1_ xS exhibits the best durability under both constant and fluctuating voltages, outperforming NixFe1_ xP and NiFe LDH. Notably, its stability is found to be positively correlated with the interval of voltage fluctuation. The degradation of NixFe1_ xS can be attributed to a combination of irreversible and reversible losses. Accelerated durability testing reveals that irreversible loss is primarily caused by the severe collapse, dissolution and agglomeration of catalyst particles on the electrode surface under fluctuating power supply. On the other hand, the reversible loss is linked to hindered contact between the electrolyte and the electrode surface, caused by gas retention within the catalyst's porous structure. This reversible loss can be mitigated by introducing a rest period, which allows for the recovery of catalyst's performance. This work provides valuable insights into the degradation mechanisms of NiFe-based OER catalysts under fluctuating power supply in AEMWE.
引用
收藏
页码:456 / 468
页数:13
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