Research Progress in Structure Evolution and Durability Modulation of Ir‐ and Ru‐Based OER Catalysts under Acidic Conditions

耐久性 催化作用 材料科学 电解 电解水 电解质 制氢 析氧 氧化物 分解水 电化学 化学工程 能量载体 纳米技术 化学 冶金 复合材料 电极 有机化学 工程类 物理化学 光催化
作者
Yunhai Zi,Chengxu Zhang,Jian-Qiang Zhao,Ying Cheng,Jinliang Yuan,Jue Hu
出处
期刊:Small [Wiley]
被引量:3
标识
DOI:10.1002/smll.202406657
摘要

Abstract Green hydrogen energy, as one of the most promising energy carriers, plays a crucial role in addressing energy and environmental issues. Oxygen evolution reaction catalysts, as the key to water electrolysis hydrogen production technology, have been subject to durability constraints, preventing large‐scale commercial development. Under the high current density and harsh acid‐base electrolyte conditions of the water electrolysis reaction, the active metals in the catalysts are easily converted into high‐valent soluble species to dissolve, leading to poor structural durability of the catalysts. There is an urgent need to overcome the durability challenges under acidic conditions and develop electrocatalysts with both high catalytic activity and high durability. In this review, the latest research results are analyzed in depth from both thermodynamic and kinetic perspectives. First, a comprehensive summary of the structural deactivation state process of noble metal oxide catalysts is presented. Second, the evolution of the structure of catalysts possessing high durability is discussed. Finally, four new strategies for the preparation of stable catalysts, “electron buffer (ECB) strategy”, combination strength control, strain control, and surface coating, are summarized. The challenges and prospects are also elaborated for the future synthesis of more effective Ru/Ir‐based catalysts and boost their future application.
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