Recent advances and modulation tactics in Ru- and Ir-based electrocatalysts for PEMWE anodes at large current densities

阳极 电流(流体) 调制(音乐) 材料科学 纳米技术 工程物理 光电子学 化学 电气工程 电极 物理 工程类 物理化学 声学
作者
Yu Wang,Haijing Yan,Honggang Fu
出处
期刊:eScience [Elsevier BV]
卷期号:5 (3): 100323-100323 被引量:62
标识
DOI:10.1016/j.esci.2024.100323
摘要

Proton exchange membrane water electrolyzer (PEMWE) technology is regarded as one of the most promising methods for green hydrogen generation. The oxygen evolution reaction (OER) at the anode is the primary bottleneck preventing the industrial-scale application of PEMWEs due to its sluggish kinetics, and it presently relies upon electrocatalysts that use scarce, costly Ru and Ir. In addition, most of the Ru- and Ir-based electrocatalysts developed to date need high noble metal loading and present good activity only at low current density and for a short period. In this review, we systematically elaborate upon various effective strategies for modulating Ru- and Ir-based catalysts to achieve large current density, high stability, and high atom economy, including single-atom designs, heteroatom doping, defect/vacancy creation, alloying, and heterojunction engineering. The structure–performance relationships of OER catalysts synthesized using different strategies are elucidated, along with the importance of substrate materials. We conclude by discussing the remaining challenges and future prospects for OER electrocatalysts in acid. • This review discusses recent advances in the design of Ru- and Ir-based electrocatalysts for PEMWE anodes. • Strategies for modulating Ru- and Ir-based acidic OER electrocatalysts to achieve large current density, high stability, and high atom economy are described in detail. • The structure–performance relationships and improvement measures for OER catalysts synthesized via different strategies are elucidated, along with the importance of substrate materials. • Perspectives on and future challenges in the design of Ru- and Ir-based catalysts for the PEMWE anode are discussed.
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