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IrW nanochannel support enabling ultrastable electrocatalytic oxygen evolution at 2 A cm(−2) in acidic media

A grand challenge for proton exchange membrane electrolyzers is the rational design of oxygen evolution reaction electrocatalysts to balance activity and stability. Here, we report a support-stabilized catalyst, the activated ~200 nm-depth IrW nanochannel that achieves the current density of 2 A cm(...

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Detalles Bibliográficos
Autores principales: Li, Rui, Wang, Haiyun, Hu, Fei, Chan, K. C., Liu, Xiongjun, Lu, Zhaoping, Wang, Jing, Li, Zhibin, Zeng, Longjiao, Li, Yuanyuan, Wu, Xiaojun, Xiong, Yujie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8192761/
https://www.ncbi.nlm.nih.gov/pubmed/34112770
http://dx.doi.org/10.1038/s41467-021-23907-1
Descripción
Sumario:A grand challenge for proton exchange membrane electrolyzers is the rational design of oxygen evolution reaction electrocatalysts to balance activity and stability. Here, we report a support-stabilized catalyst, the activated ~200 nm-depth IrW nanochannel that achieves the current density of 2 A cm(−2) at an overpotential of only ~497 mV and maintains ultrastable gas evolution at 100 mA cm(−2) at least 800 h with a negligible degradation rate of ~4 μV h(−1). Structure analyses combined with theoretical calculations indicate that the IrW support alters the charge distribution of surface (IrO(2))(n) clusters and effectively confines the cluster size within 4 (n≤4). Such support-stabilizing effect prevents the surface Ir from agglomeration and retains a thin layer of electrocatalytically active IrO(2) clusters on surface, realizing a win-win strategy for ultrahigh OER activity and stability. This work would open up an opportunity for engineering suitable catalysts for robust proton exchange membrane-based electrolyzers.