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Single Atom Iridium Decorated Nickel Alloys Supported on Segregated MoO 2 for Alkaline Water Electrolysis

Hetero-interface engineering has been widely employed to develop supported multi-component catalysts for water electrolysis, but it still remains a substantial challenge for supported single atom alloys. Herein we report a conductive oxide MoO supported Ir Ni single atom alloys (Ir Ni@MoO SAAs) bifu...

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Bibliographic Details
Published in:Advanced materials (Weinheim) 2023-12, p.e2305437
Main Authors: Wang, Bin, Li, Jiangnan, Li, Dongze, Xu, Junyuan, Liu, Shoujie, Jiang, Qike, Zhang, Yashi, Duan, Zhiyao, Zhang, Fuxiang
Format: Article
Language:English
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Summary:Hetero-interface engineering has been widely employed to develop supported multi-component catalysts for water electrolysis, but it still remains a substantial challenge for supported single atom alloys. Herein we report a conductive oxide MoO supported Ir Ni single atom alloys (Ir Ni@MoO SAAs) bifunctional electrocatalysts through surface segregation coupled with galvanic replacement reaction, where the Ir atoms are atomically anchored onto the surface of Ni nanoclusters via the Ir-Ni coordination accompanied with electron transfer from Ni to Ir. Benefiting from the unique structure, the Ir Ni@MoO SAAs not only exhibit low overpotential of 48.6 mV at 10 mA/cm and Tafel slope of 19 mV/dec for hydrogen evolution reaction, but also show highly efficient alkaline water oxidation with overpotential of 280 mV at 10 mA/cm . Their overall water electrolysis exhibits a low cell voltage of 1.52 V at 10 mA/cm and excellent durability. Experiments and theoretical calculations reveal that the Ir-Ni interface effectively weakens hydrogen binding energy, and decoration of the Ir single atoms boost surface reconstruction of Ni species to enhance the coverage of intermediates (OH*) and switch the potential-determining step. We suggest that this approach opens up a promising avenue to design efficient and durable precious metal bifunctional electrocatalysts. This article is protected by copyright. All rights reserved.
ISSN:1521-4095