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掺锶氧化铱触发直接氧-氧偶联以促进酸性水氧化电催化

Strontium Doped IrO Triggers Direct O-O Coupling to Boost Acid Water Oxidation Electrocatalysis.

作者信息

Zhang Wuyong, Zhu Caihan, Wen Yingjie, Wang Minli, Lu Zhiyi, Wang Yunan

机构信息

Key Laboratory of Advanced Fuel Cells and Electrolyzers Technology of Zhejiang Province, Ningbo Institute of Materials Technology&Engineering, Chinese Academy of Sciences, 1219 West Zhongguan Road, Zhenhai District, Ningbo, 315201, P. R. China.

University of Chinese Academy of Sciences, Beijing, 100049, P. R. China.

出版信息

Angew Chem Int Ed Engl. 2025 Feb 3;64(6):e202418456. doi: 10.1002/anie.202418456. Epub 2024 Nov 26.

Abstract

The discovery of efficient and stable electrocatalysts for the oxygen evolution reaction (OER) in acidic conditions is crucial for the commercialization of proton-exchange membrane water electrolyzers. In this work, we propose a Sr(OH)-assisted method to fabricate a (200) facet highly exposed strontium-doped IrO catalyst to provide available adjacent iridium sites with lower Ir-O covalency. This design facilitates direct O-O coupling during the acidic water oxidation process, thereby circumventing the high energy barrier associated with the generation of *OOH intermediates. Benefiting from this advantage, the resulting Sr-IrO catalyst exhibits an impressive overpotential of 207 mV at a current density of 10 mA cm in 0.5 M HSO. Furthermore, a PEMWE device utilizing Sr-IrO as the anodic catalyst demonstrates a cell voltage of 1.72 V at 1 A cm and maintains excellent stability for over 500 hours. Our work not only provides guidance for the design of improved acidic OER catalysts but also encourages the development of iridium-based electrocatalysts with novel mechanisms for other electrocatalytic reactions.

摘要

发现用于酸性条件下析氧反应(OER)的高效稳定电催化剂对于质子交换膜水电解槽的商业化至关重要。在这项工作中,我们提出了一种Sr(OH)辅助方法来制备(200)面高度暴露的掺锶IrO催化剂,以提供具有较低Ir-O共价性的可用相邻铱位点。这种设计有利于在酸性水氧化过程中直接进行O-O偶联,从而规避与*OOH中间体生成相关的高能垒。得益于这一优势,所得的Sr-IrO催化剂在0.5 M HSO中,电流密度为10 mA cm时表现出令人印象深刻的207 mV过电位。此外,使用Sr-IrO作为阳极催化剂的PEMWE装置在1 A cm时的电池电压为1.72 V,并保持超过500小时的优异稳定性。我们的工作不仅为改进酸性OER催化剂的设计提供了指导,也促进了具有新颖机制的铱基电催化剂用于其他电催化反应的发展。

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