Direct dioxygen radical coupling driven by octahedral ruthenium-oxygen-cobalt collaborative coordination for acidic oxygen evolution reaction

doi:10.1021/jacs.3c05556

淡江大學機構典藏 > 工學院 > 電機工程學系暨研究所 > 期刊論文 > Item 987654321/125578

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题名:	Direct dioxygen radical coupling driven by octahedral ruthenium-oxygen-cobalt collaborative coordination for acidic oxygen evolution reaction
作者:	Weijie Zhu, Fen Yao, Kangjuan Cheng, Mengting Zhao, Cheng-Jie Yang, Chung-Li Dong, Qiming Hong, Qiu Jiang, Zhoucheng Wang, Hanfeng Liang
日期:	2023-08-07
上传时间:	2024-07-30 12:05:47 (UTC+8)
出版者:	American Chemical Society
摘要:	The acidic oxygen evolution reaction (OER) has long been the bottleneck of proton exchange membrane water electrolyzers given its harsh oxidative and corrosive environments. Herein, we suggest an effective strategy to greatly enhance both the acidic OER activity and stability of Co3O4 spinel by atomic Ru selective substitution on the octahedral Co sites. The resulting highly symmetrical octahedral Ru–O–Co collaborative coordination with strong electron coupling effect enables the direct dioxygen radical coupling OER pathway. Indeed, both experiments and theoretical calculations reveal a thermodynamically breakthrough heterogeneous diatomic oxygen mechanism. Additionally, the active Ru–O–Co units are well-maintained upon the acidic OER thanks to the electron transfer from surrounding electron-enriched tetrahedral Co atoms via bridging oxygen bonds that suppresses the overoxidation and thus dissolution of active Ru and Co species. Consequently, the prepared catalyst, even with a low Ru mass loading of ca. 42.8 μg cm–2, exhibits an attractive acidic OER performance with a low overpotential of 200 mV and a low potential decay rate of 0.45 mV h–1 at 10 mA cm–2. Our work suggests an effective strategy to significantly enhance both the acidic OER activity and stability of low-cost electrocatalysts.
關聯:	Journal of the American Chemical Society 145(32), p.17995-18006
DOI:	10.1021/jacs.3c05556
显示于类别:	[電機工程學系暨研究所] 期刊論文

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