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Theory-driven design of high-valence metal sites for water oxidation confirmed using in situ soft X-ray absorption
Nature Chemistry ( IF 21.8 ) Pub Date : 2017-11-20 , DOI: 10.1038/nchem.2886
Xueli Zheng , Bo Zhang , Phil De Luna , Yufeng Liang , Riccardo Comin , Oleksandr Voznyy , Lili Han , F. Pelayo García de Arquer , Min Liu , Cao Thang Dinh , Tom Regier , James J. Dynes , Sisi He , Huolin L. Xin , Huisheng Peng , David Prendergast , Xiwen Du , Edward H. Sargent

Theory-driven design of high-valence metal sites for water oxidation confirmed using in situ soft X-ray absorption

Theory-driven design of high-valence metal sites for water oxidation confirmed using <i>in situ</i> soft X-ray absorption, Published online: 20 November 2017; doi:10.1038/nchem.2886

Water oxidation is key to the production of chemical fuels from electricity. Now, guided by theory, NiCoFeP oxyhydroxide catalysts have been developed that require an overpotential lower than that required by IrO2. In situ soft X-ray absorption studies of neutral-pH NiCoFeP catalysts indicate formation of Ni4+, which is favourable for water oxidation.


中文翻译:

通过原位软X射线吸收确认理论驱动的高价金属位点用于水氧化的设计

通过原位软X射线吸收确认理论驱动的高价金属位点用于水氧化的设计

使用<i>原位</ i>软X射线吸收证实了理论驱动的高价金属水氧化位点的设计,在线发布:2017年11月20日;doi:10.1038 / nchem.2886

水氧化是用电生产化学燃料的关键。现在,在理论的指导下,已开发出所需的电势低于IrO2所需的NiCoFeP羟基氧化物催化剂。中性pH NiCoFeP催化剂的原位软X射线吸收研究表明形成了Ni4 +,这对水的氧化是有利的。
更新日期:2017-11-21
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