化学
催化作用
电子转移
原子单位
电催化剂
金属
无机化学
光化学
物理化学
电化学
电极
生物化学
物理
量子力学
有机化学
作者
Yisong Yang,Lei Zhao,Yiqiang Sun,Yunxiang Lin,Yang Li,Keke Mao,Cuncheng Li,Ke Xu
出处
期刊:Inorganic Chemistry
[American Chemical Society]
日期:2023-03-15
卷期号:62 (12): 5032-5039
被引量:4
标识
DOI:10.1021/acs.inorgchem.3c00293
摘要
Developing efficient atomic-scale metal-supported catalysts is of great significance for energy conversion technologies. However, the precise modulation of electron transfer between the metal and supporter in atomic-scale metal-supported catalysts to further improve the catalytic activity is still a major challenge. Herein, we show tunable electron transfer between atomic-scale Pt and tungsten nitride/oxide supports (namely, Pt/WN and Pt/W18O49). Pt/WN with modest electron exchange and Pt/W18O49 with aggressive electron exchange exhibit notably different catalytic activities for the alkaline hydrogen oxidation reaction (HOR), in which Pt/WN shows a 5.7-fold enhancement in HOR intrinsic catalytic performance in comparison to Pt/W18O49. Additionally, the tunable electronic transfer at the interface of Pt/WN and Pt/W18O49, as proven by the theoretical calculation, resulted in the discrepancy of the adsorption free energy of the reaction intermediates, as well as catalytic activity, for the HOR process. Our work provides new insights into the design of advanced atomic-scale metal-supported catalysts for electrocatalysis.
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