催化作用
材料科学
星团(航天器)
异质结
氢
无机化学
化学工程
光电子学
化学
有机化学
计算机科学
工程类
程序设计语言
作者
Hanqing Cai,Qinghe Yang,Lulu Chen,Ruili Gao,Meihong Liao,Junyue Xing,Wenbo Zhou,Ning Pu,Jing Gu,Yichao Huang
出处
期刊:Rare Metals
[Springer Science+Business Media]
日期:2025-03-29
卷期号:44 (7): 4701-4711
被引量:7
标识
DOI:10.1007/s12598-025-03232-y
摘要
Abstract Constructing cluster heterostructures with strongly coupled interfaces is of great importance to accelerating the catalytic reactions that involve multiple intermediates. Herein, a strongly coupled cluster heterostructure composed of platinum and molybdenum carbide (Pt@Mo 2 C) derived from polyoxometalate clusters is designed to achieve excellent alkaline hydrogen evolution reaction. The Pt@Mo 2 C cluster exhibits strong electronic interactions between Pt and Mo 2 C, working together to facilitate the H 2 O dissociation by concurrently binding intermediates (Pt–H* and Mo–OH*), thus accelerating the kinetics of the rate‐determining Volmer step. The optimized Pt@Mo 2 C exhibits a high mass activity of 12.1 A·mg Pt −1 , 19.2 times higher than that of 20% Pt/C in alkaline media. Moreover, it can be stabilized at a current density of 100 mA·cm −2 for more than 200 h. This work demonstrated the superiority of the cluster heterostructures and co‐catalytic effect towards the development of highly efficient electrocatalysts.
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