材料科学
氢
Atom(片上系统)
氢原子
冶金
无机化学
纳米技术
化学工程
有机化学
化学
计算机科学
工程类
嵌入式系统
烷基
作者
Lili Xu,Yanping Xu,Bin Xia,Bingrong Guo,Khaja Mohaideen Kamal,Blaž Likozar,Xiumin Li,Feifei Dong,Siwei Li,Yufei Ma
出处
期刊:PubMed
日期:2025-04-21
卷期号:: e2502989-e2502989
标识
DOI:10.1002/adma.202502989
摘要
Single atom catalysts (SACs) achieve 100% utilization of metal atoms and have versatile support effects, whereas single atom alloys (SAAs) with metallic bonds own the free-atom-like electronic structure. Herein, surface single atom alloys (SSAAs) are developed that integrate the advantages of SACs and SAAs via incorporating an ultrathin metallic layer during the synthetic process of SACs. It is shown that the Pt single atom preferentially coordinates with metallic Mo nanolayer, thereby forming a Pt1-MoL surface atom alloy on Mo2C (marked as Pt1-MoL-Mo2C SSAAs). Comprehensive spectroscopic and theoretical calculations reveal that the Mo nanolayer in SSAAs not only functions as an electron buffer between Pt1 and Mo2C, leading to a free-atom-like d state at Pt1 sites and thereby balancing the adsorption and desorption of H, but also enhances the aggregation, adsorption, and activation of H2O. Consequently, the Pt1-MoL-Mo2C SSAAs exhibit superior alkaline hydrogen evolution reaction (HER) performance compared to Pt1/Mo2C SACs, achieving a low overpotential of 12 mV at 10 mA cm-2 and a low Tafel slope of 17 mV dec-1. This work provides novel insights into the design of advanced single-site catalysts.
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