材料科学
过电位
催化作用
贵金属
球磨机
Atom(片上系统)
电化学
金属
化学工程
纳米技术
氢
物理化学
冶金
有机化学
计算机科学
电极
工程类
化学
嵌入式系统
作者
Haiyan Jin,Siraj Sultan,Miran Ha,Jitendra N. Tiwari,Min Gyu Kim,Kwang S. Kim
标识
DOI:10.1002/adfm.202000531
摘要
Abstract Designing a facile strategy to access active and atomically dispersed metallic catalysts are highly challenging for single atom catalysts (SACs). Herein, a simple and fast approach is demonstrated to construct Pt catalysts with single atoms in large quantity via ball milling Pt precursor and N‐doped carbon support (K 2 PtCl 4 @NC‐M; M denotes ball‐milling). The as‐prepared K 2 PtCl 4 @NC‐M only requires a low overpotential of 11 mV and exhibits 17‐fold enhanced mass activity for the electrochemical hydrogen evolution compared to commercial 20 wt% Pt/C. The superior hydrogen evolution reaction (HER) catalytic activity of K 2 PtCl 4 @NC‐M can be attributed to the generation of Pt single atoms, which improves the utilization efficiency of Pt atoms and the introduction of Pt‐N 2 C 2 active sites with near‐zero hydrogen adsorption energy. This viable ball milling method is found to be universally applicable to the fabrication of other single metal atoms, for example, rhodium and ruthenium (such as Mt‐N 2 C 2 , where Mt denotes single metal atom). This strategy also provides a promising and practical avenue toward large‐scale energy storage and conversion application.
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