催化作用
铂金
化学
电化学
物理化学
氢原子
氢
纳米技术
化学工程
Atom(片上系统)
材料科学
电极
工程类
有机化学
烷基
嵌入式系统
计算机科学
作者
Xuepeng Yin,Hongjuan Wang,Shang‐Feng Tang,Xiuli Lu,Shu Miao,Rui Si,Tong‐Bu Lu
标识
DOI:10.1002/anie.201804817
摘要
Abstract Two Pt single‐atom catalysts (SACs) of Pt‐GDY1 and Pt‐GDY2 were prepared on graphdiyne (GDY)supports. The isolated Pt atoms are dispersed on GDY through the coordination interactions between Pt atoms and alkynyl C atoms in GDY, with the formation of five‐coordinated C 1 ‐Pt‐Cl 4 species in Pt‐GDY1 and four‐coordinated C 2 ‐Pt‐Cl 2 species in Pt‐GDY2. Pt‐GDY2 shows exceptionally high catalytic activity for the hydrogen evolution reaction (HER), with a mass activity up to 3.3 and 26.9 times more active than Pt‐GDY1 and the state‐of‐the‐art commercial Pt/C catalysts, respectively. Pt‐GDY2 possesses higher total unoccupied density of states of Pt 5d orbital and close to zero value of Gibbs free energy of the hydrogen adsorption (|Δ |) at the Pt active sites, which are responsible for its excellent catalytic performance. This work can help better understand the structure–catalytic activity relationship in Pt SACs.
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