催化作用
铂金
化学
吉布斯自由能
协调数
结晶学
物理化学
氢原子
制氢
氢
Atom(片上系统)
材料科学
有机化学
热力学
物理
离子
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
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 C1 -Pt-Cl4 species in Pt-GDY1 and four-coordinated C2 -Pt-Cl2 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 (|ΔGPtH* |) 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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