Pt Single-Atom collaborate with Pt Atom-Clusters by an In-Situ confined strategy for accelerating electrocatalytic hydrogen evolution

被引:21
作者
Liu, Xingyan [1 ]
Song, Xueting [1 ]
Jiang, Guangmei [1 ]
Tao, Liujun [1 ]
Jin, Zhaoyu [2 ]
Li, Fukun [1 ]
He, Youzhou [1 ]
Dong, Fan [2 ]
机构
[1] Chongqing Technol & Business Univ, Coll Environm & Resources, Chongqing Key Lab Catalysis & New Environm Mat, Chongqing 400067, Peoples R China
[2] Univ Elect Sci & Technol China, Inst Fundamental & Frontier Sci, Chengdu 610054, Peoples R China
基金
中国国家自然科学基金;
关键词
UiO-66-PtTCPP precursor; Pt single-atom; Pt atom-clusters; Mass activity; Hydrogen evolution reaction; METAL-ORGANIC FRAMEWORKS; CATALYSTS;
D O I
10.1016/j.cej.2023.148430
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Heterogeneous catalysts with atomic dispersion play an important role in electrocatalysis. In addition to the single-atom, modifying the intrinsic catalytic capacity of single-atom catalysts through cooperative atom-clusters is an effective way to increase active sites and improve mass activity. Herein, a composite electrocatalytic material (PtM@CN) with partial Pt single-atoms and partial Pt atom-clusters was obtained by pyrolysis of the thermostable UiO-66-PtTCPP precursor. Remarkably, beneficial to the synergistic effect of Pt single-atom and Pt atom-clusters as well as the strong metal-support interaction, the PtM@CN catalyst showed excellent hydrogen evolution reaction (HER) activity and stability in both acidic and alkaline electrolytes. Moreover, X-ray photoelectron spectroscopy (XPS) and density functional theory (DFT) calculations shows that the existence of Pt single-atom and Pt atom-clusters could rationally adjust electronic structure of supported metals and impact adsorption energy of reaction intermediates, which play an essential role in enhancing the electrocatalytic activity of HER.
引用
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页数:10
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