Pt Deposites on TiO2 for Photocatalytic H2 Evolution: Pt Is Not Only the Cocatalyst, but Also the Defect Repair Agent

被引:16
作者
Shu, Zhan [1 ]
Cai, Yandi [1 ,2 ]
Ji, Jiawei [1 ]
Tang, Changjin [1 ]
Yu, Shuohan [1 ]
Zou, Weixin [1 ]
Dong, Lin [1 ]
机构
[1] Nanjing Univ, Key Lab Vehicle Emiss Control, Key Lab Mesoscop Chem MOE, Sch Chem & Chem Engn,Sch Environm,Ctr Modern Anal, Nanjing 210093, Peoples R China
[2] Nanjing Tech Univ, Coll Chem & Mol Engn, Nanjing 211800, Peoples R China
基金
中国国家自然科学基金;
关键词
photocatalytic stability; electropositive defect; Pt sources; electrostatic interaction; defect repair; HYDROGEN EVOLUTION; PHOTOCORROSION INHIBITION; DOPED TIO2; MECHANISM; WATER; SEMICONDUCTORS; DEGRADATION; SINGLE; SRTIO3; ATOM;
D O I
10.3390/catal10091047
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Pt, as a common cocatalyst, has been widely used in photocatalytic H-2 evolution. However, the specific role of Pt in photocatalytic H-2 evolution has not been thoroughly studied. In this paper, by employing three Pt sources with different charges (positive, negative and neutral), we systematically studied the charge effect of Pt sources on photocatalytic H-2 evolution via TiO2 catalyst. According to the results of Raman, X-ray photoelectron spectroscopy (XPS), recycle experiments and photocurrent characterizations, it was found that TiO2 would produce electropositive defects during photocatalytic H-2 evolution, inevitably leading to the decline of H-2 production activity. Thanks to the electrostatic interaction, the electronegative Pt source not only promoted charge separation, but preferential deposited on electropositive defects, which acted as the defect repair agent, and thus resulted in the increased photocatalytic stability. This work may provide a new perspective for enhancing photocatalytic stability of hydrogen production.
引用
收藏
页码:1 / 12
页数:12
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