Electron-transfer cascade from CdSe@ZnSe core-shell quantum dot accelerates photoelectrochemical H2 evolution on TiO2 nanotube arrays

被引:56
作者
Jia, Jia [1 ]
Xue, Peng [1 ]
Hu, Xiaoyun [2 ]
Wang, Yishan [3 ]
Liu, Enzhou [1 ,2 ]
Fan, Jun [1 ]
机构
[1] Northwest Univ, Sch Chem Engn, Xian 710069, Peoples R China
[2] Northwest Univ, Sch Phys, Xian 710069, Peoples R China
[3] Chinese Acad Sci, State Key Lab Transient Opt & Photon, Xian 710119, Shaanxi, Peoples R China
基金
中国博士后科学基金; 中国国家自然科学基金;
关键词
Photoelectrochemical; H-2; evolution; Quantum dots; CdSe@ZnSe core-shell; TiO2 nanotube arrays; HIGHLY EFFICIENT; SOLAR-CELLS; PHOTOCATALYST; PERFORMANCE; SEMICONDUCTORS; LAYER; NANOCOMPOSITES; NANOSHEETS; SURFACE; STATES;
D O I
10.1016/j.jcat.2019.05.028
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
A novel TiO2-CdSe-ZnSe electron-transfer cascade heterostructure with nanoscale precision is synthesized for hydrogen evolution, exhibiting an obvious hierarchical absorption and improved separation efficiency for photocarriers. The key to this constructed structure lies in the in-situ deposition of CdSe quantum-dots onto the surface of TiO2 followed by the epitaxial growth of a ZnSe shell. In this conditions, the CdSe core can serve as a buffer layer for the electrons on the conduction band of the ZnSe shell, enabling them to rapidly migrate to the TiO2 and later to the opposite electrode to produce H-2; meanwhile, due to high injection efficiency in the cascade type II structure, holes from TiO2 are transferred to the electrolyte interface, where the oxidation reaction of hole trapping scavenger occurs. Surprisingly, this heterostructure shows a significantly enhanced photocurrent density (1.45 mA cm(-2)), favorable H-2 production rates (252 mu mol h(-1) cm(-2)) and moderate durability under light irradiation. (C) 2019 Elsevier Inc. All rights reserved.
引用
收藏
页码:81 / 94
页数:14
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