4.8 Article

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

期刊

JOURNAL OF CATALYSIS
卷 375, 期 -, 页码 81-94

出版社

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.jcat.2019.05.028

关键词

Photoelectrochemical; H-2 evolution; Quantum dots; CdSe@ZnSe core-shell; TiO2 nanotube arrays

资金

  1. National Natural Science Foundation of China [21676213, 21476183]
  2. China Postdoctoral Science Foundation [2016M600809]
  3. Natural Science Basic Research Plan in Shaanxi Province of China [2017JM2026, 2018JM5020]
  4. Open Research Fund of State Key Laboratory of Transient Optics and Photonics, Chinese Academy of Sciences [SKLST201703]
  5. Graduate Student Innovation Funds of Northwest University [YYB17015]

向作者/读者索取更多资源

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.

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