4.5 Article

Bifunctional photocatalysis of TiO2/Cu2O composite under visible light: Ti3+ in organic pollutant degradation and water splitting

期刊

JOURNAL OF PHYSICS AND CHEMISTRY OF SOLIDS
卷 72, 期 9, 页码 1104-1109

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.jpcs.2011.06.016

关键词

Semiconductors; Chemical synthesis; Sol-gel growth; Optical property; Microstructure

资金

  1. National Natural Science Foundation of China [20973070]
  2. National Key Basic Research Program of China [2009CB939704]
  3. Chinese Ministry of Education [109116]
  4. Natural Science Foundation of Jiangsu Province [BK2009724]
  5. Industry R&D program in Zhenjiang City [GY2009003]
  6. Hubei Provincial Department of Education [XD2010406]
  7. CCNU from the colleges' basic research and operation of MOE

向作者/读者索取更多资源

Photocatalytic experiment results under visible light demonstrate that both TiO2 and Cu2O have low activity for brilliant red X-3B degradation and neither can produce H-2 from water splitting. In comparison, TiO2/Cu2O composite can do the both efficiently. Further investigation shows that the formation of Ti3+ under visible light has great contribution. The mechanism of photocatalytic reaction is proposed based on energy band theory and experimental results. The photogenerated electrons from Cu2O were captured by Ti4+ ions in TiO2 and Ti4+ ions were further reduced to Ti3+ ions. Thus, the photogenerated electrons were stored in Ti3+ ions as the form of energy. These electrons trapped in Ti3+ can be released if a suitable electron acceptor is present. So, the electrons can be transferred to the interface between the composite and solution to participate in photocatalytic reaction. XPS spectra of TiO2/Cu2O composite before and after visible light irradiation were carried out and provided evidence for the presence of Ti3+. The image of high-resolution transmission electron microscopy demonstrates that TiO2 combines with Cu2O tightly. So, the photogenerated electrons can be transferred from Cu2O to TiO2. (C) 2011 Elsevier Ltd. All rights reserved.

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