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author:

Zhang, Z. (Zhang, Z..) [1] | Long, J. (Long, J..) [2] | Xie, X. (Xie, X..) [3] | Zhuang, H. (Zhuang, H..) [4] | Zhou, Y. (Zhou, Y..) [5] | Lin, H. (Lin, H..) [6] | Yuan, R. (Yuan, R..) [7] | Dai, W. (Dai, W..) [8] | Ding, Z. (Ding, Z..) [9] | Wang, X. (Wang, X..) [10] | Fu, X. (Fu, X..) [11]

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Scopus

Abstract:

This paper focuses on improving photocatalytic activity of N-doped TiO 2 photocatalyst for efficiently utilizing solar energy. A simple H 2 reduction is found to remarkably enhance the photocatalytic activity of N-doped TiO 2 for ethylene oxidation under visible light or simulated solar light irradiation. Ultraviolet/visible diffuse reflectance spectra (UV/vis DRS), X-ray photoelectron spectra (XPS) and electron paramagnetic resonance (EPR) spectra were employed to characterize the surface properties and chemical states of nitrogen dopants in H 2-reduced N-doped TiO 2. The results reveal that H 2 reduction facilitates the creation of oxygen vacancies and Ti 3+ species in N-doped TiO 2 but without removal of nitrogen species from catalyst surface. The formed oxygen vacancies and Ti 3+ species seriously influence electron excitation from doped nitrogen species and subsequently tune the generation of active oxygen species O 2 - radicals on N-doped TiO 2. The synergistic effect of oxygen vacancies and doped nitrogen species contributes to the enhancement of photocatalytic activity of N-doped TiO 2 samples, but the formed Ti 3+ ions largely suppress the photocatalytic activity. © 2012 Elsevier B.V.

Keyword:

Ethylene photooxidation; H 2 reduction; N-doped TiO 2; Oxygen vacancies; Synergistic effect

Community:

  • [ 1 ] [Zhang, Z.]Research Institute of Photocatalysis, State Key Laboratory Breeding Base of Photocatalysis, Fuzhou University, Fuzhou 350002, China
  • [ 2 ] [Long, J.]Research Institute of Photocatalysis, State Key Laboratory Breeding Base of Photocatalysis, Fuzhou University, Fuzhou 350002, China
  • [ 3 ] [Xie, X.]Research Institute of Photocatalysis, State Key Laboratory Breeding Base of Photocatalysis, Fuzhou University, Fuzhou 350002, China
  • [ 4 ] [Zhuang, H.]Research Institute of Photocatalysis, State Key Laboratory Breeding Base of Photocatalysis, Fuzhou University, Fuzhou 350002, China
  • [ 5 ] [Zhou, Y.]Research Institute of Photocatalysis, State Key Laboratory Breeding Base of Photocatalysis, Fuzhou University, Fuzhou 350002, China
  • [ 6 ] [Lin, H.]Research Institute of Photocatalysis, State Key Laboratory Breeding Base of Photocatalysis, Fuzhou University, Fuzhou 350002, China
  • [ 7 ] [Yuan, R.]Research Institute of Photocatalysis, State Key Laboratory Breeding Base of Photocatalysis, Fuzhou University, Fuzhou 350002, China
  • [ 8 ] [Dai, W.]Research Institute of Photocatalysis, State Key Laboratory Breeding Base of Photocatalysis, Fuzhou University, Fuzhou 350002, China
  • [ 9 ] [Ding, Z.]Research Institute of Photocatalysis, State Key Laboratory Breeding Base of Photocatalysis, Fuzhou University, Fuzhou 350002, China
  • [ 10 ] [Wang, X.]Research Institute of Photocatalysis, State Key Laboratory Breeding Base of Photocatalysis, Fuzhou University, Fuzhou 350002, China
  • [ 11 ] [Fu, X.]Research Institute of Photocatalysis, State Key Laboratory Breeding Base of Photocatalysis, Fuzhou University, Fuzhou 350002, China

Reprint 's Address:

  • [Zhang, Z.]Research Institute of Photocatalysis, State Key Laboratory Breeding Base of Photocatalysis, Fuzhou University, Fuzhou 350002, China

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Source :

Applied Catalysis A: General

ISSN: 0926-860X

Year: 2012

Volume: 425-426

Page: 117-124

3 . 4 1

JCR@2012

4 . 7 0 0

JCR@2023

JCR Journal Grade:1

CAS Journal Grade:2

Cited Count:

WoS CC Cited Count:

SCOPUS Cited Count:

ESI Highly Cited Papers on the List: 0 Unfold All

WanFang Cited Count:

Chinese Cited Count:

30 Days PV: 0

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