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author:

Zhang, Zizhong (Zhang, Zizhong.) [1] | Long, Jinlin (Long, Jinlin.) [2] | Xie, Xiuqiang (Xie, Xiuqiang.) [3] | Zhuang, Huaqiang (Zhuang, Huaqiang.) [4] | Zhou, Yangen (Zhou, Yangen.) [5] | Lin, Huan (Lin, Huan.) [6] | Yuan, Rusheng (Yuan, Rusheng.) [7] | Dai, Wenxin (Dai, Wenxin.) [8] | Ding, Zhengxin (Ding, Zhengxin.) [9] | Wang, Xuxu (Wang, Xuxu.) [10] | Fu, Xianzhi (Fu, Xianzhi.) [11]

Indexed by:

EI

Abstract:

This paper focuses on improving photocatalytic activity of N-doped TiO 2 photocatalyst for efficiently utilizing solar energy. A simple H2 reduction is found to remarkably enhance the photocatalytic activity of N-doped TiO2 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 H2-reduced N-doped TiO2. The results reveal that H2 reduction facilitates the creation of oxygen vacancies and Ti3+ species in N-doped TiO2 but without removal of nitrogen species from catalyst surface. The formed oxygen vacancies and Ti3+ species seriously influence electron excitation from doped nitrogen species and subsequently tune the generation of active oxygen species O2- radicals on N-doped TiO2. The synergistic effect of oxygen vacancies and doped nitrogen species contributes to the enhancement of photocatalytic activity of N-doped TiO2 samples, but the formed Ti3+ ions largely suppress the photocatalytic activity. © 2012 Elsevier B.V.

Keyword:

Doping (additives) Electron spin resonance spectroscopy Ethylene Ionization of gases Light Nitrogen Nitrogen removal Oxygen vacancies Paramagnetic resonance Photocatalytic activity Photoelectron spectroscopy Photooxidation Solar energy Titanium dioxide

Community:

  • [ 1 ] [Zhang, Zizhong]Research Institute of Photocatalysis, State Key Laboratory Breeding Base of Photocatalysis, Fuzhou University, Fuzhou 350002, China
  • [ 2 ] [Long, Jinlin]Research Institute of Photocatalysis, State Key Laboratory Breeding Base of Photocatalysis, Fuzhou University, Fuzhou 350002, China
  • [ 3 ] [Xie, Xiuqiang]Research Institute of Photocatalysis, State Key Laboratory Breeding Base of Photocatalysis, Fuzhou University, Fuzhou 350002, China
  • [ 4 ] [Zhuang, Huaqiang]Research Institute of Photocatalysis, State Key Laboratory Breeding Base of Photocatalysis, Fuzhou University, Fuzhou 350002, China
  • [ 5 ] [Zhou, Yangen]Research Institute of Photocatalysis, State Key Laboratory Breeding Base of Photocatalysis, Fuzhou University, Fuzhou 350002, China
  • [ 6 ] [Lin, Huan]Research Institute of Photocatalysis, State Key Laboratory Breeding Base of Photocatalysis, Fuzhou University, Fuzhou 350002, China
  • [ 7 ] [Yuan, Rusheng]Research Institute of Photocatalysis, State Key Laboratory Breeding Base of Photocatalysis, Fuzhou University, Fuzhou 350002, China
  • [ 8 ] [Dai, Wenxin]Research Institute of Photocatalysis, State Key Laboratory Breeding Base of Photocatalysis, Fuzhou University, Fuzhou 350002, China
  • [ 9 ] [Ding, Zhengxin]Research Institute of Photocatalysis, State Key Laboratory Breeding Base of Photocatalysis, Fuzhou University, Fuzhou 350002, China
  • [ 10 ] [Wang, Xuxu]Research Institute of Photocatalysis, State Key Laboratory Breeding Base of Photocatalysis, Fuzhou University, Fuzhou 350002, China
  • [ 11 ] [Fu, Xianzhi]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: 2

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