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Effect of Structural Parameters of TiO2 Nanotube Arrays upon Their Photocatalytic/Photoelectrocatalytic Performance 被引量:1

Effect of Structural Parameters of TiO2 Nanotube Arrays upon Their Photocatalytic/Photoelectrocatalytic Performance
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摘要 The effect of structural parameters of TiO2 nanotube arrays (TNAs) upon their photocatalytic/photoelectro- catalytic performance is studied by comparing the morphological characteristics and physicochemical properties with different tube lengths prepared from three kinds of electrolytes. The results show that the UV-Vis absorption edge of TNAs red-shifted with the increment of tube length and the short TNAs possess higher bandgap energy. The variation tendency of electrochemical window of TNAs is DMSO (5.5 V)〉Cit (3.2 V)〉HF (1.8 V). The long TNAs possess higher photocatalytic (PC) reactivity suggesting the surface roughness factor is the main determinant of PC efficiency, although, there is obvious recombination effects for the long TNAs. Evidenced by the positive correlation between tube length and photoelectrocatalytic (PEC) efficiency for TNAs from the same electrolyte, the enhancement of the tube length could lead to better PEC reactivity, but when the tube length is over a certain value, the PEC degradation rate no longer increases but decreases. The long TNAs with large surface roughness factor prepared from Cit and DMSO electrolytes exhibit comparative or even lower PEC performance compared with the short TNAs prepared from HF electrolyte, indicating that the PEC performance of TNAs was dominated by charge separation and photoelectron transfer properties rather than surface roughness coefficient and the tube length. The effect of structural parameters of TiO2 nanotube arrays (TNAs) upon their photocatalytic/photoelectro- catalytic performance is studied by comparing the morphological characteristics and physicochemical properties with different tube lengths prepared from three kinds of electrolytes. The results show that the UV-Vis absorption edge of TNAs red-shifted with the increment of tube length and the short TNAs possess higher bandgap energy. The variation tendency of electrochemical window of TNAs is DMSO (5.5 V)〉Cit (3.2 V)〉HF (1.8 V). The long TNAs possess higher photocatalytic (PC) reactivity suggesting the surface roughness factor is the main determinant of PC efficiency, although, there is obvious recombination effects for the long TNAs. Evidenced by the positive correlation between tube length and photoelectrocatalytic (PEC) efficiency for TNAs from the same electrolyte, the enhancement of the tube length could lead to better PEC reactivity, but when the tube length is over a certain value, the PEC degradation rate no longer increases but decreases. The long TNAs with large surface roughness factor prepared from Cit and DMSO electrolytes exhibit comparative or even lower PEC performance compared with the short TNAs prepared from HF electrolyte, indicating that the PEC performance of TNAs was dominated by charge separation and photoelectron transfer properties rather than surface roughness coefficient and the tube length.
出处 《Chinese Journal of Chemistry》 SCIE CAS CSCD 2011年第11期2236-2242,共7页 中国化学(英文版)
基金 Project supported by the National High Technology Research and Development Program of China (No. 2009AA063003), the State Key Development Program for Basic Research of China (No. 2009CB220004), the National Natural Science Foundation of China (No. 21177085) and the Research & Development Foundation of Shanghai Jiao Tong University.
关键词 PHOTOELECTROCATALYSIS PHOTOLYSIS TI02 NANOTUBES structural parameters photoelectrocatalysis, photolysis, Ti02, nanotubes, structural parameters
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  • 1Fujishima, A.; Honda, K. Nature 1972, 238, 37.
  • 2O'Regan, B.; Gratzel, M. Nature 1991, 353, 737.
  • 3Carey, J. H.; Lawrence, J.; Tosine, H. M. Bull. Contam. Toxicol. 1976, 16, 697.
  • 4Furube, A.; Wang, Z. S.; Sunahara, F.; Kohjiro Hara, K.; Ryuzi Katoh, R.; Tachiya, M. J. Am. Chem. Soc. 2010, 132, 6614.
  • 5Liu, H. J.; Liu, G. G.; Fan, J.; Zhou, Q. X.; Zhou, H. H.; Zhang, N.; Hou, Z. H.; Zhang, M. L.; He, Z. W. Chemosphere 2011, 82, 43.
  • 6Quan, X.; Yang, S.; Ruan, X.; Zhao, H. Environ. Sci. Technol. 2005, 39, 3770.
  • 7Varghese, O. K.; Paulose, M.; La Tempa, T. J.; Grimes, C A. Nano Lett. 2009, 9, 731.
  • 8Varghese, O. K.; Mor, G. K.; Grimes, C. A.; Paulose, M. Mukherjee, N. J. Nanosci. Nanotechnol. 2004, 4, 733.
  • 9Zheng, Q.; Zhou, B. X.; Bai, J.; Li, L. H.; Jin, Z. J.; Zhang J. L.; Li, J. H.; Liu, Y. B.; Cai, W. M.; Zhu, X. Y. Adv Mater. 2008, 20, 1044.
  • 10Kuang, D.; Brillet, J.; Chen, P.; Takata, M.; Uchida, S.Miura, H.; Sumioka, K.; Zakeeruddin, S. M.; Gratzel, M. ACS Nano 2008, 2, 1113.

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