Citation: ZHAO Wei-Rong, SHI Qiao-Meng, LIU Ying. Performance, Deactivation and Regeneration of SnO2/TiO2 Nanotube Composite Photocatalysts[J]. Acta Physico-Chimica Sinica, ;2014, 30(7): 1318-1324. doi: 10.3866/PKU.WHXB201404222 shu

Performance, Deactivation and Regeneration of SnO2/TiO2 Nanotube Composite Photocatalysts

  • Received Date: 26 January 2014
    Available Online: 22 April 2014

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  • SnO2/TiO2 nanotube composite photocatalysts were synthesized by microwave-assisted hydrothermal and micro-emulsion methods. The photocatalysts were characterized by X-ray diffraction (XRD), transmission electron microscopy with energy-dispersive X-ray spectroscopy (TEM/EDX), and electrochemical techniques. Toluene was chosen as a model pollutant to evaluate the performance, deactivation, and regeneration behavior of the photocatalysts under ultraviolet (UV) and vacuum ultraviolet (VUV) irradiation. The results show that ternary heterojunctions of SnO2/TiO2 nanotube composite photocatalysts including anatase TiO2 (A-TiO2)/rutile TiO2 (R-TiO2), A-TiO2/SnO2, and R-TiO2/SnO2 were successfully created. They were able to separate photogenerated electron-hole pairs efficiently, and promote photocatalytic activity accordingly. SnO2/TiO2 showed the best photocatalytic performance. Under UV or VUV irradiation, the toluene degradation rate of SnO2/TiO2 was 100%, and the CO2 formation rate (k2) of SnO2/TiO2 was approximately 3 times higher than that of P25. Because of the low mineralization rate under UV irradiation, the refractory intermediates generated can occupy active photocatalytic sites on the photocatalyst surface, which hinders the photocatalytic oxidation rate. After 20 h of UV irradiation, the k2 of SnO2/TiO2 decreased from 138.5 to 76.1 mg·m-3·h-1, implying that the photocatalysts can be deactivated quickly. VUV irradiation was employed to regenerate the deactivated SnO2/SnO2/TiO2 nanotube composite photocatalysts were synthesized by microwave-assisted hydrothermal and micro-emulsion methods. The photocatalysts were characterized by X-ray diffraction (XRD), transmission electron microscopy with energy-dispersive X-ray spectroscopy (TEM/EDX), and electrochemical techniques. Toluene was chosen as a model pollutant to evaluate the performance, deactivation, and regeneration behavior of the photocatalysts under ultraviolet (UV) and vacuum ultraviolet (VUV) irradiation. The results show that ternary heterojunctions of SnO2/TiO2 nanotube composite photocatalysts including anatase TiO2 (A-TiO2)/rutile TiO2 (R-TiO2), A-TiO2/SnO2, and R-TiO2/SnO2 were successfully created. They were able to separate photogenerated electron-hole pairs efficiently, and promote photocatalytic activity accordingly. SnO2/TiO2 showed the best photocatalytic performance. Under UV or VUV irradiation, the toluene degradation rate of SnO2/TiO2 was 100%, and the CO2 formation rate (k2) of SnO2/TiO2 was approximately 3 times higher than that of P25. Because of the low mineralization rate under UV irradiation, the refractory intermediates generated can occupy active photocatalytic sites on the photocatalyst surface, which hinders the photocatalytic oxidation rate. After 20 h of UV irradiation, the k2 of SnO2/TiO2 decreased from 138.5 to 76.1 mg·m-3·h-1, implying that the photocatalysts can be deactivated quickly. VUV irradiation was employed to regenerate the deactivated SnO2/TiO2 because reactive species such as ·OH, O2, O(1D), O(3P), and O3 can be generated. These play an important role in the oxidation of refractory intermediates on the photocatalyst surface, and k2 increased to 143.6 mg·m-3·h-1 accordingly. Therefore, UV photodegradation combined with VUV regeneration could be a feasible photocatalytic process because of a synergistic effect between UV and VUV.

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    1. [1]

      (1) Wang, C. H.; Shao, C. L.; Zhang, X. T.; Liu, Y. C. Inorg. Chem. 2009, 48, 7261. doi: 10.1021/ic9005983

    2. [2]

      (2) Chang, S. Y.; Chen, S. F.; Huang, Y. C. J. Phys. Chem. C 2011, 115, 1600. doi: 10.1021/jp109103a

    3. [3]

      (3) Zhou, X. F.; Cao, J. L.; Xu, M. F.;Wang, Z. S.; Lu, J. Mater. Res. Bull. 2013, 48, 4942. doi: 10.1016/j.materresbull. 2013.07.031

    4. [4]

      (4) Wu, L.; Xing, J.; Hou, Y.; Xiao, F. Y.; Li, Z.; Yang, H. G. Chem. Eur. J. 2013, 19, 8688. doi: 10.1002/chem.201390096

    5. [5]

      (5) Smith,W.;Wolcott, A.; Fitzmorris, R. C.; Zhang, J. Z.; Zhao, Y. P. J. Mater. Chem. 2011, 21, 10792. doi: 10.1039/c1jm11629k

    6. [6]

      (6) Su, C. Y.; Shao, C. L.; Liu, Y. C. J. Colloid Interface Sci. 2010, 346, 324. doi: 10.1016/j.jcis.2010.02.027

    7. [7]

      (7) Wu, Z. Y.; Zhao, G. H.; Zhang, Y. N.; Tian, H. Y.; Li, D. M. J. Phys. Chem. C 2012, 116, 12829. doi: 10.1021/jp300374s

    8. [8]

      (8) Chaguetmi, S.; Mammeri, F.; Nowak, S.; Decorse, P.; Lecoq, H.; Gaceur, M.; Naceur, J. B.; Achour, S.; Chtourou, R.; Ammar, S. RSC Adv. 2013, 3, 2572. doi: 10.1039/c2ra21684a

    9. [9]

      (9) Jovi, F.; Tomaši, V.; Davidson, A.; Nogier, J. P.; Li,W.; Kosar, V. Chem. Biochem. Eng. Q. 2013, 27, 37.

    10. [10]

      (10) Mo, J. H.; Zhang, Y. P.; Xu, Q. J.; Lamson, J. J.; Zhao, R. Y. Atmos. Environ. 2009, 43, 2229. doi: 10.1016/j.atmosenv.2009.01.034

    11. [11]

      (11) Jeong, J. Y.; Sekiguchi, K.; Sakamoto, K. Chemosphere 2004, 57, 663. doi: 10.1016/j.chemosphere.2004.05.037

    12. [12]

      (12) Huang, H. B.; Leung, D. Y. C.; Li, G. S.; Leung, M. K. H.; Fu, X. L. Catal. Today 2011, 175, 310. doi: 10.1016/j.cattod.2011.04.015

    13. [13]

      (13) Zhao,W. R.; Yang, Y. N.; Dai, J. S.; Liu, F. F.;Wang, Y. Chemosphere 2013, 91, 1002. doi: 10.1016/j.chemosphere.2013.01.086

    14. [14]

      (14) Chen, S. H.; Xu, Y.; Lu, B. L.;Wu, D. Acta Phys. -Chim. Sin. 2011, 27, 2933. [陈淑海, 徐耀, 吕宝亮, 吴东. 物理化学学报, 2011, 27, 2933.]

    15. [15]

      (15) Ou, H. H.; Lo, S. L.; Liao, C. H. J. Phys. Chem. C 2011, 115, 4000. doi: 10.1021/jp1076005

    16. [16]

      (16) Zhang, H.; Li, G. R.; An, L. P.; Yan, T. Y.; Gao, X. P.; Zhu, H. Y. J. Phys. Chem. C 2007, 111, 6143. doi:10.1021/jp0702595

    17. [17]

      (17) Zhao,W. R.;Wang, Y.; Yang, Y. N.; Tang, J.; Yang, Y. Appl. Catal. B: Environ. 2012, 115, 90.

    18. [18]

      (18) Dong, L. F.; Gari, R. R. S.; Li, Z.; Craig, M. M.; Hou, S. F. Carbon 2010, 48, 781. doi: 10.1016/j.carbon.2009.10.027

    19. [19]

      (19) Tang, Z. R.; Li, F.; Zhang, Y. H.; Fu, X. Z.; Xu, Y. J. J. Phys. Chem. C 2011, 115, 7880. doi: 10.1021/jp1115838

    20. [20]

      (20) Debono, O.; Thevenet, F.; Gravejat, P.; Hequet, V.; Raillard, C.; Lecoq, L. Appl. Catal. B: Environ. 2011, 106, 600. doi: 10.1016/j.apcatb.2011.06.021

    21. [21]

      (21) Jankulovska, M.; Berger, T.; Lana-Villarreal, T.; Gómez, R. Electrochim. Acta 2012, 62, 172. doi: 10.1016/j.electacta.2011.12.016

    22. [22]

      (22) Komaguchi, K.; Nakano, H.; Araki, A.; Harima, Y. Chem. Phys. Lett. 2006, 428, 338. doi: 10.1016/j.cplett.2006.07.003

    23. [23]

      (23) Xing, M. Y.; Zhang, J. L.; Chen, F.; Tian, B. Z. Chem. Commun. 2011, 47, 4947. doi: 10.1039/c1cc10537j

    24. [24]

      (24) Zhao, L.; Ran, J. R.; Shu, Z.; Dai, G. T.; Zhai, P. C.;Wang, S. M. Int. J. Photoenergy 2012, 2012, 1. doi: 10.1155/2012/472958

    25. [25]

      (25) Huang, H. B.; Li,W. B. Appl. Catal. B: Environ. 2011, 102, 449. doi: 10.1016/j.apcatb.2010.12.025

    26. [26]

      (26) Zhao,W. R.; Dai, J. S.; Liu, F. F.; Bao, J. Z.;Wang, Y.; Yang, Y.; Yang, Y. N.; Zhao, D. Y. Sci. Total Environ. 2012, 438, 201. doi: 10.1016/j.scitotenv.2012.08.081


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