Fabrication and Photocatalytic Activity of Pt-Inserted Titania Nanotubes
LI Hai-long1,LUO Wu-lin1,TIAN Wen-yu1,CHEN Tao1,LI Chun1,SUN Mao1,ZHU Di1, LIU Ran-ran1, ZHAO Yu-liang2, LIU Chun-li1*
1. Beijing National Laboratory for Molecular Science, College of Chemistry and Molecular Engineering, Peking University, Beijing 100871, China 2. Laboratory for Bio-Environmental Health Sciences of Nanoscale Materials and Nanosafety and Key Laboratory of Nuclear Analytical Techniques, Institute of High Energy Physics, Chinese Academy of Sciences, Beijing 100049, China
Abstract:Titania nanotubes (TNTs) were synthesized by hydrothermal treatment of rutile-phase TiO2 nanoparticals in NaOH solution at 110 ℃ for 24 hours. After drying in aceton for 36 h, the TNTs were under vacuum drying for 24 h at room temperature. The Pt-inserted titania nanotubes (Pt/TNTs) were obtained by filling H2PtCl6 ethanol solution into the TNTs after vacuum drying. The characterizations of the as-synthesized samples were confirmed by TEM, XRD, and UV-Vis. The photocatalytic activity of the Pt/TNTs was investigated by photo-induced decomposition of methyl orange(MO)under the main 365 nm UV-light. In order to comparison, the photocatalytic activity of both the rutile-phase TiO2 nanoparticles and pure TNTs were also investigated at the same time under the same experimental conditions. The TEM images show that the TNTs are hollow, a few hundred nanometers long, and the inner/outer diameter is about 6/10 nm. The crystal structure of TNTs is H2Ti2O5·H2O with a little Na. Both the shape and the crystalline of the TNTs are not changed after the modification. The oval or round Pt0 nanoparticals, about 3 nm in diameter, are found only in the nanotubes. Pt/TNTs exhibit enhanced absorption at the visible range in the UV-Vis spectra and its start absorption band edge(λ0≈457 nm)is obviously redshifted compared to the rutile-phase TiO2 nanoparticals and pure TNTs. The Pt nanoparticles are found to significantly enhance the photocatalytic activity of TNTs. Pt/TNTs are demonstrated to be highly efficient for the UV-light induced photocatalytic decomposition of MO compared to both the rutile-phase TiO2 nanoparticals and pure TNTs. After irradiation for 60 min, the photocatalysis decomposition rate of MO in rutile-phase TiO2 nanoparticals, TNTs and Pt/TNTs are 46.8%,57.2% and 84.6% respectively.
[1] Fujishim A, Honda K. Nature, 1972, 238(5358): 37. [2] ZHENG Huai-li, ZHANG Jun-hua, XIONG Wen-qiang(郑怀礼, 张峻华, 熊文强). Spectroscopy and Spectral Analysis(光谱学与光谱分析), 2004, 24(8): 1003. [3] Yu J G, Yu H G, Cheng B, et al. J. Mol. Catal. A-Chem., 2006, 249(1-2): 135. [4] Hoyer P. Langmuir, 1996, 12(6): 1411. [5] Jung J H, Kobayashi H, van Bommel K J C, et al. Chem. Matter, 2002, 14(4): 1445. [6] Gong D, Grimes C A, Varghese O K, et al. J. Mater. Res., 2001, 16(12): 3331. [7] Mor G K, Varghese O K, Paulose M, et al. Sol. Energy Mater. Sol. Cells, 2006, 90(14): 2011. [8] Kasuga T, Hiramatsu M, Hoson A, et al. Langmuir, 1998, 14(12): 3160. [9] Yao B D, Chan Y F, Zhang X Y, et al. Applied Physics Letters, 2003, 82(2): 281. [10] Suzuki Y, Yoshikawa S. J. Mater. Res., 2004, 19(4): 982. [11] Chien S H, Liou Y C, Kuo M C. Synth. Metals, 2005, 152(1-3): 333. [12] Zhu B L, Guo Q, Huang X L, et al. J. Mol. Catal. A-Chem., 2006, 249(1-2): 211. [13] Paramasivalm I, Macak J M, Schmuki P. Electrochemistry Communications, 2008, 10(1): 71. [14] Ma X Q, Feng C X, Jin Z S, et al. J. Nanopart. Res., 2005, 7(6): 681.