Photocatalytic water splitting using Pt-loaded visible light-responsive TiO2 thin film photocatalysts

被引:161
作者
Kitano, Masaaki
Takeuchi, Masato
Matsuoka, Masaya
Thomas, John A.
Anpo, Masakazu
机构
[1] Osaka Prefecture Univ, Grad Sch Engn, Dept Appl Chem, Naka Ku, Sakai, Osaka 5998531, Japan
[2] Univ Cambridge, Dept Mat Sci & Met, Cambridge CB2 3QZ, England
关键词
water decomposition; evolution of H-2 and O-2; photocatalysis; visible light-responsive TiO2 photocatalyst; thin film photocatalyst;
D O I
10.1016/j.cattod.2006.07.043
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Visible light-responsive TiO2 (Vis-TiO2) thin films which exhibit a unique declined O/Ti composition from the surface to the deep inside bulk have been successfully developed under a substrate temperature of 873 K by applying a radio-frequency magnetron sputtering deposition (RF-MS) method. By controlling the Ar gas pressure during the deposition procedure, it was possible to control the optical properties of the TiO2 thin films. These Pt-loaded Vis-TiO2 thin films were found to decompose water involving methanol (H-2 production reaction from H2O) or 0.05 M silver nitrate solution (O-2 production reaction from H2O) under visible light (lambda >= 420 nm) irradiation. In particular, the photo-oxidation of water to produce O-2 proceeds under visible light of wavelengths longer than 550 nm. The conduction and valence bands of Vis-TiO2 thin film photocatalysts were, thus, seen to have enough potential for the decomposition of water into H-2 and O-2 under visible light irradiation. These thin films were found to be stable and the declined composition could be retained even after the reaction and calcination treatment at 723 K in O-2 atmosphere. Moreover, the stoichiometric and separate evolution of H-2 and O-2 from H2O could be successfully achieved using an H-type glass container even under visible light. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:133 / 138
页数:6
相关论文
共 28 条
  • [1] Photocatalytic overall water splitting under visible light by TaON and WO3 with an IO3 -/I- shuttle redox mediator
    Abe, R
    Takata, T
    Sugihara, H
    Domen, K
    [J]. CHEMICAL COMMUNICATIONS, 2005, (30) : 3829 - 3831
  • [2] The preparation and characterization of highly efficient titanium oxide-based photofunctional materials
    Anpo, M
    Dohshi, S
    Kitano, M
    Hu, Y
    Takeuchi, M
    Matsuoka, M
    [J]. ANNUAL REVIEW OF MATERIALS RESEARCH, 2005, 35 : 1 - 27
  • [3] Preparation, characterization, and reactivities of highly functional titanium oxide-based photocatalysts able to operate under UV-visible light irradiation: Approaches in realizing high efficiency in the use of visible light
    Anpo, M
    [J]. BULLETIN OF THE CHEMICAL SOCIETY OF JAPAN, 2004, 77 (08) : 1427 - 1442
  • [4] The design and development of highly reactive titanium oxide photocatalysts operating under visible light irradiation
    Anpo, M
    Takeuchi, M
    [J]. JOURNAL OF CATALYSIS, 2003, 216 (1-2) : 505 - 516
  • [5] Utilization of TiO2 photocatalysts in green chemistry
    Anpo, M
    [J]. PURE AND APPLIED CHEMISTRY, 2000, 72 (07) : 1265 - 1270
  • [6] MECHANISM OF PHOTOCATALYTIC DECOMPOSITION OF WATER INTO H-2 AND O-2 OVER NIO - SRTIO3
    DOMEN, K
    KUDO, A
    ONISHI, T
    [J]. JOURNAL OF CATALYSIS, 1986, 102 (01) : 92 - 98
  • [7] ELECTROCHEMICAL PHOTOLYSIS OF WATER AT A SEMICONDUCTOR ELECTRODE
    FUJISHIMA, A
    HONDA, K
    [J]. NATURE, 1972, 238 (5358) : 37 - +
  • [8] ENVIRONMENTAL APPLICATIONS OF SEMICONDUCTOR PHOTOCATALYSIS
    HOFFMANN, MR
    MARTIN, ST
    CHOI, WY
    BAHNEMANN, DW
    [J]. CHEMICAL REVIEWS, 1995, 95 (01) : 69 - 96
  • [9] Explaining the enhanced photocatalytic activity of Degussa P25 mixed-phase TiO2 using EPR
    Hurum, DC
    Agrios, AG
    Gray, KA
    Rajh, T
    Thurnauer, MC
    [J]. JOURNAL OF PHYSICAL CHEMISTRY B, 2003, 107 (19) : 4545 - 4549
  • [10] Quantitative analysis of defective sites in titanium(IV) oxide photocatalyst powders
    Ikeda, S
    Sugiyama, N
    Murakami, S
    Kominami, H
    Kera, Y
    Noguchi, H
    Uosaki, K
    Torimoto, T
    Ohtani, B
    [J]. PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 2003, 5 (04) : 778 - 783