β-AgAl1-xGaxO2 Solid-Solution Photocatalysts: Continuous Modulation of Electronic Structure toward High-Performance Visible-Light Photoactivity

被引:269
作者
Ouyang, Shuxin [1 ]
Ye, Jinhua [1 ,2 ]
机构
[1] NIMS, Photocatalyt Mat Ctr PCMC, Tsukuba, Ibaraki 3050047, Japan
[2] NIMS, Int Ctr Mat Nanoarchitecton, Tsukuba, Ibaraki 3050047, Japan
关键词
BAND-STRUCTURE; DRIVEN PHOTOCATALYSTS; HYDROGEN-PRODUCTION; CRYSTAL-STRUCTURES; TITANIUM-DIOXIDE; H-2; EVOLUTION; WATER; SEMICONDUCTOR; DECOMPOSITION; SERIES;
D O I
10.1021/ja110691t
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A series of beta-AgAl1-xGaxO2 solid-solution materials were explored as novel visible-light-sensitive photocatalysts. These Ag-based solid solutions crystallize in a homogeneous crystal structure with orthorhombic symmetry but possess continuously modulated band gaps from 2.19 to 2.83 eV by decreasing the ratios of Ga/Al. Their photoactivities for iso-propanol degradation were found to be dependent on the variation of chemical compositions. Among them, the beta-AgAl0.6Ga0.4O2 sample showed the highest photocatalytic performance, which simultaneously exhibited 35 and 63 times higher activities than two terminus materials, beta-AgAlO2 and beta-AgGaO2, respectively. The apparent quantum efficiency of this sample for iso-propanol photodegradation achieved up to 37.3% at the wavelength of 425 +/- 12 nm. The theoretical calculation based on density functional theory demonstrated that the levels of valence band maximum of beta-AgAl1-xGaxO2 are similar, but the levels of conduction band minimum are gradually negatively shifted with the increase of the ratio of Ga/Al, thereby continuously narrowing the band gap. Nevertheless, the highest activity observed on beta-AgAl0.6Ga0.4O2 may be attributed to its optimized band structure, which adapts the balance between effective visible-light absorption and adequate redox potentials.
引用
收藏
页码:7757 / 7763
页数:7
相关论文
共 47 条
  • [1] Pristine simple oxides as visible light driven photocatalysts: Highly efficient decomposition of organic compounds over platinum-loaded tungsten oxide
    Abe, Ryu
    Takami, Hiticishi
    Murakami, Naoya
    Ohtani, Bunsho
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2008, 130 (25) : 7780 - +
  • [2] State of the art and perspectives on materials and applications of photocatalysis over TiO2
    Agrios, AG
    Pichat, P
    [J]. JOURNAL OF APPLIED ELECTROCHEMISTRY, 2005, 35 (7-8) : 655 - 663
  • [3] PHOTOLUMINESCENCE AND PHOTOCATALYTIC ACTIVITY OF HIGHLY DISPERSED TITANIUM-OXIDE ANCHORED ONTO POROUS VYCOR GLASS
    ANPO, M
    AIKAWA, N
    KUBOKAWA, Y
    CHE, M
    LOUIS, C
    GIAMELLO, E
    [J]. JOURNAL OF PHYSICAL CHEMISTRY, 1985, 89 (23) : 5017 - 5021
  • [4] Experimental microkinetic approach of the photocatalytic oxidation of isopropyl alcohol on TiO2.: Part 1.: Surface elementary steps involving gaseous and adsorbed C3HxO species
    Arsac, F
    Bianchi, D
    Chovelon, JM
    Ferronato, C
    Herrmann, JM
    [J]. JOURNAL OF PHYSICAL CHEMISTRY A, 2006, 110 (12) : 4202 - 4212
  • [5] Visible-light photocatalysis in nitrogen-doped titanium oxides
    Asahi, R
    Morikawa, T
    Ohwaki, T
    Aoki, K
    Taga, Y
    [J]. SCIENCE, 2001, 293 (5528) : 269 - 271
  • [6] Bard A. J., 1985, Standard Potentials in Aqueous Solution, P49
  • [7] The impact of nanoscience on heterogeneous catalysis
    Bell, AT
    [J]. SCIENCE, 2003, 299 (5613) : 1688 - 1691
  • [8] PHOTOELECTROLYSIS AND PHYSICAL-PROPERTIES OF SEMICONDUCTING ELECTRODE WO3
    BUTLER, MA
    [J]. JOURNAL OF APPLIED PHYSICS, 1977, 48 (05) : 1914 - 1920
  • [9] PREDICTION OF FLATBAND POTENTIALS AT SEMICONDUCTOR-ELECTROLYTE INTERFACES FROM ATOMIC ELECTRONEGATIVITIES
    BUTLER, MA
    GINLEY, DS
    [J]. JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1978, 125 (02) : 228 - 232
  • [10] Synergistic Effect of CdSe Quantum Dot Sensitization and Nitrogen Doping of TiO2 Nanostructures for Photoelectrochemical Solar Hydrogen Generation
    Hensel, Jennifer
    Wang, Gongming
    Li, Yat
    Zhang, Jin Z.
    [J]. NANO LETTERS, 2010, 10 (02) : 478 - 483