Mixed NaNbxTa1-xO3 perovskites as photocatalysts for H2 production

被引:30
作者
Jana, Prabhas [1 ]
de la Pena O'Shea, Victor A. [1 ]
Mata Montero, Cristina [1 ]
Galvez, Pilar [2 ]
Pizarro, Patricia [1 ,2 ]
Coronado, Juan M. [1 ]
Serrano, David P. [1 ,2 ]
机构
[1] IMDEA Energy Inst, Thermochem Proc Unit, Madrid 28935, Spain
[2] Rey Juan Carlos Univ, ESCET, Chem & Environm Engn Grp, Madrid 28933, Spain
关键词
HYDROGEN-PRODUCTION; HIGHLY EFFICIENT; TANTALATE PHOTOCATALYSTS; NATAO3; PHOTOCATALYSTS; OXYGEN VACANCY; WATER; DECOMPOSITION; SURFACE; O-2; OXIDE;
D O I
10.1039/c4gc02064b
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Mixed perovskites NaNbxTa1-xO3 were prepared by solid state reaction (SSR) as well as by hydrothermal (Hyd) methods, and their photocatalytic activity for hydrogen production was studied using the water - methanol system. The assessment of the NaNbxTa1-xO3 materials obtained by the SSR method reveals that the activity of the individual NaTaO3 and NaNbO3 perovskite semiconductors is largely improved in their combined form. Among several compositions employed, the 1 : 1 molar ratio (NaNb0.5Ta0.5O3 sample) shows the best performance for H-2 production. On the other hand, using the Hyd method, which implies lower synthesis temperature, the photocatalytic activity of NaNb0.5Ta0.5O3 is enhanced compared to the material obtained by the high temperature SSR method. The characterization of the materials reveals that catalyst properties like high surface area, a larger proportion of the monoclinic crystalline phase and lower crystal defects for the NaNb0.5Ta0.5O3 photocatalyst synthesized by the hydrothermal route may be responsible for its superior activity. Further significant improvement in the activity of the NaNb0.5Ta0.5O3 semiconductor is achieved by the addition of Pt as the co-catalyst, showing that the loading amount has a great influence on the activity. The highest H-2 production rate (37.8 mu mol g(-1) min(-1)) is obtained for the catalyst prepared by the hydrothermal method (Hyd-NaNb0.5Ta0.5O3) with 0.125 wt% of Pt loading. Moreover, the developed Hyd-NaNb0.5Ta0.5O3 sample shows a stable H-2 evolution activity for several reuse cycles.
引用
收藏
页码:1735 / 1743
页数:9
相关论文
共 47 条
  • [1] Photocatalytic degradation of organic molecules on mesoporous visible-light-active Sn(II)-doped titania
    Boppana, Venkata Bharat Ram
    Lobo, Raul F.
    [J]. JOURNAL OF CATALYSIS, 2011, 281 (01) : 156 - 168
  • [2] Semiconductor-based Photocatalytic Hydrogen Generation
    Chen, Xiaobo
    Shen, Shaohua
    Guo, Liejin
    Mao, Samuel S.
    [J]. CHEMICAL REVIEWS, 2010, 110 (11) : 6503 - 6570
  • [3] Choudhury B, 2013, INT NANO LETT, V3, DOI 10.1186/2228-5326-3-25
  • [4] Hydrogen production by molecular photocatalysis
    Esswein, Arthur J.
    Nocera, Daniel G.
    [J]. CHEMICAL REVIEWS, 2007, 107 (10) : 4022 - 4047
  • [5] Photocatalytic activity of hydrothermally synthesized tantalate pyrochlores for overall water splitting
    Ikeda, S
    Fubuki, M
    Takahara, YK
    Matsumura, M
    [J]. APPLIED CATALYSIS A-GENERAL, 2006, 300 (02) : 186 - 190
  • [6] Preparation of K2La2Ti3O10 by polymerized complex method and photocatalytic decomposition of water
    Ikeda, S
    Hara, M
    Kondo, JN
    Domen, K
    Takahashi, H
    Okubo, T
    Kakihana, M
    [J]. CHEMISTRY OF MATERIALS, 1998, 10 (01) : 72 - 77
  • [7] Photocatalytic water splitting by RuO2-loaded metal oxides and nitrides with d0- and d10-related electronic configurations
    Inoue, Yasunobu
    [J]. ENERGY & ENVIRONMENTAL SCIENCE, 2009, 2 (04) : 364 - 386
  • [8] Photochemical splitting of water for hydrogen production by photocatalysis: A review
    Ismail, Adel A.
    Bahnemann, Detlef W.
    [J]. SOLAR ENERGY MATERIALS AND SOLAR CELLS, 2014, 128 : 85 - 101
  • [9] Nanosized Au particles as an efficient cocatalyst for photocatalytic overall water splitting
    Iwase, A
    Kato, H
    Kudo, A
    [J]. CATALYSIS LETTERS, 2006, 108 (1-2) : 7 - 10
  • [10] Formation of surface nano-step structures and improvement of photocatalytic activities of NaTaO3 by doping of alkaline earth metal ions
    Iwase, A
    Kato, H
    Okutomi, H
    Kudo, A
    [J]. CHEMISTRY LETTERS, 2004, 33 (10) : 1260 - 1261