Au-TiO2 catalysts on carbon nanotibres prepared by deposition-precipitation and from colloid solutions

被引:30
作者
Hammer, Nina
Kvande, Ingvar
Xu, Xin
Gunnarsson, Vidar
Totdal, Bard
Chen, De
Ronning, Magnus [1 ]
机构
[1] Norwegian Univ Sci & Technol, Dept Chem Engn, N-7491 Trondheim, Norway
[2] Beijing Inst Petrochem Technol, Beijing 102617, Peoples R China
[3] Norwegian Univ Sci & Technol, Dept Phys, N-7491 Trondheim, Norway
关键词
Au catalyst; TiO2; carbon nanofibres; water-gas shift reaction; deposition-precipitation; Au colloids;
D O I
10.1016/j.cattod.2007.03.001
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
An catalysts have been prepared (i) on TiO2, (ii) on carbon nanofibres (CNF) and (iii) on TiO2 deposited onto CNF. Catalysts prepared from deposition-precipitation (DP) and from colloid solutions have been characterised using XRD, TEM, TGA and XAS and tested in the water-gas shift (WGS) reaction. DP yields large An particles (> 50 nm) on CNF-containing supports. High An dispersion on carbon nanofibres requires preparation via other methods such as colloid formation. An particle growth is more pronounced during the synthesis steps than during thermal treatments. This increase is not observed for the Au particles on TiO2 but only when CNF is present, indicating that the surface properties of TiO2 are altered by the CNF TiO2 XANES analyses show that distortions in the lattice symmetry of TiO2 are introduced when the oxide is deposited on CNE The distortion of the TiO2 structure by the CNF may also introduce changes that promote the turnover frequencies. The WGS activity significantly improves when titania is present. This shows that coexistence of An and TiO2 is needed to obtain high catalytic activity in the WGS reaction, indicating that the active sites are either on the Au-TiO2 interface or that the reaction follows a bifunctional mechanism. (c) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:245 / 256
页数:12
相关论文
共 62 条
  • [31] Gold catalysts supported on mesoporous titania for low-temperature water-gas shift reaction
    Idakiev, V
    Tabakova, T
    Yuan, ZY
    Su, BL
    [J]. APPLIED CATALYSIS A-GENERAL, 2004, 270 (1-2) : 135 - 141
  • [32] Water-gas shift: in situ spectroscopic studies of noble metal promoted ceria catalysts for CO removal in fuel cell reformers and mechanistic implications
    Jacobs, G
    Patterson, PM
    Williams, L
    Chenu, E
    Sparks, D
    Thomas, G
    Davis, BH
    [J]. APPLIED CATALYSIS A-GENERAL, 2004, 262 (02) : 177 - 187
  • [33] Water-gas shift: comparative screening of metal promoters for metal/ceria systems and role of the metal
    Jacobs, G
    Chenu, E
    Patterson, PM
    Williams, L
    Sparks, D
    Thomas, G
    Davis, BH
    [J]. APPLIED CATALYSIS A-GENERAL, 2004, 258 (02) : 203 - 214
  • [35] The adhesion and shape of nanosized Au particles in a Au/TiO2 catalyst
    Lopez, N
    Norskov, JK
    Janssens, TVW
    Carlsson, A
    Puig-Molina, A
    Clausen, BS
    Grunwaldt, JD
    [J]. JOURNAL OF CATALYSIS, 2004, 225 (01) : 86 - 94
  • [36] Structural and electronic properties of sol-gel titanium oxides studied by X-ray absorption spectroscopy
    Luca, V
    Djajanti, S
    Howe, RF
    [J]. JOURNAL OF PHYSICAL CHEMISTRY B, 1998, 102 (52) : 10650 - 10657
  • [37] STRUCTURAL GENESIS OF PT ON SIO2 - DETERMINATION BY X-RAY ABSORPTION-SPECTROSCOPY
    LYTLE, FW
    GREEGOR, RB
    MARQUES, EC
    SANDSTROM, DR
    VIA, GH
    SINFELT, JH
    [J]. JOURNAL OF CATALYSIS, 1985, 95 (02) : 546 - 557
  • [38] The effect of gold particle size on Au-Au bond length and reactivity toward oxygen in supported catalysts
    Miller, J. T.
    Kropf, A. J.
    Zha, Y.
    Regalbuto, J. R.
    Delannoy, L.
    Louis, C.
    Bus, E.
    van Bokhoven, J. A.
    [J]. JOURNAL OF CATALYSIS, 2006, 240 (02) : 222 - 234
  • [39] Gold on titania catalysts for the oxidation of carbon monoxide: control of pH during preparation with various gold contents
    Moreau, F
    Bond, GC
    Taylor, AO
    [J]. JOURNAL OF CATALYSIS, 2005, 231 (01) : 105 - 114
  • [40] Surface plasmon spectroscopy of nanosized metal particles
    Mulvaney, P
    [J]. LANGMUIR, 1996, 12 (03) : 788 - 800