Support effect in high activity gold catalysts for CO oxidation

被引:658
作者
Comotti, M [1 ]
Li, WC [1 ]
Spliethoff, B [1 ]
Schüth, F [1 ]
机构
[1] Max Planck Inst Kohlenforsch, D-45470 Mulheim, Germany
关键词
D O I
10.1021/ja0561441
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
In this work, we present a detailed study concerning the evaluation of the metal-support interaction in high activity gold catalysts for CO oxidation. Using the colloidal deposition method, model catalysts were prepared, which allow the isolation of the effect of the support on the catalytic activity. Prefabricated gold particles were thus deposited on different support materials. Since the deposition process did not change the particle sizes of the gold particles, only the influence of the support could be studied. TiO2, Al2O3, ZrO2, and ZnO were used as support materials. Catalytic tests and high resolution transmission electron microscopy clearly show that the support contributes to the activity. However, our results are not in line with the distinction between active and passive supports based on the semiconducting properties of the oxidic material. The most active catalysts were obtained with TiO2 and Al2O3, while ZnO and ZrO2 gave substantially less active catalysts. Furthermore, the effect of other important parameters on the catalytic activity (i.e., particles size distribution, calcination temperature, and aging time for a Au/TiO2 catalyst) has also been studied. Using this preparation route, the catalysts show high-temperature stability, size dependent activity, and a very good long-term stability.
引用
收藏
页码:917 / 924
页数:8
相关论文
共 39 条
  • [1] Oxidation of CO on gold supported catalysts prepared by laser vaporization: Direct evidence of support contribution
    Arrii, S
    Morfin, F
    Renouprez, AJ
    Rousset, JL
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2004, 126 (04) : 1199 - 1205
  • [2] Surfactant-protected gold particles: new challenge for gold-on-carbon catalysts
    Biella, S
    Porta, F
    Prati, L
    Rossi, M
    [J]. CATALYSIS LETTERS, 2003, 90 (1-2) : 23 - 29
  • [3] Au/TiO2 nanosized samples:: A catalytic, TEM, and FTIR study of the effect of calcination temperature on the CO oxidation
    Boccuzzi, F
    Chiorino, A
    Manzoli, M
    Lu, P
    Akita, T
    Ichikawa, S
    Haruta, M
    [J]. JOURNAL OF CATALYSIS, 2001, 202 (02) : 256 - 267
  • [4] Catalysis by gold
    Bond, GC
    Thompson, DT
    [J]. CATALYSIS REVIEWS-SCIENCE AND ENGINEERING, 1999, 41 (3-4): : 319 - 388
  • [5] Oxygen adsorption on well-defined gold particles on TiO2(110)
    Bondzie, VA
    Parker, SC
    Campbell, CT
    [J]. JOURNAL OF VACUUM SCIENCE & TECHNOLOGY A-VACUUM SURFACES AND FILMS, 1999, 17 (04): : 1717 - 1720
  • [6] Oxidation of alcohols and sugars using Au/C catalysts - Part 2. Sugars
    Comotti, M
    Della Pina, C
    Matarrese, R
    Rossi, M
    Siani, A
    [J]. APPLIED CATALYSIS A-GENERAL, 2005, 291 (1-2) : 204 - 209
  • [7] The catalytic activity of "Naked" gold particles
    Comotti, M
    Della Pina, C
    Matarrese, R
    Rossi, M
    [J]. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2004, 43 (43) : 5812 - 5815
  • [8] A NEW HYDROSOL OF GOLD CLUSTERS
    DUFF, DG
    BAIKER, A
    EDWARDS, PP
    [J]. JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1993, (01) : 96 - 98
  • [9] COAGULATION OF COLLOIDAL GOLD
    ENUSTUN, BV
    TURKEVICH, J
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1963, 85 (21) : 3317 - +
  • [10] Direct evidence of oxidized gold on supported gold catalysts
    Fu, L
    Wu, NQ
    Yang, JH
    Qu, F
    Johnson, DL
    Kung, MC
    Kung, HH
    Dravid, VP
    [J]. JOURNAL OF PHYSICAL CHEMISTRY B, 2005, 109 (09) : 3704 - 3706