Inhibition at Perimeter Sites of Au/TiO2 Oxidation Catalyst by Reactant Oxygen

被引:112
作者
Green, Isabel Xiaoye [1 ]
Tang, Wenjie [2 ]
McEntee, Monica [1 ]
Neurock, Matthew [1 ,2 ]
Yates, John T., Jr. [1 ,2 ]
机构
[1] Univ Virginia, Dept Chem, Charlottesville, VA 22904 USA
[2] Univ Virginia, Dept Chem Engn, Charlottesville, VA 22904 USA
关键词
CATALYTICALLY ACTIVE GOLD; CO OXIDATION; AU CLUSTERS; NANOPARTICLES; ADSORPTION; STATE; TIO2; O-2; NANOCLUSTERS; SPECTROSCOPY;
D O I
10.1021/ja304426b
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
TiO2-supported gold nanoparticles exhibit surprising catalytic activity for oxidation reactions compared to noble bulk gold which is inactive. The catalytic activity is localized at the perimeter of the Au nanoparticles where Au atoms are atomically adjacent to the TiO2 support. At these dual-catalytic sites an oxygen molecule is efficiently activated through chemical bonding to both Au and Ti4+ sites. A significant inhibition by a factor of 22 in the CO oxidation reaction rate is observed at 120 K when the Au is preoxidized, caused by the oxygen-induced positive charge produced on the perimeter Au atoms. Theoretical calculations indicate that induced positive charge occurs in the Au atoms which are adjacent to chemisorbed oxygen atoms, almost doubling the activation energy for CO oxidation at the dual-catalytic sites in agreement with experiments. This is an example of self-inhibition in catalysis by a reactant species.
引用
收藏
页码:12717 / 12723
页数:7
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共 54 条
  • [1] FTIR study of the electronic effects of CO adsorbed on gold nanoparticles supported on titania
    Boccuzzi, F
    Chiorino, A
    Manzoli, M
    [J]. SURFACE SCIENCE, 2000, 454 (01) : 942 - 946
  • [2] Unravelling the Nature of Gold Surface Sites by Combining IR Spectroscopy and DFT Calculations. Implications in Catalysis
    Boronat, M.
    Concepcion, P.
    Corma, A.
    [J]. JOURNAL OF PHYSICAL CHEMISTRY C, 2009, 113 (38) : 16772 - 16784
  • [3] Effect of alumina and titania on the oxidation of CO over Au nanoparticles evaluated by 13C isotopic transient analysis
    Calla, JT
    Bore, MT
    Datye, AK
    Davis, RJ
    [J]. JOURNAL OF CATALYSIS, 2006, 238 (02) : 458 - 467
  • [4] X-ray absorption spectroscopy and CO oxidation activity of Au/Al2O3 treated with NaCN
    Calla, JT
    Davis, RJ
    [J]. CATALYSIS LETTERS, 2005, 99 (1-2) : 21 - 26
  • [5] Nanocrystalline CeO2 increases the activity of an for CO oxidation by two orders of magnitude
    Carrettin, S
    Concepción, P
    Corma, A
    Nieto, JML
    Puntes, VF
    [J]. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2004, 43 (19) : 2538 - 2540
  • [6] Catalytically active gold: From nanoparticles to ultrathin films
    Chen, Mingshu
    Goodman, D. Wayne
    [J]. ACCOUNTS OF CHEMICAL RESEARCH, 2006, 39 (10) : 739 - 746
  • [7] The structure of catalytically active gold on titania
    Chen, MS
    Goodman, DW
    [J]. SCIENCE, 2004, 306 (5694) : 252 - 255
  • [8] Enhanced adsorption energy of Au1 and O2 on the stoichiometric TiO2(110) surface by coadsorption with other molecules
    Chretien, Steeve
    Metiu, Horia
    [J]. JOURNAL OF CHEMICAL PHYSICS, 2008, 128 (04)
  • [9] Vital role of moisture in the catalytic activity of supported gold nanoparticles
    Daté, M
    Okumura, M
    Tsubota, S
    Haruta, M
    [J]. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2004, 43 (16) : 2129 - 2132
  • [10] CO adsorption and oxidation on Au/TiO2
    Dekkers, MAP
    Lippits, MJ
    Nieuwenhuys, BE
    [J]. CATALYSIS LETTERS, 1998, 56 (04) : 195 - 197