Active role of oxide support during CO oxidation at Au/MgO.
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[1] M. Bäumer,et al. Metal deposits on well-ordered oxide films , 1999 .
[2] T. Arias,et al. Iterative minimization techniques for ab initio total energy calculations: molecular dynamics and co , 1992 .
[3] M. Boudart,et al. The kinetics and mechanism of spillover , 1974 .
[4] G. Wulff,et al. XXV. Zur Frage der Geschwindigkeit des Wachsthums und der Auflösung der Krystallflächen , 1901 .
[5] B. E. Nieuwenhuys,et al. Selective Oxidation of CO, over Supported Au Catalysts , 2001 .
[6] D. Vanderbilt,et al. Soft self-consistent pseudopotentials in a generalized eigenvalue formalism. , 1990, Physical review. B, Condensed matter.
[7] J. Nørskov,et al. Why gold is the noblest of all the metals , 1995, Nature.
[8] J. Goniakowski,et al. Theoretical study of the atomic structure of Pd nanoclusters deposited on a MgO(100) surface , 2002 .
[9] G. Ozin,et al. A metal atom model for the oxidation of carbon monoxide to carbon dioxide. The gold atom-carbon monoxide-dioxygen reaction and the gold atom-carbon dioxide reaction , 1977 .
[10] W. L Winterbottom,et al. Equilibrium shape of a small particle in contact with a foreign substrate , 1967 .
[11] K. Hayek,et al. Metal-support boundary sites in catalysis , 1997 .
[12] S. C. Parker,et al. The kinetics of CO oxidation by adsorbed oxygen on well‐defined gold particles on TiO2(110) , 1999 .
[13] M. Haruta,et al. Analytical high-resolution TEM study of supported gold catalysts: orientation relationship between Au particles and TiO2 supports. , 2000, Journal of electron microscopy.
[14] J. Hagen,et al. Coadsorption of CO and O2 on small free gold cluster anions at cryogenic temperatures: Model complexes for catalytic CO oxidation , 2002 .
[15] Jackson,et al. Atoms, molecules, solids, and surfaces: Applications of the generalized gradient approximation for exchange and correlation. , 1992, Physical review. B, Condensed matter.
[16] J. Nørskov,et al. Improved adsorption energetics within density-functional theory using revised Perdew-Burke-Ernzerhof functionals , 1999 .
[17] P. Ajayan,et al. Evidence for sinking of small particles into substrates and implications for heterogeneous catalysis , 1989, Nature.
[18] A. Sánchez,et al. Tuning the oxidation of carbon monoxide using nanoassembled model catalysts , 2000 .
[19] S. Giorgio,et al. High-resolution transmission electron microscopy study of gold particles (greater than 1 nm), epitaxially grown on clean MgO microcubes , 1991 .
[20] J. Nørskov,et al. Making gold less noble , 2000 .
[21] T. Akita,et al. Au/TiO2 Nanosized Samples: A Catalytic, TEM, and FTIR Study of the Effect of Calcination Temperature on the CO Oxidation , 2001 .
[22] R. Whetten,et al. Coadsorption of CO and O(2) on selected gold clusters: evidence for efficient room-temperature CO(2) generation. , 2002, Journal of the American Chemical Society.
[23] Jens K Nørskov,et al. Catalytic CO oxidation by a gold nanoparticle: a density functional study. , 2002, Journal of the American Chemical Society.
[24] Charles T. Campbell,et al. Ultrathin metal films and particles on oxide surfaces: structural, electronic and chemisorptive properties , 1997 .
[25] Claude R. Henry,et al. Surface studies of supported model catalysts , 1998 .
[26] Masatake Haruta,et al. Size- and support-dependency in the catalysis of gold , 1997 .
[27] Hannu Häkkinen,et al. When Gold Is Not Noble: Nanoscale Gold Catalysts , 1999 .
[28] D. Goodman,et al. Onset of catalytic activity of gold clusters on titania with the appearance of nonmetallic properties , 1998, Science.
[29] Hans-Joachim Freund,et al. Palladium Nanocrystals on Al 2 O 3 : Structure and Adhesion Energy , 1999 .
[30] U. Wille. Self-terminating, oxidative radical cyclizations: a novel reaction of acyloxyl radicals. , 2002, Journal of the American Chemical Society.
[31] Masatake Haruta,et al. Catalysis of Gold Nanoparticles Deposited on Metal Oxides , 2002 .
[32] Jens R. Rostrup-Nielsen,et al. Atom-Resolved Imaging of Dynamic Shape Changes in Supported Copper Nanocrystals , 2002, Science.