Modeling gold nanoparticles:: Morphology, electron structure, and catalytic activity in CO oxidation

被引:68
作者
Guczi, L
Horváth, D
Pászti, Z
Tóth, L
Horváth, ZE
Karacs, A
Peto, G
机构
[1] Hungarian Acad Sci, Dept Surface Chem & Catalysis, Inst Isotope & Surface Chem, CRC, H-1525 Budapest, Hungary
[2] Inst Tech Phys & Mat Sci, H-1525 Budapest, Hungary
来源
JOURNAL OF PHYSICAL CHEMISTRY B | 2000年 / 104卷 / 14期
关键词
D O I
10.1021/jp992662k
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Morphology, electron structure, and catalytic activity in CO oxidation over a Au/FeOx/SiO2/Si(100) model sample prepared by pulsed laser deposition (PLD) have been investigated by X-ray photoelectron spectroscopy (XPS), UV photoelectron spectroscopy (UPS), and transmission electron microscopy (TEM). Two types of sample were prepared denoted by PLD I and PLD II, the latter being prepared by multiple laser deposition alternatively by iron and gold. PLD I was characterized in "as prepared" oxidized and reduced states, the respective gold particle sizes being 3.8, 4.1, and 5 nm; the iron oxide support was amorphous after the first two treatments while it was partially crystallized after reduction. The activity in CO oxidation increased after oxidation of the sample, whereas it was diminished after subsequent reduction. XPS studies showed that higher activity was associated with amorphous iron oxide with Fe 2p binding energy = 711.3 eV. It was established that in developing the catalytic activity the gold should be metallic and the support should be amorphous with high binding energy and the reaction occurs at the perimeter of gold particles. PLD II has a slightly lower activity which might be the result of more crystalline phase in the iron oxide.
引用
收藏
页码:3183 / 3193
页数:11
相关论文
共 42 条
[1]  
ANDREEV A, 1996, P 8 INT S HET CAT, P141
[2]   Au/α-Fe2O3 catalyst for water-gas shift reaction prepared by deposition-precipitation [J].
Andreeva, D ;
Tabakova, T ;
Idakiev, V ;
Christov, P ;
Giovanoli, R .
APPLIED CATALYSIS A-GENERAL, 1998, 169 (01) :9-14
[3]  
Bailar J.C., 1973, COMPREHENSIVE INORGA
[4]   Fabrication of Ir/TiO2(110) planar catalysts with tailored particle size and distribution [J].
Berkó, A ;
Klivényi, G ;
Solymosi, F .
JOURNAL OF CATALYSIS, 1999, 182 (02) :511-514
[5]  
BOLDYREVA NA, 1993, P 10 INT C CAT, V3, P2621
[6]   SURFACE REACTIVITY OF SUPPORTED GOLD .1. OXYGEN TRANSFER BETWEEN CO AND CO2 [J].
CHA, DY ;
PARRAVAN.G .
JOURNAL OF CATALYSIS, 1970, 18 (02) :200-&
[7]  
CRUNWALDT JD, 1999, J CATAL, V186, P458
[8]   The relationship between the structure and activity of nanometer size gold when supported on Mg(OH)2 [J].
Cunningham, DAH ;
Vogel, W ;
Kageyama, H ;
Tsubota, S ;
Haruta, M .
JOURNAL OF CATALYSIS, 1998, 177 (01) :1-10
[9]   Model catalysts fabricated using electron beam lithography and pulsed laser deposition [J].
Eppler, AS ;
Rupprechter, G ;
Guczi, L ;
Somorjai, GA .
JOURNAL OF PHYSICAL CHEMISTRY B, 1997, 101 (48) :9973-9977
[10]   Surface characterization of Au/HY by Xe-129 NMR and diffuse reflectance IR spectroscopy of adsorbed CO. Formation of electron-deficient gold particles inside HY cavities [J].
Guillemot, D ;
Borovkov, VY ;
Kazansky, VB ;
PolissetThfoin, M ;
Fraissard, J .
JOURNAL OF THE CHEMICAL SOCIETY-FARADAY TRANSACTIONS, 1997, 93 (19) :3587-3591