EPITAXIALLY GROWN MODEL CATALYST PARTICLES OF PLATINUM, RHODIUM, IRIDIUM, PALLADIUM AND RHENIUM STUDIED BY ELECTRON-MICROSCOPY

被引:66
作者
RUPPRECHTER, G [1 ]
HAYEK, K [1 ]
RENDON, L [1 ]
JOSEYACAMAN, M [1 ]
机构
[1] UNIV NACL AUTONOMA MEXICO, INST FIS, MEXICO CITY 01000, DF, MEXICO
关键词
CATALYSIS; ELECTRON MICROSCOPY; EPITAXY; METALS;
D O I
10.1016/0040-6090(94)06429-6
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
In order to obtain oriented thin film model catalysts, small particles of Pt, Rh, Ir, Pd and Re (2-20 nm in size) were grown by high vacuum evaporation on NaCl cleavage faces or on in situ deposited NaCl films at 523-673 K. The particles were covered with a supporting film of Al2O3 or carbon and removed from the substrate. High resolution electron microscopy, selected area electron diffraction and weak-beam dark-field imaging were applied to determine the particular morphology, microstructure and orientation of the observed particles. Special attention was paid to Rh particles which appear in a variety of shapes. Pt, Ir and Pd model catalysts consist mainly of (001) oriented half octahedra which may exhibit truncations at the corners or on the top. This was also the dominant shape of Rh particles but in addition half tetrahedra in (011) epitaxy and multiply-twinned particles like decahedra in (001), (011) and (111) orientation were evident. These habits provide a definite ''initial state'' for study of the changes in structure and morphology of the particles during activating heat treatments necessary to induce catalytic activity of the Al2O3 supported metal films. Although Re films consisted of irregularly shaped particles, electron diffraction revealed a partial epitaxial alignment of both c.p.h. and f.c.c. Re.
引用
收藏
页码:148 / 155
页数:8
相关论文
共 45 条
[1]  
BACHMANN L, 1962, NATURWISSENSCHAFTEN, V49, P34
[2]   REVERSIBILITY OF STRONG METAL SUPPORT INTERACTIONS ON RH/TIO2 [J].
BRAUNSCHWEIG, EJ ;
LOGAN, AD ;
DATYE, AK ;
SMITH, DJ .
JOURNAL OF CATALYSIS, 1989, 118 (01) :227-237
[3]  
BRAUNSCHWEIG EJ, 1988, 9TH P INT C CAT, V3, P1122
[4]   COMPARISON OF MICROSTRUCTURES IN OXIDATION AND REDUCTION - RH AND IR PARTICLES ON SIO2 AND AL2O3 [J].
BURKHARDT, J ;
SCHMIDT, LD .
JOURNAL OF CATALYSIS, 1989, 116 (01) :240-251
[5]   OXIDATION REDUCTION TREATMENT OF RHODIUM SUPPORTED ON NONPOROUS SILICA SPHERES [J].
CHAKRABORTI, S ;
DATYE, AK ;
LONG, NJ .
JOURNAL OF CATALYSIS, 1987, 108 (02) :444-451
[6]   FORMATION AND CHARACTERIZATION OF SMALL PD PARTICLES DEPOSITED ON MGO AS A MODEL CATALYST [J].
CHAPON, C ;
HENRY, CR ;
CHEMAM, A .
SURFACE SCIENCE, 1985, 162 (1-3) :747-754
[7]   FACE-CENTRED CUBIC MODIFICATION IN SPUTTERED FILMS OF TANTALUM MOLYBDENUM TUNGSTEN RHENIUM HAFNIUM AND ZIRCONIUM [J].
CHOPRA, KL ;
RANDLETT, MR ;
DUFF, RH .
PHILOSOPHICAL MAGAZINE, 1967, 16 (140) :261-&
[8]   THE STUDY OF HETEROGENEOUS CATALYSTS BY HIGH-RESOLUTION TRANSMISSION ELECTRON-MICROSCOPY [J].
DATYE, AK ;
SMITH, DJ .
CATALYSIS REVIEWS-SCIENCE AND ENGINEERING, 1992, 34 (1-2) :129-178
[9]   OXIDE PARTICLES ON ULTRA THIN RHENIUM FILMS STUDIED BY ELECTRON MICROSCOPY [J].
FREDERIKSSON, H ;
KASEMO, B ;
MARKLUND, I .
THIN SOLID FILMS, 1971, 8 (01) :61-+
[10]   THE REACTION OF NEOPENTANE AND HYDROGEN ON ORIENTED AND NONORIENTED CATALYSTS OF PT ON AL2O3 [J].
GEHRER, E ;
HAYEK, K .
JOURNAL OF MOLECULAR CATALYSIS, 1987, 39 (03) :293-311