STRUCTURE AND CHEMICAL-COMPOSITION OF SURFACTANT-STABILIZED PTRU ALLOY COLLOIDS

Citation
W. Vogel et al., STRUCTURE AND CHEMICAL-COMPOSITION OF SURFACTANT-STABILIZED PTRU ALLOY COLLOIDS, JOURNAL OF PHYSICAL CHEMISTRY B, 101(51), 1997, pp. 11029-11036
Citations number
46
Journal title
JOURNAL OF PHYSICAL CHEMISTRY B
ISSN journal
15206106 → ACNP
Volume
101
Issue
51
Year of publication
1997
Pages
11029 - 11036
Database
ISI
SICI code
1089-5647(1997)101:51<11029:SACOSP>2.0.ZU;2-D
Abstract
In situ XRD has been used to study both unsupported and silica-support ed clusters PtRu[N(Oct)(4)Cl](5) (Pt:Ru approximate to 1:1). Structura l information has been gained by Debye function analysis. For the unsu pported clusters, the best fit simulation gives a 50/50 mixture of col loid particles with fcc symmetry and multiply twinned decahedral parti cles. The narrow size distribution centers around 12 Angstrom. The nea r-neighbor distance is found to be 0.9% smaller than for the bulk PtRu . XANES data provide evidence for the metallic character of the Pt com ponent. The silica-supported colloid particles oxidize rapidly in air to form an amorphous state but can be rereduced in hydrogen at room te mperature. An ''open-slit'' XRD technique was used to study the partic le growth in H-2 and He. Particles annealed to 700 degrees C in He sho w a twinned fcc symmetry with an average size of 23 Angstrom. The CO o xidation of this catalyst was studied by in situ XRD. At 280 degrees C surface oxide species are formed that slowly coalesce to RuO2 particl es. After rereduction the catalyst consists of a pure hcp ruthenium ph ase and larger alloy particles enriched in platinum.