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Time-Resolved Structural Characterization of Formation and Break-up of Rhodium Clusters Supported in Highly Dealuminated Y Zeolite

Journal Article · · J. Phys. Chem. C
DOI:https://doi.org/10.1021/jp805917g· OSTI ID:1007093

Mononuclear rhodium complexes incorporating two ethylene ligands and anchored to dealuminated zeolite Y by two Rh-O bonds were characterized by transient extended X-ray absorption fine structure (EXAFS) spectroscopy and infrared (IR) spectroscopy as they were converted in the presence of H{sub 2}. EXAFS spectra indicate reduction of the rhodium in the complex at 298 K to form rhodium clusters less than 3 {angstrom} in average diameter. Contacting of the resultant clusters with C{sub 2}H{sub 4} led to their oxidative fragmentation, and the process was reversible. When the H{sub 2} treatment was carried out at a higher temperature (373 K), larger clusters formed. The reduction and oxidation of the rhodium were confirmed by X-ray absorption near edge spectra. During the ethylene treatments, ethyl groups formed on the rhodium, as indicated by IR spectra; treatment in H{sub 2} led to hydrogenation of these groups to form ethane, and the ethyl groups are inferred to be intermediates in the catalytic hydrogenation of ethylene. Ethylene in the gas phase helps to stabilize rhodium in the form of mononuclear complexes on the zeolite during catalysis, hindering the cluster formation.

Research Organization:
Advanced Photon Source (APS), Argonne National Laboratory (ANL), Argonne, IL (US)
Sponsoring Organization:
USDOE
OSTI ID:
1007093
Journal Information:
J. Phys. Chem. C, Journal Name: J. Phys. Chem. C Journal Issue: (46) ; 11, 2008 Vol. 112; ISSN 1932-7447
Country of Publication:
United States
Language:
ENGLISH