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Molybdenum deposition from the decomposition of molybdenum hexacarbonyl

Journal Article · · J. Appl. Phys.; (United States)
DOI:https://doi.org/10.1063/1.342695· OSTI ID:6482478
Molybdenum metal deposition from the decomposition of Mo(CO)/sub 6/ adsorbed on Si(100), Mo, and Cu surfaces was studied by x-ray photoelectron spectroscopy (XPS), Auger electron spectroscopy, thermal desorption spectroscopy, and low-energy electron diffraction. Pyrolytic, photolytic, and electron-induced Mo(CO)/sub 6/ decomposition were observed and indicated different dissociation mechanisms. Thermally decomposed Mo(CO)/sub 6/ was found to leave metallic Mo in the presence of C and O. Electron-induced decomposition resulted in the formation of molybdenum carbide on the surfaces. Ultraviolet (UV) irradiation of adsorbed Mo(CO)/sub 6/ induced new peaks in XPS and TDS spectra, suggesting the formation of an unsaturated molybdenum carbonyl adsorbate. Mo(CO)/sub 6/ was found to form a multilayer on these surfaces at low temperatures, and desorb with zero-order kinetics. Although both adsorbate desorption and decomposition took place when the samples were heated, desorption was the dominant reaction path. UV irradiation of gaseous and coadsorbed Mo(CO)/sub 6/ and O/sub 2/ was also investigated. UV irradiation of the gas-phase mixture leads to MoO/sub 2/ and MoO/sub 3/ deposition; however, UV irradiation of coadsorbed Mo(CO)/sub 6/ and O/sub 2/ resulted in unsaturated molybdenum carbonyl. The effects of annealing and Ar/sup +/ bombardment on the Mo-deposited Si(100) surface are also reported.
Research Organization:
Department of Chemistry, Princeton University, Princeton, New Jersey 08544
OSTI ID:
6482478
Journal Information:
J. Appl. Phys.; (United States), Journal Name: J. Appl. Phys.; (United States) Vol. 65:8; ISSN JAPIA
Country of Publication:
United States
Language:
English