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Photoemission study of Ce/Ta(110) and Ce/W(110) interfaces and the catalytic oxidation effect

Technical Report ·
OSTI ID:5373905
Photoemission spectroscopy was used to study Ce/Ta(110) and Ce/W(110) interfaces, and the catalytic oxidation effect on both surfaces. A weak Ce/Ta interface reaction is illustrated by the reduced Ta 4f surface core-level shift (SCS) upon Ce adsorption. No Ce/Ta interdiffusion was found. The Ce layer may greatly enhance the oxidation of Ta(110). Oxidation of Ce/Ta(110) at 300 K yields on monolayer (ML) of Ta suboxide ({approximately}TaO), followed by the rapid formations of Ta{sub 2}O{sub 5}. Ce/W(110) adsorption patterns were determined by low-energy electron diffraction. For {Theta} {le} 0.5 ML, the adsorption structure is characterized by one-dimensional commensuration along the (110) direction. It changes abruptly to a hexagonal pattern after 0.5 ML. The interatomic spacing shrinks continuously from 9% larger than that for {gamma}-Ce to 3% smaller than that for {alpha}Ce. Correspondingly the Ce 4f photoelectron spectrum evolves to resemble that of {alpha}-Ce. W 4f core levels are also correlated to the adsorption. A significantly widened W SCS is found at low Ce coverages. After the formation of the hexagonal patterns, the Ce-W registration is lost, and the interaction within the Ce layer increases. The SCS for the top layer of W is partially restored. Electronic charge polarization from Ce toward the W (or Ta) substrate is believed to be the key mechanism for the Ce-induced SCS.
Research Organization:
Ames Lab., IA (United States)
Sponsoring Organization:
DOE; USDOE, Washington, DC (United States)
DOE Contract Number:
W-7405-ENG-82
OSTI ID:
5373905
Report Number(s):
IS-T-1494; ON: DE91018167
Country of Publication:
United States
Language:
English