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Ultraviolet and electron radiation induced fragmentation of adsorbed ferrocene

Journal Article · · Journal of Applied Physics
DOI:https://doi.org/10.1063/1.362474· OSTI ID:285398
; ; ;  [1]; ;  [2];  [3]
  1. Department of Physics and the Center for Materials Research and Analysis, Behlen Laboratory for Physics, University of Nebraska, Lincoln, Nebraska 68588-0111 (United States)
  2. Department of Mechanical Engineering and the Center for Materials Research and Analysis, University of Nebraska, Lincoln, Nebraska 68588-0111 (United States)
  3. Solid State Division, Oak Ridge National Laboratory, Oak Ridge, Tennessee 37831-6030 (United States)
From thermal desorption spectroscopy we find that ferrocene, Fe(C{sub 5}H{sub 5}){sub 2}, adsorbs and desorbs associatively on Ag(100). Photoemission results indicate that the initially adsorbed surface species closely resembles that of molecular ferrocene. The shift in photoemission binding energies relative to the gas phase is largely independent of the molecular orbital. We find that ultraviolet light does lead to partial fragmentation of the ferrocene and that the molecular fragments are much more strongly bound to the surface than the associatively adsorbed ferrocene. Since fragmentation occurs only in the presence of incident radiation, selective area deposition from this class of molecules is possible. Using a focused electron beam in a scanning transmission electron microscope, we show that selective area deposition of features with resolution of a few hundred angstroms is readily achieved. {copyright} {ital 1996 American Institute of Physics.}
Research Organization:
Oak Ridge National Laboratory
DOE Contract Number:
AC05-84OR21400; FG02-95ER12177
OSTI ID:
285398
Journal Information:
Journal of Applied Physics, Journal Name: Journal of Applied Physics Journal Issue: 11 Vol. 79; ISSN JAPIAU; ISSN 0021-8979
Country of Publication:
United States
Language:
English

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