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Title: Energy and Site Selectivity in O-Atom Photodesorption from Nanostructured MgO

Journal Article · · Surface Science, 602(11):1968-1973

Electronic excitation of wide gap ionic solids can induce desorption of neutral atoms with distinct hyperthermal and thermal kinetic energy distributions. Hyperthermal atomic desorption results from electronic surface excitation while thermal desorption is initiated primarily by bulk excitation. Calculations indicate that surface-localized transitions can be excited independently from bulk transitions using selected photon energies. The photon energy required to excite specific surface sites depends upon the site coordination with successively lower energies required to excite terrace, step, and corner sites. Here, we excite low-coordinated surface sites of nanostructured MgO samples using 4.7 eV UV laser pulses and observe dominant hyperthermal O-atom emission. We then selectively excite bulk sites of nanostructured MgO, using a 7.9 eV laser, and observe dominant thermal O-atom desorption. These results are analyzed in terms of laser desorption models developed previously for alkali halide crystals. We propose a multi-step mechanism for hyperthermal O-atom desorption, under surface selective excitation, based on hole trapping at 3C (corner) O-atom sites followed by exciton decomposition. The proposed “hole plus exciton” model has similarities to the surface exciton desorption model, established for alkali halides, but is more complex and requires more steps. Nonetheless, the principle of site-specific photoreaction, established for alkali halide crystals, is clearly extendable to a prototypical metal oxide.

Research Organization:
Pacific Northwest National Lab. (PNNL), Richland, WA (United States). Environmental Molecular Sciences Lab. (EMSL)
Sponsoring Organization:
USDOE
DOE Contract Number:
AC05-76RL01830
OSTI ID:
937361
Report Number(s):
PNNL-SA-58128; SUSCAS; 24794; KC0301020; TRN: US0805777
Journal Information:
Surface Science, 602(11):1968-1973, Vol. 602, Issue 11; ISSN 0039-6028
Country of Publication:
United States
Language:
English

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