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Title: Photochemical Outcomes of Adsorbed Oxygen: Desorption, Dissociation and Passivation by Coadsorbed Water

Journal Article · · Journal of Physical Chemistry C

A mixed Fe+Cr oxide surface was used to explore the photochemical fate of adsorbed O2 under ultrahigh vacuum (UHV) conditions. This mixed oxide surface possessed a magnetite-like (111) structure based on low energy electron diffraction (LEED), with its chemical behavior resembling that of Fe3O4(111). Oxygen adsorption at 40 K resulted in two chemisorption states, a strongly bound form that desorbed in temperature programmed desorption (TPD) at 230 K and a weakly bound form that evolved at 100 K. The former was assigned to charge transfer adsorption at Fe2+ sites and the latter to electrostatic binding at Fe3+ sites. A minority state of O2 was also detected in TPD at ~160 K, and tentatively assigned to adsorption at Cr3+ sites. The 230 K O2 state was the focus of photochemical studies employing four wavelengths of light from the red to the UV. Irrespective of wavelength, O2 molecules in the 230 K state preferentially photodesorbed when irradiated, with comparable rates across the visible and an order of magnitude greater in the UV. Also, approximately 10% of adsorbed O2 irreversibly photodissociated, irrespective of wavelength, with the resulting fragments blocking access to cation sites for subsequent O2 adsorption. Preadsorbed water also blocked O2 adsorption, but post-adsorbed water stabilized O2 at Fe2+ sites in TPD to 285 K. However, water-stabilized O2 molecules were insensitive to photodesorption. O2 photodissociation and photo-passivation both represent potentially adverse outcomes in the release of O2 during the heterogeneous water photooxidation reaction. The author thanks Drs. Sara Chamberlin and Scott Chambers for supplying the film used in this work. This work was supported by the US Department of Energy, Office of Science, Office of Basic Energy Sciences, Division of Chemical Sciences, Geosciences & Biosciences. Pacific Northwest National Laboratory (PNNL) is a multiprogram national laboratory operated for DOE by Battelle. The research reported here was performed using EMSL, a national scientific user facility sponsored by the Department of Energy's Office of Biological and Environmental Research and located at Pacific Northwest National Laboratory.

Research Organization:
Pacific Northwest National Lab. (PNNL), Richland, WA (United States)
Sponsoring Organization:
USDOE
DOE Contract Number:
AC05-76RL01830
OSTI ID:
1601780
Report Number(s):
PNNL-SA-111056
Journal Information:
Journal of Physical Chemistry C, Vol. 119, Issue 34
Country of Publication:
United States
Language:
English