Reflection Absorption Infrared Spectroscopy and Temperature-Programmed Desorption Studies of the Adsorption and Desorption of Amorphous and Crystalline Water on a Graphite Surface

Reflection absorption infrared spectroscopy (RAIRS) and temperature-programmed desorption (TPD) have been used to perform a detailed investigation of the adsorption of water on highly oriented pyrolytic graphite (HOPG) at 90 K. RAIRS shows that water is physisorbed on HOPG at all coverages, as expec...

Full description

Saved in:
Bibliographic Details
Published inThe journal of physical chemistry. B Vol. 109; no. 35; pp. 16836 - 16845
Main Authors Bolina, Amandeep S, Wolff, Angela J, Brown, Wendy A
Format Journal Article
LanguageEnglish
Published United States American Chemical Society 08.09.2005
Online AccessGet full text

Cover

Loading…
More Information
Summary:Reflection absorption infrared spectroscopy (RAIRS) and temperature-programmed desorption (TPD) have been used to perform a detailed investigation of the adsorption of water on highly oriented pyrolytic graphite (HOPG) at 90 K. RAIRS shows that water is physisorbed on HOPG at all coverages, as expected. Experiments at higher surface temperatures show marked changes in the O−H stretching region of the spectrum which can be assigned to the observation of the amorphous to crystalline ice phase transition. The infrared signature of both phases of solid water has been determined on HOPG and can be used to identify the phase of the ice. TPD spectra show the desorption of multilayers of crystalline ice. At high exposures a small bump appears in the TPD spectrum, on the low temperature side of the main peak, which is attributed to the amorphous to crystalline phase transition. At very low exposures of water, it is possible to distinguish the desorption of water from two- and three-dimensional islands and hence to determine the growth mode of water on the HOPG surface. Isothermal TPD studies have also been performed and show that the desorption of water does not obey perfect zero-order kinetics. Desorption orders, derived directly from the TPD spectra, confirm this observation. Desorption energies and preexponential factors have also been determined for this adsorption system.
Bibliography:istex:54B1487381883A4C41B5EF5B169C3B9E1E1C1AF5
ark:/67375/TPS-T9MDLW2C-K
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:1520-6106
1520-5207
DOI:10.1021/jp0528111