Skip to main content
U.S. Department of Energy
Office of Scientific and Technical Information

Comparisons between coverage-dependent infrared frequencies for carbon monoxide adsorbed on ordered Pt(111), Pt(100), and Pt(110) in electrochemical and ultrahigh-vacuum environments

Journal Article · · Journal of Physical Chemistry; (USA)
DOI:https://doi.org/10.1021/j100351a006· OSTI ID:7072254
Infrared spectra measured for carbon monoxide adsorbed on Pt(111), (100) and (110) surfaces in aqueous 0.1 M HClO{sub 4} as a function of CO coverage, {theta}{sub CO}, and electrode potential, E, are compared with coverage-dependent infrared spectra for the corresponding interfaces in ultrahigh vacuum (uhv). The electrochemical {theta}{sub CO} values at saturation on all three faces are similar to those in uhv. The terminal C-O stretching frequencies, {nu}{sub CO}, and band intensities are markedly dependent on the crystallographic orientation at a given electrode potential. Extrapolation of the electrochemical coverage-dependent {nu}{sub CO} values to electrode potentials corresponding to the appropriate work function for the anhydrous uhv Pt/CO surfaces yields similar {nu}{sub CO}-{theta}{sub CO} plots as are observed for the latter interfaces. This suggests that the well-known effects of the double-layer solvating environment upon {nu}{sub CO} are primarily electrostatic in origin.
OSTI ID:
7072254
Journal Information:
Journal of Physical Chemistry; (USA), Journal Name: Journal of Physical Chemistry; (USA) Vol. 93:14; ISSN 0022-3654; ISSN JPCHA
Country of Publication:
United States
Language:
English