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

In situ infrared spectroscopy of CO adsorbed at ordered Pt(100)-aqueous interfaces: Double-layer effects upon the adsorbate binding geometry

Journal Article · · Journal of Physical Chemistry; (USA)
DOI:https://doi.org/10.1021/j100375a062· OSTI ID:6330955
;  [1]
  1. Purdue Univ., West Lafayette, IN (USA)
Surface infrared spectra for carbon monoxide adsorbed on ordered Pt(100) in 0.1 M HClO{sub 4} are reported as a function of CO coverage, 0.1 {approx lt} {theta} {approx lt} 0.85, and electrode potential, {minus}0.25 V {le} E {approx lt} 0.25 V vs SCE. Vibrational C-O stretching bands, {nu}{sub co}, corresponding to both terminal and 2-fold bridging geometries are observed, with intensities that depend markedly upon E and {theta}. For coverages formed by dosing with dilute (ca. 2 {times} 10{sup {minus}5} M) CO solutions for varying times ({approx lt}15 min), alterations in {theta} at positive potentials (E {approx gt} 0.1 V) yield dramatic changes in the site occupancy in that bridging and terminal features are dominant for {theta} {approx lt} 0.3 and {theta} {approx gt} 0.7, respectively. Qualitatively similar, yet less marked, {theta}-induced alterations in the CO binding geometry are observed at negative potentials (E < 0 V vs SCE), where hydrogen rather than water constitutes the major coadsorbate.
OSTI ID:
6330955
Journal Information:
Journal of Physical Chemistry; (USA), Journal Name: Journal of Physical Chemistry; (USA) Vol. 94:12; ISSN 0022-3654; ISSN JPCHA
Country of Publication:
United States
Language:
English