The potential dependence of the extended X-ray absorption fine structure (E
XAFS) obtained at the Pt L-111 absorption edge for a carbon supported Pt el
ectrocatalyst exposed to carbon monoxide is presented, The data have been a
nalyzed using the difference file method to separate the dominant contribut
ions of the Pt neighbors from contributions to the EXAFS from the adsorbed
species. The presence of adsorbed CO is clearly observed with a Pt-C distan
ce of 1.85 Angstrom at potentials less than 0.5 V vs RHE. Increasing the po
tential above 0.5 V resulted first in the removal of the adsorbed CO and at
more positive potentials, e.g., 1.05 V, in the formation of an oxide layer
, as evidenced by the presence of a Pt-O coordination shell at 2.00 Angstro
m. These results demonstrate that in situ EXAFS of supported Pt electrocata
lysts may be used to probe adsorbate structures.