I. Villegas et al., NITRIC-OXIDE AS A PROBE ADSORBATE FOR LINKING PT(111) ELECTROCHEMICALAND MODEL ULTRAHIGH-VACUUM INTERFACES USING INFRARED-SPECTROSCOPY, Journal of physical chemistry, 99(40), 1995, pp. 14832-14839
The effects of water coadsorption on nitric oxide adlayers on Pt(111)
in ultrahigh vacuum (uhv) are examined with infrared reflection-absorp
tion spectroscopy (IRAS) along with work-function measurements with th
e objective of relating the uhv-based system to NO chemisorption at th
e Pt(111)-aqueous electrochemical interface as studied recently by in-
situ IRAS. In contrast to the corresponding (and extensively studied)
Pt(111)/CO system, solvent coadsorption apparently yields little or no
change in the NO surface binding geometry at low as well as saturated
chemisorbate coverages, the solvent-induced downshifts (ca. 35-70 cm(
-1)) in the N-O stretching (upsilon(NO)) frequencies being consistent
with the occurrence of only an electrostatic Stark effect. This behavi
or, along with the stability of the electrochemical NO adlayer at rela
tively high electrode potentials (E), facilitates intercomparison of t
he surface potentials for the aquated uhv acid in-situ interfaces by m
atching the upsilon(NO) spectrum for the former with the upsilon(NO) f
requency-E data for the latter interface. This procedure yields an est
imate of the ''absolute'' electrode potential, E(k), of the normal hyd
rogen electrode equal to 4.9 +/- 0.1 V. The approximate consistency of
this value with some previous estimates of E(k) supports the essentia
l validity of the low-temperature uhv-based approach for exploring che
misorbate solvation effects.