ON THE ELECTROCHEMICAL AND IN-SITU FOURIER-TRANSFORM INFRARED-SPECTROSCOPY CHARACTERIZATION OF UREA ADLAYERS AT PT(100) ELECTRODES

The urea adlayers formed at the surface of Pt(100) electrodes immersed in urea-containing solutions have been characterized in-situ with a c ombination of cyclic voltammetry, charge displacement, and Fourier tra nsform IR spectroscopy experiments. The infrared data indicate that th e urea molecule is bonded through the two nitrogen atoms with the C-O group normal to the electrode surface. At the same time, the cyclic vo ltammetry and charge displacement data agree with previously reported coverage data if urea adsorption takes place with a net transfer of tw o electrons per adsorbed urea molecule. The existence of lateral inter actions between neighbouring adsorbed molecules has been determined fr om the analysis of the band frequency and bandwidth together with thei r dependence on both the urea coverage and the electrode potential. At constant urea coverage the adsorbate band is shifted towards higher w avenumbers as the electrode potential increases, with a measured tunin g rate of 50 cm(-1) V-1, which does not depend significantly on the ur ea coverage. The effect of the surface charge density on the electroni c distribution in the urea molecule is suggested to play a key role on the observed potential dependent band shift and narrowing. The coexis tence of an electrochemical Stark effect can not be excluded from the present data.