ADSORPTION OF CO AND CO2 ON POLYCRYSTALLINE PT AT A POTENTIAL IN THE HYDROGEN ADSORPTION REGION IN PHOSPHATE BUFFER SOLUTION - AN IN-SITU FOURIER-TRANSFORM IR STUDY

Citation
S. Taguchi et al., ADSORPTION OF CO AND CO2 ON POLYCRYSTALLINE PT AT A POTENTIAL IN THE HYDROGEN ADSORPTION REGION IN PHOSPHATE BUFFER SOLUTION - AN IN-SITU FOURIER-TRANSFORM IR STUDY, Journal of electroanalytical chemistry [1992], 369(1-2), 1994, pp. 199-205
Citations number
30
Categorie Soggetti
Electrochemistry,"Chemistry Analytical
Journal title
Journal of electroanalytical chemistry [1992]
ISSN journal
15726657 → ACNP
Volume
369
Issue
1-2
Year of publication
1994
Pages
199 - 205
Database
ISI
SICI code
Abstract
Adsorption features of CO(ads) and reduced CO2 on a polycrystalline pl atinum electrode in phosphate buffer solution were investigated by ano dic stripping voltammetry (ASV) and in-situ Fourier transform IR (FTIR ) measurement. The ASV peak of CO(ads) at 0.45 V (with respect to a re versible hydrogen electrode did not appear in the anodic stripping vol tammogram of reduced CO2. However, sequential CO2/CO dosing at 0.05 V added the ASV peak at 0.41 V to the anodic stripping voltammogram of r educed CO2. The ASV peaks at 0.45 and 0.41 V were assigned to bridged CO by IR bands around 1850 cm-1, similar to IR bands in acidic solutio n. The sequential CO2/CO dosing gave an IR band of bridged CO of 1842 cm-1 at 0.05 V. However, the adsorption of reduced CO2 did not give a strong IR band of bridged CO. The potential dependence of the IR band feature of linear CO from CO gas was different from that from reduced CO2. The electron numbers per site for CO(ads) and reduced CO2 oxidati on processes were discussed in comparison with the results of ASV and FTIR.