Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
9634239 | Journal of Electroanalytical Chemistry | 2005 | 9 Pages |
Abstract
Nickel-underpotential deposition (UPD) on platinum electrodes has been studied in sulphuric media using cyclic voltammetry. The process seems structure-related: among the surfaces we did study, only (2Â ÃÂ 1)-reconstructed Pt(1Â 1Â 0) surface yields nickel-UPD. At low pH values, nickel-UPD peaks overlap with the hydrogen adsorption/desorption region. At higher pH (2-3) the overlapping is less severe: nickel coverage increases and can be estimated. Nickel-UPD on platinum (1Â 1Â 0) is a slow and irreversible process. The co-adsorption of sulphate or hydrogen-sulphate anions is probable. Nickel-UPD on Pt(1Â 1Â 0) occurs even in the presence of CO. Nickel submonolayer on Pt(1Â 1Â 0) exhibit remarkable activity towards CO-oxidation.
Keywords
Related Topics
Physical Sciences and Engineering
Chemical Engineering
Chemical Engineering (General)
Authors
Marian Chatenet, René Faure, Yvonne Soldo-Olivier,