The effect of the cooling atmosphere in the preparation of flame-annealed Pt(111) electrodes on CO adlayer oxidation

• Published in: Electrochemistry communications 2000-07, Vol.2 (7), p.487-490
• Main Authors: Lebedeva, Natalia P, Koper, Marc T.M, Feliu, Juan M, van Santen, Rutger A
• Format: Article
• Language: English
• Subjects: Carbon monoxide; Chemistry; Crystalline defects; Electrochemistry; Exact sciences and technology; General and physical chemistry; Kinetics and mechanism of reactions; Oxidation
• ISSN: 1388-2481; 1873-1902
• DOI: 10.1016/S1388-2481(00)00062-X

The effect of the cooling atmosphere on the rate of CO adlayer oxidation on flame-annealed Pt(111) has been studied. Cooling of a flame-annealed Pt(111) electrode in air results in a higher amount of crystalline defects compared to Pt(111) cooled in a hydrogen–argon stream. Although the blank profiles in 0.5 M H 2SO 4 of Pt(111), cooled in air and under oxygen exclusion, are virtually identical, CO adlayer oxidation occurs at significantly lower overpotentials on the former electrode. Three voltammetric peaks are observed for subsaturated CO adlayer oxidation on Pt(111), cooled in Ar+H 2 mixture, while only two peaks develop in the case of a Pt(111) surface cooled in air. Random crystalline defects, introduced via cooling of a flame-annealed Pt(111) in air, enhance CO adlayer oxidation, and apparently also suppress the third high-potential peak observed on a quasi-perfect (111) surface. The high sensitivity of the saturated CO adlayer oxidation to the presence of crystalline defects on Pt(111) can hence be used as a straightforward, sensitive, though qualitative method to assess the degree of crystalline order of the electrode.