Electrochemical characterisation of gold on Pt{ h k l} for ethanol electrocatalysis

• Published in: Journal of electroanalytical chemistry (Lausanne, Switzerland) Switzerland), 2009-01, Vol.625 (2), p.123-130
• Main Authors: Hazzazi, Omar A., Attard, Gary A., Wells, Peter B., Vidal-Iglesias, F.J., Casadesus, Meritxell
• Format: Article
• Language: English
• Subjects: Chemistry; Cyclic voltammetry; Electrochemistry; Ethanol electrooxidation; Exact sciences and technology; General and physical chemistry; Gold adsorption; Kinetics and mechanism of reactions; Pt{ h k l}
• ISSN: 1572-6657; 1873-2569
• DOI: 10.1016/j.jelechem.2008.10.016

The cyclic voltammetric (CV) behaviour of gold adsorbed on Pt{ h k l} electrodes is reported. It is found that stepped surfaces vicinal to Pt{1 1 1} exhibit preferential adsorption of gold at step sites. However, for stepped surfaces containing Pt{1 0 0} terraces, adsorption of gold at step and terrace site occurs with equal probability, although for Pt{ n 1 1} electrodes with n < 7 (i.e. electrodes containing short Pt{1 0 0} terraces), slight preference for step site adsorption is still observed. This behaviour is similar to that reported previously for Bi adsorption on Pt{ h k l} and is interpreted in terms of slower rates of gold atom surface diffusion across Pt{1 0 0} vs. Pt{1 1 1} terraces. By comparing the electrochemical response of gold adlayers on Pt{ h k l} with previously published bulk Au{ h k l} voltammetry, it is deduced that the gold overlayers on Pt{ h k l} are pseudomorphic in nature. This finding is in agreement with previous UHV and electrochemical results for gold deposition on platinum. Using such gold modified Pt{ h k l} electrodes as model surfaces, we also report, for the first time, the electrooxidation of ethanol on Au/Pt{ h k l} in alkaline aqueous solution. The ethanol oxidation reaction (EOR) is shown to be structure sensitive for submonolayer gold coverages. In fact, a maximum in the rate of EOR at platinum sites adjacent to gold islands is observed between approximately 0.4–0.6 monolayers of gold on Pt{1 0 0}, Pt{1 1 1} and Pt{1 1 0} in 0.1 M NaOH(aq). A second electrooxidation state at more positive potentials for 0 < θ Au < 1 ascribed to EOR at pure gold sites is also observed, at least for Pt{1 1 1} and Pt{1 0 0}. On Pt{1 1 1}, the potential range and activity of EOR in this second process is similar to bulk gold whereas for submonolayer gold films on Pt{1 0 0}, the peak is shifted to more negative potentials.