Surface structure and anion effects in the oxidation of ethanol on platinum nanoparticles

Ethanol oxidation on platinum nanoparticles with well-characterized surfaces is studied using cyclic voltammetry and FTIR techniques. Their behavior is compared with that obtained for platinum single crystal electrodes, in order to rationalize their performance and to understand the effects of the s...

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Published inJournal of materials chemistry. A, Materials for energy and sustainability Vol. 1; no. 24; pp. 7068 - 7076
Main Authors Busó-Rogero, Carlos, Grozovski, Vitali, Vidal-Iglesias, Francisco J., Solla-Gullón, José, Herrero, Enrique, Feliu, Juan M.
Format Journal Article
LanguageEnglish
Published 01.01.2013
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Abstract Ethanol oxidation on platinum nanoparticles with well-characterized surfaces is studied using cyclic voltammetry and FTIR techniques. Their behavior is compared with that obtained for platinum single crystal electrodes, in order to rationalize their performance and to understand the effects of the surface structure and anion adsorption on the reactivity. The results clearly demonstrate that there are strong effects of anion adsorption and surface structure on the measured current and oxidation mechanism. Thus, the main product of ethanol oxidation on (111) preferentially oriented Pt nanoparticles is acetic acid, and the amount of CO sub(2) produced can be considered negligible. On the other hand, (100) preferentially oriented Pt nanoparticles are effective for the cleavage of the C-C bond yielding adsorbed CO, which eventually is oxidized to CO sub(2). This nanoparticles electrode has the highest catalytic activity at high potentials, whereas (111) preferentially oriented Pt nanoparticles are more active at low potentials. In addition, no significant differences in the activity are reported by using different supporting electrolytes, which indicates that adsorbed acetate, which results from the adsorption of acetic acid, hinders ethanol oxidation.
AbstractList Ethanol oxidation on platinum nanoparticles with well-characterized surfaces is studied using cyclic voltammetry and FTIR techniques. Their behavior is compared with that obtained for platinum single crystal electrodes, in order to rationalize their performance and to understand the effects of the surface structure and anion adsorption on the reactivity. The results clearly demonstrate that there are strong effects of anion adsorption and surface structure on the measured current and oxidation mechanism. Thus, the main product of ethanol oxidation on (111) preferentially oriented Pt nanoparticles is acetic acid, and the amount of CO sub(2) produced can be considered negligible. On the other hand, (100) preferentially oriented Pt nanoparticles are effective for the cleavage of the C-C bond yielding adsorbed CO, which eventually is oxidized to CO sub(2). This nanoparticles electrode has the highest catalytic activity at high potentials, whereas (111) preferentially oriented Pt nanoparticles are more active at low potentials. In addition, no significant differences in the activity are reported by using different supporting electrolytes, which indicates that adsorbed acetate, which results from the adsorption of acetic acid, hinders ethanol oxidation.
Author Feliu, Juan M.
Busó-Rogero, Carlos
Solla-Gullón, José
Vidal-Iglesias, Francisco J.
Herrero, Enrique
Grozovski, Vitali
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Snippet Ethanol oxidation on platinum nanoparticles with well-characterized surfaces is studied using cyclic voltammetry and FTIR techniques. Their behavior is...
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StartPage 7068
SubjectTerms Anions
Ethanol
Ethyl alcohol
Nanoparticles
Oxidation
Platinum
Surface chemistry
Surface structure
Title Surface structure and anion effects in the oxidation of ethanol on platinum nanoparticles
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