Ethanol oxidation reactions using SnO(2)@Pt/C as an electrocatalyst


Autoria(s): SILVA, J. C. M.; SOUZA, R. F. B. De; PARREIRA, L. S.; TEIXEIRA NETO, E.; CALEGARO, M. L.; SANTOS, M. C.
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

20/10/2012

20/10/2012

2010

Resumo

This paper presents a study on the ethanol oxidation reaction using SnO(2)@Pt/C core-shell structures as electrocatalysts. All the materials used, including Pt/C and PtSn/C E-tek, were 20% (w/w) metal on carbon. The formation of core-shell nanoparticles (SnO(2)@Pt/C) was measured by UV-vis spectrophotometry. X-ray diffraction measurements showed Pt (shell) diffraction patterns without influence from the SnO(2) core and without any shift in 2 theta values for Pt. The diameters of the core-shell particle structures, measured using high-resolution transmission electron microscopy images, were in the range of 3-16 nm. The electrochemical profile for SnO(2)@Pt/C in an acidic medium (H(2)SO(4) at a concentration of 0.5 mol L(-1)) was almost the same as the typical electrochemical behavior for Pt in an acidic medium. Furthermore, the onset potential for the ethanol oxidation reaction using SnO(2)@Pt/C was almost the same as that for PtSn/C E-tek (0.23 V versus the reversible hydrogen electrode). However, the mass current peak densities for ethanol oxidation were 50% higher on SnO(2)@Pt/C than on PtSn/C E-tek. In the polarization curve, the mass current density for ethanol oxidation was higher at all potentials for SnO(2)@Pt/C when compared to Pt/C and PtSn/C E-tek. At 0.5 V, the current mass density for ethanol oxidation on SnO(2)@Pt was 2.3 times of that for the same process on the commercial material. The electrocatalytic activity of SnO(2)@Pt/C for ethanol oxidation was associated with an increase in the electrochemically active surface area. However, an electronic effect should also be considered because the Pt shell changes its electronic structure in the presence of the foreign core. (C) 2010 Elsevier B.V. All rights reserved.

CNPq[474732/2008-8]

Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)

CAPES

FAPESP[05/59992-6]

Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

FAPESP[09/09145-6]

Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

FAPESP[08/58788-4]

UFABC

UFABC

Identificador

APPLIED CATALYSIS B-ENVIRONMENTAL, v.99, n.1/Fev, p.265-271, 2010

0926-3373

http://producao.usp.br/handle/BDPI/31667

10.1016/j.apcatb.2010.06.031

http://dx.doi.org/10.1016/j.apcatb.2010.06.031

Idioma(s)

eng

Publicador

ELSEVIER SCIENCE BV

Relação

Applied Catalysis B-environmental

Direitos

restrictedAccess

Copyright ELSEVIER SCIENCE BV

Palavras-Chave #Core-shell #SnO(2)@Pt #PtSn/C #Ethanol oxidation reaction #Electrocatalysis #METHANOL FUEL-CELLS #BIMETALLIC NANOPARTICLES #STRUCTURAL-CHARACTERIZATION #METALLIC BILAYER #OXYGEN REDUCTION #ANODE CATALYSTS #ELECTROOXIDATION #PTSN/C #PT/C #NANOCRYSTALS #Chemistry, Physical #Engineering, Environmental #Engineering, Chemical
Tipo

article

original article

publishedVersion