PtSnCe/C electrocatalysts for ethanol oxidation: DEFC and FTIR ""in-situ"" studies


Autoria(s): SOUZA, R. F. B. De; PARREIRA, L. S.; SILVA, J. C. M.; SIMOES, F. C.; CALEGARO, M. L.; GIZ, M. J.; CAMARA, G. A.; Oliveira Neto, Almir; SANTOS, M. C.
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

20/10/2012

20/10/2012

2011

Resumo

The ethanol oxidation reaction (EOR) was investigated using PtSnCe/C electrocatalysts in different mass ratios (72:23:5, 68:22:10 and 64:21:15) that were prepared by the polymeric precursor method. Transmission electron microscopy (TEM) showed that the particles ranged in size from approximately 2 to 5 nm. Changes in the net parameters observed for Pt suggest the incorporation of Sn and Ce into the Pt crystalline network with the formation of an alloy between Pt, Sn and/or Ce. Among the PtSnCe catalysts investigated, the 68:22:10 composition showed the highest activity toward ethanol oxidation, and the current time curves obtained in the presence of ethanol in acidic media showed a current density 50% higher than that observed for commercial PtSn/C (E-Tek). During the experiments performed on single direct ethanol fuel cells, the power density for the PtSnCe/C 68:22:10 anode was nearly 40% higher than the one obtained using the commercial catalyst. Data from Fourier transform infrared (FTIR) spectroscopy showed that the observed behavior for ethanol oxidation may be explained in terms of a double mechanism. The presence of Sn and Ce seems to favor CO oxidation, since they produce an oxygen-containing species to oxidize acetaldehyde to acetic acid. Copyright (C) 2011, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.

CNPq

Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)

CAPES

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)

FUNDECT

FUNDECT

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

FAPESP[05/59992-6]

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

FAPESP[08/58788-4]

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

FAPESP[09/09145-6]

FAPESP[10/07831-7]

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

FAPESP[10/03037-4]

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

FAPESP[10/16511-6]

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

UFABC

UFABC

Identificador

INTERNATIONAL JOURNAL OF HYDROGEN ENERGY, v.36, n.18, p.11519-11527, 2011

0360-3199

http://producao.usp.br/handle/BDPI/31560

10.1016/j.ijhydene.2011.05.016

http://dx.doi.org/10.1016/j.ijhydene.2011.05.016

Idioma(s)

eng

Publicador

PERGAMON-ELSEVIER SCIENCE LTD

Relação

International Journal of Hydrogen Energy

Direitos

restrictedAccess

Copyright PERGAMON-ELSEVIER SCIENCE LTD

Palavras-Chave #Ethanol oxidation reaction #Electrocatalysis #Platinum-tin alloys #Ceria #Polymeric precursor method #ALCOHOL-REDUCTION PROCESS #PLATINUM-BASED ANODES #METHANOL FUEL-CELLS #FORMIC-ACID #PTSN/CEO2-C ELECTROCATALYST #PT/C ELECTROCATALYSTS #ACETIC-ACID #ELECTROOXIDATION #CATALYSTS #SN #Chemistry, Physical #Electrochemistry #Energy & Fuels
Tipo

article

original article

publishedVersion