SOUZA, R.F.B. deSILVA, J.C.M.ASSUMPCAO, M.H.M.T.NETO, A.O.SANTOS, M.C.2014-07-312014-07-312014-07-312014-07-312014SOUZA, R.F.B. de; SILVA, J.C.M.; ASSUMPCAO, M.H.M.T.; NETO, A.O.; SANTOS, M.C. Ethanol oxidation reaction using PtSn/C+ce/C electrocatalysts: aspects of ceria contribution. <b>Electrochimica Acta</b>, v. 117, p. 292-298, 2014. DOI: <a href="https://dx.doi.org/10.1016/j.electacta.2013.11.129">10.1016/j.electacta.2013.11.129</a>. Disponível em: http://repositorio.ipen.br/handle/123456789/8545.0013-4686http://repositorio.ipen.br/handle/123456789/8545The ethanol oxidation reaction (EOR) was investigated using PtSn/C + Ce/C electrocatalysts in different mass ratios (58:42, 53:47, and 42:58) prepared using the polymeric precursor method. Transmission electron microscopy (TEM) experiments showed particles sizes in the range of 3 to 7 nm. Changes in the net parameters observed for Pt suggest the incorporation of Sn into the Pt crystalline network with the formation of an alloy mixture with the SnO2 phase. Among the PtSn/C + Ce/C catalysts investigated, the 53:47 composition showed the highest activity towards the EOR. In this case, the j versus t curves obtained in the presence of ethanol in acidic media exhibited a current density 90% higher than that observed with the commercial PtSn/C (ETEK). Correspondingly, during the experiments performed on single direct ethanol fuel cells, the maximum power density obtained using PtSn/C + Ce/C (53:47) as the anode was approximately 60% higher than that obtained using the commercial catalyst. FTIR data showed that the observed behavior for ethanol oxidation may be explained in terms of a synergic effect of bifunctional mechanism with electronic effects, in addition to a chemical effect of ceria that provides oxygen-containing species to oxidize acetaldehyde to acetic acid.292-298openAccessethanoloxidationelectrocatalystsplatinumtinceriumcarbondirect ethanol fuel cellsprecursorArtigo de periódico11710.1016/j.electacta.2013.11.129https://orcid.org/0000-0002-9287-6071