OTTONI, CRISTIANE A.SILVA, SIRLANE G. daSOUZA, RODRIGO F.B. deOLIVEIRA NETO, ALMIR2016-03-082016-03-082016OTTONI, CRISTIANE A.; SILVA, SIRLANE G. da; SOUZA, RODRIGO F.B. de; OLIVEIRA NETO, ALMIR. PtAu electrocatalyst for glycerol oxidation reaction using a ATR-FTIR/Single direct alkaline glycerol/Air cell in situ study. <b>Electrocatalysis</b>, v. 7, p. 22-32, 2016. DOI: <a href="https://dx.doi.org/10.1007/s12678-015-0277-7">10.1007/s12678-015-0277-7</a>. Disponível em: http://repositorio.ipen.br/handle/123456789/25810.1868-2529http://repositorio.ipen.br/handle/123456789/25810Different ratios of PtAu/C electrocatalysts were synthesized and assessed for their capability by glycerol electrooxidation. Electrocatalysts were characterized by Xray diffraction (XRD), transmission electron microscopy (TEM), cyclic voltammetry (CV), chronoamperometry, and direct glycerol/air fuel cell coupled with a ATR-FTIR setup. XRD of PtAu/C electrocatalysts showed the presence of Pt (fcc), Au (fcc), and PtAu (fcc) phases, and TEM images for PtAu/C electrocatalysts showed particle size between 5.4 and 5.8 nm. PtAu/C (50:50) presented the best result for glycerol electrooxidation by cyclic voltammetry and chronoamperommetry measurements in comparison with other electrocatalysts prepared. All PtAu/C showed better performance in comparison with Pt/C and Au/C. Moreover, the addition of gold to platinum favored glycerol by electronic effect and bifunctional mechanism. Through ATRFTIR/direct alkaline glycerol/air cell in-situ study, it was possible to identify glycerate and tartronate as main products formed during the electrochemical glycerol oxidation.22-32openAccesselectrocatalystsglycerolfuel cellsplatinumgoldcarbonx-ray diffractiontransmission electron microscopyArtigo de periódico710.1007/s12678-015-0277-7https://orcid.org/0000-0002-9287-607168.41