SILVA, JULIO C.M.NTAIS, SPYRIDONRAJARAMAN, VISHWANATHANTEIXEIRA-NETO, ERICOTEIXEIRA-NETO, ANGELA A.NETO, ALMIR O.ANTONIASSI, RODOLFO M.SPINACE, ESTEVAM V.BARANOVA, ELENA A.2019-08-072019-08-072019SILVA, JULIO C.M.; NTAIS, SPYRIDON; RAJARAMAN, VISHWANATHAN; TEIXEIRA-NETO, ERICO; TEIXEIRA-NETO, ANGELA A.; NETO, ALMIR O.; ANTONIASSI, RODOLFO M.; SPINACE, ESTEVAM V.; BARANOVA, ELENA A. The catalytic activity of Pt:Ru nanoparticles for ethylene glycol and ethanol electrooxidation in a direct alcohol fuel cell. <b>Electrocatalysis</b>, v. 10, n. 3, p. 203-213, 2019. DOI: <a href="https://dx.doi.org/10.1007/s12678-019-00515-8">10.1007/s12678-019-00515-8</a>. Disponível em: http://repositorio.ipen.br/handle/123456789/30038.1868-2529http://repositorio.ipen.br/handle/123456789/30038In this study, we investigated the carbon-supported PtRu nanoparticles with atomic ratios of Pt:Ru of 100:0, 90:10, 70:30, and 50:50 for ethanol and ethylene glycol electrooxidation in alkaline media. The nanoparticles were synthesized using sodium borohydride method with 20 wt% of metals loading on carbon. The nanoparticle mean sizes were 7.3 nm, 5.7 nm, 5.2 nm, and 5.1 nm for Pt/C, Pt90Ru10/C, Pt70Ru30/C, and Pt50Ru50/C, respectively. X-ray diffraction (XRD) analysis revealed that Pt and PtRu electrocatalysts have face-centered cubic (fcc) structure and suggests the alloy formation for all PtRu/C materials, which was further supported by the X-ray photoelectron spectroscopy (XPS). Based on XPS analysis, Pt50Ru50/C has higher amount of Pt oxides on the surface than Pt70Ru30/C. Electrochemical results demonstrated that the addition of Ru to Pt enhances the catalytic activity towards ethanol and ethylene glycol electrooxidadion. The catalyst of Pt50Ru50/C composition showed the lowest onset potential for ethanol and ethylene glycol electrooxidation, which were 160 and 70 mV lower than for Pt/C, respectively. Furthermore, this catalyst outperformed Pt/C and other PtRu/C compositions in chronoamperometric and direct alcohol fuel cell (DAFC) experiments. DAFC experiments using Pt50Ru50/C as anode had the power density 40 and 14% higher than using Pt/C for ethanol and ethylene glycol, respectively. The promotion is due to the bi-functional mechanism and/or electronic effect of two metals in the alloy.203-213openAccessnanoparticleselectrocatalystsoxidationethanolethylene glycolselectrochemical corrosionfuel cellsdirect ethanol fuel cellsThe catalytic activity of Pt:Ru nanoparticles for ethylene glycol and ethanol electrooxidation in a direct alcohol fuel cellArtigo de periódico31010.1007/s12678-019-00515-80000-0002-7011-82610000-0001-8745-3421https://orcid.org/0000-0002-7011-8261https://orcid.org/0000-0002-9287-607145.00355.00