Michele BrandaliseMarcelo Marques TusiRita M.S. RodriguesEstevam V. SpinacéAlmir Oliveira Neto
PtSn/C, PtSn/Er2O3-C, PtSn/CeO2–C, PtSn/La2O3–C and PtSn/Nd2O3–C electrocatalysts were prepared by an alcohol-reduction process using H2PtCl6.6H2O and SnCl2.2H2O as metal sources, ethylene glycol as solvent and reducing agent, 85% Vulcan XC72-15% rare earth (Er2O3, CeO2, La2O3 and Nd2O3) as support. The platinum and tin metal loadings were always kept at 20 wt%. The electrocatalysts were characterized by EDX, XRD and TEM, while that the performance for ethanol oxidation was investigated by cyclic voltammetry and cronoamperommetry at room temperature. The PtSn/Er2O3–C electrocatalyst showed an increase of performance for ethanol oxidation in relation to PtSn/C electrocatalyst. The final current values after holding the cell potential at 0.5 V versus RHE for 30 min were the following: PtSn/Er2O3–C > PtSn/CeO2–C > PtSn/Nd2O3–C > PtSn/La2O3–C > PtSn/C. In the tests at 100oC on a single cell of a direct ethanol fuel cell (DEFC), the PtSn/Er2O3–C electrocatalyst also showed the best performance in relation to the others electrocatalysts.
Raphael RodriguesMarcelo Marques TusiM. H. ChikasawaChristina A.L.G.O. ForbiciniMarcelo LinardiEstevam V. SpinacéAlmir Oliveira Neto
Vilmária Aparecida RibeiroRyan C. SekolAndré D. TaylorAlmir Oliveira NetoEstevam V. Spinacé
Vilmária Aparecida RibeiroRyan C. SekolAndré D. TaylorAlmir Oliveira NetoEstevam V. Spinacé
Almir Oliveira NetoAndré Y. WatanabeMichele BrandaliseMarcelo Marques TusiRita M. de S. RodriguesMarcelo LinardiEstevam V. SpinacéChristina A.L.G.O. Forbicini
Almir Oliveira NetoLuciana Aparecida FariasRicardo Rodrigues DiasMichelle BrandaliseMarcelo LinardiEstevam V. Spinacé