| Texto completo | |
| Autor(es): |
Antonin, Vanessa S.
;
Parreira, Luanna S.
;
Aveiro, Luci R.
;
Silva, Fernando L.
;
Valim, Ricardo B.
;
Hammer, Peter
;
Lanza, Marcos R. V.
;
Santos, Mauro C.
Número total de Autores: 8
|
| Tipo de documento: | Artigo Científico |
| Fonte: | Electrochimica Acta; v. 231, p. 713-720, MAR 20 2017. |
| Citações Web of Science: | 11 |
| Resumo | |
In this work, materials based on core-shell W@Au type structures were found to have promise for use as electrocatalysts on the in-situ production of H2O2 by means of the oxygen reduction reaction (ORR). We describe herein the synthesis and characterization of these materials and then present a study of electrocatalytic activity towards ORR by the electrogeneration of H2O2 employing these materials supported on Vulcan XC-72R carbon corresponding to 1 and 2 wt% loading. The use of W@Au/C materials led to higher activity compared to pure carbon and commercial Pt/C, and the optimal load is 1%, which presented the highest ring current for the ORR using the rotating ring-disk electrode technique. Exhaustive electrolysis using a W@Au/C 1% gas diffusion electrode (GDE) was employed to verify the real amount of H2O2 electrogenerated comparing with a Vulcan XC-72R GDE. We verified that the W@Au/C 1% material is able to generate 50% more H2O2 than carbon. These results can be explained based on synergistic interactions presented by the W@Au/C 1% material and also by both conductivity and hydrophilicity differences provided by the nanostructures supported on carbon. (C) 2017 Elsevier Ltd. All rights reserved. (AU) | |
| Processo FAPESP: | 11/21656-6 - Materiais Nanoestruturados Binários Baseados em Metais na Eletrogeração de Peróxido de Hidrogênio para Degradação do Ciprofloxacino |
| Beneficiário: | Vanessa da Silva Antonin |
| Modalidade de apoio: | Bolsas no Brasil - Doutorado |
| Processo FAPESP: | 15/10314-8 - Nanoestruturas para a Degradação de Fenol, Ciprofloxacino e 17 alfa etinilestradiol |
| Beneficiário: | Mauro Coelho dos Santos |
| Modalidade de apoio: | Auxílio à Pesquisa - Regular |