W@Au Nanostructures Modifying Carbon as Materials for Hydrogen Peroxide Electrogeneration
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...
| Autores: | , , , , , , , |
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| Tipo de recurso: | artículo |
| Estado: | Versión publicada |
| Fecha de publicación: | 2017 |
| País: | Brasil |
| Institución: | Universidade Estadual Paulista (UNESP) |
| Repositorio: | Repositório Institucional da UNESP |
| Idioma: | inglés |
| OAI Identifier: | oai:repositorio.unesp.br:11449/178673 |
| Acceso en línea: | http://dx.doi.org/10.1016/j.electacta.2017.01.192 http://hdl.handle.net/11449/178673 |
| Access Level: | acceso abierto |
| Palabra clave: | core-shell Hydrogen peroxide electrogeneration oxygen reduction reaction W@Au |
| Sumario: | 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. |
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