Repositorio Institucional
Repositorio Institucional
CONICET Digital
  • Inicio
  • EXPLORAR
    • AUTORES
    • DISCIPLINAS
    • COMUNIDADES
  • Estadísticas
  • Novedades
    • Noticias
    • Boletines
  • Ayuda
    • General
    • Datos de investigación
  • Acerca de
    • CONICET Digital
    • Equipo
    • Red Federal
  • Contacto
JavaScript is disabled for your browser. Some features of this site may not work without it.
  • INFORMACIÓN GENERAL
  • RESUMEN
  • ESTADISTICAS
 
Artículo

Electrooxidation of ethanol and glycerol on carbon supported PtCu nanoparticles

Castagna, Rodrigo MartínIcon ; Sieben, Juan ManuelIcon ; Alvarez, Andrea ElizabethIcon ; Duarte, Marta María Elena
Fecha de publicación: 03/2019
Editorial: Elsevier
Revista: International Journal of Hydrogen Energy
ISSN: 0360-3199
Idioma: Inglés
Tipo de recurso: Artículo publicado
Clasificación temática:
Físico-Química, Ciencia de los Polímeros, Electroquímica

Resumen

Four carbon supported PtCu nanostructured catalysts with Pt:Cu atomic ratios of 1:3.20, 1:2.23, 1:0.61 and 1:0.35 were synthesized by a two-step route, involving the chemical reduction of Cu ions on the carbon support, followed by the partial galvanic replacement of Cu atoms by Pt. Bimetallic nanostructured particles with average sizes in the range of 2.3–3.2 nm were obtained. The bimetallic catalysts with surface Pt contents between 20 and 55 at. % were formed by a Cu-rich core surrounded by a Pt-Cu shell, while that with the highest Pt content presented a uniform alloy structure instead of a core-shell arrangement. The electrocatalytic performance of the as-prepared materials toward ethanol electrooxidation in acid and alkaline media and glycerol oxidation in alkaline environment was investigated by cyclic voltammetry and chronoamperometry. It was observed that the electrocatalytic activity of PtCu nanoparticles was found to depend on the surface composition, platinum utilization efficiency, structure and Pt ensemble. Among the as-prepared catalysts, Pt0·62Cu0·38/C core-shell material showed the best performance for ethanol oxidation in both acid and alkaline environments, while Pt0·24Cu0·76/C and Pt0·31Cu0·69/C core-shell catalysts exhibited the highest activity for glycerol oxidation in alkaline medium. The electrochemical results showed that the catalytic activity of the bimetallic Cu@PtCu core-shell nanostructured nanoparticles is between four and ten times higher than that of a commercial Pt0·51Ru0·49/C catalyst.
Palabras clave: CARBON SUPPORTED PtxCu1-x NANOPARTICLES , CORE-SHELL AND ALLOY STRUCTURES , ETHANOL OXIDATION , GLYCEROL OXIDATION
Ver el registro completo
 
Archivos asociados
Tamaño: 2.141Mb
Formato: PDF
.
Solicitar
Licencia
info:eu-repo/semantics/restrictedAccess Excepto donde se diga explícitamente, este item se publica bajo la siguiente descripción: Creative Commons Attribution-NonCommercial-ShareAlike 2.5 Unported (CC BY-NC-SA 2.5)
Identificadores
URI: http://hdl.handle.net/11336/104314
URL: https://linkinghub.elsevier.com/retrieve/pii/S0360319919302228
DOI: http://dx.doi.org/10.1016/j.ijhydene.2019.01.090
Colecciones
Articulos(CCT - BAHIA BLANCA)
Articulos de CTRO.CIENTIFICO TECNOL.CONICET - BAHIA BLANCA
Citación
Castagna, Rodrigo Martín; Sieben, Juan Manuel; Alvarez, Andrea Elizabeth; Duarte, Marta María Elena; Electrooxidation of ethanol and glycerol on carbon supported PtCu nanoparticles; Elsevier; International Journal of Hydrogen Energy; 44; 12; 3-2019; 5970-5982
Compartir
Altmétricas
 

Enviar por e-mail
Separar cada destinatario (hasta 5) con punto y coma.
  • Facebook
  • X Conicet Digital
  • Instagram
  • YouTube
  • Sound Cloud
  • LinkedIn

Los contenidos del CONICET están licenciados bajo Creative Commons Reconocimiento 2.5 Argentina License

https://www.conicet.gov.ar/ - CONICET

Inicio

Explorar

  • Autores
  • Disciplinas
  • Comunidades

Estadísticas

Novedades

  • Noticias
  • Boletines

Ayuda

Acerca de

  • CONICET Digital
  • Equipo
  • Red Federal

Contacto

Godoy Cruz 2290 (C1425FQB) CABA – República Argentina – Tel: +5411 4899-5400 repositorio@conicet.gov.ar
TÉRMINOS Y CONDICIONES