| Texto completo | |
| Autor(es): |
Isidoro, Roberta A.
;
Sahin, Nihat E.
;
Fonseca, Fabio C.
;
Napporn, Teko W.
;
Santiago, Elisabete I.
;
Kokoh, Kouakou Boniface
Número total de Autores: 6
|
| Tipo de documento: | Artigo Científico |
| Fonte: | HEMNANOMA; v. N/A, p. 13-pg., 2025-11-28. |
| Resumo | |
This study presents a facile synthesis of carbon-supported binarypalladium-copper (Pd-Cu/C) nanomaterials designed to achieve competitive catalytic activity while reducing material costs in solid polymer electrolyte (SPE) fuel cells. A surfactant-free, microwave-heated polyol process is employed to synthesize Pd/C and Pd-Cu/C nanomaterials with mean particle size below 4.0 nm. The electrocatalytic activity toward oxygen reduction reaction (ORR) and the corresponding kinetic parameters of Pd-Cu/C electrodes with varying compositions are systematically interrogated using rotating disk electrode (RDE) measurements. Notably, Tafel analysis reveals a slope of 60 +/- 2 mV per decade slope at low current densities indicating that the first electron transfer to molecular oxygen (O2) is the rate-determining step. At higher current densities, a slope of 144 +/- 8 mV per decade suggests a transition proton-coupled electron transfer as the dominant mechanism. Furthermore, electrochemical performance of membrane-electrode-assemblies (MEAs) reveals a peak power density of similar to 475 mW cm-2 with Pd /C cathode under optimal operating conditions. However, increasing the Cu content in the Pd-Cu/C catalysts results in a marked decrease in current density, likely due to partial Cu dissolution. These findings highlight the potential of binary Pd-Cu nanomaterials as promising alternatives to platinum-based catalysts for Pt-free SPE fuel cell applications. (AU) | |
| Processo FAPESP: | 23/14931-8 - Dispositivos eletroquímicos avançados de conversão de moléculas e produção de energia |
| Beneficiário: | Fabio Coral Fonseca |
| Modalidade de apoio: | Auxílio à Pesquisa - Temático |