Synthesis of MFe2O4 (M=Ni, Co) Nanoparticles by a Bicontinuous Microemulsion Method for the Oxygen Evolution Reaction

Author:

Sultan Faiz1,González Sepúlveda Guillermo E.2,Medina Dora I.3,Videa Marcelo1,Sánchez‐Domínguez Margarita4,Cholula‐Díaz Jorge L.1ORCID

Affiliation:

1. Tecnologico de Monterrey School of Engineering and Sciences Av. Eugenio Garza Sada 2501 64849 N.L. México

2. Universidad de Guadalajara, Centro Universitario de Tonalá Nuevo Periférico Oriente. 555, Ejido San José, Tateposco 45425 Tonalá Jal. Mexico

3. Tecnologico de Monterrey Institute of Advanced Materials for Sustainable Manufacturing Av. Eugenio Garza Sada 2501 64849 N.L. México

4. Centro de Investigación en Materiales Avanzados SC, Subsede Monterrey Alianza Norte 202, Apodaca 66628, NL Mexico

Abstract

AbstractDeveloping efficient and low‐cost electrocatalysts for the oxygen evolution reaction (OER) is crucial for sustainable hydrogen production through water splitting. In this study, CoFe2O4 and NiFe2O4 nanoparticles as electrocatalysts were prepared via an inexpensive method involving the use of bicontinuous microemulsions as nanoreactors. The crystalline structure, morphology, and elemental composition of the electrocatalysts were characterized by XRD, Raman spectroscopy, TEM, and EDS elemental mapping. The electronic structure and textural properties were examined using XPS and the nitrogen adsorption‐desorption method. The OER measurements were carried out in a standard three‐electrode system. CoFe2O4 demonstrated relatively higher OER catalytic activity than NiFe2O4 in 1 M KOH solution, with a smaller overpotential of 410 mV to achieve a current density of 10 mA cm−2 and a smaller Tafel slope of 80 mV dec−1. In contrast, NiFe2O4 offered a higher overpotential of 450 mV to reach the same current density. The superior performance of CoFe2O4 is ascribed to higher ECSA, better conductivity, and lower charge transfer resistance. However, both electrocatalysts showed stability up to more than three hours of continuous performance.

Publisher

Wiley

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