Original scientific paper
https://doi.org/10.5599/jese.3163
Nickel hydroxide enhanced nickel selenides for oxygen evolution reaction
Francisco J. García-Partida
; Universidad Autónoma de Nuevo León, UANL, Facultad de Ciencias Químicas, FCQ, Centro de Investigación en Biotecnología y Nanotecnología, CIBYN, PIIT, Apodaca, Nuevo León, C.P, 66628, Mexico
Ricardo Briones-Martínez
; Universidad Autónoma de Nuevo León, Facultad de Ciencias Químicas, Av. Universidad S/N Ciudad Universitaria, San Nicolás de los Garza, N.L, 66451, Mexico
Eduardo M. Sánchez
orcid.org/0000-0003-1255-0248
; Universidad Autónoma de Nuevo León, Facultad de Ciencias Químicas, Av. Universidad S/N Ciudad Universitaria, San Nicolás de los Garza, N.L, 66451, Mexico
Salomé M. de la Parra Arciniega
; Universidad Autónoma de Nuevo León, Facultad de Ciencias Químicas, Av. Universidad S/N Ciudad Universitaria, San Nicolás de los Garza, N.L, 66451, Mexico
Rodrigo Mayen-Mondragon
; UNITA, Universidad Nacional Autónoma de México, Vía de la Innovación 410, PIIT-Monterrey Autopista Monterrey km 10, Apodaca 66628, Nuevo León, Mexico.
Nora A. Garcia-Gomez
; Universidad Autónoma de Nuevo León, UANL, Facultad de Ciencias Químicas, FCQ, Centro de Investigación en Biotecnología y Nanotecnología, CIBYN, PIIT, Apodaca, Nuevo León, C.P, 66628, Mexico
*
* Corresponding author.
Abstract
Transition to sustainable energy systems relies on the development of efficient and cost-effective hydrogen production technologies. A major challenge in this field is designing high-performance electrocatalysts based on earth-abundant, low-cost materials. In this work, three nickel selenide phases, NiSe₂, NiSe, and Ni₃Se₂, along with their corresponding Ni(OH)₂-modified heterostructures, were synthesized on nickel foam and systematically evaluated as oxygen evolution reaction (OER) electrocatalysts in alkaline media. X-ray diffraction and scanning electron microscopy analyses revealed that the incorporation of Ni(OH)₂ profoundly influenced nucleation pathways and promoted more homogeneous active-phase distribution across the three-dimensional substrate. Electrochemical characterization demonstrated that all Ni(OH)₂-modified electrodes exhibited enhanced catalytic performance compared to their unmodified counterparts. Among them, NiSe-OH supported on nickel foam, referred to as NiSe-OH/NF, achieved the lowest overpotential of 177 mV at 10 mA cm⁻² and displayed favourable reaction kinetics, as reflected by its Tafel slope. The improved activity was attributed to synergistic interactions between Ni and Se, the activation of the Ni(OH)₂/NiOOH redox couple, and optimized charge-transfer pathways facilitated by the heterostructured interface. Long-term stability tests confirmed that the hybrid catalysts maintained over 86 % of their maximum current density after extended operation. These results establish Ni-Se/Ni(OH)₂ heterostructures as promising, earth-abundant materials for efficient alkaline OER and offer new insights into interface engineering for next-generation electrocatalyst design.
Keywords
Alkaline water splitting; electrocatalyst; heterostructured interfaces; transition metal chalcogenides
Hrčak ID:
346199
URI
Publication date:
7.3.2026.
Visits: 62 *