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Composition-controlled chemical bath deposition of Fe-doped NiO microflowers for boosting oxygen evolution reaction.

Authors :
Battiato, Sergio
Pellegrino, Anna Lucia
Pollicino, Antonino
Terrasi, Antonio
Mirabella, Salvo
Source :
International Journal of Hydrogen Energy. Jun2023, Vol. 48 Issue 48, p18291-18300. 10p.
Publication Year :
2023

Abstract

Water electrolysis for green hydrogen production is gaining tremendous attention in the quest towards sustainable energy sources. At the heart of water splitting technology are the electrocatalysts, which facilitate the two half-cell reactions, i.e., the hydrogen evolution reaction (HER) and oxygen evolution reaction (OER), with the latter being the most thermodynamically uphill. Herein, we managed to fabricate Ni 1-x Fe x O microflowers (μFs) with varying % of Fe doping (0 < x < 0.36) via an easy chemical bath deposition (CBD) method. The as-synthesized μFs drop-casted on graphene paper (GP) are then applied as electrocatalysts for OER. Compared to contrast catalysts, the electrocatalyst with x Fe = 0.1 exhibits a lower overpotential of 297 mV at a current density of 10 mA cm−2, Tafel slope of 44 mV dec−1 and unprecedented turnover frequency of 4.6 s−1 at 300 mV. It is believed that this remarkable electrochemical performance mainly stems from the synergistic effects of Ni and Fe species, working in harmony to enhance charge transfer kinetics and intrinsic activity of the catalyst. This work provides a promising avenue for developing cost-effective and highly active electrocatalysts as advanced electrodes for energy related applications. [Display omitted] • Highly active NiFe-based electrocatalysts synthesized by a simple chemical route. • Effect of Fe doping concentration on oxygen evolution reaction of NiO. • Exceptional turnover frequency of Fe-doped NiO electrodes in alkaline conditions. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
03603199
Volume :
48
Issue :
48
Database :
Academic Search Index
Journal :
International Journal of Hydrogen Energy
Publication Type :
Academic Journal
Accession number :
163768191
Full Text :
https://doi.org/10.1016/j.ijhydene.2023.01.330