Issue 47, 2023, Issue in Progress

Enhanced electrocatalytic oxygen redox reactions of iron oxide nanorod films by combining oxygen vacancy formation and cobalt doping

Abstract

A synergistic effect of Co-doping and vacuum-annealing on electrochemical redox reactions of iron oxide films is demonstrated in the present work. In this research, a series of defect-rich iron oxy/hydroxide nanorod arrays: α-FeOOH, Fe2O3, and FeOx nanorod thin film catalysts were synthesized via a hydrothermal approach followed by thermal and vacuum treatments. Besides, a cobalt doping process was employed to prepare the thin film of Co-doped FeOx nanorods. The morphology, crystallinity, and electrochemical activities of Co-doped oxygen-deficient FeOx (Co-FeOx/FTO) show strong correlations with metal concentration and thermal treatments. The electrochemical measurements demonstrated that the as-deposited Co-doped FeOx NR catalyst could achieve a maximum OER current of 30 mA cm−2, which was six times greater than that recorded by as-deposited Co-doped FeOOH NR catalysts (5.7 mA cm−2) at 1.65 V vs. RHE, confirming the superior electrocatalytic OER activity at the as-deposited Co-doped FeOx NR catalyst after cobalt doping. It is believed that these results are attributed to two factors: the synergistic effect of Co doping and the defect-rich nature of FeOx nanorod catalysts that are used in sustainable energy systems.

Graphical abstract: Enhanced electrocatalytic oxygen redox reactions of iron oxide nanorod films by combining oxygen vacancy formation and cobalt doping

Supplementary files

Article information

Article type
Paper
Submitted
21 May 2023
Accepted
19 Oct 2023
First published
13 Nov 2023
This article is Open Access
Creative Commons BY-NC license

RSC Adv., 2023,13, 33242-33254

Enhanced electrocatalytic oxygen redox reactions of iron oxide nanorod films by combining oxygen vacancy formation and cobalt doping

S. Omar ben Gubaer, M. N. Shaddad, P. Arunachalam, M. S. Amer, S. A. Aladeemy and A. M. Al-Mayouf, RSC Adv., 2023, 13, 33242 DOI: 10.1039/D3RA03394E

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