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Facile synthesis of amorphous nickel iron borate grown on carbon paper as stable electrode materials for promoted electrocatalytic urea oxidation.

Authors :
Amer, Mabrook S.
Arunachalam, Prabhakarn
Alsalman, Abdulaziz M.
Al-Mayouf, Abdullah M.
Almutairi, Zeyad A.
Aladeemy, Saba A.
Hezam, Mahmoud
Source :
Catalysis Today. Aug2022, Vol. 397, p197-205. 9p.
Publication Year :
2022

Abstract

The development of greatly stable and cost-effective electrocatalysts for urea electro-oxidation reactions (UERs) is urgent and challenging for promoting urea removal in the wastewater and advanced energy conversion devices. We demonstrated that nickel-iron borate (NiFe-B) electrocatalysts supported on carbon paper (CP) for UERs through a one-pot solvothermal method. NiFe-B electrocatalysts were obtained with numerous Ni/Fe molar ratios in the precursors, and the physicochemical features of the NiFe-B were examined by X-ray diffraction, scanning and transmission electron microscope, and X-ray photoelectron spectroscopy. The optimized NiFe-B/CP exhibited a low onset potential (E onset = 0.287 V vs. SCE) with a Tafel slope of 27.9 mV/dec on CP, demonstrating much greater performance UERs. Furthermore, the NiFe-B/CP catalysts have shown a superior activity for the UERs in alkaline solution and exhibit more than two-fold enhancement in activity than Ni-B. Facile, cost-effective fabrication and highly efficient urea oxidation create the NiFe-B electrodes as attractive materials for UERs. [Display omitted] • Amorphous Ni-Feborate/CP fabricated via facile hydrothermal process. • NiFe-B-2/CP electrode materials exhibited a lower onset potential with an overpotential of 327 mV at 10 mA cm−2. • Mass activities of NiFe-B-2/CP electrode materials reach up to 51.7 A/g. • NiFe-borate materials are a promising candidate for efficient electrocatalytic reactions. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
09205861
Volume :
397
Database :
Academic Search Index
Journal :
Catalysis Today
Publication Type :
Academic Journal
Accession number :
157218345
Full Text :
https://doi.org/10.1016/j.cattod.2021.09.036