4.7 Article

Electro-oxidation of tri(ammonium) phosphate: New hydrogen source compatible with Ni-based electro-catalysts

Journal

INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
Volume 47, Issue 60, Pages 25280-25288

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.ijhydene.2022.05.252

Keywords

Electro-oxidation; Nickel-decorated graphene; Tri(ammonium) phosphate; Hydrogen

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The reported Ni-based electro-catalysts are not suitable as anode materials for alcohol-based proton exchange membrane fuel cells due to their high onset potentials. However, these materials can be used for hydrogen generation from alcohols with small biases. In the electro-oxidation of tri(ammonium) phosphate, Ni-decorated graphene is found to be an effective catalyst, and the active layer is not consumed during the reaction.
Predominantly, the reported Ni-based electro-catalysts are not applicable anode materials for the alcohols-based proton exchange membrane fuel cells due to the high onset potentials. Alternatively, these non-precious materials can be exploited for hydrogen generation from alcohols with small biases. However, as the nickel oxy(hydroxide) active species is a reactant in the alcohols electro-oxidation reactions, so these materials are exhausted and have to be regenerated. Recently, hydrogen could be extracted from tri(ammonium) phosphate using Ni/C nanostructures as effective catalysts in a simple batch reactor. In this study, electro-oxidation of tri(ammonium) phosphate using Ni-decorated graphene is investigated. The utilized catalyst has been prepared by simple one-pot synthesis procedure; calcination of well mixed nickel acetate/commercial sugar composite. The results indicated that the prepared Ni-decorated graphene is an effective electrocatalyst for tri(ammonium) phosphate oxidation when the nickel content is optimized; 3 wt% metal is the best composition. Moreover, chronoamperometry analysis results indicated that the active layer is not being consumed during the electro-oxidation reaction of the tri(ammonium phosphate) which creates a distinct advantage for this fertilizer over alcohols. Stability of the active layer is attributed to performing Ni(OH)2/Ni(OOH) redox

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