Strategic examination of the classical catalysis of formic acid decomposition for intermittent hydrogen production, storage and supply: A review

Practically, an ideal catalyst for Formic acid-decomposition is one that best suits the reaction and significantly lowers its activation energy and improves the reaction rate under favourable conditions. Several catalysts for Formic Acid (FA)-decomposition reactions were examined. Based on the volca...

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Bibliographic Details
Main Authors: Sanni, Samuel Eshorame, Alaba, Peter Adeniyi, Okoro, Emeka, Emetere, Moses, Oni, Babalola, Agboola, Oluranti, Ndubuisi, Amanda Onyinye
Format: Article
Published: Elsevier 2021
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Online Access:http://eprints.um.edu.my/28804/
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Institution: Universiti Malaya
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Summary:Practically, an ideal catalyst for Formic acid-decomposition is one that best suits the reaction and significantly lowers its activation energy and improves the reaction rate under favourable conditions. Several catalysts for Formic Acid (FA)-decomposition reactions were examined. Based on the volcano curve and the potential of copper to give high hydrogen yields, emphasis was placed on a Cu-catalysed reaction as potential system for sustainable hydrogen production. Some recent advances in hydrogen production from formic acid were discussed and an effective system for FA-decomposition for hydrogen production was proposed. Since helium can be stored in weather balloons and weighs almost the same as hydrogen, a hydrogen buffer made from polyester fabric and coated with polyurethane or a hydrogen cylinder/tube was proposed for storing hydrogen for use as transportfuel. Also, due to the nature of the mechanisms/pathways describing FA-conversion reactions at the sites or surfaces of the copper-nanocatalysts, it is evident that the Cu(2 1 1) coordination site possesses the highest activation energy relative to those of Cu(1 0 0) and Cu(1 1 1), hence, the reason for the noticeable high or low hydrogen yields. Thus, the potential of Cu giving high hydrogen yields from FA spans from the reactions of FA at the Cu(1 1 1) and Cu(1 0 0) sites.