A rigorous electrochemical ammonia electrolysis protocol with quantitative analysis
Ammonia has emerged as an attractive liquid fuel for hydrogen production owing to its facile transportation, high capacity of hydrogen storage, and ecofriendly environmental products (N 2 and H 2 ). Moreover, the electrolysis of ammonia to produce nitrogen and hydrogen only requires an external volt...
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Veröffentlicht in: | Journal of materials chemistry. A, Materials for energy and sustainability Materials for energy and sustainability, 2021-05, Vol.9 (19), p.11571-11579 |
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Zusammenfassung: | Ammonia has emerged as an attractive liquid fuel for hydrogen production owing to its facile transportation, high capacity of hydrogen storage, and ecofriendly environmental products (N
2
and H
2
). Moreover, the electrolysis of ammonia to produce nitrogen and hydrogen only requires an external voltage of 0.06 V theoretically, which is much lower than the energy needed for water electrolysis (1.23 V). In this study, we propose a well-established procedure using
in operando
gas chromatography that enables us to reliably compare and evaluate the new catalyst for ammonia oxidation. With the protocol, we could distinguish in detail the competitive oxidation reaction between the ammonia oxidation and oxygen evolution reactions with real-time monitoring. Using a flower-like electrodeposited Pt catalyst, we have efficiently produced hydrogen with less power consumption of 734 L
H
2
kW h
−1
, which is significantly lower than that of the water-splitting process (242 L
H
2
kW h
−1
). The use of this rigorous protocol should help to evaluate the practical performances for ammonia oxidation, thus enabling the field to focus on viable pathways towards the practical electrochemical oxidation of ammonia to hydrogen.
The use of this rigorous protocol should help to evaluate the practical performances for ammonia oxidation, thus enabling the field to focus on viable pathways towards the practical electrochemical oxidation of ammonia to hydrogen. |
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ISSN: | 2050-7488 2050-7496 |
DOI: | 10.1039/d1ta00363a |