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  5. Enhancement effect of bimetallic amide K₂Mn(NH₂)₄ and in-situ formed KH and Mn₄N on the dehydrogenation/hydrogenation properties of L–Mg–N–H system

Enhancement effect of bimetallic amide K₂Mn(NH₂)₄ and in-situ formed KH and Mn₄N on the dehydrogenation/hydrogenation properties of L–Mg–N–H system

Publication date
2019-08-19
Document type
Forschungsartikel
Author
Gizer, Gökhan
Cao, Hujun
Puszkiel, Julián  
Pistidda, Claudio
Santoru, Antonio
Zhang, Weijin
He, Teng
Chen, Ping
Klassen, Thomas  
Dornheim, Martin
Organisational unit
Angewandte Werkstofftechnik  
Werkstoffkunde  
DOI
10.3390/en12142779
URI
https://openhsu.ub.hsu-hh.de/handle/10.24405/21571
Publisher
MDPI
Series or journal
Energies
ISSN
1996-1073
Periodical volume
12
Periodical issue
14
Article ID
2779
Part of the university bibliography
✅
Additional Information
Language
English
Keyword
Bimetallic amide
Hydrogen storage
Amide-hydrides
In situ X-ray diffraction
Activation energy
Reaction rate
Abstract
In this work, we investigated the influence of the K₂Mn(NH₂)₄ additive on the hydrogen sorption properties of the Mg(NH₂)₂ + 2LiH (Li–Mg–N–H) system. The addition of 5 mol% of K₂Mn(NH₂)₄ to the Li–Mg–N–H system leads to a decrease of the dehydrogenation peak temperature from 200°C to 172°C compared to the pristine sample. This sample exhibits a constant hydrogen storage capacity of 4.2 wt.% over 25 dehydrogenation/rehydrogenation cycles. Besides that, the in-situ synchrotron powder X-ray diffraction analysis performed on the as prepared Mg(NH₂)₂ + 2LiH containing K₂Mn(NH₂)₄ indicates the presence of Mn₄N. However, no crystalline K-containing phases were detected. Upon dehydrogenation, the formation of KH is observed. The presence of KH and Mn₄N positively influences the hydrogen sorption properties of this system, especially at the later stage of rehydrogenation. Under the applied conditions, hydrogenation of the last 1 wt.% takes place in only 2 min. This feature is preserved in the following three cycles.
Description
This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
Version
Published version
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