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Kinetic alteration of the 6Mg(NH2)2–9LiH–LiBH4 system by co-adding YCl3 and Li3N.

Authors :
Cao, Hujun
Zhang, Weijin
Pistidda, Claudio
Puszkiel, Julián
Milanese, Chiara
Santoru, Antonio
Karimi, Fahim
Castro Riglos, Maria Victoria
Gizer, Gökhan
Welter, Edmund
Bednarcik, Jozef
Etter, Martin
Chen, Ping
Klassen, Thomas
Dornheim, Martin
Source :
Physical Chemistry Chemical Physics (PCCP); 12/21/2017, Vol. 19 Issue 47, p32105-32115, 11p
Publication Year :
2017

Abstract

The 6Mg(NH<subscript>2</subscript>)<subscript>2</subscript>–9LiH–LiBH<subscript>4</subscript> composite system has a maximum reversible hydrogen content of 4.2 wt% and a predicted dehydrogenation temperature of about 64 °C at 1 bar of H<subscript>2</subscript>. However, the existence of severe kinetic barriers precludes the occurrence of de/re-hydrogenation processes at such a low temperature (H. Cao, G. Wu, Y. Zhang, Z. Xiong, J. Qiu and P. Chen, J. Mater. Chem. A, 2014, 2, 15816–15822). In this work, Li<subscript>3</subscript>N and YCl<subscript>3</subscript> have been chosen as co-additives for this system. These additives increase the hydrogen storage capacity and hasten the de/re-hydrogenation kinetics: a hydrogen uptake of 4.2 wt% of H<subscript>2</subscript> was achieved in only 8 min under isothermal conditions at 180 °C and 85 bar of H<subscript>2</subscript> pressure. The re-hydrogenation temperature, necessary for a complete absorption process, can be lowered below 90 °C by increasing the H<subscript>2</subscript> pressure above 185 bar. Moreover, the results indicate that the hydrogenation capacity and absorption kinetics can be maintained roughly constant over several cycles. Low operating temperatures, together with fast absorption kinetics and good reversibility, make this system a promising on-board hydrogen storage material. The reasons for the improved de/re-hydrogenation properties are thoroughly investigated and discussed. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
14639076
Volume :
19
Issue :
47
Database :
Complementary Index
Journal :
Physical Chemistry Chemical Physics (PCCP)
Publication Type :
Academic Journal
Accession number :
126591897
Full Text :
https://doi.org/10.1039/c7cp06826c