期刊
INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
卷 40, 期 33, 页码 10527-10535出版社
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.ijhydene.2015.06.168
关键词
Hydrogen storage; Complex hydrides; LiBH4; h-BN; Synergistic effects
资金
- National High Technology Research & Development Program of China [2012AA051503]
- National Natural Science Foundation of China [51471151, 51171173]
- Program for Innovative Research Team in University of Ministry of Education of China [IRT13037]
- Zhejiang Provincial Science & Technology Program of China [2015C31035, 2014C31134]
- Fundamental Research Funds for the Central Universities [2015QNA4010]
LiBH4 is an attractive material for hydrogen storage owing to its high hydrogen capacity of 13.8 wt% capacities. However, its high thermodynamic stability and sluggish kinetics limit its practical application as an onboard hydrogen storage medium. In this work, a synergetic effect of NbCl5 and hexagonal BN (h-BN) on notably improving the dehydrogenation properties of LiBH4 was investigated. It is found that the addition of NbCl5 and h-BN co-dopants can significantly enhance the dehydrogenation kinetics of LiBH4, and the catalytic effect of co-dopant is better than that of NbCl5 or h-BN dopant separately. The NbCl5/h-BN co-doped LiBH4 can release 10.78 wt% hydrogen, which is about 13 times and 5 times more than that of the NbCl5 doped LiBH4 and h-BN doped LiBH4 within 10 min at 400 degrees C, respectively. The major dehydrogenation temperature of NbCl5/h-BN co-doped LiBH4 is reduced to 377 degrees C, much lower than that of ball-milled LiBH4 (464 degrees C). The apparent activation energy (E-a) of hydrogen desorption is reduced from 195.81 kJ/mol of LiBH4 to 122.75 kJ/mol of NbCl5/h-BN co-doped LiBH4. The microstructural results reveal that the catalytic effect of NbCl5/h-BN co-dopant on improving the dehydrogenation kinetics of LiBH4 could be ascribed to the in situ formed nano NbH@h-BN, which serves as the heterogeneous nucleation site to reduce the decomposition activation energy barrier of LiBH4 and shortens the distance of the solid-liquid phase boundary movement of LiBH4 decomposition. Copyright (C) 2015, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.
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