Direct and reversible hydrogen storage of lithium hydride (LiH) nanoconfined in high surface area graphite

被引:57
作者
Wang, Lei [1 ]
Quadir, Md Zakaria [2 ,3 ]
Aguey-Zinsou, Kondo-Francois [1 ]
机构
[1] Univ New South Wales, Sch Chem Engn, Merlin Grp, Sydney, NSW 2052, Australia
[2] Univ New South Wales, Mark Wainwright Analyt Ctr, Sydney, NSW 2052, Australia
[3] Curtin Univ, JdLC, MMF, Bentley, WA 6102, Australia
关键词
Lithium hydride; Hydrogen storage; Nanoconfine; Nanosize; METAL-ORGANIC FRAMEWORKS; DESTABILIZATION; TRANSPORT; MGH2; NANOPARTICLES; CLUSTERS;
D O I
10.1016/j.ijhydene.2016.07.073
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
LiH has great potential as a high capacity hydrogen storage material (12 wt.%), however its thermodynamic stability has so far precluded practical application. Temperatures near 700 degrees C are required for hydrogen release and uptake. Herein, we report on a novel method to realise hydrogen uptake and release under milder temperature conditions without using any catalyst or alloying. Through nanoconfinement within the pores (2-20 nm) of high surface area graphite (HSAG) LiH displayed remarkable hydrogen storage properties and was able to release 1.9 wt.% of hydrogen from 200 degrees C. Reversibility was also achieved under the moderate conditions of 300 degrees C and 6 MPa hydrogen pressure. This demonstrates that the properties of LiH are particle size dependent and thus leads to new possibilities to realise the potential of LiH as a practical high capacity hydrogen storage material. (C) 2016 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:18088 / 18094
页数:7
相关论文
共 47 条
[1]   Reducing the dehydrogenation temperature of lithium hydride through alloying with germanium [J].
Abbas, Marwa A. ;
Grant, David M. ;
Brunelli, Michela ;
Hansen, Thomas C. ;
Walker, Gavin S. .
PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 2013, 15 (29) :12139-12146
[2]   Hydrogen in magnesium: new perspectives toward functional stores [J].
Aguey-Zinsou, Kondo-Francois ;
Ares-Fernandez, Jose-Ramon .
ENERGY & ENVIRONMENTAL SCIENCE, 2010, 3 (05) :526-543
[3]  
ALBERT P, 1950, B SOC CHIM FR, V17, P1165
[4]   TRANSPORT OF HYDROGEN IN LIQUID LITHIUM [J].
ALIRE, RM .
JOURNAL OF CHEMICAL PHYSICS, 1976, 65 (03) :1134-1137
[5]   In situ thermal desorption of H2 from LiNH2-2LiH monitored by environmental SEM [J].
Beattie, Shane D. ;
Langmi, Henrietta W. ;
McGrady, G. Sean .
INTERNATIONAL JOURNAL OF HYDROGEN ENERGY, 2009, 34 (01) :376-379
[6]   HYDROGEN TRANSPORT IN LITHIUM HYDRIDE AS A FUNCTION OF PRESSURE [J].
CATLETT, DS ;
SPENCER, JN ;
VOGT, GJ .
JOURNAL OF CHEMICAL PHYSICS, 1973, 58 (08) :3432-3438
[7]   Interaction between lithium amide and lithium hydride [J].
Chen, P ;
Xiong, ZT ;
Luo, JZ ;
Lin, JY ;
Tan, KL .
JOURNAL OF PHYSICAL CHEMISTRY B, 2003, 107 (39) :10967-10970
[8]   Interaction of hydrogen with metal nitrides and imides [J].
Chen, P ;
Xiong, ZT ;
Luo, JZ ;
Lin, JY ;
Tan, KL .
NATURE, 2002, 420 (6913) :302-304
[9]   Aligned carbon nanotube/sulfur composite cathodes with high sulfur content for lithium-sulfur batteries [J].
Cheng, Xin-Bing ;
Huang, Jia-Qi ;
Zhang, Qiang ;
Peng, Hong-Jie ;
Zhao, Meng-Qiang ;
Wei, Fei .
NANO ENERGY, 2014, 4 :65-72
[10]   Destabilisation of complex hydrides through size effects [J].
Christian, Meganne ;
Aguey-Zinsou, Kondo-Francois .
NANOSCALE, 2010, 2 (12) :2587-2590