Studies of covalent amides for hydrogen storage systems: Structures and bonding of the MAl(NH2)4 phases with M = Li, Na and K

被引:15
|
作者
Eymery, J. -B. [1 ]
Truflandier, L. [2 ]
Charpentier, T. [2 ]
Chotard, J. -N. [1 ]
Tarascon, J. -M. [1 ]
Janot, R. [1 ]
机构
[1] Univ Picardie Jules Verne, CNRS, UMR 6007, Lab React & Chim Solides, F-80039 Amiens, France
[2] CEA, IRAMIS, Lab Struct & Dynam Resonance Magnet SIS2M, F-91191 Gif Sur Yvette, France
关键词
Amides; DFT calculations; Hydrogen storage; Infrared spectroscopy; Thermal analysis; CRYSTAL-STRUCTURE; LITHIUM; ALUMINUM; LIMIDOALUMINATE; MECHANISM; NITROGEN; IMIDES; H-2;
D O I
10.1016/j.jallcom.2010.03.248
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
Mixtures of metallic amides and LiH are studied as hydrogen storage materials. We show that the amides decomposition temperature decreases as the polarizing effect of the metallic cation increases, hence our interest for amides with strong polarizing cations such as Al3+. Studying the MAl(NH2)(4) phases with M = Li, Na and K, we tried to rationalize such metal-decomposition temperature dependence and found from IR spectroscopy investigations supported by DFT calculations that smaller is the alkali cation M+, more the Al(NH2)(4) and M(NH2)(4) tetrahedra are interconnected in the crystal structures and higher is the decomposition temperature. Regarding applications, the possibility of using the LiAl(NH2)(4)-LiH mixture as a reversible hydrogen storage material is discussed. If such mixture is able to release up to 6.2 mass% of hydrogen at 130 degrees C, it is shown that the LiAl(NH2)(4) decomposition leads to the formation of amorphous LiAl(NH)(2) imide, which is unfortunately metastable and exothermically transformed into LiNH2 + AIN. This last reaction is highly problematic for hydrogen storage applications as it is fully irreversible and AIN does not react with hydrogen under moderate temperature and pressure conditions. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:194 / 203
页数:10
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