Reversible hydrogen decomposition of KAlH4

被引:123
作者
Morioka, H [1 ]
Kakizaki, K [1 ]
Chung, SC [1 ]
Yamada, A [1 ]
机构
[1] Sony Corp, Mat Labs, Yokohama, Kanagawa 2400036, Japan
关键词
metal hydrides; energy storage materials; gas-solid reactions; x-ray diffraction;
D O I
10.1016/S0925-8388(02)01307-5
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
We report that potassium aluminum tetrahydride. KAIH(4), exhibits a rapid reversible hydrogen decomposition reaction without any aid of external catalysts. This is significantly different from the reaction mechanism of NaAlH4 and LiAlH4, in which the homogeneous doping of the transition metal catalyst is essential for the reversibility and fast kinetics. The reversible dehydrogenation and hydrogenation were clearly observed without a catalyst over a temperature range 250-340 degreesC under <10 bar of hydrogen. Hydrogen storage ability was above 3.5 wt.% (81.4% of the theoretical value of 4.2 wt.%). KAlH4 may be a competitive option with a lightweight but high-temperature metal hydride system such as Mg2NiH4. These findings will also provide renewed guidelines for understanding the reaction mechanism of the catalyzed alanates as reversible hydrogen storage materials. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:310 / 314
页数:5
相关论文
共 23 条
[1]   Hydrogen-absorbing alloys [J].
Akiba, E .
CURRENT OPINION IN SOLID STATE & MATERIALS SCIENCE, 1999, 4 (03) :267-272
[2]   Solid state phase transformations in LiAlH4 during high-energy ball-milling [J].
Balema, VP ;
Pecharsky, VK ;
Dennis, KW .
JOURNAL OF ALLOYS AND COMPOUNDS, 2000, 313 (1-2) :69-74
[3]   Ti-doped alkali metal aluminium hydrides as potential novel reversible hydrogen storage materials [J].
Bogdanovic, B ;
Schwickardi, M .
JOURNAL OF ALLOYS AND COMPOUNDS, 1997, 253 (1-2) :1-9
[4]   Metal-doped sodium aluminium hydrides as potential new hydrogen storage materials [J].
Bogdanovic, B ;
Brand, RA ;
Marjanovic, A ;
Schwickardi, M ;
Tölle, J .
JOURNAL OF ALLOYS AND COMPOUNDS, 2000, 302 (1-2) :36-58
[5]   Reversible hydrogen storage via titanium-catalyzed LiAlH4 and Li3AlH6 [J].
Chen, J ;
Kuriyama, N ;
Xu, Q ;
Takeshita, HT ;
Sakai, T .
JOURNAL OF PHYSICAL CHEMISTRY B, 2001, 105 (45) :11214-11220
[6]  
DYMOVA TN, 1974, DOKL AKAD NAUK SSSR+, V215, P1369
[7]   Synthesis and structures of magnesium alanate and two solvent adducts [J].
Fichtner, M ;
Fuhr, O .
JOURNAL OF ALLOYS AND COMPOUNDS, 2002, 345 (1-2) :286-296
[8]   Dynamic in situ X-ray diffraction of catalyzed alanates [J].
Gross, KJ ;
Sandrock, G ;
Thomas, GJ .
JOURNAL OF ALLOYS AND COMPOUNDS, 2002, 330 :691-695
[9]   Catalyzed alanates for hydrogen storage [J].
Gross, KJ ;
Thomas, GJ ;
Jensen, CM .
JOURNAL OF ALLOYS AND COMPOUNDS, 2002, 330 :683-690
[10]   In-situ X-ray diffraction study of the decomposition of NaAlH4 [J].
Gross, KJ ;
Guthrie, S ;
Takara, S ;
Thomas, G .
JOURNAL OF ALLOYS AND COMPOUNDS, 2000, 297 (1-2) :270-281