Effect of Ti catalyst with different chemical form on Li-N-H hydrogen storage properties

被引:88
作者
Isobe, S
Ichikawa, T
Hanada, N
Leng, HY
Fichtner, M
Fuhr, O
Fujii, H
机构
[1] Hiroshima Univ, Ctr Mat Sci, N BARD, Higashihiroshima 7398526, Japan
[2] Hiroshima Univ, ADSM, Dept Quantum Matter, Higashihiroshima 7398530, Japan
[3] Forschungszentrum Karlsruhe, Inst Nanotechnol, Nanostructured Mat, D-76021 Karlsruhe, Germany
关键词
hydrogen storage materials; nanostructures; gas-solid reactions; high-energy ball milling; thermal analysis;
D O I
10.1016/j.jallcom.2004.09.081
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
The effect of some different type Ti additives on kinetics of the reaction, LiH + LiNH2 <-> Li2NH + H-2, was intensively investigated in this work. The mixture of LiH and LiNH2 powders with the 1: 1 molar ratio and Ti additives with different chemical form were mechanically ball milled under a hydrogen gas atmosphere of I MPa at 400 rpm for 2 It and the measurements of thermal hydrogen desorption spectrum (TDS), thermogravimetry (TG) and X-ray diffraction (XRD) were performed. Here, we used Ti (nano particle), Ti (micro particle), TiCl3, TiO2 (nano particle) and TiO2 (micro particle) as the additives. The results indicated that the Ti-nano, TiCl3 and TiO2nano doped composites revealed a superior catalytic effect on the TDS properties, while the Ti-micro and TiO2micro did not show so good catalytic effect being similar to the sample without any additives. In the XRD profiles, there are traces of Ti and TiO2 phases in the Ti-micro and TiO2micro doped composites, respectively, whereas no trace of Ti, TiCl3 and TiO2 was found in the Ti-nano TiCl3 and TiO2nano doped composites. These results indicate that the uniform distribution of nano particle Ti metal between LiH and LiNH2 plays an important role for catalytic effect. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:439 / 442
页数:4
相关论文
共 30 条
[11]   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
[12]   Small Ti clusters for catalysis of hydrogen exchange in NaAlH4 [J].
Fichtner, M ;
Fuhr, O ;
Kircher, O ;
Rothe, J .
NANOTECHNOLOGY, 2003, 14 (07) :778-785
[13]   Remarkable hydrogen storage, structural and optical properties in multi-layered Pd/Mg thin films [J].
Fujii, H ;
Higuchi, K ;
Yamamoto, K ;
Kajioka, H ;
Orimo, S ;
Toiyama, K .
MATERIALS TRANSACTIONS, 2002, 43 (11) :2721-2727
[14]   Catalyzed alanates for hydrogen storage [J].
Gross, KJ ;
Thomas, GJ ;
Jensen, CM .
JOURNAL OF ALLOYS AND COMPOUNDS, 2002, 330 :683-690
[15]   Hydriding properties of ordered-/disordered-Mg-based ternary Laves phase structures (vol 356, pg 429, 2003) [J].
Hanada, N ;
Orimo, S ;
Fujii, H .
JOURNAL OF ALLOYS AND COMPOUNDS, 2003, 361 (1-2) :322-322
[16]   Mechanism of novel reaction from LiNH2 and LiH to Li2NH and H2 as a promising hydrogen storage system [J].
Ichikawa, T ;
Hanada, N ;
Isobe, S ;
Leng, HY ;
Fujii, H .
JOURNAL OF PHYSICAL CHEMISTRY B, 2004, 108 (23) :7887-7892
[17]   Lithium nitride for reversible hydrogen storage [J].
Ichikawa, T ;
Isobe, S ;
Hanada, N ;
Fujii, H .
JOURNAL OF ALLOYS AND COMPOUNDS, 2004, 365 (1-2) :271-276
[18]   Development of catalytically enhanced sodium aluminum hydride as a hydrogen-storage material [J].
Jensen, CM ;
Gross, KJ .
APPLIED PHYSICS A-MATERIALS SCIENCE & PROCESSING, 2001, 72 (02) :213-219
[19]  
Kanoya L., 2002, HONDA R D TECH REV, V14, P91
[20]  
Li ZP, 2003, J ALLOY COMPD, V354, P243, DOI 10.1016/S0925-8388(03)01346-4