The effect of doping NiCl2 on the dehydrogenation properties of LiAlH4

被引:68
作者
Sun, T. [1 ]
Huang, C. K. [1 ]
Wang, H. [1 ]
Sun, L. X. [2 ]
Zhu, M. [1 ]
机构
[1] S China Univ Technol, Sch Mat Sci & Engn, Guangzhou 510640, Peoples R China
[2] Chinese Acad Sci, Dalian Inst Chem Phys, Mat & Thermochem Lab, Dalian 116023, Peoples R China
基金
中国国家自然科学基金;
关键词
Hydrogen storage; Complex hydrides; LiAlH4; NiCl2;
D O I
10.1016/j.ijhydene.2008.08.027
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
To investigate the effect of NiCl2 dopant and doping processes on the dehydrogenation behavior of LiAlH4, powder mixtures of LiAlH4 and NiCl2 dopant were prepared by designed mixing and milling processes. The microstructures of the powder mixtures were characterized by scanning electron microscopy (SEM) and X-ray diffraction (XRD). The onset decomposition temperature and isothermal dehydrogenation kinetics were measured to identify the catalyzing effect of NiCl2 on the dehydrogenation properties of LiAlH4. It has been shown that NiCl2 could greatly reduce the onset decomposition temperature and enhance the dehydriding kinetic performance of LiAlH4. The experimental result showed that milling LiAlH4 and NiCl2 together for 0.5 h can obtain a homogeneous mixture of LiAlH4, which desorbed 4.2 wt% H-2 in 3 h at only 100 degrees C, and the onset decomposition temperature of LiAlH4 is decreased by 50 degrees C. However, higher amount of dopant and unfavorable distribution of NiCl2 in LiAlH4 may cause a reduction of the catalytic efficiency. (C) 2008 International Association for Hydrogen Energy. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:6216 / 6221
页数:6
相关论文
共 18 条
[1]   Titanium catalyzed solid-state transformations in LiAlH4 during high-energy ball-milling [J].
Balema, VP ;
Wiench, JW ;
Dennis, KW ;
Pruski, M ;
Pecharsky, VK .
JOURNAL OF ALLOYS AND COMPOUNDS, 2001, 329 (1-2) :108-114
[2]   Isothermal decomposition of LiAlD4 [J].
Blanchard, D. ;
Brinks, H. W. ;
Hauback, B. C. .
JOURNAL OF ALLOYS AND COMPOUNDS, 2006, 416 (1-2) :72-79
[3]   Desorption of LiAlH4 with Ti- and V-based additives [J].
Blanchard, D ;
Brinks, HW ;
Hauback, BC ;
Norby, P .
MATERIALS SCIENCE AND ENGINEERING B-SOLID STATE MATERIALS FOR ADVANCED TECHNOLOGY, 2004, 108 (1-2) :54-59
[4]   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
[5]   Improved hydrogen storage properties of Ti-doped sodium alanate using titanium nanoparticles as doping agents [J].
Bogdanovic, B ;
Felderhoff, M ;
Kaskel, S ;
Pommerin, A ;
Schlichte, K ;
Schüth, F .
ADVANCED MATERIALS, 2003, 15 (12) :1012-+
[6]   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
[7]   Electrochemical hydrogen storage properties of La0.7Mg0.3Ni3.5-Ti0.17Zr0.08V0.35Cr0.1Ni0.3 composites [J].
Chu, Hai-Liang ;
Qiu, Shu-Jun ;
Sun, Li-Xian ;
Zhang, Yao ;
Xu, Fen ;
Zhu, Min ;
Hu, Wang-Yu .
INTERNATIONAL JOURNAL OF HYDROGEN ENERGY, 2008, 33 (02) :755-761
[8]   HYDROGEN EFFECTS ON NICKEL-CATALYZED VAPOR-PHASE METHANOL CARBONYLATION [J].
FUJIMOTO, K ;
BISCHOFF, S ;
OMATA, K ;
YAGITA, H .
JOURNAL OF CATALYSIS, 1992, 133 (02) :370-382
[9]   Ultrafast reaction between Li3N and LiNH2 to prepare the effective hydrogen storage material Li2NH [J].
Hu, Yun Hang ;
Ruckenstein, Eli .
INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, 2006, 45 (14) :4993-4998
[10]   Hydrogen release of catalyzed lithium aluminum hydride by a mechanochemical reaction [J].
Kojima, Yoshitsugu ;
Kawai, Yasuaki ;
Matsumoto, Mitsuru ;
Haga, Tetsuya .
JOURNAL OF ALLOYS AND COMPOUNDS, 2008, 462 (1-2) :275-278