Formation and Hydrogen Storage Properties of Dual-Cation (Li, Ca) Borohydride

被引:41
|
作者
Fang, Zhan-Zhao [1 ]
Kang, Xiang-Dong [1 ]
Luo, Jun-Hong [1 ]
Wang, Ping [1 ]
Li, Hai-Wen [2 ]
Orimo, Shin-ichi [2 ]
机构
[1] Chinese Acad Sci, Shenyang Natl Lab Mat Sci, Inst Met Res, Shenyang 110016, Peoples R China
[2] Tohoku Univ, Inst Mat Res, Sendai, Miyagi 9808577, Japan
来源
JOURNAL OF PHYSICAL CHEMISTRY C | 2010年 / 114卷 / 51期
基金
中国国家自然科学基金;
关键词
WELL-CRYSTALLIZED MG(BH4)(2); B-H SYSTEM; METAL-BOROHYDRIDES; COMPLEX HYDRIDES; THERMODYNAMICAL STABILITIES; 1ST-PRINCIPLES CALCULATIONS; LITHIUM BOROHYDRIDE; LIBH4; REVERSIBILITY; CA(BH4)(2);
D O I
10.1021/jp109260g
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
Lithium borohydride, LiBH4, possesses high hydrogen capacity, but cannot be used for hydrogen storage owing to the problematic H-exchange kinetics and thermodynamics. In the present study, we employed the Li+-Ca2+ combination strategy to improve the de/rehydrogenation properties of LiBH4. Our study found that mechanically milling 1:1 LiBH4/Ca(BH4)(2) mixture formed a dual-cation borohydride, Li0.9Ca(BH4)(2.9), which then transformed to stoichiometric LiCa(BH4)(3) in the heating process. The formation and decomposition behaviors of LiCa(BH4)(3) were studied using X-ray diffraction and thermogravimetry/differential scanning calorimetry/mass spectroscopy techniques. It was found that LiCa(BH4)(3) differs significantly from the component phases in terms of physical properties, decomposition behaviors, and mechanistic pathway. In particular, LiCa(BH4)(3) exhibits improved de/rehydrogenation properties relative to the component phases. These experimental findings exemplified the effectiveness of manipulation of dual-cation combination in tuning the de/rehydrogenation properties of the ionic light-metal borohydrides.
引用
收藏
页码:22736 / 22741
页数:6
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