Pressure and Temperature Influence on the Desorption Pathway of the LiBH4-MgH2 Composite System

被引:129
作者
Boesenberg, Ulrike [1 ]
Ravnsbaek, Dorthe B. [2 ,3 ]
Hagemann, Hans [4 ]
D'Anna, Vincenza [4 ]
Minella, Christian Bonatto [1 ]
Pistidda, Claudio [1 ]
van Beek, Wouter [5 ]
Jensen, Torben R. [2 ,3 ]
Bormann, Ruediger [1 ]
Dornheim, Martin [1 ]
机构
[1] GKSS Forschungszentrum Geesthacht GmbH, Inst Mat Res, D-21502 Geesthacht, Germany
[2] Univ Aarhus, Interdisciplinary Nanosci Ctr iNANO, DK-8000 Aarhus, Denmark
[3] Univ Aarhus, Dept Chem, DK-8000 Aarhus, Denmark
[4] Univ Geneva, Dept Chim Phys, CH-1211 Geneva 4, Switzerland
[5] Swiss Norwegian Beamlines ESRF, F-38043 Grenoble, France
基金
瑞士国家科学基金会;
关键词
REACTIVE HYDRIDE COMPOSITES; HYDROGEN STORAGE-SYSTEM; MAGNESIUM BOROHYDRIDE; CYCLING BEHAVIOR; MG; ALLOYS; STOICHIOMETRY; DIFFRACTION; KINETICS; NICKEL;
D O I
10.1021/jp104814u
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 decomposition pathway in LiBH4-MgH2 reactive hydride composites was investigated systematically as a function of pressure and temperature. Individual decomposition of MgH2 and LiBH4 is observed at higher temperatures and low pressures (T >= 450 degrees C and p(H-2) <= 3 bar), whereas simultaneous desorption of H-2 from LiBH4 and formation of MgB2 was observed at 400 degrees C and a hydrogen backpressure of p(H-2) = 5 bar. The simultaneous desorption of H-2 from LiBH4 and MgH2 without intermediate formation of metallic Mg could not be observed. In situ X-ray diffraction (XRD) and infrared (IR) spectroscopy reveal the present crystalline and amorphous phases.
引用
收藏
页码:15212 / 15217
页数:6
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