Enhanced dehydrogenation kinetic properties and hydrogen storage reversibility of LiBH4 confined in activated charcoal

被引:17
作者
Zhou, He [1 ]
Liu, Hai-zhen [2 ]
Gao, Shi-chao [1 ]
Wang, Xin-hua [1 ]
机构
[1] Zhejiang Univ, Sch Mat Sci & Engn, State Key Lab Silicon Mat, Hangzhou 310027, Zhejiang, Peoples R China
[2] State Grid Corp China, Global Energy Interconnect Res Inst, State Key Lab Adv Transmiss Technol, Beijing 102209, Peoples R China
基金
中国国家自然科学基金;
关键词
hydrogen storage materials; hydrogen storage properties; lithium borohydride; activated charcoal; melt infiltration; LIGHT-METAL HYDRIDES; MELT INFILTRATION; COMPLEX HYDRIDES; STABILITY; MECHANISM; RELEASE;
D O I
10.1016/S1003-6326(18)64804-6
中图分类号
TF [冶金工业];
学科分类号
0806 ;
摘要
LiBH4 was confined into activated charcoal (AC) by melt infiltration method (M), and its effects on the hydrogen sorption properties were investigated. The N-2 adsorption results reveal that melt infiltration method can effectively incorporated LiBH4 into AC. It can maintain the structural integrity of the scaffold and ensure the confinement effect. The nano-confined LiBH4/AC starts to release hydrogen at around 190 degrees C, which is 160 degrees C lower than that of pure LiBH4, and reaches a hydrogen desorption capacity of 13.6% at 400 degrees C. When rehydrogenated under the condition of 6 MPa H-2 and 350 degrees C, it has a reversible hydrogen storage capacity of 6%, while pure LiBH4 shows almost no reversible hydrogen storage capacity under the same condition. Mass spectrometry analysis (MS) results suggest that no diborane or other impurity gases are released in the decomposition process. The apparent activation energy of dehydrogenation of LiBH4 after confinement into AC decreases from 156.0 to 121.1 kJ/mol, which leads to the eminent enhancement of dehydrogenation kinetics of LiBH4.
引用
收藏
页码:1618 / 1625
页数:8
相关论文
共 34 条
[1]   Large-scale screening of metal hydride mixtures for high-capacity hydrogen storage from first-principles calculations [J].
Alapati, Sudhakar V. ;
Johnson, J. Karl ;
Sholl, David S. .
JOURNAL OF PHYSICAL CHEMISTRY C, 2008, 112 (14) :5258-5262
[2]   Using first principles calculations to identify new destabilized metal hydride reactions for reversible hydrogen storage [J].
Alapati, Sudhakar V. ;
Johnson, J. Karl ;
Sholl, David S. .
PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 2007, 9 (12) :1438-1452
[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]   Adjustment of the stability of complex hydrides by anion substitution [J].
Brinks, Hendrik W. ;
Fossdal, Anita ;
Hauback, Bjorn C. .
JOURNAL OF PHYSICAL CHEMISTRY C, 2008, 112 (14) :5658-5661
[5]   Hydrogen desorption kinetics mechanism of Mg-Ni hydride under isothermal and non-isothermal conditions [J].
Chen, Chao-yi ;
Chen, Hui-lin ;
Ma, Ya-qin ;
Liu, Jing .
TRANSACTIONS OF NONFERROUS METALS SOCIETY OF CHINA, 2016, 26 (01) :160-166
[6]   Nanoconfined light metal hydrides for reversible hydrogen storage [J].
de Jongh, Petra E. ;
Allendorf, Mark ;
Vajo, John J. ;
Zlotea, Claudia .
MRS BULLETIN, 2013, 38 (06) :488-494
[7]   Kinetic- and thermodynamic-based improvements of lithium borohydride incorporated into activated carbon [J].
Fang, Z. Z. ;
Wang, P. ;
Rufford, T. E. ;
Kang, X. D. ;
Lu, G. Q. ;
Cheng, H. M. .
ACTA MATERIALIA, 2008, 56 (20) :6257-6263
[8]   Combined Effects of Functional Cation and Anion on the Reversible Dehydrogenation of LiBH4 [J].
Fang, Zhan-Zhao ;
Kang, Xiang-Dong ;
Yang, Zhu-Xian ;
Walker, Gavin S. ;
Wang, Ping .
JOURNAL OF PHYSICAL CHEMISTRY C, 2011, 115 (23) :11839-11845
[9]   Destabilization of LiBH4 by MH2 (M = Ce, La) for hydrogen storage: Nanostructural effects on the hydrogen sorption kinetics [J].
Gennari, Fabiana C. .
INTERNATIONAL JOURNAL OF HYDROGEN ENERGY, 2011, 36 (23) :15231-15238
[10]   Nanoconfined 2LiBH4-MgH2 Prepared by Direct Melt Infiltration into Nanoporous Materials [J].
Gosalawit-Utke, Rapee ;
Nielsen, Thomas K. ;
Saldan, Ivan ;
Laipple, Daniel ;
Cerenius, Yngve ;
Jensen, Torben R. ;
Klassen, Thomas ;
Dornheim, Martin .
JOURNAL OF PHYSICAL CHEMISTRY C, 2011, 115 (21) :10903-10910