Extreme high reversible capacity with over 8.0 wt% and excellent hydrogen storage properties of MgH2 combined with LiBH4 and Li3AlH6

被引:42
作者
Lin, Wenping [1 ]
Xiao, Xuezhang [1 ,2 ,3 ]
Wang, Xuancheng [1 ]
Wong, Jie-Wei [1 ]
Yao, Zhendong [1 ]
Chen, Man [1 ]
Zheng, Jiaguang [1 ]
Hu, Zhencan [1 ]
Chen, Lixin [1 ,2 ]
机构
[1] Zhejiang Univ, Sch Mat Sci & Engn, State Key Lab Silicon Mat, Hangzhou 310027, Zhejiang, Peoples R China
[2] Key Lab Adv Mat & Applicat Batteries Zhejiang Pro, Hangzhou 310013, Zhejiang, Peoples R China
[3] South China Univ Technol, Guangdong Prov Key Lab Adv Energy Storage Mat, Guangzhou 510640, Guangdong, Peoples R China
来源
JOURNAL OF ENERGY CHEMISTRY | 2020年 / 50卷
基金
中国国家自然科学基金;
关键词
Magnesium hydride; Complex hydride; Hydrogen storage; High reversible capacity; Synergistic effect; DEHYDROGENATION PROPERTIES; GENERATION PROPERTIES; DESORPTION PROPERTIES; SORPTION PROPERTIES; MAGNESIUM; KINETICS; CARBON; THERMODYNAMICS; TI; NI;
D O I
10.1016/j.jechem.2020.03.076
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Magnesium hydride has attracted great attention because of its high theoretical capacity and outstanding reversibility, nevertheless, its practical applications have been restricted by the disadvantages of the sluggish kinetics and high thermodynamic stability. In this work, an unexpected high reversible hydrogen capacity over 8.0 wt% has been achieved from MgH2 metal hydride composited with small amounts of LiBH4 and Li3AlH6 complex hydrides, which begins to release hydrogen at 276 degrees C and then completely dehydrogenates at 360 degrees C. The dehydrogenated MgH2 + LiBH4/Li3AlH6 composite can fully reabsorb hydrogen below 300 degrees C with an excellent cycling stability. The composite exhibits a significant reduction of dehydrogenation activation energy from 279.7 kJ/mol (primitive MgH2) to 139.3 kJ/mol (MgH2 + LiBH4/Li3AlH6), as well as a remarkable reduction of dehydrogenation enthalpy change from 75.1 kJ/mol H-2 (primitive MgH2) to 62.8 kJ/mol H-2 (MgH2 + LiBH4/Li3AlH6). The additives of LiBH4 and Li3AlH6 not only enhance the cycling hydrogen capacity, but also simultaneously improve the reversible de/rehydrogenation kinetics, as well as the dehydrogenation thermodynamics. This notable improvement on the hydrogen absorption/desorption behaviors of the MgH2 + LiBH4/Li3AlH6 composite could be attributed to the dehydrogenated products including Li3Mg7, Mg17Al12 and MgAlB4, which play a key role on reducing the dehydrogenation activation energy and increasing diffusion rate of hydrogen. Meanwhile, the LiBH4 and Li3AlH6 effectively destabilize MgH2 with a remarkable reduction on dehydrogenation enthalpy change in terms of thermodynamics. In particular, the Li3Mg7, Mg17Al12 and MgAlB4 phases can reversibly transform into MgH2, Li3AlH6 and LiBH4 after rehydrogenation, which contribute to maintain a high cycling capacity. This constructing strategy can further promote the development of high reversible capacity Mg-based materials with suitable de/rehydrogenation properties. (C) 2020 Science Press and Dalian Institute of Chemical Physics, Chinese Academy of Sciences. Published by Elsevier B.V. and Science Press. All rights reserved.
引用
收藏
页码:296 / 306
页数:11
相关论文
共 74 条
[1]   Reduced Enthalpy of Metal Hydride Formation for Mg-Ti Nanocomposites Produced by Spark Discharge Generation [J].
Anastasopol, Anca ;
Pfeiffer, Tobias V. ;
Middelkoop, Joost ;
Lafont, Ugo ;
Canales-Perez, Roger J. ;
Schmidt-Ott, Andreas ;
Mulder, Fokko M. ;
Eijt, Stephan W. H. .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2013, 135 (21) :7891-7900
[2]   THERMAL DECOMPOSITION OF LITHIUM ALUMINUM HYDRIDE [J].
BLOCK, J ;
GRAY, AP .
INORGANIC CHEMISTRY, 1965, 4 (03) :304-&
[3]   Pressure and Temperature Influence on the Desorption Pathway of the LiBH4-MgH2 Composite System [J].
Boesenberg, Ulrike ;
Ravnsbaek, Dorthe B. ;
Hagemann, Hans ;
D'Anna, Vincenza ;
Minella, Christian Bonatto ;
Pistidda, Claudio ;
van Beek, Wouter ;
Jensen, Torben R. ;
Bormann, Ruediger ;
Dornheim, Martin .
JOURNAL OF PHYSICAL CHEMISTRY C, 2010, 114 (35) :15212-15217
[4]   Positive and Negative Effects of Carbon Nanotubes on the Hydrogen Sorption Kinetics of Magnesium [J].
Cai, Wupeng ;
Zhou, Xiaosong ;
Xia, Lidong ;
Jiang, Kaili ;
Peng, Shuming ;
Long, Xinggui ;
Liang, Jianhua .
JOURNAL OF PHYSICAL CHEMISTRY C, 2015, 119 (45) :25282-25290
[5]   Dual-tuning effects of In, Al, and Ti on the thermodynamics and kinetics of Mg85In5Al5Ti5 alloy synthesized by plasma milling [J].
Cao, Zhijie ;
Ouyang, Liuzhang ;
Wu, Yuyu ;
Wang, Hui ;
Liu, Jiangwen ;
Fang, Fang ;
Sun, Dalin ;
Zhang, Qingan ;
Zhu, Min .
JOURNAL OF ALLOYS AND COMPOUNDS, 2015, 623 :354-358
[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]   Formation of the Ternary Complex Hydride Mg2FeH6 from Magnesium Hydride (β-MgH2) and Iron: An Electron Microscopy and Energy-Loss Spectroscopy Study [J].
Danaie, Mohsen ;
Asselli, Alexandre Augusto Cesario ;
Huot, Jacques ;
Botton, Gianluigi A. .
JOURNAL OF PHYSICAL CHEMISTRY C, 2012, 116 (49) :25701-25714
[8]   Theoretical calculation of the energy of formation of LiBH4 [J].
Frankcombe, TJ ;
Kroes, GJ ;
Züttel, A .
CHEMICAL PHYSICS LETTERS, 2005, 405 (1-3) :73-78
[9]   Pore size effects of nanoporous carbons with ultra-high surface area on high-pressure hydrogen storage [J].
Geng, Zhen ;
Zhang, Cunman ;
Wang, Dabin ;
Zhou, Xiangyang ;
Cai, Mei .
JOURNAL OF ENERGY CHEMISTRY, 2015, 24 (01) :1-8
[10]   Remarkable improvement of hydrogen sorption kinetics in magnesium catalyzed with Nb2O5 [J].
Hanada, Nobuko ;
Ichikawa, Takayuki ;
Hino, Satoshi ;
Fujii, Hironobu .
JOURNAL OF ALLOYS AND COMPOUNDS, 2006, 420 (1-2) :46-49