Ammine Magnesium Borohydride Nanocomposites for All-Solid-State Magnesium Batteries

被引:81
作者
Yan, Yigang [1 ,2 ,3 ,4 ]
Grinderslev, Jakob B. [1 ,2 ]
Jorgensen, Mathias [1 ,2 ]
Skov, Lasse N. [1 ,2 ]
Skibsted, Jorgen [1 ,2 ]
Jensen, Torben R. [1 ,2 ]
机构
[1] Aarhus Univ, Interdisciplinary Nanosci Ctr iNANO, DK-8000 Aarhus C, Denmark
[2] Aarhus Univ, Dept Chem, DK-8000 Aarhus C, Denmark
[3] Sichuan Univ, Minist Educ, Inst New Energy & Low Carbon Technol, Chengdu 610207, Peoples R China
[4] Sichuan Univ, Minist Educ, Engn Res Ctr Sustainable Energy Mat & Devices, Chengdu 610207, Peoples R China
基金
中国国家自然科学基金;
关键词
magnesium battery; solid electrolyte; magnesium ion conduction; ammine metal borohydride; nanocomposite; POLYMER ELECTROLYTE; CONDUCTION; MECHANISM;
D O I
10.1021/acsaem.0c01599
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
Magnesium batteries are considered promising solutions for future energy storage beyond the lithium-ion battery era. However, the development of magnesium batteries is hindered by the lack of suitable electrolytes. Here we present solid Mg2+ electrolytes based on ammine magnesium borohydride composites, Mg(BH4)(2)center dot xNH(3), which have conductivities ca. three orders of magnitude higher than the parent compounds (x = 1, 2, 3, and 6). A nanocomposite formed by the Mg(BH4)(2)center dot xNH(3) composite and MgO nanoparticles exhibits outstanding Mg2+ conductivity of the order of 10(-5) S cm(-1) at room temperature and around 10(-3) S cm(-1) at moderate temperature (ca. 70 degrees C), with an activation energy for Mg2+ conduction of E-a similar to 108 kJ/mol (1.12 eV) and high thermal stability (T-dec = 120 degrees C). Characterization using solid-state nuclear magnetic resonance, powder X-ray diffraction, and transmission electron microscopy reveals that the high Mg2+ conductivity is attributed to amorphization of Mg(BH4)(2)center dot xNH(3) resulting in a highly dynamic state. This nanocomposite is compatible with a Mg metal anode and allows stable Mg plating/stripping (at least 100 cycles) in a symmetric cell. The results represent a major advancement of solid-state multivalent ion conductors here demonstrated for Mg2+.
引用
收藏
页码:9264 / 9270
页数:7
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