Boron based layered electrode materials for metal-ion batteries

被引:9
|
作者
Hao, Kuan-Rong [1 ,2 ]
Yan, Qing-Bo [2 ]
Su, Gang [1 ,3 ,4 ]
机构
[1] Univ Chinese Acad Sci, Sch Phys Sci, Beijing 100049, Peoples R China
[2] Univ Chinese Acad Sci, Coll Mat Sci & Optoelect Technol, Ctr Mat Sci & Optoelect Engn, Beijing 100049, Peoples R China
[3] Univ Chinese Acad Sci, Kavli Inst Theoret Sci, Beijing 100190, Peoples R China
[4] Univ Chinese Acad Sci, CAS Ctr Excellence Topol Quantum Computat, Beijing 100190, Peoples R China
基金
中国国家自然科学基金; 国家重点研发计划;
关键词
ELECTRICAL ENERGY-STORAGE; PROMISING ANODE MATERIAL; AB-INITIO PREDICTION; LI-ION; LITHIUM-ION; CATHODE MATERIAL; DIFFUSION; INTERCALATION; BOROPHENE; MONOLAYER;
D O I
10.1039/c9cp05318b
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
Graphite is the most commonly used electrode material, which is mainly due to two key advantages, i.e., its layered structure acts a perfect framework for the accommodation and migration of ions, and the light atomic mass of carbon is conducive to obtaining a high specific capacity. As a neighbor of carbon in the periodic table, boron is even lighter than carbon, and it can also form various layered structures. Here, we systematically investigate boron-based layered compounds to explore their potential applications as electrode materials by means of first-principle calculations. Among various types of boron compounds, MXB4 (M = Li, Na, Mg; X = Al, Ga) with the YCrB4-type structure are found to be potentially excellent electrode materials for metal-ion batteries. The adsorption and migration of Li/Na/Mg in MXB4 have been presented, and migration barriers comparable with conventional electrode materials are observed. In particular, Li2AlB4 and Li2GaB4 are found to exhibit quite high specific capacities of 754 mA h g(-1) and 470 mA h g(-1) compared to the theoretical value of graphite (372 mA h g(-1)) as well as low average voltages of 0.71 V and 0.79 V, respectively, revealing that they may be good anode materials for Lithium ion batteries.
引用
收藏
页码:709 / 715
页数:7
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