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Silicon Electrodes for Li-Ion Batteries. Addressing the Challenges through Coordination Chemistry
被引:49
|作者:
Devic, Thomas
[1
]
Lestriez, Bernard
[1
]
Roue, Lionel
[2
]
机构:
[1] Univ Nantes, CNRS, Inst Mat Jean Rouxel IMN, UMR 6502, 2 Rue Houssiniere,BP 32229, F-44322 Nantes 3, France
[2] INRS, Ctr Energie, Mat, Telecommun EMT, 1650 Blvd Lionel Boulet, Varennes, PQ J3X 1S2, Canada
来源:
ACS ENERGY LETTERS
|
2019年
/
4卷
/
02期
基金:
加拿大自然科学与工程研究理事会;
关键词:
METAL-ORGANIC FRAMEWORKS;
SI-BASED ANODES;
ALGINATE;
BINDERS;
COMPLEXES;
COMPOSITE;
NETWORK;
SURFACE;
MOFS;
D O I:
10.1021/acsenergylett.8b02433
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:
Silicon is considered as a promising negative electrode active material for Li-ion batteries, but its practical use is hampered by its very limited electrochemical cyclability arising from its major volume change upon cycling, which deteriorates the electrode architecture and the solid-electrolyte interphase. In this Perspective, we aim at critically discussing the opportunities offered by coordination chemistry to tackle these challenges. More precisely, we will show how the characteristics of the coordination bonds, notably their tunability, medium strength, and dynamic character, can be exploited to offer alternative paths for binding, templating, and coating Si particles in order to ultimately improve the cycle life of Si electrodes in Li-ion batteries.
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页码:550 / 557
页数:15
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