A graphite intercalation compound associated with liquid Na-K towards ultra-stable and high-capacity alkali metal anodes

被引:92
|
作者
Zhang, Leyuan [1 ,2 ]
Peng, Sangshan [1 ,2 ,3 ]
Ding, Yu [1 ,2 ]
Guo, Xuelin [1 ,2 ]
Qian, Yumin [1 ,2 ]
Celio, Hugo [1 ,2 ]
He, Gaohong [3 ]
Yu, Guihua [1 ,2 ]
机构
[1] Univ Texas Austin, Mat Sci & Engn Program, Austin, TX 78712 USA
[2] Univ Texas Austin, Dept Mech Engn, Austin, TX 78712 USA
[3] Dalian Univ Technol, State Key Lab Fine Chem, R&D Ctr Membrane Sci & Technol, Sch Chem Engn, Dalian 116023, Peoples R China
关键词
BATTERIES; HOST;
D O I
10.1039/c9ee00437h
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Alkali metal anodes (Li, Na, K) are highly promising for enabling high-energy-density rechargeable batteries due to their high theoretical capacities and low redox potentials. Although extensive studies have been performed on Li-metal, dendrite growth and serious interface issues are still fundamental challenges for practical alkali metal batteries (AMBs). Here, we report an in situ-formed graphite intercalation compound (GIC) framework that enables Na-K liquid alloy to be used in ultra-stable and high-capacity anodes, attributed to the synergy of fast electron and mass transport of the GIC networks associated with the self-healing behavior of the Na-K alloy. The Na-K composite electrode is highly stable; it sustains repeated stripping/deposition over 5000 hours at 20 mA cm 2 and achieves stable electrodeposition even at 80 mA cm 2 and 16 mA h cm 2. When coupled with various cathodes, versatile AMBs are realized with long cycling and high operating voltages. This framework electrode design presents new insight into developing dendrite-free alkali metal anodes.
引用
收藏
页码:1989 / 1998
页数:10
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