Mixed ionic-electronic conductor enabled effective cathode-electrolyte interface in all solid state batteries

被引:50
|
作者
Wang, Chengwei [1 ,2 ]
Zhang, Lei [1 ,2 ]
Xie, Hua [1 ]
Pastel, Glenn [1 ]
Dai, Jiaqi [1 ]
Gong, Yunhui [1 ,2 ]
Liu, Boyang [1 ]
Wachsman, Eric D. [1 ,2 ]
Hu, Liangbing [1 ,2 ]
机构
[1] Univ Maryland, Dept Mat Sci & Engn, College Pk, MD 20742 USA
[2] Maryland Energy Innovat Inst, College Pk, MD 20742 USA
关键词
All solid state battery; Garnet electrolyte; Slow pre-lithiation; Mixed ionic-electronic conductor; Cathode-garnet interface; LITHIUM; LI7LA3ZR2O12; STABILIZATION; DEPOSITION; STABILITY; ANODE;
D O I
10.1016/j.nanoen.2018.05.062
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
One of the main challenges to develop all solid state lithium (Li) metal batteries is the poor contact and thus the high interfacial resistance between electrodes and solid state electrolytes (SSEs). Recently, significant improvements have been made toward effective Li-garnet interfaces however due to the poor conductivity and rigid granular morphology of cathode materials, the cathode-garnet interface is deficient. In this work, we report an effective cathode-garnet interface using a mixed ionic-electronic (MIE) conductor, which enables cycling of all solid state batteries without a liquid or polymer electrolyte interface. The solution-processed two dimensional (2D) layered TiS2 shows MIE conductivity after slow pre-lithiation, resulting in more than 20 times lower interfacial resistance. In addition, solution-processed carbon nanotubes offer a conformal coating for an efficient cathode-current collector interface with enhanced charge transport kinetics. As a result, we demonstrated the first garnet-based truly all solid state battery using solution processed composite cathode. Given the excellent chemical stability of the Li metal anode, garnet SSE, and TiS2 cathode, the all solid state batteries can work at high temperatures from 100 degrees C to 150 degrees C for 400 cycles at current densities up to 1 mA/cm(2). The demonstrated MIE concept for addressing cathode-electrolyte interface can be further extended to other solid state battery chemistries.
引用
收藏
页码:393 / 400
页数:8
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