期刊
ENERGY STORAGE MATERIALS
卷 24, 期 -, 页码 198-207出版社
ELSEVIER
DOI: 10.1016/j.ensm.2019.08.019
关键词
Composite polymer electrolytes; All-solid-state batteries; Li-S batteries; Interfaces
资金
- Natural Sciences and Engineering Research Council of Canada (NSERC) [RGPIN-2016-03853]
- University of Calgary, Canada
Polymer-based solid electrolytes are very promising for high energy density solid-state Li-S batteries owing to their flexibility and higher safety. However, poor room temperature Li-ion conductivity of polymer-based solid electrolyte is the biggest challenge for their practical utilization. Here, a flexible composite polymer-ceramic electrolyte (CPE) comprising of PVDF and garnet-type Li6.5La2.5Ba0.5ZrTaO12 for room temperature all-solid-state-Li-S battery (ASLSB) is demonstrated. The PVDF-garnet CPE exhibits a high Li-ionic conductivity of 0.34 mS cm(-1) at 20 degrees C. PVDF-garnet-based CPEs are not electrochemically stable and undergoes severe dehydrofluorination upon galvanostatic cycling with Li electrode. For the first time, PVDF-garnet-based CPEs are modified with LiF additive, evidenced by steady galvanostatic cycling at 0.2 mA cm(-2) for more than 800 h. The effect of LiF addition on the stability of PVDF-based CPEs is explained by XPS studies and electrochemical measurements. ASLSB fabricated with the modified CPE displays a high specific capacity of 936 mA h g(-1) with 0.1C rate at 20 degrees C, along with very good stable performances over 80 continuous cycles. The ASLSB also shows very good rate capability and high Coulombic efficicency. The performance of CPE vindicates the potential applications towards room-temperature operating all-solid-state-Li-S batteries.
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