TY - JOUR
T1 - Incorporating Solvate and Solid Electrolytes for All-Solid-State Li2S Batteries with High Capacity and Long Cycle Life
AU - Shin, Minjeong
AU - Gewirth, Andrew A.
N1 - Funding Information:
The authors thank Professor Lingzi Sang and Dr. Sanghyeon Kim for helpful discussions. This work was carried out in part in the Frederick Seitz Materials Research Laboratory Central Facilities, University of Illinois. This work was supported as part of the Joint Center for Energy Storage Research, an Energy Innovation Hub funded by the U.S. Department of Energy, Office of Science, Basic Energy Sciences.
Publisher Copyright:
© 2019 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
PY - 2019/7/12
Y1 - 2019/7/12
N2 - The development of all-solid-state lithium–sulfur batteries is hindered by the poor interfacial properties at solid electrolyte (SE)/electrode interfaces. The interface is modified by employing the highly concentrated solvate electrolyte, (MeCN)2−LiTFSI:TTE, as an interlayer material at the electrolyte/electrode interfaces. The incorporation of an interlayer significantly improves the cycling performance of solid-state Li2S batteries compared to the bare counterpart, exhibiting a specific capacity of 760 mAh g−1 at cycle 100 (330 mAh g−1 for the bare cell). Electrochemical impedance spectroscopy shows that the interfacial resistance of the interlayer-modified cell gradually decreases as a function of cycle number, while the impedance of the bare cell remains almost constant. Cross-section scanning electron microscopy (SEM)/ energy dispersive X-ray spectroscopy (EDS) measurements on the interlayer-modified cell confirm the permeation of solvate into the cathode and the SE with electrochemical cycling, which is related to the decrease in cell impedance. In order to mimic the full permeation of the solvate across the entire cell, the solvate is directly mixed with the SE to form a “solvSEM” electrolyte. The hybrid Li2S cell using a solvSEM electrolyte exhibits superior cycling performance compared to the solid-state cells, in terms of Li2S loading, Li2S utilization, and cycling stability. The improved performance is due to the favorable ionic contact at the battery interfaces.
AB - The development of all-solid-state lithium–sulfur batteries is hindered by the poor interfacial properties at solid electrolyte (SE)/electrode interfaces. The interface is modified by employing the highly concentrated solvate electrolyte, (MeCN)2−LiTFSI:TTE, as an interlayer material at the electrolyte/electrode interfaces. The incorporation of an interlayer significantly improves the cycling performance of solid-state Li2S batteries compared to the bare counterpart, exhibiting a specific capacity of 760 mAh g−1 at cycle 100 (330 mAh g−1 for the bare cell). Electrochemical impedance spectroscopy shows that the interfacial resistance of the interlayer-modified cell gradually decreases as a function of cycle number, while the impedance of the bare cell remains almost constant. Cross-section scanning electron microscopy (SEM)/ energy dispersive X-ray spectroscopy (EDS) measurements on the interlayer-modified cell confirm the permeation of solvate into the cathode and the SE with electrochemical cycling, which is related to the decrease in cell impedance. In order to mimic the full permeation of the solvate across the entire cell, the solvate is directly mixed with the SE to form a “solvSEM” electrolyte. The hybrid Li2S cell using a solvSEM electrolyte exhibits superior cycling performance compared to the solid-state cells, in terms of Li2S loading, Li2S utilization, and cycling stability. The improved performance is due to the favorable ionic contact at the battery interfaces.
KW - all-solid-state batteries
KW - hybrid batteries
KW - inorganic solid electrolytes
KW - lithium sulfur batteries
KW - solvate electrolytes
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U2 - 10.1002/aenm.201900938
DO - 10.1002/aenm.201900938
M3 - Article
AN - SCOPUS:85082133606
SN - 1614-6832
VL - 9
JO - Advanced Energy Materials
JF - Advanced Energy Materials
IS - 26
M1 - 1900938
ER -