TY - JOUR
T1 - Observation of Chemomechanical Failure and the Influence of Cutoff Potentials in All-Solid-State Li-S Batteries
AU - Ohno, Saneyuki
AU - Koerver, Raimund
AU - Dewald, Georg
AU - Rosenbach, Carolin
AU - Titscher, Paul
AU - Steckermeier, Dominik
AU - Kwade, Arno
AU - Janek, Jürgen
AU - Zeier, Wolfgang G.
N1 - Funding Information:
The authors thank Dr. Joachim Sann for the assistance with the XPS measurement. The research was supported by the Federal Ministry of Education and Research (BMBF) within project LISZUBA under Grants 03XP0115A and 03XP0115D.
Publisher Copyright:
© 2019 American Chemical Society.
PY - 2019/4/23
Y1 - 2019/4/23
N2 - Because of a remarkably high theoretical energy density, the lithium-sulfur (Li-S) battery has attracted significant attention as a candidate for next-generation batteries. While employing solid electrolytes can provide a new avenue for high-capacity Li-S cells, all-solid-state batteries have unique failure mechanisms such as chemomechanical failure due to the volume changes of active materials. In this study, we investigate all-solid-state Li-S model cells with differently processed cathode composites and elucidate a typical failure mechanism stemming from irreversible Li 2 S formation in the cathode composites. Reducing the particle size is key to minimizing the influence of volume changes, and a capacity of >1000 mAh g sulfur -1 is achieved by ball milling of the cathode composites. In addition, the long-term stability of the ball-milled cathode is investigated by varying the upper and lower cutoff potentials for cycling, which results in the unveiling of the significantly detrimental role of the lower cutoff potential. Preventing a deep discharge leads to a reversible capacity of 800 mAh g sulfur -1 over 50 cycles in the optimized cell. This work highlights the importance of mitigating chemomechanical failure using microstructural engineering as well as the influence of the cutoff potentials in all-solid-state Li-S batteries.
AB - Because of a remarkably high theoretical energy density, the lithium-sulfur (Li-S) battery has attracted significant attention as a candidate for next-generation batteries. While employing solid electrolytes can provide a new avenue for high-capacity Li-S cells, all-solid-state batteries have unique failure mechanisms such as chemomechanical failure due to the volume changes of active materials. In this study, we investigate all-solid-state Li-S model cells with differently processed cathode composites and elucidate a typical failure mechanism stemming from irreversible Li 2 S formation in the cathode composites. Reducing the particle size is key to minimizing the influence of volume changes, and a capacity of >1000 mAh g sulfur -1 is achieved by ball milling of the cathode composites. In addition, the long-term stability of the ball-milled cathode is investigated by varying the upper and lower cutoff potentials for cycling, which results in the unveiling of the significantly detrimental role of the lower cutoff potential. Preventing a deep discharge leads to a reversible capacity of 800 mAh g sulfur -1 over 50 cycles in the optimized cell. This work highlights the importance of mitigating chemomechanical failure using microstructural engineering as well as the influence of the cutoff potentials in all-solid-state Li-S batteries.
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U2 - 10.1021/acs.chemmater.9b00282
DO - 10.1021/acs.chemmater.9b00282
M3 - Article
AN - SCOPUS:85064840134
SN - 0897-4756
VL - 31
SP - 2930
EP - 2940
JO - Chemistry of Materials
JF - Chemistry of Materials
IS - 8
ER -