TY - JOUR
T1 - Li-S batteries with Li2S cathodes and Si/C anodes
AU - Jha, Himendra
AU - Buchberger, Irmgard
AU - Cui, Xueyin
AU - Meini, Stefano
AU - Gasteiger, Hubert A.
N1 - Publisher Copyright:
© The Author(s) 2015. Published by ECS.
PY - 2015
Y1 - 2015
N2 - Lithium-sulfur (Li-S) batteries promise improved capacities over lithium ion batteries. While currently mostly metallic lithium anodes are used, the use of silicon-anodes might offer better safety and durability. However, in a lithium-sulfur-Silicon (Li-S-Si) battery, lithium must be introduced either on the anode or on the cathode in form of Li2S. In this study, we have prepared Li2S cathodes in combination with Si anodes (i.e., Si/Li2S full-cells) to investigate both the processes during initial charging/activation of Li2S cathodes and the effect of Li2S cathode activation on the cycling performance of Si/Li2S full-cells. We observed that the initial activation requires a substantially higher charging potential than for the subsequent cycles. In situ XRD analysis of the cathode during the first cycle clearly indicates the gradual transformation of Li2S to polysulfides and finally to crystalline sulfur, i.e., even large Li2S particles (≈20 μm) can be charged completely. The result is further confirmed by ex-situ SEM/EDS analysis, which revealed the formation of large sheets of sulfur at the cathode/separator interface. Similar cycling performance of Si/Li2S full-cells is observed at both 0.1 C and 1 C rates, a clear advantage over Li/Li2S cells, which suffer from severe dendrite formation at 1 C in the case of high Li2S loadings.
AB - Lithium-sulfur (Li-S) batteries promise improved capacities over lithium ion batteries. While currently mostly metallic lithium anodes are used, the use of silicon-anodes might offer better safety and durability. However, in a lithium-sulfur-Silicon (Li-S-Si) battery, lithium must be introduced either on the anode or on the cathode in form of Li2S. In this study, we have prepared Li2S cathodes in combination with Si anodes (i.e., Si/Li2S full-cells) to investigate both the processes during initial charging/activation of Li2S cathodes and the effect of Li2S cathode activation on the cycling performance of Si/Li2S full-cells. We observed that the initial activation requires a substantially higher charging potential than for the subsequent cycles. In situ XRD analysis of the cathode during the first cycle clearly indicates the gradual transformation of Li2S to polysulfides and finally to crystalline sulfur, i.e., even large Li2S particles (≈20 μm) can be charged completely. The result is further confirmed by ex-situ SEM/EDS analysis, which revealed the formation of large sheets of sulfur at the cathode/separator interface. Similar cycling performance of Si/Li2S full-cells is observed at both 0.1 C and 1 C rates, a clear advantage over Li/Li2S cells, which suffer from severe dendrite formation at 1 C in the case of high Li2S loadings.
UR - http://www.scopus.com/inward/record.url?scp=84937047150&partnerID=8YFLogxK
U2 - 10.1149/2.0681509jes
DO - 10.1149/2.0681509jes
M3 - Article
AN - SCOPUS:84937047150
SN - 0013-4651
VL - 162
SP - A1829-A1835
JO - Journal of the Electrochemical Society
JF - Journal of the Electrochemical Society
IS - 9
ER -