TY - JOUR
T1 - A low resistance and stable lithium-garnet electrolyte interface enabled by a multifunctional anode additive for solid-state lithium batteries
AU - Cao, Chencheng
AU - Zhong, Yijun
AU - Chandula Wasalathilake, Kimal
AU - Tadé, Moses O.
AU - Xu, Xiaomin
AU - Rabiee, Hesamoddin
AU - Roknuzzaman, Md
AU - Rahman, Rajib
AU - Shao, Zongping
N1 - Publisher Copyright:
© The Royal Society of Chemistry.
PY - 2022/2/7
Y1 - 2022/2/7
N2 - Solid-state batteries (SSBs) have attracted considerable attention due to their high intrinsic stability and theoretical energy density. As the core part, garnet electrolyte has been extensively investigated due to its high lithium-ion conductivity, wide electrochemical potential window, and easy synthesis. However, the poor and electrochemically unstable interfacial contact between the electrolyte and lithium anode greatly impedes the practical use of garnet based SSBs. Here, we report that such an interface challenge can be perfectly tackled by introducing multifunctional Li0.3La0.5TiO3 (LLTO) as an additive into the lithium anode. The limited reaction between the LLTO and lithium effectively changes the physical properties of the lithium anode, making it perfectly compatible with the garnet surface, and consequently significantly decreasing the interfacial resistance from 200 to only 48 Ω cm2 and greatly improving the interface stability and avoiding dendrite formation. Interestingly, LLTO provides additional lithium storage, and the close interface contact and the high lithium-ion conductivity of LLTO ensure high rate performance. Consequently, the symmetrical cell runs stably at 0.1 mA cm-2 for 400 h without obvious degradation. The SSB assembled with the LiFePO4 cathode and Li-LLTO composite anode demonstrates a specific capacity of 147 mA h g-1 and remarkable cycling stability with only 10% capacity decay over 700 cycles at 1C.
AB - Solid-state batteries (SSBs) have attracted considerable attention due to their high intrinsic stability and theoretical energy density. As the core part, garnet electrolyte has been extensively investigated due to its high lithium-ion conductivity, wide electrochemical potential window, and easy synthesis. However, the poor and electrochemically unstable interfacial contact between the electrolyte and lithium anode greatly impedes the practical use of garnet based SSBs. Here, we report that such an interface challenge can be perfectly tackled by introducing multifunctional Li0.3La0.5TiO3 (LLTO) as an additive into the lithium anode. The limited reaction between the LLTO and lithium effectively changes the physical properties of the lithium anode, making it perfectly compatible with the garnet surface, and consequently significantly decreasing the interfacial resistance from 200 to only 48 Ω cm2 and greatly improving the interface stability and avoiding dendrite formation. Interestingly, LLTO provides additional lithium storage, and the close interface contact and the high lithium-ion conductivity of LLTO ensure high rate performance. Consequently, the symmetrical cell runs stably at 0.1 mA cm-2 for 400 h without obvious degradation. The SSB assembled with the LiFePO4 cathode and Li-LLTO composite anode demonstrates a specific capacity of 147 mA h g-1 and remarkable cycling stability with only 10% capacity decay over 700 cycles at 1C.
UR - http://www.scopus.com/inward/record.url?scp=85124241844&partnerID=8YFLogxK
U2 - 10.1039/d1ta07804f
DO - 10.1039/d1ta07804f
M3 - 文章
AN - SCOPUS:85124241844
SN - 2050-7488
VL - 10
SP - 2519
EP - 2527
JO - Journal of Materials Chemistry A
JF - Journal of Materials Chemistry A
IS - 5
ER -