TY - JOUR
T1 - LiPF6 Induces Phosphorization of Garnet-Type Solid-State Electrolyte for Stable Lithium Metal Batteries
AU - Chen, Nan
AU - Gui, Boshun
AU - Yang, Binbin
AU - Deng, Chenglong
AU - Liang, Yaohui
AU - Zhang, Fengling
AU - Li, Bohua
AU - Sun, Wen
AU - Wu, Feng
AU - Chen, Renjie
N1 - Publisher Copyright:
© 2023 Wiley-VCH GmbH.
PY - 2024/2/22
Y1 - 2024/2/22
N2 - Garnet solid electrolyte Li6.4La3Zr1.4Ta0.6O12 (LLZTO) is an excellent inorganic ceramic-type solid electrolyte; however, the presence of Li2CO3 impurities on its surface hinders Li-ion transport and increases the interface impedance. In contrast to traditional methods of mechanical polishing, acid corrosion, and high-temperature reduction for removing Li2CO3, herein, a straightforward “waste-to-treasure” strategy is proposed to transform Li2CO3 into Li3PO4 and LiF in LiPF6 solution under 60 °C. It is found that the formation of Li3PO4 during LLZTO pretreatment facilitates rapid Li-ion transport and enhances ionic conductivity, and the LLZTO/PAN composite polymer electrolyte shows the highest Li-ion transference number of 0.63. Additionally, the dense LiF layer serves to safeguard the internal garnet solid electrolyte against solvent decomposition-induced chemical adsorption. Symmetric Li/Li cells assembled with treated LLZTO/PAN composite electrolyte exhibit a critical current density of 1.1 mA cm−2 and a long lifespan of up to 700 h at a current density of 0.2 mA cm−2. The Li/LiFePO4 solid-state cells demonstrate stable cycling performances for 141 mAh g−1 at 0.5 C, with capacity retention of 93.6% after 190 cycles. This work presents a novel approach to converting waste into valuable resources, offering the advantages of simple processes, and minimal side reactions.
AB - Garnet solid electrolyte Li6.4La3Zr1.4Ta0.6O12 (LLZTO) is an excellent inorganic ceramic-type solid electrolyte; however, the presence of Li2CO3 impurities on its surface hinders Li-ion transport and increases the interface impedance. In contrast to traditional methods of mechanical polishing, acid corrosion, and high-temperature reduction for removing Li2CO3, herein, a straightforward “waste-to-treasure” strategy is proposed to transform Li2CO3 into Li3PO4 and LiF in LiPF6 solution under 60 °C. It is found that the formation of Li3PO4 during LLZTO pretreatment facilitates rapid Li-ion transport and enhances ionic conductivity, and the LLZTO/PAN composite polymer electrolyte shows the highest Li-ion transference number of 0.63. Additionally, the dense LiF layer serves to safeguard the internal garnet solid electrolyte against solvent decomposition-induced chemical adsorption. Symmetric Li/Li cells assembled with treated LLZTO/PAN composite electrolyte exhibit a critical current density of 1.1 mA cm−2 and a long lifespan of up to 700 h at a current density of 0.2 mA cm−2. The Li/LiFePO4 solid-state cells demonstrate stable cycling performances for 141 mAh g−1 at 0.5 C, with capacity retention of 93.6% after 190 cycles. This work presents a novel approach to converting waste into valuable resources, offering the advantages of simple processes, and minimal side reactions.
KW - LiCO
KW - garnet electrolytes
KW - interface modulation
KW - solid-state batteries
UR - http://www.scopus.com/inward/record.url?scp=85173813740&partnerID=8YFLogxK
U2 - 10.1002/smll.202305576
DO - 10.1002/smll.202305576
M3 - Article
C2 - 37821400
AN - SCOPUS:85173813740
SN - 1613-6810
VL - 20
JO - Small
JF - Small
IS - 8
M1 - 2305576
ER -