TY - JOUR
T1 - Resolving electrochemical incompatibility between LATP and Li-metal using tri-layer composite solid electrolyte approaches for solid-state Li-metal batteries
AU - Kibret, Desalegn Yilma
AU - Mengesha, Tadesu Hailu
AU - Walle, Kumlachew Zelalem
AU - Wu, Yi Shiuan
AU - Chang, Jeng Kuei
AU - Jose, Rajan
AU - Yang, Chun Chen
N1 - Publisher Copyright:
© 2024 Elsevier Ltd
PY - 2024/7/30
Y1 - 2024/7/30
N2 - Due to its excellent air stability, low cost, and high ionic conductivity, Li1.3Al0.3Ti1.7(PO4)3 (LATP) has emerged as a viable option for solid-state lithium batteries (SSLBs). However, the irreversible reactivity between LATP and the Li-metal anode severely restrict its electrochemical performances. Herein, a tri-layer composite solid electrolyte (t-CSE1) comprised of LATP, PVDF-HFP, SN, and LiTFSI as the middle layer and Al-LLZO, PVDF-HFP, SN, and LiTFSI as the top and bottom layers is prepared to solve these prominent limitations since Al-LLZO is stable towards Li metal anode. As a result, the lithium plating-stripping lifetimes for the Li||Li symmetry cell is prolonged from 550 to 1950 h at 0.1 mA cm−2 without any residual redox products. In addition, the as-prepared t-CSE1 exhibited excellent ionic conductivity (ca. 6.46 × 10−4 S cm−1 at room temperature), high lithium-ion transference number (ca. 0.69) and remarkable mechanical strength (ca. 12.82 MPa). Furthermore, the Li||LiFePO4 (Li||LFP) full cell achieved significantly improved long cycle performances of 500 cycles with 80.31 % capacity retention and 99.93 % average coulombic efficiency at 0.2C. Moreover, the Li||LFP full cell showed 85.53 % capacity retention and 99.95 % coulombic efficiency after 200 cycles at 0.5C at room temperature. Thus, this study gives an insight into how to prevent the electrochemical incompatibility between LATP and Li metal for SSLBs.
AB - Due to its excellent air stability, low cost, and high ionic conductivity, Li1.3Al0.3Ti1.7(PO4)3 (LATP) has emerged as a viable option for solid-state lithium batteries (SSLBs). However, the irreversible reactivity between LATP and the Li-metal anode severely restrict its electrochemical performances. Herein, a tri-layer composite solid electrolyte (t-CSE1) comprised of LATP, PVDF-HFP, SN, and LiTFSI as the middle layer and Al-LLZO, PVDF-HFP, SN, and LiTFSI as the top and bottom layers is prepared to solve these prominent limitations since Al-LLZO is stable towards Li metal anode. As a result, the lithium plating-stripping lifetimes for the Li||Li symmetry cell is prolonged from 550 to 1950 h at 0.1 mA cm−2 without any residual redox products. In addition, the as-prepared t-CSE1 exhibited excellent ionic conductivity (ca. 6.46 × 10−4 S cm−1 at room temperature), high lithium-ion transference number (ca. 0.69) and remarkable mechanical strength (ca. 12.82 MPa). Furthermore, the Li||LiFePO4 (Li||LFP) full cell achieved significantly improved long cycle performances of 500 cycles with 80.31 % capacity retention and 99.93 % average coulombic efficiency at 0.2C. Moreover, the Li||LFP full cell showed 85.53 % capacity retention and 99.95 % coulombic efficiency after 200 cycles at 0.5C at room temperature. Thus, this study gives an insight into how to prevent the electrochemical incompatibility between LATP and Li metal for SSLBs.
KW - Al-LLZO
KW - LATP
KW - Lithium metal batteries
KW - Solid-state
KW - Tri-layer composite solid electrolyte
UR - http://www.scopus.com/inward/record.url?scp=85195578104&partnerID=8YFLogxK
U2 - 10.1016/j.est.2024.112523
DO - 10.1016/j.est.2024.112523
M3 - Article
AN - SCOPUS:85195578104
SN - 2352-152X
VL - 94
JO - Journal of Energy Storage
JF - Journal of Energy Storage
M1 - 112523
ER -