TY - JOUR
T1 - Engineering a High-Voltage Durable Cathode/Electrolyte Interface for All-Solid-State Lithium Metal Batteries via In Situ Electropolymerization
AU - Li, Qi
AU - Zhang, Xiaoyu
AU - Peng, Jian
AU - Wang, Zhihao
AU - Rao, Zhixiang
AU - Li, Yuyu
AU - Li, Zhen
AU - Fang, Chun
AU - Han, Jiantao
AU - Huang, Yunhui
N1 - Publisher Copyright:
© 2022 American Chemical Society.
PY - 2022
Y1 - 2022
N2 - Poly(ethylene oxide) (PEO)-based polymer electrolytes have been widely studied as a result of their flexibility, excellent interface contact, and high compatibility with a lithium metal anode. Owing to the poor oxidation resistance of ethers, however, the PEO-based electrolytes are only compatible with low-voltage cathodes, which limits their energy density. Here, a high-voltage stable solid-state interface layer based on polyfluoroalkyl acrylate was constructed via in situ solvent-free bulk electropolymerization between the LiNi0.8Mn0.1Co0.1O2 (NCM811) cathode and the PEO-based solid polymer electrolyte. The electrochemical oxidation window of the as-synthesized electrolyte was therefore expanded from 4.3 V for the PEO-based matrix electrolyte to 5.1 V, and the ionic conductivity was improved to 1.02 × 10-4 S cm-1 at ambient temperature and 4.72 × 10-4 S cm-1 at 60 °C as a result of the improved Li+ migration. This fabrication process for the interface buffer layer by an in situ electrochemical process provides an innovative and universal interface engineering strategy for high-performance and high-energy-density solid-state batteries, which has not been explicitly discussed before, paving the way toward the large-scale production of the next generation of solid-state lithium batteries.
AB - Poly(ethylene oxide) (PEO)-based polymer electrolytes have been widely studied as a result of their flexibility, excellent interface contact, and high compatibility with a lithium metal anode. Owing to the poor oxidation resistance of ethers, however, the PEO-based electrolytes are only compatible with low-voltage cathodes, which limits their energy density. Here, a high-voltage stable solid-state interface layer based on polyfluoroalkyl acrylate was constructed via in situ solvent-free bulk electropolymerization between the LiNi0.8Mn0.1Co0.1O2 (NCM811) cathode and the PEO-based solid polymer electrolyte. The electrochemical oxidation window of the as-synthesized electrolyte was therefore expanded from 4.3 V for the PEO-based matrix electrolyte to 5.1 V, and the ionic conductivity was improved to 1.02 × 10-4 S cm-1 at ambient temperature and 4.72 × 10-4 S cm-1 at 60 °C as a result of the improved Li+ migration. This fabrication process for the interface buffer layer by an in situ electrochemical process provides an innovative and universal interface engineering strategy for high-performance and high-energy-density solid-state batteries, which has not been explicitly discussed before, paving the way toward the large-scale production of the next generation of solid-state lithium batteries.
KW - all-solid-state lithium battery
KW - cathode electrolyte interphase
KW - high voltage
KW - interface engineering
KW - poly(trifluoroethyl methacrylate)
UR - http://www.scopus.com/inward/record.url?scp=85129946248&partnerID=8YFLogxK
U2 - 10.1021/acsami.2c02731
DO - 10.1021/acsami.2c02731
M3 - 文章
C2 - 35482579
AN - SCOPUS:85129946248
SN - 1944-8244
VL - 14
SP - 21018
EP - 21027
JO - ACS Applied Materials and Interfaces
JF - ACS Applied Materials and Interfaces
IS - 18
ER -