Nano-structured Li1.3Al0.3Ti1.7(PO4)3 coated LiCoO2 enabling compatible interface with ultrathin garnet-based solid electrolyte for stable Li metal battery

Garnet-type Li7La3Zr2O12 (LLZO) ceramics has been considered as an ideal solid-state electrolyte for Li metal cells because of its high ionic conductivity and relatively stable interface with Li. However, it is electrochemically incompatible with some high-voltage cathodes, e.g. LiCoO2. In this work, a nanoscale Li1.3Al0.3Ti1.7(PO4)(3) (LATP) fast ion conductor was coated on LiCoO2 (only 1 wt% LATP), bringing obviously enhanced interfacial compatibility with a composite electrolyte composed of Al, Nb-codoped LLZO and polyethylene oxide (PEO). A free-standing, flexible and ultrathin (20 mu m) electrolyte membrane was successfully fabricated by a facile and scalable route, even though with a high ceramics content (67 wt%). Quasi-solid-state coin and pouch-type Li cells were assembled with the LATP-coated LiCoO2 cathode, free-standing composite electrolyte and Li anode, together with soft interface modification by in-situ polymerization. The cells show stable cycling due to combined factors of enhanced electrode/electrolyte compatibility, ultrathin nature of the electrolyte membrane and the in-situ built soft interface. The pouch cells can be cycled for 300 cycles at 0.3 C and 60 degrees C with 80% retention. The pouch cells can endure abuse tests of bending, cutting and nail penetration. At a practical LiCoO2 loading of 3 mAh cm(-2), the Li vertical bar LiCoO2 pouch cell still shows stable cycling with 90% retention after 100 cycles at 60 degrees C (0.2 C charge/0.5 C discharge). This work provides a practical method to fabricate high-performance solid-state Li cells. (C) 2022 Elsevier Ltd. All rights reserved.