Solution Processing of Lithium-Rich Amorphous Li-La-Zr-O Ion Conductor and Its Application for Cycling Durability Improvement of LiCoO2 Cathode as Coating Layer
- Authors
 - Bui, Tan Tan; Yun, Boseon; Darko, Kwabena; Shin, Seung Beom; Kim, Jaehyun; Hong, Jongin; Lee, Minah; Park, Sung Kyu; Kim, Myung-Gil
 
- Issue Date
 - 2021-03
 
- Publisher
 - WILEY
 
- Citation
 - ADVANCED MATERIALS INTERFACES, v.8, no.5
 
- Abstract
 - Lithium-rich amorphous Li-La-Zr-O (a-Li-La-Zr-O) electrolyte is successfully synthesized using sol-gel processing method. With unlimited compositions of the amorphous structure, lithium-rich compositions are systematically investigated to determine optimal composition and optimized processing conditions of a-Li-La-Zr-O coatings. There is an improvement in ionic conductivity of a-Li-La-Zr-O with Li content increasing, specifically from 3.0 x 10(-8) S cm(-1) (Li8La2Zr2O11) to 1.18 x 10(-6) S cm(-1) (Li18La2Zr2O16), thereby resulting in low activation energy. The high-ionic-conductivity a-Li-La-Zr-O is implemented as an artificial solid electrolyte interface coating layer on cathode materials. The a-Li-La-Zr-O-coated LiCoO2 (LCO) and LiNi0.8Mn0.1Co0.1O2 (NMC 811) coin cells exhibit better cycling performance than the bare coin cell at the optimum compositional ratio of a-Li-La-Zr-O. A-Li-La-Zr-O can be a promising material for solid electrolyte battery and a potential coating layer for the modification of cathode surface.
 
- Keywords
 - SOLID-STATE ELECTROLYTES; GARNET-TYPE LI7LA3ZR2O12; ELECTROCHEMICAL PERFORMANCE; SURFACE-CHEMISTRY; PARTICLE-SIZE; THIN-FILMS; BATTERIES; STABILITY; PROGRESS; ORIGIN; SOLID-STATE ELECTROLYTES; GARNET-TYPE LI7LA3ZR2O12; ELECTROCHEMICAL PERFORMANCE; SURFACE-CHEMISTRY; PARTICLE-SIZE; THIN-FILMS; BATTERIES; STABILITY; PROGRESS; ORIGIN; a-Li-La-Zr-O; amorphous ion-conducting layers; cathode coatings; lithium-ion batteries; solution processing
 
- ISSN
 - 2196-7350
 
- URI
 - https://pubs.kist.re.kr/handle/201004/117313
 
- DOI
 - 10.1002/admi.202001767
 
- Appears in Collections:
 - KIST Article > 2021
 
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