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Influences of Microstructures of the Cathode/Electrolyte Interface on the Electrochemical Properties of All Solid-State Li-ion Batteries

Published online by Cambridge University Press:  26 February 2011

Kyosuke Kishida ,
Naoyuki Wada ,
Yuji Yamaguchi ,
Katsushi Tanaka ,
Yasutoshi Iriyama ,
Zempachi Ogumi  and
Haruyuki Inui
Kyosuke Kishida
Affiliation:
[email protected], Kyoto University, Department of Materials Science and Engineering, Sakyo-ku, Kyoto, 606-8501, Japan, +81-75-753-5481, +81-75-753-5461
Naoyuki Wada
Affiliation:
[email protected], Kyoto University, Department of Materials Science and Engineering, Sakyo-ku, Kyoto, 606-8501, Japan
Yuji Yamaguchi
Affiliation:
[email protected], Kyoto University, Department of Materials Science and Engineering, Sakyo-ku, Kyoto, 606-8501, Japan
Katsushi Tanaka
Affiliation:
[email protected], Kyoto University, Department of Materials Science and Engineering, Sakyo-ku, Kyoto, 606-8501, Japan
Yasutoshi Iriyama
Affiliation:
[email protected], Kyoto University, Department of Energy and Hydrocarbon Chemistry, Nishikyo-ku, Kyoto, 615-8510, Japan
Zempachi Ogumi
Affiliation:
[email protected], Kyoto University, Department of Energy and Hydrocarbon Chemistry, Nishikyo-ku, Kyoto, 615-8510, Japan
Haruyuki Inui
Affiliation:
[email protected], Kyoto University, Department of Materials Science and Engineering, Sakyo-ku, Kyoto, 606-8501, Japan
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Abstract

Two types of samples containing different La2/3-x Li3x TiO3 (LLT) solid electrolyte /LiCoO2 cathode interfaces were prepared by depositing LiCoO2 on polycrystalline LLT with two different surface finishes: cleaved and polished surfaces. Electrochemical properties of the samples were analyzed by cyclic voltammetry (CV). Microstructures of the LLT/LiCoO2 interfaces were investigated by scanning electron microscopy and transmission electron microscopy. Cyclic voltammograms of the cleaved sample show that the anodic and cathodic peaks respectively shift to higher and lower potential with the number of cycles, while those for the polished samples do not change much during cycles of potential sweeps, indicating the higher stability for the polished samples upon insertion and extraction of lithium ion. The LiCoO2 thin-film cathode is epitaxially deposited with the orientation relationships: {110}LLT//{1120}LiCoO2 and <001>LLT//<4401>LiCoO2 for both samples with different geometric configurations of the interfaces to the Li layers in the LiCoO2. Amorphous regions are observed to exist in places at the interface only in the polished samples. The geometric configuration of the interface and the existence of the amorphous regions are considered to have great influences on the stability of the LLT/LiCoO2 interfaces upon charge / discharge operations.

Keywords

defectsionic conductortransmission electron microscopy (TEM)
Type
Research Article
Information
MRS Online Proceedings Library (OPL) , Volume 972: Symposium AA – Solid-State Ionics—2006 , 2006 , 0972-AA13-05
Copyright
Copyright © Materials Research Society 2007

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