TY - JOUR
T1 - Thin-film lithium batteries with 0.3–30 μm thick LiCoO2 films fabricated by high-rate pulsed laser deposition
AU - Matsuda, Yasutaka
AU - Kuwata, Naoaki
AU - Kawamura, Junichi
N1 - Funding Information:
This study was supported by the JST ALCA-SPRING (Specially Promoted Research for Innovative Next Generation Batteries) Project. This work was also supported by JSPS KAKENHI, Grant-in-Aid for Scientific Research (B), grant number 15H03872.
Funding Information:
This study was supported by the JST ALCA-SPRING (Specially Promoted Research for Innovative Next Generation Batteries) Project. This work was also supported by JSPS KAKENHI, Grant-in-Aid for Scientific Research (B), grant number 15H03872 .
Publisher Copyright:
© 2018 The Authors
PY - 2018/7
Y1 - 2018/7
N2 - High-rate pulsed laser deposition was applied to the preparation of thick LiCoO2 cathode films, which were then used in the fabrication of thin-film batteries. The deposition rate of the LiCoO2 films was 2–3 μm/h. The thin-film batteries showed an increase in capacity up to 470 μAh/cm2 with increasing cathode film thickness. The rate dependence of discharge capacity was analyzed using a diffusion model in which the chemical diffusion coefficient of lithium in the cathode determines the dynamic capacity. For the initial stage of discharge, the chemical diffusion coefficient was estimated to be 10−10 cm2/s. Conversely, the chemical diffusion coefficient decreases to ~10−12 cm2/s at the end of discharge. From the diffusion model, the available capacity was estimated as a function of cathode thickness. Crack formation inside the LiCoO2 film is also suggested as a cause of capacity limitation.
AB - High-rate pulsed laser deposition was applied to the preparation of thick LiCoO2 cathode films, which were then used in the fabrication of thin-film batteries. The deposition rate of the LiCoO2 films was 2–3 μm/h. The thin-film batteries showed an increase in capacity up to 470 μAh/cm2 with increasing cathode film thickness. The rate dependence of discharge capacity was analyzed using a diffusion model in which the chemical diffusion coefficient of lithium in the cathode determines the dynamic capacity. For the initial stage of discharge, the chemical diffusion coefficient was estimated to be 10−10 cm2/s. Conversely, the chemical diffusion coefficient decreases to ~10−12 cm2/s at the end of discharge. From the diffusion model, the available capacity was estimated as a function of cathode thickness. Crack formation inside the LiCoO2 film is also suggested as a cause of capacity limitation.
KW - Chemical diffusion coefficient
KW - Diffusion model
KW - Lithium cobalt oxide
KW - Pulsed laser deposition
KW - Solid-state battery
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U2 - 10.1016/j.ssi.2018.02.024
DO - 10.1016/j.ssi.2018.02.024
M3 - Article
AN - SCOPUS:85042366985
SN - 0167-2738
VL - 320
SP - 38
EP - 44
JO - Solid State Ionics
JF - Solid State Ionics
ER -