Fabrication and electrochemical performance of lithium polymer battery using mesoporous silica/polymer hybrid electrolyte
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- NAKAYAMA Masanobu
- Department of Materials Science and Engineering, Nagoya Institute of Technology Japan Science and Technology Agency, PRESTO Unit of Elements Strategy Initiative for Catalysts & Batteries (ESICB), Kyoto University
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- OKAJIMA Takashi
- Department of Materials Science and Engineering, Nagoya Institute of Technology
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- YAMAMOTO Yoshihiro
- Department of Materials Science and Engineering, Nagoya Institute of Technology
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- BABA Shinji
- Department of Materials Science and Engineering, Nagoya Institute of Technology
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- IIZUKA Kaede
- Department of Materials Science and Engineering, Nagoya Institute of Technology R&D division, World Interc Co., Ltd.
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- NOGAMI Masayuki
- Department of Materials Science and Engineering, Nagoya Institute of Technology
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- MOCHIZUKI Dai
- Department of Applied Chemistry, Tokyo Institute of Technology
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- KIGUCHI Takanori
- Institute for Materials Research, Tohoku University
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- KUROKI Shigeki
- Department of Organic and Polymeric Materials, Tokyo Institute of Technology
抄録
Development of all solid-state Li secondary based on the use of dry polymer or inorganic electrolytes is vital as they will be free of solvent leakages and improve inflammability. However, both are still under development for many years due to low ionic conductivity, poor mechanical property and/or large internal impedance associated to poorly defined interfaces. In this paper, we report on a preparation and physicochemical property of mesoporous silica (MPS)/Li conductive polyethylene oxide (Li-PEO)-based polymer hybrid electrolytes (MPS+Li-PEO), and electrochemical performance of the Li/MPS+Li-PEO/LiFePO4 cell. The hybrid electrolytes showed an improvement of Li+ transportation number and a decrease of melting point and glass transition temperature, indicating a positive hybrid effect, or deviation from rule-of-mixtures behavior. The Li/MPS+Li-PEO/LiFePO4 cell showed a stable charge–discharge capacity of >70 mA h g−1 for 100 cycles at moderate temperature of 60°C and rate of 0.2 C, whereas severe capacity fade began after several of cycles for the cell using conventional Li-PEO electrolyte. AC impedance measurements revealed that the interface Li exchange between electrode and electrolytes related to the stable cyclic performance for the cell using hybrid electrolytes.
収録刊行物
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- Journal of the Ceramic Society of Japan
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Journal of the Ceramic Society of Japan 121 (1416), 723-729, 2013
公益社団法人 日本セラミックス協会
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詳細情報 詳細情報について
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- CRID
- 1390001205286775552
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- NII論文ID
- 130004480172
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- ISSN
- 13486535
- 18820743
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- 本文言語コード
- en
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- データソース種別
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- JaLC
- Crossref
- CiNii Articles
- KAKEN
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- 抄録ライセンスフラグ
- 使用不可