摘要
The isolated inorganic particles within composite polymer electrolytes (CPEs) are not correlated to the Li+ transfer network, resulting in the polymer dominating the low ionic conductivity of CPEs. Therefore, we developed novel quasi-solid-state CPEs of a Ce-doped Na super ion conductors (NASICON) Na1.3+xAl0.3CexTi1.7−x(PO4)3 (NCATP) chemically coupled poly(vinylidene fluoride-hexafluoropropylene) (PVDF-HFP)/Li-bis(trifluoromethanes-ulfonyl)imide (LiTFSI) matrix. A strong interaction between Ce3+ from NCATP and TFSI− anion from the polymer matrix contributes to the fast Li+ transportation at the interface. The PVDF-HFP/NCATP CPEs exhibit an ionic conductivity of 2.16 × 0−3 S cm−1 and a Li+ transference number of 0.88. A symmetric Li/Li cell with NCATP-integrated CPEs at 0.1 mA cm−2 presents outstanding cycling stability over 2000 h at 25 °C. The quasi-solid-state Li metal batteries of Li/CPEs/LiFePO4 at 2 C after 400 cycles and Li/CPEs/LiCoO2 at 0.2 C after 120 cycles deliver capacities of 100 and 152 mAh g−1 at 25 °C, respectively.
| 源语言 | 英语 |
|---|---|
| 页(从-至) | 311-321 |
| 页数 | 11 |
| 期刊 | Journal of Energy Chemistry |
| 卷 | 73 |
| DOI | |
| 出版状态 | 已出版 - 10月 2022 |
| 已对外发布 | 是 |
学术指纹
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