Jicheng Shan, Jun Song, Xuerong Wang, Bin Li, Haijing Zhu, Xiaosheng Qian
{"title":"为高性能固态锂电池设计具有协同传输机制的纤维素/聚环氧乙烷/EMITFSI 基复合电解质","authors":"Jicheng Shan, Jun Song, Xuerong Wang, Bin Li, Haijing Zhu, Xiaosheng Qian","doi":"10.1016/j.cej.2024.157790","DOIUrl":null,"url":null,"abstract":"Despite its theoretically high energy density, polymer solid-state lithium batteries (PSSLBs) exhibit lower actual energy density. This discrepancy arises from the low ionic conductivity of the polymer solid-state electrolyte (PSSE) due to the coupling of lithium ion (Li<sup>+</sup>) transport to the relaxation of polymer chain segments. The objective of this study is to optimize the Li<sup>+</sup> transport in PSSE. This is achieved by incorporating 1-ethyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide (EMITFSI) to plasticize both cellulose and polyethylene oxide (PEO). By leveraging the synergistic effects of cellulose and PEO, an ion-conducting network is established. This network allows Li<sup>+</sup> to form multiple Li-O coordination simultaneously with the hydroxyl group (OH) of cellulose and the ether group (EO) of PEO, thereby enabling Li<sup>+</sup> to transport between the two polymers in a decoupled manner. The PSSE demonstrated an ionic conductivity of 4 × 10<sup>-4</sup> mS/cm (at room temperature) and a Li<sup>+</sup> transference number of 0.43, significantly exceeding traditional PEO-based values of 10<sup>-5</sup> mS/cm and 0.1–0.2. Additionally, the high voltage stability of EMITFSI extends the electrochemical stability window of PSSE, achieving a stability window of 5 V. The assembled LiFePO<sub>4</sub>/Li cell achieved a specific capacity of 138 mA h/g at 50℃ (0.5C) with a capacity retention rate of 80 % after 280 cycles. This represents an innovative method for preparing high-energy–density solid-state lithium batteries.","PeriodicalId":270,"journal":{"name":"Chemical Engineering Journal","volume":"1 1","pages":""},"PeriodicalIF":13.3000,"publicationDate":"2024-11-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Design of cellulose/polyethylene oxide/EMITFSI-based composite electrolyte with synergistic transport mechanism for high-performance solid-state lithium batteries\",\"authors\":\"Jicheng Shan, Jun Song, Xuerong Wang, Bin Li, Haijing Zhu, Xiaosheng Qian\",\"doi\":\"10.1016/j.cej.2024.157790\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Despite its theoretically high energy density, polymer solid-state lithium batteries (PSSLBs) exhibit lower actual energy density. This discrepancy arises from the low ionic conductivity of the polymer solid-state electrolyte (PSSE) due to the coupling of lithium ion (Li<sup>+</sup>) transport to the relaxation of polymer chain segments. The objective of this study is to optimize the Li<sup>+</sup> transport in PSSE. This is achieved by incorporating 1-ethyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide (EMITFSI) to plasticize both cellulose and polyethylene oxide (PEO). By leveraging the synergistic effects of cellulose and PEO, an ion-conducting network is established. This network allows Li<sup>+</sup> to form multiple Li-O coordination simultaneously with the hydroxyl group (OH) of cellulose and the ether group (EO) of PEO, thereby enabling Li<sup>+</sup> to transport between the two polymers in a decoupled manner. The PSSE demonstrated an ionic conductivity of 4 × 10<sup>-4</sup> mS/cm (at room temperature) and a Li<sup>+</sup> transference number of 0.43, significantly exceeding traditional PEO-based values of 10<sup>-5</sup> mS/cm and 0.1–0.2. Additionally, the high voltage stability of EMITFSI extends the electrochemical stability window of PSSE, achieving a stability window of 5 V. The assembled LiFePO<sub>4</sub>/Li cell achieved a specific capacity of 138 mA h/g at 50℃ (0.5C) with a capacity retention rate of 80 % after 280 cycles. 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Design of cellulose/polyethylene oxide/EMITFSI-based composite electrolyte with synergistic transport mechanism for high-performance solid-state lithium batteries
Despite its theoretically high energy density, polymer solid-state lithium batteries (PSSLBs) exhibit lower actual energy density. This discrepancy arises from the low ionic conductivity of the polymer solid-state electrolyte (PSSE) due to the coupling of lithium ion (Li+) transport to the relaxation of polymer chain segments. The objective of this study is to optimize the Li+ transport in PSSE. This is achieved by incorporating 1-ethyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide (EMITFSI) to plasticize both cellulose and polyethylene oxide (PEO). By leveraging the synergistic effects of cellulose and PEO, an ion-conducting network is established. This network allows Li+ to form multiple Li-O coordination simultaneously with the hydroxyl group (OH) of cellulose and the ether group (EO) of PEO, thereby enabling Li+ to transport between the two polymers in a decoupled manner. The PSSE demonstrated an ionic conductivity of 4 × 10-4 mS/cm (at room temperature) and a Li+ transference number of 0.43, significantly exceeding traditional PEO-based values of 10-5 mS/cm and 0.1–0.2. Additionally, the high voltage stability of EMITFSI extends the electrochemical stability window of PSSE, achieving a stability window of 5 V. The assembled LiFePO4/Li cell achieved a specific capacity of 138 mA h/g at 50℃ (0.5C) with a capacity retention rate of 80 % after 280 cycles. This represents an innovative method for preparing high-energy–density solid-state lithium batteries.
期刊介绍:
The Chemical Engineering Journal is an international research journal that invites contributions of original and novel fundamental research. It aims to provide an international platform for presenting original fundamental research, interpretative reviews, and discussions on new developments in chemical engineering. The journal welcomes papers that describe novel theory and its practical application, as well as those that demonstrate the transfer of techniques from other disciplines. It also welcomes reports on carefully conducted experimental work that is soundly interpreted. The main focus of the journal is on original and rigorous research results that have broad significance. The Catalysis section within the Chemical Engineering Journal focuses specifically on Experimental and Theoretical studies in the fields of heterogeneous catalysis, molecular catalysis, and biocatalysis. These studies have industrial impact on various sectors such as chemicals, energy, materials, foods, healthcare, and environmental protection.