{"title":"A Novel Aliphatic Ketone-Based Solid Polymer Electrolyte with High Salt-Soluble Ability Enabling Highly Stable Lithium-Metal Batteries","authors":"Yuchen Jiang, Baerlike Wujieti, Yu Liu, Qinghui Zeng, Zhenfeng Li, Jiazhu Guan, Honghao Wang, Lin Chen, Yong Cao, Rongzheng Li, Yajuan Zhou, Henghui Zhou, Wei Cui, Liaoyun Zhang","doi":"10.1002/adfm.202421160","DOIUrl":null,"url":null,"abstract":"<p>Low room temperature ionic conductivity and interfacial incompatibility are the key factors that hinder the practical application of solid polymer electrolyte (SPEs) in lithium metal batteries. Increasing the ability of the SPEs to dissolve and dissociate lithium salt is helpful to enhance ion transport capacity of the SPEs. Herein, ketone groups with high solubility and dissociation ability of lithium salt are introduced into the structural design of SPE, an aliphatic ketone solid polymer electrolyte (KT@SPE) with crosslinking structure is prepared by ultraviolet (UV) polymerization. The prepared KT@SPE shows excellent viscoelastic and possess room temperature ionic conductivity of 10<sup>−4</sup> S cm<sup>−1</sup> with 200 wt% lithium bis((trifluoromethyl)sulfonyl)azanide (LiTFSI). Thanks to the contribution of high ion transport capacity, construction of multi-hydrogen bonds network structure of KT@SPE and a wettability of controlling residual dimethyl sulfoxide (DMSO) solvent to the interface, the assembled symmetrical Li cell realizes stable cycling for over 2000 h at 0.15 mA cm<sup>−2</sup>. Moreover, LiFePO<sub>4</sub> cell achieves stable long cycle at 5C and enable Li/KT@SPE<sub>3</sub>/LiFe<sub>0.6</sub>Mn<sub>0.4</sub>PO<sub>4</sub> cell operates at 4.4 V. This work not only provides a design strategy for preparing novel solid polymer electrolytes, but also exhibits the excellent application potential of aliphatic ketone-based polymer electrolyte in solid-state lithium batteries at high current density and high voltage.</p>","PeriodicalId":112,"journal":{"name":"Advanced Functional Materials","volume":"35 19","pages":""},"PeriodicalIF":19.0000,"publicationDate":"2024-12-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Advanced Functional Materials","FirstCategoryId":"88","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/adfm.202421160","RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
Abstract
Low room temperature ionic conductivity and interfacial incompatibility are the key factors that hinder the practical application of solid polymer electrolyte (SPEs) in lithium metal batteries. Increasing the ability of the SPEs to dissolve and dissociate lithium salt is helpful to enhance ion transport capacity of the SPEs. Herein, ketone groups with high solubility and dissociation ability of lithium salt are introduced into the structural design of SPE, an aliphatic ketone solid polymer electrolyte (KT@SPE) with crosslinking structure is prepared by ultraviolet (UV) polymerization. The prepared KT@SPE shows excellent viscoelastic and possess room temperature ionic conductivity of 10−4 S cm−1 with 200 wt% lithium bis((trifluoromethyl)sulfonyl)azanide (LiTFSI). Thanks to the contribution of high ion transport capacity, construction of multi-hydrogen bonds network structure of KT@SPE and a wettability of controlling residual dimethyl sulfoxide (DMSO) solvent to the interface, the assembled symmetrical Li cell realizes stable cycling for over 2000 h at 0.15 mA cm−2. Moreover, LiFePO4 cell achieves stable long cycle at 5C and enable Li/KT@SPE3/LiFe0.6Mn0.4PO4 cell operates at 4.4 V. This work not only provides a design strategy for preparing novel solid polymer electrolytes, but also exhibits the excellent application potential of aliphatic ketone-based polymer electrolyte in solid-state lithium batteries at high current density and high voltage.
低温离子电导率和界面不相容性是阻碍固体聚合物电解质在锂金属电池中实际应用的关键因素。提高spe对锂盐的溶解和解离能力有助于提高spe的离子传输能力。本文将具有高溶解度和锂盐解离能力的酮基引入SPE的结构设计中,通过紫外(UV)聚合制备了具有交联结构的脂肪族酮类固体聚合物电解质(KT@SPE)。制备的KT@SPE具有优异的粘弹性,室温离子电导率为10−4 S cm−1,含有200wt %的双((三氟甲基)磺酰基)氮化锂(LiTFSI)。由于高离子传输能力的贡献,KT@SPE的多氢键网络结构的构建以及控制二甲基亚砜(DMSO)溶剂残留在界面上的润湿性,组装的对称锂电池在0.15 mA cm−2下实现了2000 h以上的稳定循环。此外,LiFePO4电池在5C下实现了稳定的长周期,并使Li/KT@SPE3/LiFe0.6Mn0.4PO4电池在4.4 V下工作。这项工作不仅为制备新型固体聚合物电解质提供了设计策略,而且展示了脂肪族酮基聚合物电解质在高电流密度和高电压下在固态锂电池中的良好应用潜力。
期刊介绍:
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