Tao Chen , Yuncong Liu , Zhekai Jin , Lin Sun , Zeyu Liu , Hao Xu , Zhiguo Zhao , Chao Wang
{"title":"用于高压锂电池的离子-偶极相互作用调节的固体聚合物电解质","authors":"Tao Chen , Yuncong Liu , Zhekai Jin , Lin Sun , Zeyu Liu , Hao Xu , Zhiguo Zhao , Chao Wang","doi":"10.1016/j.giant.2024.100310","DOIUrl":null,"url":null,"abstract":"<div><p>Solid polymer electrolytes (SPEs) with wide electrochemically stable window and high lithium-ion transference number (<em>t</em><sub>Li</sub><sup>+</sup>) are a requirement for high energy density lithium batteries. Here, we construct a copolymer electrolyte (PDA) with ether-ester bifunctional groups that exhibits a low highest occupied molecular orbital (HOMO) energy level by in situ polymerization. Compared to the poly(1,3-dioxolane) (PDOL) pure polyether electrolyte, the weakening of the ion-dipole interaction between lithium salt and polymer in the PDA electrolyte promotes the formation of a “weak solvation” structure. Therefore, the electrolyte achieves high oxidative stability (4.6 V vs. Li<sup>+</sup>/ Li with a standard leakage current of 10 μA), high Li<sup>+</sup> transference number (0.60), and importantly, derives a stable LiF-rich composition on high voltage cathode surface. Which ultimately enables stable cycling of Li||LiNi<sub>0.5</sub>Co<sub>0.2</sub>Mn<sub>0.3</sub>O<sub>2</sub> (NCM523) batteries at a range of 3.0–4.3 V. This work provides a fundamental understanding of the design of antioxidant SPEs to achieve high energy density lithium batteries.</p></div>","PeriodicalId":34151,"journal":{"name":"GIANT","volume":"19 ","pages":"Article 100310"},"PeriodicalIF":5.4000,"publicationDate":"2024-06-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2666542524000742/pdfft?md5=0b58813171e1903c1cecfea29f9abfdb&pid=1-s2.0-S2666542524000742-main.pdf","citationCount":"0","resultStr":"{\"title\":\"Solid polymer electrolytes regulated by ion-dipole interactions for high voltage lithium batteries\",\"authors\":\"Tao Chen , Yuncong Liu , Zhekai Jin , Lin Sun , Zeyu Liu , Hao Xu , Zhiguo Zhao , Chao Wang\",\"doi\":\"10.1016/j.giant.2024.100310\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>Solid polymer electrolytes (SPEs) with wide electrochemically stable window and high lithium-ion transference number (<em>t</em><sub>Li</sub><sup>+</sup>) are a requirement for high energy density lithium batteries. Here, we construct a copolymer electrolyte (PDA) with ether-ester bifunctional groups that exhibits a low highest occupied molecular orbital (HOMO) energy level by in situ polymerization. Compared to the poly(1,3-dioxolane) (PDOL) pure polyether electrolyte, the weakening of the ion-dipole interaction between lithium salt and polymer in the PDA electrolyte promotes the formation of a “weak solvation” structure. Therefore, the electrolyte achieves high oxidative stability (4.6 V vs. Li<sup>+</sup>/ Li with a standard leakage current of 10 μA), high Li<sup>+</sup> transference number (0.60), and importantly, derives a stable LiF-rich composition on high voltage cathode surface. Which ultimately enables stable cycling of Li||LiNi<sub>0.5</sub>Co<sub>0.2</sub>Mn<sub>0.3</sub>O<sub>2</sub> (NCM523) batteries at a range of 3.0–4.3 V. This work provides a fundamental understanding of the design of antioxidant SPEs to achieve high energy density lithium batteries.</p></div>\",\"PeriodicalId\":34151,\"journal\":{\"name\":\"GIANT\",\"volume\":\"19 \",\"pages\":\"Article 100310\"},\"PeriodicalIF\":5.4000,\"publicationDate\":\"2024-06-19\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.sciencedirect.com/science/article/pii/S2666542524000742/pdfft?md5=0b58813171e1903c1cecfea29f9abfdb&pid=1-s2.0-S2666542524000742-main.pdf\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"GIANT\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2666542524000742\",\"RegionNum\":1,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"GIANT","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2666542524000742","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
Solid polymer electrolytes regulated by ion-dipole interactions for high voltage lithium batteries
Solid polymer electrolytes (SPEs) with wide electrochemically stable window and high lithium-ion transference number (tLi+) are a requirement for high energy density lithium batteries. Here, we construct a copolymer electrolyte (PDA) with ether-ester bifunctional groups that exhibits a low highest occupied molecular orbital (HOMO) energy level by in situ polymerization. Compared to the poly(1,3-dioxolane) (PDOL) pure polyether electrolyte, the weakening of the ion-dipole interaction between lithium salt and polymer in the PDA electrolyte promotes the formation of a “weak solvation” structure. Therefore, the electrolyte achieves high oxidative stability (4.6 V vs. Li+/ Li with a standard leakage current of 10 μA), high Li+ transference number (0.60), and importantly, derives a stable LiF-rich composition on high voltage cathode surface. Which ultimately enables stable cycling of Li||LiNi0.5Co0.2Mn0.3O2 (NCM523) batteries at a range of 3.0–4.3 V. This work provides a fundamental understanding of the design of antioxidant SPEs to achieve high energy density lithium batteries.
期刊介绍:
Giant is an interdisciplinary title focusing on fundamental and applied macromolecular science spanning all chemistry, physics, biology, and materials aspects of the field in the broadest sense. Key areas covered include macromolecular chemistry, supramolecular assembly, multiscale and multifunctional materials, organic-inorganic hybrid materials, biophysics, biomimetics and surface science. Core topics range from developments in synthesis, characterisation and assembly towards creating uniformly sized precision macromolecules with tailored properties, to the design and assembly of nanostructured materials in multiple dimensions, and further to the study of smart or living designer materials with tuneable multiscale properties.