{"title":"Ionic-conductive poly (vinylidene fluoride) polymer as a versatile binder to stabilize high-voltage LiCoO2 cathode materials","authors":"Yikui Wang, Jianming Tao, Jiangjie Wang, Shaoyang Chen, Yanmin Yang, Yingbin Lin","doi":"10.1007/s10832-024-00364-y","DOIUrl":null,"url":null,"abstract":"<div><p>Serious structural irreversibility and interfacial side reactions pose major challenges for the stable operation of LiCoO<sub>2</sub> cathodes at high voltages. Herein, we report a polymer-based solid electrolyte (SLP) composed succinonitrile, LiTFSI and PVDF as a binder to address these issues. The SLP binder exhibits superior performance compared to traditional PVDF and PVDF binders with LiTFSI, with higher ionic conductivity (8.46 × 10<sup>− 5</sup> S cm<sup>− 1</sup> at 30 ℃), lower activation energy of 0.38 eV and excellent adhesion. Even with just 3% SLP binder, LiCoO<sub>2</sub> cathode operating at a cutoff voltage of 4.6 V and loaded with ~ 6.0 mg cm<sup>− 2</sup> active material demonstrates improved rate capability at higher compaction densities, delivering a discharge specific capacity of 146.5 mAh g<sup>− 1</sup> after 100 cycles at 0.5 C-rate. The SLP binder not only enhances Li<sup>+</sup> conduction but also facilitates the formation of a stable cathode-electrolyte interphase, thus reducing the Li<sup>+</sup> diffusion barrier and interface polarization, and enhancing battery’s performance at low temperature. Furthermore, the SPL binder’s high compatibility and elasticity with the electrolyte mitigate irreversible structural changes and volume expansion in LiCoO<sub>2</sub> during cycling, leading to better preservation of the layered structure and lower internal stress for stable cycling under high temperatures. This strategy provides a novel interface protection idea for electroceramic cathode materials and may facilitate commercial development.</p></div>","PeriodicalId":625,"journal":{"name":"Journal of Electroceramics","volume":"52 4","pages":"303 - 313"},"PeriodicalIF":1.7000,"publicationDate":"2024-09-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Electroceramics","FirstCategoryId":"88","ListUrlMain":"https://link.springer.com/article/10.1007/s10832-024-00364-y","RegionNum":4,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"MATERIALS SCIENCE, CERAMICS","Score":null,"Total":0}
引用次数: 0
Abstract
Serious structural irreversibility and interfacial side reactions pose major challenges for the stable operation of LiCoO2 cathodes at high voltages. Herein, we report a polymer-based solid electrolyte (SLP) composed succinonitrile, LiTFSI and PVDF as a binder to address these issues. The SLP binder exhibits superior performance compared to traditional PVDF and PVDF binders with LiTFSI, with higher ionic conductivity (8.46 × 10− 5 S cm− 1 at 30 ℃), lower activation energy of 0.38 eV and excellent adhesion. Even with just 3% SLP binder, LiCoO2 cathode operating at a cutoff voltage of 4.6 V and loaded with ~ 6.0 mg cm− 2 active material demonstrates improved rate capability at higher compaction densities, delivering a discharge specific capacity of 146.5 mAh g− 1 after 100 cycles at 0.5 C-rate. The SLP binder not only enhances Li+ conduction but also facilitates the formation of a stable cathode-electrolyte interphase, thus reducing the Li+ diffusion barrier and interface polarization, and enhancing battery’s performance at low temperature. Furthermore, the SPL binder’s high compatibility and elasticity with the electrolyte mitigate irreversible structural changes and volume expansion in LiCoO2 during cycling, leading to better preservation of the layered structure and lower internal stress for stable cycling under high temperatures. This strategy provides a novel interface protection idea for electroceramic cathode materials and may facilitate commercial development.
严重的结构不可逆性和界面副反应是LiCoO2阴极在高压下稳定工作的主要挑战。在此,我们报道了一种由丁二腈、LiTFSI和PVDF组成的聚合物基固体电解质(SLP)作为粘合剂来解决这些问题。与传统PVDF和含LiTFSI的PVDF粘结剂相比,SLP粘结剂具有更高的离子电导率(30℃时为8.46 × 10−5 S cm−1)、更低的活化能(0.38 eV)和优异的附着力。即使只有3%的SLP粘结剂,LiCoO2阴极在4.6 V的截止电压下工作,并加载了~ 6.0 mg cm - 2活性材料,在更高的压实密度下表现出更高的倍率能力,在0.5 C-rate下循环100次后,放电比容量达到146.5 mAh g - 1。SLP粘结剂不仅增强了Li+的导电性,而且有利于形成稳定的阴极-电解质界面相,从而减少Li+的扩散势垒和界面极化,提高电池的低温性能。此外,SPL粘合剂与电解质的高相容性和弹性减轻了循环过程中LiCoO2中不可逆的结构变化和体积膨胀,从而更好地保留了层状结构,降低了高温下稳定循环的内应力。该策略为电陶瓷正极材料提供了一种新的界面保护思路,有利于商业化开发。
期刊介绍:
While ceramics have traditionally been admired for their mechanical, chemical and thermal stability, their unique electrical, optical and magnetic properties have become of increasing importance in many key technologies including communications, energy conversion and storage, electronics and automation. Electroceramics benefit greatly from their versatility in properties including:
-insulating to metallic and fast ion conductivity
-piezo-, ferro-, and pyro-electricity
-electro- and nonlinear optical properties
-feromagnetism.
When combined with thermal, mechanical, and chemical stability, these properties often render them the materials of choice.
The Journal of Electroceramics is dedicated to providing a forum of discussion cutting across issues in electrical, optical, and magnetic ceramics. Driven by the need for miniaturization, cost, and enhanced functionality, the field of electroceramics is growing rapidly in many new directions. The Journal encourages discussions of resultant trends concerning silicon-electroceramic integration, nanotechnology, ceramic-polymer composites, grain boundary and defect engineering, etc.