{"title":"Factors determining the Li+ conductivity in high-performance PVDF-based composite electrolytes revealed by solid-state NMR","authors":"Vestince Balidi Mbayachi , Lixin Liang , Bao Zhang , Yaru Zhang , Guiming Zhong , Kuizhi Chen , Guangjin Hou","doi":"10.1016/j.jechem.2025.06.051","DOIUrl":null,"url":null,"abstract":"<div><div>Composite polymer electrolytes (CPEs) are considered as promising electrolytes for next-generation lithium batteries due to their superior advantages in safety, mechanical stability/flexibility, cathode compatibility, etc. However, achieving high Li<sup>+</sup> conductivity remains a major challenge, particularly at low temperatures. A key obstacle lies in the limited understanding of the complex interplay among amorphous components, including fillers, plasticizers, and residual solvents, which significantly hampers the rational design of high-performing CPEs. In this contribution, a polyvinylidene fluoride (PVDF)-based composite electrolyte has been developed, exhibiting high room-temperature ionic conductivity/mobility (>1 mS cm<sup>−1</sup>/0.95 × 10<sup>−11</sup> m<sup>2</sup> s<sup>−1</sup>), along with excellent electrochemical performances, including a wide stability window (4.8 V vs. Li/Li<sup>+</sup>), superior charge/discharge capacity, and reversibility. By performing advanced solid-state nuclear magnetic resonance (ssNMR) techniques, in combination with systematic investigations into solid polymer electrolytes (SPEs), gel polymer electrolytes (GPEs), and CPEs, we establish an efficient NMR-based strategy for deconvoluting the structural and dynamic features of complex electrolyte systems. Notably, the simple <sup>1</sup>H magic-angle spinning (MAS) NMR spectroscopy enables the identification and monitoring of nearly all components in the composite matrix. Motion-sensitive <sup>1</sup>H-<sup>13</sup>C and <sup>1</sup>H-<sup>7</sup>Li correlation experiments further reveal that the rigidity of PVDF polymer chain segments and the presence of residual solvents are two critical factors governing Li<sup>+</sup> mobility. Moreover, we demonstrate that the order of the filler and plasticizer addition during the CPE fabrication significantly influences the performance of the electrolyte by regulating the retention of residual solvents. This work not only provides molecular-level insights into the structure-ion mobility relationships in the PVDF-based CPEs but also establishes a general NMR-based characterization approach for investigating other complex composite electrolyte materials.</div></div>","PeriodicalId":15728,"journal":{"name":"Journal of Energy Chemistry","volume":"110 ","pages":"Pages 165-175"},"PeriodicalIF":14.9000,"publicationDate":"2025-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Energy Chemistry","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2095495625005261","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"Energy","Score":null,"Total":0}
引用次数: 0
Abstract
Composite polymer electrolytes (CPEs) are considered as promising electrolytes for next-generation lithium batteries due to their superior advantages in safety, mechanical stability/flexibility, cathode compatibility, etc. However, achieving high Li+ conductivity remains a major challenge, particularly at low temperatures. A key obstacle lies in the limited understanding of the complex interplay among amorphous components, including fillers, plasticizers, and residual solvents, which significantly hampers the rational design of high-performing CPEs. In this contribution, a polyvinylidene fluoride (PVDF)-based composite electrolyte has been developed, exhibiting high room-temperature ionic conductivity/mobility (>1 mS cm−1/0.95 × 10−11 m2 s−1), along with excellent electrochemical performances, including a wide stability window (4.8 V vs. Li/Li+), superior charge/discharge capacity, and reversibility. By performing advanced solid-state nuclear magnetic resonance (ssNMR) techniques, in combination with systematic investigations into solid polymer electrolytes (SPEs), gel polymer electrolytes (GPEs), and CPEs, we establish an efficient NMR-based strategy for deconvoluting the structural and dynamic features of complex electrolyte systems. Notably, the simple 1H magic-angle spinning (MAS) NMR spectroscopy enables the identification and monitoring of nearly all components in the composite matrix. Motion-sensitive 1H-13C and 1H-7Li correlation experiments further reveal that the rigidity of PVDF polymer chain segments and the presence of residual solvents are two critical factors governing Li+ mobility. Moreover, we demonstrate that the order of the filler and plasticizer addition during the CPE fabrication significantly influences the performance of the electrolyte by regulating the retention of residual solvents. This work not only provides molecular-level insights into the structure-ion mobility relationships in the PVDF-based CPEs but also establishes a general NMR-based characterization approach for investigating other complex composite electrolyte materials.
复合聚合物电解质(cpe)由于其在安全性、机械稳定性/柔韧性、阴极兼容性等方面的优越优势,被认为是下一代锂电池极具发展前景的电解质。然而,实现高Li+导电性仍然是主要挑战,特别是在低温下。一个关键的障碍在于对非晶组分(包括填料、增塑剂和残留溶剂)之间复杂的相互作用的理解有限,这极大地阻碍了高性能cpe的合理设计。在这项贡献中,开发了一种基于聚偏氟乙烯(PVDF)的复合电解质,具有高室温离子电导率/迁移率(>1 mS cm−1/0.95 × 10−11 m2 s−1),以及优异的电化学性能,包括宽稳定窗口(4.8 V vs. Li/Li+),优越的充放电容量和可逆性。通过执行先进的固态核磁共振(ssNMR)技术,结合对固体聚合物电解质(spe),凝胶聚合物电解质(GPEs)和cpe的系统研究,我们建立了一种有效的基于核磁共振的策略来解卷积复杂电解质系统的结构和动态特征。值得注意的是,简单的1H魔角旋转(MAS)核磁共振波谱可以识别和监测复合基体中的几乎所有成分。运动敏感1H-13C和1H-7Li相关实验进一步揭示了PVDF聚合物链段的刚性和残留溶剂的存在是影响Li+迁移率的两个关键因素。此外,我们还证明了在CPE制造过程中,填料和增塑剂的添加顺序通过调节残余溶剂的保留来显著影响电解质的性能。这项工作不仅为基于pvdf的cpe的结构-离子迁移关系提供了分子水平的见解,而且为研究其他复杂的复合电解质材料建立了一种通用的基于核磁共振的表征方法。
期刊介绍:
The Journal of Energy Chemistry, the official publication of Science Press and the Dalian Institute of Chemical Physics, Chinese Academy of Sciences, serves as a platform for reporting creative research and innovative applications in energy chemistry. It mainly reports on creative researches and innovative applications of chemical conversions of fossil energy, carbon dioxide, electrochemical energy and hydrogen energy, as well as the conversions of biomass and solar energy related with chemical issues to promote academic exchanges in the field of energy chemistry and to accelerate the exploration, research and development of energy science and technologies.
This journal focuses on original research papers covering various topics within energy chemistry worldwide, including:
Optimized utilization of fossil energy
Hydrogen energy
Conversion and storage of electrochemical energy
Capture, storage, and chemical conversion of carbon dioxide
Materials and nanotechnologies for energy conversion and storage
Chemistry in biomass conversion
Chemistry in the utilization of solar energy