Improved ionic conductivity for amide-containing electrolytes by tuning intermolecular interaction: the effect of branched side-chains with cyanoethoxy groups

التفاصيل البيبلوغرافية
العنوان: Improved ionic conductivity for amide-containing electrolytes by tuning intermolecular interaction: the effect of branched side-chains with cyanoethoxy groups
المؤلفون: Koki Yamada, Shohei Yuasa, Hiromori Tsutsumi, Yu Katayama, Ryansu Sai, Riho Matsuoka
المصدر: Physical chemistry chemical physics : PCCP. 23(16)
سنة النشر: 2021
مصطلحات موضوعية: Steric effects, chemistry.chemical_classification, Materials science, Hydrogen bond, Intermolecular force, General Physics and Astronomy, chemistry.chemical_element, 02 engineering and technology, Polymer, Electrolyte, 010402 general chemistry, 021001 nanoscience & nanotechnology, 01 natural sciences, 0104 chemical sciences, chemistry, Side chain, Physical chemistry, Ionic conductivity, Lithium, Physical and Theoretical Chemistry, 0210 nano-technology
الوصف: Polymeric materials are considered as promising electrolytes for all-solid-state secondary lithium batteries with superior energy and power densities, long cycle lives, and high safety. To further improve the ionic conductivity of polymer electrolytes, the development of a simple and efficient method that enables precise tuning of the three key factors, polymer segmental dynamics, Li+ coordination structure, and salt dissociability, is desired. In this study, we focus on an amidation reaction, which is a simple reaction with broad applicability, to explore the impact of the side-chain structure on the intermolecular interactions within the polymer, which dictates the aforementioned key factors. We synthesized a series of polyoxetane-based polymers having different branched side-chains, i.e., methyl (PtBuOA) and bulky cyanoethoxy (P3CEOA) groups, via amidation reaction. Spectro(electro)chemical analysis verified that the large steric hindrance of the cyanoethoxy side-chain effectively breaks the hydrogen bond network and dipole interaction within the polymer, both of which decrease the polymer segmental mobility, leading to better long-range Li+ conduction. Furthermore, the unique Li+ coordination structure consisting of a cyano group, ether/carboxyl oxygen, and TFSA anion in P3CEOA electrolytes has moderate stability, which effectively promotes the short-range Li+ conduction. The amide group, with a relatively high dielectric constant, improves the dissociability of lithium salt. We confirmed a more than three orders of magnitude improvement in ionic conductivity by introducing the cyanoethoxy side-chain, than that obtained by introducing the PtBuOA electrolyte with a methyl side-chain. This work provides a holistic picture of the effect of the side-chain structure on the intermolecular interaction and establishes the new design strategy for polymer electrolytes, which enables the precise tuning of the molecular interaction using the side-chain structure.
تدمد: 1463-9084
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aaa3eceaad30fedca2cbf87cce84a9ab
https://pubmed.ncbi.nlm.nih.gov/33871005
حقوق: CLOSED
رقم الأكسشن: edsair.doi.dedup.....aaa3eceaad30fedca2cbf87cce84a9ab
قاعدة البيانات: OpenAIRE