4.8 Article

Unraveling the Role of Neutral Units for Single-Ion Conducting Polymer Electrolytes

期刊

ACS APPLIED MATERIALS & INTERFACES
卷 13, 期 43, 页码 51525-51534

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsami.1c15641

关键词

single-ion conducting; polymer electrolyte; polyethylene oxide (PEO); Coulombic interaction; activation energy

资金

  1. U.S. Department of Energy, Office of Science, Basic Energy Sciences, Materials Science and Engineering Division
  2. DOE's Scientific User Facilities Division
  3. [NIH P41-GM103311]

向作者/读者索取更多资源

Single-ion conducting polymer electrolytes (SICPEs) are considered an advanced electrolyte system with high energy efficiency for battery applications, but their relatively low ionic conductivity remains a major bottleneck. Polyethylene oxide (PEO) is recognized as a benchmark for solid polymer electrolytes due to its high salt solubility and reasonable ionic conductivity.
With the cationic transference number close to unity, single-ion conducting polymer electrolytes (SICPEs) are recognized as an advanced electrolyte system with improved energy efficiency for battery application. The relatively low ionic conductivity for most of the SICPEs in comparison with liquid electrolytes remains the major bottleneck for their practical applications. Polyethylene oxide (PEO) has been recognized as a benchmark for solid polymer electrolytes due to its high salt solubility and reasonable ionic conductivity. PEO has two advantages: (i) the polar ether groups coordinate well with lithium ions (Li+) providing good dissociation from anions, and (ii) the low T-g provides fast segmental dynamics at ambient temperature and assists rapid charge transport. These properties lead to active use of PEO as neutral plasticizing units in SICPEs. Herein, we present a detailed comparison of new SICPEs copolymerized with PEO units vs SICPEs copolymerized with other types of neutral units possessing either flexible or polar structures. The presented analysis revealed that the polarity of side chains has a limited influence on ion dissociation for copolymer-type SICPEs. The Li+-ion dissociation seems to be controlled by the charge delocalization on the polymerized anion. With good miscibility between plasticizing neutral units and ionic conductive units, the ambient ionic conductivity of synthesized SICPEs is still mainly controlled by the T-g of the copolymer. This work sheds light on the dominating role of PEO in SICPE systems and provides helpful guidance for designing polymer electrolytes with new functionalities and structures. Furthermore, based on the presented results, we propose that designing polyanions with a highly delocalized charge may be another promising route for achieving sufficient lithium ionic conductivity in solvent-free SICPEs.

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