4.8 Article

Intrinsic Ion Transport Properties of Block Copolymer Electrolytes

Journal

ACS NANO
Volume 14, Issue 7, Pages 8902-8914

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsnano.0c03713

Keywords

polymer electrolyte; block copolymer; ionic conductivity; lithium ion battery; nanomaterials

Funding

  1. U.S. Department of Energy (DOE), Basic Energy Sciences, Materials Sciences and Engineering Division
  2. Soft and Hybrid Nanotechnology Experimental (SHyNE) Resource, a node of the National Science Foundation's National Nanotechnology Coordinated Infrastructure [NSF ECCS-1542205]
  3. NSF [DMR-1420709]

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Knowledge of intrinsic properties is of central importance for materials design and assessing suitability for specific applications. Self-assembling block copolymer electrolytes (BCEs) are of great interest for applications in solid-state energy storage devices. A fundamental understanding of ion transport properties, however, is hindered by the difficulty in deconvoluting extrinsic factors, such as defects, from intrinsic factors, such as the presence of interfaces between the domains. Here, we quantify the intrinsic ion transport properties of a model BCE system consisting of poly(styrene-block-ethylene oxide) (SEO) and lithium bis(trifluoromethanesulfonyl)imide (LiTFSI) salt using a generalizable strategy of depositing thin films on interdigitated electrodes and self-assembling fully connected parallel lamellar structures throughout the films. Comparison between conductivity in homopolymer poly(ethylene oxide) (PEO)-LiTFSI electrolytes and the analogous conducting material in SEO over a range of salt concentrations (r, molar ratio of lithium ion to ethylene oxide repeat units) and temperatures reveals that between 20% and 50% of the PEO in SEO is inactive. Using mean-field theory calculations of the domain structure and monomer concentration profiles at domain interfaces-both of which vary substantially with salt concentration-the fraction of inactive PEO in the SEO, as derived from conductivity measurements, can be quantitatively reconciled with the fraction of PEO that is mixed with greater than a few volume percent of polystyrene. Despite the detrimental interfacial effects for ion transport in BCEs, the intrinsic conductivity of the SEO studied here (ca. 10(-3) S/cm at 90 degrees C, r = 0.085) is an order of magnitude higher than reported values from bulk samples of similar molecular weight SEO (ca. 10(-4) S/cm at 90 degrees C, r = 0.085). Overall, this work provides motivation and methods for pursuing improved BCE chemical design, interfacial engineering, and processing.

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