4.7 Article

Carbonyl-Containing Solid Polymer Electrolyte Host Materials: Conduction and Coordination in Polyketone, Polyester, and Polycarbonate Systems

期刊

MACROMOLECULES
卷 55, 期 24, 页码 10940-10949

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acs.macromol.2c01683

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资金

  1. ECO 2 LIB (European Union H2020 research and innovation programme) [875514]
  2. ERC [771777]
  3. Swedish Foundation for Strategic Research (project SOLID ALIBI) [139501338]
  4. Swedish Foundation for International Cooperation in Research and Higher Education (STINT)
  5. Swedish Research Council (VR) [MG2019-8467]
  6. STandUP for Energy
  7. European Research Council (ERC) [771777] Funding Source: European Research Council (ERC)

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This study compares the properties of solid polymer electrolytes (SPEs) of three different carbonyl-containing polymers. Experimental measurements and molecular dynamics simulations reveal the influence of the polymer structure on ion transport and the possibility of achieving desired transport properties by fine-tuning the polymer chemistry.
Research on solid polymer electrolytes (SPEs) is now moving beyond the realm of polyethers that have dominated the field for several decades. A promising alternative group of candidates for SPE host materials is carbonyl-containing polymers. In this work, SPE properties of three different types of carbonyl-coordinating polymers are compared: polycarbonates, polyesters, and polyketones. The investigated polymers were chosen to be as structurally similar as possible, with only the functional group being different, thereby giving direct insights into the role of the noncoordinating main-chain oxygens. As revealed by experimental measurements as well as molecular dynamics simulations, the polyketone possesses the lowest glass transition temperature, but the ion transport is limited by a high degree of crystallinity. The polycarbonate, on the other hand, displays a relatively low coordination strength but is instead limited by its low molecular flexibility. The polyester performs generally as an intermediate between the other two, which is reasonable when considering its structural relation to the alternatives. This work demonstrates that local changes in the coordinating environment of carbonyl-containing polymers can have a large effect on the overall ion conduction, thereby also showing that desired transport properties can be achieved by fine-tuning the polymer chemistry of carbonyl-containing systems.

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