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The Materials Map is an open tool for improving networking and interdisciplinary exchange within materials research. It enables cross-database search for cooperation and network partners and discovering of the research landscape.

The dashboard provides detailed information about the selected scientist, e.g. publications. The dashboard can be filtered and shows the relationship to co-authors in different diagrams. In addition, a link is provided to find contact information.

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The Materials Map is still under development. In its current state, it is only based on one single data source and, thus, incomplete and contains duplicates. We are working on incorporating new open data sources like ORCID to improve the quality and the timeliness of our data. We will update Materials Map as soon as possible and kindly ask for your patience.

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in Cooperation with on an Cooperation-Score of 37%

Topics

Publications (1/1 displayed)

  • 2023Ion transport, mechanical properties and relaxation dynamics in structural battery electrolytes consisting of an imidazolium protic ionic liquid confined into a methacrylate polymer8citations

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Chart of shared publication
Pipertzis, Achilleas
1 / 2 shared
Xu, Johanna
1 / 4 shared
Swenson, Jan
1 / 3 shared
Asp, Leif E.
1 / 13 shared
Martinelli, Anna
1 / 4 shared
Chart of publication period
2023

Co-Authors (by relevance)

  • Pipertzis, Achilleas
  • Xu, Johanna
  • Swenson, Jan
  • Asp, Leif E.
  • Martinelli, Anna
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article

Ion transport, mechanical properties and relaxation dynamics in structural battery electrolytes consisting of an imidazolium protic ionic liquid confined into a methacrylate polymer

  • Pipertzis, Achilleas
  • Xu, Johanna
  • Swenson, Jan
  • Asp, Leif E.
  • Martinelli, Anna
  • Abdou, Nicole
Abstract

<jats:p>The effect of confining a liquid electrolyte into a polymer matrix was studied by means of Raman spectroscopy, differential scanning calorimetry, temperature-modulated differential scanning calorimetry, dielectric spectroscopy, and rheology. The polymer matrix was obtained from thermal curing ethoxylated bisphenol A dimethacrylate while the liquid electrolyte consisted of a protic ionic liquid based on the ethyl-imidazolium cation [C2HIm] and the bis(trifluoromethanesulfonyl)imide [TFSI] anion, doped with LiTFSI salt. We report that the confined liquid phase exhibits the following characteristics: (i) a distinctly reduced degree of crystallinity; (ii) a broader distribution of relaxation times; (iii) reduced dielectric strength; (iv) a reduced cooperativity length scale at the liquid-to-glass transition temperature (T g); and (v) up-speeded local T g-related ion dynamics. The latter is indicative of weak interfacial interactions between the two nanophases and a strong geometrical confinement effect, which dictates both the ion dynamics and the coupled structural relaxation, hence lowering Tg by about 4 K. We also find that at room temperature, the ionic conductivity of the structural electrolyte achieves a value of 0.13 mS/cm,one decade lower than the corresponding bulk electrolyte. Three mobile ions (Im+, TFSI-, and Li+) contribute to the measured ionic conductivity, implicitly reducing the Li+ transference number. In addition, we report that the investigated solid polymer electrolytes exhibit the shear modulus needed for transferring the mechanical load to the carbon fibers in a structural battery. Based on these findings, we conclude that optimized microphase-separated polymer electrolytes, including a protic ionic liquid, are promising for the development of novel multifunctional electrolytes for use in future structural batteries. </jats:p>

Topics
  • impedance spectroscopy
  • polymer
  • Carbon
  • glass
  • glass
  • strength
  • mass spectrometry
  • thermogravimetry
  • glass transition temperature
  • differential scanning calorimetry
  • interfacial
  • Raman spectroscopy
  • crystallinity
  • liquid phase
  • dielectric strength
  • thermal curing