Materials Map

Discover the materials research landscape. Find experts, partners, networks.

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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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Topics

Publications (1/1 displayed)

  • 2016Novel Na+ ion diffusion mechanism in mixed organic-inorganic ionic liquid electrolyte leading to high Na+ transference number and stable, high rate electrochemical cycling of sodium cells241citations

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Chart of shared publication
Armand, Michel
1 / 15 shared
Forsyth, Maria
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Zhu, Haijin
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Macfarlane, Douglas
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Howlett, Patrick
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Chen, Fangfang
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2016

Co-Authors (by relevance)

  • Armand, Michel
  • Forsyth, Maria
  • Zhu, Haijin
  • Macfarlane, Douglas
  • Howlett, Patrick
  • Chen, Fangfang
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article

Novel Na+ ion diffusion mechanism in mixed organic-inorganic ionic liquid electrolyte leading to high Na+ transference number and stable, high rate electrochemical cycling of sodium cells

  • Armand, Michel
  • Forsyth, Maria
  • Yoon, Hyungook
  • Zhu, Haijin
  • Macfarlane, Douglas
  • Howlett, Patrick
  • Chen, Fangfang
Abstract

<p>Ambient temperature sodium batteries hold the promise of a new generation of high energy density, low-cost energy storage technologies. Particularly challenging in sodium electrochemistry is achieving high stability at high charge/discharge rates. We report here mixtures of inorganic/organic cation fluorosulfonamide (FSI) ionic liquids that exhibit unexpectedly high Na<sup>+</sup> transference numbers due to a structural diffusion mechanism not previously observed in this type of electrolyte. The electrolyte can therefore support high current density cycling of sodium. We investigate the effect of NaFSI salt concentration in methylpropylpyrrolidinium (C<sub>3</sub>mpyr) FSI ionic liquid (IL) on the reversible plating and dissolution of sodium metal, both on a copper electrode and in a symmetric Na/Na metal cell. NaFSI is highly soluble in the IL allowing the preparation of mixtures that contain very high Na contents, greater than 3.2 mol/kg (50 mol %) at room temperature. Despite the fact that overall ion diffusivity decreases substantially with increasing alkali salt concentration, we have found that these high Na<sup>+</sup> content electrolytes can support higher current densities (1 mA/cm<sup>2</sup>) and greater stability upon continued cycling. EIS measurements indicate that the interfacial impedance is decreased in the high concentration systems, which provides for a particularly low-resistance solid-electrolyte interphase (SEI), resulting in faster charge transfer at the interface. Na<sup>+</sup> transference numbers determined by the Bruce-Vincent method increased substantially with increasing NaFSI content, approaching &gt;0.3 at the saturation concentration limit which may explain the improved performance. NMR spectroscopy, PFG diffusion measurements, and molecular dynamics simulations reveal a changeover to a facile structural diffusion mechanism for sodium ion transport at high concentrations in these electrolytes.</p>

Topics
  • density
  • energy density
  • simulation
  • molecular dynamics
  • Sodium
  • copper
  • electrochemical-induced impedance spectroscopy
  • current density
  • interfacial
  • diffusivity
  • Nuclear Magnetic Resonance spectroscopy