Materials Map

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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 (5/5 displayed)

  • 2020Production and processing of graphene and related materials421citations
  • 2020Production and processing of graphene and related materials421citations
  • 2020Production and processing of graphene and related materials421citations
  • 2018The effect of cation chemistry on physicochemical behaviour of superconcentrated NaFSI based ionic liquid electrolytes and the implications for Na battery performance36citations
  • 2009Nanostructure and Impedance Spectroscopy of Pr0.7Sr0.3Mn1-xMxO3 (M = Fe, Co, Ni; x = 0 and 0.2) Thin Films Grown by Pulsed Laser Deposition1citations

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Armand, Michel
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Forsyth, Maria
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Macfarlane, Douglas
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Hilder, Matthias
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Saurel, Damien
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Basile, Andrew
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Howlett, Patrick C.
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Gonzalo, Elena
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Kar, Mega
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Ruiz-De-Larramendi, J. Ignacio
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Co-Authors (by relevance)

  • Armand, Michel
  • Forsyth, Maria
  • Macfarlane, Douglas
  • Hilder, Matthias
  • Saurel, Damien
  • Basile, Andrew
  • Howlett, Patrick C.
  • Gonzalo, Elena
  • Kar, Mega
  • Arriortua, M. Isabel
  • Ruiz-De-Larramendi, J. Ignacio
  • Ruiz-De-Larramendi, Idoia
  • Meatza, Iratxe
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article

The effect of cation chemistry on physicochemical behaviour of superconcentrated NaFSI based ionic liquid electrolytes and the implications for Na battery performance

  • Armand, Michel
  • Forsyth, Maria
  • Macfarlane, Douglas
  • Rojo, Teofilo
  • Hilder, Matthias
  • Saurel, Damien
  • Basile, Andrew
  • Howlett, Patrick C.
  • Gonzalo, Elena
  • Kar, Mega
Abstract

<p>There is growing interest in ionic liquid based electrolytes for Na metal and Na-ion batteries. Here we compare three quite distinct bis(fluorosulfonyl)imide (FSI) anion based ionic liquids with small alkyl phosphonium (trimethyl isobutyl phosphonium, methyl tri-isobutyl: P<sub>111i4</sub>, P<sub>1i4i4i4</sub>) or alkoxy ammonium counter cations (N-ethyl-2-(2-methoxyethoxy)-N,N-bis(2-(2-methoxyethoxy)ethyl)ethan-1-ammonium bis(fluorosulfonyl)imide: N<sub>2(2O2O1)3</sub>) mixed at near 1:1 mol ratio with NaFSI. The conductivities of these electrolytes range from 4.4 mScm<sup>−1</sup> for the smallest P<sub>111i4</sub>FSI:NaFSI system to 0.3 mScm<sup>−1</sup> for the N<sub>2(2O2O1)3</sub>FSI:NaFSI mixture at 50 °C. This difference in conductivity is interestingly not reflected in the cyclic voltammetry for Na/Na<sup>+</sup> where the maximum peak current density of 10 mAcm<sup>−2</sup> is surprisingly high for the poorly conductive N<sub>2(20201)3</sub>FSI:NaFSI solution (e.g. 17 mAcm<sup>−2</sup> for P<sub>111i4</sub>FSI:NaFSI). The overpotentials observed for Na symmetric cell cycling show very little differences after initial stabilising/conditioning for the three electrolytes being 50 mV for P<sub>111i4</sub>FSI:NaFSI and 100 mV for the others (at 0.1 mA cm<sup>−2</sup>). Also the Na<sup>+</sup> transport number is similar for the three electrolytes ranging from 0.33 to 0.37. Full cells were prepared with layered transition metal oxide cathodes: O3-Na<sub>2/3</sub>(Fe<sub>2/3</sub>Mn<sub>1/3</sub>)O<sub>2</sub>), P2-Na<sub>2/3</sub>(Fe<sub>2/3</sub>Mn<sub>1/3</sub>)O<sub>2</sub> and P2-Na<sub>2/3</sub>(Mn<sub>0.8</sub>Fe<sub>0.1</sub>Ti<sub>0.1</sub>)O<sub>2</sub>. While for the O3/P2-Na<sub>2/3</sub>(Fe<sub>2/3</sub>Mn<sub>1/3</sub>)O<sub>2</sub> structures the device performance is consistent with the electrolyte properties, with the P2-Na<sub>2/3</sub>(Mn<sub>0.8</sub>Fe<sub>0.1</sub>Ti<sub>0.1</sub>)O<sub>2</sub> cathode the N<sub>2(2O2O1)3</sub>FSI:NaFSI electrolyte cycling extremely well. The P<sub>111i4</sub>FSI and N<sub>2(2O2O1)3</sub>FSI yield almost equivalent specific capacities of approximately 180 and 160 mAhg<sup>−1</sup> respectively at C/10 rate.</p>

Topics
  • density
  • impedance spectroscopy
  • layered
  • current density
  • cyclic voltammetry