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  • 1.
    Farhat, Douaa
    et al.
    Univ Francois Rabelais Tours, UFR Sci & Tech, Lab PCM2E, EA 6296, Parc Grandmont, F-37200 Tours, France.
    Maibach, Julia
    Uppsala University, Disciplinary Domain of Science and Technology, Chemistry, Department of Chemistry - Ångström, Structural Chemistry.
    Eriksson, Henrik
    Uppsala University, Disciplinary Domain of Science and Technology, Chemistry, Department of Chemistry - Ångström, Structural Chemistry.
    Edström, Kristina
    Uppsala University, Disciplinary Domain of Science and Technology, Chemistry, Department of Chemistry - Ångström, Structural Chemistry.
    Lemordant, Daniel
    Univ Francois Rabelais Tours, UFR Sci & Tech, Lab PCM2E, EA 6296, Parc Grandmont, F-37200 Tours, France.
    Ghamouss, Fouad
    Univ Francois Rabelais Tours, UFR Sci & Tech, Lab PCM2E, EA 6296, Parc Grandmont, F-37200 Tours, France.
    Towards high-voltage Li-ion batteries: Reversible cycling of graphite anodes and Li-ion batteries in adiponitrile-based electrolytes2018In: Electrochimica Acta, ISSN 0013-4686, E-ISSN 1873-3859, Vol. 281, p. 299-311Article in journal (Refereed)
    Abstract [en]

    Due to their low vapor pressure and their promising electrochemical and thermal stability, N C- (CH2)n-C N dinitriles are proposed as an electrolyte solvent for Li-ion batteries. Adiponitrile (ADN) has substantial advantages, especially for applications requiring high potential cathodes, because it has high electrochemical/thermal stability (up to 6 V vs. Li/Li+, > 120 degrees C). However, to obtain very high voltage batteries, ADN electrolytes must also passivate the anode of the battery. In this work, reversible cycling of graphite in adiponitrile was successfully achieved by adding a few percent of fluoroethylene carbonate allowing the realization of Graphite/NMC Li-ion battery. The battery of specific capacity of 135 mAhh.g(-1) showed a cycling stability for more than 40 cycles. The composition of the solid electrolyte interphase (SEI) was determined as a function of the FEC concentration as well as the state of charge of the graphite anode using hard X-ray photoelectron spectroscopy (HAXPES) and XPS. With FEC, the SEI layer is thinner and depends on the SOC of the anode, but does not depend on the FEC concentration. SEM characterizations clearly showed that the surface of the anode is completely covered by the SEI layer, regardless of the concentration of FEC. Indeed, 2% of FEC is sufficient to suppress the reduction of adiponitrile which is explained by a specific adsorption of FEC on the graphite anode.

  • 2.
    Maibach, Julia
    et al.
    Uppsala University, Disciplinary Domain of Science and Technology, Chemistry, Department of Chemistry - Ångström, Structural Chemistry.
    Lindgren, Fredrik
    Uppsala University, Disciplinary Domain of Science and Technology, Chemistry, Department of Chemistry - Ångström, Structural Chemistry.
    Eriksson, Henrik
    Uppsala University, Disciplinary Domain of Science and Technology, Chemistry, Department of Chemistry - Ångström, Structural Chemistry.
    Edström, Kristina
    Uppsala University, Disciplinary Domain of Science and Technology, Chemistry, Department of Chemistry - Ångström, Structural Chemistry.
    Hahlin, Maria
    Uppsala University, Disciplinary Domain of Science and Technology, Physics, Department of Physics and Astronomy, Molecular and Condensed Matter Physics.
    Electric potential gradient at the buried interface between Lithium-ion battery electrodes and the SEI observed using photoelectron spectroscopy2016In: Journal of Physical Chemistry Letters, ISSN 1948-7185, E-ISSN 1948-7185, Vol. 7, no 10, p. 1775-1780Article in journal (Refereed)
    Abstract [en]

    The buried interface between the bulk electrode material and the solid electrolyte interphase (SEI) in cycled Li-ion battery anodes is suggested to incorporate an electric potential gradient. This suggestion is based on photoelectron spectroscopy (PES) results from different anode materials that all show relative binding energy shifts between the components of the SEI and the active anode. Implications of this electric potential gradient on binding energy reference points in PES as well as on charge-transfer kinetics in Li-ion batteries are discussed. Specifically, we show that the separation of surface layer and bulk material spectral contributions (depth profiling) is crucial for consistent data interpretation. We conclude that previous interpretations of lithiation as cause for changes in PES spectra may need to be revised.

  • 3.
    Valvo, Mario
    et al.
    Uppsala University, Disciplinary Domain of Science and Technology, Chemistry, Department of Chemistry - Ångström, Structural Chemistry.
    Liivat, Anti
    Uppsala University, Disciplinary Domain of Science and Technology, Chemistry, Department of Chemistry - Ångström, Structural Chemistry.
    Eriksson, Henrik
    Uppsala University, Disciplinary Domain of Science and Technology, Chemistry, Department of Chemistry - Ångström, Structural Chemistry.
    Tai, Cheuk-Wai
    Stockholm Univ, Dept Mat & Environm Chem, Arrhenius Lab.
    Edström, Kristina
    Uppsala University, Disciplinary Domain of Science and Technology, Chemistry, Department of Chemistry - Ångström, Structural Chemistry.
    Iron-Based Electrodes Meet Water-Based Preparation, Fluorine-Free Electrolyte and Binder: A Chance for More Sustainable Lithium-Ion Batteries?2017In: ChemSusChem, ISSN 1864-5631, E-ISSN 1864-564X, Vol. 10, no 11, p. 2431-2448Article in journal (Refereed)
    Abstract [en]

    Environmentally friendly and cost-effective Li-ion cells are fabricated with abundant, non-toxic LiFePO4 cathodes and iron oxide anodes. A water-soluble alginate binder is used to coat both electrodes to reduce the environmental footprint. The critical reactivity of LiPF6-based electrolytes toward possible traces of H2O in water-processed electrodes is overcome by using a lithium bis(oxalato) borate (LiBOB) salt. The absence of fluorine in the electrolyte and binder is a cornerstone for improved cell chemistry and results in stable battery operation. A dedicated approach to exploit conversion-type anodes more effectively is also disclosed. The issue of large voltage hysteresis upon conversion/de-conversion is circumvented by operating iron oxide in a deeply lithiated Fe/Li2O form. Li-ion cells with energy efficiencies of up to 92% are demonstrated if LiFePO4 is cycled versus such anodes prepared through a prelithiation procedure. These cells show an average energy efficiency of approximately 90.66% and a mean Coulombic efficiency of approximately 99.65% over 320 cycles at current densities of 0.1, 0.2 and 0.3 mAcm(-2). They retain nearly 100% of their initial discharge capacity and provide an unmatched operation potential of approximately 2.85 V for this combination of active materials. No occurrence of Li plating was detected in three-electrode cells at charging rates of approximately 5C. Excellent rate capabilities of up to approximately 30C are achieved thanks to the exploitation of size effects from the small Fe nanoparticles and their reactive boundaries.

  • 4.
    Valvo, Mario
    et al.
    Uppsala University, Disciplinary Domain of Science and Technology, Chemistry, Department of Chemistry - Ångström, Structural Chemistry.
    Liivat, Anti
    Uppsala University, Disciplinary Domain of Science and Technology, Chemistry, Department of Chemistry - Ångström, Structural Chemistry.
    Eriksson, Henrik
    Uppsala University, Disciplinary Domain of Science and Technology, Chemistry, Department of Chemistry - Ångström, Structural Chemistry.
    Tai, Cheuk-Wai
    Department of Materials and Environmental Chemistry - Arrhenius Laboratory, Stockholm University.
    Edström, Kristina
    Uppsala University, Disciplinary Domain of Science and Technology, Chemistry, Department of Chemistry - Ångström, Structural Chemistry.
    Towards more environmentally friendly iron-based Li-ion batteries2017Conference paper (Other academic)
1 - 4 of 4
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