High Power Sodium-Ion Batteries and Hybrid Electrochemical Capacitors Using Mo or Nb-Doped Nano-Titania Anodes

Dustin Bauer, Alexander J. Roberts, Sai Gourang Patnaik, Dan J. L. Brett, Paul R. Shearing, Emma Kendrick, Noriyoshi Matsumi, Jawwad A. Darr

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    Abstract

    Nano-sized anatase (TiO2) and doped anatase (Mo0.1Ti0.9O2 and Nb0.25Ti0.75O2) materials (ca. 5 nm) were synthesized using continuous hydrothermal flow synthesis and evaluated as negative electrodes in Na-ion batteries and hybrid capacitors. Na-ion half-cells (vs. Na metal counter electrodes) for the Mo-doped titania (Mo0.1Ti0.9O2) and Nb-doped titania (Nb0.25Ti0.75O2) electrodes both showed significantly higher specific discharge capacities than undoped anatase (ca. 75 mAh g−1 compared to only 30 mAh g−1 for undoped TiO2 at 1 A g−1). This improved performance was attributed to higher pseudocapacitive contributions to charge storage, as well as improved sodium ion diffusion and lower charge transfer resistance. Na-ion hybrid electrochemical capacitors (Na-HECs) were made from the electrodes with activated carbon positive electrodes. As expected, Na-HECs using doped titania showed superior performance to the undoped anatase, with power densities up to 10.5 kW kg−1 or energy densities of over 60 Wh kg−1 (based on the weight of active material in both anode and cathode). The Mo0.1Ti0.9O2/AC Na-ion hybrid capacitor also showed excellent specific capacitance retention of ca. 75% over 3000 cycles at 5 mA cm−2 (1 A g−1). © The Author(s) 2018.
    Original languageEnglish
    Pages (from-to)A1662-A1670
    Number of pages9
    JournalJournal of the Electrochemical Society
    Volume165
    Issue number9
    DOIs
    Publication statusPublished - 6 Jun 2018

    Bibliographical note

    © The Author(s) 2018. Published by ECS. This is an open access article distributed under the terms of the Creative Commons Attribution 4.0 License (CC BY, http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse of the work in any medium, provided the original work is properly cited. [DOI: 10.1149/2.0341809jes]

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