Clare P. Grey
Ionic and Electronic Conduction in TiNb2O7
Grey, Clare P.; Griffith, Kent J.; Seymour, Ieuan D.; Hope, Michael A.; Butala, Megan M.; Lamontagne, Leo K.; Preefer, Molleigh B.; Ko�er, Can P.; Henkelman, Graeme; Morris, Andrew J.; Cliffe, Matthew J.; Dutton, Si�n E.
Authors
Kent J. Griffith
Ieuan D. Seymour
Michael A. Hope
Megan M. Butala
Leo K. Lamontagne
Molleigh B. Preefer
Can P. Ko�er
Graeme Henkelman
Andrew J. Morris
MATTHEW CLIFFE Matthew.Cliffe@nottingham.ac.uk
Associate Professor
Si�n E. Dutton
Abstract
TiNb2O7 is a Wadsley–Roth phase with a crystallographic shear structure and is a promising candidate for high-rate lithium ion energy storage. The fundamental aspects of the lithium insertion mechanism and conduction in TiNb2O7, however, are not well-characterized. Herein, experimental and computational insights are combined to understand the inherent properties of bulk TiNb2O7. The results show an increase in electronic conductivity of seven orders of magnitude upon lithiation and indicate that electrons exhibit both localized and delocalized character, with a maximum Curie constant and Li NMR paramagnetic shift near a composition of Li0.60TiNb2O7. Square-planar or distorted-five-coordinate lithium sites are calculated to invert between thermodynamic minima or transition states. Lithium diffusion in the single-redox region (i.e., x ≤ 3 in LixTiNb2O7) is rapid with low activation barriers from NMR and DLi = 10–11 m2 s–1 at the temperature of the observed T1 minima of 525–650 K for x ≥ 0.75. DFT calculations predict that ionic diffusion, like electronic conduction, is anisotropic with activation barriers for lithium hopping of 100–200 meV down the tunnels but ca. 700–1000 meV across the blocks. Lithium mobility is hindered in the multiredox region (i.e., x > 3 in LixTiNb2O7), related to a transition from interstitial-mediated to vacancy-mediated diffusion. Overall, lithium insertion leads to effective n-type self-doping of TiNb2O7 and high-rate conduction, while ionic motion is eventually hindered at high lithiation. Transition-state searching with beyond Li chemistries (Na+, K+, Mg2+) in TiNb2O7 reveals high diffusion barriers of 1–3 eV, indicating that this structure is specifically suited to Li+ mobility.
Citation
Grey, C. P., Griffith, K. J., Seymour, I. D., Hope, M. A., Butala, M. M., Lamontagne, L. K., …Dutton, S. E. (2019). Ionic and Electronic Conduction in TiNb2O7. Journal of the American Chemical Society, 141(42), 16706–16725. https://doi.org/10.1021/jacs.9b06669
Journal Article Type | Article |
---|---|
Acceptance Date | Sep 1, 2019 |
Online Publication Date | Oct 14, 2019 |
Publication Date | Oct 23, 2019 |
Deposit Date | Aug 10, 2020 |
Publicly Available Date | Aug 13, 2020 |
Journal | Journal of the American Chemical Society |
Print ISSN | 0002-7863 |
Electronic ISSN | 1520-5126 |
Publisher | American Chemical Society |
Peer Reviewed | Peer Reviewed |
Volume | 141 |
Issue | 42 |
Pages | 16706–16725 |
DOI | https://doi.org/10.1021/jacs.9b06669 |
Keywords | Colloid and Surface Chemistry; Biochemistry; General Chemistry; Catalysis |
Public URL | https://nottingham-repository.worktribe.com/output/2841605 |
Publisher URL | https://pubs.acs.org/doi/10.1021/jacs.9b06669 |
Files
jacs.9b06669
(6.6 Mb)
PDF
Publisher Licence URL
https://creativecommons.org/licenses/by/4.0/
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