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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.

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Authors

Clare P. Grey

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

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

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