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Title: A reversible phase transition for sodium insertion in anatase TiO2

Abstract

Anatase TiO2 is a potential negative electrode for sodium-ion batteries. The sodium storage mechanism is, however, still under debate, yet its comprehension is required to optimize the electrochemical properties. To clarify the sodium storage mechanism occurring in anatase, we have used both electrochemical and chemical routes from which we obtained similar trends. During the first discharge, an irreversible plateau region is observed which corresponds to the insertion of Na+ within the interstitial sites of anatase and is accompanied by a drastic loss of the long-range order as revealed by X-ray diffraction, high resolution of high angle annular dark-field scanning transmission electron microscope (HAADF-STEM), and pair distribution function (PDF) analysis. Further structural analysis of the total scattering data indicates that the sodiated phase displays a layered-like rhombohedral R3m structure built from the stacking of Ti and Na slabs. Because of the initial 3D network of anatase, the reduced phase shows strong disorder due to cationic intermixing between the Ti and Na slabs and the refined chemical formula is (Na0.43Ti0.57)3a 0.22Na0.39Ti0.39)3bO2, where refers to vacancy. The presence of high valence Ti ions in the Na layers induces a contraction of the c-parameter as compared to the ordered phase. Upon desodiation, the structuremore » further amorphized and the local structure probed by PDF is shown to be similar to the anatase TiO2, suggesting that the 3D network is recovered. The reversible sodium insertion/deinsertion is thus attributed to the rhombohedral active phase formed during the first discharge, and an oxidized phase featuring the local structure of anatase. Due to the amorphous nature of the two phases, the potential-composition curves are characterized by a sloping curve. Lastly, a comparison between the intercalation of lithium and sodium into anatase TiO2 performed by DFT calculations confirmed that, for the sodiated phase, the rhombohedral structure is more stable than the tetragonal phase observed during the lithiation of nanoparticles.« less

Authors:
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Publication Date:
Research Org.:
Argonne National Lab. (ANL), Argonne, IL (United States)
Sponsoring Org.:
European Commission - Community Research and Development Information Service (CORDIS) - Seventh Framework Programme (FP7); Engineering and Physical Sciences Research Council (EPSRC); USDOE Office of Science (SC), Basic Energy Sciences (BES) (SC-22), Scientific User Facilities Division
OSTI Identifier:
1372078
Grant/Contract Number:  
AC02-06CH11357
Resource Type:
Accepted Manuscript
Journal Name:
Chemistry of Materials
Additional Journal Information:
Journal Volume: 29; Journal Issue: 4; Journal ID: ISSN 0897-4756
Publisher:
American Chemical Society (ACS)
Country of Publication:
United States
Language:
English
Subject:
36 MATERIALS SCIENCE; NaTiO2; disordered layered structure; pair distribution function; sodium-ion batteries

Citation Formats

Li, Wei, Fukunishi, Mika, Morgan, Benjamin J., Borkiewicz, Olaf J., Chapman, Karena W., Pralong, Valerie, Maignan, Antoine, Lebedev, Oleg I., Ma, Jiwei, Groult, Henri, Komaba, Shinichi, and Dambournet, Damien. A reversible phase transition for sodium insertion in anatase TiO2. United States: N. p., 2017. Web. doi:10.1021/acs.chemmater.7b00098.
Li, Wei, Fukunishi, Mika, Morgan, Benjamin J., Borkiewicz, Olaf J., Chapman, Karena W., Pralong, Valerie, Maignan, Antoine, Lebedev, Oleg I., Ma, Jiwei, Groult, Henri, Komaba, Shinichi, & Dambournet, Damien. A reversible phase transition for sodium insertion in anatase TiO2. United States. doi:10.1021/acs.chemmater.7b00098.
Li, Wei, Fukunishi, Mika, Morgan, Benjamin J., Borkiewicz, Olaf J., Chapman, Karena W., Pralong, Valerie, Maignan, Antoine, Lebedev, Oleg I., Ma, Jiwei, Groult, Henri, Komaba, Shinichi, and Dambournet, Damien. Tue . "A reversible phase transition for sodium insertion in anatase TiO2". United States. doi:10.1021/acs.chemmater.7b00098. https://www.osti.gov/servlets/purl/1372078.
@article{osti_1372078,
title = {A reversible phase transition for sodium insertion in anatase TiO2},
author = {Li, Wei and Fukunishi, Mika and Morgan, Benjamin J. and Borkiewicz, Olaf J. and Chapman, Karena W. and Pralong, Valerie and Maignan, Antoine and Lebedev, Oleg I. and Ma, Jiwei and Groult, Henri and Komaba, Shinichi and Dambournet, Damien},
abstractNote = {Anatase TiO2 is a potential negative electrode for sodium-ion batteries. The sodium storage mechanism is, however, still under debate, yet its comprehension is required to optimize the electrochemical properties. To clarify the sodium storage mechanism occurring in anatase, we have used both electrochemical and chemical routes from which we obtained similar trends. During the first discharge, an irreversible plateau region is observed which corresponds to the insertion of Na+ within the interstitial sites of anatase and is accompanied by a drastic loss of the long-range order as revealed by X-ray diffraction, high resolution of high angle annular dark-field scanning transmission electron microscope (HAADF-STEM), and pair distribution function (PDF) analysis. Further structural analysis of the total scattering data indicates that the sodiated phase displays a layered-like rhombohedral R3m structure built from the stacking of Ti and Na slabs. Because of the initial 3D network of anatase, the reduced phase shows strong disorder due to cationic intermixing between the Ti and Na slabs and the refined chemical formula is (Na0.43Ti0.57)3a 0.22Na0.39Ti0.39)3bO2, where refers to vacancy. The presence of high valence Ti ions in the Na layers induces a contraction of the c-parameter as compared to the ordered phase. Upon desodiation, the structure further amorphized and the local structure probed by PDF is shown to be similar to the anatase TiO2, suggesting that the 3D network is recovered. The reversible sodium insertion/deinsertion is thus attributed to the rhombohedral active phase formed during the first discharge, and an oxidized phase featuring the local structure of anatase. Due to the amorphous nature of the two phases, the potential-composition curves are characterized by a sloping curve. Lastly, a comparison between the intercalation of lithium and sodium into anatase TiO2 performed by DFT calculations confirmed that, for the sodiated phase, the rhombohedral structure is more stable than the tetragonal phase observed during the lithiation of nanoparticles.},
doi = {10.1021/acs.chemmater.7b00098},
journal = {Chemistry of Materials},
number = 4,
volume = 29,
place = {United States},
year = {2017},
month = {2}
}

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Cited by: 19 works
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Figures / Tables:

Figure 1 Figure 1: Galvanostatic discharge-charge curves of Na//TiO2 cells. The cells were cycled at 10 mA.g-1.

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Works referenced in this record:

Computational Dataset for "Reversible Magnesium and Aluminium-ions Insertion in Cation-Deficient Anatase TiO2"
dataset, January 2017

  • Morgan, Benjamin; Salanne, Mathieu; Dambournet, Damien
  • University of Bath
  • DOI: 10.15125/bath-00397

    Works referencing / citing this record:

    Computational Dataset for "Reversible Magnesium and Aluminium-ions Insertion in Cation-Deficient Anatase TiO2"
    dataset, January 2017

    • Morgan, Benjamin; Salanne, Mathieu; Dambournet, Damien
    • University of Bath
    • DOI: 10.15125/bath-00397

    The electrochemical storage mechanism in oxy-hydroxyfluorinated anatase for sodium-ion batteries
    journal, January 2018

    • Li, Wei; Fukunishi, Mika; Morgan, Benjamin J.
    • Inorganic Chemistry Frontiers, Vol. 5, Issue 5
    • DOI: 10.1039/c8qi00185e

    The electrochemical storage mechanism in oxy-hydroxyfluorinated anatase for sodium-ion batteries
    journal, January 2018

    • Li, Wei; Fukunishi, Mika; Morgan, Benjamin J.
    • Inorganic Chemistry Frontiers, Vol. 5, Issue 5
    • DOI: 10.1039/c8qi00185e