4.8 Article

Origin of unusual spinel-to-layered phase transformation by crystal water

Journal

CHEMICAL SCIENCE
Volume 9, Issue 2, Pages 433-438

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c7sc04114d

Keywords

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Funding

  1. Korean Government through National Research Foundation [NRF-2014R1A4A1003712, NRF-2017R1A2B3010176, NRF-2016M3D1A1021147, NRF-2015R1A2A1A15055539]
  2. R&D Convergence Program of the National Research Council of Science Technology [CAP-15-02-KBSI]
  3. Grants-in-Aid for Scientific Research [17H06519] Funding Source: KAKEN

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It is well known that many layered transition metal oxides can transform into a spinel structure upon repeated battery cycling, but a phase transition in the opposite direction is rare. Recently, the transformation from spinel Mn3O4 to layered MnO2 was observed during the operation of a Mg battery in aqueous conditions, resulting in high performance Mg batteries. We hereby use ab initio calculations to unveil the mechanism by which crystal water plays a critical role in this unique transformation. Once inserted into the spinel form, a water molecule donates an electron, offering a key structural and thermodynamic driving force to initiate the transformation process. These crystal water molecules then get favorably clustered into a planar form in the layered structure and act as a stabilizing agent for birnessite. Kinetically, the inserted crystal water dramatically promotes the necessary rearrangement of Mn during the transition by lowering the activation barrier by >2 eV. The present structural, thermodynamic and kinetic understanding of the crystal water-driven phase transition provides novel insights to further the design of related low dimensional hydrated materials for multi-valent cathodes.

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