3 research outputs found

    β‑Na<sub>1.7</sub>IrO<sub>3</sub>: A Tridimensional Na-Ion Insertion Material with a Redox Active Oxygen Network

    No full text
    The revival of the Na-ion battery concept has prompted an intense search for new high capacity Na-based positive electrodes. Recently, emphasis has been placed on manipulating Na-based layered compounds to trigger the participation of the anionic network. We further explored this direction and show the feasibility of achieving anionic-redox activity in three-dimensional Na-based compounds. A new 3D β-Na<sub>1.7</sub>IrO<sub>3</sub> phase was synthesized in a two-step process, which involves first the electrochemical removal of Li from β-Li<sub>2</sub>IrO<sub>3</sub> to produce β-IrO<sub>3</sub>, which is subsequently reduced by electrochemical Na insertion. We show that β-Na<sub>1.7</sub>IrO<sub>3</sub> can reversibly uptake nearly 1.3 Na<sup>+</sup> per formula unit through an uneven voltage profile characterized by the presence of four plateaus related to structural transitions. Surprisingly, the β-Na<sub>1.7</sub>IrO<sub>3</sub> phase was found to be stable up to 600 °C, while it could not be directly synthesized via conventional synthetic methods. Although these Na-based iridate phases are of limited practical interest, they help to understand how introducing highly polarizable guest ions (Na<sup>+</sup>) into host rocksalt-derived oxide structures affects the anionic redox mechanism

    β‑Na<sub>1.7</sub>IrO<sub>3</sub>: A Tridimensional Na-Ion Insertion Material with a Redox Active Oxygen Network

    No full text
    The revival of the Na-ion battery concept has prompted an intense search for new high capacity Na-based positive electrodes. Recently, emphasis has been placed on manipulating Na-based layered compounds to trigger the participation of the anionic network. We further explored this direction and show the feasibility of achieving anionic-redox activity in three-dimensional Na-based compounds. A new 3D β-Na<sub>1.7</sub>IrO<sub>3</sub> phase was synthesized in a two-step process, which involves first the electrochemical removal of Li from β-Li<sub>2</sub>IrO<sub>3</sub> to produce β-IrO<sub>3</sub>, which is subsequently reduced by electrochemical Na insertion. We show that β-Na<sub>1.7</sub>IrO<sub>3</sub> can reversibly uptake nearly 1.3 Na<sup>+</sup> per formula unit through an uneven voltage profile characterized by the presence of four plateaus related to structural transitions. Surprisingly, the β-Na<sub>1.7</sub>IrO<sub>3</sub> phase was found to be stable up to 600 °C, while it could not be directly synthesized via conventional synthetic methods. Although these Na-based iridate phases are of limited practical interest, they help to understand how introducing highly polarizable guest ions (Na<sup>+</sup>) into host rocksalt-derived oxide structures affects the anionic redox mechanism
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