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
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
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
AVPO<sub>4</sub>F (A = Li, K): A 4 V Cathode Material for High-Power Rechargeable Batteries
AVPO<sub>4</sub>F (A = Li, K): A 4 V Cathode Material
for High-Power Rechargeable Batterie