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      SCOPUS SCIE

      Na<sup>+</sup>/Vacancy Disordered P2-Na<sub>0.67</sub>Co<sub>1&#x2013;<i>x</i></sub>Ti<i><sub>x</sub></i>O<sub>2</sub>: High-Energy and High-Power Cathode Materials for Sodium Ion Batteries

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      https://www.riss.kr/link?id=A107451531

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      <P>Although sodium ion batteries (NIBs) have gained wide interest, their poor energy density poses a serious challenge for their practical applications. Therefore, high-energy-density cathode materials are required for NIBs to enable the utiliza...

      <P>Although sodium ion batteries (NIBs) have gained wide interest, their poor energy density poses a serious challenge for their practical applications. Therefore, high-energy-density cathode materials are required for NIBs to enable the utilization of a large amount of reversible Na ions. This study presents a P2-type Na0.67Co1-x,TixO2 (x < 0.2) cathode with an extended potential range higher than 4.4 V to present a high specific capacity of 166 mAh g(-1). A group of P2-type cathodes containing various amounts of Ti is prepared using a facile synthetic method. These cathodes show different behaviors of the Na+/vacancy ordering. Na0.67CoO2 suffers severe capacity loss at high voltages due to irreversible structure changes causing serious polarization, while the Ti-substituted cathodes have long credible cycleability as well as high energy. In particular, Na0.67Co0.90Ti0.10O2 exhibits excellent capacity retention (115 mAh g(-1)) even after 100 cycles, whereas Na0.67CoO2 exhibits negligible capacity retention (<10 mAh g(-1)) at 4.5 V cutoff conditions. Na0.67Co0.90Ti0.10O2 also exhibits outstanding rate capabilities of 108 mAh g(-1) at a current density of 1000 mA g(-1) (7.4 C). Increased sodium diffusion kinetics from mitigated Na+/vacancy ordering, which allows high Na+ utilization, are investigated to find in detail the mechanism of the improvement by combining systematic analyses comprising TEM, in situ XRD, and electrochemical methods.</P>

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