Effect of Mg Substitution on Structural Stabilization of NaxMnO2 Cathode for Na-Ion Batteries

As the Li-ion batteries market encounters numerous obstacles, such as not sufficient production to the demands, there is a need to develop post-lithium technologies, such as Na-ion batteries. Na0.67MnO2 cathode material provides high capacity; however, it suffers from phase transitions during the (de)intercalation process. Herein, it is presented that magnesium substitution in Na0.67Mg0.2Mn0.8O2 stabilizes the crystal structure during cycling, which was confirmed by operando X-ray diffraction measurements as well as the long-term cycling experiment. It also enhances the electronic conductivity from 9 x 10(-6) to 7 x 10(-5) S cm(-1) and the ionic one from 3 x 10(-6) to 4 x 10(-5) S cm(-1). X-ray absorption spectroscopy O K-edge spectra are in line with the enormous exceeding of the theoretical capacity of Na/Na+/NaxMg0.2Mn0.8O2 cell (nonreversible discharge capacity of 310 with 155 mAh g(-1) of theoretical capacity). Electronic structure calculations performed by the Korringa-Kohn-Rostoker method in the framework of local spin-density approximation + U in ordered Na2/3Mg1/3Mn2/3O2 approximant support its semiconducting properties as well as confirm that substitution of Mn with Mg markedly enhances the role of oxygen in constituting electronic states around the Fermi level and its role in the electrochemical process leading to the improved capacity.

Automated summary

As the Li-ion batteries market faces challenges in meeting demands, it is necessary to develop post-lithium technologies like Na-ion batteries. This study presents the stabilization of crystal structure in Na0.67MnO2 cathode material through magnesium substitution. The improved structure enhances electronic and ionic conductivity, resulting in an increased capacity.