Conventional cathodes of Li-ion batteries mainly operate through an insertion-extraction process involving transition metal redox. These cathodes will not be able to meet the increasing requirements until lithium-rich layered oxides emerge with beyond-capacity performance. Nevertheless, in-depth understanding of the evolution of crystal and excess capacity delivered by Li-rich layered oxides is insufficient. Herein, various in situ technologies such as X-ray diffraction and Raman spectroscopy are employed for a typical material Li Ni Mn O , directly visualizing O O (peroxo oxygen dimers) bonding mostly along the c-axis and demonstrating the reversible O /O redox process. Additionally, the formation of the peroxo OO bond is calculated via density functional theory, and the corresponding OO bond length of ≈1.3 Å matches well with the in situ Raman results. These findings enrich the oxygen chemistry in layered oxides and open opportunities to design high-performance positive electrodes for lithium-ion batteries.

A layered composite with P2 and O3 integration is proposed toward a sodium-ion battery with high energy density and long cycle life. The integration of P2 and O3 structures in this layered oxide is clearly characterized by XRD refinement, SAED and HAADF and ABF-STEM at atomic resolution. The biphase synergy in this layered P2+O3 composite is well established during the electrochemical reaction. This layered composite can deliver a high reversible capacity with the largest energy density of 640 mAh g(-1), and it also presents good capacity retention over 150 times of sodium extraction and insertion.

This article presents a comprehensive and critical review on the recent progress of titanium-based electrode materials for sodium-ion batteries.