Li-ion batteries (LIBs) have been regarded as the technology of choice for energy storage fields. The development of large-scale energy storage requires higher energy density of LIB. Li-rich cathode oxides with ultrahigh capacity have the greatest application potential for high-energy-density LIBs.

Lattice oxygen redox (l-OR) is essential for achieving the high capacity in this system materials. However, till now, the understanding of l-OR chemistry remains elusive, and a critical question is the structural effect on the stability of l-OR.

Neutron pair distribution function (nPDF), capable of emphasizing the oxygen atomic scattering, is a powerful tool to detect both the local and average oxygen lattice structure evolution upon the l-OR.

Recently, Combing the nPDF method with scanning transmission electron microscopy (STEM), ZHAO Enyue and Li Qinghao in Prof. WANG Fangwei and Prof. YU Xiqian's groups from Institute of Physics, Chinese Academy of Sciences (IOP, CAS), cooperating with Prof. GU Lin and Prof. YANG Wanli from Lawrence Berkeley National Laboratory Berkeley, USA have revealed the coupling between l-OR and structure dimensionality.

The researchers provided the direct experiment evidence for the existence of l-OR via mapping of resonant inelastic X-ray scattering.

Meanwhile, nPDF and STEM suggested that the oxygen lattice structure evolution upon the l-OR in 3D-disordered Li-rich oxides is stable, contrasting the distorted oxygen lattice in 2D/3D-ordered Li-rich oxides. It was indicated that the differentiated structure variation is directly correlated with the structure dimensionality.

The l-OR usually occur on the lattice O^2- ions with unhybridized O2p states. To reduce the energy, the distance between two oxidized O^2- ions would shrink (i.e., oxygen lattice distortion). This oxygen lattice distortion occurs only if two unhybridized O2p orbitals are coplanar.

In 3D-disordered Li-rich oxides, the formation probability of coplanar unhybridized O 2p orbitals is very low.

Thus, a stable oxygen lattice was observed in 3D-disordered Li-rich oxides, which in turn favor the stable l-OR.

This work shows that the structure dimensionality can be tuned to promote the stable l-OR with robust oxygen lattice in Li-rich cathode oxides, providing new insights for both fundamental researches and practical developments of high-energy-density cathodes relying on stable l-OR chemistry.

This study entitled "Stabilizing Oxygen Lattice and Reversible Oxygen Redox Chemistry through Structural Dimensionality in Li-rich Cathode Oxides" was published on Angew. Chem. Int. Ed.

The study was supported by the National Key R&D Program of China, National Science Foundation of China, Songshan Lake Materials Laboratory and China Spallation Neutron Source.