Air-stability is one of the most important considerations for the practical application of electrode materials in energy-harvesting/storage devices, ranging from solar cells to rechargeable batteries. The promising P2-layered sodium transition metal oxides (P2-Na_xTmO₂) often suffer from structural/chemical transformations when contacted with moist air. However, these elaborate transitions and the evaluation rules towards air-stable P2-Na_xTmO₂ have not yet been clearly elucidated. Herein, taking P2-Na_0.67MnO₂ and P2-Na_0.67Ni_0.33Mn_0.67O₂ as key examples, we unveil the comprehensive structural/chemical degradation mechanisms of P2-Na_xTmO₂ in different ambient atmospheres by using various microscopic/spectroscopic characterizations and first-principle calculations. The extent of bulk structural/chemical transformation of P2-Na_xTmO₂ is determined by the amount of extracted Na⁺, which is mainly compensated by Na⁺/H⁺ exchange. By expanding our study to a series of Mn-based oxides, we reveal that the air-stability of P2-Na_xTmO₂ is highly related to their oxidation features in the first charge process and further propose a practical evaluating rule associated with redox couples for air-stable Na_xTmO₂ cathodes.

Due to their high specific capacities beyond 250 mA h g⁻¹, lithium-rich oxides have been considered as promising cathodes for the next generation power batteries, bridging the capacity gap between traditional layered-oxide based lithium-ion batteries and future lithium metal batteries such as lithium sulfur and lithium air batteries. However, the practical application of Li-rich oxides has been hindered by formidable challenges. To address these challenges, the understanding of their electrochemical behaviors becomes critical and is expected to offer effective guidance for both materials and cell development. This review aims to provide fundamental insights into the reaction mechanisms, electrochemical challenges and modification strategies of lithium-rich oxides. We first summarize the research history, the pristine structures, and the classification of lithium-rich oxides. Then we review the critical reaction mechanisms that are closely related to their electrochemical features and performances, such as lattice oxygen oxidation, oxygen vacancy formation, transition-metal migration, layered to spinel transitions, ‘two-phase mechanism’, and lattice evolution. These discussions are coupled with state-of-the-art characterization techniques. As a comparison, the anionic redox reactions of layered sodium transition metal oxides are also discussed. Finally, after a brief overview of the correlation among the aforementioned mechanisms, we provide perspectives on the rational design of lithium-rich oxides with high energy densities and long-term cycling stability.

Layered transition metal oxides are the most important cathode materials for Li/Na/K ion batteries. Suppressing undesirable phase transformations during charge-discharge processes is a critical and fundamental challenge towards the rational design of high-performance layered oxide cathodes. Here we report a shale-like Na_xMnO₂ (S-NMO) electrode that is derived from a simple but effective water-mediated strategy. This strategy expands the Na⁺ layer spacings of P2-type Na_0.67MnO₂ and transforms the particles into accordion-like morphology. Therefore, the S-NMO electrode exhibits improved Na⁺ mobility and near-zero-strain property during charge-discharge processes, which leads to outstanding rate capability (100 mAh g⁻¹ at the operation time of 6 min) and cycling stability (>3000 cycles). In addition, the water-mediated strategy is feasible to other layered sodium oxides and the obtained S-NMO electrode has an excellent tolerance to humidity. This work demonstrates that engineering the spacings of alkali-metal layer is an effective strategy to stabilize the structure of layered transition metal oxides.

Advanced spectroscopy methods quantitatively elucidate the failure process of lithium metal batteries.