An anionic redox reaction is an extraordinary method for obtaining high-energy-density cathode materials for sodium-ion batteries (SIBs). The commonly used inactive-element-doped strategies can effectively trigger the O redox activity in several layered cathode materials. However, the anionic redox reaction process is usually accompanied by unfavorable structural changes, large voltage hysteresis, and irreversible O2 loss, which hinders its practical application to a large extent. In the present work, we take the doping of Li elements into Mn-based oxide as an example and reveal the local charge trap around the Li dopant will severely impede O charge transfer upon cycling. To overcome this obstacle, additional Zn2+ codoping is introduced into the system. Theoretical and experimental studies show that Zn2+ doping can effectively release the charge around Li+ and homogeneously distribute it on Mn and O atoms, thus reducing the overoxidation of O and improving the stability of the structure. Furthermore, this change in the microstructure makes the phase transition more reversible. This study aimed to provide a theoretical framework for further improve the electrochemical performance of similar anionic redox systems and provide insights into the activation mechanism of the anionic redox reaction.

To investigate the response of material to cavitation erosion, a comparative work was carried out on three materials, aluminum, copper alloy and titanium. Ultrasonic cavitation erosion was produced as the specimen was submerged in the deionized water. Within a cavitation erosion period of 120 min, the cumulative mass loss was measured at certain time intervals. Surface structure and cavitation damage patterns were observed for the three materials. Microhardness was measured and compared. The results indicate that the cumulative mass loss of aluminum is the highest among the three materials, while the slightest material removal is associated with titanium, which is still in the initial stage of cavitation erosion after 120 min of cavitation erosion. The surface of the aluminum specimen is eroded rapidly after the cavitation erosion commences. Large erosion pits dominate the eroded surface as the cavitation erosion progresses. The surface of the titanium specimen manifests needle-like erosion pits and cleavage cracks. Even at the later stage of the cavitation erosion, non-eroded surface elements are identifiable. The cavitation erosion pattern on the copper alloy specimen surface is related to the twin-phase crystal structure and large erosion pits are produced at the later stage of cavitation erosion. The highest resistance to the cavitation erosion of titanium is related to the close-packed hexagonal structure and the weak slip effect associated.