RESUMEN
Direct recycling is considered to be the next-generation recycling technology for spent lithium-ion batteries due to its potential economic benefits and environmental friendliness. For the spent layered oxide cathode materials, an irreversible phase transition to a rock-salt structure near the particle surface impedes the reintercalation of lithium ions, thereby hindering the lithium compensation process from fully restoring composition defects and repairing failed structures. We introduced a transition-metal hydroxide precursor, utilizing its surface catalytic activity produced during annealing to convert the rock-salt structure into a layered structure that provides fast migration pathways for lithium ions. The material repair and synthesis processes share the same heating program, enabling the spent cathode and added precursor to undergo a topological transformation to form the targeted layered oxide. This regenerated material exhibits a performance superior to that of commercial cathodes and maintains 88.4% of its initial capacity after 1000 cycles in a 1.3 Ah pouch cell. Techno-economic analysis highlights the environmental and economic advantages of surface catalytic repair over pyrometallurgical and hydrometallurgical methods, indicating its potential for practical application.
RESUMEN
The direct recycling of cathode materials in lithium-ion batteries is important for environmental protection and resource conservation. The key regeneration processes are composition replenishment and atom rearrangement, both of which depend on the migration and diffusion of atoms. However, for the direct recycling of degraded LiNi0.5Co0.2Mn0.3O2 (D-NCM523) cathode, the irreversible phase transitions that accumulate during the long-term cycles block the Li diffusion channels with a high diffusion energy barrier, making it difficult to fully repair the layered structure and resulting in rapid capacity decay. To address the challenge, fast Li replenishment channels are rebuilt to regulate the surface phase and effectively assist the regeneration process with a reduced energy barrier. This method reduces the amount of Li supplement by >75% and shortens the sintering time (only 2 h) to fully regenerate D-NCM523, compared to general direct recycling methods. The regenerated NCM523 (LCMB-NCM523) exhibits a satisfactory repaired specific capacity of 160 mAh g-1 and excellent cycling stability, retaining 78% of its capacity after 300 cycles. In addition, LCMB-NCM523 is recycled with improved thermal decomposition peak temperature and enables 200 cycles even at 60 °C, greatly improving safety. This work proposes a promising way for the large-scale direct regeneration of layered cathodes.
RESUMEN
Direct regeneration of spent lithium-ion batteries has received wide attention owing to its potential for resource reuse and environmental benefits. The repair effect of direct regeneration methods undergoing heterogeneous repair process is usually inferior, while homogenous repair process plays a vital role to achieve satisfactory repair results. However, the practical applications of current homogeneous repair methods are challenged by the complex operations and relatively high costs owing to the requirement of additional heating or pressurization. Herein, this work proposes a simple strategy to achieve homogeneous repair of spent cathode materials under relatively mild conditions by uniformly precoating lithium source at room temperature and atmospheric pressure. Followed by annealing, highly degraded LiNi0.83Co0.12Mn0.05O2 with severe Li deficiency and irreversible phase transition is repaired to have an initial capacity of 181.6 mAh g-1 and capacity retention of 80.7% after 150 cycles at 0.5 C. The lithium source used in this strategy is from the spent lithium anode. Moreover, this strategy is suitable for the direct regeneration of various layer oxide cathode materials with different failure degrees. This work provides both theoretical guidance and practical examples for the straightforward, effective, and universally applicable direct regeneration methods.
RESUMEN
Exploring the relationships between heavy metal release and salinity can help address the problems of combination of toxic heavy metals and salinization in contaminated soils. Therefore, in this study, the release characteristics of heavy metals (Cd, Cu and Zn) under different salt types and mass concentrations were investigated through batch desorption experiments. Spearman's correlation analysis was performed to assess the effects of typical physicochemical properties on metal release under salt stress. The results indicated that the types and concentration gradients of salt had notably different impacts on the release of different metals; specifically, there were significant impacts for Cd but slight impacts for Cu and Zn. MgCl2 and CaCl2 had more obvious promoting effects on Cd release, followed by a salt mixture and NaCl, and this pattern was similar for Zn release. Most salts could slightly restrain the release of Cu, except for MgCl2 and Na2SO4, which had slight promoting effects. Moreover, low levels of CaCl2 could effectively restrain the release of Cu. The results showed that the release capacities of metals followed the order of Cd > Cu > Zn, possibly attributed to the competitive adsorption among cations. Ferromanganese oxides in the soil favored the release of Cd and Zn under salt treatments, and redox potential was an important factor affecting Cu release. The results also suggested that the background values of metals could affect metal release, but the effects were varied under different salt treatments for Zn. The reason for this may be that the addition of different salts changed the effects of certain soil properties on the metal release. Overall, this study can serve as an important reference for controlling heavy metal pollution in soils in salinization and coastal areas.
