He Yujia, Jia Kai, Piao Zhihong, Cao Zhenjiang, Zhang Mengtian, Li Pengfei, Li Zhichao, Jiang Zhiyuan, Yang Guorui, Xi Huan, Zhou Guangmin, Tang Wei, Qu Zhiguo, Kumar R Vasant, Ding Shujiang, Xi Kai
School of Chemistry, Engineering Research Center of Energy Storage Materials and Devices, Ministry of Education, National Innovation Platform (Center) for Industry-Education Integration of Energy Storage Technology, Engineering Research Center of Energy Storage Material and Chemistry, Universities of Shaanxi Province, Xi'an Jiaotong University, Xi'an, 710049, China.
Tsinghua Shenzhen International Graduate School &Tsinghua-Berkeley Shenzhen Institute (TBSI), Tsinghua University, Shenzhen, 518055, China.
Angew Chem Int Ed Engl. 2025 Mar 24;64(13):e202422610. doi: 10.1002/anie.202422610. Epub 2025 Jan 15.
Direct regeneration of spent lithium-ion batteries offers economic benefits and a reduced CO footprint. Surface prelithiation, particularly through the molten salt method, is critical in enhancing spent cathode repair during high-temperature annealing. However, the sluggish Li transport kinetics, which predominantly relies on thermally driven processes in the traditional molten salt methods, limit the prelithiation efficiency and regeneration of spent cathodes. Here, we introduce a special molecular configuration (benzoate) into molten salts that facilitates rapid Li transport to the surface of LiNiCoMnO (NCM) via a quasi-Grotthuss topochemistry mechanism. This approach effectively avoids the phase transitions that could adversely degrade the electrochemical performance due to insufficient lithiation during the repair process. Computational and experimental analyses reveal that the system enables fast Li migration through the topological hopping of benzoate in organic lithium salt, rather than relying solely on thermally driven diffusion, thereby significantly improving the prelithiation and repair efficiency of spent NCM cathodes. Benefiting from the quasi-Grotthuss Li topochemistry transport, the degraded structure and Li vacancies in the spent cathode are effectively eliminated, yieding the regenerated cathode with good cycling stability comparable to commercial counterparts. The proposed Li transport mechanism presents a promising route for the efficient and sustainable regeneration of spent cathodes.
废旧锂离子电池的直接再生具有经济效益并能减少碳足迹。表面预锂化,特别是通过熔盐法进行的预锂化,对于在高温退火过程中增强废旧阴极修复至关重要。然而,传统熔盐法中主要依赖热驱动过程的缓慢锂传输动力学限制了预锂化效率和废旧阴极的再生。在此,我们将一种特殊的分子构型(苯甲酸盐)引入熔盐中,通过准Grotthuss拓扑化学机制促进锂快速传输到LiNiCoMnO(NCM)表面。这种方法有效避免了修复过程中因锂化不足而可能对电化学性能产生不利影响的相变。计算和实验分析表明,该体系通过苯甲酸盐在有机锂盐中的拓扑跳跃实现快速锂迁移,而非仅依赖热驱动扩散,从而显著提高了废旧NCM阴极的预锂化和修复效率。受益于准Grotthuss锂拓扑化学传输,废旧阴极中的退化结构和锂空位得以有效消除,得到具有与商业同类产品相当的良好循环稳定性的再生阴极。所提出的锂传输机制为废旧阴极的高效可持续再生提供了一条有前景的途径。