化学
磷酸铁锂
盐(化学)
锂(药物)
电化学
水溶液
磷酸盐
化学工程
阴极
无机化学
电池(电)
溶剂化
纳米技术
电极
离子
有机化学
材料科学
医学
功率(物理)
物理
物理化学
量子力学
工程类
内分泌学
作者
Jie Tang,Bosi Huang,Xiao Xiao,Haotian Qu,Ya Song,Junfeng Li,Yanze Song,Haocheng Ji,Junxiong Wang,Yanfei Zhu,Guangmin Zhou
摘要
Direct regeneration has emerged as a pioneering paradigm in green recycling of lithium-ion battery (LIBs) cathode materials, leveraging the inherent atomic and structural advantages of degraded materials. The solution-based regeneration strategy offers significant advantages, particularly in promoting homogeneous lithiation and mitigating the thermal instability of lithium iron phosphate (LFP) materials. However, lithium supplementation for degraded LFP (DLFP) in aqueous solutions is significantly constrained by the narrow electrochemical stability window (ESW) and the limited selection of redox agents. Herein, we propose a promising water-in-salt solution system that enables the spontaneous lithiation of DLFP. This approach not only expands the ESW of the solution but also modifies the lithium solvation structure, facilitating more efficient lithium supplementation. Using the lithium chloride-gallic acid solution as a demonstration, the regenerated cathode materials exhibit excellent electrochemical performance, achieving a specific capacity of 146 mAh g-1 at 1 C with 83% capacity retention after 500 cycles. This research offers critical insights into solution-based lithium supplementation and paves the way for the more efficient recycling of degraded LIBs.
科研通智能强力驱动
Strongly Powered by AbleSci AI