兴奋剂
材料科学
阳离子聚合
形态学(生物学)
晶体结构
锰
化学工程
结晶学
纳米技术
矿物学
冶金
化学
光电子学
地质学
高分子化学
古生物学
工程类
作者
Zhi Li,Changmeng Guo,Shuang Cao,Heng Li,Jiarui Chen,Lei Wu,Ruijuan Wang,Yansong Bai,Xianyou Wang
标识
DOI:10.1016/j.jallcom.2024.173954
摘要
Lithium-rich manganese-based cathode materials (LRMCs) can be regarded as one of the most potential cathode materials for the next-generation high-energy Li-ion batteries due to the extra oxygen redox, which can greatly increase the actual output energy density of LRMCs. Nevertheless, the structure degradation and inevitable loss of oxygen will be triggered by the irreversible oxygen redox, which will cause a significant decline in cyclic performance and limited initial Coulombic efficiency, thus restricting their industrial applicability. Herein, the LRMCs with the submicron-sized single-crystal morphology and sodium doping are prepared by molten salt treatment with NaCl. On one hand, the submicron-sized single-crystal cathode effectively reduces the diffusion path for Li+ due to the smaller particle dimensions. On the other hand, Na+ doping expands the Li slab spacing, promoting the transport of Li+. The results show that the as-prepared material can purposefully alleviate oxygen release, improve structure stability, and increase the Li+ diffusion rate for the pristine LRMCs. Moreover, the as-prepared material in this study exhibits a higher reversible capacity of 282.8 mAh g-1 at 0.1 C and displays good cyclic performance, retaining a capacity rate of 80.9% after 200 cycles at 1 C. Therefore, this study offers a potential exploration for designing LRMCs with high energy density and excellent cyclic performance, which are achieved through building submicron-sized single-crystal morphology and introducing cationic doping.
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