纳米晶材料
锂(药物)
离子
材料科学
兴奋剂
能量密度
粒子(生态学)
无机化学
化学工程
化学
纳米技术
工程物理
物理
光电子学
地质学
工程类
内分泌学
海洋学
医学
有机化学
作者
Yuanpeng Cao,Jingjing He,Wenhui Tu,Runlin Li,Wei Luo,Xinyu Zhang,Jianguo Duan,Ding Wang,Xianshu Wang,Dong Peng,Yingjie Zhang
标识
DOI:10.1016/j.ssi.2024.116576
摘要
Olivine-structured LiMnPO4-based cathode materials have been considered upgrades to LiFePO4 due to their higher energy density and highly stable polyanionic Li+ storage structure. However, the high electronic and ionic insulation has severely limited their popularization and application. In this work, the reversible specific capacity and the rate performance of LiMn0.8Fe0.2PO4@C (LMFP@C) have been promoted by incorporating particle nanocrystalline and V3+ doping. The mechanical liquid phase activation technique ensures the uniform mixing of the raw materials and reduces their particle size to nanometer scale. Based on this typical synthetic strategy, about 1 at.% of V3+ can be doped into the LMFP lattice to form a uniform solid solution, while most of the V3+ ions tend to enrich on the surface of the particles as the introducing amount is >2 at.%. Optimally, 1 at.% of V3+ doping improves the electrochemical performance of LMFP@C significantly, but >2 at.% of V3+ introduction is detrimental. The optimized material exhibits high discharge capacities of 155.4 and 115.9 mAh·g−1 at 0.1 and 5.0C, respectively, and a high capacity retention of 93.4% after 100 cycles at 1.0C rate.
科研通智能强力驱动
Strongly Powered by AbleSci AI