锂(药物)
碳纤维
共价键
兴奋剂
储能
共价有机骨架
化学
材料科学
化学工程
有机化学
物理
工程类
复合数
热力学
光电子学
复合材料
医学
功率(物理)
内分泌学
作者
Yuan Li,Kaixiang Chen,Hao Yu,Yan Du,Yonghai Song
标识
DOI:10.1016/j.est.2024.110661
摘要
Fe3O4 has the potential to be an alternative material for the anode of lithium-ion batteries (LIBs) due to its high theoretical capacity, cheapness, and environmental friendliness. However, its inevitable volume expansion and poor Li+ storage dynamics due to small lattice spacing are disadvantages that severely limit its application. Here, Ce-Fe3O4 nanoparticles with large lattice spacing and porous structure were obtained by inserting Ce with a large radius into Fe3O4 lattice. Next, the Ce-Fe3O4 nanoparticles was used as the core for the in-situ growth of COFLZU1 to form Ce-Fe3O4@ COFLZU1. Finally, high-temperature calcination was carried out to obtain flexible nano-cages of nitrogen-doped porous carbon (NC)-covered Ce-Fe3O4 (Ce-Fe3O4@NC). Flexible NC nanocages not only accommodate the volume expansion of Fe3O4 but also increase the rate of Li+ transport and provide space for Li+ storage. The successful doping of Ce effectively increases the lattice spacing of Ce-Fe3O4, improving the space and efficiency of the embedded Li+. Compared with pure Fe3O4, Ce-Fe3O4 exhibits better performance when applied to the anode of LIBs. Ce-Fe3O4@NC exhibits best electrochemical performance during lithium storage, with capacities of 662.2 and 923.7 mAh g−1 after 500 cycles at current densities of 1000 mA g−1 and 100 mA g−1. This strategy of Ce doping combined with flexible NC cladding offers options for the preparation of other core-shell type carbon nanocomposites.
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