Ce-Fe3O4@N-doped carbon derived from covalent organic framework for enhanced lithium storage

纳米笼 阳极 锂(药物) 纳米复合材料 煅烧 兴奋剂 纳米颗粒 电化学 纳米技术 化学 材料科学 化学工程 电极 冶金 工程类 物理化学 光电子学 催化作用 医学 内分泌学 生物化学
作者
Yuan Li,Kaixiang Chen,Hao Yu,Yan Du,Yonghai Song
出处
期刊:Journal of energy storage [Elsevier BV]
卷期号:83: 110661-110661 被引量:6
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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