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首页> 外文期刊>Chemical engineering journal >Crosslinking-induced spontaneous growth: A novel strategy for synthesizing sandwich-type graphene@Fe 3O 4 dots/amorphous carbon with high lithium storage performance
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Crosslinking-induced spontaneous growth: A novel strategy for synthesizing sandwich-type graphene@Fe 3O 4 dots/amorphous carbon with high lithium storage performance

机译:交联诱导的自发增长:合成夹层型石墨烯的新策略@ FE 3 O 4 锂储存性能高/无定形碳

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Graphical abstractDisplay OmittedHighlights?Crosslinking-induced spontaneous growth is developed for preparing G@Fe3O4/C.?G@Fe3O4/C shows sandwich-type structure with ultrasmall Fe3O4dots of 2–3?nm.?G@Fe3O4/C presents highly reversible capacity and superior high-rate capability.AbstractGraphene/Fe3O4hybrids have long been regarded as promising anode materials for lithium-ion batteries but remain significant bottlenecks of inhomogeneous/large Fe3O4particle size and agglomeration during the repeated lithiation/dethiation process. By carefully selecting a metallo-organic molecule of ferrocene as the building block, a novel methodology has been explored herein for the preparation of sandwich-type graphene@Fe3O4dots/amorphous carbon (G@Fe3O4/C) hybrids via a Friedel–Crafts crosslinking-induced spontaneous growth process. As prepared, ultra-small Fe3O4dots of 2–3?nm are distributed uniformly in the amorphous carbon matrix coated on the surface of graphene. The ultralow size of Fe3O4dots is able to minimize the volume change and Li+migrating distance, while the carbon matrix and graphene framework prevent Fe3O4dots from aggregation and offer a superior conductive skeleton along with a flexible framework to buffer the volume changes. In addition, the well-developed pore structure can accommodate the large volume change and facilitate the electrolyte diffusion/transfer, thereby increasing the ion accessible surface area, especially at high charge–discharge rates. Consequently, G@Fe3O4/C presents excellent lithium storage performances, including a highly reversible capacity of 1241?mAh?g?1, an outstanding cycling stability after 200 cycles (1055?mAh?g?1) and a superior high-rate capability (724?mAh?g?1at 5?A?g?1).]]>
机译:<![cdata [ 图形摘要 显示省略 突出显示 < CE:简单段ID =“SP0010”View =“全部”> 开发诱导的自发增长是为准备G @ FE 3 O 4 / c。 g @ fe 3 O 4 / C显示三明治型结构,带有UltraSMALL FE 3 O 4 DOTS 2-3?NM。 < CE:列表项ID =“O0015”> g @ fe 3 O 4 / C显示出高度可逆的容量和卓越的高速度能力。 抽象 Graphene / Fe 3 o 4 混合物长期被认为是有前途的阳极材料用于锂离子电池,但仍然是Inhomeneneo的显着瓶颈US / LARGE FE 3 O 4 重复锂化/歧视过程中的粒度和聚集。通过仔细选择二茂铁作为构建块的金属有机分子,本文探讨了一种新的方法,用于制备夹层型石墨烯@ Fe 3 O. 4 DOT /非晶碳(G @ FE 3 O 4 3 O 4 DOTS 2-3?NM在涂覆在石墨烯表面上的非晶碳基质中均匀分布。 FE 3 O 4 DOTS能够最大限度地减少音量变化和LI + 迁移距离,而碳矩阵和石墨烯框架可以防止Fe 3 O 4> 4 从聚合的点,并提供卓越的导电骨架以及灵活的框架来缓冲卷变化。此外,良好发育的孔结构可以容纳大体积变化并促进电解质扩散/转移,从而增加离子可接近的表面积,尤其是在高电荷放电速率下。因此,G @ FE 3 O 4 / C显示出优异的锂存储性能,包括a高度可逆的容量为1241?MAH?G ?1 ,200次循环后的出色的循环稳定性(1055?MAH?G ?1 )和优异的高速度能力(724?mah?g ?1 在5?a?g ?1 )。 ]]>

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