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Co3O4-C yolk-shell hollow spheres derived from ZIF-12-PVP@GO for superior anode performance in lithium-ion batteries

机译:源自 ZIF-12-PVP@GO 的 Co3O4-C 蛋黄壳空心球在锂离子电池中具有优异的阳极性能

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摘要

Transitional metal oxides have attracted increasing attention as the most promising anode material for lithium-ion batteries (LIBs). However, due to the poor ionic conductivity and great structural changes in the process of Li+ insertion and extraction, the performance of the pristine materials in batteries still has a far way to go to satisfy requirements. In this article, using spherical ZIF-12 as a pyrolysis precursor, two Co3O4 hollow core-shell carbon nanocomposites (CHS@C and CHS@CG) were fabricated via a molecular precursor pyrolysis strategy. The synergistic effect of the yolk-shell hollow nanosphere structure shortens the diffusion path of ions, increases the contact area between the electrode and electrolyte, and provides a buffer space for the volume change in the electrochemical reaction. Both materials have excellent structural stability and good electrical conductivity. In comparison, the performance of CHS@CG is better, and the reversible specific capacity reaches 831 mAh center dot g(-1) at 0.2 C after 400 cycles. In the galvanostatic charge-discharge process, the Coulombic efficiency reaches nearly 100, exhibiting a good reversible cycle. The synthesis method of these electrode materials can provide a reference for making other energy storage equipments.
机译:过渡金属氧化物作为锂离子电池(LIB)最有前途的负极材料,越来越受到关注。然而,由于离子电导率差,在Li+插入和提取过程中结构变化较大,纯材料在电池中的性能要满足要求还有很长的路要走。本文以球形ZIF-12为热解前驱体,采用分子前驱体热解策略制备了两种Co3O4空心核壳碳纳米复合材料(CHS@C和CHS@CG)。卵黄壳中空纳米球结构的协同作用缩短了离子的扩散路径,增大了电极与电解液的接触面积,为电化学反应中的体积变化提供了缓冲空间。两种材料都具有优异的结构稳定性和良好的导电性。相比之下,CHS@CG的性能更好,在0.2 C下循环400次后,可逆比容量达到831 mAh中心点g(-1)。在恒流充放电过程中,库仑效率达到近100%,表现出良好的可逆循环。这些电极材料的合成方法可为制造其他储能设备提供参考。

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