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Ge/C Nanowires as High-Capacity and Long-Life Anode Materials for Li-Ion Batteries

机译:Ge / C纳米线作为锂离子电池的高容量和长寿命阳极材料

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摘要

Germanium-based materials (Ge and GeO_x) have recently demonstrated excellent lithium-ion storage ability and are being considered as the most promising candidates to substitute commercial carbon-based anodes of lithium-ion batteries. Nevertheless, practical implementation of Ge-based materials to lithiumion batteries is greatly hampered by the poor cyclability that resulted from the huge volume variation during lithiation/delithiation processes. Herein, uniform carbonencapsulated Ge and GeO_x nanowires were synthesized by a one-step controlled pyrolysis of organic-inorganic hybrid GeO_x/ethylenediamine (GeO_x/EDA) nanowires in H_2/Ar and Ar atmospheres, respectively. The as-obtained Ge/C and GeO_x/C nanowires possess well-defined 0D-in-1D morphology and homogeneous carbon encapsulation, which exhibit excellent Li storage properties including high specific capacities (approximate 1200 and 1000 mA h g~(-1) at 0.2C for Ge/C and GeO_x/C, respectively). The Ge/C nanowires, in particular, demonstrate superior rate capability with excellent capacity retention and stability (producing high stable discharge capacities of about 770 mA h g~(-1) after 500 cycles at 10C), making them promising candidates for future electrodes for high-power Li-ion batteries. The improved electrochemical performance arises from synergistic effects of 0D-in-1D morphology and uniform carbon coating, which could effectively accommodate the huge volume change of Ge/GeO_x during cycling and maintain perfect electrical conductivity throughout the electrode.
机译:锗基材料(Ge和GeO_x)最近表现出出色的锂离子存储能力,被认为是替代锂离子电池商用碳基阳极的最有前途的候选材料。然而,由于在锂化/脱锂过程中体积的巨大变化而导致的可循环性差,极大地阻碍了将Ge基材料实际应用到锂离子电池中。本文中,通过在H_2 / Ar和Ar气氛中分别对有机-无机杂化GeO_x /乙二胺(GeO_x / EDA)纳米线进行一步控制的热解,合成了均匀的碳包封的Ge和GeO_x纳米线。所获得的Ge / C和GeO_x / C纳米线具有明确的0D-in-1D形态和均质的碳包封,显示出优异的Li储存性能,包括高比容量(在1200℃和1200 mA hg〜(-1)时)。 Ge / C和GeO_x / C分别为0.2C)。尤其是Ge / C纳米线,具有优异的倍率性能,出色的容量保持能力和稳定性(在10C下经过500次循环后可产生约770 mA hg〜(-1)的高稳定放电容量),使其有望成为未来电极的候选材料。大功率锂离子电池。电化学性能的提高归因于0D-in-1D形态和均匀碳涂层的协同效应,可有效适应循环过程中Ge / GeO_x的巨大体积变化,并在整个电极上保持完美的导电性。

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