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Co-activated Conversion Reaction of MoO2:CoMoO3 as a Negative Electrode Material for Lithium-Ion Batteries

机译:MOO2的共激化转化反应:COMO3作为锂离子电池的负极材料

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Extensive studies to develop high-capacity electrodes have been conducted worldwide to meet the urgent demand for next-generation lithium-ion batteries. In this work, we demonstrated a novel strategy to alter the lithiation mechanism of the transition metal oxide to increase the reversible capacity of the electrode material. A representative insertion-type negative electrode material, MoO_(2), was modified by introducing a heterogeneous element (Co) to synthesize the solid solution of CoO and MoO_(2) (CoMoO_(3)). CoMoO_(3) exhibited a notably improved reversible capacity of 860 mA h g~(–1), attributed to the conversion reaction, in contrast to MoO_(2) that delivers 310 mA h g~(–1), as it is limited by the insertion reaction. X-ray absorption spectroscopy and X-ray diffraction demonstrated that CoO is converted to Co and Li_(2)O, amorphizing the host structure, whereas the conversion of MoO_(2) takes place subsequently. Furthermore, the superior initial Coulombic efficiency of CoMoO_(3) (84.4%) to that of typical conversion materials is attributed to the highly conductive Co and MoO_(2), which reinforce the electronic conductivity of the active particles. The results obtained from this study provide significant insights to explore high capacity metal oxides for the advanced lithium-ion batteries.
机译:为了满足下一代锂离子电池的迫切需求,世界范围内已经开展了大量的研究来开发高容量电极。在这项工作中,我们展示了一种新的策略来改变过渡金属氧化物的锂化机制,以增加电极材料的可逆容量。通过引入非均相元素(Co)对具有代表性的插入型负极材料MoO_2进行改性,合成了CoO和MoO_2(CoMoO_3)的固溶体。由于转化反应,CoMoO_3的可逆容量显著提高,达到860 mA h g~(-1),而MoO_2的可逆容量为310 mA h g~(-1),因为它受到插入反应的限制。X射线吸收光谱和X射线衍射表明,CoO转化为Co和Li_2)O,使主体结构非晶化,而MoO_2的转化随后发生。此外,与典型转化材料相比,CoMoO_3(84.4%)的初始库仑效率更高,这归因于高导电性的Co和MoO_2,它们增强了活性粒子的电子导电性。这项研究的结果为探索用于先进锂离子电池的高容量金属氧化物提供了重要的见解。

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