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Low-temperature synthesis of CeB6 nanowires and nanoparticles as feasible lithium-ion anode materials

机译:低温合成CEB6纳米线和纳米粒子作为可行的锂离子阳极材料

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Metallic CeB6 nanomaterials were prepared via the low-temperature solution combustion method (nanoparticles) and high-pressure solid state reaction (nanowires). X-ray diffraction patterns and High-resolution transmission electron microscopy images reveal that CeB6 nanoparticles are highly crystalline and CeB6 nanowires are single crystals. The X-ray photoelectron spectroscopy analysis indicates that the cerium is present in the +3 and +4 mixed-valence state in CeB6. As lithium-ion anodes, CeB6 nanowires (nanoparticles) electrode achieves a capacity of similar to 531 (338) mA h g(-1) in the initial cycle and keeps a reversible capacity of similar to 225 (185) mA h g(-1) after 60 cycles. CeB6 nanowires are tested for 6000 cycles at 1000 mA g(-1), which shows a specific capacity approaching to the capacity at 100 mA g(-1) in spite of fluctuation within a narrow range, and keep similar to 168 mA h g(-1) after 6000 cycles, indicating a stable cycling performance owing to the excellent metal-like conductivity of (similar to 5.67 x 10(3) S m(-1)). The reason of capacity rising is that the reduction and oxidation levels of CeB6 electrodes are improved after the 2nd cycle with Li+ insertion/extraction. Meanwhile, kinetic analysis reveals that the Li+ storage mechanism is mainly controlled by a surface capacitive behavior. (C) 2019 The Society of Powder Technology Japan. Published by Elsevier B.V. and The Society of Powder Technology Japan. All rights reserved.
机译:通过低温溶液燃烧方法(纳米粒子)和高压固态反应(纳米线)制备金属CeB6纳米材料。 X射线衍射图案和高分辨率透射电子显微镜图像显示CEB6纳米颗粒是高晶体,CEB6纳米线是单晶。 X射线光电子能谱分析表明铈存在于CEB6中的+ 3和+4个混合价状态中。作为锂离子阳极,CEB6纳米线(纳米粒子)电极在初始循环中实现了类似于531(338)mA Hg(-1)的容量,并且可逆容量与225(185)Ma Hg(-1)相似60次循环后。 CEB6纳米线在1000 mA g(-1)时测试6000个循环,显示出在100mA g(-1)的容量下的特定容量,尽管在窄范围内波动,并且保持类似于168 mA hg( -1)6000次循环后,由于稳定​​的循环性能,由于(类似于5.67×10(3)S m(-1))。容量上升的原因是在具有Li +插入/提取的第二循环之后改善CEB6电极的还原和氧化水平。同时,动力学分析显示Li +储存机制主要由表面电容性能控制。 (c)2019年日本粉末技术学会。由elsevier b.v发表。和日本粉末科技会。版权所有。

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