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将微纳硅/二氧化硅(Si/SiO(x))封装于共轭氮掺杂碳中,作为用于先进锂离子电池的无粘结剂整体阳极。

Encapsulating micro-nano Si/SiO(x) into conjugated nitrogen-doped carbon as binder-free monolithic anodes for advanced lithium ion batteries.

作者信息

Wang Jing, Zhou Meijuan, Tan Guoqiang, Chen Shi, Wu Feng, Lu Jun, Amine Khalil

机构信息

School of Chemical Engineering and the Environment, Beijing Institute of Technology, Beijing Key Laboratory of Environmental Science and Engineering, Beijing, 100081, China.

出版信息

Nanoscale. 2015 May 7;7(17):8023-34. doi: 10.1039/c5nr01209k.

Abstract

Silicon monoxide, a promising silicon-based anode candidate for lithium-ion batteries, has recently attracted much attention for its high theoretical capacity, good cycle stability, low cost, and environmental benignity. Currently, the most critical challenge is to improve its low initial coulombic efficiency and significant volume changes during the charge-discharge processes. Herein, we report a binder-free monolithic electrode structure based on directly encapsulating micro-nano Si/SiOx particles into conjugated nitrogen-doped carbon frameworks to form monolithic, multi-core, cross-linking composite matrices. We utilize micro-nano Si/SiOx reduced by high-energy ball-milling SiO as active materials, and conjugated nitrogen-doped carbon formed by the pyrolysis of polyacrylonitrile both as binders and conductive agents. Owing to the high electrochemical activity of Si/SiOx and the good mechanical resiliency of conjugated nitrogen-doped carbon backbones, this specific composite structure enhances the utilization efficiency of SiO and accommodates its large volume expansion, as well as its good ionic and electronic conductivity. The annealed Si/SiOx/polyacrylonitrile composite electrode exhibits excellent electrochemical properties, including a high initial reversible capacity (2734 mA h g(-1) with 75% coulombic efficiency), stable cycle performance (988 mA h g(-1) after 100 cycles), and good rate capability (800 mA h g(-1) at 1 A g(-1) rate). Because the composite is naturally abundant and shows such excellent electrochemical performance, it is a promising anode candidate material for lithium-ion batteries. The binder-free monolithic architectural design also provides an effective way to prepare other monolithic electrode materials for advanced lithium-ion batteries.

摘要

一氧化硅作为一种很有前景的锂离子电池硅基负极材料,因其高理论容量、良好的循环稳定性、低成本和环境友好性,近年来备受关注。目前,最关键的挑战是提高其较低的初始库仑效率以及充放电过程中显著的体积变化。在此,我们报道了一种无粘结剂的整体电极结构,该结构基于将微纳米Si/SiOx颗粒直接封装到共轭氮掺杂碳骨架中,以形成整体、多核、交联的复合基体。我们利用通过高能球磨SiO还原得到的微纳米Si/SiOx作为活性材料,以及由聚丙烯腈热解形成的共轭氮掺杂碳同时作为粘结剂和导电剂。由于Si/SiOx的高电化学活性以及共轭氮掺杂碳骨架的良好机械弹性,这种特定的复合结构提高了SiO的利用效率,适应了其大体积膨胀,同时具有良好的离子和电子导电性。退火后的Si/SiOx/聚丙烯腈复合电极表现出优异的电化学性能,包括高初始可逆容量(2734 mA h g(-1),库仑效率为75%)、稳定的循环性能(100次循环后为988 mA h g(-1))和良好的倍率性能(1 A g(-1)倍率下为800 mA h g(-1))。由于该复合材料天然丰富且表现出如此优异的电化学性能,它是一种很有前景的锂离子电池负极候选材料。这种无粘结剂的整体结构设计也为制备其他用于先进锂离子电池的整体电极材料提供了一种有效方法。

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