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Heteroatom Doped-Carbon Nanospheres as Anodes in Lithium Ion Batteries

机译:杂原子掺杂碳纳米球作为锂离子电池中的阳极

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摘要

Long cycle performance is a crucial requirement in energy storage devices. New formulations and/or improvement of “conventional” materials have been investigated in order to achieve this target. Here we explore the performance of a novel type of carbon nanospheres (CNSs) with three heteroatom co-doped (nitrogen, phosphorous and sulfur) and high specific surface area as anode materials for lithium ion batteries. The CNSs were obtained from carbonization of highly-crosslinked organo (phosphazene) nanospheres (OPZs) of 300 nm diameter. The OPZs were synthesized via a single and facile step of polycondensation reaction between hexachlorocyclotriphosphazene (HCCP) and 4,4′-sulphonyldiphenol (BPS). The X-ray Photoelectron Spectroscopy (XPS) analysis showed a high heteroatom-doping content in the structure of CNSs while the textural evaluation from the N2 sorption isotherms revealed the presence of micro- and mesopores and a high specific surface area of 875 m2/g. The CNSs anode showed remarkable stability and coulombic efficiency in a long charge–discharge cycling up to 1000 cycles at 1C rate, delivering about 130 mA·h·g−1. This study represents a step toward smart engineering of inexpensive materials with practical applications for energy devices.
机译:长周期性能是储能设备中的关键要求。为了实现这个目标,已经研究了新配方和/或“常规”材料的改进。在这里,我们探索了一种新型的碳纳米球(CNS)的性能,该碳纳米球具有三种共掺杂的杂原子(氮,磷和硫)和高比表面积,可作为锂离子电池的负极材料。 CNS是通过碳化300纳米直径的高度交联的有机(磷腈)纳米球(OPZ)获得的。 OPZ是通过六氯环三磷腈(HCCP)与4,4'-磺酰基二酚(BPS)之间的简单且容易的缩合反应步骤合成的。 X射线光电子能谱(XPS)分析显示中枢神经系统结构中杂原子掺杂含量高,而N2吸附等温线的组织结构评价表明存在微孔和中孔,比表面积高875 m > 2 / g。 CNSs阳极在以1C的速率进行长达1000次循环的长充电-放电循环中显示出显着的稳定性和库伦效率,可提供约130 mA·h·g -1 。这项研究代表了将廉价材料与能源设备的实际应用进行智能工程的一步。

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