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In-Situ-Activated N-Doped Mesoporous Carbon from a Protic Salt and Its Performance in Supercapacitors

机译:质子盐原位活化氮掺杂介孔碳及其在超级电容器中的性能

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Protic salts have been recently recognized to be an excellent carbon source to obtain highly ordered N-doped carbon without the need of tedious and time-consuming preparation steps that are usually involved in traditional polymer-based precursors. Herein, we report a direct co-pyrolysis of an easily synthesized protic salt (benzimidazolium triflate) with calcium and sodium citrate at 850 degrees C to obtain N-doped mesoporous carbons from a single calcination procedure. It was found that sodium citrate plays a role in the final carbon porosity and acts as an in situ activator. This results in a large surface area as high as 1738 m(2)/g with a homogeneous pore size distribution and a moderate nitrogen doping level of 3.1%. X-ray photoelectron spectroscopy (XPS) measurements revealed that graphitic and pyridinic groups are the main nitrogen species present in the material, and their content depends on the amount of sodium citrate used during pyrolysis. Transmission electron microscopy (TEM) investigation showed that sodium citrate assists the formation of graphitic domains and many carbon nanosheets were observed. When applied as supercapacitor electrodes, a specific capacitance of 111 F/g in organic electrolyte was obtained and an excellent capacitance retention of 85.9% was observed at a current density of 10 A/g. At an operating voltage of 3.0 V, the device provided a maximum energy density of 35 W h/kg and a maximum power density of 12 kW/kg.
机译:质子盐最近被认为是获得高度有序的N掺杂碳的极佳碳源,而无需传统聚合物基前体通常涉及的繁琐且耗时的制备步骤。本文中,我们报道了易于合成的质子盐(苯并咪唑三氟甲磺酸盐)与柠檬酸钙和柠檬酸钠在850摄氏度下直接共热解,从而通过一次煅烧程序获得了N掺杂的中孔碳。发现柠檬酸钠在最终的碳孔隙率中起作用,并充当原位活化剂。这导致大表面积高达1738 m(2)/ g,孔径分布均匀,氮掺杂水平中等,为3.1%。 X射线光电子能谱(XPS)测量表明,石墨基团和吡啶基团是材料中存在的主要氮物种,其含量取决于热解过程中使用的柠檬酸钠的量。透射电子显微镜(TEM)研究表明,柠檬酸钠有助于石墨域的形成,并观察到许多碳纳米片。当用作超级电容器电极时,在有机电解质中获得的比电容为111 F / g,并且在10 A / g的电流密度下观察到85.9%的优异电容保持率。在3.0 V的工作电压下,该设备提供的最大能量密度为35 W h / kg,最大功率密度为12 kW / kg。

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