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Synthesis of Partially Graphitic Ordered Mesoporous Carbons with High Surface Areas

机译:高比表面积的部分石墨有序介孔碳的合成

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摘要

Graphitic carbons with ordered mesostructure and high surface areas (of great interest in applications such as energy storage) have been synthesized by a direct triblock-copolymer-templating method. Pluronic F127 is used as a structure-directing agent, with a low-molecular-weight phenolic resol as a carbon source, ferric oxide as a catalyst, and silica as an additive. Inorganic oxides can be completely eliminated from the carbon. Small-angle XRD and N2 sorption analysis show that the resultant carbon materials possess an ordered 2D hexagonal mesostructure, uniform bimodal mesopores (about 1.5 and 6 nm), high surface area (∼1300 m2/g), and large pore volumes (∼1.50 cm3/g) after low-temperature pyrolysis (900 °C). All surface areas come from mesopores. Wide-angle XRD patterns demonstrate that the presence of the ferric oxide catalyst and the silica additive lead to a marked enhancement of graphitic ordering in the framework. Raman spectra provide evidence of the increased content of graphitic sp2 carbon structures. Transmission electron microscopy images confirm that numerous domains in the ordered mesostructures are composed of characteristic graphitic carbon nanostructures. The evolution of the graphitic structure is dependent on the temperature and the concentrations of the silica additive, and ferric oxide catalyst. Electrochemical measurements performed on this graphitic mesoporous carbon when used as an electrode material for an electrochemical double layer capacitor shows rectangular-shaped cyclic voltammetry curves over a wide range of scan rates, even up to 200 mV/s, with a large capacitance of 155 F/g in KOH electrolyte. This method can be widely applied to the synthesis of graphitized carbon nanostructures.
机译:已经通过直接三嵌段共聚物-模板方法合成了具有有序介孔结构和高表面积(在诸如能量存储等应用中引起极大关注)的石墨碳。 Pluronic F127用作结构导向剂,低分子量酚醛甲阶酚醛树脂为碳源,三氧化二铁为催化剂,二氧化硅为添加剂。无机氧化物可以从碳中完全消除。小角XRD和N2吸附分析表明,所得碳材料具有规则的2D六角形介孔结构,均匀的双峰介孔(约1.5和6 nm),高表面积(〜1300 m2 / g)和大孔体积(〜1.50)低温热解(900°C)后进行处理。所有表面积均来自中孔。广角X射线衍射图谱表明,三氧化二铁催化剂和二氧化硅添加剂的存在导致骨架中石墨有序化的显着增强。拉曼光谱提供了石墨sp2碳结构含量增加的证据。透射电子显微镜图像证实,有序介观结构中的许多域由特征性石墨碳纳米结构组成。石墨结构的演变取决于二氧化硅添加剂和三氧化二铁催化剂的温度和浓度。当将此石墨中孔碳用作电化学双层电容器的电极材料时,进行的电化学测量显示出在宽扫描速率范围内甚至高达200 mV / s且具有155 F大电容的矩形循环伏安曲线。 / g的KOH电解质。该方法可广泛应用于石墨化碳纳米结构的合成。

著录项

  • 来源
    《Advanced energy materials 》 |2011年第1期| 1-9| 共9页
  • 作者单位

    Department of Chemistry the Key Laboratory of Resource Chemistry of Ministry of Education Shanghai Normal University Shanghai 200234 P.R. China;

    Department of Chemistry the Key Laboratory of Resource Chemistry of Ministry of Education Shanghai Normal University Shanghai 200234 P.R. China;

    Department of Chemistry Shanghai Key Laboratory of Molecular Catalysis and Innovative Materials Fudan University Shanghai 200433 P.R. China;

    Department of Chemistry Shanghai Key Laboratory of Molecular Catalysis and Innovative Materials Fudan University Shanghai 200433 P.R. China;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    energy storage; graphitic carbon; high surface area; mesoporous materials; ordered structure; synthesis;

    机译:储能石墨碳高比表面积多孔材料有序结构合成;

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