Chen Jing, Cheng Youliang, Zhang Qingling, Fang Changqing, Wu Linlin, Bai Mengsha, Yao Yongtao
Xi'an University of Technology Xi'an 710048 P. R. China
National Key Laboratory of Science and Technology on Advanced Composites in Special Environments, Harbin Institute of Technology Harbin 150001 P. R. China.
RSC Adv. 2019 Oct 10;9(55):32258-32269. doi: 10.1039/c9ra06191f. eCollection 2019 Oct 7.
Mesoporous carbon/graphene composites (MCG) have exhibited good electrochemical performances; however, the fixed mesoporous carbon, the low specific surface area, and porosity are the main obstacles in their application in supercapacitors. In this paper, mesoporous carbon microspheres/graphene composites (MCMG) were synthesized a soft template method and subsequent thermal reduction by using cetyltrimethylammonium bromide (CTAB) as the structure-directing agent, and aqueous mesophase pitch (AMP) and graphene oxide (GO) as the carbon sources. The strong electrostatic interaction between GO/CTAB and AMP promoted the self-assembly of CTAB and AMP to form the MCMG precursor. The results showed that the CTAB concentration and aging temperature have an important effect on the morphology and pore structure of the synthesized MCMG. The high aging temperature promoted the formation of mesoporous carbon spheres and its diameter increased with the increase in the concentration of CTAB. The as-prepared MCMG at the aging temperature of 140 °C had obvious spherical and layered carbon materials after carbonization at 900 °C. When the concentration of CTAB was 10.6 g L, the formed mesoporous carbon spheres with the diameter of 30-40 nm were uniformly dispersed among the layered graphenes in MCMG-140-0.2 (the aging temperature of 140 °C and the CTAB content of 0.2 g). In addition, its specific surface area was 1150.5 m g and the mesopore size was centered at 4.3 nm, 7.9 nm, and 17.1 nm. Compared with the MCMG precursor, the ordered degree of the mesopores for MCMG was reduced due to the high temperature carbonization. Importantly, the specific capacitance of MCMG-140-0.2 at the current density of 0.1 A g was as high as 356.3 F g. Moreover, the specific capacitance of MCMG-140-0.2 at 1 A g remained at 278.5 F g, the capacitance retention was 92.1% after 6000 cycles, and the coulombic efficiency was over 98% at a high current density of 2 A g. Therefore, the as-prepared MCMG can be an excellent candidate for electrode materials in supercapacitors.
介孔碳/石墨烯复合材料(MCG)已展现出良好的电化学性能;然而,固定的介孔碳、低比表面积和孔隙率是其在超级电容器应用中的主要障碍。本文采用软模板法并通过后续热还原,以十六烷基三甲基溴化铵(CTAB)作为结构导向剂,水相中间相沥青(AMP)和氧化石墨烯(GO)作为碳源,合成了介孔碳微球/石墨烯复合材料(MCMG)。GO/CTAB与AMP之间强烈的静电相互作用促进了CTAB和AMP的自组装,形成了MCMG前驱体。结果表明,CTAB浓度和老化温度对合成的MCMG的形貌和孔结构有重要影响。较高的老化温度促进了介孔碳球的形成,其直径随着CTAB浓度的增加而增大。在140℃老化温度下制备的MCMG在900℃碳化后具有明显的球形和层状碳材料。当CTAB浓度为10.6 g/L时,在MCMG - 140 - 0.2(老化温度140℃,CTAB含量0.2 g)中形成的直径为30 - 40 nm的介孔碳球均匀地分散在层状石墨烯之间。此外,其比表面积为1150.5 m²/g,中孔尺寸集中在4.3 nm、7.9 nm和17.1 nm。与MCMG前驱体相比,由于高温碳化,MCMG的中孔有序度降低。重要的是,MCMG - 140 - 0.2在电流密度为0.1 A/g时的比电容高达356.3 F/g。此外,MCMG - 140 - 0.2在1 A/g时的比电容保持在278.5 F/g,在6000次循环后电容保持率为92.1%,在2 A/g的高电流密度下库仑效率超过98%。因此,所制备的MCMG可成为超级电容器电极材料的优异候选者。