Jiang Jingui, Chen Hao, Wang Zhao, Bao Luke, Qiang Yiwei, Guan Shiyou, Chen Jianding
School of Materials Science and Engineering, East China University of Science and Technology, Mei Long Road 130, Shanghai 200237, PR China.
School of Materials Science and Engineering, East China University of Science and Technology, Mei Long Road 130, Shanghai 200237, PR China.
J Colloid Interface Sci. 2015 Aug 15;452:54-61. doi: 10.1016/j.jcis.2015.04.012. Epub 2015 Apr 18.
A porous carbon microsphere with moderate specific surface area and superior specific capacitance for supercapacitors is fabricated from polyphosphazene microsphere as the single heteroatoms source by the carbonization and subsequent KOH activation under N2 atmosphere. With KOH activation, X-ray photoelectron spectroscopy analysis confirms that the phosphorus of polyphosphazene microsphere totally vanishes, and the doping content of nitrogen and its population of various functionalities on porous carbon microsphere surface are tuned. Compared with non-porous carbon microsphere, the texture property of the resultant porous carbon microsphere subjected to KOH activation has been remarkably developed with the specific surface area growing from 315 to 1341 m(2) g(-1)and the pore volume turning from 0.17 to 0.69 cm(3) g(-1). Prepared with the KOH/non-porous carbon microsphere weight ratio at 1.0, the porous carbon microsphere with moderate specific surface area of 568 m(2) g(-1), exhibits intriguing electrochemical behavior in 1 M H2SO4 aqueous electrolyte, with superior specific capacitance (278 F g(-1) at 0.1 A g(-1)), good rate capability (147 F g(-1) remained at 10 A g(-1)) and robust cycling durability (No capacitance loss after 5000 cycles). The promising electrochemical performance could be ascribed to the synergy of nitrogen heteroatom functionalities and the porous morphology.
以聚磷腈微球为单一杂原子源,在氮气气氛下通过碳化及后续氢氧化钾活化制备了一种具有适中比表面积和优异比电容的用于超级电容器的多孔碳微球。通过氢氧化钾活化,X射线光电子能谱分析证实聚磷腈微球中的磷完全消失,且多孔碳微球表面氮的掺杂含量及其各种官能团的数量得到了调控。与无孔碳微球相比,经过氢氧化钾活化的所得多孔碳微球的织构性质得到了显著改善,比表面积从315增大到1341 m² g⁻¹,孔体积从0.17转变为0.69 cm³ g⁻¹。以氢氧化钾与无孔碳微球的重量比为1.0制备的具有568 m² g⁻¹适中比表面积的多孔碳微球,在1 M硫酸水溶液电解质中表现出有趣的电化学行为,具有优异的比电容(在0.1 A g⁻¹时为278 F g⁻¹)、良好的倍率性能(在10 A g⁻¹时仍保持147 F g⁻¹)和强大的循环耐久性(5000次循环后无电容损失)。这种有前景的电化学性能可归因于氮杂原子官能团与多孔形态的协同作用。