一步法合成具有优异循环性能的聚苯胺纳米线/自支撑石墨烯复合材料

One-step synthesis of polyaniline nanowire/self-supported graphene composite with excellent cycling stability

  • 摘要: 研究采用一步电化学剥离和电沉积法,在含Na2SO4、HCl与苯胺(An)单体的混合溶液中,以柔性石墨纸为原料,利用电场条件下电解液离子定向迁移和苯胺单体的电聚合制备聚苯胺纳米线/自支撑石墨烯(PANI/SGr)复合材料。更具活性的新生SGr与PANI结合,显著提高了PANI/SGr复合材料的稳定性。PANI呈纳米线状均匀分布在SGr上,形成的三维网络结构所呈现出的孔隙促进了电解液离子扩散到复合材料的内部结构中。将PANI/SGr复合材料作为超级电容器电极材料进行电化学测试,2 mV·s−1的扫速下获得的比电容为453 F·g−1。在0.5~10 A·g−1的电流密度范围内,PANI/SGr复合材料倍率性能达73.1%。在1 A·g−1的电流密度下PANI/SGr复合材料经10000次充放电之后的循环稳定性仍高达87.3%。这表明PANI/SGr复合材料具有良好的电容性能和优异的循环稳定性,有望作为超级电容器电极材料。

     

    Abstract: The polyaniline nanowire/self-supported graphene (PANI/SGr) composite was synthesized by one-step electrochemical exfoliation and electrodeposition method using graphite paper. The directional migration of electrolyte ions and the electropolymerization of aniline monomers through the electrical field simultaneously occurred in the mixed solution including Na2SO4, HCl and aniline (An) monomers. The stability of the PANI/SGr composite is enhanced by the combination of the new-born SGr with high activity and PANI. The uniform distribution of the nanowire-like PANI is achieved on the surface of the SGr. The PANI nanowires lead to the formation of the three-dimensional network architecture, where the existence of pores facilitates the diffusion of electrolyte ions into the internal structure of the PANI/SGr composite. The electrochemical tests of the PANI/SGr composite were conducted as a supercapacitor electrode material. The specific capacitance of 453 F·g−1 at a scan rate of 2 mV·s−1 is achieved. The rate capability of the PANI/SGr composite at the current densities of 0.5-10 A·g−1 is up to 73.1%. The cycling stability of the PANI/SGr composite is as high as 87.3% after 10000 discharge-charge cycles at the current density of 1 A·g−1. All of these results indicate that the PANI/SGr composite possesses good capacitive performance and excellent cycling stability. The PANI/SGr composite is promising for supercapacitor electrode materials.

     

/

返回文章
返回