Ghasem Hosseini Mir, Shahryari Elham
Department of Physical Chemistry, Electrochemistry Research Laboratory, University of Tabriz, Tabriz, Iran; Engineering Faculty, Department of Materials Science and Nanotechnology, Near East University, 99138 Nicosia, North Cyprus, Mersin 10, Turkey.
Department of Physical Chemistry, Electrochemistry Research Laboratory, University of Tabriz, Tabriz, Iran.
J Colloid Interface Sci. 2017 Jun 15;496:371-381. doi: 10.1016/j.jcis.2017.02.027. Epub 2017 Feb 14.
Chitosan/Graphene Oxide-MWCNT/polyaniline (CS/GM/PANI) ternary nanocomposite has been synthesized via in situ polymerization of aniline in the presence of CS/GM. The Morphology of nanocomposites was studied by Field emission scanning electron microscopy (FE-SEM), Fourier transform infrared (FT-IR) spectroscopy, as well as X-ray photoelectron spectroscopy (XPS). Furthermore, the supercapacitive behavior of the CS-based samples was investigated using cyclic voltammetry (CV), galvanostatic charge-discharge (CD) and electrochemical impedance spectroscopy (EIS) techniques in 0.5M NaSO. It is found that the CS/GM/PANI nanocomposite displays much higher specific capacitance along with better cycle stability than those of CS and CS/GM. The specific capacitance of 609.2Fg (48.5mFcm) was obtained for the CS/GM/PANI at a scan rate of 10mVs. In addition, the synthesized nanocomposite retained 96% of the initial capacitance after 500 cycles of charge-discharge at a current density of 5Ag. The improvement in the supercapacitive behavior of CS/GM/PANI may be attributed to the porous structure and pseudocapacitive mechanism of charge-storage.
壳聚糖/氧化石墨烯-多壁碳纳米管/聚苯胺(CS/GM/PANI)三元纳米复合材料是通过在CS/GM存在的情况下原位聚合苯胺合成的。通过场发射扫描电子显微镜(FE-SEM)、傅里叶变换红外(FT-IR)光谱以及X射线光电子能谱(XPS)研究了纳米复合材料的形态。此外,在0.5M NaSO中使用循环伏安法(CV)、恒电流充放电(CD)和电化学阻抗谱(EIS)技术研究了基于CS的样品的超级电容行为。结果发现,与CS和CS/GM相比,CS/GM/PANI纳米复合材料具有更高的比电容以及更好的循环稳定性。在扫描速率为10mVs时,CS/GM/PANI的比电容为609.2Fg(48.5mFcm)。此外,在5Ag的电流密度下进行500次充放电循环后,合成的纳米复合材料保留了初始电容的96%。CS/GM/PANI超级电容行为的改善可能归因于其多孔结构和赝电容电荷存储机制。