Skip navigation


Please use this identifier to cite or link to this item: http://localhost:8080/xmlui/handle/123456789/1369
Title: Chemically synthesized 3D nanostructured polypyrrole electrode for high performance supercapacitor applications
Other Titles: Journal of Materials Science: Materials in Electronics
Authors: Bhalerao, Anuradha B.
Keywords: Chemically synthesized 3D nanostructured polypyrrole electrode for high performance supercapacitor applications
Issue Date: 28-Apr-2018
Publisher: Springer Online Journals
Abstract: Three-dimensional (3D) polypyrrole (Ppy) electrodes are directly grown on Ni foam using a solution-based cost effective chemical method and an in situ controlled precipitation route for supercapacitor application. The Ppy electrodes are characterized for their structural and morphological studies using X-ray diffraction (XRD), Fourier transform infrared (FT-IR) spectroscopy, scanning electron microscopy (SEM) and transmission electron microscopy. The XRD study revealed that Ppy electrodes are amorphous. SEM shows the formation of tiny spherical grains spread over the entire electrode surface. The FT-IR study confirms the formation of Ppy film on the electrode surface. The supercapacitive performance of the Ppy electrode using the cyclic voltammetry technique in a 3M KOH electrolyte shows a maximum specific capacitance of 931 F/g at a scan rate of 5 mV/s. Performance analysis of the supercapacitive electrode carried out using electrochemical impedance spectroscopy (EIS). A distorted semicircle in the high frequency region of EIS shows reduction in charge-transfer resistance.
URI: http://192.168.3.232:8080/jspui/handle/123456789/1369
ISSN: 0957-4522
Appears in Collections:Applied Science Dept. Faculty/Staff

Files in This Item:
File Description SizeFormat 
Chemically synthesized 3D nanostructured polypyrrole electrode for high performance supercapacitor applications .pdfChemically synthesized 3D nanostructured polypyrrole electrode for high performance supercapacitor applications1.74 MBAdobe PDFView/Open


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.