Abstract

AbstractHigh‐performance composite electrode materials for supercapacitors were developed by two‐step electrochemical deposition of nano‐NiO and poly(3,4‐ethylenedioxythiophene) (PEDOT) on nickel foam (NF). NF is considered an excellent conductive substrate for preparing porous electrode materials due to its high conductivity and porosity. The electrodeposited NiO nanoparticles were uniformly and densely coated on the pore of NF to fill in the internal voids, which provides an abundant active site for the electrodeposition of PEDOT. PEDOT was prepared by simple electrodeposition and was uniformly coated on the substrate surface which has high conductivity and reversible electrochemical redox properties, as well as excellent cyclic stability. The loose surface morphology not only provides abundant redox active sites for electrode material but also contributes the good pseudocapacitance property. As expected, the maximum mass‐specific capacity of PEDOT/NiO@NF composite electrode material can reach up to 129.7 F g−1 at the current density of 1 A g−1. Moreover, the composite electrode material shows excellent electrochemical cycling stability that the specific capacity has no obvious decay compared with its initial capacity after 200 cycles of cyclic voltammetry and 100 cycles of galvanostatic charge–discharge (GCD). This work demonstrates that the composite material PEDOT/NiO@NF could be a candidate flexibility electrode material for high‐performance supercapacitor applications.

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.