Abstract
A novel unipolar pulse electro-polymerization (UPEP) method was used to prepare nanorod polyaniline (PANI) films on platinum substrates from aqueous solution containing 0.2 mol L −1 of aniline and 0.5 mol L −1 of sulphuric acid. The unipolar pulse waveform consisted of an applied anodic potential during the on-period and an open-circuit potential (zero current) during the off-period. The effects of pulse deposition parameters on the electrochemical properties of PANI films were investigated by potential cycling in 0.5 mol L −1 of H 2SO 4 solution. The supercapacitive performances of as-prepared PANI films were also investigated in the 0.5 mol L −1 of H 2SO 4 solution via charge/discharge tests as well as electrochemical impedance spectroscopy (EIS). The surface morphology and conformation of PANI films were characterized using scanning electron microscopy (SEM) and Fourier transform infrared (FT-IR) spectroscopy, respectively. Experimental results indicated that nanorod PANI films with uniform distribution on Pt were formed by using this novel method, and the anodic pulse potential should be the primary factor to influence the morphology and the conformation of PANI film. The PANI films prepared by UPEP method displayed much higher ion exchange capacity, better stability and more excellent supercapacitive performances than those by other methods such as the common cyclic voltammetric method (CVM) and potentiostatic method (PM). It should be attributed to the highly porous nano-sized PANI with short-fiber or rod-like structure and the depressed hydrolysis of aniline. The highest specific capacitance value of 907.9 F g −1 was obtained when the pulse potential, aniline concentration, pulse frequency and duty cycle were 0.85 V, 0.2 mol L −1, 1.25 s −1 and 50%, respectively.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
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.