Abstract

In this study, carbon quantum dots (Cdots) synthesized from a pencil graphite precursor using a bottom-up method were incorporated into polyaniline (PANI) to form Cdots-PANI nanocomposite. Cdots, PANI and Cdots-PANI nanocomposites were characterized using the Fourier-Transform infrared spectroscopy (FT-IR), UV–visible spectroscopy (UV–vis), X-ray diffraction (XRD) spectroscopy, scanning electron microscopy (SEM), and transmission electron microscopy (TEM). The FT-IR spectra of graphene and Cdots show the emergence of a peak at 3500 cm−1, which was initially absent in graphene, after the formation of Cdots, among other peaks. The peak at 3500 cm−1 and the stretching vibration at 1647 cm−1 suggest the presence of –OH and C=C in the Cdots. The FT-IR spectra of PANI/Cdots and PANI show that the peaks in PANI shifted to higher wavenumbers after composite formation. Similarly, the UV–visible spectra of the PANI/Cdots composite revealed a hypsochromic shift of the characteristic PANI peaks at 320 and 600 nm to 300 and 560 nm, respectively. Electrochemical characterization of Cdots, PANI and Cdots-PANI nanocomposites was done with screen-printed carbon electrodes (SPCE) and screen-printed gold electrodes (SPAuE) modified with the nanomaterials and the nanocomposites. The electrochemical properties of the as-synthesized nanomaterials and the nanocomposite were investigated with Cyclic Voltammetry (CV) and Electrochemical Impedance Spectroscopy (EIS) in 10 mM K3[Fe(CN)6] solution using the bare screen-printed electrodes and the modified electrodes. The modified electrodes gave higher anodic peak current (Ipa) responses and lower charge transfer resistance (Rct) values in the redox probe than the bare electrodes. The SPCE-Cdots-PANI nanocomposite-modified electrode exhibited better redox potentials, faster electron transfer kinetics, larger surface area, and greater stability than the bare electrodes and the other modified electrodes. The outstanding electrochemical properties of SPCE-Cdots/PANI underscores its potentials as a sensitive electrochemical sensor for a wide range of analytes.

Full Text
Published version (Free)

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