One-step electrodeposition of graphene loaded nickel oxides nanoparticles for acetaminophen detection.

An electrochemical sensor of acetaminophen (AP) based on electrochemically reduced graphene (ERG) loaded nickel oxides (Ni2O3-NiO) nanoparticles coated onto glassy carbon electrode (ERG/Ni2O3-NiO/GCE) was prepared by a one-step electrodeposition process. The as-prepared electrode was characterized by scanning electron microscopy, X-ray photoelectron spectroscopy and Raman spectroscopy. The electrocatalytic properties of ERG/Ni2O3-NiO modified glassy carbon electrode toward the oxidation of acetaminophen were analyzed via cyclic voltammetry (CV) and differential pulse voltammetry (DPV). The electrodes of Ni2O3-NiO/GCE, ERG/GCE, and Ni2O3-NiO deposited ERG/GCE were fabricated for the comparison and the catalytic mechanism understanding. The studies showed that the one-step prepared ERG/Ni2O3-NiO/GCE displayed the highest electro-catalytic activity, attributing to the synergetic effect derived from the unique composite structure and physical properties of nickel oxides nanoparticles and graphene. The low detection limit of 0.02 µM (S/N=3) with the wide linear detection range from 0.04 µM to 100 µM (R=0.998) was obtained. The resulting sensor was successfully used to detect acetaminophen in commercial pharmaceutical tablets and urine samples.

From DVD to dendritic nanostructure silver electrode for hydrogen peroxide detection.

A facile method of multi-potential step-scan has been employed to fabricate the dendritic silver nanostructures on a silver thin film based digital video disc (DVD) electrode. The morphologies of the nanostructures, the chemical composition, and the crystal structure have been characterized by field-emission scanning electron microscopy, energy-dispersed x-ray spectroscopy, and x-ray diffraction, respectively. The electrocatalytic activity of the resulting electrode toward the electro-reduction of hydrogen peroxide (H(2)O(2)) has been examined via cyclic voltammetry and amperometric analysis. The excellent linear relationship between current response and H(2)O(2) concentration is observed in the range from 5.88×10(-7) to 6.73×10(-5) mol L(-1) and the detection limit is 2×10(-7) mol L(-1) (S/N=3). The as-developed method has been employed to determine H(2)O(2) concentration in real samples.