Activated Carbon Electrodes for Supercapacitors from Purple Corncob (Zea maysL.).

Activated carbon-based supercapacitor electrodes synthesized from biomass or waste-derived biomass have recently attracted considerable attention because of their low cost, natural abundance, and power delivery performance. In this work, purple-corncob-based active carbons are prepared by KOH activation and subsequently evaluated as a composite electrode for supercapacitors using either an acidic or an alkali solution as the electrolyte. The synthesis of the material involves mixing the purple corncob powder with different concentrations of KOH (in the range of 5% to 30%) and a thermal treatment at 700 °C under an inert atmosphere. Physicochemical characterizations were performed using scanning electron microscopy, Raman spectroscopy, N2 physisorption analysis, Fourier-transform infrared spectroscopy, and X-ray photoelectron spectroscopy, while the electrochemical characteristics were determined using cyclic voltammetry, a galvanostatic charge/discharge curve, and electrochemical impedance techniques measured in a three- and two-electrode system. Composite electrodes activated with 10% KOH had a specific surface area of 728 m2 g-1, and high capacitances of 195 F g-1 at 0.5 A g-1 in 1 mol L-1 H2SO4 and 116 F g-1 at 0.5 A g-1 in 1 mol L-1 KOH were obtained. It also presented a 76% capacitance retention after 50 000 cycles. These properties depend significantly on the microporous area and micropore volume characteristics of the activated carbon. Overall, our results indicate that purple corncob has an interesting prospect as a carbon precursor material for supercapacitor electrodes.

Cd2+ Detection by an Electrochemical Electrode Based on MWCNT-Orange Peel Activated Carbon.

This study reports the development of a new electrochemical sensor based on a carbon paste electrode (CPE) composed of biomass-based orange peel activated carbon (ACOP) and multiwalled carbon nanotubes (MWCNTs), and this composite is used for the electrochemical detection of cadmium ions (Cd2+). The ACOP/MWCNT composite was characterized by FTIR, Raman, and electrochemical impedance spectroscopy. The electrochemical evaluation of Cd2+ was performed using square wave and cyclic voltammetry. The ACOP/MWCNT-CPE electrochemical sensor exhibited a coefficient of determination r2 of 0.9907, a limit of detection of 0.91 ± 0.79 µmol L-1, and a limit of quantification of 3.00 ± 2.60 µmol L-1. In addition, the developed sensor can selectively detect Cd2+ in the presence of different interferents such as Zn2+, Pb2+, Ni2+, Co2+, Cu2+, and Fe2+ with a relative standard deviation (RSD) close to 100%, carried out in triplicate experiments. The ACOP/MWCNT-CPE presented high sensitivity, stability, and reproducibility and was successfully applied for the detection of Cd2+ in river water samples with recovery rate values ranging from 97.33 to 115.6%, demonstrating to be a very promising analytical alternative for the determination of cadmium ions in this matrix.

Voltammetric Sensing of Nifedipine Using a Glassy Carbon Electrode Modified with Carbon Nanofibers and Gold Nanoparticles.

Nifedipine, a widely utilized medication, plays a crucial role in managing blood pressure in humans. Due to its global prevalence and extensive usage, close monitoring is necessary to address this widespread concern effectively. Therefore, the development of an electrochemical sensor based on a glassy carbon electrode modified with carbon nanofibers and gold nanoparticles in a Nafion® film was performed, resulting in an active electrode surface for oxidation of the nifedipine molecule. This was applied, together with a voltammetric methodology, for the analysis of nifedipine in biological and environmental samples, presenting a linear concentration range from 0.020 to 2.5 × 10-6 µmol L-1 with a limit of detection 2.8 nmol L-1. In addition, it presented a good recovery analysis in the complexity of the samples, a low deviation in the presence of interfering potentials, and good repeatability between measurements.

Hierarchical Porous Carbon-PtPd Catalysts and Their Activity toward Oxygen Reduction Reaction.

PtPd bimetallic catalysts supported on hierarchical porous carbon (HPC) with different porous sizes were developed for the oxygen reduction reaction (ORR) toward fuel cell applications. The HPC pore size was controlled by using SiO2 nanoparticles as a template with different sizes, 287, 371, and 425 nm, to obtain three HPC materials denoted as HPC-1, HPC-2, and HPC-3, respectively. PtPd/HPC catalysts were characterized by scanning electron microscopy, X-ray photoelectron spectroscopy, X-ray diffraction, and high-resolution transmission electron microscopy. The electrochemical performance was examined by cyclic voltammetry and linear sweep voltammetry. PtPd/HPC-2 turned out to be the most optimal catalyst with an electroactive surface area (ESA) of 40.2 m2 g-1 and a current density for ORR of -1285 A g-1 at 2 mV s-1 and 1600 rpm. In addition, we conducted a density functional theory computational study to examine the interactions between a PtPd cluster and a graphitic domain of HPC, as well as the interaction between the catalyst and the oxygen molecule. These results reveal the strong influence of the porous size (in HPC) and ESA values (in PtPd nanoparticles) in the mass transport process which rules the electrochemical performance.

Voltammetric sensor based on glassy carbon electrode modified with hierarchical porous carbon, silver sulfide nanoparticles and fullerene for electrochemical monitoring of nitrite in food samples.

This paper reports the development of a voltammetric sensor using glassy carbon electrode based on hierarchical porous carbon (HPC) with silver sulfide nanoparticles (Ag2SNP), Nafion and fullerene (C60) for the determination of nitrite in foods. Raman spectroscopy, scanning electron microscopy, transmission electron microscopy and energy-dispersive X-ray were used to characterize the morphology and composition of the materials. The use of HPC and C60 in the construction of the electrode contributed toward the enlargement of the specific surface area and the improvement of the electrochemical performance of the device. The electrochemical behavior of nitrite in different electrodes was evaluated by cyclic voltammetry in the potential range of 0.4 - 1 V. Using the optimal conditions, a linear response ranges of 4.0- 148 µmol L-1, a limit of detection of 0.09 µmol L-1 and a sensitivity of 0.05 µAµmol L-1 cm-2 were obtained. The results showed that the proposed method can selectively detect nitrite in the presence of other compounds without interference and with good stability. The proposed method was successfully applied for the detection of nitrite in food samples where it demonstrated a good degree of accuracy and satisfactory efficiency.