Investigating the Electrocoagulation Treatment of Landfill Leachate by Iron/Graphite Electrodes: Process Parameters and Efficacy Assessment

Electrocoagulation is a widely used method for treating leachate since it is cost effective and eco-friendly. In the present study, the electrocoagulation process was employed to remove chemical oxygen demand (COD), NH4+, total dissolved solids (TDS), total suspended solids (TSS), turbidity, and color from landfill leachate. At first, lime was used as a pretreatment, then the Fe/Gr and Ti/PbO2/steel electrodes were used, and the optimum electrode was selected. Afterwards, the effects of some variables, including pH, current density, temperature, the inter-electrode distance, and the type of electrolyte were investigated. Results showed that COD, NH4+, TSS, TDS, electrical conductivity (EC), turbidity, color, and pH of effluent pretreatment chemical reached 22,371, 385, 884, 21,820 (mg/L), 13.8 (ms/cm3), 1355 (NTU), 8500 (TCU) and 10, respectively (the removal efficiency was 0, 20.37, 32.4, 61.99, 59.18, and 56.6 percent). With the Fe/Gr electrode, the optimal condition was observed as follows: pH of 7.5, current density of 64 mA/cm2, inter-electrode distance was equal to 1.5 cm, temperature at 20 °C, and retention time 2–4 h. Overall, the electrocoagulation with the Fe/Gr electrode was a suitable technology for landfill leachate treatment due to its effectiveness for the removal of both COD and NH4+, with advantageous performance indicators.

Investigation of Fast-Charging and Degradation Processes in 3D Silicon–Graphite Anodes

The 3D battery concept applied on silicon–graphite electrodes (Si/C) has revealed a significant improvement of battery performances, including high-rate capability, cycle stability, and cell lifetime. 3D architectures provide free spaces for volume expansion as well as additional lithium diffusion pathways into the electrodes. Therefore, the cell degradation induced by the volume change of silicon as active material can be significantly reduced, and the high-rate capability can be achieved. In order to better understand the impact of 3D electrode architectures on rate capability and degradation process of the thick film silicon–graphite electrodes, we applied laser-induced breakdown spectroscopy (LIBS). A calibration curve was established that enables the quantitative determination of the elemental concentrations in the electrodes. The structured silicon–graphite electrode, which was lithiated by 1C, revealed a homogeneous lithium distribution within the entire electrode. In contrast, a lithium concentration gradient was observed on the unstructured electrode. The lithium concentration was reduced gradually from the top to the button of the electrode, which indicated an inhibited diffusion kinetic at high C-rates. In addition, the LIBS applied on a model electrode with micropillars revealed that the lithium-ions principally diffused along the contour of laser-generated structures into the electrodes at elevated C-rates. The rate capability and electrochemical degradation observed in lithium-ion cells can be correlated to lithium concentration profiles in the electrodes measured by LIBS.

Pencil Graphite Electrodes Decorated with Platinum Nanoparticles as Efficient Electrocatalysts for Hydrogen Evolution Reaction

Platinum-based materials are widely known as the most utilized and advanced catalysts for hydrogen evolution reaction. For this reason, several studies have reported alternative methods of incorporating this metal into more economical electrodes with a carbon-based support material. Herein, we report on the performance of pencil graphite electrodes decorated with electrochemically deposited platinum nanoparticles as efficient electrocatalysts for hydrogen evolution reaction. The electrodeposition of platinum was performed via pulsed current electrodeposition and the effect of current density on the electrocatalytic activity was investigated. The obtained electrodes were characterized using cyclic voltammetry, while the electrocatalytic activity was assessed through linear sweep voltammetry. Field emission scanning electron microscopy and energy-dispersive X-ray spectroscopy were utilised to gain an insight into surface morphology and chemical analysis of platinum nanoparticles. The best performing electrocatalyst, at both low and high current densities, was characterized by the highest exchange current density of 1.98 mA cm−2 and an ultralow overpotential of 43 mV at a current density of 10 mA cm−2. The results show that, at low current densities, performances closest to that of platinum can be achieved even with an ultralow loading of 50 µg cm−2 Pt.

Potentiodynamic Electrochemical Impedance Spectroscopy of Polyaniline-Modified Pencil Graphite Electrodes for Selective Detection of Biochemical Trace Elements

In this study, we analyzed the application of potentiodynamic electrochemical impedance spectroscopy (PDEIS) for a selective in situ recognition of biological trace elements, i.e., Cr (III), Cu (II), and Fe (III). The electrochemical sensor was developed using the electropolymerization of aniline (Ani) on the surface of the homemade pencil graphite electrodes (PGE) using cyclic voltammetry (CV). The film was overoxidized to diminish the background current. A wide range of potential (V = −0.2 V to 1.0 V) was investigated to study the impedimetric and capacitive behaviour of the PAni/modified PGE. The impedance behaviors of the films were recorded at optimum potentials through electrochemical impedance spectroscopy (EIS) and scrutinized by means of an appropriate equivalent circuit at different voltages and at their corresponding oxidative potentials. The values of the equivalent circuit were used to identify features (charge transfer-resistant and double layer capacitance) that can selectivity distinguish different trace elements with the concentration of 10 μM. The PDEIS spectra represented the highest electron transfer for Cu (II) and Cr (III) in a broad potential range between +0.1 and +0.4 V while the potential V = +0.2 V showed the lowest charge transfer resistance for Fe (III). The results of this paper showed the capability of PDEIS as a complementary tool for conventional CV and EIS measurement for metallic ion sensing.

Compared EC-AFM Analysis of Laser-Induced Graphene and Graphite Electrodes in Sulfuric Acid Electrolyte

Flexible and economic sensor devices are the focus of increasing interest for their potential and wide applications in medicine, food analysis, pollution, water quality, etc. In these areas, the possibility of using stable, reproducible, and pocket devices can simplify the acquisition of data. Among recent prototypes, sensors based on laser-induced graphene (LIGE) on Kapton represent a feasible choice. In particular, LIGE devices are also exploited as electrodes for sensing in liquids. Despite a characterization with electrochemical (EC) methods in the literature, a closer comparison with traditional graphite electrodes is still missing. In this study, we combine atomic force microscopy with an EC cell (EC-AFM) to study, in situ, electrode oxidation reactions when LIGE or other graphite samples are used as anodes inside an acid electrolyte. This investigation shows the quality and performance of the LIGE electrode with respect to other samples. Finally, an ex situ Raman spectroscopy analysis allows a detailed chemical analysis of the employed electrodes.