The easy and rapid analytical tool, electrochemically polymerized (EP) glycine (GN) layered carbon paste electrode (LCPE), was used for the analysis of levofloxacin (LN) using cyclic voltammogram (CV) and differential pulse voltammetry (DPV). The surface features and activities of the electrochemical sensors EPGNLCPE and bare carbon paste electrode (BCPE) were analyzed using electrochemical impedance spectroscopy (EIS), field emission scanning electron microscopy (FE-SEM), CV and DPV methods. The modified sensor (EPGNLCPE)offers a vibrant and sensitive electrochemical LN oxidation peak by controlling overpotential and the electrode material fouling effect unlike BCPE. Under improved experimental conditions, the DPV method was used to analyze LN on EPGNLCPE by varying its concentration in 0.2 M phosphate buffer solution from 30 to 90 µM, resulting in a good linear relationship(between peak current and concentration), lower limit of detection (LOD: 8.436 × 10⁻⁷ M) and lower limit of quantification (LOQ: 2.812 × 10⁻⁶ M). Finally, real-time application of the sensor was tested by analyzing LN in medicinal samples, and good LN recovery was observed.

Rutin (RU) is one of the best-known natural antioxidants with various physiological functions in the human body and other plant species. In this work, an efficient voltammetric sensor to detect RU in food samples was explicated using a poly (glutamic acid)-modified graphene paste electrode (PGAMGPE). In order to detect RU, the proposed sensor diminishes material resistance and overpotential while increasing kinetic rate, peak currents, and material conductance. Using differential pulse voltammetry (DPV) and cyclic voltammetry (CV), the analysing efficiency of a PGAMGPE and a Bare graphene paste electrode (BGPE) was evaluated in 0.2 M phosphate buffer (PB) at an ideal pH of 6.5. in a potential window of −0.25 V to 0.6 V. Electrochemical impedance spectroscopy (EIS) was used to analyse the prepared electrode materials’ conductivity, charge transfer resistance, and the kinetics of electron transport. Field emission scanning electron microscopy (FE-SEM) images were considered to compare the exterior morphology of the PGAMGPE and the BGPE. It was discovered that the PGAMGPE and the BGPE have electroactive surfaces of 0.062 cm² and 0.04 cm², respectively. It was determined that two protons and two electrons participated in the redox process. The resultant limit of detection (LOD) was found to be 0.04 µM and 0.06 µM, respectively, using DPV and CV methods. In spite of common interferents such as metal ions and chemical species, the developed sensor’s selectivity for RU detection was impressive. For the simultaneous analysis of RU in the presence of caffeine (CF), the PGAMGPE affords a good electrochemical nature for RU with good selectivity. Due to the good stability, repeatability, reproducibility, and ease of use of the present RU sensor, it is useful for real sample analysis such as food and medicinal samples with recovery ranging from 94 to 100%.

Electrode materials comprising SnO ₂ quantum dots embedded within ZnO hexagonal prisms were successfully synthesized for building cost-effective energy-storage devices. Extensive structural and functional characterizations were performed to assess the electrochemical performance of the electrodes. SEM–EDS results confirm a uniform distribution of SnO ₂ quantum dots across ZnO. The integration of SnO ₂ quantum dots with ZnO hexagonal prisms markedly improved the electrochemical behavior. The analysis of electrode functionality conducted in a 3 M KOH electrolyte revealed specific capacitances of 949.26 and 700.68 F g⁻ ¹ for SnO ₂ @ZnO and ZnO electrodes, respectively, under a current density of 2 A g⁻ ¹ . After undergoing 5,000 cycles at a current density of 15 A g⁻ ¹ , the SnO ₂ @ZnO and ZnO electrodes displayed impressive cycling stability, maintaining specific capacitance retention rates of 89.9 and 92.2%, respectively. Additionally, a symmetric supercapacitor (SSC) device constructed using the SnO ₂ @ZnO electrode showcased exceptional performance, exhibiting a specific capacitance of 83 F g⁻ ¹ at 1.2 A g⁻ ¹ . Impressive power and energy densities were achieved by the device, with values reaching 2,808 and 70.2 W kg⁻ ¹ , respectively. Notably, the SnO ₂ @ZnO SSC device maintained a capacity preservation of 75% throughout 5,000 galvanostatic charge–discharge sequences. The outcomes highlight the potential of SnO ₂ @ZnO hexagonal prisms as candidates for energy-storage applications, offering scalability and cost-effectiveness. The proposed approach enhances the electrochemical performance while ensuring affordability, facilitating the creation of effective and financially feasible energy storage solutions.

Herein, a crystalline nano-flowers structured zinc oxide (ZnO) was directly grown on carbon fiber textile (CFT) substrate via a simple hydrothermal process and fabricated with a binder-free electrode (denoted as ZnO@CFT) for supercapacitor (SC) utilization. The ZnO@CFT electrode revealed a 201 F·g⁻¹ specific capacitance at 1 A·g⁻¹ with admirable stability of >90% maintained after 3000 cycles at 10 A·g⁻¹. These impressive findings are responsible for the exceedingly open channels for well-organized and efficient diffusion of effective electrolytic conduction via ZnO and CFT. Consequently, accurate and consistent structural and morphological manufacturing engineering is well regarded when increasing electrode materials’ effective surface area and intrinsic electrical conduction capability. The crystalline structure of ZnO nano-flowers could pave the way for low-cost supercapacitors.