Cobalt-tungsten diselenide-supported nickel foam as a battery-type positive electrode for an asymmetric supercapacitor device: comparison with various MWSe2 (M = Ni, Cu, Zn, and Mn) on the structural and capacitance characteristics.

New exploration in nanomaterial research has been greatly encouraged so as to discover active electrode materials with extraordinary properties and performances. In this report, we demonstrated the synthesis of different transition metal-incorporated MWSe2 (M = Co, Ni, Cu, Zn, and Mn) and studied them using various characterization techniques. Subsequently, the proposed bimetallic chalcogenides were successfully applied as the active electrode materials for pseudocapacitor applications. The results of the electrochemical studies showed that CoWSe2 exhibited a higher specific capacitance of 3309.58 F g-1 at a constant applied current density of 1.35 A g-1, which is 1.07, 1.76, 2.04, 8.7, and 12.28-fold higher than that of NiWSe2, CuWSe2, ZnWSe2, MnWSe2, and pristine WSe2, respectively. The interconnected nanosheet structure with voids facilitates rich active sites for efficient electrolyte uptake and superior charge transfer during the faradaic redox reaction. In addition, the cycle stability of CoWSe2/NF was studied and the retention capacitance of about 82.1% was recorded, which is higher than that of NiWSe2 (60.4%), CuWSe2 (50.12%), ZnWSe2 (46.44%), MnWSe2 (40.12%), and pristine WSe2 (31.2%). Owing to the higher specific capacitance and cycle stability, CoWSe2 was proposed as a battery-type electrode material for the fabrication of an asymmetric device. The fabricated CoWSe2//AC device provided excellent energy density and power density of 182.54 W h kg-1 and 2810.81 W kg-1, respectively, at 3.51 A g-1. Based on these properties, the proposed research and studies can provide a way for the profound development of 2D-layered metal chalcogenides for energy storage applications.

Ultrasound supported synthesis of tantalum carbide integrated functionalized carbon composite for the voltammetric determination of the antibacterial drug nitrofurantoin in pharmaceutical samples.

The synthesis and fabrication of oval-shaped tantalum carbide (Ta-C) integrated functionalized-multiwalled carbon nanotube (Ta-C/f-MWCNT) as an electrocatalyst for the electrochemical determination of nitrofurantoin (NFT) is described. The Ta-C/f-MWCNT composite was prepared using the soft-template method followed by the ultrasonication process. The as-prepared Ta-C/f-MWCNT composite was characterized using powder X-ray diffraction (XRD), Raman spectroscopy, field emission scanning electron microscopy (FESEM), scanning transmission electron microscopy (STEM), and X-ray photoelectron spectroscopy (XPS) analysis. The electrochemical properties of Ta-C/f-MWCNT were investigated by electrochemical impedance spectroscopy (EIS), cyclic voltammetry (CV), and linear sweep voltammetry (LSV). The Ta-C/f-MWCNT-modified glassy carbon electrode (Ta-C/f-MWCNT/GCE) was successfully utilized as an active electrocatalyst for the detection of NFT in the presence of 0.384 mM NFT containing 0.05 M phosphate buffer (pH 7) at a scan rate of 50 mV/s. The Ta-C/f-MWCNT/GCE exhibited a wide linear response range (0.04-1047 µM) and a low detection limit (0.0011 µM). Further, the Ta-C/f-MWCNT/GCE showed appreciable results for repeatability, reproducibility, and long-term cyclic stability towards NFT sensing. The Ta-C/f-MWCNT/GCE was applied to real sample analysis such as a commercial tablet and human urine samples. The Ta-C/f-MWCNT/GCE exhibited good recovery values for the tablet (105 to 115%) and urine (101-107%) samples. The above electrochemical results suggest that the Ta-C/f-MWCNT is a promising electrocatalyst for the electrochemical sensing of NFT drug. Graphical abstract .

Ultrasound treated cerium oxide/tin oxide (CeO2/SnO2) nanocatalyst: A feasible approach and enhanced electrode material for sensing of anti-inflammatory drug 5-aminosalicylic acid in biological samples.

In this work, we developed cerium oxide/tin oxide (CeO2/SnO2) nanocatalyst with the assistance of urea by a simple sonochemical method and utilized as an efficient electrode material for electrochemical sensing of anti-inflammatory drug 5-aminosalicylic acid (Mesalamine, MES). The CeO2/SnO2 nanoparticles (NPs) were systematically characterized in terms of their crystal structure, morphologies, and physicochemical properties using XRD, Raman, FESEM, HR-TEM, EDX, mapping, and XPS analysis. The characterization results clearly confirmed that the prepared NPs was formed in the phase of CeO2/SnO2 without any other impurities. The electrochemical properties of CeO2/SnO2 NPs were investigated by EIS, CV, and DPV techniques. The CeO2/SnO2 NPs (9.6 µA) modified GCE demonstrated an excellent and improved electrocatalytic activity in terms of higher anodic peak current and lower peak potential when compared to bare GCE (6.7 µA) and CeO2 NPs/GCE (8.2 µA) for the sensing of MES. The CeO2/SnO2 NPs/GCE shows broader linear response range and lower detection limit of 0.02-1572 µM and 0.006 µM, respectively. Moreover, other potentially interfering compounds such as a similar functional group containing biological substances and inorganic species have no interference effect towards MES sensing. In addition, the practicability of the CeO2/SnO2 NPs/GCE was tested by real sample analysis in commercial MES tablet, human urine, and serum samples with the appreciable recovery results.

Electrochemical detection of toxic anti-scald agent diphenylamine using oxidized carbon nanofiber encapsulated titanium carbide electrocatalyst.

Two dimensional (2D) titanium carbide (Ti-C) is an analogues of graphene have tremendous attention in recent years due to their high electrical conductivity and catalytic activity. Herein, we have synthesized Ti-C micro particles based on the template-assisted method and subsequently integrated with oxidized carbon nanofiber (f-CNF) through ultrasonication technique. The prepared Ti-C/f-CNF composite was subjected to various structural and morphological characterization techniques including the X-ray diffraction (XRD), scanning electron microscope (SEM), Energy Dispersive X-ray (EDX) and X-ray photoelectron spectroscopy (XPS). The all followed studies confirmed the formation and crystalline nature of prepared Ti-C/f-CNF nanocomposite. Further, the proposed Ti-C/f-CNF composite modified electrode was successfully applied as an electrocatalyst for the electrochemical detection of diphenylamine (DPA) in food. DPA is known as an anti-scald agent used to post harvest treatment of fruits. However, the higher concentration of DPA causes some hazardous side effects to human. Thus, the detection of DPA is an important concern in healthcare research. Eventually, the proposed Ti-C/f-CNF/SPCE exhibited ultra-low detection limit of (0.003 µM) with a linear range of 0.04-56.82 µM towards the detection of DPA. Moreover, the practicability of the proposed sensor was tested by real sample analysis by using fresh apple extract. Remarkably, the proposed sensor showed an excellent recovery range from 106.8% to 108% for the detection of DPA in spiked apple extract. Finally, we concluded that the integration of f-CNF with Ti-C is significantly enhanced both electrical conductivity and electrocatalytic activity for sensor application.