Sense and Shoot: Unveiling the Electro-/Photocatalytic Potential of 2D White Graphene-Supported Perovskite Strontium Cobaltite from Detection to Remediation of Oxidative Stress Herbicide (Mesotrione).

In this research, we employed a strategy akin to "Feeding Two Birds with One Stone" aiming for the dual objectives of highly selective electrochemical detection and photocatalytic degradation of the environmentally hazardous herbicide mesotrione (MTN). We achieved this by utilizing hexagonal boron nitride (BN)-supported strontium cobaltite perovskite nanocomposites (SrCoO3/BN). The fabrication of the innovative bifunctional SrCoO3/BN nanocomposites involved a straightforward process of precipitation, followed by an annealing treatment and ultrasonication. The successful formation of these nanocomposites was corroborated through the application of diverse spectroscopic tools. Notably, as-prepared SrCoO3/BN nanocomposites exhibited a remarkable sensing platform for MTN, characterized by a notably low detection limit (11 nm), considerable sensitivity (3.782 µA µM-1 cm-2), and outstanding selectivity, alongside remarkable stability. Concurrently, these SrCoO3/BN nanocomposites demonstrated exceptional visible-light-driven photocatalytic efficacy for MTN degradation (99%) and complete mineralization. Our investigation systematically delved into the influence of operational parameters, including catalyst loading and the involvement of reactive oxidative species, in both the electrocatalytic and photocatalytic reactions. Drawing from these comprehensive studies, we have proposed plausible mechanisms for detecting and degrading MTN. Our findings pave the way for catalyst development, offering a unified solution for detecting and eliminating toxic organic compounds from the environment.

Facile engineering of gadolinium cobaltite anchored on functionalized carbon black as dynamic electrocatalyst for ultra-sensitive detection of nitroaromatic drug.

There has been a significant increase in the production and use of antibiotic drugs. However, the overuse and improper disposal of nitro-based antibiotics pose a significant threat to human health and the ecosystem. Specifically, the residues of antibiotic drugs such as nitrofurantoin (NFT) are dangerous to public health and pose a threat to the environment. In this study, we prepared a novel nanocomposite consisting of gadolinium cobaltite embedded functionalized carbon black (GdCoO3/f-CB) via a simple hydrothermal technique and utilized this nanocomposite as an electrode material for the electrochemical detection of NFT. The structural and morphological properties of the GdCoO3/f-CB nanocomposite was analyzed using a range of techniques, including XRD, Raman, XPS, EDX-Mapping, and HR-TEM. The electrocatalytic activity of the GdCoO3/f-CB nanocomposite was investigated using both CV and DPV techniques for the detection of NFT. Our results demonstrated that the prepared GdCoO3/f-CB nanocomposite delivered the excellent activities toward the detection of NFT at an extremely low limit of detection (LOD) of 2 nM and exhibited high sensitivity of 31 µA·µM-1·cm-2. Additionally, the proposed NFT sensor using GdCoO3/f-CB nanocomposite provided excellent reproducibility, repeatability, and selectivity, even in the presence of interfering molecules such as metal ions, biomolecules, and similar nitro compounds. These findings suggest that the GdCoO3/f-CB nanocomposite provides significant potential for the electrochemical detection of antibiotic drug residues for public health and the environment.

Raspberry-like CuWO4 hollow spheres anchored on sulfur-doped g-C3N4 composite: An efficient electrocatalyst for selective electrochemical detection of antibiotic drug nitrofurazone.

We report a highly selective and sensitive electrochemical sensor for the determination of nitrofurazone (NZ) based on sulfur-doped graphitic carbon nitride with copper tungstate hollow spheres (Sg-C3N4/CuWO4). Here, a Sg-C3N4/CuWO4 composite was synthesized by a facile ultrasonic method. The physicochemical properties of the composite were characterized by X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), energy dispersive X-ray spectroscopy (EDX) and X-ray photoelectron spectroscopy (XPS). Then, the surface morphology of the composite material was investigated by field emission scanning electron microscopy (FE-SEM) and high-resolution transmission electron microscopy (HR-TEM). Moreover, the electrochemical activity of the as-synthesized composite material was initially tested using electrochemical impedance spectroscopy (EIS). The electroanalytical techniques namely cyclic voltammetry (CV) and differential pulse voltammetry (DPV) were carried out for the electrochemical studies. The proposed sensor exhibits lower LOD and good sensitivity of about 3 nM and 1.24 µAµM-1 cm-2 to NZ detection. In addition, the Sg-C3N4/CuWO4 modified electrode showed excellent repeatability, reproducibility, long-term storage stability and excellent selectivity. The developed sensor was successfully applied for the determination of NZ in human urine and serum samples and achieved good recovery results.

A cerium vanadate interconnected with a carbon nanofiber heterostructure for electrochemical determination of the prostate cancer drug nilutamide.

Cerium vanadate resembling the shape of a hedgehog were interconnected with carbon nanofibers to give a heterostructure (referred to as CeV/CNF) that exhibits efficient catalytic activity for the electrochemical detection of the drug nilutamide (NLT). The heterostructure material and its modification were characterized by XRD, Raman spectra, XPS, FESEM, TEM, SAED, and EDX. A glassy carbon electrode was modified with the CeV/CNF nanocomposite. Best operated at -0.52 V (vs. Ag/AgCl), it exhibits a very low detection limit (2.0 nM), wide linear range (0.01-540 µM), high sensitivity (1.36 µA µM-1 cm-2) and rapid response towards NLT. It was applied to the determination of NLT in spiked human urine. Graphical abstractSchematic presentation of cerium vanadate interconnected with carbon nanofiber heterostructure for electrochemical determination of prostate cancer drug nilutamide in biological samples.

Rational design and facile synthesis of binary metal sulfides VS2-SnS2 hybrid with functionalized multiwalled carbon nanotube for the selective detection of neurotransmitter dopamine.

In this work, we report a sensitive and selective electrochemical sensor for the detection of dopamine (DA) neurotransmitter based on VS2-SnS2/f-MWCNT hybrids. Herein, the binary metal sulfide (VS2-SnS2) was synthesized via single step hydrothermal route and hybrids with f-MWCNT via the ultrasonication process. The as-prepared VS2-SnS2/f-MWCNT hybrids were characterized through the FESEM, EDX and elemental mapping, TEM, XPS, Raman and XRD techniques. The electrochemical performance and catalytic activity of the modified electrodes were probed using electrochemical impedance spectra (EIS), cyclic voltammetry (CV) and differential pulse voltammetry (DPV). Interestingly, DPV results exhibits an appreciable linear range from 0.025 to 1017 µM and LOD of 0.008 µM. The selectivity study was performed to prove the high selectivity of the VS2-SnS2/f-MWCNT hybrids modified electrode. Furthermore, the practical applicability of the DA sensor was scrutinized in human serum sample and rat brain sample.

One-step sonochemical synthesis of 1D ß-stannous tungstate nanorods: An efficient and excellent electrocatalyst for the selective electrochemical detection of antipsychotic drug chlorpromazine.

In the modern world, the contamination of ecosystem by human and veterinary pharmaceutical drugs through the metabolic excretion, improper disposal/industrial waste has been subjected to a hot issue. Therefore, exploitation of exclusive structured material and reliable technique is a necessary task to the precise detection of drugs. With this regards, we made an effort for the fabrication of novel one-dimensional (1D) stannous tungstate nanorods (ß-SnW NRs) via simple sonochemical approach and used as an electrochemical sensor for the detection of antipsychotic drug chlorpromazine (CPZ) for the first time. The crystallographic structure, surface topology, elemental compositions and their distributions and ionic states were enquired by different spectroscopic techniques such as XRD, FTIR, SEM, EDS, elemental mapping and XPS analysis. The developed ß-SnW NRs/GCE sensor exhibits a rapid and sensitive electrochemical response towards CPZ sensing with wide linear response range (0.01-457 µM), high sensitivity (2.487 µA µM-1 cm-2), low detection limit (0.003 µM) and excellent selectivity. Besides, the as-proposed electrochemical sensor was successfully applied to real sample analysis in commercial CPZ drug and biological fluids and the acquired recovery results are quite satisfactory. The proposed sonochemical method for the preparation of ß-SnW NRs is low cost, very simple, fast and efficient for sensor applications.