Bifunctional Zirconium Phosphate with Greigite for Electrochemical Detection and Simultaneous Removal of Heavy Metal Ions and Nitro Compounds.

Electrochemical sensing is emerging as a method of choice for the sensing and monitoring of contaminants in water. Various sensing platforms have been designed for sensing heavy metal ions and organic pollutants in water bodies. Herein, we report a new electrochemical platform that can be used for the detection of both heavy metal ions and nitro-based organic contaminants in water bodies. The electrochemical sensor uses a modified electrode based on Fe3S4-impregnated zirconium phosphate (ZrP) nanoparticles synthesized by a simple ultrasonication method. The ZrP@Fe3S4 nanoparticles were thoroughly characterized by power X-ray diffraction (PXRD), X-ray photoelectron spectroscopy (XPS), transmission electron microscopy (TEM), scanning electron microscopy-energy dispersive X-ray spectroscopy (SEM-EDX), and ζ-potential studies. The material exhibits an excellent electrochemical performance for the detection of Pb2+, Hg2+, nitrophenol, nitroaniline, and picric acid with low limits of detection of ca. 0.93, 0.70, 0.98, 1.10, and 1.53 ppm, respectively. Since ZrP@Fe3S4 nanoparticles are magnetically recyclable, their adsorption capacity and recyclability have been thoroughly investigated for the uptake of Pb2+ and Hg2+ ions from contaminated water. We observed that the adsorption of Pb2+ and Hg2+ ions on ZrP@Fe3S4 is best described by the Langmuir isotherm and pseudo-second-order kinetic models, with adsorption capacities of 219.44 and 118.4 mg/g, respectively. Similarly, the removal efficiency of ZrP@Fe3S4 was found to be 91, 57.6, and 31.3% for nitrophenol, nitroaniline, and picric acid, respectively. Furthermore, the theoretical calculations using density functional theory (DFT) were carried out to find the adsorption energy, affinity, and point of adsorption, which are in line with the experimental results. DFT calculations further suggest that the incorporation of Fe3S4 on ZrP improves the surface charge density and promotes efficient electron transfer between the electrode and the analyte. We have shown the real-time analysis of Dal lake water as a proof of concept, and the synthesized composite exhibits good recovery and promising results for metal ion sensing. ZrP@Fe3S4 demonstrated an excellent cycling stability and long-term stability without noticeable degradation for 1 week.

DFT Studies on a Metal Oxide@Graphene-Decorated D-π1-π2-A Novel Multi-Junction Light-Harvesting System for Efficient Dye-Sensitized Solar Cell Applications.

Graphene nanocomposites have emerged as potential photoanode materials for increased performance of the dye-sensitized solar cells (DSSCs) via charge transfer. Various metal-oxide-decorated graphene nanocomposites have widespread applications in energy devices, such as solar cells, fuel cells, batteries, sensors, electrocatalysis, and photocatalysis. However, the possible role of these composites in DSSC applications has largely remained unexplored. Herein, we studied a Sb2O3-decorated graphene-D-π1-π2-A sensitized TiO2 nanocomposite (dye-(TiO2)9/Sb2O3@GO) as a model multi-junction light-harvesting system and examined the impact of various π-bridges on the optical and photovoltaic properties of the push-pull dye system employed in this light-harvesting system. We have shown that by changing the spacer unit, the light sensitivity of nanocomposites can be varied from visible to near-infrared wavelengths. Furthermore, with the integration of metal-oxide-decorated graphene nanocomposites on D-π1-π2-A systems and D-π-A systems, composite photoelectrodes displayed better optical and photovoltaic characteristics with an enhanced absorption spectrum in the wavelength range of 800-1000 nm. The performance of the D-π1-π2-A system has been evaluated in terms of various photovoltaic parameters such as the highest occupied molecular orbital-lowest unoccupied molecular orbital energy gaps, excited-state oxidation potential (E dye *), free energy of electron injection (G inject), total reorganization energy (λtotal), and open-circuit voltage (V oc). This work throws light on the current trends and the future opportunities in graphene-metal oxide nanocomposite-based DSSCs for better harvesting of the solar spectrum and better performance of solar devices.

Electrochemical analysis of glyphosate using porous biochar surface corrosive nZVI nanoparticles.

Glyphosate [N-(phosphonomethyl)glycine] is a widely used phosphonate herbicide for different agricultural purposes. Due to its widespread use, suspected toxicity, and ubiquitous bioaccumulation, it is one of the most harmful contaminants found in drinking water. This demands efficient sensing and removal of glyphosate from contaminated water. Here, we report the decoration of novel and highly porous biochar with nanozero-valent iron (nZVI) nanoparticles to develop an efficient electrochemical sensor for the trace detection of glyphosate. The as-synthesized composite was thoroughly characterized by various state-of-the-art instrumental techniques. The electron micrographs of the composite materials revealed the cavity-like structure and the abundant loading of nZVI nanoparticles. FTIR and XPS analyses confirmed the presence of oxygen-rich functionalities and Fe(0) in the composite nanostructure. Electrochemical analysis through CV, LSV, and DPV techniques suggested efficient sensing activity with a limit of detection as low as 0.13 ppm. Furthermore, the chronopotentiometric response suggested excellent and superior stability for long-term applications. To gain more insight into the interaction between glyphosate and the composite material, DFT calculations were carried out. The Frontier Molecular Orbital study (FMO), Molecular Electrostatic Potentials (MEPs), and Density of States (DOS) suggest an increase in the electron density, an increase in the DOS, and a decrease in the HOMO-LUMO band gap by combining nZVI nanoparticles and biochar. The results suggest more facile electron transfer from the composite for trace detection of glyphosate. As a proof of concept, we have demonstrated that real-time analysis of milk, apple juice, and the as-synthesized composite shows promising results for glyphosate detection with an excellent recovery rate.

Biomass-derived carbon quantum dots: a novel and sustainable fluorescent "ON-OFF-ON" sensor for ferric ions.

Fluorescent carbon dot sensing probes have attracted much attention in recent times due to their amazing properties regarding chemical inertness, solubility, non-toxicity, optoelectronic behavior, and charge transport functionality. Herein, we report the green synthesis of lotus stem-derived carbon dots (LS-CQDs) from the naturally available lotus stem by a simple and economical hydrothermal method without the use of an oxidizing agent. HR-TEM and DLS measurements confirm the quasi-spherical shaped LS-CQDs, with a 2.5 nm average diameter. The LS-CQDs possess better aqueous dispersibility and stability due to the presence of hydrophilic hydroxyl, carboxyl, and amine surface functional groups, as manifested by FT-IR analysis. The LS-CQDs demonstrate excellent fluorescence properties that are sensitive to conditions of pH, time, and temperature. Furthermore, the prepared LS-CQDs display an interesting fluorescence "ON-OFF-ON" property. The LS-CQDs depict a selective and sensitive fluorescence quenching response in the presence of ferric ions. Moreover, the prepared LS-CQDs exhibit a quantum yield of about 0.44%. The LS-CQDs show an excellent sensing response with the limit of detection (LOD) equal to 0.212 ppm. The promising sensitivity and selectivity of LS-CQDs were utilized for the detection of ferric ions in the water samples collected from three polluted sources viz. lake water (Dal lake), underground water (tube well), and stream water. For all the collected water samples the results were reasonably good with the achievement of recovery factor above 1. Therefore, we strongly believe that the present study will serve as a good guiding star for the selective and sensitive detection of ferric ions from various polluted water bodies.

Studies on a glutathione coated hollow ZnO modified glassy carbon electrode; a novel Pb(ii) selective electrochemical sensor.

Herein, we report the electrochemical detection of heavy metal ions such as Pb(ii), Cd(ii) and Hg(ii) ions while using glutathione coated hollow ZnO modified glassy carbon electrode (Glu-h-ZnO/GCE). An excellent voltammetric response of the modified electrode towards these metal ions was observed by different voltammetric techniques. Among the different target metal ions, a selective electrochemical response (sensitivity = 4.57 µA µM-1) for the detection of Pb(ii) ions was obtained with differential pulse voltammetric (DPV) measurements. Besides, under optimal experimental conditions and in the linear concentration range of 2-18 µM, a very low detection limit of 0.42 µM was obtained for Pb(ii) ion. The observed electrochemical behaviour of Glu-h-ZnO/GCE towards these metal ions is in conformity with the band gap of the composite in the presence of various test metal ions. The band gap studies of the composite and various "Composite-Metal Ion" systems were obtained by reflectance as well as by computational methods where results are in close agreement, justifying the observed electrochemical behaviour of the systems. The lowest band gap value of the "Composite-Pb" system may be the reason for the excellent electrochemical response of the Glu-h-ZnO modified GCE towards the detection of Pb(ii) ion.

Enhanced and Selective Adsorption of Zn(II), Pb(II), Cd(II), and Hg(II) Ions by a Dumbbell- and Flower-Shaped Potato Starch Phosphate Polymer: A Combined Experimental and DFT Calculation Study.

Microwave-ultrasound-assisted facile synthesis of a dumbbell- and flower-shaped potato starch phosphate (PSP) polymer, hereafter PSP, was carried out by cross-linking the hydroxyl groups of native potato starch (NPS) using phosphoryl chloride as a cross-linking agent. Structural and morphological analysis manifested the successful formation of the dumbbell- and flower-shaped PSP biosorbent with enhanced specific surface area and thermal stability. Viscoelastic behavior of NPS and PSP suggested increased rigidity in PSP, which helped the material to store more deformation energy in an elastic manner. The synthesized PSP biosorbent material was successfully tested for efficient and quick uptake of Zn(II), Pb(II), Cd(II), and Hg(II) ions from aqueous medium under competitive and noncompetitive batch conditions with q m values of 130.54, 106.25, 91.84, and 51.38 mg g-1, respectively. The adsorption selectivity was in consonance with Pearson's hard and soft acids and bases (HSAB) theory in addition to their order of hydrated radius. Adsorption of Zn(II), Pb(II), Cd(II), and Hg(II) followed a second-order kinetics and the adsorption data fitted well with the Langmuir isotherm model. Quantum computations using density functional theory (DFT) further supported the experimental adsorption selectivity, Zn(II) > Pb(II) > Cd(II) > Hg(II), in terms of metal-oxygen binding energy measurements. What was more intriguing about PSP was its reusability over multiple adsorption cycles by treating the metal(II)-complexed PSP with 0.1 M HCl without any appreciable loss of its adsorption capacity.