CuO-NiO binary transition metal oxide nanoparticle anchored on rGO nanosheets as high-performance electrocatalyst for the oxygen reduction reaction.

To replace the existing noble-metal-based catalysts, developing highly efficient, stable electrocatalysts for oxygen reduction reactions for the increased current generation with lower overpotential is a demanding undertaking. In the present work, CuO-NiO/rGO nanocomposites were prepared using simple, cost-effective Co-precipitation methods. They act as highly effective electrocatalysts for oxygen reduction reactions in an alkaline medium. The structural characterizations demonstrate that prepared nanoparticles (≈13 nm) are tightly and effectively organized on reduced graphene oxide sheets. The electrochemical properties of the CuO, NiO nanoparticles and CuO-NiO, CuO-NiO/rGO nanocomposites were investigated. The results of the CuO-NiO/rGO nanocomposites revealed the high current density (2.9 × 10-4 mA cm-2), lower Tafel slope (72 mV dec-1) and low hydrogen peroxide yield (15%) when compared to other prepared materials (CuO, NiO, and CuO-NiO). The reduced graphene oxide increases an electron transfer during the ORR process, while the CuO-NiO has variable oxidation states that promote electro-rich features. With the combination of CuO-NiO and rGO, the hybrid electrocatalysts specific surface area and charge transfer rate drastically increase. The investigations of the rotating ring-disk electrodes experiments indicate that the oxygen reduction process takes place on CuO-NiO/rGO through an efficient four-electron pathway. Our results propose a new approach to creating highly efficient and long-lasting electrocatalysts.

Synthesis, Computational and cytotoxicity studies of aryl hydrazones of ß-diketones: Selective Ni2+ metal Responsive fluorescent chemosensors.

A new fluorescent sensor 2-(2-(3-chloro-4-fluorophenyl)hydrazono)-5,5-dimethyl cyclohexane-1,3-dione (A) and 2-(2-(4-chloro-2-nitrophenyl)hydrazono)-5,5-dimethyl cyclohexane-1,3-dione (B) composed of a ß-diketones of aryl hydrazones synthesized by simple and cost-effective method. Various analytical tools analyzed the structural investigations of the synthesized substituted ß-diketones of aryl hydrazones like FT-IR, 1H, 13C NMR and UV-Vis techniques, Single-crystal X-ray diffraction studies (SCXRD) (for A), Scanning electron microscopy (SEM), and fluorescence spectroscopy. SEM also investigates surface morphology modifications of aryl hydrazones and Ni2+ complex. Furthermore, the metal sensing (Chemo sensing) behavior of newly prepared aryl hydrazones of ß-diketones derivatives was further studied by fluorescence spectroscopy. The aryl hydrazones sensor materials show admirable fluorescence selectivity with enrichment to Ni2+ over different cations in an aqueous ethanol solution with a recognition extremity of 4 µM-7 µM. A joint experimental and theoretical investigation was led on the chemical structure employing a density functional theory (DFT) (B3LYP), engaging a 6-31G basis set. The DFT technique's enhanced geometrical bond angles and lengths exhibited great covenant with the experimental results. The highest occupied molecular (HOMO) orbital and lowest unoccupied (LUMO) molecular orbital energy has been concluded. The cytotoxicity studies show these compounds impede the growth of KB cells highly and from the studies to evaluate their capability to accurately dock aryl hydrazones to antibodies of cancer protein such as 4LRH, 4L9K, 4 EKD and 4GIW cancer proteins.

Morphology control of rutile TiO2 with tunable bandgap by preformed ß-FeOOH nanoparticles.

Rutile TiO2 are widely used for applications of coatings, cosmetics, photoelectric devices and so on. However, effective control of well-defined morphology, size and composition of rutile TiO2 nanoparticles from agglomeration has always been a challenge. A new synthesis strategy was proposed to prepare rutile TiO2 with controllable morphology varied from flower-like structures to single-separated nanorods. The ß-FeOOH nanoparticles were generated by the hydrolysis of FeCl3 solution and could prevent the aggregation of TiO2 nanocrystals at early stages of the reaction; thus, could control the morphology of rutile nanoparticles. The morphology of rutile TiO2 nanoparticles could be controllably regulated from flower-like structures to individually separated nanorods. Meanwhile, the preformed ß-FeOOH also played a role of dopant. Fe ions were substitutionally doped into the bulk lattice of TiO2 nanocrystals and reduced the bandgap, which extended the solar radiation absorption range of rutile TiO2. The prepared TiO2 may be suitable for novel UV-blue light shielding agents and many other applications in photoelectric devices, photocatalysis, and so on due to its small size, unprecedented discrete rod-like structure and unique UV-vis light permeability.

The simple hydrothermal synthesis of Ag-ZnO-SnO2 nanochain and its multiple applications.

In this article, we report the fabrication of a stable Ag-ZnO-SnO2 nanochain by template free hydrothermal method and its photocatalytic activity for the first time. This composite material represents a potential new class of photocatalysts with enhanced light absorption, hydrophobic and electronic properties of ZnO. This catalyst has been characterized by X-ray diffraction (XRD), high resolution scanning electron microscopy (HRSEM), field emission scanning electron microscopy (FESEM), elemental mapping, energy dispersive spectroscopy (EDS), X-ray photoelectron spectroscopy (XPS), UV-Vis diffuse reflectance spectroscopy (DRS) and photoluminescence spectroscopy (PL). XRD and elemental mapping reveal the presence of SnO2 and Ag in the catalyst. Ag-ZnO-SnO2 has increased absorption in the visible region when compared to ZnO. This three component nano junction system exhibits enhanced photocatalytic activity for the degradation of azo dyes, Acid Black 1 (AB 1) and Acid Violet 7 (AV 7) under UV light (365 nm), far exceeding those of the single and two component systems. Ag-ZnO-SnO2 is found to be reusable without appreciable loss of catalytic activity up to four runs. Based on the band gap energies of ZnO and SnO2, a mechanism is proposed for the photodegradation of dyes. Hydrophobicity and photoconductivity of Ag-ZnO-SnO2 have been evaluated. Nanochain exhibiting higher positive photoconductivity can be useful for soliton wave communication as well as solar cell applications. Our results provide some new insights on the fabrication of Ag-ZnO-SnO2 and its performance as an active photocatalyst, self cleaning and conducting material.

The simple, template free synthesis of a Bi2S3-ZnO heterostructure and its superior photocatalytic activity under UV-A light.

The development of a heterostructured semiconductor photocatalyst makes a significant advancement in catalytic technologies. Highly crystalline Bi2S3-ZnO nanosheets with a hierarchical structure have been successfully synthesized by a facile sonochemical process and characterized by X-ray diffraction (XRD), high resolution scanning electron microscopy (HR-SEM), X-ray photoelectron spectroscopy (XPS), UV-Vis diffuse reflectance spectroscopy (DRS), photoluminescence spectroscopy (PL) and Brunauer-Emmett-Teller (BET) surface area measurements. X-ray powder diffraction (XRD) analysis reveals that the as synthesized product has an orthorhombic phase of Bi2S3 and a hexagonal wurtzite phase of ZnO. XPS analysis shows the presence of the elements Zn, O, Bi and S and their oxidation states. Bi2S3-ZnO has increased absorption in the UV region as well as in the visible region. This heterostructured nano catalyst has a higher photocatalytic activity for the degradation of Acid Black 1 (AB 1) under UV-A light than pure ZnO, Bi2S3 and commercial Degussa P25. The heterojunction in the Bi2S3-ZnO photocatalyst has led to low recombination rates of photoinduced electron-hole pairs and an enhanced photocatalytic activity. Bi2S3-ZnO is advantageous in AB 1 degradation because of its reusability and higher efficiency at neutral pH 7.