Search

Advanced photo-active materials have attracted attention for their potential uses in water purification. In this study, a novel and facile route was used for designing nanohybrids to be valuable sources for producing effective photocatalysts for purifying water from the colored pollutants. Host-guest interaction and intercalation reactions used long chains of hydrocarbons of n-capric acid and stearic acid to facilitate incorporation of fine particles of cobalt iron oxide nanocomposite with the internal surface of the nanolayers of Al/Zn for building nanohybrids. The thermal decomposition of the prepared nanohybrids led to formation of zinc oxide nanoparticles doped with multi-oxides of magnetic and non-magnetic dopants. These dopants created new optical centers causing a strong reduction in the band gap energy from 3.30 eV to 2.60 eV. This positive effect was confirmed by a complete removal of the dye of Naphthol green B from water after 15 min of light irradiation. Moreover, a kinetic study showed that the reaction rate of photocatalytic degradation of the pollutants was faster than that of the conventional photocatalysts. Finally, this route was effective for producing benign and fast solutions for purifying water in addition to environment-related problems. [ABSTRACT FROM AUTHOR]

Herein we have fabricated AuTiO2 from a one-dimensional (1D) nanocomposite by the simple oxidation method of the Ti sheet for supercapacitor applications. We intended on fabricating a microlayer extended into the sheet body to form a selfstanding electrode. Raman spectra and XRD patterns confirmed the formation of the rutile phase of the TiO2 bulk, and FESEM confirmed the growth of the 1D nanostructure made of Au/TiO2, where the Au nanoparticles reside on the tip of the TiO2 nanorods. The growth of 1D TiO2 by this method is supported by a growth mechanism during the oxidation process. Three electrodes were fabricated based on pure and doped TiO2. These electrodes were used as a selfstanding supercapacitor electrode. The Au-doped TiO2 exhibited a great improvement in the electrochemical performance at low Au concentrations, whereas the excessive Au concentration on the TiO2 surface exhibited a negative effect on the capacitance value. The highest areal capacitance of 72 mFcm−2 at a current density of 5 µAcm−2 was recorded for TiO2 doped with a low Au concentration. The mechanism of the electrochemical reaction was proposed based on Nyquist and Bode plots. The obtained results point out that the effect of Au on the TiO2 surface makes Au/TiO2 ceramic electrodes a promising material as selfstanding energy storage electrodes. [ABSTRACT FROM AUTHOR]

In this work, we report the development of separators coated with hexagonal boron nitride (hBN) to improve the thermal stability of Li-ion batteries (LIBs). Aiming to achieve a synergistic effect of separators and anodes on thermal stability and electrochemical performance, multiwalled carbon nanotubes (MWCNTs) were prepared via plasma-enhanced chemical vapor deposition (PECVD) method and used as potential anode materials for LIBs. The grown MWCNTs were well characterized by using various techniques which confirmed the formation of MWCNTs. The prepared MWCNTs showed a crystalline structure and smooth surface with a diameter of ~9–12 nm and a length of ~10 μm, respectively. Raman spectra showed the characteristic peaks of MWCNTs and BN, and the sharpness of the peaks showed the highly crystalline nature of the grown MWCNTs. The electrochemical studies were performed on the fabricated coin cell with a MWCNT anode using a pristine and BN-coated separators. The results show that the cell with the BN-coated separator in a conventional organic carbonate-based electrolyte and MWCNTs as the anode resulted in a discharge capacity (at 65 °C) of ~567 mAhg−1 at a current density of 100 mAg−1 for the first cycle, and delivered a capacity of ~471 mAhg−1 for 200 cycles. The columbic efficiency was found to be higher (~84%), which showed excellent reversible charge–discharge behavior as compared with the pristine separator (69%) after 200 cycles. The improved thermal performance of the LIBs with the BN-coated separator and MWCNT anode might be due to the greater homogeneous thermal distribution resulting from the BN coating, and the additional electron pathway provided by the MWCNTs. Thus, the fabricated cell showed promising results in achieving the stable operation of the LIBs even at higher temperatures, which will open a pathway to solve the practical concerns over the use of LIBs at higher temperatures without compromising the performance. [ABSTRACT FROM AUTHOR]

Doping processes for optical materials are one of the driving forces for developing efficient and clean technologies for decontamination of aquatic effluents through lowering their band gap energy to become effective in sunlight. The current study has used a non-conventional technique for doping zinc oxide by multi metals, non-metals and organic dyes through a one-step process. In this trend, Zn-Al nanolayered structures have been used as hosts for building host–guest interactions. Organic dyes that have inorganic species of iron, nitrogen and sulfur have been used as guests in the intercalation reactions of Zn-Al layered double hydroxides. By intercalating green dyes, organic–inorganic nanohybrids were formed as nanolayered structures with expanding interlayered spacing to 2.1 nm. By changing the concentration of green dyes and thermal treatment, series of nanofibers and nanoplates of zinc oxides were formed and doped by aluminum, iron and sulfur in addition to colored species. The optical properties of the multi-doped zinc oxide indicated that it became suitable for solar applications because its band gap energy decreased from 3.30 eV to 2.80 eV. The experimental and kinetic results of the multi-doped zinc oxide concluded that the colored pollutants were effectively removed during 50 min of sunlight irradiation. [ABSTRACT FROM AUTHOR]

Bio-inspired synthesis is a novel and attractive environmentally friendly route to generating inorganic materials. In this work, the preparation of CeO2 NPs using egg white and investigation of their antibacterial properties both in liquid and solid growth medium against Escherichia coli and Staphylococcus aureus bacteria were reported. The CeO2 nanoparticles were characterized using X-ray diffraction (XRD), Field emission transmission electron microscope (FETEM), UV-Vis, Raman, and antibacterial measurements. The results from XRD and TEM analysis showed that the prepared nanoparticles were a single phase in the nano regime (5–7 nm) with spherical shape and uniform size distribution. Optical properties reflected the characteristics peaks of CeO2 in the UV-Vis range with a bandgap ~2.80 eV. The antibacterial activity of the synthesized NPs was achieved under ambient conditions with different bacteria and the results showed that the properties were different for both the bacteria. The highest activity with an inhibition zone of about 22 mm against S. aureus was obtained as compared with the 19 mm zone of inhibition obtained with E.coli. This finding will be of major significance that indicates a possibility to develop CeO2 NPs as antibacterial agents against extensive microorganisms to control and prevent the spread and persistence of bacterial infections. [ABSTRACT FROM AUTHOR]

The present study aims to enhance the optical properties of barium titanate through narrowing its band gap energy to be effective for photocatalytic reactions in sunlight and be useful for solar cells. This target was achieved through growth of the hollandite phase instead of the perovskite phase inside the barium titanate crystals. By using solvent thermal reactions and thermal treatment at different temperatures (250 °C, 600 °C, and 900 °C), the hollandite phase of barium titanate was successfully obtained and confirmed through X-ray diffraction (XRD), Raman spectra and scanning electron microscopy techniques. XRD patterns showed a clear hollandite phase of barium titanium oxides for the sample calcined at 900 °C (BT1-900); however, the samples at 600 °C showed the presence of mixed phases. The mean crystallite size of the BT1-900 sample was found to be 38 nm. Morphological images revealed that the hollandite phase of barium titanate consisted of a mixed morphology of spheres and sheet-like features. The optical properties of barium titanate showed that its absorption edge shifted to the visible region and indicated band gap energy tuning ranging from 1.75 eV to 2.3 eV. Photocatalytic studies showed the complete and fast decolorization and mineralization of green pollutants (naphthol green B; NGB) in the prepared barium titanate with hollandite phase after illumination in sunlight for ten minutes. Finally, it can be concluded that the low band gap energy of barium titanate having the hollandite phase introduces beneficial structures for optical applications in sunlight. [ABSTRACT FROM AUTHOR]