ABSTRACT
In this paper, a unique hybrid approach to design and synthesize 2D/3D Al2O3-ZnO nanostructures by simultaneous deposition is presented. Pulsed laser deposition (PLD) and RF magnetron sputtering (RFMS) methods are redeveloped into a single tandem system to create a mixed-species plasma to grow ZnO nanostructures for gas sensing applications. In this set-up, the parameters of PLD have been optimized and explored with RFMS parameters to design 2D/3D Al2O3-ZnO nanostructures, including nanoneedles/nanospikes, nanowalls, and nanorods, among others. The RF power of magnetron system with Al2O3 target is explored from 10 to 50 W, while the ZnO-loaded PLD's laser fluence and background gases are optimized to simultaneously grow ZnO and Al2O3-ZnO nanostructures. The nanostructures are either grown via 2-step template approach, or by direct growth on Si (111) and MgO<0001> substrates. In this approach, a thin ZnO template/film was initially grown on the substrate by PLD at ~300 °C under ~10 milliTorr (1.3 Pa) O2 background pressure, followed by growth of either ZnO or Al2O3-ZnO, using PLD and RFMS simultaneously under 0.1-0.5 Torr (13-67 Pa), and Ar or Ar/O2 background in the substrate temperate range of 550-700 °C. Growth mechanisms are then proposed to explain the formation of Al2O3-ZnO nanostructures. The optimized parameters from PLD-RFMS are then used to grow nanostructures on Au-patterned Al2O3-based gas sensor to test its response to CO gas from 200 to 400 °C, and a good response is observed at ~350 °C. The grown ZnO and Al2O3-ZnO nanostructures are quite exceptional and remarkable and have potential applications in optoelectronics, such in bio/gas sensors.
ABSTRACT
In this work, we report an easy, efficient method to synthesize high quality lithium-based upconversion nanoparticles (UCNPs) which combine two promising materials (UCNPs and lithium ions) known to enhance the photovoltaic performance of perovskite solar cells (PSCs). Incorporating the synthesized YLiF4:Yb,Er nanoparticles into the mesoporous layer of the PSCs cells, at a certain doping level, demonstrated a higher power conversion efficiency (PCE) of 19%, additional photocurrent, and a better fill factor (FF) of 82% in comparison to undoped PSCs (PCE = ~16.5%; FF = 71%). The reported results open a new avenue toward efficient PSCs for renewable energy applications.
ABSTRACT
The present work describes the synthesis of Ag-CoFe2O4/rGO nanocomposite as a photocatalyst through the hydrothermal process by the attachment of silver and cobalt ferrite (CoFe2O4) nanoparticles on the surface of reduced graphene oxide. The effect of Ag and reduced graphene oxide (rGO) on the structure, optical, magnetic, photocatalytic, and electrochemical performance of the CoFe2O4 is systematically explored through various analytical techniques. The analyses of the observed outcomes reveal that the graphene sheets are exfoliated and decorated with well-dispersed Ag and CoFe2O4 nanoparticles. UV-vis spectra indicate a gradual shift in the absorption edge toward the higher wavelength with the addition of Ag ions, which signifies variation in the energy gap of the samples. Photoluminescence results divulge that graphene can decline the electron-hole recombination rate and improve the photocatalytic activity of the Ag-CoFe2O4/rGO nanocomposite. In this context, the Ag-CoFe2O4/rGO sample presents good catalytic activity as compared to the CoFe2O4 and Ag-CoFe2O4 photocatalysts for the degradation of methylene blue (MB) dye and suggests that the rGO plays a vital role in the Ag-CoFe2O4/rGO nanocomposite. The deterioration rate of the samples is found to be in the order of CoFe2O4(78.03%) < Ag-CoFe2O4(83.04%) < Ag-CoFe2O4/rGO(93.25%) in 100 min for MB dye, respectively, under visible-light irradiation. The room-temperature ferromagnetic behavior of the samples is confirmed by the M-H hysteresis loop measurements. Overall, the Ag-CoFe2O4/rGO nanocomposite promises to be a strong magnetic photocatalyst for contaminated wastewater treatment. The electrochemical performance of all of the samples was examined by the cyclic voltammetry (CV) that exhibits a superior rate performance and cycle stability of the Ag-CoFe2O4/rGO nanocomposite as compared to the other samples.
ABSTRACT
Currently, chemotherapy is an important method for the treatment of various cancers. Nevertheless, it has many limitations, such as poor tumour selectivity and multi-drug resistance. It is necessary to improve this treatment method by incorporating a targeted drug delivery system aimed to reduce side effects and drug resistance. The present work aims to develop pH-sensitive nanocarriers containing magnetic mesoporous silica nanoparticles (MMSNs) coated with pH-responsive polymers for tumour-targeted drug delivery via the folate receptor. 2-Diethyl amino ethyl methacrylate (DEAEMA) was successfully grafted on MMSNs via surface initiated ARGET atom transfer radical polymerization (ATRP), with an average particle size of 180 nm. The end groups of poly (2-(diethylamino)ethyl methacrylate) (PDEAEMA) brushes were converted to amines, followed by a covalent bond with folic acid (FA) as a targeting agent. FA conjugated to the nanoparticle surface was confirmed by X-ray photoelectron spectroscopy (XPS). pH-Responsive behavior of PDEAEMA brushes was investigated by Dynamic Light Scattering (DLS). The nanoparticles average diameters ranged from ca. 350 nm in basic media to ca. 650 in acidic solution. Multifunctional pH-sensitive magnetic mesoporous nanoparticles were loaded with an anti-cancer drug (Doxorubicin) to investigate their capacity and long-circulation time. In a cumulative release pattern, doxorubicin (DOX) release from nano-systems was ca. 20% when the particle exposed to acidic media, compared to ca. 5% in basic media. The nano-systems have excellent biocompatibility and are minimally toxic when exposed to MCF-7, and -MCF-7 ADR cells.
ABSTRACT
In this study, rods of magnesium alloy and titanium alloy were cut to have similar height of about 5mm and size of 10 mm × 10 mm to fabricate three Mg-Ti couples. The Mg-Ti couple was heat treated at 540 °C, 570 °C, and 600 °C. The corrosion of these couples have been investigated and compared with AZ31 alloy. Potentiodynamic polarization and electrochemical impedance spectroscopy measurements were employed to study the corrosion behavior after 1.0 h and 48 h exposure to 3.5% NaCl solutions. The morphology of surfaces was examined by scanning electron microscopy (SEM) and the profile analysis was collected using an energy dispersive X-ray (EDX) analyzer after 5 days immersion in the chloride solutions. It is found that coupling Mg with Ti reduces the corrosion of AZ31 alloy, which further decreased with the increase of the temperature of treatment. Prolonging the time of exposure from 1.0 h to 48 h remarkably decreased the corrosion of the couples as well.
ABSTRACT
Visual inspection through image processing of welding and shot-peened surfaces is necessary to overcome equipment limitations, avoid measurement errors, and accelerate processing to gain certain surface properties such as surface roughness. Therefore, it is important to design an algorithm to quantify surface properties, which enables us to overcome the aforementioned limitations. In this study, a proposed systematic algorithm is utilized to generate and compare the surface roughness of Tungsten Inert Gas (TIG) welded aluminum 6061-T6 alloy treated by two levels of shot-peening, high-intensity and low-intensity. This project is industrial in nature, and the proposed solution was originally requested by local industry to overcome equipment capabilities and limitations. In particular, surface roughness measurements are usually only possible on flat surfaces but not on other areas treated by shot-peening after welding, as in the heat-affected zone and weld beads. Therefore, those critical areas are outside of the measurement limitations. Using the proposed technique, the surface roughness measurements were possible to obtain for weld beads, high-intensity and low-intensity shot-peened surfaces. In addition, a 3D surface topography was generated and dimple size distributions were calculated for the three tested scenarios: control sample (TIG-welded only), high-intensity shot-peened, and low-intensity shot-peened TIG-welded Al6065-T6 samples. Finally, cross-sectional hardness profiles were measured for the three scenarios; in all scenarios, lower hardness measurements were obtained compared to the base metal alloy in the heat-affected zone and in the weld beads even after shot-peening treatments.
ABSTRACT
The microstructural, optical and photocatalytic properties of undoped and 5% Zn doped CeO2 nanocrystals (NCs) have been explored through various analytical techniques, viz. powder x-ray diffraction (PXRD), x-ray photoelectron spectroscopy (XPS), transmission electron microscopy (TEM), UV-visible, Raman and photoluminescence (PL) spectroscopy. XRD data analysis revealed face centred cubic (FCC) crystal symmetry of the samples with average crystallite size in the range of 19-24 nm. XPS results confirmed that the Zn ions exist in +2 states and successfully incorporated into the CeO2 matrix. Internal structure and morphology observed by TEM exhibited almost uniform cubical shape of the particles of average size ~20-26 nm. The enegy bandgap of undoped and Zn doped CeO2 NCs had a direct transition of 3.46 eV and 3.57 eV respectively as estimated by the optical absorption data. The increase in the bandgap revealed blue shift of absorption edge due to the quantum confinement effects. The NCs exhibited an inherent luminescence emission peak at ~408 nm in PL spectra. Improvement in the photocatalytic activity was observed for Zn incorporated sample attributed to the enhanced light absorption or/and fall in charge recombination rate between CeO2 and Zn.
