Conformal zinc sulfide coating of vertically aligned ZnO nanorods by two-step hydrothermal synthesis on wide bandgap seed layers for lead-free perovskite solar cells.

Vertically aligned ZnO nanorods (NRs) were grown hydrothermally on the wide bandgap (∼3.86 - 4.04 eV) seed layers (SLs) of grain size ∼162 ± 35 nm, prepared using ball-milled derived ZnO powder. The synthesized ZnO NRs were further decorated with ZnS nanocrystals to achieve a ZnO NR-ZnS core-shell (CS)-like nano-scaffolds by a subsequent hydrothermal synthesis at 70 °C for 1 h. UV-Vis-NIR spectroscopy, x-ray diffractometry (XRD), Raman spectroscopy and Field emission scanning electron microscopy (FESEM) coupled with Energy dispersive x-ray spectroscopy (EDX) analyses confirmed the formation of ZnS atop the vertically aligned ZnO NR arrays of ∼1.79 ± 0.17µm length and ∼165 ± 27 nm diameter. Transmission electron microscopy (TEM)/EDX analyses revealed that vertically aligned ZnO NRs (core dia. ∼181 ± 12 nm) arrays are conformally coated by an ultrathin ZnS (∼25 ± 7 nm) shell layer with a preferential ZnS{111}/ZnO{10-10}-like partial epitaxy. The ZnO NRs exhibited a sharp band edge near ∼384 nm having optical bandgap energy (Eg) of ∼3.23 eV. However, the ZnO NR-ZnS CS exhibited double absorption bands atEg∼ 3.20 eV (ZnO-core) andEg∼ 3.78 eV (ZnS-shell). The ZnS{111}/ZnO{10-10}-nano-scaffolds could be utilized to facilitate the enhanced absorption of UV photons as well as the radial junction formation between the Pb-free perovskite absorber and ZnS/ZnO NRs layers.

Calcined chicken eggshell-derived biomimetic nano-hydroxyapatite as a local drug-delivery aid for doxycycline hyclate: characterization, bio-activity, cytotoxicity, antibacterial activity and in vitro release study.

The integration of bioactive substances with antibiotics has been extensively pursued for the treatment of osteomyelitis. These materials, also known as biomaterials, can serve both as bone replacements and targeted drug delivery systems for antibiotics. In this study, biomimetic nano-hydroxyapatite (nHAp) was synthesized via the coprecipitation technique where waste chicken eggshell (WCE) was employed as the source of Ca. Heat treatment was performed at four different temperatures (100 °C, 300 °C, 600 °C and 900 °C). Subsequently, the samples were characterized using XRD, FTIR spectroscopy, Raman spectroscopy, FESEM, EDX, XPS, DLS hydrodynamic size and zeta potential analysis. Also, their biomedical effectiveness was evaluated in terms of cytotoxicity, hemolysis, antibacterial performance, and bioactivity. Doxycycline hyclate (DOXh) was loaded in the synthesized nHAp samples, and subsequently its in vitro release was studied under stirring in simulated body fluid (SBF). The DOXh release kinetics was evaluated, and it was found that the first-order model was the best fitted kinetic model describing the release of DOXh from the nHAp samples, except for nHAp100, which was best described by the Korsmeyer-Peppas model. The nHAp synthesized utilizing WCE showed excellent potential for biomedical application and can be used as a drug delivery agent for antibiotics, such as DOXh.

Influence of Y3+ and La3+ ions on the structural, magnetic, electrical, and optical properties of cobalt ferrite nanoparticles.

In the current study, nanocrystalline CoY0.5xLa0.5xFe2-xO4 (where x = 0.00, 0.02, 0.04, 0.06, 0.08, and 0.10) ferrites have been synthesized via a sol-gel auto combustion process. The synthesized powders were pressed into pellet forms and sintered at 900 °C for 4 h in the air. X-ray diffractometry (XRD) confirmed the single-phase cubic spinel structure of the synthesized samples having the mean crystallite domain sizes ranging from 122 and 54 nm. FTIR spectroscopic analyses revealed two strong bands within the range of 600 to 350 cm-1, further confirming the cubic inverse spinel structure of the prepared materials. The surface morphologies and composition were investigated by Field Emission Scanning Electron Microscopy (FE-SEM) and Energy Dispersive X-ray (EDX) Spectroscopy. The magnetic hysteresis curves recorded at room temperature exhibit ferrimagnetic behavior. The highest coercivity (Hc∼1276 Oe) was found at a high doping (x = 0.10) concentration of Y3+ and La3+ in cobalt ferrite. Dielectric constant increase with increased doping concentration whereas real-impedance and dielectric loss decrease with increased in doping concentration and applied frequency. The band gap energy increased from 1.48 to 1.53 eV with increasing Y3+ and La3+concentrations in the UV-Vis region. The elevated levels of magnetic and dielectric substances in the ferrite nanoparticles suggest that the material could be used for magnetic recording media and high-frequency devices.

Facile extraction and characterization of calcium hydroxide from paper mill waste sludge of Bangladesh.

Herein, paper mill waste sludge (PMS) from two different sources has been investigated to extract calcium hydroxide, Ca(OH)2 by a facile and inexpensive extraction process. PMS samples, collected from local paper mill plants of Bangladesh, were the main precursors wherein HCl and NaOH were used for chemical treatment. The as-synthesized products were analysed by a variety of characterization tools including X-ray diffraction (XRD), Fourier transform infrared (FTIR) spectroscopy, Raman spectroscopy, scanning electron microscopy (SEM) and energy dispersive X-ray (EDX) elemental analyses. Our studies confirm that the extracted product contains Ca(OH)2 as a major content, albeit it also includes CaCO3 phase owing to the inescapable carbonation process from the surrounding environment. The particle size of the synthesized products is in the range of 450-500 nm estimated from SEM micrographs. The crystallite domain size of the same estimated from XRD analyses and was found to be approximately 47 and 31 nm respectively for product-A and product-B considering major (101) Bragg peak of Ca(OH)2. The yield percentage of the isolated products is about 65% for samples collected from both sources.

Effects of yttrium doping on structural, electrical and optical properties of barium titanate ceramics.

In this report, we study the Yttrium-doped Barium Titanate (Y-BT) Ba1 - xYxTiO3 (with x = 0.00, 0.01, 0.03, 0.05, 0.07 mmol) perovskite ceramics synthesized by sol-gel method. The as-made powder samples were pressed into a pellet shape and subsequently sintered at 1300 °C for 5 h in air. The structural, morphological, electrical, and optical properties of the synthesized samples were investigated by X-ray diffraction (XRD), field emission scanning electron microscopy (FESEM), impedance analyzer, and UV-Vis-NIR Spectroscopy respectively. The XRD study revealed the formations of single phase tetragonal structure of Barium Titanate (BT) with ∼23-33 nm mean crystallite size. The crystallite size increases initially with Y-doping, found at about 33 nm for x = 0.01, and reduces for increase in Y3+ concentration further. The microstructural study from FESEM depicts the uniform distribution of compact and well-faceted grain growth for Y-BT in contrast with undoped barium titanate. The average grain size (∼0.29-0.78 µm) of the Y-BT decreases with increasing doping concentration. Frequency-dependent impedance analyses show enhanced dielectric properties like dielectric constant, quality factor, and conductivity with low dielectric loss in the presence of Yttrium. The optical bandgap energy (∼2.63-3.72 eV) estimated from UV-Vis-NIR diffuse reflection data shows an increasing trend with a higher concentration of yttrium doping.

Facile synthesis of Cu2O nanorods in the presence of NaCl by successive ionic layer adsorption and reaction method and its characterizations.

Cuprous oxide (Cu2O) nanorods have been deposited on soda-lime glass substrates by the modified successive ionic layer adsorption and reaction technique by varying the concentration of NaCl electrolyte into the precursor complex solution. The structural, electrical and optical properties of synthesized Cu2O nanorod films have been studied by a variety of characterization tools. Structural analyses by X-ray diffraction confirmed the polycrystalline Cu2O phase with (111) preferential growth. Raman scattering spectroscopic measurements conducted at room temperature also showed characteristic peaks of the pure Cu2O phase. The surface resistivity of the Cu2O nanorod films decreased from 15 142 to 685 Ω.cm with the addition of NaCl from 0 to 4 mmol and then exhibited an opposite trend with further addition of NaCl. The optical bandgap of the synthesized Cu2O nanorod films was observed as 1.88-2.36 eV, while the temperature-dependent activation energies of the Cu2O films were measured as about 0.14-0.21 eV. Scanning electron microscope morphologies demonstrated Cu2O nanorods as well as closely packed spherical grains with the alteration of NaCl concentration. The Cu2O phase of nanorods was found stable up to 230°C corroborating the optical bandgap results of the same. The film fabricated in presence of 4 mmol of NaCl showed the lowest resistivity and activation energy as well as comparatively uniform nanorod morphology. Our studies demonstrate that the nominal presence of NaCl electrolytes in the precursor solutions has a significant impact on the physical properties of Cu2O nanorod films which could be beneficial in optoelectronic research.

Influence of the Substrate, Process Conditions, and Postannealing Temperature on the Properties of ZnO Thin Films Grown by the Successive Ionic Layer Adsorption and Reaction Method.

Here, we report the effect of the substrate, sonication process, and postannealing on the structural, morphological, and optical properties of ZnO thin films grown in the presence of isopropyl alcohol (IPA) at temperature 30-65 °C by the successive ionic layer adsorption and reaction (SILAR) method on both soda lime glass (SLG) and Cu foil. The X-ray diffraction (XRD) patterns confirmed the preferential growth thin films along (002) and (101) planes of the wurtzite ZnO structure when deposited on SLG and Cu foil substrates, respectively. Both XRD and Raman spectra confirmed the ZnO and Cu-oxide phases of the deposited films. The scanning electron microscopy image of the deposited films shows compact and uniformly distributed grains for samples grown without sonication while using IPA at temperatures 50 and 65 °C. The postannealing treatment improves the crystallinity of the films, further evident by XRD and transmission and reflection results. The estimated optical band gaps are in the range of 3.37-3.48 eV for the as-grown samples. Our experimental results revealed that high-quality ZnO thin films could be grown without sonication using an IPA dispersant at 50 °C, which is much lower than the reported results using the SILAR method. This study suggests that in the presence of IPA, the SLG substrate results in better c-axis-oriented ZnO thin films than that of deionized water, ethylene glycol, and propylene glycol at the optimum temperature of 50 °C. Air annealing of the samples grown on Cu foils induced the formation of Cu x O/ZnO junctions, which is evident from the characteristic I-V curve including the structural and optical data.