4,4′-Dimethylazobenzene as a chemical actinometer

Chemical actinometers are a useful tool in photochemistry, which allows to measure the photon flux of a light source to carry out quantitative analysis on photoreactions. The most commonly employed actinometers so far show minor drawbacks, such as difficult data treatment, parasite reactions, low stability or impossible reset. We propose herewith the use of 4,4′-dimethylazobenzene as a chemical actinometer. This compound undergoes a clean and efficient E/Z isomerization, approaching total conversion upon irradiation at 365 nm. Thanks to its properties, it can be used to determine the photon flux in the UV–visible region, with simple experimental methods and data treatment, and with the possibility to be reused after photochemical or thermal reset. Graphical abstract

The behavior of hydrothermally synthesized hematite nanorods prepared on spin coated seed layers

Herein we report on the effect of varied spin-coated seed layer concentrations of Iron (III) chloride hexahydrate (FeCl3.6H2O) on the photoelectrochemical performance of hydrothermally synthesized hematite nanorods. The seed layers were prepared from 0.05, 0.07, 0.09, 0.11, and 0.13 M concentrations of FeCl3.6H2O. The nanorods were vertically aligned with slight inclinations over the seed layers with the two lowest molar concentrations (0.05 and 0.07 M) of FeCl3.6H2O. A further increase in seed layer concentrations transformed the nanorods as they grew over others and agglomerated into clusters. Structural analysis using X-ray diffraction (XRD) and Raman spectroscopy demonstrated uniform hematite crystalline peaks for all the samples. All samples absorbed highly in the visible region within an onset absorption edge wavelength ranging from 624 to 675 nm. Overall, the nanorods synthesized over the lowest seed layer concentration of 0.05 M of FeCl3.6H2O exhibited the highest photocurrent density of 0.077 mA/cm2 at 1.5 V vs. reversible hydrogen electrode. The results obtained provide important information about the structural, optical, and photoelectrochemical properties of hematite nanorods synthesized over varied seed layer concentrations. This is a key contribution in understanding and enhancing the hematite nanorods performance for photocatalytic applications.

Spatial profile of Al-ZnO thin film on polycarbonate deposited by ring-shaped magnetized rf plasma sputtering with two facing cylindrical Al2O3 - ZnO targets

Radial profiles of the ion saturation current are measured in a ring-shaped magnetized radio-frequency plasma sputtering process with two facing cylindrical ZnO targets including Al2O3 (2% wt.). The profile has a non-uniform shape with a peak whose position corresponds to the target near the electrode due to the effect of the magnetic field distribution. It becomes uniform at large distances between the substrate and a target (d st ≥ 50 mm). The radial profile of the resistivity of the Al-ZnO (AZO) films deposited on a polycarbonate plate at Ar gas pressure of 0.27 Pa is uniform at about 10-3 Ω·cm for d st ≥ 50 mm. The films deposited at various positions and room-substrate-temperature also show a good crystallinity based on an X-ray diffraction peak of about 33.95 - 34.44°. The grains exhibit a preferential orientation along the [002] axis with its size ranging from 18.15 to 28.17 nm. A higher transmittance of 95.6 % in the visible region is also obtained.

Numerical Study of a Wide-angle Near-Perfect Absorber for the Visible Regime Incorporating Metal-Dielectric-Metal Subwavelength Grating Structure

A near-perfect absorber for the visible regime based on metal-dielectric-metal subwavelength grating structure with the refractory metals is designed and demonstrated numerically. The absorber presents an average absorption over 98.4% in the visible regime at normal incidence. Angle-relative analysis shows that the proposed structure has good angle-tolerance. The high average absorption (86.6%) in the visible region can be maintained with the incident angles up to 60°. Through the analysis of the magnetic field, the physical origin is verified that this excellent absorption performance mainly stems from the cooperative effect of surface plasmonic resonances and the intrinsic broadband spectral responses by the refractory metals. In addition, the dependence of the absorption spectrum of the proposed absorber on the structural parameters is analyzed. This work provides an idea for the design of high-performance absorbers and has potential applications in advanced light energy capture and integration systems.

Photocatalytic Degradation of Fluoroquinolone Antibiotics in Solution

The photocatalytic degradation of two quinolone-type antibiotics (ciprofloxacin and levofloxacin) in aqueous solution was studied, using catalysts based on ZnO nanoparticles, which were synthesized by a thermal procedure. The efficiency of ZnO was subsequently optimized by incorporating different co-catalysts of gC3N4, reduced graphene oxide and nanoparticles of gold. The catalysts were fully characterized by electron microscopy (TEM and SEM), XPS, XRD, Raman, and BET surface area. The most efficient catalyst was 10%Au@ZnONPs-3%rGO-3%gC3N4, allowing to obtain degradations of both pollutants above 96%. This catalyst has the largest specific area, and its activity has been related to a synergistic effect, involving factors as relevant as the surface of the material and the ability to absorb radiation in the visible region, mainly produced by the incorporation of rGO and gC3N4 to the semiconductor. The use of different scavengers during the catalytic process, was used to establish the possible photodegradation mechanism of both antibiotics.

Tracking the changes in the structural, optical and photoluminescent properties of CuCo2O4/MnS nanocomposites with different composition ratios

(1−x)CuCo2O4/xMnS (x = 0, 0.25, 0.5) nanocomposite samples were formed using hydrothermal and thermolysis procedures. X-ray diffraction (XRD) phase analysis showed the formation of only CuCo2O4 phase necessitating the inclusion of Mn and S ions into the CuCo2O4 lattice. Fourier-transform infrared spectroscopy (FTIR) analyses confirmed the presence of Mn and S ions in the nanocomposite samples. Rietveld refinement method was applied to determine the cation distribution of the different ions between different sites. The cell parameter (a) has no fixed trend of change. The average crystallite size is almost the same for all samples with an average of 15 nm. The effect of insertion of Mn and S ions into the CuCo2O4 on the diffused absorbance, extinction coefficient, refractive index, dielectric properties, and nonlinear optical parameters was discussed in detail. The pristine CuCo2O4 nanoparticles have two direct optical band gaps (1.65, 2.74) eV which are decreased to (1.59, 2.56) and (1.58, 2.54) eV for the MnS content x = 0.25 and 0.5, respectively. The two indirect optical band gaps of pristine CuCo2O4 changed irregularly as the MnS amount increased in the nanocomposite. The PL spectrum of CuCo2O4 is shifted to higher wavelength in the visible region upon alloying with MnS. The photoluminescence (PL) intensity of the nanocomposite samples is smaller than that of CuCo2O4 sample. The emitted PL colors depended on the amount of Mn and S ions in the CuCo2O4 matrix.

One-Step Preparation of RGO/Fe3O4-Fevo4 Nanocomposites As Highly Effective Photocatalysts Under Natural Sunlight Illumination

The study used a one-step hydrothermal method to prepare Fe3O4-FeVO4 and xRGO/Fe3O4-FeVO4 nanocomposites. XRD, TEM, EDS, XPS, DRS, and PL techniques were used to examine the structurally and morphologically properties of the prepared samples. The XRD results appeared that the Fe3O4-FeVO4 has a triclinic crystal structure. Under hydrothermal treatment, (GO) was effectively reduced to (RGO) as illustrated by XRD and XPS results. UV-Vis analysis revealed that the addition of RGO enhanced the absorption in the visible region and narrowed the band gap energy. The photoactivities of the prepared samples were evaluated by degrading methylene blue (MB), phenol and brilliant green (BG) under sunlight illumination. As indicated by all the nanocomposites, photocatalytic activity was higher than the pure Fe3O4-FeVO4 photocatalyst, and the highest photodegradation efficiency of MB and phenol was shown by the 10%RGO/Fe3O4-FeVO4. In addition, the study examined the mineralization (TOC), photodegradation process, and photocatalytic reaction kinetics of MB and phenol.

Ti Doped Cu2O Thin Films: DC Magnetron Sputtering and Structural and Optical Studies

Ti doped Cu2O thin films were prepared at distinct Argon/Oxygen gas flow ratio of 34/1, 33/2,32/3 and 31/4 with net flow (Ar+O2) of 35 sccm by using DC magnetron sputtering system on glass substrates at room temperature. The gas mixture influence on the film properties studied by using X-ray diffraction, Field emission scanning electron microscopy and UV-Visible spectroscopy. From XRD results, it is evident that, with a decrease in oxygen content, the amplitude of (111) peak increased, peak at a 35.67o scattering angle and the films shows a simple cubic structure. The FESEM images indicated the granularity of thin films was distributed uniformly in a homogenous model and also includes especially pores and cracks. The film deposited at 31/4 showed a 98% higher transmittance in the visible region.

Chemical redox-induced chiroptical switching of supramolecular assemblies of viologens

Chiral assemblies of viologen-modified glutamide derivatives exhibit a unique orange-color and CD signals by CT complexes of viologen groups and electro-responsive chiroptical switching behaviors in the visible region in water.