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For a safe environment, humanity should be oriented towards renewable energy technology. Water splitting (WS), utilizing a photoelectrode with suitable thickness, morphology, and conductivity, is essential for efficient hydrogen production. In this report, iridium oxide (IrOx) films of high conductivity were spin-cast on glass substrates. FE-SEM showed that the films are of nanorod morphology and different thicknesses. UV-Vis spectra indicated that the absorption and reflectance of the films depend on their thickness. The optical band gap (Eg) was increased from 2.925 eV to 3.07 eV by varying the spin speed (SS) of the substrates in a range of 1.5 × 103–4.5 × 103 rpm. It was clear from the micro-Raman spectra that the films were amorphous. The Eg vibrational mode of Ir–O stretching was red-shifted from 563 cm−1 (for the rutile IrO2 single crystal) to 553 cm−1. The IrOx films were used to develop photoelectrochemical (PEC) hydrogen production catalysts in 0.5M of sodium sulfite heptahydrate Na2SO3·7H2O (2-electrode system), which exhibits higher hydrogen evaluation (HE) reaction activity, which is proportional to the thickness and absorbance of the used IrOx photocathode, as it showed an incident photon-to-current efficiency (IPCE%) of 7.069% at 390 nm and −1 V. Photocurrent density (Jph = 2.38 mA/cm2 at −1 V vs. platinum) and PEC hydrogen generation rate (83.68 mmol/ h cm2 at 1 V) are the best characteristics of the best electrode (the thickest and most absorbent IrOx photocathode). At −1 V and 500 nm, the absorbed photon-to-current conversion efficiency (APCE%) was 7.84%. Electrode stability, thermodynamic factors, solar-to-hydrogen conversion efficiency (STH), and electrochemical impedance spectroscopies (EISs) were also studied.

We examine how the weak excitation regime of a quantum well confined in a semiconductor microcavity (SM) influences the dynamics of quantum coherence and the total phase. We analyze the impact of the physical parameters on different quantumness measures, and illustrate their numerical results. We show that the amount of the coherence and total phase in the SMs for multi-photon excitation can be improved and controlled by the strength of the field, exciton-photon coupling, cavity dissipation rate, and excitonic spontaneous emission rate. We illustrate how the fidelity varies depending on the physical parameters. These results might have far-reaching ramifications not just in quantum information processing and optics, but also in physics at large.

A p-n nanocomposite based on TiO2 nanotubes (NTs) and NiO nanoparticles (NPs) was designed and optimized in this study to improve the photocatalytic performance of methylene blue (MB). The hydrothermal technique has been used to produce TiO2/NiO nanocomposites with different NiO NPs weight ratios; 1TiO2:1NiO, 1TiO2:2NiO, and 1TiO2:3NiO. The crystal phase, chemical composition, optical properties, and morphology of TiO2/NiO were explored by various techniques. TiO2 NTs have a monoclinic structure, while NiO NPs have a cubic structure, according to the structural study. The bandgap of TiO2 NTs was reduced from 3.54 eV to 2.69 eV after controlling the NiO NPs weight ratio. The TiO2/2NiO nanocomposite showed the best photodegradation efficiency. Within 45 min of solar light irradiation, the efficiency of MB dye degradation using TiO2/2NiO hits 99.5% versus 73% using pure TiO2 NTs. Furthermore, the catalytic photodegradation efficiency did not deteriorate significantly even after five reusability cycles, intimating the high stability of the TiO2/2NiO nanocomposite. This suggests that the loading of NiO NPs into TiO2 NTs lowers the recombination of photo-produced electron/hole pairs and enlarged solar spectral response range, which results in improved photocatalytic activity. The mechanism of charge transfer in the TiO2/NiO and kinetic models were discussed for the photodegradation of MB.