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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.

Obtaining H2 energy from H2O using the most abundant solar radiation is an outstanding approach to zero pollution. This work focuses on studying the effect of Co doping and calcination on the structure, morphology, and optical properties of spin-coated SnO2 films as well as their photoelectrochemical (PEC) efficiency. The structures and morphologies of the films were investigated by XRD, AFM, and Raman spectra. The results confirmed the preparation of SnO2 of the rutile phase, with crystallite sizes in the range of 18.4–29.2 nm. AFM showed the granular structure and smooth surfaces having limited roughness. UV-Vis spectroscopy showed that the absorption spectra depend on the calcination temperature and the Co content, and the films have optical bandgap (Eg) in the range of 3.67–3.93 eV. The prepared samples were applied for the PEC hydrogen generation after optimizing the sample doping ratio, using electrolyte (HCl, Na2SO4, NaOH), electrode reusability, applied temperature, and monochromatic illumination. Additionally, the electrode stability, thermodynamic parameters, conversion efficiency, number of hydrogen moles, and PEC impedance were evaluated and discussed, while the SnO2 films were used as working electrodes and platinum sheet as an auxiliary or counter electrode (2-electrode system) and both were dipped in the electrolyte. The highest photocurrent (21.25 mA/cm2), number of hydrogen moles (20.4 mmol/h.cm2), incident photon-to-current change efficiency (6.892%@307 nm and +1 V), and the absorbed photon-to-current conversion efficiency (4.61% at ~500 nm and +1 V) were recorded for the 2.5% Co-doped SnO2 photoanode that annealed at 673 K.

For a safe environment, harmful-gas sensors of low cost and high performance are essential. For CO2 gas sensing applications, Ba-doped CuO thin films with 4 mol% and 6 mol% Ba were produced on glass substrates using the successive ionic layer adsorption and reaction approach. Utilizing various techniques, crystallographic structures, nanomorphologies, and elemental compositions were examined to assess the impact of doping on the characteristics of the films. According to the structural and morphological analyses, the nanocrystalline films consisted of irregularly shaped nanoparticles, which assembled to form a rough surface with unequal grain sizes. Because of its nanoporous nature, the CuO:6% Ba thin film exhibited the most substantial nanomorphological change and the highest gas sensing capability. At varied CO2 gas flow rates, the maximum sensor response (9.4%) and Rair/RCO2 ratio (1.12) at room temperature (RT = 30 °C) were observed at 100 SCCM. By optimizing the sensor’s operating temperature, the sensor response value reached 82.2% at 150 °C, which is approximately eight times the value at RT. Selectivity, reusability, repeatability, detection limit, and quantification limit were all tested. It shows excellent response and recovery times of 5.6 and 5.44 s. In comparison to prior literature, the improved sensor is suited for use in industrial applications. Graphical abstract

In this work, a low-cost, high-yield hydrothermal treatment was used to produce nanozeolite (Zeo), nanoserpentine (Serp), and Zeo/Serp nanocomposites with weight ratios of 1:1 and 2:1. At 250 °C for six hours, the hydrothermal treatment was conducted. Various methods are used to explore the morphologies, structures, compositions, and optical characteristics of the generated nanostructures. The morphological study revealed structures made of nanofibers, nanorods, and hybrid nanofibril/nanorods. The structural study showed clinoptilolite monoclinic zeolite and antigorite monoclinic serpentine with traces of talcum mineral and carbonates. As a novel photoelectrochemical catalyst, the performance of the Zeo/Serp (2:1) composite was evaluated for solar hydrogen generation from water splitting relative to its constituents. At −1 V, the Zeo/Serp (2:1) composite produced a maximum current density of 8.44 mA/g versus 7.01, 6.74, and 6.6 mA/g for hydrothermally treated Zeo/Serp (1:1), Zeo, and Serp, respectively. The Zeo/Serp (2:1) photocatalysts had a solar-to-hydrogen conversion efficiency (STH) of 6.5% and an estimated hydrogen output rate of 14.43 mmole/h.g. Consequently, the current research paved the way for low-cost photoelectrochemical catalytic material for efficient solar hydrogen production by water splitting.