Hydrogen (H 2 ) is a well-known reduction gas and for safety reasons is very important to be detected. The most common systems employed along its detection are metal oxide-based elements. However, the latter demand complex and expensive manufacturing techniques, while they also need high temperatures or UV light to operate effectively. In this work, we first report a solution processed hybrid mixed halide spin coated perovskite films (CH 3 NH 3 PbI 3−x Cl x ) that have been successfully applied as portable, flexible, self-powered, fast and sensitive hydrogen sensing elements, operating at room temperature. The minimum concentrations of H 2 gas that could be detected was down to 10 ppm. This work provides a new pathway on gases interaction with perovskite materials, poses new questions that must be addressed regarding the sensing mechanisms involved. The utilization of halide perovskite sensing elements demonstrates their potential beyond solar cell applications. OPEN ACCESS RECEIVED

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CoNiTiO systems evaluated as photo- and electrocatalytic materials for oxygen evolution reaction (OER) from water have been studied. These materials have shown promising properties for this half-reaction both under (unbiased) visible-light photocatalytic approach in the presence of an electron scavenger and as electrocatalysts in dark conditions in basic media. In both situations, CoNiTiO exhibits the best performance and is proved to display high faradaic efficiency. A synergetic effect between Co and Ni is established, improving the physicochemical properties such as surface area and pore size distribution, besides affecting the donor density and the charge carrier separation. At higher Ni content, the materials exhibit behavior more similar to that of NiTiO, which is a less suitable material for OER than CoTiO.

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Hydrogen is attractive as an abundant source for clean and renewable energy. However, due to its highly flammable nature in a range of concentrations, the need for reliable and sensitive sensor/monitoring technologies has become acute. Here a solid-state hydrogen sensor based on solution-processable p-type semiconductor copper thiocyanate (CuSCN) is developed and studied. Sensors incorporating interdigitated electrodes made of noble metals (gold, platinum, palladium) show excellent response to hydrogen concentration down to 200 ppm while simultaneously being able to operate reversibly at room temperature and at low power. Sensors incorporating Pd electrodes show the highest signal response of 179% with a response time of ≈400 s upon exposure to 1000 ppm of hydrogen gas. The experimental findings are corroborated by density functional theory calculations, which highlight the role of atomic hydrogen species created upon interaction with the noble metal electrode as the origin for the increased p-type conductivity of CuSCN during exposure. The work highlights CuSCN as a promising sensing element for low-power, all-solid-state printed hydrogen sensors.

The increasing air pollution taking place in virtue of human activity has a novel impact in our health. Heterogeneous photocatalysis is a promising way of degrading volatile organic compounds (VOCs) that makes the quest of new and improved photocatalysts of great importance. Herein, perovskite-related materials ATiO3 with A = Mg, Ni, Co, Zn were synthesized through an ethylene glycol-mediated root, with ethylene glycol being used as a solvent and ligand. Characterization techniques such as X-ray diffraction (XRD), scanning electron microscopy, and energy dispersive X-ray spectroscopy (SEM/EDX), transmission electron microscopy (TEM), UV-vis spectroscopy, Raman spectroscopy, Fourier transform infrared (FT-IR), and photoluminescence spectroscopy (PL) were used in order to confirm the structure, the nanorod morphology, their absorption in UV-vis, and the separation efficiency of photogenerated charge carriers. The highest photoactivity was observed for ZnTiO3 in which 62% of toluene was decomposed after 60 min under LED illumination (54 mW/cm2).