The outstanding versatility of graphene for surface functionalization has been exploited by its decoration with synthesized polypyrrole (PPy) nanoparticles (NPs). A green, facile, and easily scalable for mass production nanocomposite development was proposed, and the resulting [email protected] was implemented in chemoresistive gas sensors able to detect trace levels of ammonia (NH₃) under room-temperature conditions. Gas exposure for 5 min revealed that the presence of nanoparticles decorating graphene entail greater sensitivity (13-fold) in comparison to the bare graphene performance. Noteworthy, excellent repeatability (0.7% of relative error) and a low limit of detection of 491 ppb were obtained, together with excellent long-term stability. Besides, an extensive material characterization was conducted, and vibration bands obtained via Raman spectroscopy confirmed the formation of PPy NPs, while X-ray spectroscopy (XPS) revealed the relative abundance of the different species, as polarons and bipolarons. Additionally, XPS analyses were conducted before and after NH₃ exposure to assess the PPy aging and the changes induced in their physicochemical and electronic properties. Specifically, the gas sensor was tested during a 5-month period, demonstrating significant stability over time, since just a slight decrease (11%) in the responses was registered. In summary, the present work reports for the first time the use of PPy NPs decorating graphene for gas-sensing purposes, revealing promising properties for the development of unattended gas-sensing networks for monitoring air quality.

During the few last years, indoor and outdoor Air Quality Monitoring (AQM) has gained a lot of interest among the scientific community due to its direct relation with human health. The Internet of Things (IoT) and, especially, Wireless Sensor Networks (WSN) have given rise to the development of wireless AQM portable systems. This paper presents the development of a LoRa (short for long-range) based sensor network for AQM and gas leakage events detection. The combination of both a commercial gas sensor and a resistance measurement channel for graphene chemoresistive sensors allows both the calculation of an Air Quality Index based on the concentration of reducing species such as volatile organic compounds (VOCs) and CO, and it also makes possible the detection of NO₂, which is an important air pollutant. The graphene sensor tested with the LoRa nodes developed allows the detection of NO₂ pollution in just 5 min as well as enables monitoring sudden changes in the background level of this pollutant in the atmosphere. The capability of the system of detecting both reducing and oxidizing pollutant agents, alongside its low-cost, low-power, and real-time monitoring features, makes this a solution suitable to be used in wireless AQM and early warning systems.

Lead halide perovskites have been attracting great attention due to their outstanding properties and have been utilized for a wide variety of applications. However, the high toxicity of lead promotes an urgent and necessary search for alternative nanomaterials. In this perspective, the emerging lead-free perovskites are an environmentally friendly and harmless option. The present work reports for the first time gas sensors based on lead-free perovskite nanocrystals supported on graphene, which acts as a transducing element owing to its high and efficient carrier transport properties. The use of nanocrystals enables achieving excellent sensitivity toward gas compounds and presents better properties than those of bulky perovskite thin films, owing to their quantum confinement effect and exciton binding energy. Specifically, an industrially scalable, facile, and inexpensive synthesis is proposed to support two different perovskites (Cs₃CuBr₅ and Cs₂AgBiBr₆) on graphene for effectively detecting a variety of harmful pollutants below the threshold limit values. H₂ and H₂S gases were detected for the first time by utilizing lead-free perovskites, and ultrasensitive detection of NO₂ was also achieved at room temperature. In addition, the band-gap type, defect tolerance, and electronic surface traps at the nanocrystals were studied in detail for understanding the differences in the sensing performance observed. Finally, a comprehensive sensing mechanism is proposed.

Dysprosium-doped zinc oxide (ZnO) thin films have been prepared through spray pyrolysis onto glass substrates. Cross-sections of the deposited thin films were assessed through Scanning Electron Microscopy (SEM), showing thicknesses between 200 and 300 nm. The thin film roughness was evaluated using the obtained images from the Atomic Force Microscope (AFM) micrographs. The crystallographic structure of the samples was analyzed by X-ray diffraction (XRD) revealing polycrystalline thin films. However, the slight shift towards a higher 2θ angle in Dy-doped ZnO films as compared to the pure ones indicates the incorporation of Dy³⁺ into the ZnO crystal lattice. The analysis of the oxidation state via X-ray photoelectron spectroscopy (XPS) confirms the incorporation of Dy ions in the ZnO matrix. Besides, UV-Vis-NIR spectrophotometry analysis and photoluminescence (PL) spectroscopy showed that bandgap energy values of ZnO decreased when dysprosium doping increased. Therefore, Dy doped ZnO thin films can be potentially used as a solar-light-driven photocatalyst. Among the different doping yields, the ZnO doped with 6% dysprosium provides the highest degradation rate for methylene blue (MB) under solar irradiation. Specifically, 9% of dye degradation was achieved under sunlight irradiation for 120 minutes.

This paper explores the gas sensing properties of graphene nanolayers decorated with lead halide perovskite (CH₃NH₃PbBr₃) nanocrystals to detect toxic gases such as ammonia (NH₃) and nitrogen dioxide (NO₂). A chemical-sensitive semiconductor film based on graphene has been achieved, being decorated with CH₃NH₃PbBr₃ perovskite (MAPbBr₃) nanocrystals (NCs) synthesized, and characterized by several techniques, such as field emission scanning electron microscopy, transmission electron microscopy and X-ray photoelectron spectroscopy. Reversible responses were obtained towards NO₂ and NH₃ at room temperature, demonstrating an enhanced sensitivity when the graphene is decorated by MAPbBr₃ NCs. Furthermore, the effect of ambient moisture was extensively studied, showing that the use of perovskite NCs in gas sensors can become a promising alternative to other gas sensitive materials, due to the protective character of graphene, resulting from its high hydrophobicity. Besides, a gas sensing mechanism is proposed to understand the effects of MAPbBr₃ sensing properties.