The present work reports the influence of zinc oxide (ZnO) seed layer annealing temperature on structural, optical and electrical properties of ZnO nanorod arrays, synthesized by hydrothermal method assisted by microwave radiation, to be used as UV sensors. The ZnO seed layer was produced using the spin-coating method and several annealing temperatures, ranging from 100 to 500 °C, have been tested. X-ray diffraction (XRD), scanning electron microscopy (SEM), atomic force microscopy (AFM) and spectrophotometry measurements have been used to investigate the structure, morphology, and optical properties variations of the produced ZnO nanorod arrays regarding the seed layer annealing temperatures employed. After the growth of ZnO nanorod arrays, the whole structure was tested as UV sensors, showing an increase in the sensitivity with the increase of seed layer annealing temperature. The UV sensor response of ZnO nanorod arrays produced with the seed layer annealed temperature of 500 °C was 50 times superior to the ones produced with a seed layer annealed at 100 °C.

The degradation of organic pollutants in wastewaters assisted by oxide semiconductor nanostructures has been the focus of many research groups over the last decades, along with the synthesis of these nanomaterials by simple, eco-friendly, fast, and cost-effective processes. In this work, porous zinc oxide (ZnO) nanostructures were successfully synthesized via a microwave hydrothermal process. A layered zinc hydroxide carbonate (LZHC) precursor was obtained after 15 min of synthesis and submitted to different calcination temperatures to convert it into porous ZnO nanostructures. The influence of the calcination temperature (300, 500, and 700 °C) on the morphological, structural, and optical properties of the ZnO nanostructureswas investigated. All ZnO samples were tested as photocatalysts in the degradation of rhodamine B (RhB) under UV irradiation and natural sunlight. All samples showed enhanced photocatalytic activity under both light sources, with RhB being practically degraded within 60 min in both situations. The porous ZnO obtained at 700 °C showed the greatest photocatalytic activity due to its high crystallinity, with a degradation rate of 0.091 and 0.084 min−1 for UV light and sunlight, respectively. These results are a very important step towards the use of oxide semiconductors in the degradation of water pollutants mediated by natural sunlight.

In this work, zinc oxide (ZnO) and titanium dioxide (TiO 2 ) nanostructures were grown on different cellulose paper substrates, namely, Whatman, office, and commercial hospital papers, using a hydrothermal method assisted by microwave irradiation. Pure ZnO and TiO 2 nanostructures were synthesized; however, the growth of TiO 2 above ZnO was also investigated to produce a uniform heterostructure. Continuous ZnO nanorod arrays were grown on Whatman and hospital papers; however, on office paper, the formation of nanoplates originating nanoflower structures could be observed. TiO 2 nanoparticles homogeneously covered all the substrates, in some conditions forming uniform TiO 2 films. Structural characterization was carried out by scanning electron microscopy (SEM) coupled with energy-dispersive X-ray spectroscopy (EDS), X-ray diffraction (XRD), and Raman spectroscopy. The optical characterization of all the materials was carried out. The produced materials were investigated for multifunctional applications, like photocatalyst agents, bacterial inactivators, and ultraviolet (UV) sensors. To evaluate the photocatalytic activity under UV and solar radiations, rhodamine B was the model-test contaminant indicator and the best photocatalytic activity was achieved with Whatman paper. Hospital paper with TiO 2 nanoparticles showed significant antibacterial properties against Staphylococcus aureus. ZnO-based UV sensors demonstrated a responsivity of 0.61 μA W -1 .

An increase in the demand for the next generation of “Internet‐of‐Things” (IoT) has motivated efforts to develop flexible and affordable smart electronic systems, in line with sustainable development and carbon neutrality. Cellulose holds the potential to fulfil such demands as a low‐cost green material due to its abundant and renewable nature and tunable properties. Here, a cellulose‐based ionic conductive substrate compatible with printing techniques that combines the mechanical robustness, thermal resistance and surface smoothness of cellulose nanofibrils nanopaper with the high capacitance of a regenerated cellulose hydrogel electrolyte, is reported. Fully screen‐printed electrolyte‐gated transistors and universal logic gates are demonstrated using the engineered ionic conductive nanopaper and zinc oxide nanoplates as the semiconductor layer. The devices exhibit low‐voltage operation (<3 V), and remarkable mechanical endurance under outward folding due to the combination of the robustness of the nanopaper and the compliance of the semiconductor layer provided by the ZnO nanoplates. The printed devices and the ion‐conductive nanopaper can be efficiently recycled to fabricate new devices, which is compatible with the circular economy concept.

The fabrication of low-cost, flexible, and recyclable electronic devices has been the focus of many research groups, particularly for integration in wearable technology and the Internet of Things (IoT). In this work, porous zinc oxide (ZnO) nanostructures are incorporated as a UV sensing material into the composition of a sustainable water-based screen-printable ink composed of carboxymethyl cellulose (CMC). The formulated ink is used to fabricate flexible and foldable UV sensors on ubiquitous office paper. The screen-printed CMC/ZnO UV sensors operate under low voltage (≤2 V) and reveal a stable response over several on/off cycles of UV light exposure. The devices reach a response current of 1.34 ± 0.15 mA and a rise and fall time of 8.2 ± 1.0 and 22.0 ± 2.3 s, respectively. The responsivity of the sensor is 432 ± 48 mA W−1, which is the highest value reported in the literature for ZnO-based UV sensors on paper substrates. The UV-responsive devices display impressive mechanical endurance under folding, showing a decrease in responsivity of only 21% after being folded 1000 times. Their low-voltage operation and extreme folding stability indicate a bright future for low-cost and sustainable flexible electronics, showing potential for low-power wearable applications and smart packaging.