Hybrid perovskites, materials composed of metals and organic substances in their structure, have emerged as potential materials for the new generation of photovoltaic cells due to a unique combination of optical, excitonic and electrical properties. Inspired by sensitization techniques on TiO₂ substrates (DSSC), CH₃NH₃PbBr₃ and CH₃NH₃PbI₃ perovskites were studied as a light-absorbing layer as well as an electron–hole pair generator. Photovoltaic cells based on per-ovskites have electron and hole transport layers (ETL and HTL, respectively), separated by an ac-tive layer composed of perovskite itself. Major advances subsequently came in the preparation methods of these devices and the development of different architectures, which resulted in an efficiency exceeding 23% in less than 10 years. Problems with stability are the main barrier to the large-scale production of hybrid perovskites. Partially or fully inorganic perovskites appear promising to circumvent the instability problem, among which the black perovskite phase CsPbI₃ (α-CsPbI₃) can be highlighted. In more advanced studies, a partial or total substitution of Pb by Ge, Sn, Sb, Bi, Cu or Ti is proposed to mitigate potential toxicity problems and maintain device efficiency.

The nanostructured lanthanide-silica materials of the Ln–SiO₂ type (Ln = La, Ce, Pr, Nd, Eu, Gd, Dy, Yb, Lu) were synthesized by the hydrothermal method at 100 °C, using cetyltrimethylammonium as a structural template, silica gel and sodium silicate as a source of silicon, and lanthanide oxides, with Si/Ln molar ratio = 50. The resulting materials were calcined at 500 °C using nitrogen and air, and characterized by X-ray diffraction (XRD), Fourier-Transform infrared absorption spectroscopy, scanning electron microscopy, thermogravimetry (TG), surface area by the BET method and acidity measurements by n-butylamine adsorption. The XRD and chemical analysis indicated that the SiO₂ presented a hexagonal structure and the incorporation of lanthanides in the structure changes the properties of the Ln–SiO₂ materials. The heavier the lanthanide element, the higher the Si/Ln ratio. The TG curves showed that the decomposition of the structural template occurs in the materials at temperatures below 500 °C. The samples showed variations in specific surface area, mean pore diameter and silica wall thickness, depending on the nature of the lanthanide. The incorporation of different lanthanides in the silica generated acid sites of varied strength. The hydrothermal stability of the Ln–SiO₂ materials evaluated at high temperatures, evidenced that the properties can be controlled for application in adsorption and catalysis processes.

In the past few years, wind power has become a viable alternative in Brazil to diversify the energy mix and mitigate pollutant emissions from fossil fuels. Significant wind energy generation potential is inherent in the Brazilian Northeast state of Rio Grande do Norte, due to prevailing strong winds along the coastline and elevated regions. However, clean and renewable wind energy may lead to potential biodiversity impacts, including the removal of native vegetation during plant construction and operation. This case study explores the flash pyrolysis-based valorization of three commonly suppressed species, namely Cenostigma pyramidale (CP), Commiphora leptophloeos (CL), and Aspidosperma pyrifolium (AP), in a wind farm situated within the Mato Grande region of Rio Grande do Norte State. The study centers on determining their bioenergy-related properties and assessing their potential for producing phenolic-rich bio-oil. The investigation of three wood residues as potential sources of high-value chemicals, specifically phenolic compounds, was conducted using a micro-furnace type temperature programmable pyrolyzer combined with gas chromatography/mass spectrometry (Py–GC/MS setup). The range of higher heating values observed for three wood residues was 17.5–18.4 MJ kg⁻¹, with the highest value attributed to AP wood residue. The bulk density ranged from 126.5 to 268.7 kg m⁻³, while ash content, volatile matter content, fixed carbon content, and lignin content were within the respective ranges of 0.8–2.9 wt.%, 78.5–89.6 wt.%, 2.6–9.5 wt.%, and 19.1–30.6 wt.%. Although the energy-related properties signifying the potential value of three wood residues as energy resources are evident, their applicability in the bioenergy sector can be expanded via pelleting or briquetting. Yields of phenolic compounds exceeding 40% from the volatile pyrolysis products of CL and AP wood residues at 500 °C make them favorable for phenolic-rich bio-oil production. The findings of this study endorse the utilization of wood residues resulting from vegetation suppression during the installation of wind energy plants as potential feedstocks for producing bioenergy and sustainable phenolic compounds. This presents a solution for addressing a regional environmental concern following the principles of green chemistry.