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CsPbI3 inorganic perovskite is synthesized by a solvent-free, solid-state reaction, and its structural and optical properties can be deeply investigated using a multi-technique approach. X-ray Diffraction (XRD) and Raman measurements, optical absorption, steady-time and time-resolved luminescence, as well as High-Resolution Transmission Electron Microscopy (HRTEM) imaging, were exploited to understand phase evolution as a function of synthesis time length. Nanoparticles with multiple, well-defined crystalline domains of different crystalline phases were observed, usually surrounded by a thin, amorphous/out-of-axis shell. By increasing the synthesis time length, in addition to the pure α phase, which was rapidly converted into the δ phase at room temperature, a secondary phase, Cs4PbI6, was observed, together with the 715 nm-emitting γ phase.

The need to find a rapid and worthwhile technique for the in situ detection of the content of delta-9-tetrahydrocannabinol (THC) and cannabidiol (CBD) in Cannabis sativa L. is an ever-increasing problem in the forensic field. Among all the techniques for the detection of cannabinoids, Raman spectroscopy can be identified as the most cost-effective, fast, noninvasive, and nondestructive. In this study, 42 different samples were analyzed using Raman spectroscopy with 1064 nm excitation wavelength. The use of an IR wavelength laser showed the possibility to clearly identify THC and CBD in fresh samples, without any further processing, knocking out the contribution of the fluorescence generated by visible and near-IR sources. The results allow assigning all the Raman features in THC- and CBD-rich natural samples. The multivariate analysis underlines the high reproducibility of the spectra and the possibility to distinguish immediately the Raman spectra of the two cannabinoid species. Furthermore, the ratio between the Raman bands at 1295/1440 and 1623/1663 cm –1 is identified as an immediate test parameter to evaluate the THC content in the samples.

Halide perovskite colloidal nanocrystals have recently gained much attention thanks to their superior stability compared with their bulk counterpart and to their unique optical properties. In this paper, two systems combining nanocrystals and nanoporous gold are studied to create an optimal metal semiconductor heterojunction that can be used in photocatalysis and photovoltaic devices. The perovskite degradation phenomenon is observed when the nanoporous gold powder is mixed into the hexane suspension of nanocrystals, while the charge separation efficiency is increased by synthesizing the nanocrystals directly onto the gold porous structure. The analysis of the structural and optical properties evidences an energy transfer efficiency of 47%, along with the high structural stability of the hybrid system.

Totally inorganic perovskites are playing an increasingly important role for their potential applications in optoelectronics devices. However, a big problem to be solved is the role of the different phases, the presence of which is closely linked to the growth method and to the role of impurities. In this article, we propose a solvent-free, solid-state growth method, which allows to obtain samples free of any organic residues. The analysis of structural (XRD and Raman measurements), optical (absorption, steady-time and time-resolved luminescence) and morphological (HRTEM imaging), permitted to understand the phase evolution during the synthesis as a function of the temporal duration. The dynamic equilibrium process at high temperature between the CsPbI3 and the starting precursors, CsI and PbI2, plays a fundamental role in the final phase. If, from one side, the α and δ phases are related to the exact stoichiometry, on the other hand an excess of CsI permits the formation of room temperature stable perovskite γ-phase and, with a further excess, the secondary Cs4PbI6 phase is obtained.