In this work, iron oxide nanoparticles produced using the laser ablation technique were studied in order to determine the characteristics of these nanoparticles as a function of the laser energy for the possible application in magnetic hyperthermia. Nanoparticles were obtained by varying the power of the laser considering values of 90, 173, 279 and 370 mJ. The morphology of these nanoparticles was determined using the dynamic light scattering (DLS) and scattering transmission electron microscopy (STEM) techniques, confirming that the size of the particles was in the order of nanometers. A great influence of the laser power on the particle size was also observed, caused by the competition between the energy and the temperature. The composition was determined by X-ray diffraction and Raman spectroscopy, showing the presence of magnetite, maghemite and hematite. The hyperthermia measurements showed that the temperature rise of the iron oxide nanoparticles was not greatly influenced by the energy change, the heating capacity of magnetic NPs is quantified by the specific absorption rate (SAR), that tends to decrease with increasing energy, which indicates a dependence of these values on the nanoparticles concentration.

Perovskite-based materials have been considered as the most promising materials in several solar-driven processes, especially photovoltaics. Some features such as high sunlight harvesting and improved carrier transport have been highlighted to have an impact on the efficiency of the above topics, but limited studies have pointed out their surface composition, which mainly influence the above abilities. As a starting point to recognize the surface environment and chemical states of these materials, x-ray photoelectron spectroscopy measurements were performed. Trication-mixed halide perovskite films based on Cs0.08MA0.18FA0.78PbBr0.42I2.58 were prepared by a one step process and deposited on an indium tin oxide substrate by spin-coating. Survey spectra, Pb 4f, I 3d, Br 3d, Cs 3d, C 1s, N 1s, Pb 4d, and Pb 5d core levels, and valence band spectra were measured for the semiconductor sample. Results exhibit symmetrical peaks, indicating that a homogenous solid solution was achieved. Main chemical states of this kind of perovskites such as Cs-Br and Pb-I species are also shown. We deduced that the later signals are associated with the [PbI6]4− octahedra existing in the perovskite lattice, while the former one is related to Cs+ bounded to [PbBr6]4− units on the perovskite surface. Interestingly, the NR4+ signal was also identified, associated with the presence of methylammonium and formamidinium cations.

Cadmium selenide was analyzed using x-ray photoelectron spectroscopy. The specimen is a powder purchased from Chemsavers. The sample was fixed to a stainless-steel sample holder with copper 3MTM double-sided adhesive tape. Survey spectra, Cd 3d, Se 3d, O 1s, Cd 3p, Cd MNN, Se LMM, Se 3p, C 1s, and Cd 4d core level along with the valence band spectra were recorded. Results point out a stoichiometry of 0.95 on surface.

Bismuth (III) acetate was analyzed using x-ray photoelectron spectroscopy. The specimen is a powder purchased from Sigma Aldrich. The sample was fixed to a stainless-steel sample holder with copper 3MTM double-sided adhesive tape. Survey spectra, Bi 4f, O 1s, C 1s, Bi 4d, Bi 5d, Bi 6s core levels, and valence band spectra were acquired. The results showed how the elements in the structure of bismuth acetate are related.

This study shows the energy optimization and stabilization in the time of solutions composed of H₂O + TX-100 + Multi-Wall Carbon Nanotubes (MWCNTs), used to improve the mechanical properties of Portland cement pastes. For developing this research, sonication energies at 90, 190, 290, 340, 390, 440, 490 and 590 J/g are applied to a colloidal substance (MWCNTs/TX-100 + H₂O) with a molarity of 10 mM. Raman spectroscopy analyses showed that, for energies greater than 440 J/g, there are ruptures and fragmentation of the MWCNTs; meanwhile at energies below 390 J/g, better dispersions are obtained. The stability of the dispersion over time was evaluated over 13 weeks using UV-vis spectroscopy and Zeta Potential. With the most relevant data collected, sonication energies of 190, 390 and 490 J/g, at 10 mM were selected at the first and the fourth week of storage to obtain Portland cement specimens. Finally, we found an improvement of the mechanical properties of the samples built with Portland cement and solutions stored for one and four weeks; it can be concluded that the MWCNTs improved the hydration period.