Apresentação

O nosso departamento congrega docente que atuam em diversas áreas de pesquisa, notadamente Ciências dos Materiais, Física Computacional, Astrofísica, Cosmologia e Gravitação, Big Bang, Matéria Escura, Energia Escura, Relatividade Geral e teorias gravitacionais alternativas.. Temos um curso de bacharelado em física com ênfases em ciências dos materiais e física básica e um curso de Licenciatura em Física. Atuamos nos cursos de Pós-graduação em Física de Materiais (FIMAT), Rede Temática em Engenharia de Materiais - REDEMAT, Mestrado Profissional em Estudo de Ciência (MPEC) e outros programas em colaboração com outros departamentos da UFOP. 

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Publicações Recentes do Departamento de Física

Martins LGP, Silva DL, Smith JS, Lu A-Y, Su C, Hempel M, Occhialini C, Ji X, Pablo R, Alencar RS, et al. Hard, transparent, sp3-containing 2D phase formed from few-layer graphene under compression. Carbon [Internet]. 2020. Publisher's VersionAbstract
Despite several theoretically proposed two-dimensional (2D) diamond structures, experimental efforts to obtain such structures are in initial stage. Recent high-pressure experiments provided significant advancements in the field, however, expected properties of a 2D-like diamond such as sp3 content, transparency and hardness, have not been observed together in a compressed graphene system. Here, we compress few-layer graphene samples on SiO2/Si substrate in water and provide experimental evidence for the formation of a quenchable hard, transparent, sp3-containing 2D phase. Our Raman spectroscopy data indicates phase transition and a surprisingly similar critical pressure for two-, five-layer graphene and graphite in the 4-6 GPa range, as evidenced by changes in several Raman features, combined with a lack of evidence of significant pressure gradients or local non-hydrostatic stress components of the pressure medium up to ≈ 8 GPa. The new phase is transparent and hard, as evidenced from indentation marks on the SiO2 substrate, a material considerably harder than graphene systems. Furthermore, we report the lowest critical pressure (≈ 4 GPa) in graphite, which we attribute to the role of water in facilitating the phase transition. Theoretical calculations and experimental data indicate a novel, surface-to-bulk phase transition mechanism that gives hint of diamondene formation.
Farias G, Salla CAM, da Silva Heying R, Bortoluzzi AJ, Curcio S, Cazati T, dos Santos PL, Monkman AP, de Souza B, BECHTOLD IVANH. Reducing Lifetime in Cu(I) Complexes with Thermally Activated Delayed Fluorescence and Phosphorescence promoted by Chalcogenolate-Diimine Ligand. J. Mater. Chem. C [Internet]. 2020 :-. Publisher's VersionAbstract
Luminescent copper(I) complexes have drawn attention due to their promising performance as alternative optoelectronic materials to the well-known heavy transition metals complexes. Herein, we report the synthesis of six luminescent Cu(I) complexes with phosphines and 1,10-phenanthroline-derived ligands with thiadiazole and selenodiazole groups in order to evaluate the effect of heavy atom on their photophysical properties. Steady-state and time-resolved spectroscopy confirmed delayed fluorescence emission via a thermally activated delayed fluorescence mechanism in all cases. The experimental spectroscopic data was analyzed with detailed quantum-chemical calculations. Interestingly, these complexes did not show the expected “heavy atom effect”, that enhances the spin-orbit coupling matrix elements, but nevertheless the addition of the heavier chalcogens contributed to reduce the photoluminescence lifetime to roughly 800 ns, which is the lowest reported so far for such TADF materials.
dos Teixeira AR, Teixeira RR, Ribeiro IML, Pereira WL, Manhabosco TM, de Brito ACF, Oliveira LAM, de Oliveira K, Nogueira PC. Association of electroanalytical and spectrophotometric methods to evaluate the antioxidant activity of isobenzofuranone in primary cultures of hippocampal neurons. Toxicology in Vitro [Internet]. 2020 :104970. Publisher's VersionAbstract
The isobenzofuran-1(3H)-ones (phthalides) exhibit various biological activities, including antioxidant activity on reactive oxygen species (ROS). An excess of ROS that cannot be naturally contained by cellular enzymatic systems is called redox imbalance, which damage cell membranes, proteins, and DNA, thereby possibly triggering neuronal death in several neurodegenerative diseases. Considering our ongoing efforts to find useful compounds to control redox imbalance, herein we evaluated the antioxidant activity of two phtalides (compounds 3 and 4), using primary cultures of hippocampal neurons. Spectrophotometric assays showed that compound 3 significantly reduced (p ≤ 0.05) ROS levels and lipid peroxidation compared to the control treatment, while compound 4 was unable at any of the tested concentrations. Despite their structural similarity, these compounds behave differently in the intracellular environment, which was reliably corroborated by the determination of oxidation potentials via cyclic voltammetry. It was demonstrated that compound 3 presents a lower oxidation potential. The combination of the mentioned methods allowed us to find a strong correlation between the chemical structure of compounds and their biological effects. Taking together, the results indicate that compound 3 presents desirable characteristics to act as a candidate pharmacological agent for use in the prevention and treatment of neurodegenerative diseases.
Paez EBA, Curcio S, Neme N, Matos M, Correa RS, Pereira FJ, Hilário FF, Cazati T, Taylor JG. Synthesis, Photophysical and Electrochemical Properties of Novel and Highly Fluorescent Difluoroboron Flavanone β-Diketonate Complexes. New J. Chem. [Internet]. 2020 :-. Publisher's VersionAbstract
Difluoroboron β-diketonates complexes are highly luminescent with extensive properties such as their fluorescence both in solution and in solid state and their high molar extinction coefficients. Due to their rich optical properties, these compounds have been studied for their applications in organic electronics such as in self-assembly and applications in biosensors, bio-imaging and optoelectronic devices. The easy and fast synthesis of difluoroboron β-diketonate (BF2dbm) complexes makes their applications even more attractive. Although many different types of difluoroboron β-diketonates complexes have been studied, the cyclic flavanone analogues of these compounds have never been reported in the literature. Therefore, the present work aims to synthesize difluouroboron flavanone β-diketonate complexes, study their photophysical and electrochemical properties and assess their suitability for applications in optoelectronic devices. The synthesis was based on a Baker–Venkataraman reaction which initially provided substituted diketones, which were subsequently reacted with aldehydes to afford the proposed flavanones. The complexation was achieved by reacting flavanones and BF3. Et2O and in total 9 novel compounds were obtained. A representative difluoroboron flavanone complex was subjected to single crystal X-ray diffraction to unequivocally confirm the chemical structure. A stability study indicated only partial degradation of these compounds over a few days in a protic solvent at elevated temperatures. Photophysical studies revealed that the substituent groups and the solvent media significantly influence the electrochemical and photophysical properties of the final compounds, especially the molar absorption coefficient, fluorescence quantum yields, and the band gap. Moreover, the compounds exhibited a single excited-state lifetime in all studied solvent. Computational studies were employed to evaluate ground and excited states properties and carry out DFT and TDDFT level analysis. These studies clarify the role of each state in the experimental absorption spectra as well as the effect of the solvent.
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Publicações de Livros do Departamento de Física

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