KATIUSSE SOARES DE SOUZA

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  • Resumo IPEN-doc 31004
    Molybdenum (II) acetate as a precursor for molybdenum trioxide
    2024 - SOUZA, KATIUSSE S. de; SILVA, CRYSTIAN W.C. da; BURIMOVA, ANASTASIA; PEREIRA, LUCIANO F.; OTUBO, LARISSA; CARBONARI, ARTUR W.; FREITAS, RAFAEL S. de
    Transition metal structures (such as cobalt, nickel, and molybdenium) have been the subject of studies in recent years due to their electrical, catalytic and magnetic properties. Orthorhombic molybdenum trioxide (α-MoO3) is relevant because it is an antioxidant material, leading to its catalytic properties that are influenced by the valence state of molybdenum ions and the local environment where they are inserted. These structures have been investigated in developments of sensors, energy storage and the formulation of gels for the treatment of chronic diseases [1]. In this perspective, the present work proposes the use of the molybdenum (II) acetate as a metallic precursor for obtaining α-MoO3 structures by the thermal decomposition method [2]. The Mo (II) acetate belongs to a group of metal complexes composed of two highly correlated Mo ions, in which each cations are connected to complexes containing oxygen. This reagent could favor, in specific chemical route, the crystallization of MoxOy [2][3]. The syntheses yields were characterized by X-ray diffraction (XDR), scanning electron microscopy (SEM), and energy-dispersive analysis (EDS). The X-ray diffraction results suggested α-MoO3 crystallite of the 77 nm (by the Scherrer equation). By means of microscopy analysis were observed that the obtained morphology is microrod-like, with a of approximately 774 nm and a length of the 37 micrometers. The EDS analysis only showed energies related to molybdenum (Mo) and oxygen (O), confirming the purity of the obtained material.
  • Resumo IPEN-doc 30996
    Development of flexible magnetic films by the incorporation of Ni/Ni3C nanoparticles in a matrix of Amazonian tannic extract (Myrcia atramentifera)
    2024 - SILVA, CRYSTIAN W.C. da; SOUZA, KATIUSSE S. de; SILVA, BARBARA P.G.; FREITAS, RAFAEL S. de; LAZAR, DOLORES R.R.; PASCA, GABRIEL A.C.; CARBONARI, ARTUR W.; OTUBO, LARISSA
    The development of nanostructured magnetic materials based on Ni and its compounds (Ni/Ni3C) has been the objective of scientific research due to the versatility of applications that these materials. In this context, magnetic films can be applied in a variety of technologies such as data storage, flexible spintronics, chemical detection, and magnetic sensors.[1] Additionally, the growing prospect of obtaining environmentally eco-friendly materials has promoted the use of vegetable matrices for film synthesis, such as tannins, for example. In this work, we report the fabrication of flexible magnetic films on paper substrates by adding Ni/Ni3C nanoparticles to the tannin extract matrix of the Amazonian species Myrcea atramentífera.[2] The tannin extract solution was obtained by processing the species' bark through grinding, sieving, and water extraction for 8 hours at 70°C, followed by filtration and concentration. After this step, a tannin extract suspension containing 0.1% Ni/Ni3C was prepared by dispersion in an ultrasonic processor. The suspension was dispersed onto a paper substrate and dried at 30 °C for 10 minutes. The films were characterized by XRD, SEM, AFM, and TGA/DSC measurements. The structural and morphological results indicate the formation of continuous films with dispersed nanoparticles. Thermal analysis results suggest that the nanoparticles dispersed in the films maintain structural stability up to 350 °C. The films present macroscopic magnetic response at room temperature, which can be attributed to the presence of nanoparticles with a coercive field of 100 Oe and saturation magnetization of 26 emu/g. [3]
  • Artigo IPEN-doc 30786
    Synthesis and local characterization of CoO nanoparticles in distinct phases
    2024 - SANTOS, SUZILENE V.; COSTA, CLEIDILANE S.; PARAGUASSU, WALDECI; SILVA, CRYSTIAN W.C.; OTUBO, LARISSA; SOUZA, KATIUSSE S.; CORREA, BRUNO S.; MIRANDA-FILHO, ARNALDO A.; FERREIRA, WANDERSON L.; CARBONARI, ARTUR W.; CABRERA-PASCA, GABRIEL A.
    The advancement of functional nanomaterials has become a major focus of recent research, driven by the exceptional properties these materials display compared to their macroscopic (bulk) counterparts. Cobalt oxide nanoparticles (CoO-NPs) stand out primarily for their catalytic and magnetic properties, which can enable a range of technological applications, such as advanced catalysts, drug delivery systems, implants, prosthetics, sensors. However, in addition to the dependence on factors such as size, morphology, and functionalization, the properties of CoO-NPs are significantly influenced by the crystal structure. Therefore, local investigation into the polymorphic structures of CoO at the nanometric scale may provide new insights into the local structural and magnetic characteristics of these systems. In this report, we address the synthesis and local characterization of cobalt oxide (CoO) nanoparticles in the rock-salt cubic fcc-CoO and Wurtzite hpc-CoO phases, obtained through thermal decomposition. We analyze the influence of oleylamine and oleic acid ligands on the structural and morphological control of these systems. The obtained nanoparticles were characterized using conventional techniques such as X-ray diffraction (XRD), transmission electron microscopy, Raman spectroscopy, and Fourier-transform infrared spectroscopy. Local characterization was carried out by the perturbed angular correlation (PAC) nuclear technique using the radioactive tracer 111In(111Cd). Measurements were conducted at 295 and 10 K to investigate possible magnetic phase transitions in these systems. XRD results confirmed the formation of fcc-CoO and hcp-CoO phases. The phase fcc was obtained with the pair of oleylamine and oleic acid ligands, while the phase hcp phase was synthesized using only oleylamine. Additionally, nanoparticles synthesized with oleylamine and oleic acid exhibited better morphological control compared to those produced with only oleylamine. Raman spectroscopy analyses suggest a phase transformation process resulting in Co3O4. PAC results for hyperfine interactions at the 111In(111Cd) probe nucleus, indicate that the hcp-CoO phase shows smaller hyperfine magnetic interactions (Bhf = 1 T) compared to the fcc-CoO phase (Bhf = 17 T). This suggests the mechanism of superexchange interactions, which are strongly influenced by the Co-O-Co bond angle, which is 110° for the hpc-CoO phase and 180° for the fcc-CoO phase due to the geometries of the systems.