Transparent p-AgCoO2/n-ZnO diode heterojunction fabricated by pulsed laser deposition

Transparent diode heterojunction on ITO coated glass substrates was fabricated using p-type AgCoO2 and n-type ZnO films by pulsed laser deposition (PLD). The PLD of AgCoO2 thin films was carried out using the pelletized sintered target of AgCoO2 powder, which was synthesized in-house by the hydrothermal process. The band gap of these thin films was found to be ~3.89 eV and they had transmission of~55% in the visible spectral region. Although Hall measurements could only indicate mixed carrier type conduction but thermoelectric power measurements of Seebeck coefficient confirmed the p-type conductivity of the grown AgCoO2 films. The PLD grown ZnO films showed a band gap of ~3.28 eV, an average optical transmission of ~85% and n-type carrier density of~4.6×1019 cm− 3. The junction between p-AgCoO2 and n-ZnO was found to be rectifying. The ratio of forward current to the reverse current was about 7 at 1.5 V. The diode ideality factor was much greater than 2.

Mn2þ-induced room-temperature ferromagnetism and spin-glass behavior in hydrothermally grown Mn-doped ZnO nanorods

The magnetic properties of Mn-doped ZnO (ZnO:Mn) nanorods grown by hydrothermal process at a temperature of 200 8C and a growth time of 3 h have been studied. The samples were characterized by using powder X-ray diffraction with Rietveld refinement, scanning electron microscopy, energy-dispersive X-ray analysis and SQUID magnetometry. Mn (3 wt%) and (5 wt%)-doped ZnO samples exhibit paramagnetic and ferromagnetic behavior, respectively, at room temperature. The spin-glass behavior is observed from the samples with respect to the decrease of temperature. At 10 K, both samples exhibit a hysteresis loop with relatively low coercivity. The room-temperature ferromagnetism in 5 wt% Mn-doped ZnO nanorods is attributed to the increase in the specific area of grain boundaries, interaction between dopant Mn2þ ions substituted at Zn2þ site and the interaction between Mn2þ ions and Zn2þ ions from the ZnO host lattice

Titanium-based shape memory alloys and scaffolds for biomedical applications

Porous Ti-50.5Ni shape memory alloys with different porosities were produced using a space-holder sintering method. A new Ni-free Ti-based shape memory alloy, Ti-18Nb-5Mo-5Sn, was developed for potential biomedical applications, and a novel one-step hydrothermal process was applied to produce hydroxyapatite coatings on the surface of Ti alloy.

In vitro osteoblast-like cell proliferation on nano-hydroxyapatite coatings with different morphologies on a titanium-niobium shape memory alloy

The morphology of nanomaterials significantly affects their physical, chemical, and biological properties. In the present study, nano-hydroxyapatite coatings with different morphologies were produced on the surface of a titanium-niobium shape memory alloy via a hydrothermal process. The effect of the nano-hydroxyapatite coatings on the in vitro proliferation of SaOS-2 osteoblast-like cells was investigated. Factors including crystallinity, surface micro-roughness, and surface energy of the nano-hydroxyapatite coatings were discussed. Results show that in vitro proliferation of the osteoblast-like cells was significantly enhanced on the nano-hydroxyapatite-coated titanium-niobium alloy compared to the titanium-niobium alloy without coating. The cell numbers on the nano-hydroxyapatite-coated titanium-niobium alloy changed consistently with the surface energy of the hydroxyapatite coatings. This study suggests that surface energy as a characteristic parameter influencing the in vitro proliferation of osteoblast-like cells was predominant over the crystallinity and surface micro-roughness of the nano-hydroxyapatite coatings.

Preparation of size-selective Mn3O4 hexagonal nanoplates with superior electrochemical properties for pseudocapacitors

Porous Mn3O4 hexagonal nanoplates were synthesized through annealing the hydrohausmannite precursor obtained by a one-pot hydrothermal process and by precisely controlling the concentrations of potassium hydroxide and glucose. The effect of potassium hydroxide and glucose on the growth of hexagonal nanoplates was investigated, and a growth mechanism was also proposed. Due to its abundant pores, the pure Mn3O4-based electrode exhibits excellent cycling stability with 100% capacity retention after 5000 cycles. The asymmetric supercapacitor exhibited high performance with an energy density of 17.276 W h kg^-1 at a power density of 207.3 W kg^-1 in a wide potential window of 1.5 V.

Síntese, processamento em hidrotermal convencional/microondas e propriedades fotoluminescentes dos pós de BaW 'O IND. 4'

Pós-graduação em Ciência e Tecnologia de Materiais - FC

Mineralizações auríferas hospedadas na faixa metavulcano-sedimentar Jacuí-Bom Jesus da Penha - Sudoeste de Minas Gerais

Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

Síntese de nanofios de óxidos semicondutores para aplicações em dispositivos ópticos e eletrônicos

Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

Síntese hidrotérmica de nanopartículas de 'TI''O IND.2', de nanocompósitos metal/'TI''O IND.2' e degradação oxidativa de 4-clorofenol em reator membranar fotocatalítico

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)

Diagênese e alteração hidrotermal em rochas sedimentares da formação Corumbataí, Permiano Superior, Mina Granusso, Cordeirópolis/SP

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)

Síntese e caracterização de analcina obtida a partir de rejeito caulim com aplicação em adsorção

Neste trabalho foi utilizado rejeito de caulim da região do Ipixuna-PA, com objetivo de sintetizar zeólita tipo analcina na forma sódica como fase cristalina predominante, através do processo hidrotérmico. O rejeito foi submetido à calcinação por 4 horas a 700°C, para conversão em metacaulinita. A partir desta metacaulinita foi preparada uma mistura reacional contendo diatomito e hidróxido de sódio, que foi levada à autoclave a uma temperatura de 215°C por 24 horas. Diversas variáveis do processo de síntese foram investigadas, entre elas destacam-se: disponibilidade de sódio, proporção de silício, natureza da fonte de sílica, pH na mistura reacional e tempo de autoclavagem. Isso com o intuito de se determinar quais asalterações que os produtos reacionais sofrem com tais modificações, definindo desta forma a condição ideal de síntese da analcina. Foram avaliadas também algumas propriedades importantes do adsorvente, tais como: estabilidade térmica, onde foi aplicado o método de Rietveld para identificar as modificações na estrutura cristalina; estabilidade em presença ácida; cinética de dessorção gerada pelo íon hidrogênio; comportamento das isotermas de adsorção de cobre, cádmio, zinco e níquel bem como avaliar a seletividade de tais cátions no adsorvente. A síntese de analcina mostrou-se possível usando rejeito de caulim. Quando analcina foi calcinada a 400°C foi observado deslocamento nos planos (h,k,l) e manteve-se constante até 600°C, gerado pela saída de oxigênio da posição 1/8 da analcina, isso gera uma diminuição na célula unitária provocando uma diminuição nos canais e sítios ativos da zeólita o que afetou a capacidade de adsorção.

Caracterização mineralógica, petrológica e química da sulfetação nos reef's da mina Canavieiras, Jacobina, Bahia

In the Serra de Jacobina, localized in the North Central portion of the state of Bahia, occours the Jacobina Group. It’s a sedimentary basin and the gold deposit is stocked on the basal portion, which consist on quartzites intercalated with oligomítico metaconglomerates of Serra do Córrego Formation. There are controversies about the origin of the gold mineralization, but the currently most accepted hypothesis corresponds to a paleoplacer deposit with subsequent ore remobilization and concentration by hydrothermal process. The sulphidation is one of the main results of hydrothermal process, which was more detail characterized, besides identifying if there was more than one sulfides phase generation and its relationship with gold mineralization. The analyzes were performed from the main reef's (metaconglomerates mineralized levels) of Mine Canavieiras: Maneira, Holandez, Liberino, Piritoso, MU and LU. Chemical analyzes semi-quantitative were developed with EDS in MEV and also petrographics analyses. The main sulfide is pyrite, followed by chalcopyrite. Six groups of pyrite were classified according with chemical composition, however they show similarities in their habit and occurrence. Were identified four types of chlorite, labeled A, B, C, D. Gold occurs in free form, associate to pyrites, to Fe-Ti-Muscovite, to chlorite type B and to microfractures with iron hydroxide. Gold presents three different compositions: pure, with Ag or associated with U-Zr. The results of chemical analysis showed that the hydrothermal process have as their main source, ultramafic rocks present in the Jacobina Basin

Chemical composition and accumulation rates of chemical elements in metalliferous sediments from axial zones of the East Pacific Rise and the Mid-Atlantic Ridge

In the monograph metalliferous sediments of the East Pacific Rise near 21°S are under consideration. Distribution trends of chemical, mineral and grain size compositions of metalliferous sediments accumulated near the axis of this ultrafast spreading segment of the EPR are shown. On the basis of lithological and geochemical investigations spatial and temporal variations of hydrothermal activity are estimated. Migration rates of hydrothermal fields along the spreading axis are calculated. The model of cyclic hydrothermal process is suggested as a result of tectono-magmatic development of the spreding centre.

Supercapattery based on binder-free Co3 (PO4)2·8H2O multilayer nano/microflakes on nickel foam

A binder-free cobalt phosphate hydrate (Co3(PO4)2·8H2O) multilayer nano/microflake structure is synthesized on nickel foam (NF) via a facile hydrothermal process. Four different concentrations (2.5, 5, 10, and 20 mM) of Co2+ and PO4–3 were used to obtain different mass loading of cobalt phosphate on the nickel foam. The Co3(PO4)2·8H2O modified NF electrode (2.5 mM) shows a maximum specific capacity of 868.3 C g–1 (capacitance of 1578.7 F g–1) at a current density of 5 mA cm–2 and remains as high as 566.3 C g–1 (1029.5 F g–1) at 50 mA cm–2 in 1 M NaOH. A supercapattery assembled using Co3(PO4)2·8H2O/NF as the positive electrode and activated carbon/NF as the negative electrode delivers a gravimetric capacitance of 111.2 F g–1 (volumetric capacitance of 4.44 F cm–3). Furthermore, the device offers a high specific energy of 29.29 Wh kg–1 (energy density of 1.17 mWh cm–3) and a specific power of 4687 W kg–1 (power density of 187.5 mW cm–3).

Processing and characterization of srTiO₃-TiO₂ nanoparticle-nanotube heterostructures on titanium for biomedical applications

Surface properties such as physicochemical characteristics and topographical parameters of biomaterials, essentially determining the interaction between the biological cells and the biomaterial, are important considerations in the design of implant materials. In this study, a layer of SrTiO3-TiO2 nanoparticle-nanotube heterostructures on titanium has been fabricated via anodization combined with a hydrothermal process. Titanium was anodized to create a layer of titania (TiO2) nanotubes (TNTs), which was then decorated with a layer of SrTiO3 nanoparticles via hydrothermal processing. SrTiO3-TiO2 heterostructures with high and low volume fraction of SrTiO3 nanoparticle (denoted by 6.3-Sr/TNTs and 1.4-Sr/TNTs) were achieved by using a hydrothermal processing time of 12 and 3 h, respectively. The in vitro biocompatibility of the SrTiO3-TiO2 heterostructures was assessed by using osteoblast cells (SaOS2). Our results indicated that the SrTiO3-TiO2 heterostructures with different volume fractions of SrTiO3 nanoparticles exhibited different Sr ion release in cell culture media and different surface energies. An appropriate volume fraction of SrTiO3 in the heterostructures stimulated the secretion of cell filopodia, leading to enhanced biocompatibility in terms of cell attachment, anchoring, and proliferation on the heterostructure surface.