The depletion of conventional energy sources and the concern with the environmental impacts of the use of fossil fuels sparked interest in researching new energy sources and improving existing processes. In this context, the solar energy presents itself as one of the most promising energy sources on the planet, given its wide availability and applicability in thermal processes. However, its use still represents a great technological and economic challenge, because many systems that use this energy still have low efficiency and high cost, which makes them uncompetitive in competition with systems using other energies. With that, the search for the improvement of the processes awakens the researches in more adequate and cheaper materials, which represents a great scientific potential in the evolution of these technologies. Thus, the present work proposes to obtain and analyze a selective surface for applications in solar-thermal collectors, using CRFO (compound formed by chromium and iron oxides), varying the percentage by weight, and then mixed with aluminum oxide. For the tests, an experimental bench was built to simulate a flat plate solar-thermal collector in real operating conditions. Some characterizations were carried out, such as: techniques scanning electron microscopy (SEM), infrared analysis and UV-VIS absorptivity determination, as well as the graphs with surface temperatures and with radiation during the tests in the Sun for the composite (CRFO and aluminum oxide) and for the commercial surface (MRTiNOX). With the results obtained, it was verified in the field test that one of the produced selective surfaces obtained a result of absorptivity of 0.94 and 0.0349 of emissivity, which is close to that of the commercial surface. The results were confirmed in the characterization by UV-VIS, which showed high absorptivity values in the visible light range.

Abstract Founding new materials and structures for solar cells is a challenge in the photovoltaic field. This work evaluated the effect of the lignin in the photovoltaic activity by compounding with TiO2/lignin as photoanode for the dye sensitized solar cells (DSSC’s). Hybrid films (TiO2/lignin) with different concentrations of lignin (5, 10 and 15%) were deposited by spin coating over commercial TiO2 thin films. The cells were sandwich assembled. The characterizations were done through analysis of absorbance, band gap, x-ray diffraction, morphological and electrical. The lignin at 15% reduced the TiO2 band gap from 3.66 to 2.84 eV, favoring the short current density to 11.06 mA/cm2 and efficiency of 4.65%, an increase of 103.95% compared to the TiO2 structure without lignin.

ABSTRACT Nanoparticles of TiO2 have been the main semiconductor applied in Dye-sensitized solar cells (DSSCs). In this work, solar cells were developed from the electrophoretic deposition of anatase titanium dioxide (TiO2) films on conductive glasses. The electrophoretic deposition was perfomed with a constant voltage of 80V for 2 minutes and, after drying, the films were sintered at three different temperatures: 450 °C, 550 °C and 600 °C. In the assembly of the cells, the titanium dioxide films were sensitized by Ruthenizer 535-bisTBA dye (N719) and an electrolyte containing the iodide / tri-iodide redox pair and a commercial transparent platinum counter electrode were used. TiO2 films were characterized by scanning electron microscopy, dispersive energy spectroscopy and X-ray diffraction and photo-electrochemical techniques. The energy conversion rates were 0.2646% for the sintered film at 450 °C, 0.1209% for the sintered film at 550 °C and 0.1137% for the film sintered at 600 °C.

RESUMO Filmes de estanho/óxido de zinco foram depositados em óxido condutor transparente por banho químico, a porcentagens de 5, 10 e 15% de estanho (Sn) na estrutura de óxido de zinco (ZnO). Todos os filmes foram tratados termicamente para melhorar sua cristanilidade. Os filmes produzidos foram caracterizados por difração de raios x e medidas ópticas, como absorbância, transmitância e reflectância. O espectro de raios x mostrou a formação de ZnO na forma de wurtzite e os tamanhos dos cristalitos foram de 53,74; 79,59 e 66,38 nm para os fotoanodos a 5, 10 e 15% de estanho (Sn), respectivamente, na estrutura do óxido de zinco. Os valores calculados para a energia de banda proibida dos filmes revelaram que a presença de estanho pode reduzir o valor da energia até aproximadamente 3,2 eV. Esses filmes foram usados como fotoanodos em células solares sensibilizadas por corante (CSSC) para observar os efeitos do estanho (Sn) na atividade fotovoltaica do semicondutor de óxido de zinco (ZnO). Parâmetros como eficiência e densidade de corrente de curto- circuito foram particularmente afetados pela presença de estanho na composição, com o filme de ZnO a 5% de Sn apresentando os melhores resultados de 7,56% de eficiência e 34,35 mA/cm2 de densidade de corrente de curto-circuito, os demais filmes apresentaram menores valores para a eficiência, o que pode ser atribuído aos menores valores alcançados para a corrente de curto circuito.

ABSTRACT Tin Zinc Oxide thin films were deposited on transparent conductive oxide by chemical bath, at percentages of 5, 10 and 15% of tin (Sn) on the zinc oxide (ZnO) structure. All films were thermally treated to improve its crystallinity. The produced films with tin were characterized by x-ray diffraction and optical measurements, such as absorbance, transmittance and reflectance. The x-ray spectrum showed the formation of the ZnO wurtzite and the crystallite size of the films were calculated to be 53.74; 79.59 and 66.38 nm for the photoanodes at 5, 10 and 15% of tin (Sn), respectively, on the zinc oxide structure. The calculated band gap energy of the films revealed that the presence of tin can reduce the band gap energy to about 3.2 eV. Those films were used as photoanodes on dye sensitized solar cells (DSSC) to observe the effects of the tin (Sn) on the photovoltaic activity of the zinc oxide (ZnO) semiconductor. Parameters such as efficiency and short circuit current density were particularly affected by the presence of tin in the composition, with the 5% Sn ZnO film presenting the best results of 7.56 % efficiency and 34.35 mA/cm2, short circuit current density, the other films presented lower values for efficiency, which can be attributed to lower values of short-current density.

This paper presents the study of the addition of the polyaniline polymer (PANI), at the junction of the cadmium telluride and cadmium sulfide (CdTe/CdS) layers in order to improve the contact between the layers, to decrease the air gap that limit the conversion photovoltaic. The morphology of CdS, CdTe and polyaniline (PANI) were characterized with multiple techniques including scanning electron microscopy (SEM), energy dispersive spectroscopy (EDS), X-ray diffraction (XRD) and optical absorption. The Metrohm Autolab LED Driver Kit system was used for data collection, and it was possible to obtain the current and voltage parameters of the cells. The inclusion of PANI thin film in CdS/CdTe hybrid solar cells increases the energy conversion efficiency from 0.0075% to 0.15%, this gives a 20-fold increase in efficiency.

Abstract A low cost spin coater was constructed in this work for the deposition of thin films of titanium dioxide (TiO2) on conductive substrate of FTO (fluoride doped tin oxide) with application on dye sensitized solar cells. The results showed a 95% precision between the speed values obtained by the software of C#sharp language and the spin values observed directly on the device. The TiO2 films deposited through the spin coater with different angular speeds were characterized by UV-Vis optical spectrum, scanning electron microscopy (SEM), atomic force microscopy (AFM) and electrical measurements on an active area of 0.25 cm2. The DSSCs assembled with the TiO2 films of double layer deposited by the spin coater had an efficiency value of 12.74%, while the cell with a single layer presented 4.05% efficiency. Therefore, it is concluded that the spin coater assembled in this study at low costs successfully can produce TiO2 electrodes for DSSCs.

ABSTRACT The depletion of fossil fuel reserves and climate change caused by atmospheric pollution has led the human being to seek alternatives that are less damaging to the environment. The concern and the awareness of the population open space for the study of renewable energies to be deepened, among them the best use of solar energy. The use of alternative materials to replace selective surfaces is a natural trend, since improvements in surface efficiency are usually sought while attempting to reduce costs. Composite substances are already used to obtain some selective surfaces, and, as a result, the search for better processes awakens research on more appropriate and lower cost materials, which represents a great scientific potential in the evolution of these technologies. Thus, the present work consisted in obtaining and studying selective surfaces for applications in low-cost flat plate solar collectors, using residues from the granite industry. Five different surfaces were studied, varying the weight percentage: 100% granite powder, 75% granite powder + 25% chromium oxide, 50% granite powder + 50% chromium oxide, 25% granite powder + 75% chromium oxide and 100% chromium oxide. For the tests, an experimental wooden stand was built, and it was possible to simulate the conditions of a flat plate solar collector. To characterize the surfaces, scanning electron microscope (SEM) techniques, infrared analysis, X-ray diffraction and UV-VIS absorbance determination, as well as graphs with surface temperatures and with radiation, during the tests in the sun, were used. The surfaces` efficiency was determined by the ratio of the absorptivity by the emissivity, as well as the trademark MRTiNOX, a commercial selective surface applied on copper substrate. For this, an efficiency of 23.56 was obtained, while for the 50% granite and 50% chromium surfaces the value of 23.27 (closest to the trade mark) was calculated. Therefore, replacing the traditional components of selective surfaces with granite proved to be a satisfactory solution, contributing to the reduction of costs with work involving solar energy.

ABSTRACT Titanate nanotubes (TiNTs) with the chemical composition Na2Ti3O7.nH2O (NaTiNT) were obtained through a hydrothermal method in highly alkaline medium. Protonated titanates nanotubes (H-TiNTs), with the composition H2Ti3O7.nH2O, were prepared by ion exchange reaction through a suspension of Na2Ti3OγnH2O nanotubes in HCl medium, promoting the exchange of Na+ ions by H+. Both Na2Ti3O7.nH2O and H2Ti3O7.nH2O products, as well the TiO2 used as raw material for the nanotubes processing, were used as starting material for the solar cells photoelectrodes sensitized using mesoporphyrin extracted from a precursor of cashew nut shell. Exposing the NaTiNT sample to solar radiation of 1258 W/m2, a short-circuit current density (ISC) of 13 µA/cm2 and an open-circuit voltage (VOC) of 370 mV were registered and, a current density of 7.6 µA/cm2 and a voltage of 256 mV for the prototype cell based on H-TiNTs. A current density of 1.1 µA/cm2 and an open-circuit voltage of 1.6 mV were obtained for the cell using TiO2 as electrode.

RESUMO Quantificar o tamanho de materiais em escala nanométrica é um dos desafios a serem superados, uma vez que existem técnicas diferentes. A equação de Scherrer modificada foi usada para estimar o tamanho das partículas de dióxido de titânio em escala nanométrica. Dióxido de titânio com tamanho nominal de nanopartícula de 21 nm foi usado como padrão para determinar a precisão da equação modificada. A partir dos dados de raios-X, para a amostra sem tratamento térmico foi obtido um valor médio do tamanho das nanopartículas de 20,63 nm. Um tratamento estatístico foi usado para fazer uma correlação entre o valor estimando pela equação de Scherrer modificada e o valor nominal de 21nm. Um desvio de 0,70 foi encontrado entre o valor calculado e o valor nominal, indicando uma concordância entre os valores. Adicionalmente, a influência da temperatura sobre o tamanho médio das nanopartículas de dióxido de titânio foi pesquisada.

ABSTRACT The materials sizing in nano-scale is a challenge to be overcome, because the size determined by various methods differ. In order to shed light about the nanomaterials sizing, a modified Scherrer's equation was applied to estimate more accurately the nanostructured titanium dioxide crystal size. The manufactured titanium dioxide-nanostructured powder with nominal average size about 21nm was used as the reference standard to determine the accurate of modified equation. From X-ray diffraction data, an average crystal size about 20.63 nm was achieved for unheated sample. To establish a relation between the result obtained with modified Scherrer's equation and the nominal average crystal size, a statistical treatment and a comparative assessment were performed. The average absolute divergence does not exceed 0.70 nm. The value of crystal size determined from X-ray data was in good agreement with that informed by the supplier. Additionally, the behavior of sample was studied as a function of temperature.

Nanoparticles of TiO2 have been the main semiconductor applied in Dye-sensitized solar cells (DSSCs). In this work, titanate nanotubes (NaTiNT) and nanoribbons, were obtained by the hydrothermal method from TiO2 anatase. These materials were deposited on conductive substrate by electrophoresis, with and without thermal treatment, sensitized by ruthenium-based dye and used as work electrode. Exposing those photovoltaic devices to visible radiation, with films before thermal treatment, a short-circuit current density (JSC) of 0.0012 mA/cm2 was observed for the cell with NaTiNT, a current density of 0.0398 mA/cm2 for the cell with Nanoribbons, and a current density of 0.4028 mA/cm2 for the cell with TiO2 as electrode. After thermal treatment, a short-circuit current density of 0.4269 mA/cm2 was observed for the cell with NaTiNT, a current density of 0.0765 mA/cm2 for the Nanoribbons cell, and, finally, a current density of 0.3310 mA/cm2 for the cell with TiO2 as electrode. The new morphological, structural and optical characteristics of these nanoparticles may contribute for the development and research of new generation photovoltaic devices.

Amongst the many parts of a silicon cells photovoltaic module, silicon is the most important and expensive constituent. Thus, research on silicon recycling from damaged cells can lead to economic and environmental benefits. In this work, the broken silicon cells were tailored to function along with the fluorine-doped tin oxide as the transparent electric conductors. The broken silicon cells were analyzed by the current density versus voltage plots, together with the Mott-Schottky, X-rays diffraction and fluorescence analysis. Under light, the damaged cells sandwiched between the two transparent electric conductors presented photovoltaic effect. However, such effect was not obtained after the removal of the antireflection layer due to the destruction of the n-type layer as demonstrated by the Mott-Schottky analysis. The X-rays diffraction revealed samples rich on silicon atoms and the presence of aluminum atoms as impurity.

RESUMO A eletrodeposição tem sido empregada para a obtenção de materiais semicondutores; todavia, ainda não estão bem esclarecidos os mecanismos envolvidos neste processo. Neste sentido, este trabalho apresenta a investigação deste processo, evidenciando a caracterização do CdTe eletrodepositado sobre substrato platina em solução ácida. A deposição ocorre a partir de 0,0 V, em relação ao eletrodo Ag/AgCl,KClsat, com etapas de controle ativado e de difusão. Os filmes finos de CdTe foram eletrodepositados sobre o substrato de platina a temperatura ambiente (~24°C) a partir de uma solução ácida. A influência do potencial aplicado foi investigada utilizando técnicas de caracterização de superfície, como a difração de raios X e Microscopia eletrônica de varredura. A caracterização elétrica foi realizada por medidas de capacitância (Mott-Schottky). Os filmes finos de CdTe apresentaram pico de maior intensidade no plano (220), demostrando ter um crescimento preferencial para esse plano. Os filmes apresentam uma morfologia granular influenciado pelo potencial de deposição e uma condutividade característica de um semicondutor tipo n.

ABSTRACT The electrodeposition has been used for obtaining semiconductor materials; however, remain unclear the mechanisms involved in this process. Thus, this paper presents the research of this process, showing the characterization of electrodeposited CdTe on platinum substrate in acid solution. The deposition occurs from 0.0 V relative to the electrode Ag/AgCl KClsat with step activated control and diffusion. The thin film of CdTe was electrodeposited on the platinum substrate at room temperature (~ 24 ° C) from an acidic solution. The influence of the applied potential was investigated using surface characterization techniques such as X-ray diffraction analyses and scanning electron microscopy. The electrical properties of the films were performed capacitance measurements (Mott-Schottky plot). The thin CdTe films presented the prominent (220) planes, showing have a preferential growth in that plane. The films show a granular morphology influenced by deposition potential and property of an n-type semiconductor.

Este trabalho apresenta um modelo teórico que relaciona a potência elétrica com a potência química numa célula fotossensibilizada com corante. O mesmo é baseado na junção dos conceitos presentes nos modelos de potencial químico e de potência química. Assim, a partir destas duas considerações é possível a realização de testes sob diversas condições físicas e ambientais, durante o processo de conversão de energia solar. Consequentemente, o modelo teórico proposto permite relacionar a potência química aos parâmetros solares: ângulo sólido, temperatura da fonte de radiação, comprimento de onda e temperatura da célula fotossensibilizada com corante. A geração do fluxo de elétrons dentro da célula é promovida pela absorção da energia solar incidente sobre o corante. Por isso, a principal condição consubstanciada neste trabalho baseia-se que a superfície de absorção da energia incidente seja o corante.

This paper presents a theoretical model relating the electrical power to the chemical power in a photosensitized dye-cell. The same is based on the junction of present concepts of chemical potential models and chemical power. Thus, from these two considerations is possible to perform tests under various physical and environmental conditions during the solar conversion process. Consequently, the proposed theoretical model allows relating the power to solar chemical parameters: solid angle, temperature of the radiation source, wavelength and temperature of the photosensitized dye-cell. The electrons flow generation within the cell is promoted by absorption of solar energy incident on the dye. Therefore, the main condition embodied in this work is based on the incident energy absorption surface is the dye.