108,236 research outputs found

    Enhanced electrical and optical properties of room temperature deposited Aluminium doped Zinc Oxide (AZO) thin films by excimer laser annealing

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    High quality transparent conductive oxides (TCOs) often require a high thermal budget fabrication process. In this study, Excimer Laser Annealing (ELA) at a wavelength of 248 nm has been explored as a processing mechanism to facilitate low thermal budget fabrication of high quality aluminium doped zinc oxide (AZO) thin films. 180 nm thick AZO films were prepared by radio frequency magnetron sputtering at room temperature on fused silica substrates. The effects of the applied RF power and the sputtering pressure on the outcome of ELA at different laser energy densities and number of pulses have been investigated. AZO films deposited with no intentional heating at 180 W, and at 2 mTorr of 0.2% oxygen in argon were selected as the optimum as-deposited films in this work, with a resistivity of 1×10−3 Ω.cm, and an average visible transmission of 85%. ELA was found to result in noticeably reduced resistivity of 5×10−4 Ω.cm, and enhancing the average visible transmission to 90% when AZO is processed with 5 pulses at 125 mJ/cm2. Therefore, the combination of RF magnetron sputtering and ELA, both low thermal budget and scalable techniques, can provide a viable fabrication route of high quality AZO films for use as transparent electrodes

    Grazing Incidence X-ray Scattering from Magnetic Thin Films and Nanostructures

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    Grazing incidence scattering of synchrotron x-rays has been used to characterize the structure of magnetic thin films and periodic nanostructures. The combined metal and metal oxide films have been chosen to clarify the effects of growth processing techniques in technologically important magnetic and magnetoresistive thin film materials, and have particular relevance to the magnetic tunnel junction (MTJ) class of magnetic sensor. Co/Al2O3 thin films and Co/MgO multilayer thin films have been characterized using x-ray reflectivity and diffuse scatter analysis to explain how preparatory oxidation of the lower ferromagnet in an MTJ can reduce Néel interlayer coupling and improve the consistency of magnetoresistance. Measurements reveal differing effects for Al2O3 and MgO tunnel barrier materials. In Co/Al2O3 systems, preoxidation is found to reduce significantly chemical interdiffusion at the interface between the two layers, implying a more uniform oxidation of the barrier layer. In Co/MgO multilayers, an increased in-plane correlation length of the inherited interface roughness is seen after preoxidation. This implies that preoxidation suppresses the short wavelength undulations on both sides of the tunnel barrier that cause Néel coupling. Grazing incidence in-plane diffraction measurements on epitaxial Fe/MgO/Fe [001] and Fe/Au/MgO/Fe [001] films during annealing to 600 K have shown that, in both cases, the MgO lattice is initially strained towards being commensurate with the iron and gold layers, but relaxes after annealing towards a typical bulk MgO lattice. The iron and gold layers display linear thermal expansion at rates consistent with the bulk material. These in-plane lattice measurements demonstrate how the strain and strain dispersion in an epitaxial MgO barrier layer can be relieved under controlled annealing conditions. Finally, patterned thin film surfaces with submicron periodic symmetries have been studied by grazing incidence x-ray scattering. A novel semi-kinematical theory has been developed into a numerical algorithm capable of simulating the scatter from a wide range of arbitrary and disordered nanoscale arrays. This has allowed key structural parameters including array periodicity, symmetry and array coherence lengths to be extracted from experimental data

    Las Islas de la Calma, 1966 (complete work)

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    X Films presenta ; Operador, Juan Manuel de la Chica; Ayudante, Pedro Hueros; Commenntarios en la voz de, Simon Ramirez; "Se Llarga": Ballado por el groupo folklorico de sas Jose Ibiza; Jefe de production, Jose Maria Gonzalez Sinde; Montaje, Elena Jaumandren; Ingeniero de Sonido, Jesus Jimenez; Labortorio, Fotofilm Madrid S.A. Sonoriacion: Iberson; Deposito Legal M-14229 1966; Gulon y Direccion, Ramon Masats.To order a reproduction, inquire about permissions, or for information about prices, see: http://www.lib.washington.edu/specialcollections/services/reproduction/reproductio

    Characterization of SiGe thin films using a laboratory X-ray instrument

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    The technique of reciprocal space mapping using X-rays is a recognized tool for the nondestructive characterization of epitaxial films. X-ray scattering from epitaxial Si0.4Ge0.6 films on Si(100) substrates using a laboratory X-ray source was investigated. It is shown that a laboratory source with a rotating anode makes it possible to investigate the material parameters of the super-thin 2–6 nm layers. For another set of partially relaxed layers, 50–200 nm thick, it is shown that from a high-resolution reciprocal space map, conditioned from diffuse scattering on dislocations, it is possible to determine quantitatively from the shape of a diffraction peak (possessing no thickness fringes) additional parameters such as misfit dislocation density and layer thickness as well as concentration and relaxation

    Correlation of Raman and X-Ray Diffraction Measurements of Annealed Pulsed Laser Deposited ZnO Thin Films.

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    Raman spectroscopy, X-ray diffractometry and atomic force microscopy have been used to characterise ZnO thin films grown by pulsed laser deposition as a function of the post-growth annealing temperature. The results show substantial enhancement and broadening of certain Raman features which correlate excellently with the change in width of the X-ray diffraction peaks. The 570 cm[-1] Raman feature showed pronounced asymmetry and enhanced intensity in the unannealed sample. An increase in grain size observed after subsequent annealing produced a substantial reduction in both the asymmetry and intensity of this peak. Our experimental data suggest that electric fields, due to charge trapping at grain boundaries, in conjunction with localised and surface phonon modes are the cause of the intensity enhancement and asymmetry of this feature

    Pyroelectricity in langmuir-blodgett films

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    The fabrication of pyroelectric devices using the Langmuir-Blodgett (LB) technique is described. Studies of a wide range of materials are reported; however, the thesis concentrates on electrical and structural investigations of two specific alternate layer films: 22-tricosenoic acid/l-docosylamine and 22-tricosenoic acid/4-octadecylaniline. The latter system possesses a pyroelectric coefficient of 0.65 nCcm(^-2)K(^-1), representing the largest reported value, to date, for an LB film. The pyroelectric figure of merit (p/e(^1)(_T)) of such films is approximately 0.22 nCcm(^-2)K(^-1), which is comparable with the values for commercially available materials. The difference in pyroelectric coefficient of the two types of alternate layer film is attributed to differences in inter-layer bonding, as revealed by infrared spectroscopy. The dependence of the pyroelectric coefficients on parameters such as film thickness, substrate thickness and temperature is investigated. Structural studies, performed using electron and X-ray diffraction techniques, are also described. These provide information on the orientation of the molecules relative to the substrate and on the d-spacing of the LB films. It is shown that the substrate has a deleterious effect on the responsivity of LB film devices, and studies of films deposited onto different substrate materials indicate that there is a significant piezoelectric ally induced secondary effect contributing to the overall pyroelectric coefficient. This secondary effect is small at low temperatures, but becomes dominant at around 250 K. The results of thermally stimulated discharge experiments indicate that both free charges and dipolar groups are incorporated in the films during deposition, and become tightly bound within the polar structure

    Deposition and characterisation of sputtered Nickel manganate thin films

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    This work investigates the structural and electrical properties of both bulk and r magnetron sputtered thin films of spinel structured Ni(_x)Mn(_3-x)0(_4=8) material system. The distribution of the LDOS of the thin films is also studied using STS. A rf magnetron sputtering system capable of reactive sputtering in a range of argon/oxygen ambients was designed, constructed and commissioned in the first phase of this work. The system was optimised in terms of the effect of various process parameters on the growth rate using factorial experimental design technique. Incident power, substrate to target distance and oxygen percentage in the ambient was found to be the most significant. The effect of different sintering temperatures was investigated for five different compositions of the NhMn3-x04+s material system. Monophase material could not be prepared without prolonged annealing at 800 C after sintering at higher temperatures. This was in contradiction with the published phase diagram of the material and hence a modified scheme was proposed. The lattice parameter of the spinel phase increased with decreasing nickel content. Grain growth was found to be exponentially dependent on the sintering temperature. The R-T characteristics below 300K followed the Shklovskii and Efros VRH model (To -2x10(^5) K) and a change to the NNH model (∆E -330 meV) was observed above 300K. The resistivity of the material was dependent on both the ratio of Ni:Mn and the oxygen stoichiometry (varying from 1.2 Kohm-cm up to 30 Kohm-cm).The as-deposited films showed poor crystallinity, hence post deposition annealing at 800 C was required. The microstructure and the degree of preferred orientation were found to be dependent on the substrate temperature and post deposition annealing. The lattice parameter of the films was lower than the target. The NNH model best described the R-T characteristics of the films deposited at low oxygen content <2.5% (∆E -360 meV) whereas films deposited at higher oxygen content could be better described by the Shklovskii and Efros VRH model {To -2.4 x 10^ K). The resistivity of the films decreased with increasing oxygen in the ambient in the as-deposited state, however after annealing the resistivity of all the films became similar and much lower than the target. The distribution of the LDOS of the films, using STS, was found to be parabolic and in agreement with the assumption in the Shklovskii and Efros VRH model. Additional features were observed in the LDOS with increasing temperatures (~±0.15 eV and ~+1.6 eV) however the changes were completely reversible with temperature

    Strontium titanate based films for tunable device applications

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    Doutoramento em Ciência e Engenharia de MateriaisO SrTiO3 (ST) cristaliza com a estrutura da perovesquite e apresenta propriedades de um paraeléctrico quântico; isto é, exibe um aumento continuo da permitividade dieléctrica com o decréscimo da temperatura até 4K, seguido de um patamar de valor constante até cerca de 0K. A presença de imperfeições na rede, tais como defeitos pontuais, impurezas e tensões podem modificar apreciavelmente as propriedades do ST puro e mesmo induzir ferroelectricidade. Neste trabalho foi conduzido um estudo sistemático da estrutura, microestrutura e comportamento dieléctrico de filmes finos não dopados e dopados de ST policristalino preparados por sol gel e depositados sobre diferentes substratos. As propriedades dieléctricas foram estudadas numa gama alargada de temperatura e frequência do campo eléctrico. A caracterização dieléctrica dos filmes foi efectuada em função da temperatura e frequência desde o regime das frequências rádio (rf), terahertz (THz-TDS) e infra vermelho (IR). As características cristalográficas e microestuturais dos filmes de ST foram analisadas por difracção de raios X (DRX), espectroscopia de Raman, microscopia electrónica de varrimento (SEM) e de transmissão (TEM), espectroscopia de Rutherford Backscattering (RBS). Foi feito um estudo detalhado da dinâmica de rede destes materiais. É mostrado neste trabalho que filmes finos de ST não dopados e crescidos em diferentes substratos (Al2O3/Pt, Si/SiO2/TiO2/Pt, (LaAlO3)0.3- (Sr2AlTaO6)0.7/Pt, SrTiO3/Pt and MgO/Pt) apresentam diferentes características estruturais e propriedades eléctricas, directamente dependentes das tensões criadas nos filmes. Nos grãos dos filmes de ST depositados sobre substratos de MgO/Pt devido às elevadas tensões compressivas originadas pelo substrato observam-se deslocações do tipo “slip band dislocations”, Enquanto que o modo TO1 de filmes de ST depositados sobre Al2O3 se comporta de maneira muito semelhante aos cristais de ST na gama de temperatura entre 300K e 150K, o modo TO1 dos filmes de ST depositados sobre substratos de MgO apresenta-se endurecido, o que se pode explicar pela influência das tensões geradas nos filmes pelo substrato. Filmes de ST com as tensões compressivas mais elevadas, depositados sobre substratos de MgO/Pt exibem os valores mais elevados da parte real da permitividade dieléctrica (ε′), a maior resposta histerética da polarização em função do campo eléctrico aplicado e os maiores valores da sintonabilidade dieléctrica (nr), em oposição aos filmes de ST, depositados sobre substratos de Al2O3/Pt com as tensões tractoras mais elevadas. Neste trabalho é também salientada a importância dos aspectos tecnológicos da preparação por sol gel, na qualidade dos filmes finos de ST, que se reflecte nos valores elevados de ε′ and nr, que são obtidos por pela introdução de camadas intermédias tampão (buffer layers) e pelo aumento da temperatura de queima de 750o C para 900o C. Com base em previsões teóricas, de que o deslocamento de iões de pequenas dimensões (“off centre”) como o Mg, nos locais dos iões Sr da rede induzem uma anomalia na resposta dieléctrica do ST, foi estudada a incorporação de Mg na rede dos filmes de ST. Foi observado que o limite de solubilidade sólida de Mg na rede de ST é dependente do local da rede no qual ocorre a incorporação do dopante e da temperatura do tratamento térmico. Aumentando a temperatura do tratamento térmico decresce a solubilidade do magnésio nos filmes de Sr1-xMgxTiO3 de x > 0.30 a 750o C para x < 0.15 a 900o C. De acordo com este estudo, o Mg não induz um estado ferroeléctrico nem um comportamento do tipo relaxor em filmes finos de titanato de estrôncio preparados por sol gel, quer quando a substituição ocorre nos locais A ou B da rede do ST. A estrutura, dinâmica de rede e propriedades dieléctricas de filmes finos de ST dopados com Bi são também apresentados neste trabalho e discutidos pela primeira vez. Nos filmes de Sr1-1.5xBixTiO3 o modo TO1 torna-se mais duro e independente da temperatura e uma relaxação a baixas frequências aparece com o aumento do conteúdo de Bi. A posição do máximo de ε′ dos filmes estudados desloca-se para temperaturas mais altas com o aumento da concentração de Bi e com o aumento da frequência. A presença de “clusters” de dimensões nanométricas e dos iões de Bi em posição “off centre” causa uma relaxação dieléctrica complexa. A relaxação dieléctrica induzida segue, a lei de Arrhenius para as amostras com baixo teor de Bi (x < 0.04), e a relação de Vogel-Fulcher para as amostras com as concentrações de dopante mais elevadas (0.04 ≤ x ≤ 0.167). A dispersão da frequência de ε′ em filmes finos de Sr1-1.5xBixTiO3 com pequenos teores de Bi é ligeiramente suprimida, quando em comparação com os cerâmicos correspondentes, o que pode ser explicado pela influência do substrato no caso dos filmes finos. Este estudo ilustra que a incorporação de Bi na rede de ST origina um comportamento do tipo relaxor, aumentando a tunabilidade dieléctrica. Filmes finos de Sr1-1.5xBixTiO3 com elevados factores de qualidade (> 2000 numa gama de temperatura alargada) são candidatos apropriados para utilização em sintonizadores.SrTiO3 (ST), crystallizing in the perovskite type structure, is a quantum paraelectric, i.e., it exhibits a continuous increase of the dielectric permittivity with decreasing temperature down to 4K, followed by the levelling off of the permittivity to near 0K. The presence of lattice imperfections such as strain, point defects, grain boundaries, and impurity atoms can appreciably modify the properties of pure ST and even induce ferroelectricity. In this work, systematic research on the structure, microstructure and dielectric behaviour of polycrystalline SrTiO3 - based thin films prepared by solgel is performed. The dielectric properties are studied in a wide temperature, frequency and electric field ranges. For some films the dielectric characterisation is assessed at radio-frequency (rf), time-domain terahertz (THz-TDS), and infrared (IR) spectroscopy. The crystallographic and micro structures of the undoped and doped ST films are analysed by X-ray diffraction (XRD), Raman spectroscopy, scanning and transmission electron microscopy (SEM and TEM) and Rutherford Backscattering Spectrometry (RBS) techniques. Detailed investigations of the lattice dynamics in a wide frequency range is undertaken as well. It was observed, that undoped ST films grown on different substrates (Al2O3/Pt, Si/SiO2/TiO2/Pt, (LaAlO3)0.3-(Sr2AlTaO6)0.7/Pt, SrTiO3/Pt and MgO/Pt) have different structural and dielectric properties dependent on the strain/stress effect induced by the substrate. For the case of ST films on MgO substrates the appearance of some “slip band dislocations” within the film grains was detected due to the high compressive stresses from the substrate. Whereas TO1 mode of ST films deposited on Al2O3 behaves similarly to that of ST single crystals in the temperature range from 300K to 150K. TO1 mode of ST films deposited on MgO substrate is stiffened, what can also be explained by influence of the stresses. ST films, with the highest compressive stress, deposited on MgO/Pt substrate shows the highest value of the real part of the dielectric permittivity (ε′), the largest hysteresis loop, and the highest value of the dielectric tunability (nr) in opposition to ST films, with the highest tensile stress, deposited on Al2O3/Pt substrates. The role of the technological aspects associated with the preparation of highquality sol-gel ST films is reflected in the elevated ε′ and nr of ST films, obtained by introducing buffer layers, intermediately annealed at 600o C, and by increasing films annealing temperature from 750o C to 900o C. As a consequence ε′ and nr of ~700 and ~50% are attained, being among the highest values reported for ST sol gel based films. Based on the theoretical prediction, that the off-centre displacements of small Mg ions at the large Sr sites can induce dielectric anomalies in ST, the incorporation of Mg in ST films was addressed in this work. Solid solubility limit of Mg was found to depend on the lattice site of incorporation and annealing temperature. Increasing annealing temperature decreases the solubility in Sr1-xMgxTiO3 thin films from x > 0.30 for 750o C to x < 0.15 at 900o C. Moreover Mg does not induce ferroelectricity or relaxor-like behaviour in strontium titanate, either located in A- or B-site of the SrTiO3 lattice. Within this work, the structure, low temperature lattice dynamics and dielectric properties of Bi doped ST films are described and discussed for the first time. In Sr1-1.5xBixTiO3 films TO1 mode becomes harder and, concomitantly a temperature independent and low-frequency relaxation appears with increasing of Bi content. The position of the maximum of ε′ of the investigated films shifts to high temperatures with increasing Bi content and frequency. The presence of nanoclusters and off-centred Bi ions causes a complex relaxation dynamics in these films. The induced dielectric relaxation follows the Arrhenius law for the samples with low Bi content (x < 0.04) and the Vogel-Fulcher law for the samples with a higher doping concentration (0.04 ≤ x ≤ 0.167). The frequency dispersion of ε′ in Sr1-1.5xBixTiO3 thin films with small amount of the Bi is slightly suppressed, compared to the corresponding ceramics, what can be explained by the influence of substrate. Bi incorporation in ST lattice leads to a relaxortype dielectric response, increasing the dielectric tunability. Sr1-1.5xBixTiO3 thin films with high value of the quality factor (> 2000 in wide temperature range) are appropriate candidates for using in tunable applications

    Crystallographic properties and elemental migration in two-stage prepared CuIn1−xAlxSe2 thin films for photovoltaic applications

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    Two-stage fabrication of CuIn1−xAlxSe2 thin films for photovoltaic absorbers using sputtered Cu–In–Al metallic precursors has been investigated. Precursors containing different relative amounts of Al were selenised and their structural and chemical properties characterised. X-ray diffraction (XRD) analyses revealed that the Al was only incorporated into the chalcopyrite structure for precursor composition ratios x = [Al]/([Al] + [In]) ⩾ 0.38, while chemical analysis of the cross-section indicated partial segregation of Al near the back of the film. Precursor films in the range of compositions that yielded no Al incorporation were then selenised at four different temperatures. Glow discharge optical emission spectroscopy, plasma profiling time-of-flight mass spectrometry and XRD analyses provided an insight into the diffusion processes and reactions taking place during the selenisation stage. The effect of post-selenisation annealing without additional Se was also investigated, and led to partial incorporation of the Al into the CuInSe2 lattice but no rediffusion

    Electrical, morphological and structural properties of RF magnetron sputtered Mo thin films for application in thin film photovoltaic solar cells

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    Molybdenum (Mo) thin films were deposited using radio frequency magnetron sputtering, for application as a metal back contact material in ‘‘substrate configuration’’ thin film solar cells. The variations of the electrical, morphological, and structural properties of the deposited films with sputtering pressure, sputtering power and post-deposition annealing were determined. The electrical conductivity of the Mo films was found to increase with decreasing sputtering pressure and increasing sputtering power. X-ray diffraction data showed that all the films had a (110) preferred orientation that became less pronounced at higher sputtering power while being relatively insensitive to process pressure. The lattice stress within the films changed from tensile to compressive with increasing sputtering power and the tensile stress increased with increasing sputtering pressure. The surface morphology of the films changed from pyramids to cigar-shaped grains for a sputtering power between 100 and 200 W, remaining largely unchanged at higher power. These grains were also observed to decrease in size with increasing sputtering pressure. Annealing the films was found to affect the resistivity and stress of the films. The resistivity increased due to the presence of residual oxygen and the stress changed from tensile to compressive. The annealing step was not found to affect the crystallisation and grain growth of the Mo films
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