We report on a novel silicon nanowire-based field effect transistor with integrated ferroelectric gate oxide. The concept allows tuning the carrier transport in a non-volatile approach by switching the polarization in the ferroelectric layer close to the source Schottky-junction. We interpret the results in terms of tuning the transmissibility of the Schottky-junction for charge carriers. The experimental results provide a first step towards the integration of memory-in-logic concepts with reconfigurable nanowire transistors.

Low cost, rapid and high thermal by IR heating, rapid cooling and high efficiency, there are RTP (Rapid Thermal Processing) properties. We can use RTP for annealing, diffusion, contacting, oxidation and others. Rapid temperature change and IR heating can be followed positive effects in the silicon substrate. This paper is focused on annealing by RTP. Wafers were p-type monocrystalline CZ silicon with different bulk minority carrier lifetime. Minority carrier lifetime was measured by MW-PCD (Microwave Photoconductance Decay) before and after thermal processing.

Metal-semiconductor contacts have been widely studied in the past 60 years. These structures are of importance in the microelectronics industry. As the scaling down of silicon-based complementary metal-oxide-semiconductor (CMOS) devices becomes more and more challenging, new material and device structures to relax this physical limitation in device scaling are now required. Germanium (Ge) has been proposed as a potential alternative to silicon. In this thesis a systematic study of the thermally induced reaction of transition metals with the n-Ge substrate is outlined. Investigations in the change of the electrical properties of the metal germanide structures is studied in a wide range of temperatures. Current-voltage (I-V), capacitance-voltage (C-V), deep level transient spectroscopy (DLTS) and high-resolution Laplace-DLTS (L-DLTS) techniques have been used for the electrical characterization of the fabricated Schottky contacts. Results obtained indicate the variation of the electrical properties of these Schottky contacts can be attributed to combined effects of interfacial reactions and phase transformation during the annealing process. The barrier height distribution in identically prepared Schottky contacts on n-Ge (100) showed that the barrier heights and ideality factors varied from diode to diode even though they were identically fabricated. The properties of the n-Ge Schottky contacts have revealed a strong dependence on temperature. The current transport mechanism has been shown to be predominantly thermionic emission at high temperatures while at low temperatures, the Schottky contacts have exhibited the dominance of the generation-recombination current mechanism. The variation of the Schottky barrier heights at low temperatures have been attributed to barrier inhomogeneities at the metal-semiconductor (MS) interface. Results from defect characterization by DLTS show that the E-centre is the dominant defect introduced in n-Ge by electron beam deposition during contact fabrication and substitutional related defects are induced during the annealing process. The identification of some of the defects was achieved by using defect properties, defect signature, annealing mechanisms and annealing behaviour and comparing these properties to the results from theoretical defect models. Annealing showed that defects in Ge can be removed by low thermal budget of between 250–350°C. Finally, structural characterization of these samples was performed by scanning electron microscopy (SEM) and Rutherford backscattering spectrometry (RBS) techniques. From the SEM images it can be observed that the onset temperature for agglomeration in the 30 nm Ni/n-Ge (100), and Pt/-, Ir/- and Ru/n-Ge (100) systems occur at 500–600°C and 600–700°C, respectively. / Thesis (PhD)--University of Pretoria, 2010. / Physics / unrestricted

Integration of high-K Metal-Insulator-Metal (MIM) capacitors in the Back-end-of-line (BEOL) is a topic of interest for the further development of the process at KTH Royal Institute of Technology. MIM-capacitors benefit from having constant capacitance values over a range of voltages and/or frequencies. One significant limitation in the development of better MIM-capacitors is the temperature consideration for BEOL processes. For the process at KTH Institute of Technology the temperature should not exceed 600 °C, as this would damage underlying devices. This work aims to fabricate aluminium oxide MIM-capacitors as a standard BEOL process performed at low temperature, which has been achieved via atomic layer deposition (ALD). The fabricated aluminium oxide MIM-capacitors had a good quality factor, series resistance and low dissipation. The capacitance for a 10 nm thick aluminium oxide insulator layer was 1 µF/cm2, which exceeds the set requirement. This work also aimed to make ferroelectric aluminium doped hafnium oxide MIM-capacitors using ALD. The doping ratio was varied in ALD as this had been found to affect formation of the ferroelectric crystal phase after a rapid thermal annealing step. Three wafers of 20 nm thick hafnium oxide and differing ratios were found to not be ferroelectric. The intermediate doping ratio was found to appear slightly anti-ferroelectric. A 10 nm thick doped hafnium oxide of intermediate doping was also fabricated and was found to be ferroelectric with a remnant polarisation of 1 µC/cm2. Though this polarisation is relatively small, it shows that top electrode induced strain due to lattice mismatch could be responsible for the ferroelectric properties of the capacitor. The quality of the hafnium based capacitors seemed worse in comparison to the aluminium oxide capacitors, which is suspected to be due to oxygen vacancies, resulting in a high loss tangent. While this first experiment showed promising results, the ferroelectric remnant polarisation should be increased by an order of magnitude and the electrical benchmark values should be improved before these hafnium oxide MIM-capacitors can be used in the BEOL process. / Integratie van high-K MIM-condensatoren in de Back-end-of-line (BEOL) is een onderwerp van belang voor de ontwikkeling van het proces bij de KTH. MIM-condensatoren profiteren van een constante capaciteitswaarde over een reeks spanningen en/of frequenties. Een belangrijke beperking bij de ontwikkeling van betere MIM-condensatoren is het temperatuur limiet voor BEOL-processen. Bij de KTH moet de temperatuur niet hoger zijn dan 600 °C, omdat dit de onderliggende apparaten zou beschadigen. Dit werk heeft tot doel aluminiumoxide MIM-condensatoren te fabriceren als een standaard BEOL-proces met lage temperatuur, en heeft dit inderdaad bereikt via atomaire laagafzetting (ALD). De gefabriceerde aluminiumoxide MIM-condensatoren hadden een goede kwaliteitsfactor, serieweerstand en lage dissipatie. De capaciteit voor een 10 nm dikke aluminiumoxide-isolatorlaag was 1µF/cm2, hoger dan de gestelde eisen. Dit werk was ook gericht op het maken van ferro-elektrische aluminium gedoteerde hafniumoxide MIM-condensatoren met behulp van ALD. De doteringsverhouding werd gevarieerd in ALD, aangezien bleek dat dit de vorming van de ferro-elektrische kristalfase faciliteerde na een snelle thermische gloeistap. Drie wafers van 20 nm dik hafniumoxide en verschillende verhoudingen bleken niet ferro-elektrisch te zijn. De tussenliggende doteringsverhouding bleek enigszins anti-ferro-elektrisch te zijn. Een 10 nm dik gedoteerd hafniumoxide met intermediaire dotering werd ook gefabriceerd en bleek ferro-elektrisch te zijn met een restpolarisatie van 1 µC/cm2. Hoewel deze polarisatie relatief klein is, toont het aan dat de door de topelektrode geïnduceerde spanning als gevolg van roostermismatch verantwoordelijk zou kunnen zijn voor de ferro-elektrische eigenschappen van de condensator. De kwaliteit van de op hafnium gebaseerde isolator leek slechter in vergelijking met die van aluminiumoxide, hetgeen kan worden toegeschreven aan gebrek van zuurstof in het rooster, wat in een groot verlies resulteert. De ferro-elektriciteit moet met een orde van grootte worden verhoogd en de elektrische benchmarks moeten ook verhoogd worden voordat deze hafniumoxide MIM-condensatoren kunnen worden gebruikt in het BEOLproces. Sleutelwoorden: atomaire laagafzetting (ALD), Ferro-elektrisch, Metaal-Isolator- Metaal (MIM) condensator, lage temperatuur, snelle thermische gloeiing.

No description available.

Del A: Polyetylentereftalat fibrer I detta arbete presenteras olika metoder för att framställa monofilament av polyetylentereftalat (PET) (diameter: 30-50 µm) med en radiell gradient. Nyutvecklad Raman-spektroskopiteknik har använts för att kartlägga dessa inducerade radiella gradienter i t.ex. kristallinitet. På liknande sätt har FTIR-ATR teknik modifierats och anpassats för att studera ytegenskaperna hos dessa filament. Industriella filamentprover och egna smältspunna PET-filament har framgångsrikt modifierats med användning av olika termiska och kemiska behandlingar för att erhålla fibrer med förbättrade mekaniska egenskaper och minskad fibrillering. De strukturella förändringar som uppträdde i filamenten på mikroskopisk nivå karakteriserades med bl a infraröd analys, termisk analys, Raman-mikroskopi och röntgenteknik (SAXS och WAXD). Tester av fibrilleringsegenskaper utfördes av industriella partners med egenutvecklad teknik följt av testning av masterbatch-fibrer på en vävningssimulator. Resultaten i laboratorieskala avslöjade fibrernas strukturella anisotropi och radiella gradienter, vilka visade en minskad fibrillering med en viss inverkan på de mekaniska egenskaperna.  Del B: Poly(3-hydroxybutyrat) fibrer Detta arbete presenterar studier av poly(3-hydroxybutyrat) (P3HB) fibrer med reversibla strukturförändringar. Tidigare studier har visat att kristallisationen hos P3HB fibrer i huvudsakligen sker i ortorombisk α-kristallform. Stress-anlöpning resulterar dock i en förändring i beteendet hos P3HB-materialet. Strukturen hos P3HB fibrer består av amorfa och kristallina regioner samt en mesofas. Mesofasen antas vara belägen mellan α-kristallerna och uppträder som starkt orienterade bindningskedjor, s k “tie-chains”. Denna studie syftar till att observera effekten av stress-anlöpning på mesofasen och dess beroende av anlöpningsförhållandena. Förändringarna i mesofasen observeras med en anpassad och polariserad Attenuated Total Reflection Fourier Transform Infrared Spectroscopy (ATR-FTIR) samt med Differential Scanning Calorimetry (DSC). Resultaten från ATR-FTIR visar att mesofasen är närvarande i spunna och högt stress-anlöpta fibrer, medan den är frånvarande i fibrer som är lågt stress-anlöpta. Mesofasen kan emellertid återupptas i lågt stress-anlöpta fibrer genom dragning. In situ ATR-FTIR användes för att studera förändringarna i materialbeteendet under en dragningsprocess för att observera periodiciteten i förekomsten av mesofasen. Det visade sig att förekomsten av mesofasen är en starkt reversibel process som observeras som en funktion av topparnas intensitet i ATR-FTIR. / Part A: Poly(ethylene terephthalate) fibres In this work, various methods to produce Poly(ethylene terephthalate) (PET) monofilaments (diameter: 30-50µm) with a radial gradient are presented along with a newly developed Raman spectroscopy technique to map these induced radial gradients in e.g. crystallinity. On similar lines, FTIR-ATR technique has been modified and adapted to study the surface properties of these fine filaments. Industrial filament samples and in-house melt-spun PET filaments have been successfully modified using various thermal and chemical treatments to obtain fibres with improved mechanical properties and reduced fibrillation. The structural changes occurring in the filaments on the microscopic level were characterized using infrared analysis, thermal analysis, Raman microscopy and X-ray techniques (SAXS and WAXD) among others. The fibrillation properties were tested by the industrial partners using a technique developed in-house followed by testing of masterbatch fibres on a weaving simulator. Lab-scale results revealed the structural anisotropy and radial gradient maps of the fibres which also demonstrated reduced fibrillation with some impact on mechanical properties also being observed. Part B: Poly(3-hydroxybutyrate) fibres This work presents studies on poly(3-hydroxybutyrate) (P3HB) fibres with reversible structural changes. Previously reported literature shows that crystallization of P3HB fibres takes place majorly in the orthorhombic α-crystal form. However, the stress-annealing results in a change of the material behaviour of P3HB. P3HB fibres compose of amorphous regions, crystalline regions and mesophase in their structure. The mesophase is supposed to be located in between the α-crystals of the material as highly oriented tie-chains. This study targets to observe the effect of stress-annealing of the mesophase present in the P3HB fibres and its dependence on the annealing conditions. The changes in the mesophase content are observed with the help of a highly adapted polarized Attenuated Total Reflection Fourier Transform Infrared spectroscopy (ATR-FTIR) and Differential Scanning Calorimetry (DSC). The presented results from polarized ATR-FTIR show that the mesophase is present in as-spun and high stress annealed fibres while it is absent in fibres annealed with low stress. However, the mesophase can be re-obtained in low stress annealed fibres through tensile drawing. In-situ ATR-FTIR was utilized to study the changes in the material behaviour during a tensile drawing process to observe the cyclicity in the occurrence of the mesophase. It was found that the existence of mesophase is a highly reversible process observed as a function of the peak intensities of the polarized ATR-FTIR spectroscopy.

In dieser Arbeit wird das epitaktische Wachstum von GaP/Si Heterostrukturen zur Herstellung von rauscharmen GaP/Si Nanodiodenarrays untersucht, wobei eine top-down Ätztechnik zur Herstellung der verwendeten Nanodiodenarrays genutzt wurde. Zur Untersuchung der gewachsenen Schichten wurden Röntgenstreuung (XRD), Rasterelektronenmikroskopie sowie die elektrische Charakterisierung mittels Strom-Spannungs und Kapazität-Spannungsmessungen verwendet. Zudem wurde die Grenzfläche zwischen epitaktischer Schicht und Substrat mittels Niederfrequenter Rauschspektroskopie (LFN) untersucht. Die GaP-Schichten wurden auf p-dotierten Si (100) Substraten mittels eines Riber-32P Gasquellen-Molekularstrahlepitaxiesystems gewachsen. Die Abhängigkeit der Oberflächenbeschaffenheit und Kristallqualität von denWachstumsbedingungen, wie der Wachstumstemperatur, wurden intensiv untersucht, um die Defektdichte zu minimieren. Dafür wurden nominal 500 nm dicke Heterostrukturschichten beiWachstumstemperaturen von 550 °C, 400 °C und 250 °C gewachsen, wobei 400 °C als die optimale Wachstumstemperatur bestimmt wurde. Trotzdem waren die erhaltenen Schichten aufgrund der hohen Versetzungsdichte von schlechter Qualität. Eine nur sehr geringe Qualitätsverbesserung konnte durch einen in situ durchgeführten thermischen Annealingschritt bei 500 °C für 10 Minuten erreicht werden. Daher wurde eine neue Annealingmethode vorgeschlagen, die in dieser Arbeit step-graded annealing (SGA) genannt wird. Bei dieser Methode wurde die Temperatur schrittweise von 400 °C auf 480 °C innerhalb von 90 Minuten erhöht. Dabei wurde die Oberfläche die gesamte Zeit mittels Reflexion hochenergetischer Elektronen (RHEED) untersucht. Die Oberflächenrekonstruktion, die während des Annealens mittels RHEED beobachtet wurde, zeigte schließlich eine große Verbesserung der Kristallqualität. Die Gitterparameter von GaP wurden mittels asymmetrischer XRD gemessen, wobei festgestellt wurde, dass sie exakt denen von Volumen-GaP entsprechen. Zudem wurde festgestellt, dass die GaP-Schicht automatisch n-dotiert ist und diodentypisches Gleichrichtungsverhalten aufweist. Interessante Informationen über Fallenzustände in den Heterostrukturfilmen konnten mittels LFN-Messungen gefunden werden. In einer nicht annealten Probe wurden beispielsweise zwei Fallenzustände im Bereich der Bandlücke festgestellt. In den mittels der SGA-Methode annealten Proben wurde hingegen ein rauscharmes und fallenfreies System erhalten. Anschließend wurde Elektronenstrahllithografie (EBL) zum Erstellen von Nanomustern auf der Oberfläche genutzt, die zur Herstellung von Nanodrähten genutzt werden sollen. Zur Optimierung der Elektronenstrahllithografie wurden dabei GaPSubstrate aufgrund der im Vergleich zu den epitaktischen Schichten besseren und glatteren Oberflächenstruktur genutzt. Dabei konnten in einer Goldschicht 200 nm große Löcher in einem Gitter mit hoher Dichte auf GaP erstellt und in die GaPSchicht übertragen werden. Die metallunterstütztes chemisches Ätzen (MacEtch) genannte Technik wurde kürzlich vorgeschlagen und eignet sich für die Herstellung von Nanodrähten. Die Anwendung zur Herstellung von Nanodrähten aus GaP war herausfordernd aufgrund bisher begrenzter Anwendung für III-V Halbleiter. Zur Optimierung der MacEtch Technik wurde zunächst wieder GaP-Substrat verwendet, um den Einfluss von Kristalldefekten und der Oberflächenrauigkeit auf die Ergebnisse zu minimieren. Genutzt wurde ein Gemisch aus Lösungen von HF/KMnO4 mit verschiedenen Konzentrationen. Mit den so bestimmten Prozessbedingungen konnten erfolgreich GaP Nanodrähte aus GaP-Epilayern hergestellt werden. GaP/Si Heteroübergangsnanodioden wurden anschließend unter Nutzung von Au-Ge/Ni Kontakten zu GaP-Schicht und Al/Ni Kontakten zum rückseitigen Si hergestellt. Die Transporteigenschaften des Nanodiodenarrays bestätigen die Möglichkeit, diese Arrays als elektronische NiederLärmbauelemente einzusetzen. / An epitaxial growth of GaP/Si heterostructures for the fabrication of low-noise GaP/Si nanodiode array based on nanowires is reported. The grown films were characterized using X-ray diffraction, scanning-electron microscopy, atomic-force microscopy and electrical measurements. Besides that, the interface between the epilayer and the substrate was deeply studied using a low-frequency noise (LFN) spectroscopy. The GaP epilayers were grown on p-type Si (100)substrates using gas-source molecular-beam epitaxy system. The dependence of surface morphology and crystal quality on the growth conditions was intensively investigated for minimizing the defects. The heterostructure films were grown at an optimal growth temperature of 400 °C and a nominal thickness of 500 nm. In order to improve the crystalline quality of the heterostructures, a new thermal annealing method was proposed, and referred to as step-graded annealing (SGA). In this method, the temperature was increased gradually to the annealing temperature to reduce the strain relaxation in the epilayers. A highly improvement in the crystal quality was confirmed using the SGA method. In addition, the epilayers were found to be n-type autodoped, and exhibited diode rectification behavior. Furthermore, the trap levels in the band gap, which were revealed via LFN measurements, were found to be suppressed in the annealed films. Thereafter, gold-mesh nanopatterns on the GaP surfaces were fabricated using an electron-beam lithography, as a step for the fabrication of GaP nanowires. A metal-assisted chemical etching technique with a mixture of HF:KMnO4 was carried out to fabricate GaP nanowires. GaP/Si heterojunction nanodiodes were then fabricated using an Au-Ge/Ni contact on the top of the GaP nanowires as well as an Al/Ni contact on the backside of Si. Transport properties of the nanodiode array confirmed the possibility of using the array as a low-frequency electronic device.

L’imbibition est d’une importance fondamentale dans de nombreuses applications technologiques et intervient par ailleurs dans de nombreux phénomènes naturels (industrie textile, industrie pharmaceutique, érosion des sols ….). Malgré l’importance de ce phénomène, la description et la modélisation des mécanismes d’imbibition sont encore sujettes à discussion dans la littérature, en particulier, la prédiction des cinétiques d’imbibition à partir de la connaissance de la topographie du milieu poreux. L’objectif de ce travail de thèse a été de relier les cinétiques d’imbibition à la structure du milieu poreux imbibé. Pour cela, nous avons étudié l’imbibition capillaire (ou spontanée) en suivant une démarche expérimentale dans laquelle nous avons utilisé des substrats poreux modèles dont nous contrôlons le volume et la structure de pores. La configuration d’imbibition choisie dans ce travail est celle d’une goutte sessile (ou posée).Ces travaux ont permis de mettre en œuvre une technique de construction de pastilles macroscopiques, autosupportées et cohésives, par assemblage de microbilles de polymère. Ces systèmes modèles ont été utilisés pour étudier les cinétiques d’imbibition capillaire de liquides dans des supports tridimensionnels à structure de pores complexe en fonction de la taille des microbilles constituant la pastille poreuse, de la reconstruction thermique, de la perméabilité pour une structure poreuse bicouches et de la force capillaire. Ces études ont permis entre autres de mettre en évidence des régimes cinétiques et des transitions d’imbibition inattendues dans ces systèmes (régimes visqueux et inertiel). / Imbibition is of fundamental importance in many technological applications, and is also involved in many natural phenomena (textile industry, pharmaceutical industry, soil erosion ....). Despite the importance of this phenomenon, the description and modelling of imbibition mechanisms are still subject to discussion in the literature, in particular, the prediction of the kinetics of imbibition from the knowledge of the morphology of the porous medium.The aim of this thesis was to relate the imbibition kinetics with the structure of a model porous medium. For this, we studied the capillary imbibition (or spontaneous) following an experimental approach in which we used a model porous substrate with both a controlled porous volume and pore structure. The experimental configuration for studying this imbibition was that of a sessile drop. In this work we developed a technique for the fabrication of self-supported and cohesive macroscopic pellets of polymer microbeads. These model porous systems have been characterized for their internal structure and used to study the capillary imbibition kinetics as a function of i) the size of the microbeads, ii) the temperature of the thermal annealing, iii) the permeability in the case of bilayered porous structures and iv) the capillary force (concentration of ethanol in water, nature of the liquid). This approach allowed observing and discussing unexpected imbibition regimes and transitions (inertial and viscous regimes).

De maneira a melhorar o desempenho de um Transistor de Efeito de Campo Metal-Óxido-Semicondutor (MOSFET), o germânio (Ge) é um forte candidato para substituir o silício (Si) como semicondutor, devido a sua alta mobilidade dos portadores de carga. Contudo, o filme de dióxido de germânio (GeO2) sobre Ge é solúvel em água e suas propriedades elétricas inferiores. Nesse sentido, a proposta desta dissertação de Mestrado é oxinitretar termicamente filmes de GeO2 em atmosfera de óxido nítrico (15NO), de maneira a melhorar as propriedades elétricas e físico-químicas dessas estruturas. Inicialmente, as amostras foram limpas quimicamente usando uma mistura de peróxido de hidrogênio (H2O2) e ácido clorídrico + água (HCl + H2O, 4:1). Os filmes de GeO2 foram crescidos termicamente sobre Ge usando atmosfera de oxigênio enriquecido 97% no isótopo de massa 18 (18O), com parâmetros na qual geraram um filme com espessura de ~5 nm. As oxinitretações foram realizadas em um forno térmico rápido com atmosfera de 15NO, nas temperaturas variando de 400-600°C, nos tempos de 1 a 5 minutos. O objetivo da oxinitretação foi criar um filme de oxinitreto de germânio (GeOxNy) com propriedades físico-químicas satisfatórias para a indústria de microeletrônica. Também foram realizados recozimentos térmicos em atmosfera inerte com objetivo de testar a estabilidade térmicas dos filmes de GeOxNy. Análise com Reação Nuclear (NRA) e Espectrometria de Retroespalhamento Rutherford em geometria de canalização (RBS-c) foram utilizadas para quantificar a quantidade total de oxigênio 18O e 16O, respectivamente. NRP também foi utilizada de modo a determinar o perfil de concentração em função da profundidade para as espécies de 18O e 15N. De modo a investigar a composição química das amostras, Espectroscopia de Fotoelétrons induzidos por raio-X (XPS) foi utilizada. Pelas análises por RBS e NRA do 18O, podemos observar que ocorre troca entre os isótopos de 18O e 16O para todas das temperaturas de oxinitretação. Este resultado corrobora com estudos recentes da literatura. Para as amostras oxinitretadas em 5 minutos a 500°C e todas as amostras oxinitretadas a 550°C e 600°C, ocorre troca isotópica completa. Observamos ainda por NRP que o 15N é incorporado mais superficialmente para as temperaturas de oxinitretação até 550°C. Resultados de XPS indicam formação maior de GeOxNy próximos da superfície das amostras e para temperaturas e/ou tempos maiores. Testes de estabilidade térmica indicam que a incorporação de nitrogênio mais próximo das superfície da amostra inibe a dessorção das espécies de GeO. As amostras que não foram oxinitretadas acabam dessorvendo quase por completo o filme de GeO2 quando realizados os recozimentos térmicos. Este efeito do nitrogênio incorporado próximo da superfície tem grande potencial para uso em camadas interfaciais entre semicondutor e dielétricos de porta. / In order to improve the performance of Metal-Oxide-Semiconductor Field Effect Transistor (MOSFET), germanium is a good candidate to replace silicon as semiconductor due to its higher charge carrier mobility. However, the germanium dioxide (GeO2) film over Ge is water soluble and produces poor electrical characteristics. In this way, this Master dissertation proposes thermal oxinitridation of the GeO2 films in nitric oxide (15NO) atmosphere in order to improve its electrical and physico-chemical characteristics. Samples were first cleaned using a mixture of hydrogen peroxide (H2O2) and hydrogen chloride + water (HCl + H2O, 4:1). GeO2 films were thermally grown on Ge using oxygen enriched in 97% in the isotope of mass 18, which generated ~5 nm thick film. Oxinitridation was performed in a rapid thermal furnace under 15NO atmosphere, at the 400-600°C temperature range, and 1-5 minutes time range. The goal was to form a germanium oxinitride film (GeOxNy) with physico-chemical properties that are satisfactory for microelectronics industry. We also performed thermal annealing in inert atmosphere to test the thermal stability of GeOxNy films. Nuclear Reaction Analysis (NRA) and Rutherford Backscattering Spectrometry in channeled geometry (RBS-c) were used to quantify the total amount of oxygen 18O and 16O, respectively. NRP was also performed to determine the 18O and 15N depth distribution. In order to investigate the chemical composition of the samples, X-ray Photoelectron Spectroscopy (XPS) was performed. RBS and NRA analysis showed isotopic exchange between 18O and 16O for all temperatures investigated. This result corroborates previous literature studies. Samples oxynitrided in 5 minutes at 500°C and all the samples oxinitrided at 550-600°C showed complete isotopic exchange. We also observed by NRP that nitrogen incorporation occurs more superficially until 550°C. XPS results indicate more formation of GeOxNy near the surface of the samples and for higher temperatures and/or time of oxinitredation. Thermal stability results indicated that the nitrogen incorporation near the sample surface inhibit the GeO desorption. On the other hand, samples that were not oxynitrided have almost all the GeO2 desorbed when thermal annealing is performed.

De maneira a melhorar o desempenho de um Transistor de Efeito de Campo Metal-Óxido-Semicondutor (MOSFET), o germânio (Ge) é um forte candidato para substituir o silício (Si) como semicondutor, devido a sua alta mobilidade dos portadores de carga. Contudo, o filme de dióxido de germânio (GeO2) sobre Ge é solúvel em água e suas propriedades elétricas inferiores. Nesse sentido, a proposta desta dissertação de Mestrado é oxinitretar termicamente filmes de GeO2 em atmosfera de óxido nítrico (15NO), de maneira a melhorar as propriedades elétricas e físico-químicas dessas estruturas. Inicialmente, as amostras foram limpas quimicamente usando uma mistura de peróxido de hidrogênio (H2O2) e ácido clorídrico + água (HCl + H2O, 4:1). Os filmes de GeO2 foram crescidos termicamente sobre Ge usando atmosfera de oxigênio enriquecido 97% no isótopo de massa 18 (18O), com parâmetros na qual geraram um filme com espessura de ~5 nm. As oxinitretações foram realizadas em um forno térmico rápido com atmosfera de 15NO, nas temperaturas variando de 400-600°C, nos tempos de 1 a 5 minutos. O objetivo da oxinitretação foi criar um filme de oxinitreto de germânio (GeOxNy) com propriedades físico-químicas satisfatórias para a indústria de microeletrônica. Também foram realizados recozimentos térmicos em atmosfera inerte com objetivo de testar a estabilidade térmicas dos filmes de GeOxNy. Análise com Reação Nuclear (NRA) e Espectrometria de Retroespalhamento Rutherford em geometria de canalização (RBS-c) foram utilizadas para quantificar a quantidade total de oxigênio 18O e 16O, respectivamente. NRP também foi utilizada de modo a determinar o perfil de concentração em função da profundidade para as espécies de 18O e 15N. De modo a investigar a composição química das amostras, Espectroscopia de Fotoelétrons induzidos por raio-X (XPS) foi utilizada. Pelas análises por RBS e NRA do 18O, podemos observar que ocorre troca entre os isótopos de 18O e 16O para todas das temperaturas de oxinitretação. Este resultado corrobora com estudos recentes da literatura. Para as amostras oxinitretadas em 5 minutos a 500°C e todas as amostras oxinitretadas a 550°C e 600°C, ocorre troca isotópica completa. Observamos ainda por NRP que o 15N é incorporado mais superficialmente para as temperaturas de oxinitretação até 550°C. Resultados de XPS indicam formação maior de GeOxNy próximos da superfície das amostras e para temperaturas e/ou tempos maiores. Testes de estabilidade térmica indicam que a incorporação de nitrogênio mais próximo das superfície da amostra inibe a dessorção das espécies de GeO. As amostras que não foram oxinitretadas acabam dessorvendo quase por completo o filme de GeO2 quando realizados os recozimentos térmicos. Este efeito do nitrogênio incorporado próximo da superfície tem grande potencial para uso em camadas interfaciais entre semicondutor e dielétricos de porta. / In order to improve the performance of Metal-Oxide-Semiconductor Field Effect Transistor (MOSFET), germanium is a good candidate to replace silicon as semiconductor due to its higher charge carrier mobility. However, the germanium dioxide (GeO2) film over Ge is water soluble and produces poor electrical characteristics. In this way, this Master dissertation proposes thermal oxinitridation of the GeO2 films in nitric oxide (15NO) atmosphere in order to improve its electrical and physico-chemical characteristics. Samples were first cleaned using a mixture of hydrogen peroxide (H2O2) and hydrogen chloride + water (HCl + H2O, 4:1). GeO2 films were thermally grown on Ge using oxygen enriched in 97% in the isotope of mass 18, which generated ~5 nm thick film. Oxinitridation was performed in a rapid thermal furnace under 15NO atmosphere, at the 400-600°C temperature range, and 1-5 minutes time range. The goal was to form a germanium oxinitride film (GeOxNy) with physico-chemical properties that are satisfactory for microelectronics industry. We also performed thermal annealing in inert atmosphere to test the thermal stability of GeOxNy films. Nuclear Reaction Analysis (NRA) and Rutherford Backscattering Spectrometry in channeled geometry (RBS-c) were used to quantify the total amount of oxygen 18O and 16O, respectively. NRP was also performed to determine the 18O and 15N depth distribution. In order to investigate the chemical composition of the samples, X-ray Photoelectron Spectroscopy (XPS) was performed. RBS and NRA analysis showed isotopic exchange between 18O and 16O for all temperatures investigated. This result corroborates previous literature studies. Samples oxynitrided in 5 minutes at 500°C and all the samples oxinitrided at 550-600°C showed complete isotopic exchange. We also observed by NRP that nitrogen incorporation occurs more superficially until 550°C. XPS results indicate more formation of GeOxNy near the surface of the samples and for higher temperatures and/or time of oxinitredation. Thermal stability results indicated that the nitrogen incorporation near the sample surface inhibit the GeO desorption. On the other hand, samples that were not oxynitrided have almost all the GeO2 desorbed when thermal annealing is performed.