Les propriétés magnétiques détaillées des solides peuvent être vu comme le résultat de l'interaction de plusieurs sous-systèmes: celui des spins effectifs, portant l'aimantation, celui des électrons et celui du réseau crystallin. Différents processus permettent à ces sous-systèmes d'échanger de l'énergie. Parmis ceux-ci, les phénomènes de relaxation jouent un rôle prépondérants. Cependant, la complexité de ces processus en rend leur modélisation ardue. Afin de prendre en compte ces interactions de façon abordable aux calculs, l'approche de Langevin est depuis longtemps appliquée à la dynamique d'aimantation, qui peut être vue comme la réponse collective des spins. Elle consiste à modéliser les interactions entre les trois sous-systèmes par des interactions effectives entre le sous-système d'intérêt, les spins, et un bain thermique, dont seulement la densité de probabilité constituerait une quantité pertinente. Après avoir présenté cette approche, nous verrons en quoi elle permet de bâtir une dynamique atomique de spin. Une fois son implémentation détaillée, cette méthodologie sera appliquée à un exemple tiré de la littérature et basé sur le superparamagnétisme de nanoaimants de fer. / Detailed magnetic properties of solids can be regarded as the result of the interaction between three subsystems: the effective spins, that will be our focus in this thesis, the electrons and the crystalline lattice. These three subsystems exchange energy, in many ways, in particular, through relaxation processes. The nature of these processes remains extremely hard to understand, and even harder to simulate. A practical approach, for performing such simulations, involves adapting the description of random processes by Langevin to the collective dynamics of the spins, usually called the magnetization dynamics. It consists in describing the, complicated, interactions between the subsystems, by the effective interactions of the subsystem of interest, the spins, and a thermal bath, whose probability density is only of relevance. This approach allows us to interpret the results of atomistic spin dynamics simulations in appropriate macroscopic terms. After presenting the numerical implementation of this methodology, a typical study of a magnetic device based on superparamagnetic iron monolayers is presented, as an example. The results are compared to experimental data and allow us to validate the atomistic spin dynamics simulations.

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior / Samples of Bi 2Fe4O9 mullite and ReFe 0.5M0.5O3 (Re = Nd, Sm, Eu, Gd, Dy; M = Mn, Al) complex perovskites were successfully synthesized by using the combustion synthesis method. While the mullite was obtained after thermal treatment at temperatures below 1000ºC, complex perovskites are produced after thermal treatments between 1250ºC and 1500ºC for at most 24 h. The X-ray diffraction data analysis suggests the formation of single phase orthorhombic structure, after suitable heat treatment. Scanning electron microscopy (SEM) revealed the formation of micrometric grain size, giving to the sample the relative density. EDS spectra confirmed the homogeneity and purity of complex perovskites. Magnetization measurements as a function of field and temperature showed the diversity of magnetic behavior of the samples. Among the behaviors we can highlight the reorientation of spin for ortoferritas ReFe0.5Mn0.5O3 (Re = Dy, Gd, Eu, Sm, Eu) and ReFe0.5Al0.5O3 (Re = Dy, Nd). Another interesting finding was the effect of magnetic reversal of the samples ReFe0.5Al0.5O3 (Re = Nd, Gd) and EuFe0.5Mn0.5O3. Raman spectra show anomalous bands of second order in the perovskite DyFe0.5Al0.5O3 with characteristics of resonant effects. The evolution of the band associated with the symmetric vibrational mode of the octahedron shows hardening at the temperature range of ordered magnetic phase, thus suggesting a possible spin-phonon coupling. Depolarization current measurements highlights a relaxation process due to charge carriers in the samples ReFe0.5Mn0.5O3 (Re = Dy, Gd). The application of magnetic field profoundly influences the depolarization current behavior of DyFe0.5Mn0.5O3. Dielectric permittivity measurements showed no anomalies between 10 K and 300 K, that could can be associated to a ferroelectric phase. / Amostras da mulita Bi2Fe4O9 e das perovskitas complexas ReFe0.5M0.5O3 (Re= Nd, Sm, Eu, Gd, Dy; M = Mn, Al) foram sintetizadas com sucesso utilizando o método de síntese por reação de combustão. Enquanto a mulita foi obtida após tratamento térmico com temperaturas abaixo de 1000ºC, as perovskitas complexas foram produzidas após tratamentos térmicos entre 1250ºC e 1500ºC por, no máximo, 24 h. A análise de dados de difração de raios X sugerem a formação de estruturas ortorrômbicas de fase única, após os tratamento térmico apropriado. Medidas de microscopia evidenciaram formação de grãos micrométricos conferindo às amostras relativa densidade. Os espectros EDS confirmaram a homogeneidade e pureza das perovskitas complexas. As medidas de magnetização em função do campo e da temperatura evidenciaram a diversidade de comportamentos magnéticos das amostras estudadas. Entre os comportamentos destacamos reorientação de spin para as ortoferritas ReFe0.5Mn0.5O3 (Re = Dy, Gd, Eu, Sm, Eu) e ReFe0.5Al0.5O3 (Re = Dy,Nd). Outro interessante achado foi o efeito de inversão magnética das amostras ReFe0.5Al0.5O3 (Re = Nd, Gd) e EuFe0.5Mn0.5O3. Espectros Raman demonstram bandas anômalas de segunda ordem na perovskita DyFe0.5Al0.5O3 com características de efeitos ressonantes. A evolução da banda associada ao modo vibracional simétrico do octaedro apresenta endurecimento em temperaturas na faixa da fase magnética ordenada, sugerindo assim, um possível acoplamento spin-f onon. Medidas de corrente de despolarização destaca um processo de relaxação devido aos portadores de cargas nas amostras ReFe0.5Mn0.5O3 (Re=Dy,Gd). A aplicação de campo magnético influencia profundamente o comportamento da corrente de despolarização do DyFe0.5Mn0.5O3. Medidas de permissividade dielétrica não exibiram anomalias entre 10 K e 300 K que possam a ser associadas a uma fase ferroelétrica.

[pt] No presente trabalho foram realizadas medidas de capacidade térmica à pressão constante do espinélio Al2MnO4 na faixa entre 2 e 873 K. No intervalo entre 2 e 300 K empregou-se um calorímetro de relaxação térmica. Os dados evidenciaram a presença de uma anomalia em torno de 33 K, cuja componente magnética pôde ser constatada mediante medidas de capacidade calorífica com campo magnético constante, bem como também medidas de magnetização específica como função da temperatura. A contribuição entrópica associada à mencionada anomalia foi considerada no cálculo da entropia molar a 298.15 K do óxido em questão (116.05 mais ou menos 5.2 J/mol.K), valor este consistente com valores da literatura para outros espinélios. Na faixa entre 323 e 873 K empregou-se um calorímetro diferencial de varredura. Os dados foram ajustados quantitativamente com o modelo de Berman e Brown, incluindo-se no ajuste o valor de capacidade térmica a 298.15 K, obtido via calorimetria de relaxação térmica. Empregando-se o valor de entropia molar determinado no presente trabalho, os parâmetros do modelo de Berman e Brown estimados com os dados em temperaturas elevadas, e uma estimativa disponível na literatura para a entalpia de formação do óxido Al2MnO4, construiu-se um modelo para a dependência térmica da energia de Gibbs do referido composto válido na faixa entre 298.15 e 2114 K. O modelo foi testado com sucesso no acesso termodinâmico das propriedades do sistema Al2O3-MnO. / [en] In the present work the constant pressure molar heat capacity of the spinel Al2MnO4 was measured between 2 K and 873 K. In the interval between 2 K and 300 K a relaxation calorimeter was employed. The data indicated the presence of a thermal anomaly around 33 K, whose magnetic component could be evidenced through measurements of the heat capacity with a constant applied magnetic field, and also through specific magnetization data as a function of temperature. The entropic contribution of the thermal anomaly was considered in the calculation of the molar entropy of the oxide at 298.15 K (116.05 more or less 5.2 J/mol.K), and the calculated value has proven to be consistent with values published earlier for other spinel compounds. In the interval between 323 and 873 K a differential scanning calorimeter was employed. The data were quantitatively modeled with the function proposed by Berman and Brown, including the heat capacity value obtained at 298.15 K accessed through the relaxation calorimeter route. By using the molar entropy at 298.15 K, the values of the parameter estimated for the Berman and Brown model with the heat capacity data at elevated temperatures, and an estimative for the heat of formation of the spinel Al2MnO4 extracted from the literature, it was possible to construct a model for the thermal dependence of the Gibbs energy of this compound valid between 298.15 K and 2114 K. The model was successfully tested in the thermodynamic assessment of the properties of the system Al2O3-MnO.

In the present thesis, magnetization reversal in both out-of-plane and in-plane magnetized thin lms and in devices fabricated out of those lms are explored. Pt/Co/Pt stacks with ultrathin Co layer were in-estimated initially for understanding their magnetic properties in this thesis. These perpendicular magnetized systems are good candidates for magnetic hard disc drives due to their large anisotropy, which may allow miniaturization of magnetic data storage devices. The spin Hall e ect mediated current-induced magnetization reversal in patterned Pt/Co/Pt devices were extensively investigated. Investigation of the magnetization reversal by means of a current instead of a magnetic eld is necessary to explore the possibilities of solid state magnetic memory devices. This is the primary motivation behind the investigation of current-induced magnetization reversal in Pt/Co/Pt system, in this thesis. Another important proposal for magnetic data storage is the race track memory, where the domain walls separating magnetic domains (in in-plane or out-of-plane magnetized materials) are moved by using a current. This involves a great deal of understanding of the domain wall motion in Nano-conduits under applied magnetics ends, and currents and also its interaction with engineered geometrical features. In this thesis work, magnetic led-driven domain wall pinning and deepening experiments on in-plane magnetized nanowires of perm alloy were performed to un-distend this interaction and the e act of domain wall chirality. In chapter 1, a general introduction to di errant data storage technologies and the current progress in the leg of spintronic is presented. This will highlight a perspective of this thesis work with respect to the present day research in spintronic and magnetization reversal studies. In chapter 2, a basic background of magnetism using the micromag-netic framework is illustrated. A brief introduction to magnetic domain walls is also presented. The Landau-Lifshitz-Gilbert dynamical equation is discussed and some case studies applied to a single domain particle with uniaxial anisotropy under the effect of spin-orbit torque are illu trated. The basics of spin-orbit coupling leading to spin Hall e ect is also explain In chapter 3, most of the essential experimental tools along with their basic working principles are described. Extensive e orts have been in-vested in designing and building the experimental tools. These include custom designs of a sputter deposition system, an ultra-high vacuum chamber for pulsed laser ablation, a magneto-optic Kerr e ect magne-tometer, a Kerr imaging system and a magneto-transport setup. All of these experimental setups have been automated, details of which are brie y discussed in this chapter. The Kerr imaging system was designed to measure hysteresis loops, observe domain wall motion and to measure domain wall velocity under applied magnetic elds and electric current. The magneto-transport setup was used for studying the domain wall pinning and depinning experiments in permalloy nanowires. In chapter 4, the optimization process for obtaining perpendicular mag-netic anisotropy in Pt/Co/Pt lms is described. The spin reorientation transition with varying thickness of Co (from 1.5 nm down to 0.35 nm) was studied. The magnetization easy axis direction changes from in-plane to out-of-plane as the thickness of Co is reduced. The dependence of Curie temperatures of ultrathin Co lms, with thickness as low as 0.35 nm, on the underlayer Pt thickness and its crystallinity was studied in detail. The e act of Ta but err layer on the texture of the Pt lm, and on the Curie temperature of the Pt/Co/Pt system was evaluated. To gain further insight of the role of the bottom Pt/Co and the top Co/Pt interfaces, ultrathin Cu lbs were inserted at the respective interfaces, and the anisotropy and magnetization reversal behaviour of these lbs were investigated. In chapter 5, studies on current-induced magnetization reversal in mi-corn sized wires of Pt/Co/Pt trilete is presented. The spin Hall e act assisted spin-orbit torque was used to reversibly switch the magnetization of these devices with and without the help of an external magnetic led. Since both the top and bottom layers are Pt, any contribution from Rashia e act towards spin-orbit torque could be ignored. By preparing devices with unequal top and bottom Pt thicknesses, a net spin-orbit torque could be applied to the magnetization of the Co layer. The thickness gradient/induced anisotropy in the Co layer was utilized to experimentally investigate current-induced deterministic switching. Sin-gel domain simulations with spin-orbit torque were also carried out to understand the mechanism of deterministic switching of magnetization in Pt/Co/Pt devices. This study is expected to have made sign cant contributions and to open up the possibilities of further investigation in the studies of spin-orbit torque in Pt/Co/Pt systems for solid state magnetic memory devices. In chapter 6, magnetic led-induced reversal in systems with in-plane magnetic anisotropy is presented. Here the e act of the width of a Nanos-trip on the anisotropy of a soft magnetic material like perm alloy was in-estimated. By introducing a nucleation pad to one end of the perm alloy nanowire, a single domain wall was generated at the junction with apple-cation of a proper magnetic led sequence. This domain wall could be in-jested into the nanowire by a magnetic led and pinned at a geometrical constriction inside the nanowire. The statistics of domain wall pinning and deepening processes indicated two di errant types of domain walls involved in the reversal process. With the assistance of micro magnetic simulations the domain walls were ident end as vortex walls of di errant chirality’s. Thus the interaction of domain walls with a Nano constriction and its dependence on the chirality of domain walls are understood. In chapter 7, a brief summary of the results obtained during the course of investigations is presented. An outlook presented at the end will help the readers of this thesis to understand the important research problems in this area and their potential future aspects.

Un des objectifs du Femtomagnetisme est de contrôler l’aimantation des matériaux avec des impulsions laser femtoseconde. Il a été démontré qu’une réponse magnéto-optique (MO) cohérente a lieu avant la thermalisation des populations de spins dans une configuration pompe-sonde MOKE. Elle résulte du couplage cohérent spin-photon dû à l’interaction spin-orbite. Une description simplifiée de cet effet a été faite en tenant compte d’un système à huit niveaux couplés au champ laser. La cohérence MO est définie par le temps de déphasage dépendent du champ T2MO. Dans ce travail, il est montré que la réponse MO cohérente d’un grenat dopé au bismuth peut être mesurée directement avec différentes configurations de mélange à quatre ondes MO. L’importance de connaître la phase spectrale de l’impulsion pour obtenir T2MO a été étudié. Avec des impulsions de 10fs dans le proche infra-rouge, une mesure de T2MO donne (2.8+/-1)fs, c. à d., du même ordre de grandeur que le temps de déphasage des charges. / One of the goals of Femtomagnetism is to manipulate the magnetization of materials using femtosecond optical pulses. It has been shown in ferromagnetic films that a magneto-optical (MO) coherent response takes place before the thermalization of the spins populations in a pump and probe MOKE experiment. It results from the coherent spin-photon coupling mediated by the spin-orbit interaction. A simplified description of this effect has been made by considering an eight-level system coupled with the laser field. The MO coherence can be defined by the magnetic field dependent dephasing time T2MO. In the present work, it is shown that the coherent MO response of a bismuth-doped garnet can be directly measured in different degenerated MO four-wave mixing configurations. The importance of well-knowing the spectral phase of the pulse to measure T2MO was studied. Using 10fs near infra-red pulses, T2MO was shown to be (2.8+/-1)fs that is of the same order of the charges dephasing time.

In this work we study the interesting physics of the rare earths, and the microscopic state after ultrafast magnetization dynamics in iron. Moreover, this work covers the development, examination and application of several methods used in solid state physics. The first and the last part are related to strongly correlated electrons. The second part is related to the field of ultrafast magnetization dynamics. In the first part we apply density functional theory plus dynamical mean field theory within the Hubbard I approximation to describe the interesting physics of the rare-earth metals. These elements are characterized by the localized nature of the 4f electrons and the itinerant character of the other valence electrons. We calculate a wide range of properties of the rare-earth metals and find a good correspondence with experimental data. We argue that this theory can be the basis of future investigations addressing rare-earth based materials in general. In the second part of this thesis we develop a model, based on statistical arguments, to predict the microscopic state after ultrafast magnetization dynamics in iron. We predict that the microscopic state after ultrafast demagnetization is qualitatively different from the state after ultrafast increase of magnetization. This prediction is supported by previously published spectra obtained in magneto-optical experiments. Our model makes it possible to compare the measured data to results that are calculated from microscopic properties. We also investigate the relation between the magnetic asymmetry and the magnetization. In the last part of this work we examine several methods of analytic continuation that are used in many-body physics to obtain physical quantities on real energies from either imaginary time or Matsubara frequency data. In particular, we improve the Padé approximant method of analytic continuation. We compare the reliability and performance of this and other methods for both one and two-particle Green's functions. We also investigate the advantages of implementing a method of analytic continuation based on stochastic sampling on a graphics processing unit (GPU).

Les travaux réalisés lors de cette thèse ont pour but la caractérisation magnétique et structurale de réseaux ultra-denses de nanofils monocristallins de cobalt de structure hcp avec l’axe c parallèle à l’axe des nanofils. Ces réseaux sont obtenus par une méthode physico-chimique dite croissance hybride. Le nanomatériau obtenu est un réseau de nanofils monocristallins de Co verticaux épitaxiés sur un film de platine. La cristallinité des nanofils induit une forte anisotropie perpendiculaire au réseau faisant émerger des propriétés physiques qui pourraient répondre au cahier des charges pour constituer des média magnétiques à haute capacité. Le manuscrit s’organise en quatre parties. Il convient dans un premier temps d’exposer une revue de la littérature décrivant le comportement magnétique d’un nano-cylindre isolé puis d’un réseau hexagonal de nano-cylindres. La méthode de magnétométrie utilisée pour caractériser ces réseaux est appelée méthode FORC (First Order Reversal Curves). La mesure et le traitement associé permettent de tracer des diagrammes dits FORC dans lesquels peuvent être lus les caractéristiques magnétiques des nanofils et leurs interactions. La lecture de ces diagrammes n’étant pas directe, le chapitre II est consacré à la description de la méthode FORC appliquée à des assemblées d’hystérons. Cette investigation a demandé d’être soutenue par des simulations micromagnétiques afin d’appuyer les hypothèses formulées lors de l’interprétation des diagrammes FORC mesurés. Il apparait ainsi une famille en très bon accord avec les modèles théoriques exposés dans le chapitre I, puis une seconde famille dont la description précise nécessite l’ajout d’une interaction magnétisante entre nanofils en plus de l’interaction magnétostatique. / The work carried out during this thesis aims at the magnetic and structural characterization of ultra-dense arrays of single crystalline cobalt hcp nanowires with the c axis parallel to the wires axis. These arrays are obtained by a physicochemical method called hybrid growth. The resulting nanomaterial is an array of vertical Co nanowires epitaxially grown on a platinum film, with diameters of 6 to 15 nm and coated with organic ligands. The crystallinity of the nanowires induces a strong anisotropy perpendicular to the substrate, giving rise to physical properties that could meet the specifications to constitute high density magnetic media. The manuscript is organized in four parts. First, a review of the literature describing the behavior of isolated magnetic nano-cylinders and dense arrays of nano-cylinders is presented. The magnetometry method used to characterize these arrays is called the FORC (First Order Reversal Curves) method. This measurement and analysis lead to the plot of FORC diagrams which contain the magnetic properties of nanowires and their interactions. The reading of these FORC diagrams being undirect, the chapter II is devoted to the description of the FORC method applied to assemblies of hysterons. Because of its reproducibility, the physico-chemical synthesis is a critical point of this study which is detailed in Chapter III. FORC magnetometry applied to two families of synthesized samples is described in Chapter IV. This investigation has required numerous micromagnetic simulations to support the assumptions made in the interpretation of FORC diagrams. This deep analysis reveals a first family in very good agreement with the theoretical models exposed in chapter I, and a second family for which the precise description requires the addition of a magnetizing interaction between nanowires in addition to the magnetostatic one.

Im Rahmen der Dissertation wurde das Phänomen der Wechselwirkungsdomänen sowohl experimentell als auch unter Zuhilfenahme mikromagnetischer Simulationen untersucht. Gegenstand der Untersuchungen waren einphasige NdFeB-Magnete, die durch Heißpressen und anschließender Warmumformung hergestellt wurden. Zusätzlich wurden über den gleichen Herstellungsweg Kompositproben aus NdFeB und Fe mit unterschiedlichen Partikelausgangsgrößen erhalten und studiert. Korrelationsuntersuchungen verschiedener Messmethoden haben gezeigt, dass im thermisch entmagnetisierten Zustand die Grenzen der Wechselwirkungsdomänen an der Oberfläche größtenteils entlang von Korngrenzen verlaufen. Mittels in-situ MFM wurden erstmalig Untersuchungen von Wechselwirkungsdomänen an massiven NdFeB-Magneten im Magnetfeld durchgeführt. Die Ummagnetisierung erfolgt dabei über die Bewegung der Domänengrenze durch schrittweises Wandern von einer Korngrenze zur benachbarten. Die Beweglichkeit der Domänengrenzen ist durch das Haften an den Korngrenzen gehemmt, was sich in der geringeren Suszeptibilität der warmumgeformten Magnete im Vergleich zu Sintermagneten bemerkbar macht. Aufgrund der eingestellten Mikrostruktur in den warmumgeformten Magneten kann folglich gesagt werden, dass die Ummagnetisierungsprozesse sowohl Merkmale von klassischen Nukleations-, als auch von klassischen Pinningmagneten aufweisen. Mit Hilfe von mikromagnetischen Simulationen konnte eine Eindomänenteilchengröße prismatischer Partikel mit quadratischer Grundfläche ermittelt werden. Außerdem konnte gezeigt werden, dass der Winkel des Streufeldvektors eine entscheidende Rolle bei Ummagnetisiserungsprozessen in solchen Partikeln spielt. Die Superposition des Streufeldvektors mit dem Vektor des angelegten Feldes führt zu einem Gesamtfeldvektor, dessen Winkelabhängigkeit ein Stoner-Wohlfarth ähnliches Verhalten zeigt.

In the present work, the implications of ion irradiation on the magnetostatic and dynamic properties of soft magnetic Py/Ta (Py = Permalloy: Ni80Fe20) single and multilayer films have been investigated with the main objective of finding a way to determine their saturation magnetization. Both polar magneto-optical Kerr effect (MOKE) and vector network analyzer ferromagnetic resonance (VNA-FMR) measurements have proven to be suitable methods to determine µ0MS, circumventing the problem of the unknown effective magnetic volume that causes conventional techniques such as SQUID or VSM to fail. Provided there is no perpendicular anisotropy contribution in the samples, the saturation magnetization can be determined even in the case of strong interfacial mixing due to an inherently high number of Py/Ta interfaces and/or ion irradiation with high fluences. Another integral part of this work has been to construct a VNA-FMR spectrometer capable of performing both azimuthal and polar angle-dependent measurements using a magnet strong enough to saturate samples containing iron. Starting from scratch, this comprised numerous steps such as developing a suitable coplanar waveguide design, and writing the control, evaluation, and fitting software. With both increasing ion fluence and number of Py/Ta interfaces, a decrease of saturation magnetization has been observed. In the case of the 10×Py samples, an immediate decrease of µ0MS already sets in at small ion fluences. However, for the 1×Py and 5×Py samples, the saturation magnetization remains constant up to a certain ion fluence, but then starts to rapidly decrease. Ne ion irradiation causes a mixing and broadening of the interfaces. Thus, the Py/Ta stacks undergo a transition from being polycrystalline to amorphous at a critical fluence depending on the number of interfaces. The saturation magnetization is found to vanish at a Ta concentration of about 10–15 at.% in the Py layers. The samples possess a small uniaxial anisotropy, which remains virtually unaffected by the ion fluence, but slightly reduces with an increasing number of Py/Ta interfaces. In addition to magnetostatics, the dynamic properties of the samples have been investigated as well. The Gilbert damping parameter α increases with both increasing number of Py/Ta interfaces and higher ion fluences, with the former having a stronger influence. The inhomogeneous linewidth broadening ΔB0 increases as well with increasing number of Py/Ta interfaces, but slightly decreases for higher ion fluences. / In dieser Dissertation ist der Einfluss von Ionenbestrahlung auf die magnetostatischen und dynamischen Eigenschaften von weichmagnetischen Py/Ta-Einzel- und Multilagen (Py = Permalloy: Ni80Fe20) untersucht worden, wobei das Hauptziel gewesen ist, eine Methode zur Bestimmung der Sättigungsmagnetisierung zu finden. Sowohl polare magneto-optische Kerr-Effektmessungen (MOKE) als auch ferromagnetische Resonanzmessungen mittels eines Vektornetzwerkanalysators (VNA-FMR) haben sich als geeignet erwiesen, um µ0MS zu bestimmen, wobei das Problem des unbekannten effektiven magnetischen Volumens umgangen wird, welches bei der Verwendung von Techniken wie SQUID oder VSM auftreten würde. Unter der Voraussetzung, dass die Proben keinen senkrechten magnetischen Anisotropiebeitrag besitzen, kann die Sättigungsmagnetisierung selbst im Fall starker Grenzflächendurchmischung infolge einer großen Anzahl an Py/Ta-Grenzflächen und/oder Ionenbestrahlung mit hohen Fluenzen bestimmt werden. Ein weiterer wesentlicher Bestandteil dieser Arbeit ist die Konstruktion eines VNA-FMR-Spektrometers gewesen, welches vollautomatisiert ist, polare und azimutale Winkelabhängigkeiten messen kann und einen Magneten besitzt, der Proben, die Eisen beinhalten, sättigen kann. Von Grund auf beginnend umfasste dies zahlreiche Schritte wie z. B. die Entwicklung eines geeigneten koplanaren Wellenleiterdesigns sowie das Schreiben von Steuerungs-, Auswertungs- und Fitprogrammen. Mit steigender Fluenz und Zahl an Py/Ta-Grenzflächen ist eine Abnahme der Sättigungsmagnetisierung beobachtet worden. Im Fall der 10×Py-Proben findet diese bereits bei kleinen Fluenzen statt. Im Gegensatz dazu bleibt µ0MS der 1×Py- und 5×Py-Proben bis zu einer bestimmten Fluenz konstant, bevor sie sich dann umso schneller verringert. Die Bestrahlung mit Ne-Ionen verursacht eine Durchmischung und Verbreiterung der Grenzflächen. Infolgedessen erfahren die Py/Ta-Proben bei einer kritischen Fluenz, die von der Zahl der Grenzflächen abhängig ist, einen Phasenübergang von polykristallin zu amorph. Die Sättigungsmagnetisierung verschwindet ab einer Ta-Konzentration von etwa 10–15 Atom-% in den Py-Schichten. Die Proben besitzen eine kleine uniaxiale Anisotropie, die praktisch unbeeinflusst von der Fluenz ist, sich jedoch mit steigender Zahl an Py/Ta-Grenzflächen leicht verringert. Neben den statischen sind auch die dynamischen magnetischen Eigenschaften der Proben untersucht worden. Der Gilbert-Dämpfungsparameter α erhöht sich sowohl mit steigender Zahl an Py/Ta-Grenzflächen als auch mit höheren Fluenzen, wobei Erstere einen größeren Einfluss hat. Die inhomogene Linienverbreiterung ΔB0 nimmt ebenfalls mit steigender Zahl an Py/Ta-Grenzflächen zu, verringert sich jedoch bei größeren Fluenzen leicht.

The presented thesis includes investigations to fully characterize the electronic structure and magnetic properties ofselected manganese containing high-spin molecules by means of various X-ray spectroscopic, magnetic and theoretical methods. The investigations on the Mn4 star-shaped molecule havelead to a number of interesting results. Magneto-chemical studies exhibit very weak exchange coupling constantsbetween the four Mn(II) ions, leading to complicated low lying states in which the ground state is not well separated, resulting from a dominant weak ferromagnetic coupling and a giant moment of up to 20 µB/f.u. XMCD measurements revealed that almost the completemagnetic moment is located around the Mn(II) ions.This is in agreement with only a few charge transfer states foundwithin the detailed X-ray absorption spectroscopic study. The electronic structure and detailed magnetic properties of the star-shaped heteronuclear CrIIIMnII3 complex have been precisely investigated.With XPS the homovalency of Mn and Cr have been verified. The XA-spectra of the manganese and chromium L edges were measured and compared to earlier investigated Mn4 spectra.The combination high-magnetic field magnetic measurements and element selective XMCD of Mn and Cr L edges and quantum model calculations lead to a complete analysis of the magnetic structure of the CrMn3 magnetic core. The III valence state of the manganese ions in MnIII6O2Salox has been verified. From X-ray diffraction, typical Jahn-Teller distorted oxygen octahedra have been found for Mn(III) ions. Comparisons of XPS and XAS spectra of the complex to corresponding spectraof maganite and tetranuclear manganese(II) cluster it was definitely possible to identify MnIII6O2Salox as a pure Mn(III) compound.