Dans cette thèse nous avons développé trois techniques de mesures dynamiques du renversement de l'aimantation à l'échelle de la nanoseconde en utilisant des micro bobines comme source de champ pulsé. Le comportement dynamique de plusieurs systèmes magnétiques sous la forme de couches minces a été étudié. Avec la technique de Dichroïsme Circulaire Magnétique de Rayons X (XMCD) résolu en temps développée à l'ESRF on obtient la sélectivité en espèce chimique outre à une résolution temporelle de 100 ps. Cela nous a permis d'effectuer des études du renversement de l'aimantation et du couplage dynamique dans des structures du type vanne de spins et jonctions tunnel. Dans certaines conditions de champ pulsé le temps de renversement de l'aimantation de la couche libre (FeNi) est de l'ordre de la nanoseconde. Dans ces structures, suivant l'épaisseur de la couche non magnétique, le couplage dynamique entre les couches libre et dure peut être très différent de celui statique. La technique de mesure dynamique Kerr/Faraday s'est montrée assez efficace pour l'étude dynamique des couches minces à forte anisotropie perpendiculaire grâce aux possibilités de champs importants (jusqu'à 10 T) associées à une haute sensibilité (~2 x 10(+8) µB). Avec la technique d'imagerie Kerr/Faraday résolue en temps on a pu suivre le renversement d'un grenat magnétique suite à une impulsion de champ. Les processus du renversement sont facilement identifiés par la visualisation dynamique des domaines magnétiques. Avec les micro bobines développées en collaboration avec le LETI, nous avons pu montrer la possibilité d'obtenir des champs magnétiques très forts (jusque 50 T) à un très bas coût comparé aux installations conventionnelles. Pour la suite de ce travail nous envisageons le développement d'une technique d'imagerie dynamique avec haute résolution spatiale (dizaine de nm) et sélectivité chimique basée sur un microscope PEEM (Microscope à photoémission d'électrons).

Le système des nano-colonnes auto-assemblées de GeMn, riches en Mn et entourées d'une matrice de germanium quasi pure, est un matériau prometteur pour la spintronique. Selon les paramètres de croissance, les échantillons contiennent des nano-colonnes de type cohérents sur la matrice de Ge, de type amorphe, ou/et des nano-inclusions de Ge3Mn5. Ce manuscrit présente notre étude des propriétés électroniques, magnétiques et structurales des nano-colonnes de GeMn à l'aide du rayonnement synchrotron. Les mesures de la diffusion et diffraction des rayons X en incidence rasante dans des échantillons contenant des nano-colonnes cohérentes et sans précipités de Ge3Mn5 montrent un certain désordre dans les nano-colonnes. Les cartographies de l'espace réciproque ont pu être quantitativement expliquées en considérant la déformation de la matrice de germanium due à l'inclusion des nano-colonnes dans celle-ci, ainsi que par leurs corrélations de position, sans avoir recours à d'autres phases cristallines. La spectroscopie d'absorption et le dichroïsme circulaire magnétique de rayons X ont permis de sonder spécifiquement les propriétés magnétiques des atomes de Mn dans des échantillons sans précipités de Ge3Mn5. On observe une allure des spectres XAS-XMCD des nano-colonnes très similaire à celle observée dans le cas de Ge3Mn5. Le moment magnétique local sur le manganèse possède une composante orbitale faible mais non-nulle et une amplitude totale (0.8 +/- 0.1 µB) plus faible que celle attendue pour Ge3Mn5 (~2.6 µB) ou pour des atomes de Mn substitutionnels (~3 µB). Ceci indique une origine différente de la phase des nano-colonnes. Les spectres XAS-XMCD ont été calculés pour différentes structures modèles, incluant des défauts simples ainsi de nouvelles phases cristallines, les paramètres critiques des calculs ayant été identifiés. Le meilleur accord est observé pour une nouvelle phase de type Ge2Mn.

<p>In this Thesis the magnetic and structural properties of thin epitaxial Fe, Co, and Ni films are discussed. Some of the in-situ prepared samples were used to characterize the degree of circular polarization of the newly installed beamline D1011 at MAX-lab. By means of x-ray magnetic circular dichroism (XMCD) and utilizing the associated magneto optic sum rules, the orbital (<i>m</i><i>l</i>) and spin (<i>m</i><i>s</i>) moments are determined directly in <i>m</i><i>B</i>/atom with elemental specificity. The extended x-ray absorption fine structure (EXAFS) measurements yield site specific information on the local crystallographic structure.</p><p>These measurements were performed using the circular x-rays of several beamlines. The influence of the degree of spatial source coherence <i>l</i><i>spat</i> of the x-rays was characterized by means of Fresnel diffractometry. A correlation between enhanced XAS white line intensities and higher values of <i>l</i><i>spat</i> was established for 20 ML Fe, Co, and Ni films on Cu(100).</p><p>The degree of circularly polarized x-rays (<i>P</i><i>c</i>) at beamline D1011 at MAX-lab was characterized by studying Fe films on Cu(100) by means of XMCD. The maximum value of <i>P</i><i>c</i> is experimentally determined to <i>P</i><i>c</i> =0.85.</p><p>The Au/Co/Au trilayer system was studied as a function of Co thickness, temperature, and Au cap thickness. A 10 mono-layer (ML) Co film, with an Au cap of 20 Å, shows a spin reorientation transition (SRT) from an in-plane to an out-of-plane easy direction as the temperature is lowered from 300 K to 200 K. The magnetic properities of these Co films are very different to what is found for bulk samples due to, in particular, the broken symmetry at the interfaces.</p><p>The thickness dependent spin reorientation transition in the Fe/Ag(100) system was characterized by means of XMCD and EXAFS measurements. 3 ML Fe films show an out-of-plane easy direction with an 125% enhanced orbital moment as compared to the 25 ML Fe in-plane film. Simulations of the Fe <i>L</i>-edge EXAFS indicate the bulk Fe bcc structure for film thicknesses of 6-25 ML Fe. For 3 ML Fe strong deviations from this bcc phase is observed.</p><p>Ultrathin Co films deposited on flat and vicinal Cu(111) in the thickness region 1-25 ML were studied by means of XMCD and scanning tunneling microscopy (STM). The vicinal Cu(111) Co deposition leads to the formation of elongated islands preferentially oriented along the step edges. In connection to this particular Co growth mode we observe an increase of both the orbital and the spin moment on the vicinal Cu(111) of about 25% relative to what was observed for Co on flat Cu(111).</p>

<p>In this thesis the magnetic and structural properties of ultra-thin 3d transition metals films have been investigated, in particular Fe, Ni and Co films. X-ray Magnetic Circular Dichroism (XMCD) has provided element specific spin (m_s ) and orbital (m_l ) moments per atom by utilizing the magneto optic sum-rules. Element specific hysteresis curves have been measured by means of X-ray Resonant Magnetic Scattering (XRMS), and the local crystallographic structure has been investigated using Extended X-ray Absorption Fine Structure (EXAFS). </p><p>By performing XMCD on Fe/Ag(100) we observe a spin reorientation from in-plane to out-of-plane as the Fe thickness is lowered. At temperatures below 300K it occurs around 5-7 mono layers (ML) of Fe. While reorienting the magnetization out-of-plane the orbital moment increases with 125% but only a minor increase (5%) of the spin moment is observed. Extended X-ray Absorption Fine Structure (EXAFS) measurements indicate that films 6 ML and thicker have a bulk-like bcc structure. For the thin out-of-plane films, the local crystallographic structure is more complicated. </p><p>The spin reorientation of the Au/Co/Au tri-layer system has been studied as a function of temperature, Co layer and Au cap thickness. An unexpected behavior of the orbital moment upon spin reorientation is found in these systems. An ex-situ prepared sample shows a smooth spin reorientation from an in-plane to an out-of-plane easy magnetization direction as the temperature is lowered from 300K to 200K. In-situ prepared samples have also been investigated and a novel phase diagram has been identified. The Au/Co interface has been explored during the Au capping by means of photoemission measurements. </p><p>In the bi- and tri-layer system of Fe and Ni we have been able to manipulate the spin reorientation by varying the Fe and Ni thickness. A novel non-collinear interlayer exchange interaction for 3d ferro magnets in direct contact has been discovered for a set of samples. This exchange interaction is found to be strongly dependant on the preparation conditions.</p>

Materials exhibiting new functionalities due to interdependent electric (e.g. conductivity) and magnetic properties are potentially interesting for spintronics applications. We have investigated electronic and magnetic properties by means of x-ray spectroscopies and SQUID magnetometry in several magnetic materials, often in the form of thin films, which have shown promising properties for applications. One of the main subjects has been studies of inter-diffusion between layers in multilayer structures, which is an important factor for spin-dependent transport and magnetic properties. These studies have been performed by high kinetic (HIKE) photoemission spectroscopy where high photon energies increase the bulk sensitivity in comparison to soft x-ray photoemission spectroscopy. Cu/Ni multilayers were studied mainly as a model system and revealed a diffusion process that was dependent on layer thicknesses and capping materials. CoFeB/MgO/CoFeB, which is used as a magnetic field sensor in hard drives, has recently been shown to exhibit a perpendicular magnetic anisotropy (PMA) switchable by electric fields. We have studied both the interface quality and magnetic properties of thin CoFeB layers exhibiting PMA. Layered structures of full Heusler alloys Co2MnGe/Rh2CuSn have been proposed as a promising candidate for current-perpendicular-to-plane giant magneto-resistance sensors. Using HIKE,we have shown that diffusion of atoms, mainly Mn, occurs at temperatures lower than what is used in device fabrication, which likely contributes to the limited magneto-resistance values obtained. Lately, a large body of research has been performed on semiconductors doped with transition metal elements with the hope to find a ferromagnetic semiconductor at room temperature, a foundation for new devices combining spin and charge in their functionality. We have investigated Co and Fe doping in ZnO for different concentrations of the dopants and different annealing temperatures. The Co and Fe atoms are shown to forms clusters for which antiferromagnetic interactions are dominating.

In this Thesis the magnetic and structural properties of thin epitaxial Fe, Co, and Ni films are discussed. Some of the in-situ prepared samples were used to characterize the degree of circular polarization of the newly installed beamline D1011 at MAX-lab. By means of x-ray magnetic circular dichroism (XMCD) and utilizing the associated magneto optic sum rules, the orbital (ml) and spin (ms) moments are determined directly in mB/atom with elemental specificity. The extended x-ray absorption fine structure (EXAFS) measurements yield site specific information on the local crystallographic structure. These measurements were performed using the circular x-rays of several beamlines. The influence of the degree of spatial source coherence lspat of the x-rays was characterized by means of Fresnel diffractometry. A correlation between enhanced XAS white line intensities and higher values of lspat was established for 20 ML Fe, Co, and Ni films on Cu(100). The degree of circularly polarized x-rays (Pc) at beamline D1011 at MAX-lab was characterized by studying Fe films on Cu(100) by means of XMCD. The maximum value of Pc is experimentally determined to Pc =0.85. The Au/Co/Au trilayer system was studied as a function of Co thickness, temperature, and Au cap thickness. A 10 mono-layer (ML) Co film, with an Au cap of 20 Å, shows a spin reorientation transition (SRT) from an in-plane to an out-of-plane easy direction as the temperature is lowered from 300 K to 200 K. The magnetic properities of these Co films are very different to what is found for bulk samples due to, in particular, the broken symmetry at the interfaces. The thickness dependent spin reorientation transition in the Fe/Ag(100) system was characterized by means of XMCD and EXAFS measurements. 3 ML Fe films show an out-of-plane easy direction with an 125% enhanced orbital moment as compared to the 25 ML Fe in-plane film. Simulations of the Fe L-edge EXAFS indicate the bulk Fe bcc structure for film thicknesses of 6-25 ML Fe. For 3 ML Fe strong deviations from this bcc phase is observed. Ultrathin Co films deposited on flat and vicinal Cu(111) in the thickness region 1-25 ML were studied by means of XMCD and scanning tunneling microscopy (STM). The vicinal Cu(111) Co deposition leads to the formation of elongated islands preferentially oriented along the step edges. In connection to this particular Co growth mode we observe an increase of both the orbital and the spin moment on the vicinal Cu(111) of about 25% relative to what was observed for Co on flat Cu(111).

In this thesis the magnetic and structural properties of ultra-thin 3d transition metals films have been investigated, in particular Fe, Ni and Co films. X-ray Magnetic Circular Dichroism (XMCD) has provided element specific spin (ms ) and orbital (ml ) moments per atom by utilizing the magneto optic sum-rules. Element specific hysteresis curves have been measured by means of X-ray Resonant Magnetic Scattering (XRMS), and the local crystallographic structure has been investigated using Extended X-ray Absorption Fine Structure (EXAFS). By performing XMCD on Fe/Ag(100) we observe a spin reorientation from in-plane to out-of-plane as the Fe thickness is lowered. At temperatures below 300K it occurs around 5-7 mono layers (ML) of Fe. While reorienting the magnetization out-of-plane the orbital moment increases with 125% but only a minor increase (5%) of the spin moment is observed. Extended X-ray Absorption Fine Structure (EXAFS) measurements indicate that films 6 ML and thicker have a bulk-like bcc structure. For the thin out-of-plane films, the local crystallographic structure is more complicated. The spin reorientation of the Au/Co/Au tri-layer system has been studied as a function of temperature, Co layer and Au cap thickness. An unexpected behavior of the orbital moment upon spin reorientation is found in these systems. An ex-situ prepared sample shows a smooth spin reorientation from an in-plane to an out-of-plane easy magnetization direction as the temperature is lowered from 300K to 200K. In-situ prepared samples have also been investigated and a novel phase diagram has been identified. The Au/Co interface has been explored during the Au capping by means of photoemission measurements. In the bi- and tri-layer system of Fe and Ni we have been able to manipulate the spin reorientation by varying the Fe and Ni thickness. A novel non-collinear interlayer exchange interaction for 3d ferro magnets in direct contact has been discovered for a set of samples. This exchange interaction is found to be strongly dependant on the preparation conditions.

Cette thèse concerne l'étude des transformations structurelles et magnétiques qui se produisent dans les métaux 3d quand ils sont comprimés jusqu'à des pressions extrêmes. L'étude a été réalisée en utilisant les techniques de polarisation absorption des rayons X (Dichroïsme circulaire magnétique de rayons X ou XMCD) et diffraction des rayons X couplées à les calculs DTF, et appliquée à les cas du cobalt, du nickel et des alliages de fer et cobalt (FeCo). En particulier, pour le cobalt, on présente la première preuve expérimentale de la suppression du son ferromagnétisme induite par la pression et on explore la relation entre les changements structurels et magnétique. Le cas du nickel, qui est structurellement stable sur une large gamme de pressions, permet d'aller plus loin dans l'interprétation du signal XMCD à la seuil K, encore débattue aujourd'hui. Enfin l'enquête sur les alliages FeCo vise à comprendre le rôle joué par l'ordre chimique dans les propriétés de réglage haute pression structurales et magnétiques.

The magnetic and structural properties of nano magnet arrays and ferromagnetic thin films are investigated. Circular x-rays are used and extensive use is made in this Thesis of the X-ray Magnetic Circular Dichroism (XMCD) technique. By means of the XMCD magneto-optic sum rules the values of the orbital and spin moments are determined. In the case of the nano magnet arrays studied, the XMCD technique is used in a spatially resolved mode using Photo Electron Emission Microscopy (PEEM) after circular light excitation. The Extended X-ray Absorption Fine Structure (EXAFS) is studied in both the Co K- and L-edges. In situ Co L-edge X-ray XMCD spectroscopy measurements are presented, in combination with spectro-microscopy results, on Co/Pt and Co/Au based nano-dot arrays, of typical dot lateral size 250×100 nm2, on self organized Si0.5Ge0.5. The Co is only a few atomic layers thick. The dot arrays display a high degree of lateral order and the individual dots, in several cases, exhibit a stable magnetic moment at 300 K. It is found possible to characterize the spin reorientation of these dot arrays. For both systems the in- versus out-of-plane orbital moment anisotropy, is not always related with an out-of-plane magnetization and the occurrence of a spin reorientation. By performing Co K-edge EXAFS measurements the local atomic structure around the Co atoms is characterized. The feasibility of a high precision quantitative structural analysis of L-EXAFS is studied on the system Au/Co/Au/W(110). The spin reorientation transition is studied as a function of the Co thickness and Au cap thickness. The L-edge EXAFS indicates that this reorientation is correlated to a lattice expansion in the perpendicular direction. High precision angle dependent XMCD work is performed on a high temperature exchange bias system. Pinned or frozen magnetic moments are studied within an exchange biased NiFe ferromagnet at the NiFe/FeMn, ferromagnet/antiferromagnet interface by XMCD and complemented by x-ray resonant reflectivity experiments, at the Ni, Fe and Mn L-edges. The Mn L-edge XMCD MnSb and of (Ga, Mn)As layers modified by high temperature annealing is studied. For MnSb an enhanced value is obtained versus theoretical calculations. This result can be explained by means of the enhanced surface to volume ratio for the samples studied. For (Ga, Mn)As differences are found in the local environment of the Mn atoms upon annealing.

Les analogues du bleu de Prusse contenant du Fe et du Co (Fe/Co PBA) sont des complexes moléculaires qui présentent des propriétés physiques bistables. Par conséquent, ils sont considérés comme des candidats potentiels pour le stockage d'informations à base de molécules. Cette thèse vise à étudier la structure électronique et magnétique de Fe/Co PBA en utilisant des techniques expérimentales et théoriques avancées. Les techniques X-ray Absorption Spectroscopy (XAS) et X-ray magnetic circular dichroism (XMCD) combinées avec la théorie des multiplets en champ de ligands (LFM) sonde le changement dans les propriétés magnétiques macroscopiques de Fe/Co PBA et peuvent donner des informations locales sur les centres métalliques des complexes. Le composé tridimensionnel RbCoFe PBA, deux complexes de dinucléaire photomagnétiques et les précurseurs de Fe sont étudiés. L'étude de XMCD combinée avec la LFM a révélé une grande valeur du moment magnétique d'orbite du précurseur FeTp. Une étude détaillée a été effectuée pour vérifier les règles de somme d'orbite et de spin dans le cas des ions de Fe(III) bas spin et il a été constaté que la règle spin somme n'était pas valide à cause de l'entremélange des seuils L2 et L3. L'enquête XMCD des complexes dinucléaires photomagnétiques a confirmé le transfert d'électrons métal-métal. Cette enquête XMCD de la plus petite unité de la famille Fe / Co PBA est utile pour comprendre les propriétés magnétiques de la famille de Fe / Co PBA. L'étude XMCD sur aux seuils K du Fe et du Co d'un composé tridimensionnel RbCoFe PBA a prouvé l'existence d'une interaction antiferromagnétique entre les ions métalliques de Fe et de Co dans l'état photoinduit. / The Fe/Co Prussian Blue Analogues (PBA) are molecular complexes that exhibit externally controlled bistable physical properties. Thus, they are considered as potential candidates for photoswitchable molecule-based information storage. This thesis aims to investigate the electronic and magnetic structure of Fe/Co PBA using advanced experimental and theoretical techniques. X-ray Absorption Spectroscopy (XAS) and X-ray Magnetic Circular Dichroism (XMCD) techniques combined with Ligand Field Multiplet (LFM) theory probe the change in the macroscopic magnetic properties of PBA and can give local information about the metal centers existing in the complexes. The XAS and XMCD spectra at Fe and Co L2,3 edges are simulated using Ligand Field Multiplet (LFM) Calculations. The tridimensional RbCoFe PBA, two photomagnetic dinculear complexes and the building blocks Fe-bearing precursors are investigated. The XMCD study combined with LFM investigation revealed a large value of orbital magnetic moment in FeTp precursor of the dinuclear complex. A detailed study has been performed to check for the orbit and spin sum rules in the case of low spin FeIII ions and it was found that the spin sum rule does not hold because of intermixing between L2 and L3 edges. The XMCD investigation of the photomagnetic dinuclear complexes confirmed the metal-to-metal electron transfer. This XMCD investigation of the smallest unit of Fe/Co PBA family is helpful to understand the magnetic properties of the family of Fe/Co PBA. The XMCD study at Fe and Co K edges of a tridimensional RbCoFe PBA proved the existence of an antiferromagnetic interaction between Fe and Co metal ions in the photoinduced state.