Ce 5d and Fe 3d magnetic profiles in CeH2/Fe multilayers probed by XRMS

The element and electronic shell specificities of X-ray resonant magnetic scattering have been used to investigate the magnetization of Ce 5d and Fe 3d states in [CeH₂(19.6 ?)/Fe(25.4 ?)]*38 a multilayer. We show that the measurement of the magnetic contribution to the intensities reflected at low angles at the Ce L₂ and Fe L_2,3 edges allows us to investigate the profile of the Ce 5d and Fe 3d magnetic polarization. The Fe 3d polarization is found to be uniform across the Fe layer and the Ce 5d polarization appears to be restricted close to the interface with Fe. Received: 22 May 2001 / Accepted: 4 July 2001 / Published online: 5 October 2001     

Spin reorientation transition in Fe/CeH2 multilayers probed by soft X-ray resonant magnetic scattering

The magnetic domain configurations of Fe 3d spins in Fe/CeH₂ multilayers were measured by soft X-ray resonant magnetic scattering. The interface region could be probed by setting up X-ray standing waves due to the multilayer periodicity. By resolving first- and second-order magnetic scattering contributions, we show that the latter probe directly the magneto-crystalline anisotropy which is dominated by the Fe interface layers causing a spin reorientation transition when the temperature is lowered. Received: 30 May 2001 / Accepted: 4 July 2001 / Published online: 5 October 2001     

Ferromagnetism induced by double impurities Mn and Cr in 3C–SiC

Using first principles calculations based on KKR Korringa Kohn Rostoker method related to the Coherent Potential Approximation (CPA), we have investigated the magnetic properties of silicon-carbide doped by transition metals (TM). In addition, for some concentrations of the TM elements (Mn, Cr), we have found that the ferromagnetic states appear in the 3C–Si_1?x?yMnxCr_yC system. Moreover, the total magnetic moment of 3C–Si_1?xTM_xC increases with increasing TM (TM?=?Mn or Cr) concentrations. As well, our results indicate that the Curie temperature of 3C–Si_1?xTM_xC and 3C–Si_1?x?yMnxCr_yC increases with increasing transition metal concentration. Finally, we have found that the double exchange interaction between Cr and Mn is the mechanism responsible for the ferromagnetism in 3C–Si_1?xTM_xC and 3C–Si_1?x?yMn_xCr_yC systems.     

Hydrogen-controlled interlayer exchange coupling in Fe/LaHx multilayers

Magneto-optic Kerr magnetometry and neutron reflectometry reveal that Fe layers exhibit magnetic exchange coupling through LaH_x spacer layers. Ferromagnetic and antiferromagnetic coupling is observed on multilayers of these materials depending on the thickness of the hydride layers, but without oscillatory behavior. Starting from metallic La dihydride spacer layers the effect of dissolving increasingly more hydrogen was examined. Sign and value of the coupling depend crucially on the hydrogen content x. The coupling can be inverted from antiferromagnetic to ferromagnetic and vice versa. These alterations are due to modifications of the electronic structure of the hydride. When the hydrogen absorption saturates the hydride layers become insulating and the exchange coupling is likely to disappear. In this final state the multilayers are always characterized by a very soft ferromagnetic rectangular hysteresis curve. Upon removal of the hydrogen to the initial concentration the original magnetic structure is restored.     

Interface reactions in [Fe/B]<Subscript>n</Subscript> multilayers: a way to tune from crystalline/amorphous layer sequences to homogeneous amorphous Fe<Subscript>x</Subscript>B<Subscript>100-x</Subscript> films

[Fe/B]_{n ≥2} multilayers were prepared by thermal evaporation, ion-beam sputtering and laser ablation. By applying in situ electron spectroscopies (UPS, XPS) and monitoring the electrical resistance during layer growth, evidence could be provided for the occurrence of interface reactions within the range of studied deposition temperatures (77 K ≤T ≤300 K). These reactions result in amorphous Fe_xB_100-x phases, which are spatially restricted to a width of less than 3 nm at the original interface. The amorphicity of the reacted interlayers was unequivocally proven by additional high-resolution electron microscopy (HRTEM) and their characteristically changed magnetic properties. Due to the well-defined width of the interface reaction, homogeneous amorphous Fe_xB_100-x films can be obtained by reducing the individual Fe and B layer thicknesses to below the above reaction depth, while for larger thicknesses layer sequences of the crystalline/amorphous/crystalline type will result. Received: 30 January 2002 / Accepted: 31 January 2002 / Published online: 10 September 2002 RID="*" ID="*"Corresponding author. Fax: +49-731/502-2963, E-mail: hans-gerd.boyen@physik.uni-ulm.de     

Electronic structure and magnetism of disordered bcc Fe alloys

We study the electronic structure and magnetic properties of disordered bcc Co_xFe_1-x, Cr_xFe_1-x and Mn_xFe_1-x alloys in their ferromagnetic phases using the Augmented Space Recursion (ASR) technique coupled with the tight-binding linearized muffin tin orbital (TB-LMTO) method. We calculate the density of states and magnetic moment of these alloys to show the variation upon alloying Fe with the other neighbouring 3d transition metals using arguments based on charge transfer, exchange splitting and hybridization effects. Received 10 April 2001 and Received in final form 15 August 2001     

Mössbauer effect studies of Sm(Rh1−xFex)3B2, x=0.005

Sm(Rh_1–xFe_x)₃B₂ compound (x=0.005) was studied by⁵⁷Fe Mossbauer spectroscopy as a function of temperature. The Fe doped compound has high temperature magnetic transition T_c ^*580 K in addition to the transition at T_c90 K exhibited by the pure SmRh₃B₂ compound. For Tc ^* the spectrum comprises of a quadrupole doublet along with magnetic splitting which merges into a single quadrupole doublet above T_c ^*. The results indicate that Fe induces a large polarization in the Rh-4d band due to the enhanced density of states at the Fermi level in the presence of the hybridized Sm 4f-electrons.     

Transmission X-ray microscopy using X-ray magnetic circular dichroism

X-ray magnetic circular dichroism (X-MCD) was used as a large, element-specific and quantitative magnetic contrast mechanism in the soft X-ray microscopes at BESSY I (Berlin) and the ALS (Berkeley). The present state and potential of magnetic transmission X-ray microscopy (MTXM) is outlined. The possibility to record images in varying magnetic fields and the high spatial resolution down to 25 nm were used to image out-of-plane magnetized (4 ?Fe / 4 ?Gd)×75 systems. Magnetic domains could be studied in arrays of circular and square dots with lateral dimensions down to 180 nm. Hysteresis loops of individual dots were deduced using the direct proportionality of the X-MCD contrast to the sample magnetization. Images of a 3 nmCr / 50 nmFe / 6 nmCr film demonstrate for the first time that MTXM is also able to observe in-plane magnetized domains. In the future the possible applications of MTXM will be extended with regard to the strength of the external field, the available energy range and the sample conditions by building a dedicated transmission X-ray microscope for magnetic imaging at BESSY II. Received: 22 May 2001 / Accepted: 4 July 2001 / Published online: 5 October 2001     

A new study on the catalytic mechanism of Fe-based alloys in diamond formation by Mössbauer spectroscopy

M?ssbauer spectroscopy has been used to systemically study the catalytic mechanism of Fe-based alloys in diamond formation at high temperature–high pressure (HTHP) for the first time. M?ssbauer spectra reveal the magnetic state of the 3d electrons of a Fe atom in the Fe-based alloy catalyst during diamond formation at HTHP. During carburization at lower temperatures than that required for diamond formation and diamond formation in the diamond-stability region using Fe-based alloys as a catalyst, both the quadrupole splitting QS and the isomer shift IS change from negative to positive, especially reaching a state in which they are zero. It was indicated that the state of the 3d-shell electrons of the iron atom changes greatly during carburization and diamond formation and that the incomplete 3d sub-bands of Fe atoms in the catalyst alloys could be filled up in proper order by electrons of interstitial carbon atoms. During diamond formation, the unpaired 3d-shell electrons of an iron atom in the Fe-based alloy absorb and interact with 2P_z electrons of the carbon atoms. There exist a Fe–C bonding and an electron charge transfer stage. The 2P_z electrons of the carbon atoms could be dragged into the metal atoms in the catalyst alloy and would make a transition of triangular (sp²π) hybridization of valence electrons to tetrahedral (sp³) hybridization of valence electrons (a transition of sp²π bonds of graphite to sp³ bonds of diamond), resulting in a transition of graphite structure to diamond. Although the conclusion of this study is strictly applicable only to Fe-based alloy catalysts, it could be considered more general because of the chemical similarities between the transition elements used as solvent catalysts for diamond synthesis. Received: 2 March 2001 / Accepted: 20 August 2001 / Published online: 2 October 2001     

Microstructures and dielectric properties of compositionally graded (Ba1-xSrx) TiO3 thin films prepared by pulsed laser deposition

Compositionally graded (Ba_1-xSr_x)TiO₃ (BST) (x:0.0∼0.25) thin films were grown on Pt (111)/TiO₂/SiO₂/Si (100) substrates using layer-by-layer pulsed laser deposition in the temperature range 550–650 °C. Both downgraded (Ba/Sr ratio varying from 100/0 at the bottom surface to 75/25 at the top surface) and upgraded (Ba/Sr ratio varying from 75/25 at the bottom surface to 100/0 at the top surface) BST films were prepared. Their microstructures were systematically studied by X-ray diffractometry and scanning electron microscopy. A grain morphology transition from large ‘rosettes’ (>0.30 μm) to small compact grains (70–110 nm) was observed in the downgraded BST films as the deposition temperature was increased from 550 to 650 °C. No such grain morphology transition was detected in the upgraded BST films. Dielectric measurements with metal electrodes revealed an enhanced dielectric behavior in the downgraded films. This enhancement is mainly attributed to the large compressive stress field built up near the interface between the downgraded film and substrate. Furthermore, the BaTiO₃ layer in the downgraded BST films not only serves as a bottom layer but also as an excellent seeding layer for enhancing the crystallization of the subsequent film layers in the downgraded films. Received: 10 December 2001 / Accepted: 12 March 2002 / Published online: 19 July 2002 RID="*" ID="*"Corresponding author. Fax: 86-25/359-5535, E-mail: xhzhu@public1.ptt.js.cn     

A Mössbauer study of the quasi two-dimensional antiferromagnet TlFe2−x Se2

TlFe_2?x Se₂ compounds withx from 0.36 to 0.40 have been examined with Mössbauer spectroscopy. The compounds order antiferromagnetically with broad magnetic transition regions whose width increases with decreasing Fe content. The Néel temperature decreases with x and the temperature variation of the magnetic hyperfine field indicates that the transition is of first order. In samples without vacancy ordering the Fe nuclei experience a different temperature variation of the hyperfine field than in compounds with ordered vacancies.     

Spin fluctuation and local magnetism of isolated Fe impurities in Pd<Subscript>1−x</Subscript>V<Subscript>x</Subscript> alloys studied by time differential perturbed angular distribution spectroscopy

The magnetic moment and spin fluctuation temperature of isolated Fe impurity atoms in Pd_1?xV_x (0 ≤ x ≤ 0.15) alloys have been studied by time differential perturbed angular distribution (TDPAD) technique. With increasing V content in Pd matrix, a large non-linear reduction of the local magnetic moment accompanied with an exponential increase of the spin fluctuation temperature T_SF has been observed. At and beyond x = 0.12, the Fe atoms are found to be nonmagnetic. As an important new feature, T_SF is observed to vary quadratically with composition dependent changes in host spin polarization.     

Electronic structure of thin film iron-tetracyanoethylene: Fe(TCNE)<Subscript><Emphasis Type="Italic">x</Emphasis></Subscript>

Thin film iron-tetracyanoethylene Fe(TCNE) _x , x∼2, as determined by photoelectron spectroscopy, was grown in situ under ultra-high vacuum conditions using a recently developed physical vapor deposition-based technique for fabrication of oxygen- and precursor-free organic-based molecular magnets. Photoelectron spectroscopy results show no spurious trace elements in the films, and the iron is of Fe²⁺ valency. The highest occupied molecular orbital of Fe(TCNE) _x is located at ∼1.7 eV vs. Fermi level and is derived mainly from the TCNE⁻ singly occupied molecular orbital according to photoelectron spectroscopy and resonant photoelectron spectroscopy results. The Fe(3d)-derived states appear at higher binding energy, ∼4.5 eV, which is in contrast to V(TCNE)₂ where the highest occupied molecular orbital is mainly derived from V(3d) states. Fitting ligand field multiplet and charge transfer multiplet calculations to the Fe L-edge near edge X-ray absorption fine structure spectrum yields a high-spin Fe²⁺ (3d⁶) configuration with a crystal field parameter 10Dq∼0.6 eV for the Fe(TCNE) _x system. We propose that the significantly weaker Fe-TCNE ligand interaction as compared to the room temperature magnet V(TCNE)₂ (10Dq∼2.3 eV) is a strongly contributing factor to the substantially lower magnetic ordering temperature (T _C ) seen for Fe(TCNE) _x -type magnets.     

Ferromagnetic-to-antiferromagnetic transition in (Hf1−xTix)Fe2 intermetallic compounds induced by geometrical frustration of the Fe(2a) sites

The ferromagnetic-to-antiferromagnetic transition in the hexagonal (Hf_1−xTi_x)Fe₂ (0?x?1) intermetallic compounds has been investigated by ⁵⁷Fe Mössbauer spectroscopy. At 10 K, the transition occurs within rather narrow concentration limits, around x=0.55–0.65. We found that the key factor governing the unexpected quick change of the magnetic structure is the magnetic frustration of the Fe(2a) sites. The magnetic frustration is caused by the noncollinearity of the Fe(6h) magnetic sublattice. The noncollinearity arises from the rotation of the magnetic moments due to the competition between the ferromagnetic exchange interactions and the antiferromagnetic Fe(6h)–Ti–Fe(6h) interaction. In the compounds with x=0.4–0.6, the temperature transitions to the antiferromagnetic state are observed. As an example, the Hf_0.4Ti_0.6Fe₂ compound is completely antiferromagnetic above 200 K.     

Magnetic and electric properties of (Fe,Co)/(Si,Ge) multilayers

We review selected results concerning the interlayer exchange coupling in Fe/Si _x Fe_1−x , Fe/Ge and Co/Si layered structures. Among the ferromagnet/semiconductor systems, Fe/Si structures are the most popular owing to their strong antiferromagnetic interlayer coupling. We show that such interaction depends not only on semiconducting sublayer thickness, but also on deposition techniques and on the chemical composition of the sublayer as well. In similar heterostructures e.g. Fe/Ge, antiferromagnetic coupling was observed only in ion-beam deposited trilayers at low temperatures. In contrast, in Fe/Ge multilayers deposited by sputtering, no such coupling was found. However, when the Ge is partially substituted by Si, antiferromagnetic interlayer coupling appears. For Co/Si multilayers, we observed a very weak exchange coupling and its oscillatory behavior. The growth of Co on Si occurs in an island growth mode. The evolution of magnetic loop shapes can be successfully explained by the interplay between interlayer coupling and anisotropy terms.     

Inscription of holographic gratings using circularly polarized light: influence of the optical set-up on the birefringence and surface relief grating properties

The polarization properties of the optical set-up used for holographic recording of diffraction gratings on azopolymer thin films are analyzed. The state of polarization of circularly polarized light is fully analyzed after reflection on a mirror at various incidences (Lloyd-mirror set-up). The Stokes analysis is performed using a photopolarimeter and the phase shift, the ellipticity and the azimuth orientation are compared with those calculated from Fresnel formulae. At large angles of incidence, an initially right circularly polarized (RCP) beam becomes elliptically polarized with an azimuth of nearly +45°. From these results, holographic diffraction gratings are recorded on an azobenzene-containing polymer thin film using (i) co- and contra-circularly polarized beams and (ii) a right circularly polarized beam interfering with a +45° linearly polarized light beam. Using Jones-matrix formalism, the polarization states of the diffracted orders from the birefringence (Δn) and the surface-relief (2Δd) gratings are derived and compared with experimental measurements. Finally, the induced local birefringences and surface-relief amplitudes are discussed in connection with atomic force microscopy measurements. The diffraction efficiencies obtained under the (+45°+RCP) and (LCP + RCP) (where LCP = left circularly polarized) configurations are thus compared and discussed. Received: 5 October 2001 / Revised version: 26 November 2001 / Published online: 17 January 2002     

Complex magnetism in ultra-thin films: atomic-scale spin structures and resolution by the spin-polarized scanning tunneling microscope

In this paper we present a density functional theory investigation of complex magnetic structures in ultra-thin films. The focus is on magnetically frustrated antiferromagnetic Cr and Mn monolayers deposited on a triangular lattice provided by a Ag (111) substrate. This involves non-collinear magnetic structures, which we treat by first-principles calculations on the basis of the vector spin-density formulation of the density functional theory. We find for Cr/Ag (111) a coplanar non-collinear periodic 120° Néel structure, for Mn/Ag (111) a row-wise antiferromagnetic structure, and for Fe/Ag (111) a ferromagnetic structure as magnetic ground states. The spin-polarized scanning tunneling microscope (SP–STM) operated in the constant-current mode is proposed as a powerful tool to investigate complex atomic-scale magnetic structures of otherwise chemically equivalent atoms. We discuss a recent application of this operation mode of the SP–STM on Mn/W (110), which led to the first observation of a two-dimensional antiferromagnet on a non-magnetic metal. The future potential of this approach is demonstrated by calculating SP–STM images for different magnetic structures of Cr/Ag (111). The results show that the predicted non-collinear magnetic ground state structure can clearly be discriminated from competing magnetic structures. A general discussion of the application of different operation modes of the SP–STM is presented on the basis of the model of Tersoff and Hamann. Received: 07 May 2001 / Accepted: 23 July 2001 / Published online: 3 April 2002     

57Fe Mössbauer study YBa2Cu3−xFexO7−y

Mössbauer measurement is made on the system YBa₂Cu_3?xFe_xO_7?y (0.03≤x≤1.0) at various temperatures. It is found that the sites occupied by Fe ions can be classified into major two and minor one groups. The isomer shifts for the major two groups are nearly zero relative to metallic iron, and their quadrupole splittings are large (about 1.9 and 1.1 mm/s). By comparison of the spectra measured before and after a heat-treatment in vacuum, it is concluded that the Fe ions with the largest quadrupole splitting occupy the pyramidal sites, and the other the planer sites. Two different hyperfine magnetic fields (240 and 442 k0e) are observed at 1.7 K for the specimen with x=0.2. It is proposed that the valence states of Fe ions of the major two groups are pentavalent.     

Reactivity and magnetism of Fe/InAs(100) interfaces

Interface reaction and magnetism of epitaxially-grown Fe on InAs(100) are studied by core-level photoemission (As 3d and In 4d) and Fe 2p X-ray magnetic circular dichroism using synchrotron radiation. The reactivity of Fe/InAs(100) is relatively low compared to that of other interfaces involving deposition of 3d metals on III-V semiconductors. As a consequence, we observe a magnetic signal at Fe L_{2, 3} edges for the lowest thicknesses studied (1 ML). The atomic magnetic moment reaches a value close to that of the bulk α-Fe (2.2 μ _B) for Fe coverages exceeding 5 ML. A ferromagnetic compound with approximate stoichiometry of FeAs is formed at the interface. The orbital magnetism represents between 12 and 20% of the total momentum, due to 3d density of states depletion and to crystal-field modification of the electronic levels. These properties make the Fe/InAs(100) interface very promising for spin-tunneling devices. Received 4 April 2002 / Received in final form 13 May 2002 Published online 31 July 2002