(0 0 1) Exchange-coupled FCC/L10 FePt bilayers

Exchange coupling between hard and soft magnetic materials has implications for both permanent magnet and magnetic recording technologies. This paper looks at exchange coupling of FCC FePt epitaxially grown onto (0 0 1) oriented L1₀ FePt deposited on (0 0 1) MgO substrates at elevated temperature. By varying the thickness of the FCC layer there is a relaxation of the single crystal FCC layer that produces a polycrystalline microstructure as evidenced by the development of rings in the electron diffraction pattern. A concurrent decoupling of the layers is apparent from magnetization curves with two distinct switching fields as the FCC layer thickness is increased above 20 nm. The results shown here confirm the importance of the epitaxial relationship between materials of disparate anisotropies in maintaining strong exchange coupling.     

On the phenomena occurring at the interface between iron and iron–platinum thin films

FePt films were rf sputtered at room temperature and 550?C on MgO monocrystalline substrates. Room temperature films were post-annealed at 550?C. The high temperature growth induces a tetragonal distortion of the structure with the formation of L1₀-FePt phase. Soft iron layers, with different thickness, were e-beam deposited on these hard films. The phenomena occurring at the interface have been analysed and connected with the final magnetic behaviour of the system. It has been found that a strong exchange coupling between soft and hard layers has been established through the formation of an interfacial layer constituted by FePt small particles.     

Exchange-spring magnets based on L10-FePt ordered phase

Thin bi-layers constituted by a hard L1₀-FePt layer and a soft Fe layer were obtained using respectively an rf sputtering device and an UHV e-beam evaporation technique. Magneto-Optical Kerr Effect magnetometry, Atomic/Magnetic Force Microscopy and Conversion Electron Mössbauer Spectroscopy were used in order to correlate the magnetic properties of the bi-layers with the effects of the interdiffusion at the interfaces. It has been found that the evaporated Fe can easily diffuse into the hard film, giving raise to the formation of a region containing small particles of both Fe and Fe-rich FePt which show a superparamagnetic behaviour. The ferromagnetic Fe film can grow only on this region. The system shows (i) a preferred orientation of the easy magnetization axis along the direction normal to the film plane, and (ii) a single-phase magnetic behaviour due to the strong exchange coupling which established between the constituent phases.     

Influence of the phenomena occurring at the interface between L1<Subscript>0</Subscript>-ordered-FePt and Fe on the coercivity behavior

L1₀-ordered FePt/Fe thin bi-layers were grown using a molecular beam epitaxy onto (100)-MgO substrates changing the soft Fe layer thickness. The study of the intermixing phenomena occurring at the hard/soft interfaces was carried out using surface Mössbauer spectroscopy. The magnetic properties of the samples were analyzed with a magneto-optical Kerr effect magnetometer. The surface morphology and the magnetic domains were analyzed with an UHV atomic and magnetic force microscopy in tapping and lift mode respectively.The present work clearly demonstrates that the degree of interface intermixing and reactions is the responsible for the coercivity behavior in exchange-spring magnets.     

Control of crystallographic orientation in L10 FePt films by using Cr and CrW underlayers

The microstructure and magnetic properties of FePt films grown on Cr and CrW underlayers were investigated. The FePt films that deposited on Cr underlayer show (2 0 0) orientation and low coercivity because of the diffusion between FePt and Cr underlayer. The misfit between FePt magnetic layer and underlayer increases by small addition of W element in Cr underlayer or using a thin Mo intermediate layer, which is favorable for the formation of (0 0 1) orientation and the transformation of FePt from fcc to fct phase. A good FePt (0 0 1) texture was obtained in the films with Cr₈₅W₁₅ underlayer with substrate temperature of 400 °C. The FePt films deposited on Mo/Cr underlayer exhibit larger coercivity than that of the films grown on Pt/Cr₈₅W₁₅ because 5 nm Mo intermediate layer depressed the diffusion of Cr into magnetic layer.     

Thickness dependence of microstructure and magnetic properties in FePt/B<Subscript>4</Subscript>C multilayer thin films

FePt/B₄C multilayer films with different single FePt layer thickness were prepared by magnetron sputtering and subsequently annealing in vacuum. Influence of single FePt layer thickness on microstructure and magnetic property of FePt/B₄C films is investigated. Experimental results suggest that the Fe and Pt rich regions will appear in the interior of single FePt layer. The increasing of FePt layer thickness leads to the increase of grain size and volume fraction of order phase f ₀, which eventually induce satisfied coercivity (5.8 kOe).     

缓冲层Ta对FePt薄膜L10有序相转变及矫顽力的影响

制备了Ta/FePt/C系列多层膜，研究了样品在不同温度退火后的磁特性和微结构.实验结果表明，不同厚度的Ta缓冲层具有不同的微结构特征，显著影响FePt层的L1₀有序相的形成及相应的矫顽力.当Ta缓冲层较薄，Ta层为非晶态，且较为粗糙，由此使FePt在界面处产生较多的缺陷并导致较高密度的晶界，在退火过程中，受束缚相对较弱的非晶态的Ta原子比较容易沿FePt的缺陷和晶界处向FePt层扩散，使FePt在相变过程中产生的应力比较容易释放，同时，Ta在扩散过程中产生的缺陷，降低了FePt有序 关键词： FePt薄膜 0相')" href="#">L1₀相 原子扩散     

Electronic states of self stabilized L10 FePt alloy nanoparticles

The ligand capped bimetallic FePt alloys were prepared by using the chemical coreduction method in the presence of oleic acid and oleylamine. An X-ray photoelectron spectroscopy (XPS) study on the as prepared and annealed samples reveals the degradation of hydrocarbon capping with annealing temperature along with a phase transformation to a L1₀ phase. This degradation of organic capping results in formation of capping layer over FePt which has been observed using High Resolution Transmission electron microscopy (HRTEM). This capping layer over the FePt nanoparticles was further investigated with Raman studies confirming the presence of the graphitic carbon. The presence of the graphitic layer enhances the stability of FePt nanoparticles by protecting the surface against oxidation. This was confirmed by the magnetic measurements which show a high coercivity of 11.8 kOe, retained over a period of one year.     

Dependence of microstructure and magnetic properties of FePt films on Cr90Ru10 underlayers

The effect of the thickness of Cr₉₀Ru₁₀ underlayers on the microstructure and magnetic properties of FePt films has been studied. Experimental results showed that the FePt films grown on the Cr₉₀Ru₁₀ underlayers exhibited a (0 0 1) preferred orientation with out-of-plane magnetic anisotropy. The degree of the FePt(0 0 1) preferred orientation was closely related to that of the Cr(0 0 2) preferred orientation. The degree of ordering of the FePt films increased with the thickness of the Cr₉₀Ru₁₀ underlayers. The angular dependence of the coercivity curves suggested that an incoherent curling rotational mode be a dominant magnetic reversal mechanism in the FePt films at various Cr₉₀Ru₁₀ underlayer thicknesses.     

Structural and magnetic properties of RF sputtered FePt/Fe multilayers

Series of [FePt(4min)/Fe(t_Fe)]₁₀ multilayers have been prepared by RF magnetron sputtering and post-annealing in order to optimize their magnetic properties by structural designs. The structure, surface morphology, composition and magnetic properties of the deposited films have been characterized by X-ray diffractometer (XRD), Rutherford backscattering (RBS), scanning electron microscope (SEM), energy dispersive X-ray spectroscope (EDX) and vibrating sample magnetometer (VSM). It is found that after annealing at temperatures above 500 °C, FePt phase undergoes a phase transition from disordered FCC to ordered FCT structure, and becomes a hard magnetic phase. X-ray diffraction studies on the series of [FePt/Fe]_n multilayer with varying Fe layer thickness annealed at 500 and 600 °C show that lattice constants change with Fe layer thickness and annealing temperature. Both lattice constants a and c are smaller than those of standard ones, and lattice constant a decreases as Fe layer deposition time increases. Only a slight increase in grain size was observed as Fe layer decreased in samples annealed at 500 °C. However, the increase in grain size is large in samples annealed at 600 °C. The coercivities of [FePt/Fe]_n multilayers decrease with Fe layer deposition time, and the energy product (BH)_max reaches a maximum in the samples with Fe layer deposition time of 3 min. Comparison of magnetic properties with structure showed an almost linear relationship between the lattice constant a and the coercivities of the FePt phase.     

垂直取向FePt/Ag纳米颗粒薄膜的结构和磁性

用磁控溅射法在单晶MgO(100)基片上制备了［FePt 2 nm/Ag dnm］₁₀多层膜， 经真空热处理后，得到具有高矫顽力的垂直取向L1₀-FePt/Ag颗粒膜.x射线衍射结 果表明，在250 ℃的热基片上溅射，当Ag层厚度d=3—11 nm时，FePt颗粒具有很好的［001］取向，随着Ag层厚度的增加，FePt颗粒尺寸减小.［FePt 2 nm/Ag 9 nm］₁₀经过6 00 ℃真空热处理15 min后，颗粒大小仅约8 nm，垂直矫顽力达到692 kA/m.这种无磁耦合作用的颗粒膜，适合用作超高密度的垂直磁记录介质. 关键词： 磁控溅射 垂直磁记录 纳米颗粒膜 0-FePt/Ag')" href="#">L1₀-FePt/Ag     

各向同性纳米结构Fe-Pt薄膜的结构和磁性

采用直流溅射和热处理技术制备了两个各向同性的纳米结构Fe-Pt永磁合金薄膜系列,并研究了它们的结构和磁性.研究表明,在富Fe双相纳米结构Fe-Pt永磁合金薄膜中,仅由硬磁的FePt相与软磁的Fe₃Pt相组成;在同一系列中,随Fe层厚度的增加,饱和磁极化强度和剩磁明显增大.由Kelly-Henkel图研究指出,在上述Fe-Pt纳米结构永磁合金薄膜中,磁相互作用主要由近邻纳米晶粒间的铁磁交换相互作用控制. 关键词： 磁性薄膜 纳米结构 矫顽力     

Influence of Fe cap layer on the structural and magnetic properties of Fe49Pt51/Fe bi-layers

The influences of an Fe cap layer on the structural and magnetic properties of FePt/Fe bi-layers are investigated. Compared with single FePt alloy films, a thin Fe layer can affect the crystalline orientation and improve the chemical ordering of L10 FePt films. Moreover, the coercivity increases when a thin Fe layer covers the FePt layer.Beyond a critical thickness, however, the Fe cover layer quickens the magnetization reversal of Fe49Pt51/Fe bi-layers by their exchange coupling.     

L10 Stacked Binaries as Candidates for Hard‐Magnets: FePt,MnAl and MnGa

We present a novel approach for designing new hard magnets by forming stacks of existing binary magnets to enhance the magneto crystalline anisotropy. This is followed by an attempt at reducing the amount of expensive metal in these stacks by replacing it with cheaper metal with similar ionic radius. This strategy is explored using examples of FePt, MnAl and MnGa. In this study a few promising materials are suggested as good candidates for hard magnets: stacked binary FePt₂MnGa₂ in structure where each magnetic layer is separated by two non‐magnetic layers, FePtMnGa and FePtMnAl in hexagonally distorted Heusler structures and FePt_0.5Ti_0.5MnAl.     

Structural and magnetic properties of FePt films grown on Cr1-xMox underlayers

FePt films were deposited on Cr_1-xMo_x underlayers by dc magnetron sputtering. The effects of the Mo content in the underlayers, underlayer thickness, substrate temperature, and FePt film thickness on the structural and magnetic properties of the FePt films were studied. Experimental results showed that the (200) textured Cr₉₀Mo₁₀ film was a promising underlayer for promoting the growth of the L1₀ FePt films with (001) preferred orientation at relatively low temperatures. With the Cr₉₀Mo₁₀ underlayers, the ordering process of the FePt films could start at 200 °C. Both the ordering degree and the out-of-plane coercivity (H_c) of the FePt films increased with an increase in substrate temperature. When the substrate temperature was ≥250 °C, the FePt films grown on the Cr₉₀Mo₁₀ underlayers could have the (001) preferred orientation. The FePt films grown on the Cr₉₀Mo₁₀ underlayers at different temperatures showed a continuous microstructure. The out-of-plane coercivities H_c decreased while the ordering degree increased with increased FePt film thickness, which could be due to the variation of the magnetic reversal mechanism from rotation predominant mode to domain wall motion predominant mode. PACS 68.55.Jk; 75.50.Ss     

Enhancement of L10 ordered FePt by Pt buffer layer

L₁₀-ordered FePt thin films prepared by molecular-beam epitaxy on MgO (0 0 1) substrate at 320 °C with different thickness of Pt buffer layer have been investigated. The out-of-plane coercivity increases with increasing thickness of Pt buffer. The maximum values of the long-range order parameter and uniaxial magnetic anisotropy energy are 0.72 and 1.78×10⁷ erg/cm³, respectively, for films with 12 nm thick Pt buffer layer, where the c/a ratio (0.976) shows the minimum value. The reason for the enhancement in ordering is due to the proper lattice strains Pt buffer bestows on FePt layer, these strains are equal to the contraction in lattice parameter c and the expansion in a. Studies of angular-dependent coercivity revealed that the magnetization reversal behaviour shifts from a domain-wall motion dominated case towards a near rotational mode with increasing thickness of Pt buffer layer.     

Effects of Cr underlayer and Pt buffer layer on the interfacial structure and magnetic characteristics of sputtered FePt films

This work develops a new method for growing L1₀ FePt(0 0 1) thin film on a Pt/Cr bilayer using an amorphous glass substrate. Semi-coherent epitaxial growth was initiated from the Cr(0 0 2) underlayer, continued through the Pt(0 0 1) buffer layer, and extended into the L1₀ FePt(0 0 1) magnetic layer. The squareness of the L1₀ FePt film in the presence of both a Cr underlayer and a Pt buffer layer was close to unity as the magnetic field was applied perpendicular to the film plane. The single L1₀ FePt(1 1 1) orientation was observed in the absence of a Cr underlayer. When a Cr underlayer is inserted, the preferred orientation switched from L1₀ FePt(1 1 1) to L1₀ FePt(0 0 1) and the magnetic film exhibited perpendicular magnetic anisotropy. However, in the absence of an Pt intermediate layer, the Cr atoms diffused directly into the FePt magnetic layer and prevented the formation of the L1₀ FePt(0 0 1) preferred orientation. When a Pt buffer layer was introduced between the FePt and Cr underlayer, the L1₀ FePt(0 0 1) peak appeared. The thickness of the Pt buffer layer also substantially affected the magnetic properties and atomic arrangement at the FePt/Pt and Pt/Cr interfaces.     

Assembly of high-anisotropy L10 FePt nanocomposite films

In this paper we report results on the synthesis and magnetic properties of L1₀ FePt nanocomposite films. Three fabrication methods have been developed to produce high-anisptropy FePt films: non-epitaxial growth of (0 0 1)-oriented FePt:X (X=Ag, C) composite films that might be used for perpendicular media; monodispersed FePt(CF_x) core–shell nanocluster-assembled films grown with a gas-aggregation technique and having uniform cluster size and narrow size distribution; and template-mediated self-assembled FePt clusters prepared with chemical synthesis by a hydrogen reduction technique, which has a high potential for controlling both cluster size and orientation. The magnetic properties are controllable through variations in the nanocluster properties and nanostructure. Analytical and numerical simulations have been done for these films, providing better understanding of the magnetization reversal mechanisms. The films show promise for development as magnetic recording media at extremely high areal densities.     

Magnetization reversal in a preferred oriented (111) L1(0) FePt grown on a soft magnetic metallic glass for tilted magnetic recording

L1(0) FePt is an important material for the fabrication of high density perpendicular recording media, but the ultrahigh coercivity of L1(0) FePt restricts its use. Tilting of the magnetic easy axis and the introduction of a soft magnetic underlayer can solve this problem. However, high temperature processing and the requirement of epitaxial growth conditions for obtaining an L1(0) FePt phase are the main hurdles to be overcome. Here, we introduce a bilayered magnetic structure ((111) L1(0) FePt/glassy Fe(71)Nb(4)Hf(3)Y(2)B(20)/SiO(2)/Si) in which the magnetic easy axis of L1(0) FePt is tilted by ~36° from the film plane and epitaxial growth conditions are not required. The soft magnetic underlayer not only promotes the growth of L1(0) FePt with the preferred orientation but also provides an easy cost-effective micro/nanopatterning of recording bits. A detailed magnetic characterization of the bilayered structure in which the thickness of (111) L1(0) FePt with the soft magnetic Fe(71)Nb(4)Hf(3)Y(2)B(20) glassy underlayer varied from 5 to 60 nm is carried out in an effort to understand the magnetization switching mechanism. The magnetization switching behavior is almost the same for bilayered structures in which FePt layer thickness is >10 nm (greater than the domain wall thickness of FePt). For FePt film ~10 nm thick, magnetization reversal takes place in a very narrow field range. Magnetization reversal first takes place in the soft magnetic underlayer. On further increase in the reverse magnetic field, the domain wall in the soft magnetic layer compresses at the interface of the hard and soft layers. Once the domain wall energy becomes sufficiently large to overcome the nucleation energy of the domain wall in L1(0) FePt, the magnetization of the whole bilayer is reversed. This process takes place quickly because the domain walls in the hard layer do not need to move, and the formation of a narrower domain wall may not be favorable energetically. Our results showed that the present bilayered structure is very promising for the fabrication of tilted bit-patterned magnetic recording media.     

Exchange interaction effect of TbCo/FePt bilayers

Interlayer exchange coupling in dc-magnetron sputtered Tb_29.6Co_70.4/FePt bilayers with different annealing temperatures of the FePt film have been investigated. The dependence of ordering degree on perpendicular magnetic properties of the FePt film was studied. The Tb_29.6Co_70.4/FePt film has high perpendicular coercivity and high saturated magnetization about 7.5 kOe, and 302 emu/cm³, respectively as the substrate temperature is 500 °C and annealing at 500 °C for 30 min. It also shows a strong exchange coupling between this FePt layer and Tb_29.6Co_70.4 layer. We also examined the interface wall energy in the exchange coupled Tb_29.6Co_70.4/FePt double layers.