Nd28Fe66B6/Fe50Co50双层纳米复合膜的结构和磁性

利用磁控溅射法制备了Nd28F66B6/Fe50Co50双层纳米复合磁性薄膜,研究了其结构和磁性.经873K退火处理15min后,利用x射线衍射仪测定薄膜晶体结构,采用俄歇电子能谱仪估算薄膜厚度和超导量子干涉仪测量其磁性.磁性测量表明,1)该系列薄膜具有垂直于膜面的磁各向异性.从起始磁化曲线和小回线的形状特征可知,矫顽力机制主要是由畴壁钉扎控制.2)对于固定厚度(10nm)层的硬磁相Nd-Fe-B和不同厚度(dFeCo=1-100nm)层软磁相FeCo双层纳米复合膜,剩磁随软磁相FeCo厚度的增加快速增加,而矫顽力则减少.当dFeCo=5nm时,最大磁能积达到160×103A/m.磁滞回线的单一硬磁相特征说明,硬磁相Nd-Fe-B层和软磁相FeCo层之间的相互作用使两相很好地耦合在一起.剩磁和磁能积的提高是由于两相磁性交换耦合所致.     

Nd-Fe-B/FeCo多层纳米复合膜的结构和磁性

制备了Nd₂₈Fe₆₆B₆/Fe₅₀Co₅₀多层纳米复合磁性薄膜，对溅射态和650℃退火处理15 min试样的相成分分析和微结构的观察显示，溅射态薄膜呈非晶态，经650℃退火处理15 min后，薄膜主要相成分为硬磁性Nd₂Fe₁₄B相和软磁性相FeCo(110)相.Nd₂Fe₁₄B相呈柱状，其易磁化c轴垂直于膜面，尺寸约10 nm.在硬磁性相和软磁性相之间存在少量富Nd相和非晶态，富Nd相大小约7 nm.磁性测量和分析表明，1)该系列薄膜退火态具有垂直于膜面的磁晶各向异性.2)对于固定厚度(10 nm)层Nd-Fe-B和不同厚度(t_FeCo=1—100 nm)层FeCo多层纳米复合膜,剩磁随软磁相FeCo 厚度的增加快速增加，而矫顽力则减小.当t_FeCo=5 nm时，最大磁能积达到200 kJ/m³. 3)硬磁相Nd-Fe-B层和软磁相FeCo层之间交换耦合导致剩磁和磁能积增强. 关键词： Nd-Fe-B/FeCo多层纳米复合膜 交换耦合 磁各向异性     

Ag对CoPt/Ag纳米复合膜的结构与磁性的影响

采用直流磁控溅射的方法制备了一系列(CoPt/Ag)_n多层膜，然后在不同温度下 进行了退火处理，并对其结构和磁性做了初步的表征，研究了Ag的含量以及薄膜中每一单元 厚度与总厚度对退火后薄膜的结构以及磁性能的影响.结果表明，膜厚较薄时(大约20 nm)有 利于薄膜沿(001)取向生长，Ag的加入不但能够抑制CoPt晶粒的过分长大还可以诱导薄膜的( 001)取向，使退火后的薄膜在垂直于膜面方向上的矫顽力大大增强.对于特定组分为Co ₄₀Pt₄₃Ag₁₇的薄膜，经600℃退火后已经显示了明显的(001) 取向，垂直于膜面方向上的矫顽力为5.6×10⁵ A/m，饱和磁化强度为0.65T, 并 且磁滞回线具有很好的矩形度，剩磁比(s)为0.95. 关键词： 磁记录材料 磁性薄膜 CoPt/Ag纳米复合膜     

纳米超微晶Fe73.5Cu1Mo3Si13.5B9合金显微结构和磁性的研究

对纳米晶Fe_73.5Cu₁Mo₃Si_13.5B₉合金的原始制备态和各退火态样品进行了室温Mossbauer谱研究,结果表明晶化态的合金存在α-Fe(Si)微晶相和晶界的非晶相。晶相和非晶相内场和面积随退火温度的变化是退火时Cu,Mo,B等成分的扩散和在各相中的再分配引起的。最佳磁性能对应非晶相中的铁量占合金铁总量的30％左右,超微晶合金的双相无规各向异性模型表明,一定量的非晶相对保持纳米晶优异的软 关键词：     

Fe39.4－xCo40Si9B9Nb2.6Cux纳米晶合金的有效磁各向异性研究

采用多晶材料趋近饱和定律研究了非晶Fe_39.4-xCo₄₀Si₉B₉Nb_2.6Cu_x(x=0.5,1,1.5) 合金在不同温度纳米晶化后的有效磁各向异性常数〈K〉.结果表明， Cu含量较低(x=0.5)时，纳米晶粒较大并且在较低的退火温度(550℃)下析出硬磁相，〈K〉随退火温度T_a升高显著增加；随着Cu含量的增加，有效地细化了晶粒，并且抑制了硼化物的析出，〈K〉明显减小.讨论了〈K〉与晶粒尺寸D及初始磁导率的关系. 关键词： 纳米晶 有效磁各向异性 磁导率 FeCo基合金     

衬底层对Fe65Co35合金薄膜结构与磁性的影响

采用磁控溅射法制备了具有不同衬底层(Cu, Co和Ni₈₀Fe₂₀)的FeFe₆₅Co₃₅双层合金薄膜.研究了不同衬底材料以及NiFe衬底层厚度对FeCo合金薄膜结构与磁性的影响.研究结果表明:衬底层的引入可以增加薄膜的面内单轴各向异性,且薄膜的软磁性能显著提升,获得良好软磁性的原因归结为晶粒的细化、层间的偶极相互作用以及表面粗糙度的降低,并且对于相同厚度的不同衬底层, NiFe衬底层对FeCo薄膜软磁性能的提升最为明显;通过改变NiFe衬底层厚度,实现了对薄膜各向异性的调控, NiFe/FeCo表现出良好的高频响应和低的阻尼系数,同时较小的薄膜厚度能够减小涡流损耗,因此,促进了其在高频微波磁性器件方面的应用.     

Co50Fe50-xSix合金的结构相变和磁性

利用实验测量和理论计算相结合的方法,研究了介于B2结构CoFe低有序合金和L2₁结构Co₂FeSi高有序合金之间的Co₅₀Fe_50-xSi_x合金的结构相变、磁相变、分子磁矩和居里温度.采用考虑Coulomb相互作用的广义梯度近似(GGA+U)方法计算了合金的能带结构.研究发现,合金出现较强的原子有序倾向,表现出较强的共价成相作用.合金的晶格常数、磁矩、居里温度随Si含量的增加而线性地降低,极限成分Co₂FeSi合金的分子磁矩和居里温度分别达到5.92μ_B和777 ℃.原子尺寸效应导致合金晶格发生变化,但并未成为居里温度和分子磁矩变化的主导因素.分子磁矩的变化符合Slater-Pauling原理,但发现原子磁矩的变化并非线性,据此提出了共价成相对磁性影响的观点.采用Stearns理论解释了居里温度的变化趋势,排除了原子间距对居里温度的主导影响作用.能带计算的结果还表明,Co₂FeSi作为半金属材料并非十分完美,可能在实际应用中会出现自旋极化率降低的问题.发现该系列合金的结构相变和磁相变随着成分的变化聚集在窄小的成分和温度范围内. 关键词： 磁性 Heusler合金 结构相变     

Fe2O3/Au/Ag磁性核壳纳米粒子的制备及其SERS研究

本文介绍了一种制备多功能磁性Fe2O3/Au/Ag纳米粒子的简捷方法, 制备的粒子直径大约在100 nm左右, 采用UV-vis和SEM对该结构进行了表征。并通过调节硝酸银的用量, 制备了一系列具有不同壳层厚度和表面结构的多重核壳纳米粒子。以苯硫酚(TP)为探针分子, 研究了不同银壳厚度的磁性纳米粒子的表面增强拉曼散射(SERS)活性。结果表明随Ag:Au比例的不断增加, 其SERS活性呈现先增大后减小的趋势, 这与表面结构的改变有关。     

纳米晶复合SrFe12O19γ-Fe2O3永磁铁氧体的制备和交换耦合作用

采用solgel方法制备M型六角锶铁氧体.利用X射线衍射,透射电子显微镜和VSM对纳米晶样品进行了研究.当焙烧温度小于或等于800℃,样品存在复相.在同样条件下,压成薄片的样品呈现了硬磁与软磁SrFe12O19γFe2O3的纳米复合相的磁性交换耦合作用.800℃焙烧的薄片样品的比饱和磁化强度σS为75.6A·m2kg,内禀矫顽力HcJ为478.9kAm,最大磁能积(BH)max为14.9kJm3,而粉末样品相应的分别为75.9A·m2kg,509.6kAm和12.1kJm3.当焙烧温度大于850℃时,只有 关键词： 六角锶铁氧体 纳米复合 交换耦合 磁性     

非晶Nd3Fe81B16合金的晶化及其对磁性和M?ssbauer谱的影响

本文报道利用单辊方法制备的非晶Nd₃Fe₈₁B₁₆合金的晶化及其对磁性和M?ssbauer谱的影响。发现在非晶Fe₈₁B₁₉合金中用3at％Nd取代B,使非晶Fe₈₁B₁₉合金的晶化温度提高88℃。在适当的退火条件下晶化后样品在室温下的磁性是:σ_s=189emu/g,σ_r/σ_s=0.7,_iH_c=2.15kOe,B_r≈12kG,_bH_c=2kOe,(BH)_max≈8MGOe。与目前广泛使用的六角铁氧体相比,_bH_c相近,但B_r和(BH)_max远比六角铁氧体高。这种材料仅含有少量的Nd,因此可能开发为一种新的廉价永磁材料。本文对少量Nd的添加对非晶FeB合金的晶化温度,磁性和M?ssbauer谱的影响进行了讨论。初步探讨了高矫顽力的来源,认为它的磁化和反磁化过程可以用畴壁钉扎理论解释。 关键词：     

Improvement of the magnetic properties of Nd9.5Fe81Zr3B6.5 nanocomposite magnets by semi-melt spinning

Nd_9.5Fe₈₁Zr₃B_6.5 ribbons are prepared by single roller melt-spinning technique at 1150 °C which is in the solid and liquid coexistence zone. The phase evolution and magnetic properties were studied by X-ray diffraction, differential scanning calorimetry, transmission electron microscopy observations, and magnetization measurements. The experimental results show that in comparison to the ribbons quenching at higher temperature, the thickness of ribbons prepared at 1150 °C are insensitive to the wheel speed and an uniform nanoscale structure with fine grains can be obtained directly from the semi-melt and the exchange coupling interaction between the grains was enhanced for the nanocomposite permanent alloy which can contributed to excellent magnetic properties.     

Effects of oblique-incidence evaporation on magnetic properties of Fe20Ni80/Fe70Co30 bilayer film

Evaporative deposition at oblique incidence is shown to enhance the magnetic anisotropy of an Fe₂₀Ni₈₀ magnetic film and induce magnetic anisotropy in an overlying, strongly isotropic Fe₇₀Co₃₀ film. This deposition method for the formation of an underlayer of several lattice parameters in thickness and semi-hard overlayer of a few thousands Angstroms in thickness achieves a significant change in the magnetization process and strong suppression of the coercive forces of Fe₇₀Co₃₀ in the hard magnetization direction. Soft magnetization of the Fe₇₀Co₃₀ overlayer is not achieved when one of the layers is deposited at oblique incidence. It is anticipated that shape magnetic anisotropy is responsible in part for the magnetic anisotropy induced in both in Fe₂₀Ni₈₀ under- and Fe₇₀Co₃₀ overlayer by oblique incidence evaporation.     

Domain structures of Nd13Fe80B7 magnets during HDDR process

The domain structures of Nd13Fe80B7 alloy at different stages of the HDDR process have been revealed using a magnetic force microscope. In the as-cast samples, the columnar crystals with easy axis perpendicular to one another are clearly characterized by their different domain structures. For the insufficient and sufficient HD treatment, an obvious change of domain structure occurs, which is related to the variation of composition and crystalline microstructure during the HD process. And for the samples after sufficient DR processing, it is confirmed that the configuration of the columnar crystals is retained by the detected domain structures.     

纳米复合永磁Pr9Fe74Co12B5Snx(x=0, 0.5)的磁化行为与磁黏滞性

用熔体快淬法制备了纳米复合永磁样品Pr₉Fe₇₄Co₁₂B₅ 与Pr₉Fe₇₄Co₁₂B₅Sn_0.5，分析了样品的起始磁化、反磁化过程，测得样品的总磁化率、可逆磁化率以及样品的磁黏滞性.结果表明，两样品在室温下均表现为单一硬磁相磁化行为，在低温下表现为双相行为，且由于添加Sn后使晶粒均匀化从而导致样品低温下的双相行为更加明显.添加Sn后引起样品中软磁相含量和软磁相晶粒尺寸的增加，使磁化反转中可逆磁化部分增多，且使反磁化形核场降低.磁黏滞性研究表明，热激活体积与软磁相晶粒的大小有关. 关键词： 纳米复合永磁 磁化反转 磁粘滞     

Co0.9Fe0.1薄膜面内元素分辨的磁各向异性

利用X射线磁性圆二色技术对Co_0.9Fe_0.1薄膜面内元素分辨的磁各向异性进行了研究，通过剩磁模式测量不同磁化方向的样品组分原子单位空穴磁矩的变化，发现除了在生长的磁诱导方向存在易磁化轴外，在与该轴垂直的方向还存在一个类似易轴的软磁化轴；面内的两个难磁化轴与易磁化轴取向大约成66°夹角，从而构成了面内双轴磁各向异性；对不同组分元素，其单位空穴磁矩随磁化方向的变化趋势基本相同，不同磁化方向Fe原子单位空穴的磁矩值约为Co的对应值的87%，反映了Fe原子和Co原子之间存在着强烈的铁磁性耦合. 关键词： 磁各向异性 X射线磁性圆二色 铁磁耦合 CoFe合金薄膜     

BiFeO3/Ni81Fe19磁性双层膜中的交换偏置及其热稳定性研究

研究了磁场诱导生长的BiFeO₃/Ni₁₈Fe₁₉磁性双层膜中 的交换偏置及其热稳定性. 结果表明: BiFeO₃/Ni₁₈Fe₁₉双层膜中的交换偏置场H_ex未表现出明显的磁练习效应. 在负饱和磁场等待过程中, BiFeO₃/Ni₁₈Fe₁₉双层膜磁滞回线的前支和后支曲 线都随着在负饱和磁场中等待时间t_sat的增加向正场方向偏移. 交换偏置场H_ex的大小随着等待时间t_sat的增加而减小, 矫顽力H_c基本不变. 交换偏置场H_ex的大小随测量温度T_m的升高变化不明显, 表现出良好的热稳定性; 但矫顽力H_c随T_m的升高而显著减小. 良好的热稳定性应该来源于铁电性和反铁磁性间的共同耦合作用. 关键词： 多铁性 磁性薄膜 交换偏置 热稳定性     

Preparation,microstructure, and magnetic properties of a nanocrystalline Nd12Fe82B6 alloy by HDDR combined with mechanical milling

Nanocrystalline Nd₁₂Fe₈₂B₆ (atomic ratio) alloy powders with Nd₂Fe₁₄B/α-Fe two-phase structure were prepared by HDDR combined with mechanical milling. The as-cast Nd₁₂Fe₈₂B₆ alloy was disproportionated via ball milling in hydrogen, and desorption–recombination was then performed. The phase and structural change due to both the milling in hydrogen and the subsequent desorption–recombination treatment was characterized by X-ray diffraction (XRD). The desorption–recombination behavior of the as-disproportionated alloy was investigated by differential scanning calorimetry (DSC) and thermal gravimetric analysis (TGA). The morphology and microstructure of the final alloy powders subject to desorption–recombination treatment were observed by scanning electron microscopy (SEM) and transmission electron microscopy (TEM), respectively. The results showed that, by milling in hydrogen for 20 h, the matrix Nd₂Fe₁₄B phase of the alloy was fully disproportionated into a nano-structured mixture of Nd₂H₅, Fe₂B, and α-Fe phases with average size of about 8 nm, and that a subsequent desorption–recombination treatment at 760 °C for 30 min led to the formation of Nd₂Fe₁₄B/α-Fe two-phase nanocomposite powders with average crystallite size of 30 nm. The remanence B_r, coercivity H_c, and maximum energy product (BH)_max of such nanocrystalline Nd₁₂Fe₈₂B₆ alloy powders achieved 0.73 T, 610 kA/m, and 110.8 kJ/m³, respectively.     

Structural transformations and magnetic properties of Fe60Pt15B25 and Fe60Pt25B15 nanocomposite alloys

Structural and magnetic properties of two rapidly solidified and post-annealed Fe₆₀Pt₁₅B₂₅ and Fe₆₀Pt₂₅B₁₅ alloys are compared. The as-quenched Fe₆₀Pt₁₅B₂₅ ribbon was fully amorphous whereas in the Fe₆₀Pt₂₅B₁₅ alloy the amorphous phase coexists with an fcc FePt disordered solid solution. Differential scanning calorimetry curves of both alloys reveal a single exothermal peak with onset temperatures of 873 and 847 K for Fe₆₀Pt₁₅B₂₅ and Fe₆₀Pt₂₅B₁₅, respectively. Magnetically hard, tetragonal ordered L1₀ FePt and magnetically soft Fe₂B nanocrystalline phases were formed due to the annealing of the alloys, as indicated by X-ray diffraction and Mössbauer spectroscopy measurements. Two-phase behavior was detected in the temperature dependence of magnetization of the annealed samples. A magnetic hardening was observed for all annealed ribbons. Magnetic properties of the annealed alloys, studied by hysteresis loop measurements, were related to the differences in the relative fractions of the hard and soft magnetic phases calculated from Mössbauer spectra. The alloy with 25 at% Pt exhibits better hard magnetic properties (H_c=437 kA/m, M_r/M_s=0.74) than the alloy with smaller Pt content (H_c=270 kA/m, M_r/M_s=0.73) mainly due to the larger abundance of the ordered tetragonal FePt phase.