H2（V=3）+H2（He）碰撞中的转动能量转移

激发态Na₂与H₂碰撞,使H₂（V=3,J=3）得到布居,在H₂和He总气压为800 Pa及温度为700 K的条件下,利用相干反斯托克斯拉曼散射（CARS）光谱技术研究了H₂（3,3）与H₂（He）间转动能量转移过程.改变CARS激光束与激发Na₂的激光之间的延迟时间,测量He不同摩尔配比时H₂（3,J）态CARS谱强度的时间演化,得到H₂（3,3）的总弛豫速率系数分别为k_3,3^H₂=（21士5）×10^-3cm³·s^-1和k_3,3^H_e=（5.6士1.6）×10^-13cm³·s^-1.测量H₂（3,J）各转动态的相对CARS谱强度,由速率方程分析,得到H₂（3,3）+H₂→H₂（3,J）+H₂中,对于J=2,4,转移速率系数分别为（11±4）×10^-13cm³·s^-1和（8.2±3.1）×10^-13cm³·s_<sup>-1.在H₂（3,3）+He→H₂（3,J）+He中,对于J=2,4,转移速率系数分别为（3.1±1.2）×10^-13cm³·s^-1和（2.1士0.7）×10¹³cm³·s^-1.对于H₂（3,3）,单量子弛豫|△J|=1约占该态总弛豫率的90%.     

磁共振法研究(Fe1-xCox)84Zr3.5Nb3.5B8Cu1纳米晶薄带的磁各向异性

铁磁共振(FMR)实验研究(Fe1-xCox)84Zr3.5 Nb3.5B8Cu1(x=0.0,0.2,0.4,0.6, 0.8)合金薄带的各向异性,易轴在薄带的横向方向,同等宽度样品的各向异性常数K′随Co掺杂量的增加而减小, K′值在4.67×10-5 J/m(x=0.0)到2.54×10-5 J/m4(x=0.8)之间.由于磁化率的虚部χ″(H)随磁场强度H非线性变化,在低场(0-12 mT)有一个与FMR信号强度相当的低场非共振信号.特别是对Fe84Zr3.5 Nb3.5B8Cu1合金薄带的磁化,在可逆磁化(0-2.0 mT)和趋近饱和磁化(9.0-12 mT)区域, dχ″/dH=0;不可逆畴壁移动过程中,交流磁化率虚部χ″(H)与磁场强度的n次方即Hn(n≥3)有关;在磁畴转动过程中χ″(H)正比于H2(瑞利区),(dχ″)/(dH)为常数;而且发现,有不可逆畴壁移动-磁畴转动三段交替变化的过程,此过程对应三种磁畴的消失过程.     

Li2Mo2O6多晶材料的结构与电性能的研究

本文用固相反应烧结制备出Li₂Mo₂O₆多晶材料。经X射线分析、红外光谱和电子顺磁共振谱(EPR)的研究,确定了它的结构是Li₂Mo₂O₄和MoO₂两个晶相组成的烧结体。钼离子以四价状态存在于MoO₂晶相结构中。采用交流阻抗谱分析了晶界与温度变化的相关性。测得了样品的ln(σ_总T)-1/T 曲线是由两段直线和一段曲线所组成;总电导率化能σ_27℃=1.36×10^-3(Ω·cm)^-1,σ_115℃=1.49×10^-3(Ω·cm)^-1,σ_300℃=9.71×10^-3(Ω·cm)^-1,σ_370℃=2.42×10^-3(Ω·cm)^-1;电导活化能E₁=0.043eV,E₂=0.235eV,E_平均=0.76eV。采用维格纳极化电池法测得电子电导率σ_e,σ_e27℃=2.240×10^-5(Ω·cm)^-1,σ_e300℃=4.476×10^-3(Ω·cm)^-1。实验证明,室温下材料为固体电解质,300℃附近为良好的离子与电子混合导体。 关键词：     

钙钛矿（La1-yTby)0.67Sr0.33MnO3的磁致伸缩效应

采用固相反应烧结法制备了（La_1-yTb_y)_0.67Sr_0.33MnO₃系列样品（y=0,0.05,0.15,0.20,0.25,0.33,0.40,0.50,0.60,1.00).X射线衍射表明,随着y值增大钙钛矿型晶体结构从菱面对称性向正交对称性转变.180K时,μ₀H=7T条件下,在y=0.40样品的巨磁电阻可达900％.μ₀H=1.7T时,y=0.20样品的室温磁致伸缩为-50×10^-6.210K时,y=0.33样品的磁致伸缩可达-130×10^-6. 关键词：     

金属玻璃(Fe1-xCox)78Si10B12的感生各向异性

本文研究了金属玻璃(Fe_1-xCO_x)₇₈Si₁₀B₁₂的磁化感生各向异性、应变感生各向异性随成分和温度的变化。磁化感生各向异性常数K_um为正值,x=0.7时为最大;不可逆的应变感生各向异性常数K_usi为正值,x=0.5时为最大;可逆的应变感生各向异性常数K_usr除了x>0.975区均为负值,在x=0.7时为最大;感生各向异性常数在温度变化时与M_s^α成正比,α在3.4和7.5之间随成分和退火工艺而变化。用短程有序模型解释了部分实验结果。 关键词：     

Y3Fe5-xMnxO12的磁结构和磁性能

对多晶Y₃Fe₃Fe_5-xMn_xO₁₂(x=0.05和0.09),得到300K下的中子衍射曲线。发现当x=0.05时,Mn³⁺离子占据16a和24d位置的几率分别为0.72和0.28;当x=0.09时,Mn³⁺离子全部占据16a位置;还得到两种组分16a和24d位置各自的磁矩值。在外磁场(800—10KOe)下测量Y₃Fe_5-xMn_xO₁₂(x=0—0.11)的磁化曲线,温度范围是1.5—300K。得到饱和磁矩值;并利用趋近饱和定律确定1.5K下的磁晶各向异性常数k₁值,发现|k₁|值随含锰量增加而减小。 关键词：     

高位振动态RbH（X1∑+,v"≥15）与CO2碰撞转移中的能量相关性

研究了高位振动态RbH（X¹∑⁺,v″=15～21）与CO₂碰撞转移过程.脉冲激光激发RbH至高位态,利用激光感应荧光光谱（LIF）得到RbH（X¹∑⁺,v″）与CO₂的猝灭速率系数k_v″（CO₂）,k_v″=21（CO₂）=2.7k_vⁿ=15（CO₂）.利用激光泛频光谱技术,测量了CO₂（00⁰,J）高转动态分布,得到了转动温度,从而获得了平均转动能rot>和转动能的变化<△E_rot>,发现<△E_rot>_v″=21≈2.9<△E_rot>_v″=15.对于v″=16,证实了振动—振动能量转移的4-1近共振过程.在一次碰撞条件下,通过速率方程分析,得到RH（v″）-CO₂振转速率系数.对于v″=15,J=32-48,速率系数在1.25-0.33×10^-13cm³s^-1.之间;对于v″=21,速率系数在2.47-1.53×10^-13cm³s^-1之间,其能量相关性是明显的.     

CdTe/CdS的合成及其作为VB1高灵敏荧光探针的应用

以CdTe/CdS量子点为荧光探针,荧光猝灭为理论基础,设计出一种快速、超灵敏且高选择性的检测片剂与注射剂中VB₁含量的方法。结果表明,VB₁在2.0×10^-7—5.0×10^-5mg/mL的范围内线性良好,相关系数为0.9994,检出限（S/N=3）为0.12ng/mL。将3×10^-5mg/mL的VB₁标准溶液平行测定7次,RSD为0.64%,加标回收实验结果满意。     

注入Mo 在Zr57Nb5Cu15.4Ni12.6Al10非晶合金中的扩散

通过二次离子质谱仪（SIMS）研究了Mo在Zr₅₇Nb₅Cu_15.4Ni_12.6Al₁₀非晶合金中的扩散，并计算出其扩散激活能Q和前置系数D₀分别为1.95 eV和1.13×10^-5m²s^-1.根据Stokes-Einstern关系式研究了玻璃转变温度以下593—673 K之间Zr₅₇Nb 关键词： 扩散 离子注入 二次离子质谱（SIMS） 黏滞特性     

电子对Cl2的离解附着

在电子平均能量为3—5电子伏的范围内,测定了Ar/Cl₂混合物中,电子对Cl₂的离解附着速率常数。结果表明,电子平均能量为3.5电子伏时,离解附着速率常数为(3.2±0.4)×10^-10厘米³/秒,并考察了速率常数与电子平均能量的关系。这些实验结果与最近Los Alamos国家实验室研究者们的类似工作的结果是一致的。 关键词：     

Fe84Zr3.5Nb3.5B8Cu1薄带的动态磁化过程

由于铁磁性样品的交流磁化率虚部χ″随磁场强度H的变化是非线性的，在低场(0～12 mT)有一个与铁磁共振信号强度相当的低场非共振信号. 利用ESR谱仪测量交流磁化率虚部χ″对磁场强度H的一次微分随磁场强度的变化dχ″/dH～H，研究Fe₈₄Zr_3.5Nb_3.5B₈Cu₁合金薄带的动态磁化特性. 合金薄带样品是各向异性的，易磁化轴（易轴）在薄带的横向方向，外加磁场H在易轴方向. 样品在可逆磁化区域(0～2.0 mT)和趋近饱和的磁化区域(9.0 mT以上)，dχ″/dH=0；在不可逆畴壁移动过程中，当H为4.2 mT 时, χ″(H)达到最大值χ_max；在磁畴转动过程中，χ″(H)正比于H²（瑞利区）；而实验中却发现，在某些区域交流磁化率虚部χ″(H) 与磁场强度H的n次方即Hⁿ(n≥3)有关；而且发现，在一定区域，有三段不可逆畴壁移动和磁畴转动交替出现的现象. 在这一过程中，dχ″/dH为常数的磁场范围分别为4.8～5.2mT, 5.8～6.4 mT, 8.0～8.5 mT, 其常数相对值分别为1：0.85：0.60. 样品的交流磁化率虚部χ″对磁场H的微分dχ″/dH随磁场H的这一变化规律反映了不可逆畴壁移动和磁畴转动交替发生的微观过程.     

Effects of Nb substitution for Zr on the phases,microstructure and magnetic properties of Co80Zr18−xNbxB2 melt-spun ribbons

The phases, microstructure, and magnetic properties of Co₈₀Zr_18−xNb_xB₂ (x=1, 2, 3, and 4) melt-spun ribbons were investigated. The small substitution of Nb for Zr in the Co–Zr–B melt-spun ribbons resulted in the improvement of magnetic properties, especially the coercivity. The main effect of added Nb on the coercovity of Co–Zr–Nb–B melt-spun ribbons, originated from modification of the grain size of Co₁₁Zr₂ phase. The coercivity of the Co–Zr–Nb–B melt-spun ribbons depends on the annealing temperature. The optimal magnetic properties of H_c=5.1 kOe, and (BH)_max=3.4 MGOe were obtained in the Co₈₀Zr₁₅Nb₃B₂ melt-spun ribbons annealed at 600 °C for 3 min.     

具有宽过冷液相区的Fe62Co8-x(Cr,Mo)xNb4Zr6B20非晶态合金的热稳定性与磁性

根据制备块状非晶态合金的三条经验准则,选择了成分为Fe₆₂Co_8-xCr_xNb₄Zr₆B₂₀和Fe₆₂Co_8-xMo_xNb₄Zr₆B₂₀(x=0,2,4)的合金系.利用单辊急冷法制备出厚为30μm宽为5mm左右的条带,并用差热分析、X射线衍射以及 关键词： 过冷液相区 铁磁性 非晶态合金     

Exchange interactions and magnetization reversal of nanocrystalline (NdDyTb)12.3(FeZrNbCu)81.7B6.0 ribbons with Co substitution

Alloys of composition Nd_10.8Dy_0.75Tb_0.75Fe_79.7−xCo_xZr_0.8Nb_0.8Cu_0.4B_6.0 (x=0, 3, 6, 9, 12, 15) were prepared by melt spinning at 22 m/s and subsequent annealing. Phase analysis revealed single-phase materials. Magnetic structure and remanence analysis indicated strong exchange coupling between neighboring grains in all samples. The remanence polarization J_r and maximum energy product (BH)_max increased first and then decreased with further increasing Co content x although the intrinsic coercivity H_ci decreased with increasing x. The increase in remanence polarization J_r by the substitution of Co for Fe is mainly caused by the increase in the saturation polarization J_s rather than by the improvement of exchange-coupling interactions. Optimum magnetic properties with J_r=1.041 T, H_ci=944.9 kA/m and (BH)_max=155.1 kJ/m³ were achieved for x=12 ribbons. The mechanism of magnetic hardening in all samples was of pinning type by analyzing initial magnetization and the dependence on applied magnetizing field of the coercivity and remanence.     

Field annealing effect on amorphous (FexCo1-x)85Nb15 alloys

The magnetic anisotropy induced by magnetic field annealing was examined for amorphous (Fe_xCo_1-x)₈₅Nb₁₅ alloys produced by a sputtering technique. An appreciably large uniaxial anisotropy was observed even at x = 0. The anisotropy constant (K_u) obtained was 2.3x10³ erg/cm³ at x=0, and it increased with x, showing a maximum of about 5.4x10³ erg/cm³ near x = 0.2. This compositional change in K_u was explained in terms of the directional ordering of magnetic Fe-Co atom pairs under the negative nonmagnetic interaction energy leading to a precipitation.     

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.     

The magnetic susceptibility of hydrogen-doped partially crystalline (Zr76Ni24)1−xHx metallic glasses

The magnetizations of Zr₇₆Ni₂₄ metallic glass and hydrogen-doped partially crystalline (Zr₇₆Ni₂₄)_1−xH_x metallic glasses have been measured in the temperature range 10-300 K and magnetic fields up to 2 T for various dopant concentrations (x=0, 0.024, 0.043, 0.054). It is found that the samples are paramagnetic and magnetic susceptibility at room temperature, χ(300 K), shows a nonmonotonic behaviour upon hydrogenation. The values of χ(300 K) of the hydrogen-doped partially crystalline (Zr₇₆Ni₂₄)_1−xH_x metallic glasses are reduced with increase in hydrogen content up to x=0.043, whereas for x=0.054, an enhancement of χ(300 K) has been revealed. The magnetic susceptibility is weakly temperature dependent down to 110 K, below which an increase is observed. A shallow minimum exists between 90 and 120 K. The form and magnitude of the observed temperature dependence of the magnetic susceptibility are well accounted for by the sum of the quantum corrections to the magnetic susceptibility. Hydrogen reduces the electronic diffusion constant and influences strongly the quantum interference at defects, slowing down the spin diffusion and enhancing the magnetic susceptibility in the temperature range from 110 down to 10 K.     

Structural,microstructural and magnetic properties of nanocomposite isotropic Sm(CobalFe0.1MyZr0.04B0.04)7.5 ribbons with M=Ni,Cu and y=0.09 and 0.12

In boron-substituted melt-spun Sm(Co,Fe,Cu,Zr)_7.5-type alloys a nanocomposite microstructure and high coercivities in both as-spun and short-time annealed ribbons can be obtained. In the present study three different compositions, namely Sm(Co_0.73Fe_0.1Cu_0.09Zr_0.04B_0.04)_7.5, Sm(Co_0.70Fe_0.1Cu_0.12Zr_0.04B_0.04)_7.5 and Sm(Co_0.70Fe_0.1Ni_0.12Zr_0.04B_0.04)_7.5 have been examined in order to investigate the influence of composition on the magnetic properties and the microstructure. Melt-spun ribbons have been obtained and annealing has been followed under argon atmosphere for 30–75 min at 600–870 °C. For the as-spun ribbons the TbCu₇-type of structure and fcc-Co as a secondary phase have been identified in the X-ray diffraction patterns. For the annealed ribbons above 700 °C the 1:7 phase transforms into 2:17 and 1:5 phases. The TEM studies have shown a homogeneous nanocrystalline microstructure with average grain size of 30–80 nm. Coercivity values of 15–27 kOe have been obtained from hysteresis loops traced in non-saturating fields. The coercivity decreases with temperature, but it is sufficiently large to maintain values higher than 5 kOe at 380 °C.     

单轴M型SrFe12-xCrxO19超细粒子结构与磁性研究

采用溶胶-凝胶法制备了单轴M型锶铁氧体SrFe12-x_12-xCrx_xO 19₁₉(x=0—1)超细晶粒.实验结果表明, 随掺杂量x的增大，质量饱和磁化强 度σs_s在x≤04范围内增大，在x=02附近达到极大值.矫顽力Hc_c在x＜05的范围 内单调降低，这对于用作高密度磁记录材料非常有利.当x≤04时，样品是单相结构， 在 x=06以后出现非磁性相α-Fe2₂O3< 关键词： 锶铁氧体 3+')" href="#">Cr3+³⁺ 结构 磁性     

电流退火铁基薄带巨磁阻抗效应的影响

研究了电流退火工艺对铁基非晶合金Fe₈₄Zr₈Nb_3.5B_3.5Cu_{1〈/sub>薄带巨磁阻抗效应的影响.实验结果表明,该铁基合金的巨磁阻抗ΔZ/Z随退火电流的增加而增强,当电流为820mA时,ΔZ/Z达到最大值62％,阻抗变化灵敏度可达约0.23％（A/m)^-1.结合此合金在电流退火燧后电性能和软磁性能的演变,讨论了材料的巨磁阻抗效应借助趋肤效应与交流频率和外加纵向磁场的关系. 关键词：}