Amorphous Fe–Mg alloy thin films: magnetic properties and atomic vibrational dynamics

Amorphous (a-) Fe _x Mg_1?x alloys are interesting materials for the investigation of non-Debye-like low-energy vibrational excitations. We have prepared a-Fe _x Mg_1?x alloy thin films (0.3 ≤ × ≤0.7) by vapour quenching. The amorphous state was confirmed by conversion electron Mössbauer spectroscopy between 4.2–300 K, and the x- and temperature-dependence of the isomer shift and hyperfine magnetic field was measured. For x= 0.6 and 0.7, magnetic ordering occurs below ~150 K. The atomic vibrational density of states, g(E), was determined by nuclear resonant inelastic scattering, providing clear evidence for the non-Debye-like low-energy vibrational excitations.     

Mössbauer spectroscopy study of spin structure and its in-field and temperature dynamics in B2 ordered Fe(Al) alloys

The experimental data from Mössbauer spectroscopy and magnetic measurements are presented as functions of the temperature and external magnetic field for a B2-type ordered Fe ₆₆ Al ₃₄ alloy.     

Mössbauer studies on ultraporous Fe-Oxide/SiO2 aerogel

Magnetic aerogels with very low volume density of ～0.2 g/cm³ were prepared by sol-gel method and supercritical drying. The resulting materials were monolithic and displayed high surface area. By X-ray diffraction and Mössbauer spectroscopy the crystalline phase formed inside the mesopores of the SiO₂ matrix was identified as a spinel iron oxide. Comparison of the magnetic measurements with Mössbauer spectra at various temperatures contributed to the elucidation of the magnetic state of this nanocomposite system with restricted magnetic interactions, in particular its transition to a superparamagnetic state.     

The Mössbauer spectrum of synthetic hureaulite: Fe5 2+(H2O)4(PO4H)2(PO4)2

The crystal structure of synthetic ferrous hureaulite, Fe₅ ²⁺ (H₂O)₄(PO₄H)₂(PO₄)₂, was refined from single-crystal X-ray data. It is monoclinic, space group C2/c, with a=17.487(4), b=9.017(2), c=9.338(2) Å, β=96.27(3)°, V=1463.6(6) Å³, Z=4 and D _calc=3.327 g/cm³. This end member of the hureaulite series was crystallized under distinctly acidic conditions, by a method that gives perfect crystals, large enough for X-ray single crystal studies. The main feature of the hureaulite structure is that it has an equal number of normal (PO₄)³⁺ and acid (PO₄H)²⁺ tetradentate groups. These are centered on Fe²⁺ atoms and share corners with edge-linked octahedra, forming pentamer units. The five Fe²⁺ atoms are distributed on three distinct sites in these units. This can be directly observed in the Mössbauer spectrum at 295 K, which contains three doublets whose relative intensities correspond to the 1:2:2 distributions of crystallographic sites.     

Mössbauer studies of mixed-valence spin-crossover iron complexes with a hexadentate tripod ligand

The spin-crossover behaviors of mixed-valence iron compounds [Fe^IIH₃L][Fe^IIIL](NO₃)₂ (1) and [Fe^IIH₃L^Me][Fe^IIIL^Me](NO₃)₂ (2) have been investigated by ⁵⁷Fe Mössbauer spectroscopy, where H₃L is a hexadentate N₆ tripod ligand containing three imidazole groups and H₃L^Me is its 2-methylimidazole derivative. Deconvolution analyses of the Mössbauer spectra revealed that a two-step SCO (LS Fe^II–LS Fe^III→HS Fe^II–LS Fe^III→HS Fe^II–HS Fe^III) proceeds in each compound on elevating the temperature. Compound 2 exhibited lower spin-transition temperatures than 1. “Frozen-in effect” was observed below 120 and 50 K for 1 and 2, respectively.     

Mössbauer study of nanodimensional nickel ferrite – mechanochemical synthesis and catalytic properties

Iron–nickel spinel oxide NiFe₂O₄ nanoparticles have been prepared by the combination of chemical precipitation and subsequent mechanical milling. For comparison, their analogue obtained by thermal synthesis is also studied. Phase composition and structural properties of iron–nickel oxides are investigated by X-ray diffraction and Mössbauer spectroscopy. Their catalytic behavior in methanol decomposition to CO and methane is tested. An influence of the preparation method on the reduction and catalytic properties of iron–nickel samples is established.     

基于双透镜外腔结构的窄线宽可调谐半导体激光器

设计了一种具有独特双透镜外腔结构的可调谐窄线宽激光器,利用一个温控50 GHz的标准具提供ITU标准波长序列,通过一个压电陶瓷驱动的Fabry-Pérot可调谐滤波器选择一个标准波长实现单波长输出。实验结果表明:该激光器的调谐范围达到了1 525～1 580 nm,覆盖整个C波段,线宽为37.5 kHz,400 mA电流条件下的输出功率超过50 mW,边模抑制比超过50 dB,达到或超过相干通讯应用的要求和其他单片集成类器件的指标。另外,本结构具有位置容差大、调谐速度快(<3 ms)、易于实现超窄线宽以及波长微调等优点,待实现小型化和标准封装,其大规模应用将成为可能。     

空间扫描型光纤法布里珀罗传感解调系统中CCD的光照度数学模型研究

针对空间扫描型光纤法布里珀罗（F-P）传感解调系统中CCD的光照度分布建立了数学模型,研究了不同帧扫描频率下CCD输出信号和信噪比。利用已设计的解调模块进行了CCD光照度分布的实验,实验结果表明,当帧扫描频率不同时,CCD各个像素输出信号电压的实验值与计算值的相对误差均小于2.5%,同一像素输出信号电压的实验值与计算值的相对误差变化数值均小于0.005,随实验所用CCD帧扫描频率变化,信噪比以184 Hz为分界点以两种变化斜率改变,验证了数学分析模型的有效性。     

金属网栅法布里珀罗干涉仪测量太赫兹波波长

设计并制作了用于测量波长大于150 μm(频率低于2 THz)的太赫兹波波长的金属网栅法布里珀罗干涉仪(FPI)。采用光电子微纳制造工艺制作了五组周期不大于40 μm,线宽不大于10 μm的有衬底方形金属网栅,利用太赫兹时域光谱技术测量了金属网栅的太赫兹波段光电特性,得到了各组金属网栅在感兴趣频段的反射率和金属网栅FPI的反射精细度,结果表明所制作的金属网栅FPI均可用于测量波长大于150 μm的太赫兹波。实验搭建金属网栅FPI扫描测量了212 μm的太赫兹波波长,与理论结果吻合。研究了金属网栅FPI对太赫兹波偏振方向的依赖性以及对FPI腔镜平行度的要求,结果表明,方形金属网栅FPI对正入射太赫兹波偏振方向不敏感,而对FPI腔镜平行度很敏感。