90°视向角口腔内窥镜光学系统设计

基于实际应用设计了一个90°视向角的光学系统,可用于1/4″CCD口腔内窥镜成像.系统具有62°视场角,孔径为F/7,各视场的光学传递函数在80 lp/mm处取值良好、景深大、像面照度均匀,整个系统的最大镜头口径小于4.6 mm.     

含三层衍射元件的60°视场折/衍混合头盔目镜

设计了一种含有三层衍射光学元件的60°视场头盔显示目镜,并给出了系统优化过程和结果.在整个视场和设计波段范围内三层衍射光学元件的衍射效率均在90%以上,提高了系统的光能利用率和像的对比度.此目镜光学系统的出瞳直径为8 mm,出瞳距离为22 mm.整个系统重量仅为8 g,总长度为26.8 mm,结构轻便紧凑,具有良好的光学性能,满足头盔显示目镜的使用需求.     

180°圆弧形钝感炸药的爆轰波传播

 采用贴体坐标下与Level Set方法相结合的爆轰冲击波动力学（DSD）计算方法,研究了180°圆弧形钝感炸药中非理想爆轰波的传播过程。通过数值模拟计算和实验测量的对比分析,得到了180°圆弧形炸药中爆轰波传播的一些规律：圆弧形钝感炸药可以实现定常爆轰,即在极坐标中整个爆轰波以固定角速度转动。这种定常阵面的形状和角速度与圆弧的外半径无关,定常体系依赖于圆弧形炸药的内半径和覆盖圆弧的外壳物质。对描述圆弧形炸药中爆轰波传播规律的经验公式进行了研究,结果表明这些经验公式能够准确描述爆轰波速度的变化,在实验测量和预估方面具有一定的参考价值。     

45°倾斜镜多自由度精调结构设计研究

对于高准确度光学系统,光学元件及其支撑机构之间的简单连接很难使光路对准并满足公差要求,本文介绍了一种在光学系统中能够对光路进行折转或分束的45°倾斜镜的精调支撑机构.该倾斜镜支撑结构采用了多自由度精调方式,能够在实现两维倾斜调整的同时,实现相互垂直光路的方向平移.设计中使用的柔性元件使结构的倾斜调整准确度达到角秒级,实现0~10 mm的位移,同时借鉴现有的燕尾槽导轨平移技术节省加工成本和减小周期,并且借助有限元分析软件,对机构中的关键部分进行了详尽的分析和论证.整个研究方法可作为同类光机系统设计时的参考,在光学系统的光路调整中有较大的应用价值.     

Formation of γ-Fe2O3 hierarchical nanostructures at 500 °C in a high magnetic field

Three-dimensional (3-D) hierarchical nanostructures of γ-Fe₂O₃ are prepared by a solvothermal process combined with subsequent thermal treatment in air at 500 or 350 °C with the aid of a high magnetic field. The experimental results indicate that γ-Fe₂O₃ instead of α-Fe₂O₃ forms in air at 500 °C in a 12 T field. The products are characterized by X-ray powder diffraction (XRD), scanning electron microscopy (SEM) and transmission electron microscopy (TEM). The magnetization curves measured at room temperature exhibit superparamagnetic characteristics.     

Phase coexistence between the (√3 × √3)R30° - β and (1 × 1) phases on Pb/Ge(1 1 1)

We have characterized the phase transition between the (1 × 1) and (√3 × √3)R30° - β phases on Pb/Ge(1 1 1) using low energy electron microscopy (LEEM). We show that the transition is first-order and that, in the coexistence region of the two phases, the dominant mechanism for phase separation changes critically with Pb coverage, from nucleation and growth at 1.33 ML (saturation coverage of the β phase) to spontaneous domain switching due to thermal fluctuations of the local Pb density for slightly smaller coverage. As the Pb coverage decreases, the concentration of vacancies in the β phase increases, making additional possible Pb adsorption sites available. The larger resulting local density fluctuation of Pb becomes comparable to the density difference of the two phases, manifesting itself in the observed domain switching.     

Z→li±lj干 processes in the BLMSSM

In a supersymmetric extension of the Standard Model (SM) where baryon and lepton numbers are local gauge symmetries (BLMSSM), we investigate the charged lepton flavor violating (CLFV) processes Z→l_i^±l_j^干 after introducing new gauginos and right-handed neutrinos. In this model, the branching ratios of Z→l_i^±l_j^干 are around (10^-8-10^-10), which approach the present experimental upper bounds. We hope that the branching ratios for these CLFV processes can be detected in the near future.     

High-Resolution Study of the Atilde;A′→X?A″ Transition of DO2: Analysis of the 000-000 Band

The near-infrared emission spectrum of the Atilde;²A′→X?²A″ transition of DO₂ has been studied by Fourier-transform spectrometry. The 000→000 band has been recorded at high spectral resolution. ΔK_a=±1 subbands up to K_a′=12→K_a″=11 and K_a′=9→K_a″=10, comprising lines from rotational levels up to N′=34, have been observed. With about a factor of 5-10 lower intensity, ΔK_a=0 subbands 0-0 to 6-6 were found, which are due to magnetic dipole transitions. Several local perturbations extending over 3-10 N″ values were observed. Two prominent perturbations in the F₁ levels of the òA′, 000, K_a″=11 and 12 states are attributed to ΔK_a=0, ΔJ=0, ΔN=±1 interactions with the 211 level of the X?²A″ ground state. The rotational constants for HO₂ and DO₂ have been used to deduce the molecular geometry of HO₂ at the zero point levels of the X?²A″ and òA′ states.     

Crossing of the πd<Subscript>5/2</Subscript> and πg<Subscript>7/2</Subscript> orbitals in the <Subscript>51</Subscript>Sb isotopes

Self-consistent calculations using the D1S Gogny force have been performed in order to study the mechanism involved in the crossing of the πd _5/2 and πg _7/2 orbitals in the Sb isotopes. This inversion is well predicted by the HFB + blocking calculations with spherical symmetry performed for the odd-A Sb isotopes. In addition, several HFB and HF calculations have been performed for even-even nuclei of the five neighbouring isotopic chains (Z = 46 to 54, from the proton dripline to N = 82). The results obtained for the binding energies of the two proton orbitals indicate that the radii of the systems play an important role in the crossing, even though some particular πν interactions also give a contribution. The spin-orbit interaction, which is known to be concentrated mainly at the nuclear surface, is proposed to be the main responsible of the crossing.     

On the nature of the lowest 1/2<Superscript>-</Superscript> baryon nonet and decuplet<Superscript>⋆</Superscript>

From our recent study of properties of the lowest spin-parity 1/2^- baryons, N ^*(1535) and Δ^*(1620) , new pictures for the internal structure of the lowest 1/2^- baryon nonet and decuplet are proposed. While the lowest 1/2^- baryon nonet may have large diquark-diquark-antiquark component, the lowest 1/2^- baryon decuplet is proposed to have large vector-meson-baryon components. Evidence for “missing" members of the new pictures is pointed out and suggestions are made for detecting these predicted states from forthcoming experiments.     

An ab Initio Study of the ÃΠ State and the ÃΠ←X?Σ Electronic Transition of MgNC

We use the RENNER program system (see, for example, P. Jensen, G. Osmann, and P. R. Bunker, in “Computational Molecular Spectroscopy” (P. Jensen and P. R. Bunker, Eds.), Wiley, Chichester, 2000, and references therein) to make a detailed calculation of the rovibronic energies in the first excited electronic state, òΠ, of the MgNC radical. This calculation is based on ab initio data (supplemented here with points for larger bending displacements from linearity) calculated at the level of MR-SDCI(+Q)/[TZ3P+f(Mg), aug-cc-pVQZ (N and C)] by T. E. Odaka, T. Taketsugu, T. Hirano, and U. Nagashima (J. Chem. Phys.115, 1349-1354 (2001)). These authors employed ab initio derived spectroscopic constants to calculate vibronic energies using perturbation expressions (J. T. Hougen and J. P. Jesson, J. Chem. Phys.38, 1524-1525 (1963)), and their results suggested that an observed vibronic band belonging to the òΠ←X?²Σ⁺ electronic transition (R. R. Wright and T. A. Miller, J. Mol. Spectrosc.194, 219-228 (1999)) should be reassigned. The present work confirms this conclusion, which is further substantiated by the rotational structures calculated in the vibronic states and by Franck-Condon theory predicting relative intensities.     

The 1-v″ bands progression of the BΣ → XΣ system of CO

The B²Σ⁺ → X²Σ⁺ (0-1, 2, 3, 4 progression) electronic transition of ¹²C¹⁷O⁺ was first observed and analyzed by Szajna and Ke¸pa [Spectrochim. Acta A 65 (2006) 1014-1020]. We have now extended our previous studies. The use of high resolution conventional spectroscopic techniques has allowed first rotational analysis of the 1-2, 1-3, 1-4 and 1-5 bands of the first negative system in the 37,000-43,000 cm⁻¹ spectral region. Approximately 500 transition wavenumbers were measured with an estimated accuracy of 0.005 cm⁻¹. The present data were combined with the previous measurements to yield an improved set of molecular constants for the B²Σ⁺(v′ = 0, 1) and X²Σ⁺(v″ = 1, 2, 3, 4, 5). The v′ = 1 and v″ = 5 vibrational levels were observed for the first time and the main molecular constants are (in cm⁻¹, one standard deviation in parentheses)

B2Σ+		X2Σ+
B1 = 1.710792(20)		B5 = 1.825694(23)
D1 = 7.799(15) × 10−6		D5 = 6.085(21) × 10−6
γ1 = 1.9491(37) × 10−2		γ5 = [8.381] × 10−3

Full-size table

     

一种基于超材料的宽带、反射型90°极化旋转体设计

根据各向异性媒质理论, 设计了一种宽带、反射型超材料极化旋转体, 能够将线极化波极化方向旋转90°, 极化转化率大于90%的工作带宽为5.5–14.5 GHz. 该极化旋转体由两层介质板、金属双开口谐振环和金属底板周期排列构成, 具有各向异性的特点, 单元两对角线方向的电场分量反射系数相同, 反射相位相差180°, 导致其极化旋转特性. 利用表面电流分布图, 分析不同极化波入射时该极化旋转体的谐振状态, 实验和仿真结果符合较好. 该极化旋转体在新型天线设计和隐身技术等方面具有广阔的应用前景.     

Spectroscopy of AlO: Combined analysis of the AΠi → XΣ and BΣ → XΣ transitions

A combined analysis of the A²Π_i → X²Σ⁺ and B²Σ⁺ → X²Σ⁺ band systems of AlO, involving 21,500 line assignments, has been performed. The analysis indicates that the previously reported γ values of the B²Σ⁺ state are questionable. The present analysis shows that γ(B²Σ⁺) ≈ 0.014 cm⁻¹, essentially independent of the vibrational level. The positive sign is consistent with second order interaction with the higher-lying C²Π_r and lower-lying A²Π_i states. It also appears that many of the previously reported γ and γ_D values of X²Σ⁺ (v > 0) are doubtful. In fact, γ(X²Σ⁺) is observed to become increasingly negative for v″ > 1, due to second order interaction with the low-lying A²Π_i state. The present results are based on models where the hyperfine structure of the ²Σ⁺ states has been taken into account explicitly. Intensity patterns of the branches of the B²Σ⁺ → X²Σ⁺ system have been shown to be influenced by the case bβ_S coupling in the ground state v = 0,1 levels. This gives rise to intensity differences of around 10 percent in the R₁/R₂ and P₁/P₂ doublet components. The synthesized intensity patterns are fully in accord with the F₁/F₂ assignments of the present work.     

Catalysis of the hydrogen oxidation reactions by Sr-doped LaMn1 − yCryO3 ± δ oxides

Sr-doped and Sr-free La_1 − xSr_xMn_1 − yCr_yO_3 ± δ (LSMC, x(Sr) = 0-0.2, y(Cr) = 0.4-0.6) perovskite-type oxides were synthesized and evaluated as single phase anodes for use in intermediate temperature solid oxide fuel cell applications. Their thermo-chemical and chemical stabilities were investigated in hydrogen at high temperatures and correlated with their oxygen non-stoichiometry (3 ± δ), determined by permanganate titration. The catalytic activity towards hydrogen oxidation was examined as a function of oxide sintering time, operating temperature, and the Sr and Cr contents, using a Pt mesh current collector. While all of the perovskite oxides studied here showed some irreversible performance degradation with time under both open circuit and anodically polarized conditions, La_0.9Sr_0.1Mn_0.6Cr_0.4O_3.03 (LSMC9164), sintered at 1200 °C for 10 h, was found to be the most catalytically active and also the most stable.     

New spectroscopic investigations of the fourth-positive (AΠ → XΣ) system bands in the CO molecule

The present work puts forward the results of the recordings carried out under high resolution by conventional, photographic spectroscopy and modern analysis of thirteen bands with v′ = 7-12 and v″ = 16-24 of the fourth-positive (A¹Π → X¹Σ⁺) band system. The current investigations include the region of the observed ¹³C¹⁶O molecule spectrum, much greater now than before. Especially, new transitions connected with not hitherto observed v′ = 12 vibrational level of the A¹Π state, were recorded and studied. Moreover, the region of perturbations observed in the upper state of the fourth-positive system was significantly enlarged. The observed perturbations were confronted with those predicted from theoretical calculations.     

Critical evolution of the local order parameters related to the nanopolar domains in Pb(Mg<Subscript>1/3</Subscript>Nb<Subscript>2/3</Subscript>)O<Subscript>3</Subscript> ceramics

In the present paper, Pb(Mg_1/3Nb_2/3)O₃ (PMN) ceramics prepared by the columbite method were investigated. The dielectric study indicates typical relaxor properties, with a frequency dispersion in the range of 200–350 K. The relaxor-to-paraelectric phase transition was evidenced by the continuous decrease of the local order parameter derived from the permittivity-temperature data. As a result of the critical behavior, the main Raman modes show anomalies at: (i) ∼150 K; (ii) ∼220 K (i.e. close to the critical temperature reported for the field-induced ferroelectric state in PMN single crystal); (iii) ∼260 K (i.e. the temperature of the permittivity maximum); (iv) ∼350 K (the temperature for initiation of the cluster freezing process T ^*); (v) ∼620 K (Burns temperature). The frequency split of the doublet at ∼605 and ∼500 cm⁻¹ presents a critical behavior related to the local symmetry lowering and to the structure ordering due to a phase transformation which takes place below T ^*. The tunability in the paraelectric state was interpreted in terms of reorientation of the non-interacting nanopolar clusters in a double-well potential. The temperature dependence of the nanopolar domain size also shows anomalies in the range of T ^*. The size and dynamics of the polar nanodomains is essential in determining the functional properties of the Pb(Mg_1/3Nb_2/3)O₃ relaxor.     

Direct observation of the D′ 2g(P2)-A′ Π(2u) system for Cl2 by laser induced fluorescence spectroscopy: Determination of the absolute position of the A′ state

In a discharged supersonic jet of Cl₂, transitions of the D′ 2_g(³P₂)-A′ ³Π(2_u) system for ³⁵Cl₂ were observed directly by laser induced fluorescence spectroscopy. By a discharge in Cl₂, the Cl₂ molecules were populated into the A′ state, which is a metastable and optically forbidden state, from the state. An ultraviolet laser radiation excites the molecules to the D′ ion-pair state. A set of Dunham parameters for the A′ state is determined from a global least-squares fitting for 59 vibronic bands with v″ = 0-7. In the fitting, the previously reported data, T(v) and B(v) for the v = 14 and 15 bands of the A′ state [T. Ishiwata, A. Ishiguro, K. Obi, J. Mol. Spectrosc. 147 (1991) 300-320], were included. Y₀₀ = 57295.723(5) cm⁻¹ of the D′ state [J.-H. Si, T. Ishiwata, K. Obi, J. Mol. Spectrosc. 147 (1991) 334-345] was also included in the global fitting in order to determine the absolute position of the A′ state. The determined parameters of the A′ state are Y₀₀ = 17171.506(14), Y₁₀ = 255.915(85), Y₂₀ = −4.465(70), Y₃₀ = −8.7(23) × 10⁻², Y₄₀ = 6.3(35) × 10⁻³, Y₅₀ = −4.9(26) × 10⁻⁴, Y₆₀ = 1.43(69) × 10⁻⁵, Y₀₁ = 0.16282(15), Y₁₁ = −2.363(68) × 10⁻³, Y₂₁ = −5.01(93) × 10⁻⁵, and Y₃₁ = −3.01(36) × 10⁻⁶ (in cm⁻¹ and one standard deviations of the fit in parentheses). The absolute position of the A′ state is determined with good accuracy.