在BEPC上建造γ束线站的分析

考虑电子的反冲并利用康普顿散射,研究了激光同步辐射光源(LSS)辐射的光子波长、光子能量。结果表明,对于不同的γ,LSS辐射的光子波长和能量有不同的近似公式。当γ<<λ1/4λe时,LSS辐射的光子波长λ2≈λ1/4γ2,能量(εc2≈4γ2εc1;当γ>>λ1/4λe时,LSS辐射的光子波长λ2≈λe/γ,能量cε2≈m0γc2;结果表明,LSS辐射的条件是种子激光的波长λ1大于电子的物质波波长λm;LSS辐射的极值波长是λ2m ax=h/m0γv,极值能量是cε2m ax=βeε;本文后半部分提出了利用北京正负电子对撞机的强流高亮度电子束与激光的康普顿背散射产生单色γ射线的建议。     

The role of emitter quasi-bound state and scattering on intrinsic bistability in resonant tunneling diodes

Usually, numerical self-consistent calculations predict a much larger intrinsic bistability region than actually is measured in resonant tunneling diodes (RTDs). In addition, numerical calculations have shown that scattering in the well reduces bistability. We used a unified treatment of current flowing from continuum states and emitter quasi-bound states to show numerically and analytically that not only the scattering in the quantum well but also the scattering in the emitter reduces bistability. Moreover, within the Hartree approximation, bistability occurs by tunneling resonantly between emitter quasi-bound state and well quasi-bound state as a pitchfork bifurcation.     

Wavelength dependence in photochemical vapor deposition of aluminum film using dimethylaluminum hydride

In photochemical vapor deposition of aluminum film on silicon using dimethylaluminum hydride, (CH₃)₂AlH, a surface reaction dominated below a (CH₃)₂AlH pressure of 0.3 m Torr at 200°C, which was induced only with the 160 nm band emitted from a deuterium lamp. A gas-phase reaction occurred above 0.3 mTorr at 200°C, which could be induced by both 160 nm and 240 nm emission bands from the lamp. To distinguish between surface ad gas-phase reactions, a thickness profile was used. At 240°C the surface reaction could be induced even by the 240 nm band, while the deposits formed under illumination of the two bands were thinner than those obtained with only the 240 nm band, indicating occurrence of vacuum ultraviolet (VUV)-enhanced desorption. The mechanism responsible for the observed wavelength dependence in unclear. The electrical resistivity of the films deposited at 200°C was 4.5 μΩ cm, which did not change with wavelength.     

荧光波长对共焦显微镜成像特性的影响

导出了共焦显微镜中不同荧光波长情况下的荧光功率传输函数、三维脉冲响应函数（3D－PSF）和三维光学传递函数（3D－OTF）。结果表明，不同的荧光波长对共焦显微镜的空间截止频率、分辨率、光学传递函数存在明显的影响。当激发波长与荧光波长的比值下降到一定程度时，可以看到明显的失锥现象。     

InAs/GaSb/AlSb resonant tunneling spin device concepts

We discuss device concepts for creating spin-polarized current sources without external magnetic fields, using non-magnetic 6.1 Å semiconductor resonant tunneling structures. Spin filters, spin pumps, and spin transistors that exploit structural and bulk inversion asymmetries will be examined.     

双波长分光光度法同时测定岩石矿物中的微量金和钯

本文提出以硫代米蚩酮为显色剂，用双波长分光光度法同时测定岩石矿物中的微量金和钯的方法，消除了测定金钯的相互干扰，该方法简便，快速，选择性好，用于矿石样品中金和钯的测定，结果满意。     

Solid Phase Extraction and Simultaneous Spectrophotometric Determination of Trace Amounts of Copper and Iron Using Mixture of Ligands

 A novel sensitive and simple method for rapid and selective extraction, preconcentration and determination of iron (as its bathophenanthroline complex) and copper (as its neocuproine complex) using octadecyl silica cartridges and dual wavelength spectrophotometry is presented. The dual wavelength method (533 nm for the iron-bathophenanthroline and 454 nm for the copper-neocuproine as the analytical wavelength) is used to eliminate spectral interferences. Extraction efficiency and the influence of flow rates of sample solution and eluent, pH, amount of neocuproine, bathophenanthroline and hydroxylamine hydrochloride, type and least amount of eluent for elution of iron and copper complexes from cartridge, break-through volume and limit of detection are evaluated. The effects of various cationic and anionic interferences on percent recovery of iron and copper are also studied. Extraction efficiencies >95% are obtained by elution of cartridges with minimal amount of organic solvent. Iron and copper were determined in the range of 3–100 ng mL⁻¹. The limits of detection are 0.98 and 1.13 ng mL⁻¹ for iron and copper, respectively. The proposed method is applied successfully to the determination of both analytes in river, tap and well water samples. Author for correspondence. E-mail: yyamini@modares.ac.ir Received September 18, 2002; accepted December 12, 2002 Published online May 5, 2003     

Synthesis and characterization of hollandite-type material intended for the specific containment of radioactive cesium

The hollandite Ba₁Cs_0.28Fe_0.82Al_1.46Ti_5.72O₁₆, which has been proposed for the cesium-specific conditioning, can be synthesized either by an alcoxyde or a dry route. In both cases, a two-step protocol is applied, i.e., a calcination at 1000 °C followed by a sintering at 1200 °C. After sintering, both synthetic processes lead to a tetragonal form. According to the X-ray diffraction (XRD) patterns collected at the barium and the cesium K absorption edges, the different positions of these two elements have been evidenced with a more centered position in the oxygen cubic site of the tunnel for Ba than for Cs. On the contrary, after calcination, the two synthetic routes yield different products. The alcoxyde route gives rise to a mixture of the aforementioned Cs- and Ba-containing tetragonal I4/m hollandite, a Cs-only-containing monoclinic I2/m hollandite and an unidentified phase with a weak coherence length containing only Ba. The dry route yields a single tetragonal hollandite material containing Ba and Cs slightly different in composition from the targeted compound.     

Quantitative millimetre wavelength spectrometry at pressures approaching atmospheric: II. Determination of oxygen at atmospheric pressure

A millimetre wavelength (MMW) Fabry-Perot cavity spectrometer described in earlier work has been applied to the measurement of oxygen absorption at 60 GHz and atmospheric pressure in a gas matrix of nitrogen. The spectrometer has also been modified such that the MMW source is stabilised by a sub-harmonic microwave signal transmitted by an infrared carrier on a single mode telecommunications fibre optic. This is a step towards developing an instrument comprising minimal electronic components that can perform MMW spectrometry remotely. Oxygen determinations were achieved by monitoring the change in the quality factor (Q) of a resonant Fabry-Perot cavity due to the presence of an absorbing sample. The MMW absorption of the sample was determined by incrementing the frequency modulation (FM) deviation of the source frequency scanning the cavity resonance profile. The response curve of absorption signal versus fraction of oxygen in nitrogen was found to be linear throughout the working range of 1-100% O₂ (v/v) in N₂ with a slope of (1.407±0.007)×10⁻⁴ m⁻¹ (% O₂)⁻¹. The detection limit (3× standard deviation of the background) was found to be ∼0.8% (v/v). The MMW technique employed is advantageous since, unlike common MMW techniques, there is no vacuum requirement. Application of this method, to the monitoring of oxygen in gas mixtures of practical importance, is proposed. Values of the oxygen spectral absorption coefficients of lines between 55 and 60 GHz were measured at reduced pressure and found to be within ±2% of previous literature values. A pressure correction coefficient for O₂ absorption at 60 GHz in the 45-121 kPa range was obtained and found to be (1.354±0.014)×10⁻⁴ m⁻¹ kPa⁻¹.