用CARS技术确定拉曼退偏比的一种数据处理新方法

Yuika等人利用偏振CARS技术可以准确地确定分子的拉曼退偏比.其方法是，首先对不同检偏角_d所对应CARS谱峰的频率分布进行数学模拟，然后由所得系数随检偏角φ_d的变化求得使CARS信号中共振项消失的偏振角φ^０_d，最后由消失条件ρ＝-1/(tanθtanφ⁰_d)求出退偏比ρ，θ为产生CARS光的Pump光与Stokes光偏振方向的夹角.本文提出的数据处理方法，即交点法.同Yuika等人处理数据的方法相比，交点法毋需关于谱峰频率分布的知识，做法也更为简便.     

带有电子-双声子相互作用的一维铁磁性介观环的非经典本征态和非经典本征持续电流

在一维铁磁性织构介观环的基础上, 计及电子-双声子相互作用, 介入了三项非经典效应抑制电子-单声子相互作用引起的量子涨落效应: 1) 跳步电子-单声子相干态关联效应;2) 由压缩相干态引起的声子压缩态-单声子相干态间过程关联效应;3) 声子位移-声子压缩态的表象关联效应．从结果来看, 电子-双声子相互作用明显加强了压缩效应(增大压缩参量), 而跳步电子-单声子相干态关联效应引起本征能量大幅度下降, 持续电流大幅度增加．特别是介入了声子压缩态-单声子相干态间过程关联效应后, 声子压缩参量远大于理想压缩态相应的压缩参量, 有效地抑制了Debye-Waller(D-W)效应．当声子压缩态-单声子相干态间过程关联与声子位移重整化效应结合在一起时, 声子场的压缩将更大幅度地增加, D-W效应(参量w_ph)将更大幅度地减小, w_ph << w_ph⁽⁰⁾, 从而极大幅度地抑制了电子-单声子相互作用导致的量子涨落效应. 这样一来, 非经典态本征能量E_n极大幅度地下降, E_n << E_n⁽⁰⁾, 与此同时, 本征持续电流振幅I_n 则极大幅度地增大, I_n >> I_n⁽⁰⁾.     

宽带腔增强吸收光谱技术应用于痕量气体探测及气溶胶消光系数测量

基于氙灯的非相干宽带腔增强吸收光谱系统, 并将其应用于痕量气体及气溶胶消光系数的测量. 该系统的探测灵敏度通过测量NO₂在520—560 nm波长范围内的吸收得到验证, 最小可探测灵敏度为1.8× 10^-7cm^-1 (1σ, 0.12 s积分时间, 50次平均), 对应的NO₂探测极限～33 nmol/mol. 结合标准气溶胶粒子发生系统, 测量了不同浓度的单分散硫酸铵气溶胶粒子在532 nm波长处的消光系数, 得到粒径为600 nm的硫酸铵气溶胶的消光截面为1.12× 10^-8cm², 与文献报道值1.167× 10^-8cm²相一致, 验证了气溶胶测量的可行性和准确性.     

邻碘甲苯分子光解动力学的飞秒时间分辨质谱研究

利用飞秒时间分辨质谱技术研究了邻碘甲苯分子在266 nm激发下的光解动力学. 光解产物碎片通过800 nm强激光场下的多光子电离实现探测. 拟合光解产物C₇H₇自由基和I原子随泵浦-探测延迟时间变化的信号,得到解离时间为38±50 fs,它反映的是266 nm同时激发nσ^*和ππ^*态后C-I键的平均解离时间. 此外,还利用基态碘原子的共振波长298.23 nm作为探测光,通过共振增强多光子电离方法对解离生成的基态碘原子进行了选择性探测. 拟合I⁺随泵浦-探测延迟时间变化的信号,得到解离时间为40±50 fs,这与通过800 nm多光子电离得到的解离时间一致,表明解离生成的主要产物是基态碘原子.     

一种新型的多模虚偶相干态光场的等阶N次方Y压缩与等阶N次方H压缩

本文利用新近建立的多模压缩态理论,详细研究了一种新型的多模虚偶相干态光场|Ψ_i,e⁽²⁾>_q的广义非线性等阶N次方Y压缩与等阶N次方H压缩特性.结果发现:1)态|Ψ_i,e⁽²⁾>_q是一种典型的多模非经典光场,当压缩阶数N为奇数时,态|Ψ_i,e⁽²⁾>_q在一定条件下总可呈现出周期性变化的、任意阶的等阶N次方Y压缩效应;当腔模总数q与压缩阶数N这两者的乘积q·N为奇数时,则在一定条件下态|Ψ_i,e⁽²⁾>_q又可呈现出周期性变化的、任意阶的等阶N次方H压缩效应.2)态|Ψ_i,e⁽²⁾>_q的等阶N次方Y压缩与等阶N次方H压缩效应这两者的压缩程度和压缩深度分别与几率幅γ_q^(e)、压缩参数R_j、各模的初始相位φ_j(或者各模的初始相位和 φ_j)、压缩阶数N以及腔模(指纵模)总数q等呈较强的非线性关联,等阶N次方H压缩效应与上述诸参量之间的非线性关联程度要比等阶N次方Y压缩效应的更强.3)多模虚偶相干态光场|Ψ_i,e⁽²⁾>_q与多模偶相干态光场|Ψ_,e>_q及多模复共轭偶相干态光场|Ψ*_,e⁽²⁾>_q这后两者的等阶N次方Y压缩效应和等阶N次方H压缩效应的压缩条件和压缩特性正好相反,这种现象就称为相反压缩.     

第Ⅶ类两态叠加多模叠加态光场的偶数阶等阶N次方Y压缩

本文构造了由多模相干态|{Z_j}>_q与多模虚相干态的相反态|{-iZ_j}>_q这两者的线性叠加所组成的第Ⅶ类两态叠加多模叠加态光场|ψ₇⁽²⁾>_q.利用多模压缩态理论,研究了态|ψ₇⁽²⁾>_q的偶数阶等阶N次方Y压缩特性.结果发现:在压缩阶数N=2p、并且P=2m+1(m=0,1,2,3,…,…)的条件下,如果各模的初始相位φj(j=1,2,3,…,q)、态间的初始相位差与各单模相干态光场的平均光子数之和 等分别满足一定的取值条件,则在这种情况下态|ψ₇⁽²⁾>_q可呈现出周期性变化的偶数阶等阶N次方Y压缩效应.     

第Ⅵ类两态叠加多模叠加态光场的等阶N次方Y压缩特性研究

本文构造了由多模相干态|{Z_j}〉q与多模虚相干态|{iZ_j}〉q这两者的线性叠加所组成的第Ⅵ类两态叠加多模叠加态光场|Ψ₆⁽²⁾〉q.利用多模压缩态理论,研究了态|Ψ₆⁽²⁾〉q的广义非线性等阶N次方Y压缩特性.结果发现:1)在压缩阶数N＝2p且p＝2l(l＝1,2,3,…,…)的条件下,无论各模的初始相位φ_j(j＝1,2,3,…,q)、态间的初始相位差(θ_pq^(R)-θ_pq^(I))以及各单相干态光场的平均光子数之和 R_j²等如何变化,态|ψ₆⁽²⁾〉q总是恒处于偶数阶等阶N-Y最小测不准态.2)在压缩阶数N＝2p且p＝2l+1(l＝0,1,2,3,…,…)的条件下,当各模的初始相位φj、态间的初始相位差(θ_pq^(R)-θ_pq^(I))以及各单模相干态光场的平均光子数之和 R_j²等分别满足一定的量子化条件(或者在特定的区间内连续取值)时,态|ψ₆⁽²⁾〉q的第一及第二这两个正交分量总可分别呈现出周期性变化的偶数阶的等阶N次方Y压缩效应.     

增加光子奇偶q相干态的高阶压缩效应

通过数值计算研究了增加光子奇q相干态a_q^+m|α>_q^o和增加光子偶q相干态a_q^+m|α>_q^e的高阶压缩效应.结果表明:当q较小时,态a_q^+m|α>_q^o和a_q^+m|α>_q^e都能呈现出强烈的奇次方阶压缩效应,但无偶次方阶压缩效应,而且奇次方阶压缩随m的增大而增强.当m=0时a_q^+m|α>_q^o和a_q^+m|α>_q^e为光场振幅偶次幂的最小测不准态,但当m≠0时它们不是光场振幅偶次幂的最小测不准态.     

Tm3+/Yb3+共掺碲酸盐玻璃的近红外发光及能量传递机理

采用高温熔融法制备了组分为TeO₂-ZnO-Na₂O的Tm³⁺离子单掺和Tm³⁺/Yb³⁺共掺碲酸盐玻璃,应用Judd-Ofelt理论计算分析了玻璃样品的强度参量Ω_t(t=2, 4, 6),自发辐射跃迁几率A,荧光分支比β和荧光辐射寿命τ_rad等光谱参量,测量得到了不同Yb³⁺离子掺杂浓度下玻璃样品的Tm³⁺离子上转换发光谱.结果显示,在980 nm泵浦光激励下玻璃样品发射出强烈的近红外上转换荧光.对Tm³⁺离子上转换发光分析表明,强烈的Tm³⁺离子近红外上转换发光主要来自于Yb³⁺/Yb³⁺离子间的共振能量传递以及基于单声子和双声子辅助的Yb³⁺/Tm³⁺离子间的非共振能量传递过程,并进一步计算得到了声子贡献比和能量传递系数.最后,计算分析了Tm³⁺:³F₄→³H₆能级间跃迁的1.8 μm波段吸收截面、受激发射截面和增益系数.研究表明,Yb³⁺/Tm³⁺共掺TeO₂-ZnO-Na₂O玻璃可以作为近红外波段固体激光器的潜在增益基质.     

γ-LiAlO2上a面ZnO薄膜的光谱特性研究

利用激光脉冲沉积(PLD)技术在(302)γ-LiAlO₂衬底上成功生长了非极性的a面(1120)ZnO薄膜，光致发光谱(PL)带边发射峰半峰宽仅为115meV.研究了非极性ZnO薄膜光谱特性的面内各向异性，发现随着入射光偏振方向改变，在偏振透射光谱上，吸收边移动了20meV，这与A、B激子和C激子的能量差一致；而在拉曼光谱上，激发光偏振方向的改变导致E₂模式的强度发生明显改变.     

Nanoscale C‐Rich SixC1−x Bus/Ring Waveguide Based Cross‐Wavelength Data Converter

The carbon‐rich silicon carbide (C‐rich Si_xC_1?x) micro‐ring channel waveguide with asymmetric core aspect is demonstrated for all‐optical cross‐wavelength pulsed return‐to‐zero on‐off keying (PRZ‐OOK) data conversion. Enhanced nonlinear optical Kerr switching enables 12‐Gbit per second data processing with optimized modulation depth. The inverse tapered waveguide at end‐face further enlarges the edge‐coupling efficiency, and the asymmetric channel waveguide distinguishes the polarization modes. To prevent data shape distortion, the bus/ring gap spacing is adjusted to control the quality factor (Q‐factor) of the micro‐ring. Designing the waveguide cross section at 500 × 350 nm² provides the C‐rich Si_xC_1?x channel waveguide to induce strong transverse electric mode (TE‐mode) confinement with a large Kerr nonlinearity of 2.44 × 10^?12 cm² W^?1. Owing to the trade‐off between the Q‐factor and the on/off extinction ratio, the optimized bus/ring gap spacing of 1400 nm is selected to provide a coupling ratio at 5–6% for compromising the modulation depth and the switching throughput. Such a C‐rich Si_xC_1?x micro‐ring with asymmetric channel waveguide greatly enhances the cross‐wavelength data conversion efficiency to favor its on‐chip all‐optical data processing applications for future optoelectronic interconnect circuits.     

Production of a highly polarized sodium atomic beam

Two experimental techniques for preparing atoms in selected states were combined in order to obtain a highly polarized sodium beam: Firstly state selection by an inhomogeneous magnetic field and secondly optical pumping with laser light. This results in a dominating population of the 3s ² S _1/2 ground state levelF=2M _F=+2 (or alternativelyF=2M _F=−2) corresponding to high electron as well as nuclear spin polarization. Polarization values of 0.85±0.05 were easily obtained. The sign of the polarization can be reversed by changing the light polarization. The method can also be applied to other atoms. In addition, it is demonstrated that the optical pumping process allows a determination of the spin-selectivity of hexapole magnets.     

Observation of oriented 23 S 1 helium atoms in a sodium-helium plasma irradiated by polarization-modulated laser radiation

An experiment on the observation of spin polarization of metastable helium atoms interacting with optically oriented sodium atoms under continuous rf discharge conditions is described. Laser radiation with alternating-sign circular polarization, tuned to the resonance excitation of the 3² S _1/2–3² P _1/2 transition in Na atoms, is used as the source for optical pumping of ground-state sodium atoms. Pis’ma Zh. éksp. Teor. Fiz. 65, No. 5, 385–387 (10 March 1997)     

双折射晶体中旋光效应的耦合波理论

与传统的旋光效应理论不同，采用三阶赝张量κ⁽²⁾_jkl描述旋光现象，并将相关的电极化强度作微扰处理，直接从Maxwell方程组出发推导出了双折射晶体中自然旋光效应的耦合波方程组并得到解析解.该解析解包含了已有的旋光效应宏观理论结果，可方便地用于描述任意偏振态的单色光波在任意点群的双折射旋光晶体中沿任意方向的传播行为.最后，以石英晶体为例,通过对出射光波的偏振态分析，研究了波矢失配对旋光效应的影响. 关键词： 耦合波理论 旋光效应 非线性光学     

Doppler-free optical double resonance spectroscopy using a single-frequency laser and modulation sidebands

Principles and applications are described for a form of Doppler-free optical double resonance spectroscopy which uses amplitude modulation sidebands (v _L ±v) imposed on a single laser frequency (v _L ). The sidebands are generated by passing the carrier radiationv _L through an electro-optic modulator, driven at a radiofrequency ν, which enables the intensity and polarization characteristics of the emerging radiation to be varied for enhancement of selected double-resonance processes. The technique has been applied to infrared-infrared double-resonance studies of the Stark effects of a variety of molecules—¹³CH₃F,¹²CH₃F, PH₃,¹⁵NH₃, GeH₄, SiH₄, and CH₃D—for which physical results are presented and discussed. These results include determination of extremely small electric dipole moments (10⁻³–10⁻⁵ debye) for GeH₄ and CH₃D and, for the dipole moment of PH₃, a vibrational state dependence which is extremely small (Δμ=0.0028(5) debye for ∣Δv ₂∣=1) and a rotational state dependence which is of an unexpected sign. The spectra recorded in some cases display unusual polarization and optical saturation effects which deviate markedly from the predictions of a simple three-wave polarization theory.     

DWBA Analysis of Polarization of Protons from the 9Be(d,p1)10Bex Reaction at Ed = 5.5, 15.0, and 20.5 MeV

The polarization of protons from the ⁹Be(d, p₁)¹⁰Be^x reaction has been analyzed in terms of the DWBA theory at deuteron energies 5.5, 15.0 and 20.5 MeV. Good fits were obtained which show the usefulness of the DWBA theory for describing polarization by using the optimum optical model parameters.     

Anisotropy of absorption spectra of the rare-earth orthoaluminate TbAlO<Subscript>3</Subscript> in polarized light

Polarized spectra of the optical absorption of the 4f → 4f transition ⁷ F ₆ → ⁵ D ₄ in rare-earth orthoaluminate TbAlO₃ were experimentally studied at temperature T = 78 K. It was shown that the nontrivial character of the absorption anisotropy of TbAlO₃ at low temperatures could be related either to the symmetry of wave functions of the Stark sublevels of ⁷ F ₆ and ⁵ D ₄ multiplets combining in the optical transitions under study or to optical experiment geometry that takes into account the orientation of incident light polarization relative to the crystal axes and the axes of local coordinate systems of a rare-earth ion in orthoaluminate.     

NMR studies on polarized12B implanted in highly oriented pyrolytic graphite

NMR measurements on¹²B nuclei implanted in a thin sheet of highly oriented pyrolytic graphite (Grafoil) have been made to study the magnitude of the polarization of¹²B and its electric quadrupole coupling. The magnitude of the residual polarization of¹²B held in carbon material is of crucial importance to the experiment measuring the average polarization of¹²B produced in the muon capture by¹²C. It was found that the polarization of¹²B can be maintained at 101.0±2.2% in Grafoil under a magnetic field of 3 kG. The electric quadrupole coupling was determined to bee ² qQ/h=+1207.3±8.2 kHz. From the magnitude and the sign of the electric field gradienteq, the location of¹²B was found to be a substitutional site in the carbon lattice. The anomalous B-C bond involving thesp ₂ hybrid orbitals with partially filledp _z electrons is also discussed.     

Polarization of Luminescence in the Nanostructure Si/CaF<Subscript>2</Subscript> Upon Polarization of the Nuclear Spins of Fluorine

The laws governing polarization of luminescence in the nanostructure Si/CaF₂ upon polarization of the spins of the fluorine nuclei by means of optical excitation of charge carriers are considered theoretically. The possibility of studying experimentally the properties of nuclear spins in analyzing luminescence is shown. The polarization of luminescence is most informative in the range of excitation rates of charge carriers from 3⋅10⁷ to 3⋅ 10⁸ sec⁻¹ with the CaF₂ layer of thickness from 0.6 to 0.8 nm and optical excitation polarization degree of 0.1. __________ Translated from Zhurnal Prikladnoi Spektroskopii, Vol. 72, No. 4, pp. 524–529, July–August, 2005.     

Raman studies and optical properties of some (PbO)x(Bi2O3)0.2(B2O3)0.8−x glasses

Five (PbO)_x(Bi₂O₃)_0.2(B₂O₃)_0.8−x glasses, where x = 0, 0.2, 0.3, 0.4 and 0.6, were prepared. The dilatometric glass transition temperature (T_g) was found in the region 470 (x = 0)≥ T_g ( °C) ≥ 347 (x = 0.6), and the density (ρ) varied within 4.57 (x = 0) ≤ ρ (g/cm³) ≤ 8.31 (x = 0.6). Raman spectra indicated the conversion of BO₃ to BO₄ entities for low x values but for x > 0.3, namely, for x → 0.6, back‐conversion occurred, most probably. From the measurements of the optical transmission on very thin bulk samples, the room temperature optical gap values (E_g) were determined to be in the range 4.03 (x = 0)≥ E_g (eV) ≥ 3.08 (x = 0.6). The temperature (T) dependence of the optical gap (E_g(T)) in the region 300 ≤ T(K) ≤ 600 was examined and approximated by a linear relationship of the form of E_g(T) = E_g(0)− γT, where γ × 10⁻⁴(eV/K) varied from 5.1 to 6.8. The non‐linear refractive index (n₂) was estimated from the optical gap values and it was found to correspond to the n₂ values calculated from the experimental third‐order non‐linear optical susceptibility taken from the literature. Copyright © 2008 John Wiley & Sons, Ltd.