铯6S1/2 -6P3/2 -8S1/2阶梯型系统中超精细能级的多重电磁感应透明

基于铯原子6S_1/2 -6P_3/2 -8S_1/2的阶梯型能级系统,对室温下铯原子气室中的电磁感应透明(EIT)谱进行了研究.由于探测光的频率锁定于基态6S_1/2(F=3)到中间态6P_3/2的超精细跃迁线上,耦合光在中间态6P_3/2和激发态8S_1/2之间扫描,得到的EIT谱具有平坦的背景,提高了光谱的精度.理论上,采用了一个多能级的EIT模型,将其计算结果与所观察的实验现象进行了比较,二者符合得比较好. 关键词： 电磁感应透明 光抽运 超精细结构 阶梯型系统     

Double-resonance optical-pumping effect and ladder-type electromagnetically induced transparency signal without Doppler background in cesium atomic vapour cell

In a Doppler-broadened ladder-type cesium atomic system (6S_1/2-6P_3/2-8S_1/2), this paper characterizes electromagnetically induced transparency (EIT) in two different experimental arrangements, and investigates the influence of the double-resonance optical-pumping (DROP) effect on EIT in both arrangements. When the probe laser is weak, DROP is explicitly suppressed. When the probe laser is moderate, population of the intermediate level (6P_3/2 F'=5) is remarkable, therefore DROP is mixed with EIT. An interesting bimodal spectrum with the broad component due to DROP and the narrow part due to EIT has been clearly observed in cesium 6S_1/2 F=4-6P_3/2 F'=5-8S_1/2 F"=4 transitions.     

Influence of atomic alignment on crossover signals in saturation spectroscopy

The crossover resonance between the atomic transitions² S _1/2(F=2)→² P _1/2(F′=1, 2), observed in the saturation spectrum of sodium, was found to be sensitive to the atomic orientation of the ground state, produced by velocity selective optical pumping. For zero magnetic field and the same linear polarization of saturating and probing beam, a negative signal was recorded for the crossover, corresponding to an increase in absorption of the probing beam. Application of a sufficiently strong magnetic field perpendicular to the polarization vector causes the destruction of the alignment, leading to a change in sign for the crossover intensity, i.e., to an enhanced transmission of the probing beam. It was shown experimentally that an increase in the atomic transit time has the same effect. Using optical pumping theory all qualitative features could be accounted for.     

Saturated absorption spectroscopy: Elimination of crossover resonances with the use of a nanocell

It is demonstrated that the velocity-selective optical pumping/saturation resonances of the reduced absorption in a Rb vapor nanocell with thickness L = λ, 2λ, and 3λ (resonant wavelength λ = 780 nm) allow for the complete elimination of crossover (CO) resonances. We observe well-pronounced resonances corresponding to the F _g = 3 → F _e = 2, 3, and 4 hyperfine transitions of the ⁸⁵Rb D₂ line with line widths close to the natural width. A small CO resonance located midway between F _g = 3 → F _e = 3 and F _g = 3 → F _e = 4 transitions appears only for L ≥ 4λ. The D₂ line (λ = 852 nm) in a Cs nanocell exhibits a similar behavior. From the amplitude ratio of the CO and VSOP resonances, it is possible to determine the thickness of the column of alkali vapor in the range of 1–1000 μm. The absence of the CO resonances for nanocells with L ～ λ is attractive for the frequency reference application and for studying the transitions between the Zeeman sublevels in external magnetic fields.     

Multiple fluorescence and the electronic relaxation processes of coronene vapor: The fluorescence from the S1, S2, and S3 states

Fluorescence and excitation spectra of coronene vapor have been measured under different conditions. Weak emission which can be regarded as the fluorescence from the third excited singlet state, S₃(¹E_1u), was observed in addition to the S₁(¹B_2u) and S₂(¹B_1u) fluorescence. The observed S₂ and S₃ fluorescence are substantially different from those reported previously for coronene vapor. Addition of oxygen resulted in significant decrease of the S₁ fluorescence intensity, but did not affect the S₂ fluorescence intensity, indicating the faster decay rate of the S₂ state than that of S₁. Excitation energy dependence of the S₁, S₂ and S₃ fluorescence quantum yields (Φ_F(S₁), Φ_F(S₂) and Φ_F(S₃), respectively) revealed that Φ_F(S₁) decreases with increasing excitation energy, while Φ_F(S₂) and Φ_F(S₃) increase significantly. The quantum yield ratios, Φ_F(S₂)/Φ_F(S₁) and Φ_F(S₃)/Φ_F(S₂), obtained as a function of excitation energy are correlated with the ratios of the relative internal conversion rates.     

Exchange currents in electric transitions and the rôle of siegert's theorem: A case study in deuteron photodisintegration

The hyperfine structure (hfs) splittings of the metastable 1s2s ³ S ₁ state of⁷Li⁺ have been measured with combined laser optical pumping and microwave resonance. A lowenergy Li⁺ ion beam, optically excited by an intersecting laser beam, passed a waveguide where radio frequency transitions were induced. The resulting population transfer among the hfs levels of the³ S ₁ was detected via the change in intensity of the fluorescence light from a second crossing region of laser light and ion beam located past the waveguide. The magnetic hfs constantA(⁷Li⁺, 1s2s ³S₁) was measured and compared with theory. A deviation of the two transition frequenciesν(F=3/2?F=5/2) andν(F=1/2?F=3/2) from the interval rule is due to a depression of theF=3/2 hfs sublevel, caused by mixing of the 2³ S ₁ and 2¹ S ₀ states via hyperfine interaction. This shift was never observed so far in a two-electron spectrum, because of absence ofI>1/2 isotopes in He, the only two-electron atom investigated spectroscopically with high precision. The size of the shift is in fair agreement with a theoretical estimate.     

Analysis of the high-resolution 5-μm spectra of the ν4(E) and 2ν2(A1) bands of 12CD3F

The infrared spectrum of the ν₄(E) and 2ν₂(A₁) bands of ¹²CD₃F have been recorded and deconvolved to ∼0.005 cm⁻¹ resolution. More than 1890 transitions have been assigned to one of the 37 subbands (−18≤KΔK≤+18) comprising the spectrum of the ν₄ band with a maximum assigned J value of 41. The weak 2ν₂(A₁) band has never been reported in the infrared prior to this work. A total of 358 transitions in K ≤ 8 subbands have been assigned to the 2ν₂ band. The two bands are members of the 24 interacting state complex of ¹²CD₃F spectra in the 5-μm region. The ν₄ and 2ν₂ spectra are highly perturbed, exhibiting local and global resonances. Effective parameters of the two bands were obtained by fitting the data in a restricted manner leaving out the obviously perturbed transitions. The effective parameters, the identification of the different resonances affecting the bands, and estimates of some of the coupling constants are reported.     

Study of absorption spectra of Er<Superscript>3+</Superscript> in KTaO<Subscript>3</Subscript> crystals

The first results of the study of optical absorption spectra of KTaO₃: Er³⁺ crystals are presented. In the 350–660-nm region, lines are observed deriving from intraconfigurational electronic transitions from the ⁴ I _15/2 ground state to levels of the ⁴ F _9/2, ⁴ S _3/2, ² H _11/2, ⁴ F _7/2, ⁴ F _5/2(⁴ F _3/2), ² G _9/2, and ⁴ G _11/2 excited states of the Er³⁺ ions. A comprehensive study of transitions to the ⁴ F _9/2, ⁴ S _3/2, ² H _11/2, and ⁴ F _7/2 levels at 77 K is carried out. The number of lines observed for the above transitions fits the theoretically possible number for ?-? electronic transitions in Er³⁺ ions in the cubic crystal field. In the case of a differently charged substituted ion, this situation occurs only under nonlocal impurity charge compensation. The energies of the excited state levels for the transitions under study are determined.     

V.L. Ginzburg’s elliptic screw polarization modes in an optical medium with linear birefringence and twist: Determination of their parameters by the method of Jones matrices

The effect of electromagnetically induced transparency (EIT) has been experimentally implemented for the first time for the (4S _1/2–4P _1/2–4S _1/2) Λ-system of potassium atom levels in a nanocell with a 770-nm-thick column of atomic vapor. It is shown that, at such a small thickness of the vapor column, the EIT resonance can be observed only when the coupling-laser frequency is in exact resonance with the frequency of the corresponding atomic transition. The EIT resonance disappears even if the coupling-laser frequency differs slightly (by ~50 MHz) from that of the corresponding atomic transition, which is due to the high thermal velocity of K atoms. The EIT resonance and related velocity selective optical pumping resonances caused by optical pumping (formed by the coupling) can be simultaneously recorded because of the small (~462 MHz) hyperfine splitting of the lower 4S _1/2 level.     

Thermal phase transition of RbMnFe(CN)6 observed by X-ray emission and absorption spectroscopy

The thermal phase transition of RbMnFe(CN)₆ has been observed by Mn and Fe 3p-1s X-ray emission spectroscopy (XES) and 1s X-ray absorption spectroscopy (XAS). The thermal variations of the spin states and the valences of Mn and Fe were determined to be Mn²⁺(S=5/2)-NC-Fe³⁺(S=1/2) for the high-temperature (HT) phase and Mn³⁺(S=2)-NC-Fe²⁺(S=0) for the low-temperature (LT) phase. These transitions are thus caused by charge transfer between Mn and Fe. The temperature dependences of Mn and Fe 3p-1s XES and 1s XAS were observed as the composition of the spectra of the HT and LT phases. The ratios of the HT component in each spectrum show good agreement with the thermal transition curves observed with magnetic susceptibility measurements.     

Absolute intensity measurements of the CO2 bands 401III←000 and 411III←010

The absolute intensities of the transitions 401_III←000 and 411_III←010 of CO₂ have been measured from spectra obtained under high resolution. Both the vibration-rotation line intensities and the integrated band intensities are reported. The rotationless transition moment of 401_III←000 is deduced and a vibration-rotation interaction factor F(m) = 1+(4.92×10^?4)m+(4.4×10^?7)m² is determined. The values obtained are: S_Band(401_III←000) = (25.54±0.22)×10^?5 cm^?2atm_{(293 K)}^?1, |R₀₀₀^401_III| = (1.87±0.02)×10^?4D, and S_Band(411_III←010) = (1.83±0.13)×10^?5 cm^?2atm_{(293 K)}^?1.     

Highly resolved electronic absorption and luminescence spectra of some phenanthrolines in Shpolskii matrices: Part II. Fluorescence and S1←S0 absorption spectra

Highly resolved fluorescence and S₁←S₀ absorption spectra of some phenanthrolines in n-alkane matrices were obtained at 77 K. The vibrational analysis of the spectra was carried out. Mirror symmetry distortions of the fluorescence and absorption spectra were attributed to vibronic coupling between ¹(π, π¹) states. It was shown that vibronic mixing of S₁(π, π¹) and S₂(π, π¹) states occurs in phenanthroline molecules with S₁-S₂ energy gap not exceeding 3000 cm^-1 (i.e., 4,7-, 1,7- and 1,10-Phen), whereas in other phenanthrolines the coupling of S₁ and S₃(π, π¹) plays a dominant role. Fluorescence quantum yields of phenanthroline liquid solutions were measured. Changes of luminescence efficiencies due to the change of the polarity of the media point to a weak coupling of the lowest ¹(π, π¹) and ¹(n, π¹) states.     

FTS-Raman flame spectroscopy of high-J lines in H2 and D2

High-J rotational transitions in the ground vibrational state of molecular hydrogen and deuterium have been recorded using the FTS-Raman technique. Transitions above those recorded previously at room temperature were observed in diffusion flames burning H₂ with air, and D₂ with air. For H₂ the v = 0-0 S(6) and S(7) transitions, which had not been observed previously, were recorded in the flame spectra. For D₂ the flame spectra yielded measurements of the S(7) through S(12) lines for the first time. By combining flame and room-temperature Raman and infrared measurements it has been possible to improve H₂ ground state rotation constants to fifth order. For D₂, the combination of flame and room-temperature Raman measurements required an extension to fifth-order constants, as compared with the third-order fit which was adequate for the room-temperature data alone. Our improved line positions can be applied to transitions observed in the Orion Molecular Cloud.     

ωNN vertex function and the γπππ anomaly

We show that the empirical ωNN form factor (cut-off 1400–C1500 MeV) can be understood as arising from a combination of a quark model form factor (typical cut-off 700–C800 MeV) and an anomalous form factor ～ q ² arising from the 3π-intermediate state. The anomaly contributes to the Dirac form factor F ₁(q ²) with F ₁(0) = 0, (and sizable), and to the Pauli form factor F ₂(q ²) with F ₂(0) ≠ 0. The resulting tensor coupling F2(0) is sensitive to the cut-off of the pion momenta in the two-loop integrals and turns out to be small for values around 1 GeV. The quark model ωNN tensor coupling F ²(0) vanishes for point-like quarks. The anomaly, however, contributes a non-vanishing tensor coupling which can be seen to effectively enhance the vector coupling in NN models which do not include a tensor coupling.     

红色LiMBO3 : Re3+(Re=Eu,Sm) 发光材料的特性

采用固相法制备了红色LiM(M=Ca, Sr, Ba)BO₃ : Re³⁺(Re=Eu, Sm)发光材料,研究了材料的发光性能。研究发现LiM(M=Ca, Sr, Ba)BO₃ : Eu³⁺材料呈现多峰发射,最强发射分别位于610,615,613 nm处,分别监测这三个最强峰,所得激发光谱峰值位于369,400,470 nm。LiM(M=Ca, Sr, Ba)BO₃ : Sm³⁺材料也呈多峰发射,分别对应Sm³⁺的⁴G_5/2→⁶H_5/2、⁴G_5/2→⁶H_7/2和⁴G_5/2→⁶H_9/2跃迁发射;分别监测602,599,597 nm三个最强发射峰,所得激发光谱峰值位于374,405 nm。研究了激活剂浓度对材料发射强度的影响,结果随激活剂浓度的增大,发射强度先增强后减弱,即,存在浓度猝灭效应。实验表明,加入电荷补偿剂Li⁺、Na⁺或K⁺均可提高LiM(M=Ca, Sr, Ba)BO₃ : Re³⁺(Re=Eu, Sm)材料的发射强度。     

Spectroscopy of coherent dark resonances in multilevel atoms for the example of samarium vapor

A universal theory for calculating coherent population trapping resonances in multilevel atoms is suggested. The theory allows arbitrary schemes of multilevel atoms and their excitations to be calculated taking into account the influence of relaxation effects in atoms, applied magnetic field, and the Doppler effect. The experimental data obtained by high-precision diode spectroscopy of coherent dark resonances in samarium vapor are systematically analyzed using the suggested theory. In the absence of a magnetic field, the model of samarium is based on consideration of a degenerate Λ system of the 4f⁶6s²(⁷F₀) ? 4f⁶(⁷F)6s6p(³P⁰)⁹F ₁ ⁰ ?4f⁶6s²(⁷F₁) active transitions. If the fourth 4f⁶6s²(⁷F₂) level is taken into account, this Λ system becomes open. Numerical simulation of coherent population trapping resonances shows that the open character of the system decreases the contrast of resonance curves in absorption spectra without changing resonance widths. The system under applied external longitudinal and transverse magnetic fields is correctly described by 7-and 12-level models of atomic transitions, respectively.     

Selective laser pumping of magnetic sublevels in the hyperfine structure of the cesium atom

The evolution of the populations of the magnetic sublevels of the cesium atom (¹³³Cs isotope) in resonant laser fields with linear polarization is analyzed using the equations for the density matrix. Analytic expressions are derived for stationary populations resulting from laser-induced optical transitions on the hyperfine structure components F _g = 3 ? F _e = 2, 3 and F _f = 4 ? F _e = 3, 4 of lines D ₁ (6² S _1/2 → 6² P _1/2) and D ₂ (6² S _1/2 → 6² P _3/2) depending on the initial values of the populations. The numerical solution of the evolution equations gives the characteristic times of stabilization of the steady regime as functions of laser field intensities and detuning from optical resonance. We determine the sequences of optical transitions increasing (by more than an order of magnitude) the population of the lower sublevel 6² S _1/2 F _g = 3 M = 0 of the “clock” microwave transition F _g = 3 M = 0 ? F _f = 4 M = 0 in the cesium frequency standard, which increases the signal intensity in the recording system by the same proportion.     

Frequency modulation spectroscopy of coherent dark resonances of multi-level atoms in a magnetic field

The resonances of coherent population trapping (CPT) excited by a frequency-modulated (FM) field at the Zeeman sublevels during the transition F _g = 2 → F _e = 1 of the ⁸⁷Rb D ₁-absorption line were studied theoretically. The influence of the nonlinear Zeeman effect on the structure of the observed resonances was considered. The spectra of CPT resonances were calculated for different values of magnetic field induction and compared with the experimental data.     

Electromagnetically induced transparency resonances inverted in magnetic field

The phenomenon of electromagnetically induced transparency (EIT) is investigated in a Λ-system of the ⁸⁷Rb D ₁ line in an external transverse magnetic field. Two spectroscopic cells having strongly different values of the relaxation rates γ_rel are used: an Rb cell with antirelaxation coating (L ~ 1 cm) and an Rb nanometric- thin cell (nanocell) with a thickness of the atomic vapor column L = 795 nm. For the EIT in the nanocell, we have the usual EIT resonances characterized by a reduction in the absorption (dark resonance (DR)), whereas for the EIT in the Rb cell with an antirelaxation coating, the resonances demonstrate an increase in the absorption (bright resonances (BR)). We suppose that such an unusual behavior of the EIT resonances (i.e., the reversal of the sign from DR to BR) is caused by the influence of an alignment process. The influence of alignment strongly depends on the configuration of the coupling and probe frequencies as well as on the configuration of the magnetic field.     

Radiative properties of α-ZnAl2S4:V spinel type single crystals

The absorption and luminescent properties of α-ZnAI₂S₄:V spinel type crystals in the temperature range 10-300 K are investigated. The spectra are assigned to the electronic transitions of trivalent vanadium ions located in octahedral sites. It is shown that at low temperatures the three main components of the revealed IR luminescence spectra are caused by the ¹A_1g(¹G)→¹E_g(¹D), ¹T_2g(¹D), ³T_2g(³F)→³T_1g(³F), and ¹E_g(¹D)→³T_1g(³F) transitions. The observed dependencies of the emission components intensities on temperature are explained assuming that there is a phonon assisted tunnelling between ³T_2g(³F) and ¹E_g(¹D) states. On temperature rise, the ³T_2g(³F)→³T_1g(³F) vibronic transitions suppress other emission channels, which leads to the enhancement of the integral luminescence intensity and to the broadening of the spectrum centred at λ=1.4 μm.