由激光诱导荧光方法探测光碎片分子取向的理论研究

采用密度矩阵方法 ,推导了从激光诱导荧光 (LIF)强度中抽出光碎片取向参数的表达式 .光碎片的取向由分子态多极矩描述 .用于解离母分子和激发碎片分子的激光均为线偏振光 ,而探测荧光为非偏振光 .激光诱导荧光强度是光碎片分子初始态多极矩、线强度因子和解离—激发几何因子的函数 .光碎片的取向参数可以由测量荧光偏振比和计算动力学因子而获得     

Attenuation corrections for in-cylinder NO LIF measurements in a heavy-duty Diesel engine

Quantification of the nitric oxide (NO) concentration inside the cylinder of a Diesel engine by means of laser-induced fluorescence (LIF) measurements requires, amongst others, knowledge of the attenuation of the ultraviolet radiation involved. We present a number of laser diagnostic techniques to assess this attenuation, enabling a correction for laser intensity and detection efficiency of the raw NO LIF data. Methods discussed include overall laser beam transmission, bidirectional laser scattering (bidirectional LIF), spectrally resolved fluorescence imaging, and Raman scattering by N₂. A combination of techniques is necessary to obtain the complete attenuation of laser beam and NO fluorescence. The overall laser beam transmission measurements and bidirectional LIF measurements (the latter yielding spatially resolved transmission) provide evidence of a non-uniform attenuation distribution, with predominant attenuation within or near the piston bowl. Fluorescence imaging of multiple vibrational bands through a spectrograph is shown to be a powerful method for obtaining spatially resolved data on the transmission losses of fluorescence. Special attention is paid to the role of CO₂ and O₂ as UV light absorbers, and the consequences to different excitation-detection schemes for NO. PACS 82.33.Vx; 42.62.Fi; 33.20.t     

Integrated state multipoles and plane asymmetry

The relationship between the integral alignment and orientation coefficients and the polarizations of the decay photons measured in an experiment where the scattered electrons are not observed is expounded. The determination of some integrated state multipoles is shown to provide also a simple checking of the plane symmetry invariance of an atomic collision.     

Angular momentum polarization in molecular collisions : Classical and quantum theory for measurements using resonance fluorescence

Inelastic or reactive collisions typically produce an anisotropic distribution of rotational angular momentum. An explicit and general treatment is given for the intensity and polarization of resonance fluorescence from molecules produced in such processes. Both classical and quantum results are expressed in terms of bipolar harmonics and state multipoles formed from linear combinations of density matrix elements. The treatment provides an inversion procedure for determining moments of the rotational angular momentum distribution ; twelve independent moments can be obtained. The combinations of angular momentum operators involved are even in eight of these moments and odd in four, with respect to reflection in a plane containing the initial and final relative velocity vectors. Measurements of the even moments require linearly polarized excitation and fluorescence, whereas measurements of the odd moments require circularly polarized excitation. The requisite experimental geometry and other practical aspects are discussed. In the three appendices are discussed the classical limits of transition intensities, a density matrix treatment of atom-rigid-rotor collisions, including analysis of state multipole symmetries ; and the coupling coefficients for parallel angular momenta.     

Role of rotational state-selected for nonadiabatic alignment: OCS molecules in femtosecond laser fields

Nonadiabatic alignment by intense nonresonant laser fields is a versatile technique to manipulate the spatial direction of molecules. By solving the time-dependent Schrödinger equation numerically the degree of alignment of the molecules initially in different rotational state are calculated and the results show that the degree of alignment strongly depends on the initial rotational state. Thus, the present study indicates that, for obtaining a high degree of alignment for molecules, appropriate selection of molecular rotational states is necessary.     

Optical pumping with laser-induced-fluorescence

We describe a new procedure for optical pumping that is based on laser-induced fluorescence (LIF). The procedure is demonstrated by optically exciting a sample of Rb⁸⁵ atoms, which then creates a population imbalance between the ground state hyperfine levels of Rb⁸⁷ by “LIF depopulation pumping”. Though optical pumping with this technique increases the intensity dependent light-shift coefficient (i.e., ac Stark shift) of the Rb⁸⁷ 0-0 hyperfine transition, it reduces the frequency dependent light-shift coefficient by at least an order of magnitude. Since the stabilization of the diode laser wavelength is a significant challenge in the development of laser-pumped gas-cell atomic clocks, it is anticipated that optical pumping with LIF will be of benefit to atomic clock technology.     

Effect of tunneling ionization on dynamic alignment and post-ionization alignment of nitrogen molecules irradiated by different laser intensities

The dynamic alignment and post-ionization alignment of nitrogen molecules are investigated while considering the effect of tunneling ionization. The effects of tunneling ionization on the angular distribution are calculated when the molecules are irradiated by different laser intensities. The results show that laser intensity directly affects the time and extent of dynamic alignment. Furthermore, the extent of post-ionization alignment is not only determined by laser intensity but also affected by the final extent of dynamic alignment. The post-ionization alignment will dominate during the process of molecular (or molecular ion) rotational alignment for femtosecond laser pulse. The time of tunneling ionization is a significant factor to the final ensemble angular distribution of molecular ions when laser intensity is low.     

Laser coupling to nuclei via collective electronic oscillations—a simple heuristic model study

The induction field coupling of laser-driven collective electronic oscillations has been proposed as an interlevel transfer mechanism for a gamma-ray laser. Using a heuristic classical model for the electron oscillations, we verify in the model six general features which we conjecture are valid for laser-induced collective oscillations: (1) enhancement of the electric field seen by the nucleus, (2) harmonic generation, (3) generation of higher multipoles, (4) odd (even) order multipoles couple to odd (even) harmonics, (5) there exists an optimum laser intensity for each multipole order and harmonic, and (6) for a given multipole order, the optimum intensity increases with harmonic number. We briefly discuss the relevance of these results to a proposed interlevel transfer experiment in ²³⁵U.     

Experimental investigation of the effect of collisions and temperature on degenerate four-wave mixing

An experimental investigation (including a comparison with a simple theoretical model) of the effect of buffer-gas composition, pressure and temperature on resonant Degenerate Four-Wave Mixing (DFWM) has been performed. The DFWM signal from NO in a quartz cell was measured and the effect of quenching as well as elastic (phase-changing) collisions was studied by varying the total and partial pressures of N₂ and CO₂ as buffer gases. It was found that the DFWM signal first slowly increased with buffer-gas pressure (up to 10 mbar) and then rapidly decreased. It was furthermore found that the DFWM signal was considerably less sensitive to quenching collisions as compared to Laser-Induced Fluorescence (LIF) (for laser intensities approximately equal to half the DFWM saturation intensity of the transition). On the other hand, while LIF is virtually insensitive to elastic collisions, DFWM displays a larger sensitivity to elastic collisions than to quenching collisions. The DFWM saturation intensity was found to increase with buffer-gas pressure (although slower than expected). When varying the temperature of the gas composition, it was found that the DFWM signal decreased markedly with increasing temperature. This decrease is too fast to be explained solely by a change in the population of the molecular state probed by the laser.     

Molecular multipoles and (hyper) polarizabilities from the Buckingham expansion:revisited

The Buckingham expansion is important for understanding molecular multipoles and (hyper) polarizabilities. In this study, we give a complete derivation of the Buckingham expansion in the traced form using successive Taylor series. Based on the derivation results, a general Buckingham expansion in the traced form is proposed, from which highly accurate numerical calculations using the finite field method can be achieved. The transformations from the traced multipoles and multipole-multipole polarizabilities to the corresponding traceless counterparts are realized with an auxiliary traced electric field gradient. The applications of thefinite field method in this study show good agreements with previous theoretical calculations and experimental measurements.