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.     

Stereodynamics of the Ca + HCl → CaCl + H molecular reaction imposed by the rotational-excited states of HCl

The effects of the initial rotational-excited states of the HCl molecule on the stereodynamics properties of the Ca + HCl molecular reaction are investigated using the quasiclassical trajectory theory and the analytical potential energy surface. The orientation and alignment behaviors for the rotational angular momentum of the product, along with the generalized differential cross section (PDDCS)-dependent polarization, are calculated to explore the stereodynamics properties. The initial rotational-excited states of the HCl molecule impose a remarkable effect on the vector correlation distributions, regardless of the orientation, alignment, or PDDCS. The forward, backward, and weak sideway scatterings are found in the Ca + HCl → CaCl + H molecular reaction. The results demonstrate that the initial rotational-excited state of j = 3 results in more obvious stereodynamics effects.     

State dependence of rayleigh scattering from an=2 state of hydrogenlike atoms

We consider Rayleigh scattering from a hydrogenlike atom in an arbitrary excitedn=2 state, and we investigate theoretically the dependence of the scattered radiation intensity and Stokes parameters on the state multipoles for the case of unpolarized incident radiation. Because in then=2 case Rayleigh scattering can not be accompanied by the change of the electron angular momentum, only 10 out of the 16 state multipoles influence the scattered radiation attributes. Our study reveals the existence of a measurable quantity which is determined only by Rayleigh scattering from 2p states. For the particular case of excitation by electron impact, some quantitative predictions are made, at the photon scattering angle ?=π/2, based on values for the state multipoles extracted from the literature (Blum and Kleinpoppen, Band). The vicinity of Balmer α and Lyman α resonances are studied in detail.     

Electronic angular momentum polarizations of photofragments: a case study of ICN photodissociation from a perpendicular transition

A quantum treatment on ICN photodissociation from an initial perpendicular transition (Omega'=+/-1<--Omega"=0) to the asymptote CN(|Sigma+,J'M'N'1/2>)+I(2P3/2) is presented. Density matrices of both photofragments are derived and explicit expressions of the state multipoles in terms of the angular momentum coupling coefficients and the rotation-bending factors have been obtained. To perceive the physical origin of electronic angular momentum polarizations of the iodine photofragments, a correlation scheme which considers the magnetic dipolar and the electrostatic dipole-quadrupole interactions between I and CN cofragments is proposed. For ICN precursors in the vibrational ground state or in the equally populated l-type split levels, the alignment parameters of the iodine photofragments in the molecular frame can be calculated according to this long-range interaction model. For the perpendicular transition |1Pi1><--|1Sigma0+>, its alignment parameters of I(2P3/2) from the incoherent and coherent transitions to the |Omega'=1> and |Omega'=-1> components are rho(0)2(1Pi1)=0.756 and rho2(2)(1Pi1)=-0.656, respectively. For the perpendicular transition to |3Pi1>, rho(0)2(3Pi1)=-0.878 and rho2(2)(3Pi1)=0.328 are from the incoherent transition, whereas rho(0)2(3Pi1)=0.122 and rho2(2)(3Pi1)=0.328 are from the coherent transition. To analyze the photoion images of iodine photofragments, angular distributions of I+ from the 2+1 resonance-enhanced multiphoton ionization detection scheme are derived.     

Orientation and alignment in charge exchange processes involving sodium atoms studied by semi-classical molecular theory

The semi-classical molecular model is applied to study the charge exchange processes in the H⁺-Na 3p and Li⁺-Na 3p systems in the keV energy range. The dependence of the charge exchange on the orientation and the alignment of the initial or final state is obtained for the transition probabilities and for the differential cross sections. The 14 state present model for the H⁺-Na system is in good agreement with the experimental differential cross sections. The alignment is explained by orientation occurring in the transfer region. The cross sections predicted with a 28 state model for Li⁺-Na exhibit similar behaviour as for H⁺-Na.     

Optimal molecular alignment and orientation through rotational ladder climbing

We study the control by electromagnetic fields of molecular alignment and orientation in a linear, rigid-rotor model. With the help of a monotonically convergent algorithm, we find that the optimal field is in the microwave part of the spectrum and acts by resonantly exciting the rotation of the molecule progressively from the ground state, i.e., by rotational ladder climbing. This mechanism is present not only when maximizing orientation or alignment, but also when using prescribed target states that simultaneously optimize the efficiency of orientation/alignment and its duration. The extension of the optimization method to consider a finite rotational temperature is also presented.     

Alignment mechanism of a nematic liquid crystal on a pre-rubbed polyimide film with laser-induced periodic surface structure

A periodic surface structure was prepared on a pre-rubbed polyimide (PI) film surface with a pulsed UV laser polarized perpendicular to the rubbing direction. The experimental results demonstrate that the rubbing-induced molecular anisotropic orientation was relaxed by the pulsed laser irradiation, and the laser induced molecular orientation was perpendicular to the line of the laser-induced periodic structure. The dichroism of the anisotropy of molecular orientation increased with the increase of laser energy. Since the direction of the laser-induced molecular anisotropy was perpendicular to the surface groove direction of the pre-rubbed PI surface, the effects of surface microgroove and anisotropic molecular orientation of the PI chain on liquid crystal (LC) alignment can be distinguished from each other. LC alignment was investigated by evaluating the anchoring energy of the PI surface, which was calculated according to Berreman's theory using the twist angle of the LC in the cells. The experimental results demonstrate that the exact alignment direction of the LC molecules is determined by the relative strength of both factors.     

Achieving a robust homogenously aligned liquid crystal layer with reactive mesogen for in-plane switching liquid crystal displays

Uniformly aligned liquid crystals (LCs) are of crucial importance in a practical application, such as displays, phase modulators and virtual reality devices. Although an alignment layer using polyimide-type polymers can almost perfectly align the LCs, polymer-stabilisation at the surface using pre-mixed monomers has been attempted to reduce the fabrication process, i.e. eliminating the alignment layer, thereby reducing the fabrication cost. Here, we propose an approach to achieve a homogeneous alignment of LCs by controlling the molecular structure of reactive monomers mixed in LCs without using conventional polyimide alignment layer. The result shows an excellent initial dark state and acceptable electro-optic performance which implies that the polymer stabilisation at the surface successfully anchors the homogenous orientation of LCs. We believe that the proposed fabrication method can contribute to cost-effective fabrication process by eliminating an alignment layer with no fabrication step of a surface treatment.     

Alignment mechanism of a nematic liquid crystal on a pre-rubbed polyimide film with laser-induced periodic surface structure

A periodic surface structure was prepared on a pre-rubbed polyimide (PI) film surface with a pulsed UV laser polarized perpendicular to the rubbing direction. The experimental results demonstrate that the rubbing-induced molecular anisotropic orientation was relaxed by the pulsed laser irradiation, and the laser induced molecular orientation was perpendicular to the line of the laser-induced periodic structure. The dichroism of the anisotropy of molecular orientation increased with the increase of laser energy. Since the direction of the laser-induced molecular anisotropy was perpendicular to the surface groove direction of the pre-rubbed PI surface, the effects of surface microgroove and anisotropic molecular orientation of the PI chain on liquid crystal (LC) alignment can be distinguished from each other. LC alignment was investigated by evaluating the anchoring energy of the PI surface, which was calculated according to Berreman's theory using the twist angle of the LC in the cells. The experimental results demonstrate that the exact alignment direction of the LC molecules is determined by the relative strength of both factors.     

Force related atomic multipoles in planar molecules. Derivation of atomic quadrupole and octupole moments

Atomic multipoles as defined by current methods generally do not account for forces in molecules that arise from external electrostatic fields. It is pointed out that such forces and the electrostatic potential that the molecule itself generates are both determined by the molecular multipolar tensors. The latter constitute therefore the fundamental molecular constants that determine the molecular electrostatics apart from polarization. In general the multipolar tensors include contributions from the atomic multipoles and their fluxes. In planar molecules, however, the perpendicular charge flux is zero by symmetry. This gives rise to a (previously introduced) formalism that extracts analytical, force-related, atomic multipoles from the molecular multipolar tensors. This formalism is extended in this work to include force-related (FR) atomic quadrupoles and octupoles in planar molecules. The properties of the FR atomic multipoles, including their perpendicular fluxes, are discussed and some formal theoretical and computational advantages that characterize them are indicated. As an example, the electrostatics of OCS, including the molecular electrostatic potential and the forces on the nuclei due to an external point charge, is discussed.     

Generation, characterisation, and applications of atomic and molecular alignment and orientation

The gas phase is generally defined as a state of matter in which atoms or molecules are in constant, rapid, random Brownian motion. However, a range of techniques exist for preparing distributions of gas phase atoms and molecules whose motion is far from random, and whose orientation in space is well defined. In this Perspective, we will explore the nature of atomic and molecular alignment and orientation, the various techniques by which samples of spatially oriented species may be prepared and characterised, and some of the ways in which oriented molecules are being exploited to further our knowledge of molecular structure and dynamics.     

Infrared intensities of lattice vibrations in molecular crystals

From the dynamic multipoles model an expression is derived for the dipole moment derivative governing the intensity of infrared absorption by lattice modes in molecular crystals. The result depends on non-local susceptibilities which take proper account of the local electric field in a way consistent with dielectric theory. It is shown that the non-local rsponse follows naturally from microscopic lattice dynamical theory. It arises from dipolar coupling and is intimately connected with the delocalized exciton states produced by the same mechanism. Intensities calculated for the iodine crystal are inproved by including the local field, but a point quadrupole field proves too anisotropic to yield the measured intensity ratio. The treatment shows that infrared intensities can be used to obtain unique effective molecular polarizabilities.     

Small-angle neutron scattering from a hexagonal phase under shear

Summary The shear orientation of a micellar hexagonal liquid crystalline phase was investigated by small-angle neutron scattering. The hexagonal phase in the quiescent state showed a symmetrical scattering pattern typical of a polydomain structure. Enhanced scattering along the flow direction was observed during shear and the anisotropy of scattering intensity became stronger with increasing shear rate. The anisotropic scattering pattern corresponds to an orientation perpendicular to the flow direction and can be interpreted as a log-rolling state. The oriented sample did not relax after cessation of shear. The results from small-angle neutron scattering confirm data obtained previously from rheo-small angle light scattering measurements and are discussed in comparison to shear alignment of lyotropic liquid crystalline polymer solutions.     

Quantum stereodynamics of Li + HF reactive collisions: the role of reactants polarization on the differential cross section

A complete quantum study for the state-to-state Li + HF(v,j,m) → LiF(v',j',Ω') + H reactive collisions has been performed using a wave packet method, for different initial rotational states and helicity states of the reactants. The state-to-state differential cross section has been simulated, and the polarization of products extracted. It is found that the reactivity is enhanced for nearly collinear collisions, which produces a vibrational excitation of HF, needed to overcome the late barrier. It is also found that LiF(v' = 0) products are preferentially forward scattered, while vibrationally excited LiF(v' = 1 and 2) are backward scattered. These results are interpreted with a simple reaction mechanism, based on the late character and bent geometry of the transition state, originating from a covalent/ionic crossing, which consists of two steps: the arrival at the transition state and the dissociation. In the first step, in order to get to the saddle point some HF vibrational excitation is required, which favors head-on collisions and therefore low values of m. In the second step a fast dissociation of H atom takes place, which is explained by the ionic Li(+)F(-)H character of the bent transition state: the FH(-) is repulsive making that H depart rapidly leaving a highly rotating LiF molecule. For the higher energy analyzed, where resonances slightly contribute, the orientation and alignment of product rotational states, referred to as reactants frame (with the z-axis parallel to k), are approximately constant with the scattering angle. The alignment is close to -1, showing that j' is perpendicular to k, while starting from initial states with well defined rotational orientation, as states with pure m values, the final rotational are also oriented. It is also found that when using products frame (with the z'-axis parallel to k') the rotational alignment and orientation of products varies a lot with the scattering angle just because the z' axis changes from being parallel to anti-parallel to k when varying from θ = 0 to π.     

The lifetime of the A2Sigmau+ state of the N3 radical

The lifetime of the A 2Sigmau+ state of N3 has been determined from line broadening in the rotationally resolved laser-induced fluorescence (LIF) spectrum of the A 2Sigmau+-X 2Pig transition. N3 radicals, produced by fluorine atom abstraction from HN3, were probed with an intracavity doubled ring laser operating near 272 nm. Careful examination of the LIF spectrum indicates a significant Lorentzian component to the line shape due to a rapid predissociation in the A 2Sigmau+ state. The predissociation lifetime is found to be 132+/-21 ps for the 000 vibrational level and 64+/-10 ps for the 010 level. The short lifetime is consistent with the low intensity of the LIF signal especially for the 010-010 hot band.     

Quantum Theory of ICN Photodissociation: Density Matrices of Photofragments from a Parallel Transition

A quantum treatment on ICN photodissociation from an initial parallel transition (Ω′ = 0 ← Ω″ = 0) to 1 the asymptote CN(|)+ I(²P_1/2) is presented. Density matrices of both photofragments are derived, and explicit expressions of the state multipoles in terms of the angular momentum coupling coefficients and the rotation‐bending factors have been obtained. The present theoretical framework provides a foundation to study photofragments with non‐null electronic and/or spin angular momenta. To investigate the angular momentum polarizations phenomena, these density matrices can play a prime role in laser‐based detections of state‐selected photofragments.     

Detection of collision-induced rotational alignment in counterpropagating beam scattering

Collision-induced rotational alignment of NH₃ scattered from He is detected in a counterpropagating pulsed molecular beam scattering experiment. Starting from an isotope distribution of the initial rotational angular momentum, the generation of a highly aligned product ensemble due to inelastic scattering is observed. For all probed state-resolved differential cross sections the alignment changes from negative values for backward scattering to positive values at small deflection angles which is in qualitative agreement with predictions from a geometric apse model. The degree of alignment strongly depends on the final rotational state, indicating a correlation with the involved energy transfer.     

Orbital alignment in N2O photodissociation. I. Determination of all even rank anisotropy parameters

We present a general method for determination of the photofragment K=4 state multipoles in an ion imaging experiment. These multipoles are important for determining the full density matrix for any photofragment with j(a)> or =2. They are expressed in terms of laboratory frame anisotropy parameters that have distinct physical origins and possess characteristic angular distributions. The explicit expression for the (2+1) resonant multiphoton ionization absorption signal for the case of arbitrarily polarized probe light is derived and a procedure for isolation of the rank-4 state multipoles from all others is shown. This treatment is applied to the case of O((1)D) produced in the 193 nm photodissociation of N2O. The results show nonzero values for all K=4 anisotropy parameters, indicating the complexity of the photodissociation dynamics in this system.     

UNDERSTANDING STRUCTURAL EFFECTS OF MULTIPOLE MOMENTS ON AQUEOUS SOLVATION OF IONS USING THE SOFT-STICKY DIPOLE-QUADRUPOLE-OCTUPOLE WATER MODEL

The effects of water multipole moments on the aqueous solvation of ions were determined in Monte Carlo simulations using soft-sticky dipole-quadrupole-octupole (SSDQO) water. Water molecules formed linear hydrogen bonds to Cl(-) using the new SSDQO1 parameters, similar to multi-site models. However, the dipole vector was tilted rather than parallel to the oxygen-Na(+) internuclear vector as in most multi-site model, while experiment and ab initio molecular dynamics simulations generally indicate a range of values between tilted and parallel. By varying the multipoles in SSDQO, the octupole was found to determine the orientation around Na(+). Moreover, analysis of the multipoles of more conventional models is predictive of their performance as solvents.     

Laser-induced fluorescence and pure rotational spectroscopy of the CH2CHS (vinylthio) radical

Laser-induced fluorescence (LIF) excitation spectra of the B-X (2)A(") electronic transition of the CH(2)CHS radical, which is the sulfur analog of the vinoxy (CH(2)CHO) radical, were observed under room temperature and jet-cooled conditions. The LIF excitation spectra show very poor vibronic structures, since the fluorescence quantum yields of the upper vibronic levels are too small to detect fluorescence, except for the vibrationless level in the B state. A dispersed fluorescence spectrum of jet-cooled CH(2)CHS from the vibrationless level of the B state was also observed, and vibrational frequencies in the X state were determined. Precise rotational and spin-rotation constants in the ground vibronic level of the radical were determined from pure rotational spectroscopy using a Fourier-transform microwave (FTMW) spectrometer and a FTMW-millimeter wave double-resonance technique [Y. Sumiyoshi et al., J. Chem. Phys. 123, 054324 (2005)]. The rotationally resolved LIF excitation spectrum for the vibronic origin band of the jet-cooled CH(2)CHS radical was analyzed using the ground state molecular constants determined from pure rotational spectroscopy. Determined molecular constants for the upper and lower electronic states agree well with results of ab initio calculations.