Classical and quantum mechanical resonance fluorescence

We study resonance fluorescence from a two-level atom illuminated by coherent and incoherent light. Especially, we treat the case of an intense incoherent component which is broad band and chaotic in character.New insights into the phenomenon of resonance fluorescence are obtained by constructing certain analogies with the precession of a classical (Bloch) vector around a classical stochastic field. The analogies are based on a representation of the density operator of the two-level atoms as a diagonal mixture of directed angular momentum states.As long as the whole light field is an imposed one the weight function of the mixture mentioned above describes a random sequence of rotations of the Bloch vector and obeys a simple Fokker Planck equation. If, however, the incoherent component of the light field acts as a zero- or finite temperature heat bath, the equation of motion for the weight function is no longer a Fokker Planck equation. Nontheless, we find the exact solution and calculate the correlation functions relevant to a discussion of the spectrum and of antibunching effects.     

Angular uncertainty of momentum correlations in parametric fluorescence

Uncertainty in determining the emission angles of the signal and idler photons is investigated. The role of the pump beam divergence, the pump-spectrum width, and the crystal size is elucidated. Experimental data obtained using an intensified CCD camera are in good agreement with a numerical model that provides angular and spectral characteristics of the signal and idler fields.     

Classical correlations and entanglement in quantum measurements

We analyze a quantum measurement where the apparatus is initially in a mixed state. We show that the amount of information gained in a measurement is not equal to the amount of entanglement between the system and the apparatus, but is instead equal to the degree of classical correlations between the two. As a consequence, we derive an uncertainty-like expression relating the information gain in the measurement and the initial mixedness of the apparatus. Final entanglement between the environment and the apparatus is also shown to be relevant for the efficiency of the measurement.     

Single-spin measurements for quantum computation using magnetic resonance force microscopy

The quantum theory of a single-spin measurement using magnetic resonance force microscopy is presented. We use an oscillating cantilever-driven adiabatic reversal technique. The frequency shift of the cantilever vibrations is estimated. We show that the frequency shift causes the formation of a Schrödinger cat state for the cantilever. The interaction between the cantilever and the environment quickly destroys the coherence between the two cantilever trajectories. It is shown that using partial adiabatic reversals one can obtain a significant increase in the frequency shift. We discuss the possibility of sub-magneton spin density detection in molecules using magnetic resonance force microscopy.     

Classical and quantum conformal field theory

We define chiral vertex operators and duality matrices and review the fundamental identities they satisfy. In order to understand the meaning of these equations, and therefore of conformal field theory, we define the classical limit of a conformal field theory as a limit in which the conformal weights of all primary fields vanish. The classical limit of the equations for the duality matrices in rational field theory together with some results of category theory, suggest that (quantum) conformal field theory should be regarded as a generalization of group theory.On leave of absence from the Department of Physics, Weizmann Institute of Science, Rehovot 76100, Israel     

Angular momentum polarization of the molecules in the Li + HF reaction

A theoretical analysis of the orientation and alignment of the rotational angular momenta of the reactants and products of the Li + HF(v _r = 0, j _r = 3) → LiF(v, j) + H reaction at a collision energy of E _coll = 0.317 eV is performed. The polarization of the angular momentum of the molecules involved in the reaction is based on the technique of spherical tensor operators (state multipoles). Quantum-mechanical calculations of the S-matrix of the reaction are carried out using the wave packet method. In particular, the influence of the orientation of the angular momentum of the HF reactant on the differential cross section is examined. It is shown that the contribution to the differential cross section comes only from be reactants with an angular momentum perpendicular to the reaction plane. In addition, the angular dependence of the orientation and alignment of the angular momenta of the reaction products are examined. It is shown that, for an isotropic distribution of reactant molecules, the orientation of the angular momenta of the products differs from zero only in the direction perpendicular to the reaction plane. Different experimental geometries, based on radiation enhanced multiphoton ionization, are proposed to detect the predicted effects.     

Energy and angular momentum transfer in atom-diatom collisions from polarized laser fluorescence

We report a study of collisional reorientation of diatomic lithium molecules by rare gas atoms using high resolution circularly polarized laser fluorescence. As in the case of I₂ we find that elastic collisions are very inefficient at reorienting Li₂ molecules and a selection rule ΔM′ _J = 0 appears to be in operation. Rotationally inelastic collisions, particularly those with argon, cause some degree of reorientation and are the result of relatively long range intermolecular interactions. Vibrational transfer features are more strongly depolarized. Optical pumping studies of oriented ¹Σ _g Li₂ molecules have yielded a cross section for inelastic transfer of 35 ± 15 Ų.     

Statistical theory of angular momentum polarization in chemical reactions

A general statistical treatment applicable to any vector property of reactive scattering is derived from angular correlation theory. This pertains to the usual experimental situation in which two or three vector directions are observed but numerous other vectors are random or unobserved, particularly various angular momentum vectors. The dependence of the cross section on the angles relating the observed vectors is expanded as a Legendre polynomial series, with coefficients which represent averages of angular momentum functions over the unobserved vectors. An algorithm for calculating these angular correlation coefficients is provided by the statistical theory. All non-vanishing terms involve only even-order Legendre polynomials. In many experiments, one or two terms are predominant. Classical and quantal versions give the same algorithm in the correspondence principle limit, which often holds for chemical reactions. The angular correlations involving the initial and final relative velocity vector directions [kcirc] and [kcirc]′ and the product rotational angular momentum j′ are treated in detail, including both pairwise and triple correlations. Explicit formulae are given for three choices of the quantization axis : along [kcirc], along [kcirc]′, and along [kcirc] × [kcirc]′. Coefficients for the ([kcirc], [kcirc]′, j′) correlations are tabulated for seven reactions as examples and comparison made with recent experimental measurements of the spatial orientation or polarization of j′ in reactions of alkali atoms with hydrogen halides and with methyl iodide.     

Statistical theory of angular momentum polarization in chemical reactions

A general statistical treatment applicable to any vector property of reactive scattering is derived from angular correlation theory. This pertains to the usual experimental situation in which two or three vector directions are observed but numerous other vectors are random or unobserved, particularly various angular momentum vectors. The dependence of the cross section on the angles relating the observed vectors is expanded as a Legendre polynomial series, with coefficients which represent averages of angular momentum functions over the unobserved vectors. An algorithm for calculating these angular correlation coefficients is provided by the statistical theory. All non-vanishing terms involve only even-order Legendre polynomials. In many experiments, one or two terms are predominant. Classical and quantal versions give the same algorithm in the correspondence principle limit, which often holds for chemical reactions. The angular correlations involving the initial and final relative velocity vector directions [kcirc] and [kcirc]′ and the product rotational angular momentum j′ are treated in detail, including both pairwise and triple correlations. Explicit formulae are given for three choices of the quantization axis: along [kcirc], along [kcirc]′, and along [kcirc] × [kcirc]′. Coefficients for the ([kcirc], [kcirc]′, j′) correlations are tabulated for seven reactions as examples and comparison made with recent experimental measurements of the spatial orientation or polarization of j′ in reactions of alkali atoms with hydrogen halides and with methyl iodide.     

Energy and momentum as observables in quantum field theory

The spectrum condition implies that energy and momentum are limits of local observables.     

Angular correlation and linear polarization measurements on unresolved gamma-ray cascades

A method for the determination of transition multipolarity and neighbouring level spins by means of direction- and polarization-correlation measurements on an unresolved mixture of gamma-ray cascades with one common transition is presented. The applicability of this method in particular problems is briefly discussed.The author wishes to thank Ing. J. Honzátko and Dr. J. Kopecký for helpful discussions and comments.     

Fock-tani representation for the quantum theory of reactive collisions

A previously-developed second-quantization representation for nonrelativistic systems of composite bound states and their constituents is extended to any number of composite species. The result is an explicit representation for the kinematics and dynamics of reactive scattering processes (rearrangement collisions). A single Hamiltonian in the new representation simultaneously exhibits the various possible scattering and reaction channels, thus circumventing problems associated with “different Hamiltonians for different channels”. The “unperturbed” Hamiltonian describes the free propagation of all possible bound composites as well as their unbound constituents, while the interaction Hamiltonian describes only true scattering and reaction processes, each term corresponding to a collision process with specified initial and final bound composites and/or unbound constituents. The key to the generalization is a suitable ordering of the composite species and a corresponding ordered-product form of the unitary transformation to the new representation.     

Wave packets in the quantum theory of collisions

Two methodological difficulties of the quantum theory of collisions are considered. The first is the undesirable interference of the incident and scattered waves in the stationary approach to scattering. The second concerns the nonstationary approach to the theory of collisions of the type a + b → c + d. In order to calculate the cross section one uses the matrix element 〈cd|S|ab〉 of the S-matrix. The element is proportional to δ-function expressing the energy conservation. The corresponding probability |〈cd|S|ab〉|² contains δ², which is mathematically meaningless. The known regular way to overcome the difficulty seems to be unsatisfactory. In this paper, both the problems are resolved using wave packets of incident particles. The text was submitted by the author in English.     

Classical and quantum hall effect measurements in GaInNAs/GaAs quantum wells

We have performed magneto-transport experiments in modulation-doped Ga_0.7In_0.3N_yAs_1−y/GaAs quantum wells with nitrogen mole fractions 0.4%, 1.0% and 1.5%. Classical magnetotransport (resistivity and low-field Hall effect) measurements have been performed in the temperatures between 1.8 and 275 K, while quantum Hall effect measurements in the temperatures between 1.8 and 47 K and magnetic fields up to 11 T.The variations of Hall mobility and Hall carrier density with nitrogen mole fractions and temperature have been obtained from the classical magnetotransport measurements. The results are used to investigate the scattering mechanisms of electrons in the modulation-doped Ga_0.7In_0.3N_yAs_1−y/GaAs quantum wells. It is shown that the alloy disorder scattering is the major scattering mechanism at investigated temperatures.The quantum oscillations in Hall resistance have been used to determine the carrier density, effective mass, transport mobility, quantum mobility and Fermi energy of two-dimensional (2D) electrons in the modulation-doped Ga_0.7In_0.3N_yAs_1−y/GaAs quantum wells. The carrier density, in-plane effective mass and Fermi energy of the 2D electrons increases when the nitrogen mole fraction is increased from y=0.004 to 0.015. The results found for these parameters are in good agreement with those determined from the Shubnikov-de Haas effect in magnetoresistance.     

Special topics in the quantum theory of angular momentum

Two special topics in the quantum theory of angular momentum are discussed in this article. They are: (i) the relationship between the coupling and recoupling coefficients (for two and three angular momenta, respectively) and sets of generalized hyper-geometric functions of unit argument; and (ii) the ‘non-trivial’ or polynomial zeros of angular momentum coefficients and their classification.     

A comparative study of model ingredients: Fragmentation in heavy-ion collisions using quantum molecular dynamics model

We aim to understand the role of NN cross-sections, equation of state as well as different model ingredients such as width of Gaussian, clusterization range and different clusterization algorithms in multifragmentation using quantum molecular dynamics model. We notice that all model ingredients have sizable effect on the fragment pattern.