Determination of the excited state density for an optically thick resonance line

The transverse profile of the monochromatic radiance of an optically thick resonance line from a cylindrical discharge is inverted exactly to give the radial distribution of radiating atoms. In contrast to the Abel transform, this result is valid for all optical depths.     

The line shape of Coherent Antistokes Raman Scattering excited under resonance conditions

If Coherent Antistokes Raman Scattering (CARS) is excited by a biharmonic pump in resonance with one photon molecular transition, the Raman line shape is significantly changed compared to the case of nonresonant excitation. This is due to an essential alteration of the 3rd order susceptibility responsible for CARS. Aside from a considerable enhancement of the Raman signal (which makes it possible to detect dissolved molecules in concentration lower than 10^-4 mole/l) the most marked effects are a reversal of the spectral sequence of the Raman maximum and minimum in the CARS-spectrum and for a specially chosen concentration an enhanced contrast of the signal. The factors determining the CARS line shape are discussed theoretically and preliminary experimental results concerning resonance CARS spectra are reported.     

Crossed-coil detection of two-photon excited nuclear quadrupole resonance

Applying a recently developed theoretical framework for determining two-photon excitation Hamiltonians using average Hamiltonian theory, we calculate the excitation produced by half-resonant irradiation of the pure quadrupole resonance of a spin-3/2 system. This formalism provides expressions for the single-quantum and double-quantum mutation frequencies as well as the Bloch-Siegert shift. The dependence of the excitation strength on RF field orientation and the appearance of the free-induction signal along an axis perpendicular to the excitation field provide an unmistakable signature of two-photon excitation. We demonstrate single- and double-quantum excitation in an axially symmetric system using 35Cl in a single crystal of potassium chlorate (omega(Q) = 28 MHz) with crossed-coil detection. A rotation plot verifies the orientation dependence of the two-photon excitation, and double-quantum coherences are observed directly with the application of a static external magnetic field.     

Near resonance charge transfer from a laser excited donor state

A laser induced charge transfer from Na(3p) to hydrogen-ions at different kinetic energies has been studied. An enhancement factor of about 90% in the production rate of Lyman-α radiation has been demonstrated to occur only with H⁺ and Na(3p) atoms reaction; no enhancement was observed with either H ₂ ⁺ or H ₃ ⁺ ions. Absolute cross-section for the production of Lyman-α radiation during the collision of H⁺, H ₂ ⁺ and H ₃ ⁺ ions and Na(3p) and Na(3s) atoms have been measured in the energy range 1–600eV. The charge exchange reactions involving hydrogen-ions and Na(3p) atoms created by two different methods have also been compared.     

Magnetic resonance in an atomic vapor excited by a mechanical resonator

We demonstrate a direct resonant interaction between the mechanical motion of a mesoscopic resonator and the spin degrees of freedom of a sample of neutral atoms in the gas phase. This coupling, mediated by a magnetic particle attached to the tip of the miniature mechanical resonator, excites a coherent precession of the atomic spins about a static magnetic field. The novel coupled atom-resonator system may enable development of low-power, high-performance sensors, and enhance research efforts connected with the manipulation of cold atoms, quantum control, and high-resolution microscopy.     

Polarization spectroscopy of an excited state transition

We demonstrate polarization spectroscopy of an excited state transition in room-temperature cesium vapor. An anisotropy induced by a circularly polarized pump beam on the D2 transition is observed using a weak probe on the 6P(3/2)→7S(1/2) transition. At high pump power, a subfeature due to Autler-Townes splitting is observed that theoretical modeling shows is enhanced by Doppler averaging. Polarization spectroscopy provides a simple modulation-free signal suitable for laser frequency stabilization to excited state transitions.     

Observation of the coherent state in a system of nuclear spin-wave pairs excited by microwave noise pumping

The parametric excitation of nuclear magnons by a microwave noise field was observed in an antiferromagnet. Two critical pumping amplitudes were found to exist. The first one corresponds to the onset of nonlinear microwave absorption. Above the second amplitude, strong phase correlations appear in a system of excited magnon pairs to form a nonequilibrium Bose condensate, which produces intense coherent electromagnetic radiation from the sample and gives rise to the coherent response of parametric magnons to the modulation of their spectrum (modulation response). It was found that, for the noise pumping, the contribution from the processes of elastic magnon relaxation to the threshold pumping amplitudes becomes nonadditive.     

Recoil distance half-life measurements of the excited states in 145Sm

A recoil distance method was used to measure half-lives of the excited states of ₁₄₅Sm. The reaction used was ₁₃₉La(₁₀B, 4n)₁₄₅Sm. A plunger system was used. Half-lives were determined for two excited states for the first time. The yrast 27/2₊ state was found to have a half-life of 1.1 ± 0.2 ns corresponding to the retardation of 3.1 × 10₋₄ comparing with the single particle estimate of M1. The excitation energy of this state was well reproduced by the shell model calculation having a mixed configuration of [π{h^11/2(g^7/2)₋₂ (d^5/2)₋₁}¹⁰⁻, νf^7/2] + [π{h^11/2(g^7/2)₋₁}⁹⁻,νh^9/2]. Another retarded E1 transition was also found in a decay of a 21/2₊ state. Its retardation was 1.6 × 10₋₄ comparing with the single particle value. Received: 9 September 1997 / Revised version: 12 June 1998     

Features of the bremsstrahlung accompanying collisions with a hydrogen atom in an excited state

The features of the bremsstrahlung appearing during a collision of a fast charged particle with a hydrogen atom (or hydrogenic ion) in an excited state are investigated. It is shown that the emission spectrum of photons with energies greater than the ionization potential of a given excited state (except the 2s state) displays narrow lines, which are caused by de-excitation of the atom in an intermediate state. It is demonstrated that the scattering of a charged particle on an excited hydrogen atom produces a feature which is not observed in the case of scattering on a ground-state hydrogen atom. Expressions are obtained for the generalized dynamic polarizability of the hydrogen atom and hydrogenic ions in the 1s, 2s, and 3s states. A method is developed for deriving expressions for the generalized dynamic polarizabilities of other excited states through the use of the Coulomb Green’s function and representation of the electronic wave function in terms of the differentiation of the generating functions of Laguerre polynomials. The bremsstrahlung cross sections for electrons and positrons colliding with hydrogen atoms in the 1s, 2s, and 3s states are calculated. Zh. Tekh. Fiz. 69, 7–13 (October 1999)     

The structure of the triethylenediamine molecule in an excited electronic state

Ultraviolet absorption spectrum has been observed of triethylenediamine (1,4 diazabicyclo[2.2.2]octane) ($\text{D}{}_{\mathrm{<mtext>3</mtext><mtext>A</mtext><mtext>?</mtext>}}$) vapor in the 2200–2600 Å region, and an analysis has been made of its vibrational structure. The vibronic 0-0 transition was determined to be at 2513.65 Å (39782.8 cm^?1), and in the 2540–2590 Å region there were four hot bands found: two from the a₁′-type vibrational levels and two from the a₂″-type vibrational levels of the ground electronic state. The fine structures of these hot bands were examined with 0.49 Å/mm dispersion (slit width = 50 μm). For each of the two a₂″-type hot bands, a progression with 30 ～ 40 cm^?1 spacings was observed; whereas, no such progressions were found for the a₁′-type hot bands, in which absorption peaks are much more concentrated within narrow ranges. These progressions were attributed to a large-amplitude twisting motion of triethylene-diamine molecule. For explaining the whole energy-level structure, another large-amplitude motion, has been postulated. That is a double-minimum deformation motion along the molecular axis; in each minimum, one of the two NC₃ umbrellas is half-way open and the other NC₃ umbrella is half-way closed. The height of the potential barrier between these two minima has been estimated to be 1586 cm^?1.     

The interaction between first excited state hydrogen atoms and a different non-degenerate atom: an example of second-order resonance forces

The interaction of a first excited state hydrogen atom with a different non-degenerate atom is considered in the R ^-1 multiple approximation. The interaction energies for the Π states arising from this interaction have the form usually associated with second-order dispersion energies while those for the Σ states behave quite differently as a function of R. Because of a second-order ‘resonance within one molecule effect’ the second-order Σ-state energies do not possess single R ^-1 expansions that are formally valid for all values of R consistent with the multipole treatment. The expansions of these Σ-state energies, that are valid for ‘small’ R, contain terms varying as both even and odd powers of R ^-1; the lead R ^-7 ‘odd’ term competes strongly with the usual R ^-6 dispersion energy. The expansions that are valid for ‘large’ R contain terms varying as even powers of R ^-1 only and usually have little physical meaning. The He(¹S)-H(n=2) interaction is considered as a specific example of these results and the interaction energies for this system are evaluated through O(R ^-8) by using one-centre pseudostate methods. The general significance of the results is also discussed briefly.     

Ionization of ytterbium atoms from an excited state

The cross sections of the photoionization and the electron impact-induced ionization of Yb atoms from the excited 6s6p(³ P ₁) state are numerically calculated. Matrix elements are computed in multielectron relativistic and nonrelativistic approximations with allowance for the superposition of configurations and a relaxation effect. The radial part of the electron wavefunction in a continuous spectrum is calculated using the solutions to one-configuration Hartree-Fock and Dirac-Fock equations. The cross sections calculated by a relativistic method are compared to those for a nonrelativistic approximation. The ratios of the radiation reduced matrix elements and the phase shifts of the wavefunctions of a continuous spectrum calculated for the 6p ɛs and 6p → ɛd transitions are compared to the values obtained by approximating the experimental dependences of the angular distribution of photoelectrons for the photoionization by ultraviolet radiation from an oriented excited state.     

Competition between benzene and styrene in forming radicals under different solvent conditions observed by muon level crossing resonance

The muon level-crossing-resonance technique has been used to resolve major discrepancies that exist in muon-spin-resonance studies (both free-radical formation and muonium decay rates) in the competition between benzene and styrene. The results, obtained for 30 mM solutions in ethanol and for 2.5 mM aqueous micelles solutions, show that muonium atoms (Mu) react 8 (±2) times faster with styrene than with benzene. In the above cases thermalized Mu is unquestionably the reactive species, which is known to show nucleophilic intra-molecular selectivity in the case of styrene. But a similar value, 9 (±2), was also obtained for undiluted mixtures of liquid benzene and styrene (neat mixture) — where the precursor might have been hot Mu (which should display weaker selectivity than Mu) or cations derived from ⁺ (which should show higher selectivity). These results support the view that thermalized Mu is the predominant reactive species in liquid benzene and styrene.     

Microstructure of excited nuclear states in the vicinity of an yrast line

The microscopic model describing the wobbling motion in fast rotating nuclei is presented and the connection of the parameters describing it with the Coriolis effects at low spins is discussed.     

Electron spin resonance in the relaxed excited state of F-centres detected via saturated optical pumping

A fairly simple and effective method is described to detect spin resonances in the relaxed excited state (RES) of F-and similar color centres in alkali halides. It has been applied to F-centers in CsCl and CsBr, yielding g-factors of 1.77(4) and 1.54(4), respectively, for the RES.     

The decay of the18O giant dipole resonance to excited residual nuclear states

The decay of the¹⁸O GDR to excited residual nuclear states has been examined by measuring spectra of prompt deexcitationγ-rays. The target was irradiated by bremsstrahlung with endpoint energies of 23.5 and 28 MeV. “Bremsstrahlung-weighted” integrated cross sections are given for the population of the residual nuclear states in¹⁷O,¹⁷N,¹⁶O and¹⁴C. Proton decay to excited states in¹⁷N is remarkably weak. It seems that 1p _3/2 excitations play only a minor role in the¹⁸O GDR.