14 research outputs found

    A large-scale R-matrix calculation for electron-impact excitation of the Ne2+^{2+} O-like ion

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    The five JΠ\Pi levels within a np2np^2 or np4np^4 ground state complex provide an excellent testing ground for the comparison of theoretical line ratios with astrophysically observed values, in addition to providing valuable electron temperature and density diagnostics. The low temperature nature of the line ratios ensure that the theoretically derived values are sensitive to the underlying atomic structure and electron-impact excitation rates. Previous R-matrix calculations for the Ne2+^{2+} O-like ion exhibit large spurious structure in the cross sections at higher electron energies, which may affect Maxwellian averaged rates even at low temperatures. Furthermore, there is an absence of comprehensive excitation data between the excited states that may provide newer diagnostics to compliment the more established lines discussed in this paper. To resolve these issues, we present both a small scale 56-level Breit-Pauli (BP) calculation and a large-scale 554 levels R-matrix Intermediate Coupling Frame Transformation (ICFT) calculation that extends the scope and validity of earlier JAJOM calculations both in terms of the atomic structure and scattering cross sections. Our results provide a comprehensive electron-impact excitation data set for all transitions to higher nn shells. The fundamental atomic data for this O-like ion is subsequently used within a collisional radiative framework to provide the line ratios across a range of electron temperatures and densities of interest in astrophysical observations.Comment: 17 pages, 8 figure

    K-shell photoionization of ground-state Li-like boron ions [B2+^{2+}]: Experiment and Theory

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    Absolute cross sections for the K-shell photoionization of ground-state Li-like boron [B2+^{2+}(1s2^22s 2^2S)] ions were measured by employing the ion-photon merged-beams technique at the Advanced Light Source synchrotron radiation facility. The energy ranges 197.5--200.5 eV, 201.9--202.1 eV of the [1s(2s\,2p)3^3P]2^2Po{\rm ^o} and [1s(2s\,2p)1^1P] 2^2Po{\rm ^o} resonances, respectively, were investigated using resolving powers of up to 17\,600. The energy range of the experiments was extended to about 238.2 eV yielding energies of the most prominent [1s(2\ell\,n\ell^{\prime})]2^2Po^o resonances with an absolute accuracy of the order of 130 ppm. The natural linewidths of the [1s(2s\,2p)3^3P] 2^2Po{\rm ^o} and [1s(2s\,2p)1^1P] 2^2Po{\rm ^o} resonances were measured to be 4.8±0.64.8 \pm 0.6 meV and 29.7±2.529.7 \pm 2.5 meV, respectively, which compare favourably with theoretical results of 4.40 meV and 30.53 meV determined using an intermediate coupling R-matrix method.Comment: 6 figures and 2 table

    K-shell photoionization of ground-state Li-like carbon ions [C3+^{3+}]: experiment, theory and comparison with time-reversed photorecombination

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    Absolute cross sections for the K-shell photoionization of ground-state Li-like carbon [C3+^{3+}(1s2^22s 2^2S)] ions were measured by employing the ion-photon merged-beams technique at the Advanced Light Source. The energy ranges 299.8--300.15 eV, 303.29--303.58 eV and 335.61--337.57 eV of the [1s(2s2p)3^3P]2^2P, [1s(2s2p)1^1P]2^2P and [(1s2s)3^3S 3p]2^2P resonances, respectively, were investigated using resolving powers of up to 6000. The autoionization linewidth of the [1s(2s2p)1^1P]2^2P resonance was measured to be 27±527 \pm 5 meV and compares favourably with a theoretical result of 26 meV obtained from the intermediate coupling R-Matrix method. The present photoionization cross section results are compared with the outcome from photorecombination measurements by employing the principle of detailed balance.Comment: 3 figures and 2 table

    Convergent close-coupling method for positron scattering from noble gases

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    We present the convergent close-coupling formulation for positron scattering from noble gases (Ne, Ar, Kr and Xe) within the single-center approximation. Target functions are described in a model of six p-electrons above an inert Hartree–Fock core with only one-electron excitations from the outer p6 shell allowed. Target states have been obtained using a Sturmian (Laguerre) basis in order to model coupling to ionization and positronium (Ps) formation channels. Such an approach is unable to yield explicit Ps-formation cross sections, but is valid below this threshold and above the ionization threshold. The present calculations are found to show good agreement with recent measurements

    Theory and applications of atomic and ionic polarizabilities

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    Atomic polarization phenomena impinge upon a number of areas and processes in physics. The dielectric constant and refractive index of any gas are examples of macroscopic properties that are largely determined by the dipole polarizability. When it comes to microscopic phenomena, the existence of alkaline-earth anions and the recently discovered ability of positrons to bind to many atoms are predominantly due to the polarization interaction. An imperfect knowledge of atomic polarizabilities is presently looming as the largest source of uncertainty in the new generation of optical frequency standards. Accurate polarizabilities for the group I and II atoms and ions of the periodic table have recently become available by a variety of techniques. These include refined many-body perturbation theory and coupled-cluster calculations sometimes combined with precise experimental data for selected transitions, microwave spectroscopy of Rydberg atoms and ions, refractive index measurements in microwave cavities, ab initio calculations of atomic structures using explicitly correlated wave functions, interferometry with atom beams, and velocity changes of laser cooled atoms induced by an electric field. This review examines existing theoretical methods of determining atomic and ionic polarizabilities, and discusses their relevance to various applications with particular emphasis on cold-atom physics and the metrology of atomic frequency standards.Comment: Review paper, 44 page
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