317 research outputs found

    Isotope shift in the dielectronic recombination of three-electron ^{A}Nd^{57+}

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    Isotope shifts in dielectronic recombination spectra were studied for Li-like ^{A}Nd^{57+} ions with A=142 and A=150. From the displacement of resonance positions energy shifts \delta E^{142,150}(2s-2p_1/2)= 40.2(3)(6) meV (stat)(sys)) and \delta E^{142,150}(2s-2p_3/2) = 42.3(12)(20) meV of 2s-2p_j transitions were deduced. An evaluation of these values within a full QED treatment yields a change in the mean-square charge radius of ^{142,150}\delta = -1.36(1)(3) fm^2. The approach is conceptually new and combines the advantage of a simple atomic structure with high sensitivity to nuclear size.Comment: 10 pages, 3 figures, accepted for publication in Physical Review Letter

    Relativistic quantum dynamics in strong fields: Photon emission from heavy, few-electron ions

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    Recent progress in the study of the photon emission from highly-charged heavy ions is reviewed. These investigations show that high-ZZ ions provide a unique tool for improving the understanding of the electron-electron and electron-photon interaction in the presence of strong fields. Apart from the bound-state transitions, which are accurately described in the framework of Quantum Electrodynamics, much information has been obtained also from the radiative capture of (quasi-) free electrons by high-ZZ ions. Many features in the observed spectra hereby confirm the inherently relativistic behavior of even the simplest compound quantum systems in Nature.Comment: Version 18/11/0

    High-resolution measurement of the time-modulated orbital electron capture and of the ÎČ+\beta^+ decay of hydrogen-like 142^{142}Pm60+^{60+} ions

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    The periodic time modulations, found recently in the two-body orbital electron-capture (EC) decay of both, hydrogen-like 140^{140}Pr58+^{58+} and 142^{142}Pm60+^{60+} ions, with periods near to 7s and amplitudes of about 20%, were re-investigated for the case of 142^{142}Pm60+^{60+} by using a 245 MHz resonator cavity with a much improved sensitivity and time resolution. We observed that the exponential EC decay is modulated with a period T=7.11(11)T = 7.11(11)s, in accordance with a modulation period T=7.12(11)T = 7.12(11) s as obtained from simultaneous observations with a capacitive pick-up, employed also in the previous experiments. The modulation amplitudes amount to aR=0.107(24)a_R = 0.107(24) and aP=0.134(27)a_P = 0.134(27) for the 245 MHz resonator and the capacitive pick-up, respectively. These new results corroborate for both detectors {\it exactly} our previous findings of modulation periods near to 7s, though with {\it distinctly smaller} amplitudes. Also the three-body ÎČ+\beta^+ decays have been analyzed. For a supposed modulation period near to 7s we found an amplitude a=0.027(27)a = 0.027(27), compatible with a=0a = 0 and in agreement with the preliminary result a=0.030(30)a = 0.030(30) of our previous experiment. These observations could point at weak interaction as origin of the observed 7s-modulation of the EC decay. Furthermore, the data suggest that interference terms occur in the two-body EC decay, although the neutrinos are not directly observed.Comment: In memoriam of Prof. Paul Kienle, 9 pages, 1 table, 5 figures Phys. Lett. B (2013) onlin

    Isotope Shift in the Dielectronic Recombination of Three-electron \u3csup\u3eA\u3c/sup\u3eNd⁔⁷âș

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    Isotope shifts in dielectronic recombination spectra were studied for Li-like ANd57+ ions with A = 142 and A = 150. From the displacement of resonance positions energy shifts ÎŽE142 150(2s-2p1/2) = 40.2(3)(6) meV [(stat)(sys)] and ÎŽE142 150(2s - 2p3/2) = 42.3(12)(20)meV of 2s - 2pj transitions were deduced. An evaluation of these values within a full QED treatment yields a change in the mean-square charge radius of 142 150ή⟹ r2⟩ = -1.36(1)(3) fm2. The approach is conceptually new and combines the advantage of a simple atomic structure with high sensitivity to nuclear size

    Excitonic AND Logic Gates on DNA Brick Nanobreadboards

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    A promising application of DNA self-assembly is the fabrication of chromophore-based excitonic devices. DNA brick assembly is a compelling method for creating programmable nanobreadboards on which chromophores may be rapidly and easily repositioned to prototype new excitonic devices, optimize device operation, and induce reversible switching. Using DNA nanobreadboards, we have demonstrated each of these functions through the construction and operation of two different excitonic AND logic gates. The modularity and high chromophore density achievable via this brick-based approach provide a viable path toward developing information processing and storage systems
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