Radiation detected resonance ionization spectroscopy on208Tl and242fAm

An ultra-sensitive laser spectroscopic method has been developed for the hyperfine spectroscopy of short-lived isotopes far off stability produced by heavy ion induced nuclear reactions at very weak intensity (> 1/s). It is based on resonance ionization spectroscopy in a buffer gas cell with radiation detection of the ionization process (RADRIS). As a first on-line application of RADRIS optical spectroscopy at^242fAm fission isomers is in progress at the low target production rate of 10/s. The resonance ionization has been performed in two steps utilizing an excimer dye laser combination with a repetition rate of 300 Hz. The first resonant step proceeds through terms which correspond to wavelengths of 466.28, 468.17 or 426.56 nm; the second non-resonant step is achieved with the 351 nm radiation of the excimer laser itself, running with XeF. The frequency scans of the tuneable dye laser at 466.28 and 468.17 nm exhibit broad resonance ionization signals, the latter with a large isotope shift between^242fAm and²⁴³Am which is in accordance with the large quadrupole moment of the^242fAm fission isomer.Work supported by the Bundesministerium für Forschung und Technologie under contract 06 MZ 188 I.     

First observation of a resonance ionization signal on242mAm fission isomers

The feasibility of a hyperfine spectroscopy on^242mAm fission isomers has been demonstrated at the low target production rate of 10/s. The experimental method employed is based on resonance ionization spectroscopy in a buffer gas cell with detection of the ionization process by means of the fission decay of the isomers. The resonance ionization has been performed in two steps, utilizing an excimer dye laser combination with a repetition rate of 300 Hz. The first resonant step proceeds through theJ=7/2 term at 21440.35 cm⁻¹, which has been excited with the tuncable dye laser beam of a wavelength of 466.28 nm, the second non-resonant step is achieved with the 351 nm radiation of the excimer laser itself, running with XeF. The frequency scan of the tuneable dye laser exhibits a broad resonance ionization signal, the width of which is most likely explained by the magnetic hyperfine interaction.     

Isotope shift and hyperfine structure measurements at the242f Am fission isomer

Istope shift and hyperfine structure measurements have been performed for the^242fAm fission isomer with target production rates of only a few per second. The method is based on resonance ionization spectroscopy (RIS) in a buffer gas cell with radioactive decay detection of the ionization process (RADRIS). A relative isotope shift ratioX _exp=IS^242f,241/ IS^243,241=41.7±0.9 has been measured for the 500.02 nm transition corresponding to a nuclear parameter ^242f,241=5.4±0.3 fm². The analysis of the quadrupole moment based on the deformed Fermi-model of the nuclear charge distribution including second order corrections results inQ ₂₀=38.2 ±1.4( _–0.8 ^+0.4 )_model eb. The measurement of the hyperfine structure splitting of the transition at 466.28 nm yields a negativeg-factor and a nuclear spin ofI=2 orI=3.Work supported by the Bundesministerium für Bildung und Forschung under contract 06 MZ 5661.     

Isotope shift measurement at 244fAm *

Strips of Fe_62.5Co₆Ni_7.5Zr₆Cu₁Nb₂B₁₅, prepared by rapid quenching from the melt, were annealed at different temperatures and studied performing Mössbauer and magnetoelastic measurements. By increasing annealing temperature, the long range order increases strengthening the exchange interactions. The maximum of magnetoelastic response corresponds to the maximum of the out of plane magnetization. A possible explanation for the onset of the perpendicular magnetic anisotropy is proposed.