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.     

碘分子单频及双频多光子光谱

采用多光子离化谱和荧光激发谱技术，对碘分子单频和双频五光子离化谱和三光子荧光谱进行了研究和标识．对OODR五光子离化谱中一组间隔为72cm^-1的振动序列进行了归属，并确定了其激发、发射和离化通道 关键词：     

Laser Spectroscopic Investigation of the Element Fermium (Z = 100)

The level scheme and hyperfine structure of the element fermium (Z = 100) has been investigated with the method of resonance ionization spectroscopy in a buffer gas cell. The experiments were carried out on a 46 pg sample of the isotope ²⁵⁵Fm with a half-life time of 20.1 h, produced in the high flux nuclear reactor of the ORNL, Oak Ridge, USA. A wave number scan from 27,100 to 28,400 cm⁻¹ was carried through to search for three levels with large Einstein-coefficients, as predicted by ab initio Multi-Configuration-Dirac-Fock (MCDF) calculations, and five new levels were found. In addition, the two known levels at wave numbers (25,099.8 ± 0.2) and (25,111.8 ± 0.2) cm⁻¹ were studied with a laser band width of 1.5 GHz and hyperfine broadenings were observed.     

Resonance ionization spectroscopy of thorium

Here we describe experiments aimed at developing an element-selective ion source for thorium (Th). The technique applied is resonance ionization spectroscopy (RIS) with a thermal atom beam. Ionization schemes for isotopically nonselective ionization of Th as well as for isotopically selective ionization of ²³⁰Th are proposed. The RIS-scheme used is two-photon two-colour ionization with excitation in the ultraviolet spectral range between 244 nm and 267 nm or in the visible spectral range between 485 nm and 529 nm. Ionization of the excited atoms is performed either by ultraviolet photons or by visible photons, depending on the energy required for this process.     

Laser Based Techniques for Ultra Trace Isotope Production, Spectroscopy and Detection

A variety of research activities in the field of fundamental and applied nuclear physics has evolved in the last years using resonantly tuned radiation from powerful lasers. The technique of resonance ionization spectroscopy has delivered outstanding results and found broad acceptance in the last years as a particularly efficient and highly selective method for rare and exotic radioisotope studies. It is used for production, spectroscopy and detection of these species and provides complete isobaric, high isotopic and even some isomeric selection, which altogether is needed for on-line investigation of short lived species far off stability as well as for ultra trace determination. Good overall efficiency pushes the experimental limits of detection in elemental trace analysis down to below 10⁶ atoms per sample, and additionally isotopic selectivity as high as 3 × 10¹² has been demonstrated. The widespread potential of resonance ionization techniques is discussed, focusing on the experimental arrangements for applications in selective on-line isotope production, spectroscopy of rare radioisotopes and ultra trace determination of radiotoxic isotopes like ²³⁸Pu to ²⁴⁴Pu, ^135,137Cs, ^89,90Sr or ⁴¹Ca in environmental, technical and biomedical samples.     

Study of the neutron deficient 182–190Pb isotopes by simultaneous atomic- and nuclear-spectroscopy

Mean-square charge radii and magnetic moments have been measured for the neutron deficient lead isotopes, ^182–190Pb. The measurement was performed at the ISOLDE online mass separator, using the in-source resonance ionization spectroscopy technique. The wavelength of the first excitation step for the resonance ionization laser ion source (RILIS) was scanned over the resonance(s) whilst the α- and γ-ray spectra from the decay of the Pb isotopes were recorded as a function of the wavelength. The isotope shift and, in the case of odd-A isotopes, the hyperfine splitting were deduced. The rms-charge radii of the very neutron deficient Pb isotopes follow the smooth trend of the heavier isotopes. This finding indicates a spherical shape for the lead ground states at the neutron mid-shell (N = 104), where the excitation energy of the oblate 0⁺ state in the even isotopes reaches its minimum.     

Fully rotationally resolved ZEKE photoelectron spectroscopy of C6H6 and C6D6: photoionization dynamics and geometry of the benzene cation

A comprehensive set of spectra for the benzene cation and the perdeuterated benzene cation has been recorded with full rotational resolution using zero kinetic energy photoelectron spectroscopy (ZEKE) at high resolution (up to 0.2 cm^?1), using a slow-rising extraction pulse. With different rovibronic levels in the S₁ 6^l state as intermediate resonance, the rotational transitions to the vibronic ground state of the cation have been recorded using two-colour, two-photon resonance enhanced multiphoton ionization. A simple spectator model has been employed to simulate the intensities of the ZEKE transitions. By fitting the simulations to the recorded spectra, improved values for the rotational constants and the Coriolis coupling parameters of benzene and perdeuterated benzene have been obtained. The CC and CH bond lengths of the cation have been deduced. The spectator model is shown to be reliable despite the fact that no specific allowance is made for the effect of final state interactions on the signal intensity.     

Investigation of highly excited states of samarium

Highly excited even-parity states of the samarium atom in the range between 34104 and 39155 cm⁻¹ have been studied by the method of one-color three-photon resonance ionization spectroscopy. The energies and total angular momenta of 342 states have been determined. Seven new even-parity states of samarium have been discovered.     

Isotope shift and hyperfine structure measurements for 155Yb by laser ion source technique

The change in the mean square charge radius and electromagnetic moments of the neutron deficient ¹⁵⁵Yb isotope have been determined using resonance ionization spectroscopy in a laser ion source. The data point to an absence of a marked deformation change for Yb isotopes with N=84−86. Received: 2 October 1997 / Revised version: 24 October 1997     

Collision-energy-resolved Penning ionization electron spectroscopy of toluene and chlorotoluenes

Stereodynamics in ionization of toluene and o-, p-chlorotoluenes by collision with He^*(2³S) metastable atoms were investigated by two-dimensional collision-energy/electron-energy-resolved Penning ionization electron spectroscopy. Anisotropic interactions around the molecule were studied by the collision energy dependence of partial ionization cross-sections (CEDPICS) as well as model potential calculations, and shielding effect by the methyl group was observed in CEDPICS for ionization from Cl lone-pair orbitals of o- chlorotoluene. Attractive interaction with He^*(2³S) around the π orbital region was found to be larger for toluene rather than o-, p- chlorotoluenes. Exterior electron density (EED) calculation of partial ionization cross-sections in Penning ionization and negative CEDPICS for ionization band observed in ca. 4 eV in electron energy indicated that π^-2π⁺¹ shake-up state was observed in Penning ionization electron spectroscopy of toluene.     

Ru原子高Rydberg态研究

本文描述用激光共振激发-场电离实验方法测定Ru原子的4d⁷(⁴F)ns(n=28—45)和4d⁷(⁴F)nd(n=26—48)系列Rydberg能级,并应用非线性拟合得到了Ru原子的第一电离阈值。采用相对论性自洽场方法对所得能级以及相应的量子亏损作了计算,理论与实验结果符合得很好。此外还将本文所得的第一电离阈值与已有数据作了比较。 关键词：     

Towards the determination of the charge radius of 11Li by laser spectroscopy

Isotope shift measurements by means of laser resonance ionization spectroscopy are a unique tool to determine the charge radii of halo nuclei. The most prominent halo nucleus ¹¹Li is at the same time the best accessible candidate for such studies. The experimental method to determine the charge radius of this exotic nucleus and first test results on ⁷Li will be presented in this paper. This revised version was published online in August 2006 with corrections to the Cover Date.     

(2 + 1) Resonance enhanced multiphoton ionization of hydrogen chloride in a pulsed supersonic jet: Vacuum wavenumbers of rotational lines with detailed band analysis for excited electronic states of HCl

A comprehensive study of the excited electronic states of HCl is reported. Using resonance enhanced multiphoton ionization ((2 + 1) REMPI) and time-of-flight mass spectrometry (TOFMS) over 120 band systems are analyzed. Supersonic jet techniques are used to prepare rotationally cold species for laser spectroscopy in the 77 000 to 96 000 cm⁻¹ region. At least 50 new electronic states are characterized as well as several features only tentatively assigned previously. A long vibrational progression consisting of 29 vibrational levels of the deeply bound V¹Σ⁺(0⁺) valence/ion-pair state is studied. We also extend the identification and analysis to high vibrational levels of low-lying Rydberg states. The assignments of [²Π_i] Rydberg state complexes are evaluated in terms of spin-orbit coupling and united-atom calculations. In several band systems, the spectra exhibit anomalous rotational line intensities and broadened linewidths which are consistent with predissociation. Multiphoton ionization with mass spectrometry permits the investigation of isotope effects as well as the appearance of fragment species associated with repulsive potential curves.     

Resonance ionization spectroscopy of bismuth at the IGISOL facility

A programme of research has commenced at the IGISOL facility, Jyväskylä, combining the technique of resonance ionization spectroscopy with the development of the highly selective laser ion source trap (LIST). The first element of interest is bismuth, which contains three isomers of multi-quasiparticle states in near-spherical nuclei, namely ²⁰⁷Bi (21/2⁺, 182 μs), ²⁰⁴Bi (10^?, 13 ms) and ²⁰⁴Bi (17⁺, 1.07 ms). A measurement of the optical isomer shift provides a direct comparison of the mean?square charge radii between the isomer and the nuclear ground state. Due to the short isomer lifetimes the spectroscopy will be done either within the ion guide or in a sextupole ion beam guide (SPIG), located after the ion guide and used in the development of the LIST. A mixed dye-Ti:Sapphire laser ionization scheme has been successfully tested for bismuth and first off-line results have been obtained.     

Electronic Spectra of Radical Ions

Abstract

Organic molecules may accept an extra electron to form radical anions, R⁺, or give up an electron by ionization to form radical cations, R⁺. Some of the radical ions are relatively stable in their ground states in solution phase and can be readily characterized by spectroscopic methods. Electron spin resonance spectroscopy provides an ideal tool for the study of the unshared electron in these radical ions. Most radical ions are intensely colored and give characteristic absorption bands in the electronic spectra. Further, electronic spectroscopy is one of the few tools available for the study of the dianions, which are generally diamagnetic. Electronic spectroscopy is used not merely for the characterization of the ionic species in solution but also for the study of the chemical equilibria involving various kinds of ionic species.     

Ionization Scheme Development at the ISOLDE RILIS

The resonance ionization laser ion source (RILIS) of the ISOLDE on-line isotope separation facility is based on the method of laser step-wise resonance ionization of atoms in a hot metal cavity. The atomic selectivity of the RILIS complements the mass selection process of the ISOLDE separator magnets to provide beams of a chosen isotope with greatly reduced isobaric contamination. Using a system of dye lasers pumped by copper vapour lasers, ion beams of 24 elements have been generated at ISOLDE with ionization efficiencies in the range of 0.5–15%. As part of the ongoing RILIS development off-line resonance ionization spectroscopy studies carried out in 2003 and 2004 have determined the optimal three-step ionization schemes for scandium, antimony, dysprosium and yttrium.     

New laser setup at the IRIS facility. Magnetic moments and mean squared charge radii of neutron deficient Tl isotopes

A new laser installation for the resonance ionization spectroscopy in a laser ion source and for rare isotope production has been put into operation at the IRIS mass-separator, working on-line with the 1 GeV proton beam of the Petersburg Nuclear Physics Institute synchrocyclotron. Isotope shift and hyperfine splitting of 276.9 nm atomic transition in the long chain of Tl isotopes and isomers have been measured. New data on the magnetic moments and changes in mean squared charge radius for ^{183,184,185,185m,186m2,195m,197m}Tl have been obtained.     

Accurate isotope shift measurements on short lived neon isotopes

We report on fast beam collinear laser spectroscopy measurements that demonstrate the feasibility of accurate isotope shift measurements for short lived Ne isotopes including the proton halo candidate ¹⁷Ne. Ultra high sensitivity is achieved by the application of an efficient resonance detection scheme based on collisional ionization and ion counting via the β decay. A direct measurement of the kinetic energy of the atomic Ne beam provides the required high accuracy. This revised version was published online in August 2006 with corrections to the Cover Date.     

碘分子高激发态光学双共振多光子离化光谱

本文利用双色双共振多光子离化技术（ＯＯＤＲ－ＭＰＩ）,对Ｉ２分子离子对态Ｆ０＋ｕ态进行了较为仔细的研究,利用已知的分子常数,对所得谱线进行了标识和归属,将Ｔｅ＝５２４００ｃｍ－１,间隔为３７ｃｍ－１的振动序列归属为Ｆ０＋ｕ态的高振动激发态,并确定了多光子激发及离化的跃迁通道