Target ion source and charge exchange cell development for the EXCYT facility

The EXCYT facility at the INFN-LNS is based on a K-800 superconducting cyclotron delivering stable ion beams on a Target Ion Source (TIS) assembly to produce the required nuclear species, and on a 15 MV Tandem for post-accelerating the radioactive beams. For some ion beams such as for Li, the extraction efficiency from the TIS is higher when obtained by positive ionisation, while the injection into the Tandem is possible only after a charge exchange to obtain negative ions. In this work we present the procedures together with the results of the production of ^6,7,8,9Li beams extracted at EXCYT during the last year. The production of the radioactive elements was performed by sending a ¹³C⁴⁺ primary beam of 45 MeV/u on a graphite target. The ionisation of the production species was achieved by a tungsten positive surface ioniser. The Li⁺ has been extracted from TIS at different energies to cross-check the transmission and the charge exchange efficiency. To perform the conversion from positive to negative ions we employed a Charge Exchange Cell (CEC) containing Cs vapours. The Li beam interacts with the latter in a two-step reaction, thus converting its charge from +1 to –1. The CEC was already characterised during off-line tests; the results obtained at EXCYT confirmed both the isotopic shift effect and the efficiency values at several given extraction energies. Future improvements of the TIS and the CEC are discussed.     

ISAC-I and ISAC-II: Present status and future perspectives

The ISAC facility at TRIUMF utilizes up to 100 μA from the 500 MeV H^- cyclotron to produce the RIB using the Isotopic Separation On Line (ISOL) method. The ISAC-I facility comprised the RNB production target stations, the mass separator and the beam delivery to low energy area and to a room temperature linear accelerator composed of a 4-rod RFQ and an inter-digital H type structure Drift Tube LINAC. ISAC-I linear accelerator can provide beam from A = 3 to 30 amu with an energy range from 0.15 to 1.5 A MeV. Since the beginning of operations target development program has been to increase proton beam currents on targets. Now we routinely operate our target at 50 to 85 μA and recently we have operated our target at 100 μA. Other developments are in place to add other ion sources, laser, FEBIAD and ECRIS to the actual surface ion source. The last two five year plans were mainly devoted to the construction of a heavy ion superconducting LINAC (ISAC-II), that will upgrade the mass and the energy range from 30 to 150 and 1.5 to 6.5 A MeV, respectively. We are now commissioning the medium β section and first experiment is scheduled for the fall 2006.     

Laser spectroscopy of trapped 7Be and 10Be at a prototype slow RI-beam facility of RIKEN

A next-generation slow radioactive nuclear ion beam facility (SLOWRI) which provides slow, high-purity and small emittance ion beams of all elements is being build as one of the principal facilities at the RIKEN RI-beam factory (RIBF). High energy radioactive ion beams from the projectile fragment separator BigRIPS are thermalized in a large gas catcher cell. The thermalized ions in the gas cell are guided and extracted to a vacuum environment by a combination of dc electric fields and inhomogeneous rf fields (rf carpet ion guide). From there the slow ion beam is delivered via a mass separator and a switchyard to various devices: such as an ion trap, a collinear fast beam apparatus, and a multi-reflection time of flight mass spectrometer. In the R&D works at the present RIKEN facility, an overall efficiency of 5% for a 100A MeV ⁸Li ion beam from the present projectile fragment separator RIPS was achieved and the dependence of the efficiency on the ion beam intensity was investigated. Recently our first spectroscopy experiment at the prototype SLOWI was performed on Be isotopes. Energetic ions of ¹⁰Be and ⁷Be from the RIPS were trapped and laser cooled in a linear rf trap and the specific mass shifts of these isotopes were measured for the first time.     

Nuclear-matter distributions of halo nuclei from elastic proton scattering in inverse kinematics

Proton-nucleus elastic scattering at intermediate energies, a well-established method for probing nuclear-matter density distributions of stable nuclei, was applied for the first time to exotic nuclei. This method is demonstrated to be an effective means for obtaining accurate and detailed information on the size and radial shape of halo nuclei. Absolute differential cross-sections for small-angle scattering were measured at energies near 700 MeV/u for the neutron-rich helium isotopes ⁶He and ⁸He, and more recently for the lithium isotopes ⁶Li, ⁸Li, ⁹Li and ¹¹Li, using He and Li beams provided by the fragment separator FRS at GSI Darmstadt. Experiments were performed in inverse kinematics using the hydrogen-filled ionization chamber IKAR which served simultaneously as target and recoil-proton detector. For deducing nuclear-matter distributions, differential cross-sections calculated with the aid of the Glauber multiple-scattering theory, using various parametrizations for the nucleon density distributions as input, were fitted to the experimental cross-sections. The results on nuclear-matter radii and matter distributions are presented, and the significance of the data for a halo structure is discussed. Nuclear-matter distributions obtained for ⁶He and ⁸He conform with the concept that both nuclei compose of α-particle like cores and significant neutron halos. The matter distribution in ¹¹Li exhibits, as expected from previous reaction cross-section studies with nuclear targets, the by far most extended halo component of all nuclei being investigated. In addition the present data allow a quantitative comparison of the structure of the He and Li isobares of either the mass number A = 6 or A = 8. The measured differential cross-sections have also been used for probing density distributions as predicted from various microscopic calculations. A few examples are presented. Received: 21 March 2002 / Accepted: 16 May 2002 / Published online: 31 October 2002 RID="a" ID="a"e-mail: p.egelhof@gsi.de     

Design study of an in-flight projectile fragment separator for rare isotope beams

Radioactive isotope(RI) beams are used to investigate the characteristics of unstable nuclei. Fragment separators, which have large angular and energy acceptances, were required to obtain high RI beam intensity. Careful design is required due to the large high order aberrations induced by the large aperture magnets, which are used to collect rare isotopes obtained from a high energy primary heavy-ion beam hitting a target [1]. In our design study, a high energy ¹²C primary beam was used to produce neutron rich medium mass heavy ions such as ⁹Li. Mirror symmetric optics provides smaller high order aberration and thus a design study of a mirror symmetric in-flight projectile fragment separator was performed to obtain large angular and energy acceptances. We investigated the optimal material and thickness of the target for the production of a ⁹Li beam. Based on the simulation, a beryllium target was selected to give a large yield with a smaller energy spread of the secondary beam. We also investigated the optimal thickness of the aluminum energy degrader. The selections of the target material and thickness were investigated by using the code LISE++.After optimization of the material and the thickness of the target, we performed a design study of the optics of the in-flight separator for a high resolution with high acceptance. The designed optics of the in-flight separator consists of the four normal conducting quadrupole triplets, three sextupoles and two normal conducting dipoles. The horizontal and vertical angular acceptances of the designed separator are 40 mrad and 70 mrad, respectively. The separator has a mass resolution of 640 when the object size is taken to be 1 mm. The correction of the second order aberration in the designed optics was performed by three sextupole magnets. The path length of the designed separator is 20.183 m. The optics design and the high order aberrations were investigated by using the code ORBIT.     

Isotope shifts and hyperfine structure in the transitions in calcium II

The isotope shift and hyperfine structure in the three - transitions in Ca II have been studied by fast ion beam collinear laser spectroscopy for all stable Ca isotopes. The metastable 3d states were populated within the surface ionization source of a mass separator with a probability of about 0.1%. After resonant excitation to the 4p levels with diode laser light around 850 nm the uv photons from the transitions to the ground state were used for detection. Hyperfine structure parameters A and B for the odd isotope ⁴³Ca, as evaluated from the splittings observed, agree well with theoretical predictions from relativistic many-body perturbation theory. Field shift constants and specific mass shift constants were extracted from the measured isotope shifts and are discussed in comparison with expectation values from theory. Received: 19 September 1997 / Revised: 5 December 1997 / Accepted: 27 January 1998     

Commissioning of the MAGNEX large-acceptance spectrometer

The MAGNEX large-acceptance spectrometer has been commissioned with beams from the Tandem accelerator at INFN-LNS Catania. The optics were tested with elastically-scattered ⁷Li, ¹⁶O and ⁴⁸Ti beams with various apertures mounted after the target. The momentum dispersion was verified to be in agreement with the optics calculations. A demonstration of the particle identification capabilities of the PSD start detector and the focal plane detector was given by a measurement of the ²⁷Al(⁷Li,⁶Li)²⁸Al transfer reaction at a mean angle of 25°. The measured charge state distribution of ⁴⁸Ti ions is in agreement with predictions for a gold stripping foil. Preliminary results of the software reconstruction of incident angle and excitation energy, obtained through matrices based on a 3D-interpolation of the measured field maps, are encouraging.     

CARIBU: a new facility for the study of neutron-rich isotopes

The Californium Rare Ion Breeder Upgrade (CARIBU) to the ATLAS superconducting linac facility is currently being commissioned. It provides low-energy and re-accelerated beams of neutron-rich isotopes obtained from ²⁵²Cf fission. The fission products from a ²⁵²Cf source are stopped in a large high-intensity gas catcher, thermalized and extracted through an RFQ cooler, accelerated to 50 kV and mass separated in a high-resolution separator before being sent to either an ECR charge breeder for post-acceleration through the ATLAS linac or to a low-energy experimental area. This approach gives access to beams of very neutron-rich isotopes, many of which have not been available at low or Coulomb barrier energies previously. These beams provide unique opportunities for measurements along the r-process path. To take advantage of these unique possibility, the reaccelerated beams from CARIBU will be made available at the experimental stations of ATLAS to serve equipment such as Gammasphere, HELIOS and the reaction spectrometers. In addition, the Canadian Penning Trap (CPT) mass spectrometer has been moved to the CARIBU low-energy experimental area and a new injection line has been built. The new injection line consists of a RFQ buncher sitting on a 50 kV high-voltage platform that will accumulate the mass separated 50 kV radioactive beams, cool and extract them as a pulsed beam of 3 keV. This beam can be sent either to a tape station for diagnostics and tuning, or a cryogenic linear trap for preparation before transfer to the high-precision Penning trap where the mass measurements will take place. Initial CARIBU commissioning is proceeding with a 2 mCi source that will be replaced by a 100 mCi source as the commissioning proceeds. Final operation will use a 1 Ci source and attain yield in excess of 10⁷ ions/sec for the most intense beams at low energy, an order of magnitude less for reaccelerated beams.     

Resonance lonization mass spectroscopy with a pulsed thermal atomic beam

Resonance ionization mass spectroscopy (RIMS) and pulsed-laser induced desorption (PLID) have been combined for ultrasensitive detection and spectroscopy of very small samples of refractive elements. The method has been tested and applied to laser spectroscopy of 5×10⁹ atoms (1.5 pg) of¹⁹⁵Au (T _1/2= 183d) implanted at the ISOLDE online mass separator with 60 keV into graphite. A pulsed thermal atomic beam was formed by laser desorption with a 10 ns NdYag laser pulse. Subsequently the atoms were photoionized in a three-colour, three-step resonant excitation to an autoionizing state. The selectivity was enhanced by a time-of-flight measurement of the photo ions. In resonance, one ion was detected per 10⁵ atoms implanted resulting in a gain in detection efficiency by three orders of magnitude in comparison to the use of a continuous atomic beam. In the course of the experiments several unknown autoionizing states were found, and the lifetime of the 6d ² D ^3/2 state of gold was determined to be=10.7(6) ns.     

Reaction cross section measurements of the neutron-rich isotopes8,9,11Li at 80 MeV/nucleon

Total interaction cross sections have been measured for⁸Li on C and Pb targets, for⁹Li on C, Al, Cu, Sn and Pb targets as well as for¹¹Li on C, Sn and Pb targets. For each beam, we also used a plastic scintillator as target. The measurements with the scintillator targets are used to extract reduced nuclear radii of the lithium isotopes. These radii are then used for the calculation of the nuclear part of the total cross section for the other targets. The total electromagnetic-dissociation (EMD) cross sections have been deduced and are compared to different models. A strong target-charge-dependent EMD cross section is measured for¹¹Li reaching 2.96 _–0.82 ^+0.84 b for the Pb target. In the⁹Li case, a large EMD cross section for high-Z targets has been observed which amounts to 0.75 ± 0.45 b for the Pb target. The EMD cross sections of both,⁹Li and¹¹Li, may be understood by the giantdipole-resonance model.This work forms part of the PhD Thesis of B. Blank     

RI beam facility project at RIKEN and physics programs

In the Radioactive-Isotope Beam Factory (RIBF) project in RIKEN, intense primary beams can be provided at the energies E = 350−400MeV over the whole range of atomic number in the cascade-cyclotron acceleration scheme, for which three cyclotrons, fRC, IRC, and SRC, have been newly constructed. The project proceeds through two phases. In the phase-I program, the superconducting in-flight radioactive-isotope beam separator BigRIPS and the following ZeroDegree spectrometer have been installed as well as the three cyclotrons. In the commissioning, after the successful extraction of a ²³⁸U beam from SRC at E = 345 A MeV in the cascade-acceleration scheme, radioactive-isotope beams were produced and isotope-separated with BigRIPS as designed. The RIBF project is fully capitalized in the phase-II program, in which the construction of several experimental key devices has been proposed. The upgrade of the former fragment separator RIPS is also included there. It allow for a scheme to use intense primary beams at the intermediate energy E = 115 A MeV with RIPS. Remarkably, the produced radioactive-isotope beams at this energy can be spin-polarized taking the advantage of the fragmentation-induced spin orientation phenomena. on behalf of the RIBF project     

Laser Spectroscopy Programme at the Jyväskylä IGISOL

This paper reviews the status of the laser spectroscopy programme being carried using the IGISOL mass separator in combination with an RFQ cooler-buncher. Measurements in the zirconium region are being extended to the yttrium isotopes. Two K = 8 isomers, in ¹⁷⁶Yb and ¹³⁰Ba, are found to have smaller mean square charge radii than their ground states, and the isotope shifts of stable osmium isotopes have been measured off-line by collinear laser spectroscopy.     

Advances in laser spectroscopy of lithium

A number of recent experiments have employed novel spectroscopic techniques to precisely measure the fine and hyperfine structure splittings as well as the isotope shifts for several transitions at optical frequencies for the stable ^6,7Li and radioactive isotopes ^8,9,11Li. These data offer an important test of theoretical techniques that have been developed over the last decade by two groups to accurately calculate effects due to Quantum Electrodynamics and the finite nuclear size in 2 and 3 electron atoms. Theory and experiment have studied several transitions in both singly ionized and neutral lithium. The work by multiple groups permits a critical examination of the consistency of separately, the experimental work as well as the theoretical calculations. Combining the measured isotope shifts with the calculated energy shifts passing these consistency tests, permits the determination of the relative nuclear charge radius with an uncertainty approaching 1 × 10^?18 meter. These results are more than an order of magnitude more accurate than those obtained by electron scattering experiments and give insight into the mass and charge distributions of the nuclear constituents. Prospects for a precision measurement of the fine structure constant are also discussed.     

NMR at single crystal surfaces

15 sites on 1 cm². To overcome this for the important class of alkali adsorbates on metals and semiconductors, two methods are presented. Common to both is the preparation of a highly nuclear spin-polarized atomic beam of ⁶Li in the one case and ⁸Li in the other. The latter isotope is radioactive and undergoes a β-decay with a half-life of 0.84 s. Li adsorbed on the close-packed Ru(001) surface is investigated. The longitudinal relaxation time, T₁, is the main observable and is used to deduce the local electronic density of states [LDOS(E_F,r=0)] and Li diffusion barriers. The second experiment uses ⁶Li as an adsorbate, also studied on Ru(001). The nuclear polarization is measured by beam foil spectroscopy. A novel particle detected (photon counting) Fourier transform NMR technique is demonstrated. This is done by observing the time-dependent flux of circularly polarized light emitted behind the foil after a 90° pulse has been employed at the surface. Electric field gradients and transverse relaxation times, T₂, are thus determined. A large difference between T₁ and T₂ is traced to the dimensionality of the system. Received: 21 March 1997/Accepted: 12 August 1997     

ISOLTRAP: An on-line Penning trap for mass spectrometry on short-lived nuclides

ISOLTRAP is a Penning trap mass spectrometer for high-precision mass measurements on short-lived nuclides installed at the on-line isotope separator ISOLDE at CERN. The masses of close to 300 radionuclides have been determined up to now. The applicability of Penning trap mass spectrometry to mass measurements of exotic nuclei has been extended considerably at ISOLTRAP by improving and developing this double Penning trap mass spectrometer over the past two decades. The accurate determination of nuclear binding energies far from stability includes nuclei that are produced at rates less than 100 ions/s and with half-lives well below 100ms. The mass-resolving power reaches 10⁷ corresponding to 10keV for medium heavy nuclei and the uncertainty of the resulting mass values has been pushed down to below 10^-8. The article describes technical developments achieved since 1996 and the present performance of ISOLTRAP.     

Polarized beam of unstable nuclei via ion beam surface interaction at grazing incidence

We have measured the polarization of unstable nuclei produced by the technique of ion beam surface interaction at grazing incidence (IBSIGI). A 60 keV ¹²⁴Cs beam from the on-line mass separator was used. The NMR technique was employed for the observation of the nuclear polarization. A small polarization of 0.22(13)% was observed. The small value was interpreted in terms of the velocity dependence of nuclear polarization, comparing with the results observed with stable nuclei. This revised version was published online in August 2006 with corrections to the Cover Date.     

Integrated target-ion source unit for on-line production of radioactive short-lived isotopes

A new version of integrated target-ion source unit (ionising target) has been developed for the on-line production of radioactive single-charged ions. The target is able to withstand temperatures up to 2500 ^°C and acts also as an ion source of the surface and laser ionisation. Off-line and on-line experiments with the ionising target, housing tantalum foils as a target material, have been carried out at the IRIS (Investigation of Radioactive Isotopes on Synchrocyclotron) facility. The off-line surface ionisation efficiency measured for stable atoms of Li, Rb and Cs was correspondingly 6% , 40% and 55% at the target temperature of 2000 ^°C and 3-10% for atoms of rare-earth elements Sm, Eu, Tm and Yb at a temperature of 2200 ^°C. The off-line measured values of the ionisation efficiency for stable Gd and Eu atoms by the laser beam ionisation inside the target were 1% and 7%, respectively. The radioactive beam intensities of neutron-deficient rare-earth nuclides from Eu to Lu produced by the integrated target-ion source unit have been measured at a temperature of 2500 ^°C. The results of the integrated target-ion source unit use for on-line laser resonance ionisation spectroscopy study of neutron-deficient Gd isotopes have been also presented.     

Magneto-optical trap and mass-separator system for the ultra-sensitive detection of <Superscript>135</Superscript>Cs and <Superscript>137</Superscript>Cs

We report the first magneto-optical trapping of radioactive ¹³⁵Cs and ¹³⁷Cs and a promising means for detecting these isotopes at ultra-sensitive levels by coupling a magneto-optical trap (MOT) to a mass separator. A sample containing both isotopes was placed in the source of a mass separator, ionized, mass-separated, and implanted in a Zr foil within the trapping cell. After implantation, atoms were released from the foil by inductive heating and then captured in a MOT that used large-diameter beams and a dry-film-coated cell to achieve high trapping efficiency. Trapped-atom numbers in the case of either isotope ranged from 10⁴ to 10⁷, as determined from the MOT fluorescence signal. Over this trapped-atom range, the MOT fluorescence signal was found to increase linearly with the number of atoms implanted in the foil and without isotopic bias to within 4%. In principle, this method can then provide a measurement of the ¹³⁷Cs/¹³⁵Cs ratio accurate to within 4% through the direct ratio of MOT fluorescence signals. The fluorescence signal from stable ¹³³Cs, when implanted and released from the foil, was suppressed relative to MOT signals by more than seven orders of magnitude when the system was tuned to trap ¹³⁵Cs or ¹³⁷Cs. When combined with the isotopic selectivity of ≥10⁵ for the mass separator, the overall suppression of ¹³³Cs is expected to exceed 10¹². At present our system delivers atoms from sample to MOT with an efficiency of 0.5%, has a trapped-atom detection limit of 4000 atoms, and achieves a sample-detection sensitivity of one million atoms. Received: 23 August 2002 / Published online: 8 January 2003 RID="*" ID="*"Corresponding author. Fax: +1-505/667-0440, E-mail: mdd@lanl.gov     

The β decay of tellurium 135 and 137

Tellerium 135 and 137 nuclei were produced in thermal neutron fission of²³⁵U separated by on-line isotope separator and deposited on a movable tape. Gamma ray singles,γ-γ, β-γ coincidences and time sequencedγ spectra were collected using Ge(Li) detectors and scintillator (NE 102 A) telescope. The half-lives and mass excesses of¹³⁵Te and¹³⁷Te were measured and level schemes of¹³⁵I and¹³⁵I have been established. The level scheme of¹³⁵I has been compared to different shell model calculations.     

Exploring new mass regions with the ISOLTRAP spectrometer

First direct mass measurements on rare earth isotopes around ¹⁴⁶Gd have been performed with the Penning trap mass spectrometer ISOLTRAP at ISOLDE/CERN. More than 40 isotopes of the elements Pr, Nd, Pm, Sm, Eu, Dy and Ho have been measured with an accuracy of typically 1 × 10^-7. In the case of ¹⁴¹Sm isomeric and ground state (ΔE = 175 keV) were resolved. Since isobaric contaminations are present in the ISOLDE beam, these measurements on rare earth isotopes became only possible after the installation of a new cooler trap which acts an isobar separator. This revised version was published online in August 2006 with corrections to the Cover Date.