Search for a Neutron Dark Decay in

Neutron dark decays have been suggested as a solution to the discrepancy between bottle and beam experiments, providing a dark matter candidate that can be searched for in halo nuclei. The free neutron in the final state following the decay of ^{6}He into ^{4}He+n+χ provides an exceptionally clean detection signature when combined with a high efficiency neutron detector. Using a high-intensity ^{6}He^{+} beam at Grand Accélérateur National d'Ions Lourds, a search for a coincident neutron signal resulted in an upper limit on a dark decay branching ratio of Br_{χ}≤4.0×10^{-10} (95% C.L.). Using the dark neutron decay model proposed originally by Fornal and Grinstein, we translate this into an upper bound on a dark neutron branching ratio of O(10^{-5}), improving over global constraints by one to several orders of magnitude depending on m_{χ}.

Addressing three-body fragmentation of methane dication using "native frames": Evidence of internal excitation in fragments.

The three body fragmentation of methane dication has been studied using the technique of cold target recoil ion momentum spectroscopy. The process is initiated by impact of energetic Ar9+ ions on neutral methane and the data is subsequently collected in coincidence with Ar8+ projectile. By analysing the dissociation channels leading to (H + H+ + CH2+) and (H + H2+ + CH+) fragments, it is concluded that these fragments are formed in a sequential manner via formation of molecular intermediates CH3+ and CH2+ respectively. It is shown that these molecular intermediates carry a few eVs as their internal energies, part of which is released when they emit an H-atom with the open possibility that the final detected fragments may still be internally excited. This was accomplished by analysing the two-steps of the sequential process in their own native frames. For a molecular system having three-dimensional structure, our results prove to be an ideal example to highlight the importance of using native frames for correct interpretation of the obtained results. Our results indicate that the dissociation of methane dication can be a major source of production of H-atoms in addition to H+ fragments with the probability of the two being of similar order.

ß-Nuclear-Recoil Correlation from

We report the first precise measurement of a ß-recoil correlation from a radioactive noble gas (^{6}He) confined via a magneto-optical trap. The measurement is motivated by the search for exotic tensor-type contributions to the charged weak current. Interpreted as tensor currents with right-handed neutrinos, the measurements yield |C_{T}/C_{A}|^{2}≤0.022 (90% confidence limit, C.L.). On the other hand, for left-handed neutrinos the limits are 0.007

Unexplained dissociation pathways of two-body fragmentation of methane dication.

The ion-induced fragmentation of CH4 2+ into H+ and CH3 + is studied using a cold target recoil ion momentum spectroscopy in coincidence with the charge state of the post-collision projectile. Using constant velocity Ar9+ and N3+, results from four different datasets are presented, with a selection on the final charge state of the projectile (Ar8+ or Ar7+ and N2+ or N+). Three distinct dissociation pathways (I, II, and III) are observed for each dataset, with the mean kinetic energy release values of around 4.7, 5.8, and 7.9 eV, respectively. The electronic states that are populated correspond to electronic configurations (1t2)-2 and (2a1)-1(1t2)-1 of the methane dication, CH4 2+. The relative branching ratios between the three pathways are discussed as a function of the charge state of the post-collision projectile, and a strong correlation with the specific nature of the ion-molecule interaction is found. The existing ab initio calculations have provided an explanation only for pathway II. In this article, we propose an explanation for pathway III, but pathway I still remains unexplained and requires further theoretical efforts. A discussion of the dependence of dissociation on the mode of excitation is presented.

Role of a Neighbor Ion in the Fragmentation Dynamics of Covalent Molecules.

Fragmentation of molecular nitrogen dimers (N_{2})_{2} induced by collision with low energy 90 keV Ar^{9+} ions is studied to evidence the influence of a molecular environment on the fragmentation dynamics of N_{2} cations. Following the capture of three or four electrons from the dimer, the three-body N_{2}^{+}+N^{m+}+N^{n+} [with (m,n)=(1,1) or (1, 2)] fragmentation channels provide clean experimental cases where molecular fragmentation may occur in the presence of a neighbor molecular cation. The effect of the environment on the fragmentation dynamics within the dimer is investigated through the comparison of the kinetic energy release (KER) spectra for these three-body channels and for isolated N_{2}^{(m+n)+} monomer cations. The corresponding KER spectra exhibit energy shifts of the order of 10 eV, attributed to the deformation of the N^{m+}+N^{n+} potential energy curves in the presence of the neighboring N_{2}^{+} cation. The KER structures remain unchanged, indicating that the primary collision process is not significantly affected by the presence of a neighbor molecule.

Towards high-resolution laser ionization spectroscopy of the heaviest elements in supersonic gas jet expansion.

Resonant laser ionization and spectroscopy are widely used techniques at radioactive ion beam facilities to produce pure beams of exotic nuclei and measure the shape, size, spin and electromagnetic multipole moments of these nuclei. However, in such measurements it is difficult to combine a high efficiency with a high spectral resolution. Here we demonstrate the on-line application of atomic laser ionization spectroscopy in a supersonic gas jet, a technique suited for high-precision studies of the ground- and isomeric-state properties of nuclei located at the extremes of stability. The technique is characterized in a measurement on actinium isotopes around the N=126 neutron shell closure. A significant improvement in the spectral resolution by more than one order of magnitude is achieved in these experiments without loss in efficiency.

Interatomic Coulombic decay as a new source of low energy electrons in slow ion-dimer collisions.

We provide the experimental evidence that the single electron capture process in slow collisions between O^{3+} ions and neon dimer targets leads to an unexpected production of low-energy electrons. This production results from the interatomic Coulombic decay process, subsequent to inner-shell single electron capture from one site of the neon dimer. Although pure one-electron capture from the inner shell is expected to be negligible in the low collision energy regime investigated here, the electron production due to this process overtakes by 1 order of magnitude the emission of Auger electrons by the scattered projectiles after double-electron capture. This feature is specific to low charge states of the projectile: similar studies with Xe^{20+} and Ar^{9+} projectiles show no evidence of inner-shell single-electron capture. The dependence of the process on the projectile charge state is interpreted using simple calculations based on the classical over the barrier model.

Atomic site-sensitive processes in low energy ion-dimer collisions.

Electron capture processes for low energy Ar(9+) ions colliding with Ar(2) dimer targets are investigated, focusing attention on charge sharing between the two Ar atoms as a function of the molecular orientation and the impact parameter. A preference for charge-asymmetric dissociation channels is observed, with a strong correlation between the projectile scattering angle and the molecular ion orientation. The measurements here provide clear evidence that projectiles distinguish each atom in the target and that electron capture from near-site atoms is favored. Monte Carlo calculations based on the classical over-the-barrier model, with dimer targets represented as two independent atoms, are compared to the data. They give new insight into the dynamics of the collision by providing, for the different electron capture channels, the two-dimensional probability maps p(b), where b is the impact parameter vector in the molecular frame.

High-resolution probe of coherence in low-energy charge exchange collisions with oriented targets.

The trapping lasers of a magneto-optical trap have been used to bring Rb atoms into well defined oriented states. Coupled to recoil-ion-momentum spectroscopy, this provided a unique MOTRIMS setup which was able to probe scattering dynamics, including the coherence features, with unprecedented resolution. The technique was applied to the low-energy charge exchange reactions Na+ + Rb(5p±1)→Na(3p,4s)+Rb+. The measurements revealed detailed features of the collisional interaction which were employed to improve the theoretical description. As such, it was possible to ascertain the validity of the intuitive models used to predict the most likely capture transitions.

First measurement of pure electron shakeoff in the ß decay of trapped 6He+ ions.

The electron shakeoff probability of 6Li2+ ions resulting from the ß- decay of 6He+ ions has been measured with high precision using a specially designed recoil ion spectrometer. This is the first measurement of a pure electron shakeoff following nuclear ß decay, not affected by multielectron processes such as Auger cascades. In this ideal textbook case for the application of the sudden approximation, the experimental ionization probability was found to be P(so)(exp)=0.02339(36) in perfect agreement with simple quantum mechanical calculations.

Asymmetry in multiple-electron capture revealed by radiative charge transfer in Ar dimers.

We measured kinetic energies of the fragment ions of argon dimers multiply ionized by low-energy Ar(9+) collisions. For (Ar2)(4+) dissociation, the asymmetric channel (Ar(3+) + Ar(+)) yield is found unexpectedly higher than the symmetric channel (Ar(2+) + Ar(2+)) yield in contrast with previous observation for covalent molecules or clusters. For the dissociation channel (Ar2)(2+)→Ar(+) + Ar(+), two well-separated peaks were observed, clearly evidencing that the direct Coulombic dissociation and the radiative charge transfer followed by ionic dissociation alternatively occur for the dicationic dimers. The respective intensity of these two peaks provides a direct mean to unravel the respective proportion of one-site and two-site double-electron capture, which are found equal for this collision system.

A new magneto-optical trap-target recoil ion momentum spectroscopy apparatus for ion-atom collisions and trapped atom studies.

A new magneto-optical trap-target recoil ion momentum spectroscopy apparatus has been built and tested at the LPC-CAEN. Dedicated to ion-atom collisions studies and excited fraction measurements, the setup combines a projectile ion beam line, a target of cold rubidium atoms provided by a magneto-optical trap (MOT), and a recoil ion momentum spectrometer. In a test experiment using a beam of Na(+) projectiles, we demonstrate its capability to measure, with a very high signal over background ratio, fully differential cross sections in scattering angle, initial state, and final state of the system. We detail, in this work, features that had not been described previously in the literature: an extraction of the recoil ions transverse to the ion beam axis, and a fast switch for the MOT magnetic field. Advantages of transverse versus longitudinal extraction are discussed, and future possibilities for the setup are presented.

Paul trapping of radioactive 6He+ ions and direct observation of their beta decay.

We demonstrate that abundant quantities of short-lived beta unstable ions can be trapped in a novel transparent Paul trap and that their decay products can directly be detected in coincidence. Low energy 6He+ (807 ms half-life) ions were extracted from the SPIRAL source at GANIL, then decelerated, cooled, and bunched by means of the buffer gas cooling technique. More than 10(8) ions have been stored over a measuring period of six days, and about 10(5) decay coincidences between the beta particles and the 6Li++ recoiling ions have been recorded. The technique can be extended to other short-lived species, opening new possibilities for trap assisted decay experiments.

Kinematically complete study of dissociative ionization of by ion impact.

We present a kinematically complete study of dissociative ionization of D(2) by 13.6 MeV/u S(15+) ions. The experiment allows us to unravel the competing mechanisms, namely, direct single ionization, autoionization of doubly excited states, ionization excitation, and double ionization, and to analyze the corresponding electron angular distribution from fixed-in-space molecules. The conclusions are supported by theoretical calculations in which the correlated motion of all electrons and nuclei and the interferences between them are described from first principles.

First Tests of (6) Li Doped Glass Scintillators for Ultracold Neutron Detection.

We report the results of test measurements aimed at determining the performances of (6)Li doped glass scintillators for the detection of ultra-cold neutrons. Four types of scintillators, GS1, GS3, GS10 and GS20, which differ by their (6)Li concentrations, have been tested. The signal to background separation is fully acceptable. The relative detection efficiencies have been determined as a function of the neutron velocity. We find that GS10 has a higher efficiency than the others for the detection of neutrons with velocities below 7 m/s. Two pieces of scintillators have been irradiated with a high flux of cold neutrons to test the radiation hardness of the glasses. No reduction in the pulse height has been observed up to an absorbed neutron dose of 1 × 10(13) cm(-3).

State selective charge transfer cross sections for Na+ with excited rubidium: a unique diagnostic of the population dynamics of a magneto-optical trap.

It is shown how the newly developed technique of magneto-optical-trap recoil-ion momentum spectroscopy can be used to measure the temporal evolution of excited state fraction in such a trap. In this case, the fraction of atoms in a 5p state is measured. The technique can be generalized to allow the measurement of more complicated systems, e.g., a Rb sample having a mixture of 5s, 5p, 4d, and Rydberg states.

Kinematically complete charge exchange experiment in the Cs(+)+Rb collision system using a MOT target.

Charge exchange is examined with unprecedented precision using the newly developed magneto-optical trap-target recoil ion momentum spectroscopy (MOTRIMS) technique. Initial and final state selective, charge exchange cross sections are obtained for 6 keV Cs+ colliding with rubidium in 5s and 5p states. For each charge transfer channel, cross sections differential in scattering angle are measured. These data are used to overturn previous long-standing conjecture as to the origin of oscillations seen in total charge exchange cross section measurements, and compare well with an enhanced Demkov model calculation.