Time-resolved fast-neutron imaging with a pulse-counting image intensifier

A new imaging method that combines high-efficiency fast-neutron detection with sub-ns time resolution is presented. This is achieved by exploiting the high neutron detection efficiency of a thick scintillator and the fast timing capability and flexibility of light-pulse detection with a dedicated image intensifier. The neutron converter is a plastic scintillator slab or, alternatively, a scintillating fibre screen. The scintillator is optically coupled to a pulse counting image intensifier which measures the 2-dimensional position coordinates and the Time-Of-Flight (TOF) of each detected neutron with an intrinsic time resolution of less than 1 ns. Large-area imaging devices with high count rate capability can be obtained by lateral segmentation of the optical readout channels

Wide-field time-correlated single photon counting-based fluorescence lifetime imaging microscopy

Wide-field time-correlated single photon counting detection techniques, where the position and the arrival time of the photons are recorded simultaneously using a camera, have made some advances recently. The technology and instrumentation used for this approach is employed in areas such as nuclear science, mass spectroscopy and positron emission tomography, but here, we discuss some of the wide-field TCSPC methods, for applications in fluorescence microscopy. We describe work by us and others as presented in the Ulitima fast imaging and tracking conference at the Argonne National Laboratory in September 2018, from phosphorescence lifetime imaging (PLIM) microscopy on the microsecond time scale to fluorescence lifetime imaging (FLIM) on the nanosecond time scale, and highlight some applications of these techniques

Mechanisms of photo double ionization of helium by 530 eV photons

We have measured fully differential cross sections for photo double ionization of helium 450eV above the threshold. We have found an extremely asymmetric energy sharing between the photoelectrons and an angular asymmetry parameter β≃2 and β≃0 for the fast and slow electrons, respectively. The electron angular distributions show a dominance of the shakeoff for 2eV electrons and clear evidence of an inelastic electron-electron scattering at an electron energy of 30eV. The data are in excellent agreement with convergent close-coupling calculations

State Selective Scattering Angle Dependent Capture Cross Sections Measured by Cold Target Recoil Ion Momentum Spectroscopy

We have developed a new kind of recoil ion momentum spectroscopy technique, using a precooled supersonic gas jet target, to determine state selective, scattering angle dependent cross sections for swift ion-atom collisions ( 0. 25 , ..., , 1 MeV He2+ on He), by measuring the transverse and longitudinal momentum of the recoil ion. A longitudinal momentum resolution of ± 0.13 a. u. was achieved, about a factor of 30 better than ever obtained before, which enables a clear separation of K and L shell capture. In the transverse direction a resolution corresponding to a projectile scattering angle uncertainty of Δ ϑ P = ±1 μ rad was obtained

Complete photo-fragmentation of the deuterium molecule

All properties of molecules, from binding and excitation energies to their geometry, are determined by the highly correlated initial state wavefunction of the electrons and nuclei. Perhaps surprisingly, details of these correlations can be revealed by studying the break-up of these systems into their constituents. The fragmentation might be initiated by the absorption of a single photon [1, 2, 3, 4, 5, 6], collision with a charged particle [7, 8] or exposure to a strong laser pulse [9, 10]. If the exciting interaction is sufficiently understood, one can use the fragmentation process as a tool to learn about the bound initial state [11, 12]. However, often the interaction and the fragment motions pose formidable challenges to quantum theory [13, 14, 15]. Here we report the coincident measurement of the momenta of both nuclei and both electrons from the single photon induced fragmentation of the deuterium molecule. The results reveal that the correlated motion of the electrons is strongly dependent on the inter-nuclear separation in the molecular ground state at the instant of photon absorption