Scintillation characteristics of the EJ-299-02H scintillator.

A study of the dead layer thickness and quenching factor of a plastic scintillator for use in ultracold neutron (UCN) experiments is described. Alpha spectroscopy was used to determine the thickness of a thin surface dead layer to be 630 ± 110 nm. The relative light outputs from the decay of 241Am and Compton scattering of electrons were used to extract Birks' law coefficient, yielding a kB value of 0.087 ± 0.003 mm/MeV, consistent with some previous reports for other polystyrene-based scintillators. The results from these measurements are incorporated into the simulation to show that an energy threshold of (∼9 keV) can be achieved for the UCNProBe experiment. This low threshold enables high beta particle detection efficiency and the indirect measurement of UCN. The ability to make the scintillator deuterated, accompanied by its relatively thin dead layer, gives rise to unique applications in a wide range of UCN experiments, where it can be used to trap UCN and detect charged particles in situ.

Improved Neutron Lifetime Measurement with UCNτ.

We report an improved measurement of the free neutron lifetime τ_{n} using the UCNτ apparatus at the Los Alamos Neutron Science Center. We count a total of approximately 38×10^{6} surviving ultracold neutrons (UCNs) after storing in UCNτ's magnetogravitational trap over two data acquisition campaigns in 2017 and 2018. We extract τ_{n} from three blinded, independent analyses by both pairing long and short storage time runs to find a set of replicate τ_{n} measurements and by performing a global likelihood fit to all data while self-consistently incorporating the ß-decay lifetime. Both techniques achieve consistent results and find a value τ_{n}=877.75±0.28_{stat}+0.22/-0.16_{syst} s. With this sensitivity, neutron lifetime experiments now directly address the impact of recent refinements in our understanding of the standard model for neutron decay.

Search for the Neutron Decay n→X+γ, Where X is a Dark Matter Particle.

Fornal and Grinstein recently proposed that the discrepancy between two different methods of neutron lifetime measurements, the beam and bottle methods, can be explained by a previously unobserved dark matter decay mode, n→X+γ. We perform a search for this decay mode over the allowed range of energies of the monoenergetic γ ray for X to be dark matter. A Compton-suppressed high-purity germanium detector is used to identify γ rays from neutron decay in a nickel-phosphorous-coated stainless-steel bottle. A combination of Monte Carlo and radioactive source calibrations is used to determine the absolute efficiency for detecting γ rays arising from the dark matter decay mode. We exclude the possibility of a sufficiently strong branch to explain the lifetime discrepancy with 97% confidence.

Decomposition of Methanol on Mixed CuO-CuWO4 Surfaces.

Mixed CuO(2 × 1)-CuWO4 layers on a Cu(110) surface have been prepared by the on-surface reaction of the CuO(2 × 1) surface oxide with adsorbed (WO3)3 clusters. The adsorption and decomposition of methanol on these well-defined CuO-CuWO4 surfaces has been followed by high-resolution X-ray photoelectron spectroscopy (XPS), high-resolution electron energy loss spectroscopy (HREELS), and temperature-programmed desorption (TPD) to assess the molecular surface species and their concentration, while the state of the surface oxide phases before and after methanol decomposition has been characterized by scanning tunneling microscopy (STM), low energy electron diffraction (LEED), and XPS. Surface methoxy species form the primary methanol decomposition products, which desorb partly by recombination as methanol at 200-300 K or decompose into CHx and possibly CO. The most reactive surfaces are mixed CuO-CuWO4 phase, with CuWO4 coverages 0.5-0.8 monolayer, thus pointing at the importance of oxide phase boundary sites. In a minority reaction channel, a small amount of formaldehyde is detected on the CuWO4 surface. The CuWO4 oxide phase becomes modified as a result of reduction and a morphology transition triggered by the methanol decomposition, but the pristine surface state can be recovered by a postoxidation treatment with oxygen.

Phase behaviour of 2D MnWO x and FeWO x ternary oxide layers on Pd(1 0 0).

The structure and properties of ternary oxide materials at the nanoscale are poorly explored both on experimental and theoretical levels. With this work we demonstrate the successful on-surface synthesis of two-dimensional (2D) ternary oxide, MnWO x and FeWO x , nanolayers on a Pd(1 0 0) surface and the understanding of their new structure and phase behaviour with the help of state-of-art surface structure and spectroscopy techniques. We find that the 2D MnWO x and FeWO x phases, prepared under identical thermodynamic conditions, exhibit similar structural properties, reflecting the similarity of the bulk MnWO4 and FeWO4 phases with the wolframite structure. Structure models of prototypical 2D ternary oxide phases are proposed and discussed in the light of new structure architecture concepts which have no analogues in the bulk.