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Register a new userAn apparatus to manipulate and identify individual Ba ions from bulk liquid Xe
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We describe a system to transport and identify barium ions produced in liquid xenon, as part of R&D towards the second phase of a double beta decay experiment, nEXO. The goal is to identify the Ba ion resulting from an extremely rare nuclear decay of the isotope $^{136}$Xe, hence providing a confirmation of the occurrence of the decay. This is achieved through Resonance Ionization Spectroscopy (RIS). In the test setup described here, Ba ions can be produced in liquid xenon or vacuum and collected on a clean substrate. This substrate is then removed to an analysis chamber under vacuum, where laser-induced thermal desorption and RIS are used with time-of-flight (TOF) mass spectroscopy for positive identification of the barium decay product.
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The optical properties of LXe in the vacuum ultra violet (VUV), determining the performance of a scintillation calorimeter, are discussed in detail. The available data, measured in a wider spectral region from visible to UV light, and in a large range of Xe densities, from gas to liquid, are examined. It is shown that this information can be used for deriving the LXe optical properties in the VUV. A comparison is made with the few direct measurements in LXe for VUV light resulting from the LXe excitation by ionizing particles. A useful relation is obtained which connects the Rayleigh scattering length to the refractive index in LXe.
Vacuum ultraviolet light emission from xenon-doped liquid argon is described in the context of liquid noble gas particle detectors. Xenon concentrations in liquid argon from 0.1 ppm to 1000 ppm were studied. The energy transfer from the second excimer continuum of argon ($sim$127 nm) to the second excimer continuum of xenon ($sim$174 nm) is observed by recording optical emission spectra. The transfer almost saturates at a xenon concentration of $sim$10 ppm for which, in addition, an intense emission in the infrared at a peak wavelength of 1.17 $mu$m with (13000$pm$4000) photons per MeV deposited by electrons had been found. The corresponding value for the VUV emission at a peak wavelength of 174 nm (second excimer continuum of xenon) is determined to be (20000$pm$6000) photons per MeV electron energy deposited. Under these excitation conditions pure liquid argon emits (22000$pm$3000) photons per MeV electron energy deposited at a peak wavelength of 127nm. An electron-beam induced emission spectrum for the 10 ppm Ar-Xe liquid mixture ranging from 115 nm to 3.5 $mu$m is presented. VUV emission spectra from xenon-doped liquid argon with exponentially varied xenon concentrations from 0.1 ppm to 1000 ppm are also shown. Time structure measurements of the light emissions at well-defined wavelength positions in the vacuum ultraviolet as well as in the near-infrared are presented.
An experimental setup is being developed to extract Ba ions from a high-pressure Xe gas environment. It aims to transport Ba ions from 10 bar Xe to vacuum conditions. The setup utilizes a converging-diverging nozzle in combination with a radio-frequency (RF) funnel to move Ba ions into vacuum through the pressure drop of several orders of magnitude. This technique is intended to be used in a future multi-ton detector investigating double-beta decay in $^{136}$Xe. Efficient extraction and detection of Ba ions, the decay product of Xe, would allow for a background-free measurement of the $^{136}$Xe double-beta decay.
We study the stability of three types of popularly employed TPB coatings under immersion in liquid argon. TPB emanation from each coating is quantified by fluorescence assay of molecular sieve filter material after a prolonged soak time. Two of the coatings are shown to emanate a detectable concentration of TPB into argon over a 24 hour period, which corresponds to tens of parts per billion in argon by mass. In an independent setup, the dissolved or suspended TPB is shown to produce a wavelength shifting effect in the argon bulk. Interpretations of these results and implications for present and future liquid argon time projection chamber experiments are discussed.
We have constructed an apparatus to study DC electrical breakdown in liquid helium at temperatures as low as 0.4 K and at pressures between the saturated vapor pressure and $sim$600 torr. The apparatus can house a set of electrodes that are 12 cm in diameter with a gap of $1-2$ cm between them, and a potential up to $pm 50$ kV can be applied to each electrode. Initial results demonstrated that it is possible to apply fields exceeding 100 kV/cm in a 1 cm gap between two electropolished stainless steel electrodes 12 cm in diameter for a wide range of pressures at 0.4 K. We also measured the current between two electrodes. Our initial results, $I<1$ pA at 45 kV, correspond to a lower bound on the effective volume resistivity of LHe of $rho_V > 5times10^{18}$ $Omegacdot$cm. This lower bound is 5 times larger than the bound previously measured. We report the design, construction, and operational experience of the apparatus, as well as initial results.
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