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Radio Frequency and DC High Voltage Breakdown of High Pressure Helium, Argon, and Xenon

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 Added by Katherine Woodruff
 Publication date 2019
  fields Physics
and research's language is English




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Motivated by the possibility of guiding daughter ions from double beta decay events to single-ion sensors for barium tagging, the NEXT collaboration is developing a program of R&D to test radio frequency (RF) carpets for ion transport in high pressure xenon gas. This would require carpet functionality in regimes at higher pressures than have been previously reported, implying correspondingly larger electrode voltages than in existing systems. This mode of operation appears plausible for contemporary RF-carpet geometries due to the higher predicted breakdown strength of high pressure xenon relative to low pressure helium, the working medium in most existing RF carpet devices. In this paper we present the first measurements of the high voltage dielectric strength of xenon gas at high pressure and at the relevant RF frequencies for ion transport (in the 10 MHz range), as well as new DC and RF measurements of the dielectric strengths of high pressure argon and helium gases at small gap sizes. We find breakdown voltages that are compatible with stable RF carpet operation given the gas, pressure, voltage, materials and geometry of interest.



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As noble liquid time projection chambers grow in size their high voltage requirements increase, and detailed, reproducible studies of dielectric breakdown and the onset of electroluminescence are needed to inform their design. The Xenon Breakdown Apparatus (XeBrA) is a 5-liter cryogenic chamber built to characterize the DC high voltage breakdown behavior of liquid xenon and liquid argon. Electrodes with areas up to 33~cm$^2$ were tested while varying the cathode-anode separation from 1 to 6~mm with a voltage difference up to 75~kV. A power-law relationship between breakdown field and electrode area was observed. The breakdown behavior of liquid argon and liquid xenon within the same experimental apparatus was comparable.
High pressure gas time projection chambers (HPGTPCs) are made with a variety of materials, many of which have not been well characterized in high pressure noble gas environments. As HPGTPCs are scaled up in size toward ton-scale detectors, assemblies become larger and more complex, creating a need for detailed understanding of how structural supports and high voltage insulators behave. This includes the identification of materials with predictable mechanical properties and without surface charge accumulation that may lead to field deformation or sparking. This paper explores the mechanical and electrical effects of high pressure gas environments on insulating polymers PTFE, HDPE, PEEK, POM and UHMW in Argon and Xenon, including studying absorption, swelling and high voltage insulation strength.
We report new measurements of the drift velocity and longitudinal diffusion coefficients of electrons in pure xenon gas and in xenon-helium gas mixtures at 1-9 bar and electric field strengths of 50-300 V/cm. In pure xenon we find excellent agreement with world data at all $E/P$, for both drift velocity and diffusion coefficients. However, a larger value of the longitudinal diffusion coefficient than theoretical predictions is found at low $E/P$ in pure xenon, below the range of reduced fields usually probed by TPC experiments. A similar effect is observed in xenon-helium gas mixtures at somewhat larger $E/P$. Drift velocities in xenon-helium mixtures are found to be theoretically well predicted. Although longitudinal diffusion in xenon-helium mixtures is found to be larger than anticipated, extrapolation based on the measured longitudinal diffusion coefficients suggest that the use of helium additives to reduce transverse diffusion in xenon gas remains a promising prospect.
Within the framework of xenon-based double beta decay experiments, we propose the possibility to improve the background rejection of an electroluminescent Time Projection Chamber (EL TPC) by reducing the diffusion of the drifting electrons while keeping nearly intact the energy resolution of a pure xenon EL TPC. Based on state-of-the-art microscopic simulations, a substantial addition of helium, around 10 or 15~%, may reduce drastically the transverse diffusion down to 2.5~mm/$sqrt{mathrm{m}}$ from the 10.5~mm/$sqrt{mathrm{m}}$ of pure xenon. The longitudinal diffusion remains around 4~mm/$sqrt{mathrm{m}}$. Light production studies have been performed as well. They show that the relative variation in energy resolution introduced by such a change does not exceed a few percent, which leaves the energy resolution practically unchanged. The technical caveats of using photomultipliers close to an helium atmosphere are also discussed in detail.
Radio-frequency carpets with ultra-fine pitches are examined for ion transport in gases at atmospheric pressures and above. We develop new analytic and computational methods for modeling ion behavior on phased radio-frequency (RF) carpets in gas densities where ion dynamics are strongly influenced by buffer gas collisions. The analytic theory of phased RF arrays is obtained by generalizing the conventional Dehmelt potential treatment, and the emergence of levitating and sweeping forces from a single RF wave is demonstrated. We consider the effects of finite electrode width and demonstrate the existence of a surface of no return at around 0.25 times the carpet pitch. We then apply thermodynamic and kinetic theory arguments to calculate ion loss rates from RF carpets in the presence of stochastic effects from ion-neutral collisions. Comparison to collision-by-collision simulations in SIMION validate this new and efficient approach to calculation of transport efficiencies. We establish the dependence of transport properties on array phasing, and explore a parameter space that is of special interest to neutrinoless double beta decay experiments using xenon gas: RF transport of barium ions in xenon gas at pressures from 1 to 10 bar, which could represent a promising technique for barium daughter ion tagging. We explore the allowed parameter space for efficient transport, accounting for the detailed microphysics of molecular ion formation and pressure dependent mobility, as well as finite temperature effects for both room temperature and cooled gases. The requirements of such systems lie significantly beyond those of existing devices in terms of both voltage and electrode pitch, and we discuss the challenges associated with achieving these operating conditions with presently available or near-future technologies.
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