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P. Herrero-Gómez

Publications and source records attributed to P. Herrero-Gómez.

21 records · Page 2Linked to original sources

Measurement of the ${}^{136}$Xe two-neutrino double beta decay half-life via direct background subtraction in NEXT

We report a measurement of the half-life of the ${}^{136}$Xe two-neutrino double beta decay performed with a novel direct background subtraction technique. The analysis relies on the data collected with the NEXT-White detector operated with ${}^{136}$Xe-enriched and ${}^{136}$Xe-depleted xenon, as well as on the topology of double-electron tracks. With a fiducial mass of only 3.5 kg of Xe, a half-life of $2.34^{+0.80}_{-0.46}\textrm{(stat)}^{+0.30}_{-0.17}\textrm{(sys)}\times10^{21}~\textrm{yr}$ is derived from the background-subtracted energy spectrum. The presented technique demonstrates the feasibility of unique background-model-independent neutrinoless double beta decay searches.

nucl-ex↗

Ba$^{2+}$ ion trapping by organic submonolayer: towards an ultra-low background neutrinoless double beta decay detector

If neutrinos are their own antiparticles, the otherwise-forbidden nuclear reaction known as neutrinoless double beta decay ($ββ0ν$) can occur, with a characteristic lifetime which is expected to be very long, making the suppression of backgrounds a daunting task. It has been shown that detecting (``tagging'') the Ba$^{+2}$ dication produced in the double beta decay ${}^{136}\mathrm{Xe} \rightarrow {}^{136}$Ba$^{+2}+ 2 e + (2 ν)$ in a high pressure gas experiment, could lead to a virtually background free experiment. To identify these \Bapp, chemical sensors are being explored as a key tool by the NEXT collaboration . Although used in many fields, the application of such chemosensors to the field of particle physics is totally novel and requires experimental demonstration of their suitability in the ultra-dry environment of a xenon gas chamber. Here we use a combination of complementary surface science techniques to unambiguously show that Ba$^{+2}$ ions can be trapped (chelated) in vacuum by an organic molecule, the so-called fluorescent bicolour indicator (FBI) (one of the chemosensors developed by NEXT), immobilized on a surface. We unravel the ion capture mechanism once the molecules are immobilised on Au(111) surface and explain the origin of the emission fluorescence shift associated to the trapping of different ions. Moreover, we prove that chelation also takes place on a technologically relevant substrate, as such, demonstrating the feasibility of using FBI indicators as building blocks of a Ba$^{+2}$ detector.

hep-ex↗

The Dynamics of Ions on Phased Radio-frequency Carpets in High Pressure Gases and Application for Barium Tagging in Xenon Gas Time Projection Chambers

Radio-frequency (RF) 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 RF ion transport at densities where dynamics are strongly influenced by buffer gas collisions. An analytic description of levitating and sweeping forces from phased arrays is obtained, then thermodynamic and kinetic principles are used to calculate ion loss rates in the presence of collisions. This methodology is validated against detailed microscopic SIMION simulations. We then explore a parameter space of special interest for neutrinoless double beta decay experiments: transport of barium ions in xenon at pressures from 1 to 10 bar. Our computations account for molecular ion formation and pressure dependent mobility as well as finite temperature effects. We discuss the challenges associated with achieving suitable operating conditions, which lie beyond the capabilities of existing devices, using presently available or near-future manufacturing techniques.

physics.ins-det↗