Molecular Dynamics Simulations of Bubble Nucleation in a Liquid-Noble Scintillator

TL;DR

This study uses molecular dynamics simulations to analyze bubble nucleation in a liquid-noble scintillator, revealing that scintillation effects significantly increase the energy threshold for bubble formation, impacting detector sensitivity.

Contribution

It introduces a detailed molecular dynamics simulation incorporating scintillation effects in liquid argon, providing new insights into bubble nucleation thresholds in scintillating media.

Findings

Scintillation doubles the energy needed for bubble formation.

Excited molecular states with longer lifetimes do not significantly aid bubble nucleation.

Simulations show increased thresholds with longer excited state lifetimes.

Abstract

The Scintillating Bubble Chamber collaboration is searching for Weakly Interacting Massive Particles using a novel bubble chamber with intended thresholds as low as 100eV. Existing molecular dynamics simulations of bubble formation in bubble chambers were conducted with non-scintillating target materials and therefore do not account for the energy transfer to photons or time-delayed releases that occur in atomic de-excitation. In this study, we use the HOOMD-blue molecular dynamics framework to simulate bubble formation in liquid argon, including photon creation, ionization, and direct nuclear recoils. A multi-stage bubble growth process similar to that reported in the literature was observed. When comparing simulated thresholds with and without scintillation effects, we found that scintillation raises the average energy required to form a bubble by a factor of 2.16. This is larger than the fraction of energy lost to photon creation, and demonstrates that energy stored in excited molecular states with lifetimes longer than the rapid growth phase of nucleation (~250 ps) does not contribute significantly to bubble formation. This conclusion was further supported by simulations showing increased bubble nucleation thresholds when the excited molecular state lifetimes were increased, even under identical thermodynamic conditions.