$\textit{Ab initio}$ calculation of the calorimetric electron capture spectrum of $^{163}$Holmium: Intra-atomic decay into bound-states
M. Bra\ss, C. Enss, L. Gastaldo, M.W. Haverkort

TL;DR
This paper presents an extit{ab initio} calculation of the electron capture spectrum of $^{163}$Ho, accounting for intra-atomic decay channels, and assesses the impact of many-body interactions and relativistic effects on spectral features relevant for neutrino mass determination.
Contribution
The study introduces a detailed theoretical framework for calculating the $^{163}$Ho electron capture spectrum, including intra-atomic decay channels and many-body effects, providing critical insights for neutrino mass experiments.
Findings
Relativistic effects cause minor spectral shifts.
Multiplet structures significantly alter resonance appearance.
Auger decay peaks are weak and do not affect neutrino mass analysis.
Abstract
The determination of the electron neutrino mass by electron capture in Ho relies on a precise understanding of the deexcitation of a core hole after an electron capture event. We here present an \textit{ab intio} calculation of the electron capture spectrum in Ho, including all intra-atomic decay channels into bound-states. We use theoretical methods developed for the calculation of core level spectroscopy on correlated electron compounds. Our comparison critically tests the reality of these theories. We find that relativistic interactions beyond the Dirac equation, i.e. quantum-electro dynamics, only lead to minor shifts of the spectral peaks. The electronic relaxation after an electron capture event due to the changed nuclear potential leads to a mixing of different edges, but due to conservation of angular momentum of each scattered electron, no additional structures…
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