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Nuclear electric quadrupole moments of unstable isotopes are commonly extracted from laser spectroscopy of the atomic hyperfine structure, where the accuracy is limited to the several-percent level by the available electric-field-gradient (EFG) calculations. In this study, we determine the spectroscopic quadrupole moment of ²²³Ra (half-life t1/2 = 11.4 d) from hyperfine-resolved collinear resonance ionization spectroscopy of the radioactive molecule ²²³Ra¹⁹F. The X\,²Σ⁺ electronic ground state of RaF provides a large axial EFG at the radium nucleus that can be calculated with relativistic coupled-cluster theory to sub-percent accuracy. Together with a three-fold improvement in spectral resolution over previous fast-beam measurements of radioactive molecules, this yields Qₛ = +1.211(7)ₛtat(2)ₛyst(5)ₜheo\,eb for ²²³Ra with a total uncertainty of 0.73%, approximately three times better than atomic and ionic determinations. This result demonstrates that molecular spectroscopy can provide access to the electromagnetic structure of unstable nuclei with a precision competitive with, and in favorable cases better than, atomic spectroscopy, and may thus be envisioned for studies beyond the limitations of current radioactive-atom experiments.
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Fajardo-Zambrano et al. (2026) studied this question.
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