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O. Ahmad

Publications and source records attributed to O. Ahmad.

4 recordsLinked to original sources

Precise and accurate nuclear electric quadrupole moment of $^{223}$Ra from molecular spectroscopy

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 $^{223}$Ra (half-life $t_{1/2} = 11.4$ d) from hyperfine-resolved collinear resonance ionization spectroscopy of the radioactive molecule $^{223}$Ra$^{19}$F. 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 $Q_s = +1.211(7)_\mathrm{stat}(2)_\mathrm{syst}(5)_\mathrm{theo}\,e\mathrm{b}$ for $^{223}$Ra 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.

nucl-ex↗

Energies and lifetimes of the 9p and 10p excited states in atomic francium

We present the first measurement of 9p 2P1/2,3/2 and 10p 2P1/2,3/2 excited levels absolute wavenumbers and radiative lifetime in francium. We used the Collinear Resonance Ionization Spectroscopy (CRIS) technique, applied on a beam of 221Fr atoms. Prior to this work, no experimental data existed for francium p-states with n > 8. The results provide a precision experimental test of relativistic coupled-cluster theory for the heaviest alkali, showing good agreement for lifetimes and relative excitation energies, despite a residual global offset in absolute energies.

physics.atom-ph↗

Pinning down electron correlations in RaF via spectroscopy of excited states and high-accuracy relativistic quantum chemistry

We report the spectroscopy of the 14 lowest excited electronic states in the radioactive molecule radium monofluoride (RaF). The observed excitation energies are compared with fully relativistic state-of-the-art Fock-space coupled cluster (FS-RCC) calculations, which achieve an agreement of >=99.64% (within ~12 meV) with experiment for all states. Guided by theory, a firm assignment of the angular momentum and term symbol is made for 10 states and a tentative assignment for 4 states. The role of high-order electron correlation and quantum electrodynamics effects in the excitation energy of excited states is studied, found to be important for all states. Establishing the simultaneous accuracy and precision of calculations is an important step for research at the intersection of particle, nuclear, and chemical physics, including searches of physics beyond the Standard Model, for which RaF is a promising probe.

physics.atom-ph↗

Radiative lifetime of the A 2Π1/2 state in RaF with relevance to laser cooling

The radiative lifetime of the $A$ $^2 Π_{1/2}$ (v=0) state in radium monofluoride (RaF) is measured to be 35(1) ns. The lifetime of this state and the related decay rate $Γ= 2.86(8) \times 10^7$ $s^{-1}$ are of relevance to the laser cooling of RaF via the optically closed $A$ $^2 Π_{1/2} \leftarrow X$ $^2Σ_{1/2}$ transition, which makes the molecule a promising probe to search for new physics. RaF is found to have a comparable photon-scattering rate to homoelectronic laser-coolable molecules. Thanks to its highly diagonal Franck-Condon matrix, it is expected to scatter an order of magnitude more photons than other molecules when using just 3 cooling lasers, before it decays to a dark state. The lifetime measurement in RaF is benchmarked by measuring the lifetime of the $8P_{3/2}$ state in Fr to be 83(3) ns, in agreement with literature.

physics.atom-ph↗