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Register a new userQED radiative corrections to the $^2$P$_{1/2}$-$^2$P$_{3/2}$ fine-structure in fluorinelike ions
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Ab initio calculations of QED radiative corrections to the $^2P_{1/2}$ - $^2P_{3/2}$ fine-structure transition energy are performed for selected F-like ions. These calculations are nonperturbative in $alpha Z$ and include all first-order and many-electron second-order effects in $alpha$. When compared to approximate QED computations, a notable discrepancy is found especially for F-like uranium for which the predicted self-energy contributions even differ in sign. Moreover, all deviations between theory and experiment for the $^2P_{1/2}$ - $^2P_{3/2}$ fine-structure energies of F-like ions, reported recently by Li et al., Phys. Rev. A 98, 020502(R) (2018), are resolved if their highly accurate, non-QED fine-structure values are combined with the QED corrections ab initially evaluated here.
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The workhorse of atomic physics, quantum electrodynamics, is one of the best-tested theories in physics. However recent discrepancies have shed doubt on its accuracy for complex atomic systems. To facilitate the development of the theory further we aim to measure transition dipole matrix elements of metastable helium (He*) (the ideal 3 body test-bed) to the highest accuracy thus far. We have undertaken a measurement of the `tune-out wavelength which occurs when the contributions to the dynamic polarizability from all atomic transitions sum to zero; thus illuminating an atom with this wavelength of light then produces no net energy shift. This provides a strict constraint on the transition dipole matrix elements without the complication and inaccuracy of other methods. Using a novel atom-laser based technique we have made the first measurement of the tune-out wavelength in metastable helium between the $3^{3}P_{1,2,3}$ and $2^{3}P_{1,2,3}$ states at 413.07(2) nm which compares well with the predicted valuecite{Mitroy2013} of 413.02(9) nm. We have additionally developed many of the methods necessary to improve this measurement to the 100 fm level of accuracy where it will form the most accurate determination of transition rate information ever made in He* and provide a stringent test for atomic QED simulations. We believe this measurement to be one of the most sensitive ever made of an optical dipole potential, able to detect changes in potentials of $sim$200 pK and is widely applicable to other species and areas of atom optics.
Despite quantum electrodynamics (QED) being one of the most stringently tested theories underpinning modern physics, recent precision atomic spectroscopy measurements have uncovered several small discrepancies between experiment and theory. One particularly powerful experimental observable that tests QED independently of traditional energy level measurements is the `tune-out frequency, where the dynamic polarizability vanishes and the atom does not interact with applied laser light. In this work, we measure the `tune-out frequency for the $2^{3!}S_1$ state of helium between transitions to the $2^{3!}P$ and $3^{3!}P$ manifolds and compare it to new theoretical QED calculations. The experimentally determined value of $725,736,700,$$(40_{mathrm{stat}},260_{mathrm{syst}})$ MHz is within ${sim} 2.5sigma$ of theory ($725,736,053(9)$ MHz), and importantly resolves both the QED contributions (${sim} 30 sigma$) and novel retardation (${sim} 2 sigma$) corrections.
Isotope shifts of the 2$p_{3/2}$-2$p_{1/2}$ transition in B-like ions are evaluated for a wide range of the nuclear charge number: Z=8-92. The calculations of the relativistic nuclear recoil and nuclear size effects are performed using a large scale configuration-interaction Dirac-Fock-Sturm method. The corresponding QED corrections are also taken into account. The results of the calculations are compared with the theoretical values obtained with other methods. The accuracy of the isotope shifts of the 2$p_{3/2}$-2$p_{1/2}$ transition in B-like ions is significantly improved.
Laser spectroscopy of short-lived radium isotopes in a linear Paul trap has been performed. The isotope shifts of the $6d,^2$D$_{3/2},$ - $7p,^2$P$_{1/2},$ transition in $^{209-214}$Ra$^+$ were measured, which are sensitive to the short range part of the atomic wavefunctions. The results are essential experimental input for improving the precision of atomic structure calculation. This is indispensable for parity violation in Ra$^+$ aiming at the determination of the weak mixing angle.
We measured the isotope shift in the $^2$S$_{1/2}$-$^2$P$_{3/2}$ (D2) transition in singly-ionized calcium ions using photon recoil spectroscopy. The high accuracy of the technique enables us to resolve the difference between the isotope shifts of this transition to the previously measured isotopic shifts of the $^2$S$_{1/2}$-$^2$P$_{1/2}$ (D1) line. This so-called splitting isotope shift is extracted and exhibits a clear signature of field shift contributions. From the data we were able to extract the small difference of the field shift coefficient and mass shifts between the two transitions with high accuracy. This J-dependence is of relativistic origin and can be used to benchmark atomic structure calculations. As a first step, we use several ab initio atomic structure calculation methods to provide more accurate values for the field shift constants and their ratio. Remarkably, the high-accuracy value for the ratio of the field shift constants extracted from the experimental data is larger than all available theoretical predictions.
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