Splitting Isotope Shift in the 1s2p\,3\!P0,1,2 Fine-Structure Triplet in 12,13,14C4+: Experiment and Theory
Abstract
We report measurements and theoretical calculations of the fine-structure splittings in all three 1s2s\,3\!S1→\,1s2p\,3\!P0,1,2 transitions in the heliumlike systems of the isotopes 12,13,14C. The metastable triplet state was efficiently populated in an electron beam ion source and the C4+ ions were electrostatically accelerated to 50\,keV to perform collinear laser spectroscopy. From the determined transition frequencies, the splitting isotope shift (SIS), i.e., the difference in fine-structure splittings between different isotopes of the same element, was extracted. In the SIS, theoretical uncertainties due to higher-order quantum electrodynamic corrections are strongly suppressed since they are independent of both nuclear mass and the fine-structure quantum number J in lowest order. Comparison with theory provides an important test of experimental accuracy, particularly in the 13C4+ case, for which the nuclear spin leads to hyperfine-induced fine-structure mixing. At the same time, the even-even isotopes 12,14C4+ without nuclear spin can be used to confirm theory. Theoretical values of the SIS are given for all the heliumlike ions with 2 Z 10.
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