Wavelength meters are widely used for frequency determinations and stabilization purposes since they cover a large wavelength range, provide a high read-out rate and have specified accuracies of up to 10 −8 . More accurate optical frequency measurements can be achieved with frequency combs but only at the price of considerably higher costs and complexity. In the context of precise and accurate frequency determinations for high-resolution laser spectroscopy, the performance of five different wavelength meters was quantified with respect to a frequency comb. The relative precision as well as the absolute accuracy has been investigated in detail, allowing us to give a sophisticated uncertainty margin for the individual instruments. We encountered a prominent substructure on the deviation between both device types with an amplitude of a few MHz that is repeating on the GHz scale. This finally limits the precision of laser scans which are monitored and controlled with wavelength meters. While quantifying its uncertainty margins, we found a high temporal stability in the characteristics of the wavelength meters which enables the preparation of wavelength-dependent adjustment curves for wide-and short-ranged scans. With this method, the absolute accuracy of wavelength meters can be raised up to the MHz level independently from the wavelength of the reference laser used for calibrating the device. Since this technique can be universally applied, it can lead to benefits in all fields of wavelength meter applications.
We present the results of high-voltage collinear laser spectroscopy measurements on the 5 ppm relative uncertainty level using a pump and probe scheme at the transition of involving the metastable state. With two-stage laser interaction and a reference measurement we can eliminate systematic effects such as differences in the contact potentials due to different electrode materials and thermoelectric voltages, and the unknown starting potential of the ions in the ion source. Voltage measurements were performed between −5 kV and −19 kV and parallel measurements with stable high-voltage dividers calibrated to 5 ppm relative uncertainty were used as a reference. Our measurements are compatible with the uncertainty limits of the high-voltage dividers and demonstrate an unprecedented (factor of 20) increase in the precision of direct laser-based high-voltage measurements.
We present a new collinear laser spectroscopy setup that has been designed to overcome systematic uncertainty limits arising from high-voltage and frequency measurements, beam superposition, and collisions with residual gas that are present in other installations utilizing this technique. The applied methods and experimental realizations are described, including an active stabilization of the ion-source potential, new types of ion sources that have not been used for collinear laser spectroscopy so far, dedicated installations for pump-and-probe measurements, and a versatile laser system referenced to a frequency comb. The advanced setup enables us to routinely determine transition frequencies, which was so far demonstrated only for a few cases and with lower accuracy at other facilities. It has also been designed to perform accurate high-voltage measurements for metrological applications. Demonstration and performance measurements were carried out with Ca+ and In+ ions.
Nuclear charge radii of 55;56 Ni were measured by collinear laser spectroscopy. The obtained information completes the behavior of the charge radii at the shell closure of the doubly magic nucleus 56 Ni. The trend of charge radii across the shell closures in calcium and nickel is surprisingly similar despite the fact that the 56 Ni core is supposed to be much softer than the 48 Ca core. The very low magnetic moment μð 55 NiÞ ¼ −1.108ð20Þ μ N indicates the impact of M1 excitations between spin-orbit partners across the N; Z ¼ 28 shell gaps. Our charge-radii results are compared to ab initio and nuclear density functional theory calculations, showing good agreement within theoretical uncertainties.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.