We report on a study to determine the efficiency of various buffer gases in quenching the population trapping states of laser-excited ytterbium ions. The ions were confined in an rf-dc hybrid trap, and their
2S1/2${\mathrm{\ensuremath{\leftrightarrows}}}^{2}$
P3/2 transition was excited with 329-nm laser light. Buffer gases used include
H2,
N2,
CO2, Ar, and He at several different pressure regimes. We have identified
N2 to be highly efficient in quenching the population of the trapping states and thus be the most suitable buffer gas to use with ytterbium for the development of a trapped-ion microwave frequency standard.
We report on a study to determine the efficiency of various buffer gases in quenching the population trapping states of laser excited ytterbium ions. The ions were confined in an rf/dc hybrid trap, and their /sup 2/S/sub 1/2//spl hArr//sup 2/P/sub 3/2/ transition was excited with 329 nm laser light. Buffer gases used include H/sub 2/, N/sub 2/, CO/sub 2/, Ar, and He at several different pressure regimes. We have identified N/sub 2/ to be highly efficient in quenching the population of the trapping states, and thus be the most suitable buffer gas to use with ytterbium for the development of a trapped ion microwave frequency standard.
We report that methane, CH4, can be used as an efficient F-state quenching gas for trapped ytterbium ions. The quenching rate coefficient is measured to be (2.8 ± 0.3) × 106 s−1 Torr−1. For applications that use microwave hyperfine transitions of the ground-state 171Y b ions, the CH4 induced frequency shift coefficient and the decoherence rate coefficient are measured as δν/ν = (−3.6 ± 0.1) × 10−6 Torr−1 and 1/T2 = (1.5 ± 0.2) × 105 s−1 Torr−1. In our buffer-gas cooled 171Y b+ microwave clock system, we find that only ≤10−8 Torr of CH4 is required under normal operating conditions to efficiently clear the F-state and maintain ≥85% of trapped ions in the ground state with insignificant pressure shift and collisional decoherence of the clock resonance.
Long-lived metastable states of
Yb+ ions are used for atomic frequency standards, precision measurements, and quantum information research. The effect of population trapping and transfer in these states must be well understood. We report here the transfer of
Yb+ ions into the long-lived
2F7/2 state by means of collisions between He buffer gas and
Yb+ ions held in a linear Paul trap. Transfer rates were measured as functions of buffer-gas pressure and repump-laser power, and the collisional population transfer rates were extracted. The measured transfer rate coefficients are $8.32(75)\ifmmode\times\else\texttimes\fi{}{10}^{\ensuremath{-}11}$ and $8.65(33)\ifmmode\times\else\texttimes\fi{}{10}^{\ensuremath{-}11}\text{ }{\text{cm}}^{3}/\text{s}$ for the collisional processes ${^{2}P}_{1/2}\ensuremath{\rightarrow}{^{2}D}_{5/2}$ and ${^{2}D}_{3/2}\ensuremath{\rightarrow}{^{2}F}_{7/2}$, respectively.
It is known that fluorescence of trapped
Yb+ ions fades with continuous driving of the
2 S1/2${\mathrm{\ensuremath{-}}}^{2}$
P1/2 transition in the presence of buffer gases. This phenomenon has been interpreted as being caused by population trapping in the
2 F7/2 state of
Yb+ . As another cause of the fluorescence disappearance, we found the production of
YbH+ by chemical reaction of
Yb+ in excited states with
H2 gas. We found that the wavelengths of 369.482, 369.202, and 368.947 nm, formerly assigned as wavelengths for deexcitation of
Yb+ in the
2 F7/2 state to the
2 S1/2 ground state, are actually photodissociation lines of
YbH+ . The change of the resonance point of rf resonance absorption signals indicates the production and dissociation of
YbH+ ions. The production of
YbH+ may be a problem in establishing frequency standards using buffer-gas-cooled
Yb+ , owing to difficulty in removing
H2 gas from vacuum systems.
Resonant laser excitation of Yb ions confined in an rf ion trap is found to result in perfect population trapping in the highly metastable
2F7/2 state. The lifetime of this level is measured to be greater than 8 days. Population and depopulation of this level under narrow- and broad-band laser excitation conditions is investigated and its potentiality for ultimate-resolution laser spectroscopy indicated.