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Register a new userProton-electron mass ratio by high-resolution optical spectroscopy of ion ensembles in the resolved-carrier regime
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Optical spectroscopy in the gas phase is a key tool to elucidate the structure of atoms and molecules and of their interaction with external fields. The line resolution is usually limited by a combination of first-order Doppler broadening due to particle thermal motion and of a short transit time through the excitation beam. For trapped particles, suitable laser cooling techniques can lead to strong confinement (Lamb-Dicke regime, LDR) and thus to optical spectroscopy free of these effects. For non-laser coolable spectroscopy ions, this has so far only been achieved when trapping one or two atomic ions, together with a single laser-coolable atomic ion [1,2]. Here we show that one-photon optical spectroscopy free of Doppler and transit broadening can also be obtained with more easily prepared ensembles of ions, if performed with mid-infrared radiation. We demonstrate the method on molecular ions. We trap approximately 100 molecular hydrogen ions (HD$^{+}$) within a Coulomb cluster of a few thousand laser-cooled atomic ions and perform laser spectroscopy of the fundamental vibrational transition. Transition frequencies were determined with lowest uncertainty of 3.3$times$10$^{-12}$ fractionally. As an application, we determine the proton-electron mass ratio by matching a precise ab initio calculation with the measured vibrational frequency.
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Molecules with deep vibrational potential wells provide optical intervals sensitive to variation in the proton-electron mass ratio ($mu$). On one hand, polar molecules are of interest since optical state preparation techniques have been demonstrated for such species. On the other hand, it might be assumed that polar species are unfavorable candidates, because typical molecule-frame dipole moments reduce vibrational state lifetimes and cause large polarizabilities and associated Stark shifts. Here, we consider single-photon spectroscopy on a vibrational overtone transition of the polar species TeH$^+$, which is of practical interest because its diagonal Franck-Condon factors should allow rapid state preparation by optical pumping. We point out that all but the ground rotational state obtains a vanishing low-frequency scalar polarizability from coupling with adjacent rotational states, because of a fortuitous relationship between rigid rotor spacings and dipole matrix elements. We project that for good choices of spectroscopy states, demonstrated levels of field control should make possible uncertainties of order $1 times 10^{-18}$, similar to those of leading atomic ion clocks. The moderately long lived vibrational states of TeH$^+$ make possible a frequency uncertainty approaching $1 times 10^{-17}$ with one day of averaging for a single trapped ion. Observation over one year could probe for variation of $mu$ with a sensitivity approaching the $1 times 10^{-18}/textrm{yr}$ level.
Molecular transitions recently discovered at redshift z_abs=2.059 toward the bright background quasar J2123-0050 are analysed to limit cosmological variation in the proton-to-electron mass ratio, mu=m_p/m_e. Observed with the Keck telescope, the optical spectrum has the highest resolving power and largest number (86) of H_2 transitions in such analyses so far. Also, (7) HD transitions are used for the first time to constrain mu-variation. These factors, and an analysis employing the fewest possible free parameters, strongly constrain mus relative deviation from the current laboratory value: dmu/mu =(+5.6+/-5.5_stat+/-2.7_sys)x10^{-6}. This is the first Keck result to complement recent constraints from three systems at z_abs>2.5 observed with the Very Large Telescope.
We present a new derivation of the proton-electron mass ratio from the hydrogen molecular ion, HD$^+$. The derivation entails the adjustment of the mass ratio in highly precise theory so as to reproduce accurately measured ro-vibrational frequencies. This work is motivated by recent improvements of the theory, as well as the more accurate value of the electron mass in the recently published CODATA-14 set of fundamental constants, which justifies using it as input data in the adjustment, rather than the proton mass value as done in previous works. This leads to significantly different sensitivity coefficients and, consequently, a different value and larger uncertainty margin of the proton-electron mass ratio as obtained from HD$^+$.
UV frequency metrology has been performed on the a3Pi - X1Sigma+ (0,0) band of various isotopologues of CO using a frequency-quadrupled injection-seeded narrow-band pulsed Titanium:Sapphire laser referenced to a frequency comb laser. The band origin is determined with an accuracy of 5 MHz (delta u / u = 3 * 10^-9), while the energy differences between rotational levels in the a3Pi state are determined with an accuracy of 500 kHz. From these measurements, in combination with previously published radiofrequency and microwave data, a new set of molecular constants is obtained that describes the level structure of the a3Pi state of 12C16O and 13C16O with improved accuracy. Transitions in the different isotopologues are well reproduced by scaling the molecular constants of 12C16O via the common mass-scaling rules. Only the value of the band origin could not be scaled, indicative of a breakdown of the Born-Oppenheimer approximation. Our analysis confirms the extreme sensitivity of two-photon microwave transitions between nearly-degenerate rotational levels of different Omega-manifolds for probing a possible variation of the proton-to-electron mass ratio, mu=m_p/m_e, on a laboratory time scale.
Great advances in precision quantum measurement have been achieved with trapped ions and atomic gases at the lowest possible temperatures. These successes have inspired ideas to merge the two systems. In this way one can study the unique properties of ionic impurities inside a quantum fluid or explore buffer gas cooling of the trapped ion quantum computer. Remarkably, in spite of its importance, experiments with atom-ion mixtures remained firmly confined to the classical collision regime. We report a collision energy of 1.15(0.23) times the $s$-wave energy (or 9.9(2.0)~$mu$K) for a trapped ytterbium ion in an ultracold lithium gas. We observed a deviation from classical Langevin theory by studying the spin-exchange dynamics, indicating quantum behavior in the atom-ion collisions. Our results open up numerous opportunities, such as the exploration of atom-ion Feshbach resonances, in analogy to neutral systems.
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