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Chinese Physics Letters

Rotational Population Measurement of Ultracold 85 Rb 133 Cs Molecules in the Lowest Vibrational Ground State

Zhonghua Ji, Zhonghao Li, Ting Gong, Yanting Zhao, Liantuan Xiao, Suotang Jia

Published Oct 1, 2017• 5 citations
Publisher

Abstract

We measure the rotational populations of ultracold 85 Rb 133 Cs molecules in the lowest vibrational ground state by a depletion spectroscopy and quantify the molecular production rate based on the measurement of single ion signal area. The 85 Rb 133 Cs molecules in the are formed from the short-range molecular state. A home-made external-cavity diode laser is used as the depletion laser to measure the rotational populations of the formed molecules. Based on the determination of single ion signal, the production rates of molecules in the J = 0 and J = 2 rotational levels are derived to be 4800 mole/s and 7200 mole/s, respectively. The resolution and quantification of molecules in rotational states are facilitative for the manipulation of rotational quantum state of ultracold molecules.

DOI
10.1088/0256-307x/34/10/103301

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We measure the rotational populations of ultracold 85 Rb 133 Cs molecules in the lowest vibrational ground state by a depletion spectroscopy and quantify the molecular production rate based on the measurement of single ion signal area. The 85 Rb 133 Cs molecules in the are formed from the short-range molecular state. A home-made external-cavity diode laser is used as the depletion laser to measure the rotational populations of the formed molecules. Based on the determination of single ion signal, the production rates of molecules in the J = 0 and J = 2 rotational levels are derived to be 4800 mole/s and 7200 mole/s, respectively. The resolution and quantification of molecules in rotational states are facilitative for the manipulation of rotational quantum state of ultracold molecules.
We investigate the production of ultracold ground state X 1 σ + (v = 0) RbCs molecules in the lowest vibrational level via short-range photoassociation followed by spontaneous emission. The starting point is the laser cooled 85 Rb and 133 Cs atoms in a dual species, forced dark magneto-optical trap. The special intermediate level (5)0 + (v = 10) correlated to the (2) 3 π electric state is achieved by the photoassociation process. The formed ground state X 1 σ + (v = 0) molecule is resonantly excited to the 2 1 π intermediate state by a 651 nm pulse laser and is ionized by a 532 nm pulse laser and then detected by the time-of-flight mass spectrum. Saturation of the photoionization spectroscopy at large ionization laser energy is observed and the ionization efficiency is obtained from the fitting. The production of ultracold ground state 85 Rb 133 Cs molecules is facilitative for the further research about the manipulation of ultracold molecules in the rovibrational ground state.
We report on the use of depletion spectroscopy to detect ultracold ground-state KRb molecules with rotational resolution. The population of a specific ground-state vibrational level ${v}^{\ensuremath{''}}$, produced by photoassociation of ultracold atoms, is monitored by one-color two-photon pulsed-laser ionization. When a cw laser is resonant with a rovibrational transition to an excited state, the ground-state population, and hence the ion signal, is depleted. This narrow-band spectroscopic technique allows the individual rotational levels in both ground and excited states to be resolved, and thus the population of a single ground-state rovibrational level to be monitored. These resolved transitions are a necessary first step in transferring population from high vibrational levels of the ground state, such as produced by photoassociation, to the absolute molecular ground state $X\phantom{\rule{0.2em}{0ex}}^{1}\ensuremath{\Sigma}^{+}$ (${v}^{\ensuremath{''}}=0$, ${J}^{\ensuremath{''}}=0$). This technique can also be used to determine binding energies of high-${v}^{\ensuremath{''}}$ molecules. Combining our binding energy measurement with the results of previous spectroscopy yields an improved dissociation energy of the XXX state: ${D}_{e}=4217.822\ifmmode\pm\else\textpm\fi{}0.003\phantom{\rule{0.3em}{0ex}}{\mathrm{cm}}^{\ensuremath{-}1}$. We also report on the two-color pulsed-laser ionization used to locate the depletion transitions.
This thesis describes the spectroscopy work on ultracold 39K 85Rb molecules as part of our effort towards producing ground-state ultracold polar molecules. ^ The starting points of our experiment are laser cooled and trapped K and Rb atoms in dual-species MOTs and the molecule formation method is photoassociation (PA). A fraction of the PA-produced excited-state molecules can spontaneously emit to the two lowest electronic states, the X 1Σ + state and the a 3Σ + state, to form high vibrational level molecules. In order to develop a population transfer scheme to make deeply bound molecules, we have studied the spectroscopy of KRb in several steps. Besides the PA step, we have also carried out a state-selective detection experiment to study the population distribution of the high vibrational level molecules formed via spontaneous emission. The detection method is pulsed-laser based ion time-of-flight mass spectroscopy. Due to the linewidth limitations of the pulsed laser, this detection method can only resolve vibrational structures. A cw laser induced ion depletion spectroscopy technique has been developed in order to obtain rotational resolution. Using this ion depletion method, we have studied a possible stimulated Raman transfer scheme via the 3 1Σ+ state. To this end, we have obtained all the spectroscopic information required to produce deeply bound KRb molecules in a single vibrational and rotational level. ^ Several other spectroscopic studies using the high vibrational level ultracold molecules are also discussed. ^
We demonstrate measurement of the permanent electric dipole moment (EDM) of 85 Rb 133 Cs molecules in the absolute vibrational ground state by microwave (MW) coherent spectroscopy. The rotational states of the considered molecules, which are formed from short-range photoassociation of mixed cold atoms, are nondegenerated under external electric field. To measure the EDM based on electric-field-induced shifts of the sublevels of X 1 Σ + ( v = 0, J = 1) rotational state, we utilized a MW coherent spectroscopy, which has a higher resolution than depletion spectroscopy and one-photon MW spectroscopy and can also eliminate the influence from Stark shift of the excited state existing in both spectroscopies above. In order to acquire accurate electric intensity, electromagnetic induced transparency spectroscopy of 85 Rb Rydberg atoms is used to implement the calibration. The permanent EDM of 85 Rb 133 Cs molecules is finally determined to be 1.266(15) D, which agrees with the theoretical calculations and is comparable with the value of its isotopic molecule.
We present the formation of ultracold (85)Rb(133)Cs molecules in the (5)0(+) electronic state by photoassociation and their detection via resonance-enhanced two-photon ionization. Up to v = 47 vibrational levels including the lowest v = 0 vibrational and lowest J = 0 levels are identified with rotationally resolved high resolution photoassociation spectra. Precise Dunham coefficients are determined for the (5)0(+) state with high accuracy, then the Rydberg-Klein-Rees potential energy curve is derived. The electric dipole moments with respect to the vibrational numbers of the (5)0(+) electronic state of (85)Rb(133)Cs molecule are also measured in the range between 1.9 and 4.8 D. These comprehensive studies on previously unobserved rovibrational levels of the (5)0(+) state are helpful to understand the molecular structure and discover suitable transition pathways for transferring ultracold atoms to deeply bound rovibrational levels of the electronic ground state.
We have developed an approach to continuously load ultracold ^{85}Rb_{2} vibrational ground-state molecules into a crossed optical dipole trap from a magneto-optical trap. The technique relies on a single high-power light beam with a broad spectrum superimposed onto a narrow peak at an energy of about 9400 cm^{-1}. This single laser source performs all the required steps: the short-range photoassociation creating ground-state molecules after radiative emission, the cooling of the molecular vibrational population down to the lowest vibrational level v_{X}=0, and the optical trapping of these molecules. Furthermore, we probe by depletion spectroscopy and determine that 75% of the v_{X}=0 ground-state molecules are in the three lowest rotational levels J_{X}=0, 1, 2. The lifetime of the ultracold molecules in the optical dipole trap is limited to about 70 ms by off-resonant light scattering. The proposed technique opens perspectives for the formation of new molecular species in the ultracold domain, which are not yet accessible by well-established approaches.