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Raman Setup for Optical Cooling of Trapped Lithium Atoms outside the Lamb Dicke Regime / Raman Setup zum optischen Kühlen gefangener Lithium Atome außerhalb des Lamb Dicke Regimes

S. Krumm

Published Jan 1, 2023• 0 citations
OpenAlex

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Motion-selective coherent population trapping for subrecoil cooling of optically trapped atoms outside the Lamb-Dicke regime

Hyun Gyung Lee, Sooyoung Park, Meung Ho Seo +1 more

We propose a scheme that combines velocity-selective coherent population trapping (CPT) and Raman sideband cooling (RSC) for subrecoil cooling of optically trapped atoms outside the Lamb-Dicke regime. This scheme is based on an inverted $\mathsf{Y}$ configuration in an alkali-metal atom. It consists of a $\mathrm{\ensuremath{\Lambda}}$ formed by two Raman transitions between the ground hyperfine levels and the $D$ transition, allowing RSC along two paths and formation of a CPT dark state. Using the state-dependent difference in vibration frequency of the atom in a circularly polarized trap, we can tune the $\mathrm{\ensuremath{\Lambda}}$ to make only the motional ground state a CPT dark state. We call this scheme motion-selective coherent population trapping (MSCPT). We write the master equations for RSC and MSCPT and solve them numerically for a $^{87}\mathrm{Rb}$ atom in a one-dimensional optical lattice when the Lamb-Dicke parameter is 1. Although MSCPT reaches the steady state slowly compared with RSC, the former consistently produces colder atoms than the latter. The numerical results also show that subrecoil cooling by MSCPT outside the Lamb-Dicke regime is possible under a favorable, yet experimentally feasible, condition. We explain this performance quantitatively by calculating the relative darkness of each motional state. Finally, we discuss the application of the MSCPT scheme to an optically trapped diatomic polar molecule whose Stark shift and vibration frequency exhibit large variations depending on the rotational quantum number.

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We present the results of simulations of optical sideband cooling of atomic ions in a trap with a shallow potential well. In such traps, an ion cannot be Doppler cooled near to the Lamb-Dicke regime $\mathrm{[}{\ensuremath{\eta}}^{2}(2\ensuremath{\langle}n\ensuremath{\rangle}+1)\ensuremath{\ll}1]$. Outside the Lamb-Dicke regime, the sideband cooling dynamics are altered by the existence of various Fock states with weak coupling where the cooling becomes very slow. A $^{40}\mathrm{Ca}^{+}$ ion trapped in our Penning trap realizes such a situation; hence single stage cooling is inefficient to prepare the ion in the motional ground state. For these systems, it is necessary to study the cooling dynamics in detail and we show that it is possible to implement an optimized cooling sequence to achieve efficient ground-state cooling. We also present the simulated cooling dynamics of two ions trapped in a Penning trap, where the presence of an additional motional mode requires a complicated cooling sequence in order to cool both axial modes to the ground state simultaneously. Additionally, we demonstrate the dissipative preparation of Fock states outside the Lamb-Dicke regime by sideband heating a single ion in a Penning trap.

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Preparation of 87Rb and 133Cs in the motional ground state of a single optical tweezer

Stefan Spence, R V Brooks, Daniel K. Ruttley +2 more

Abstract We report simultaneous Raman sideband cooling of a single 87Rb atom and a single 133Cs atom held in separate optical tweezers at 814 nm and 938 nm, respectively. Starting from outside the Lamb-Dicke regime, after 45 ms of cooling we measure probabilities to occupy the three-dimensional motional ground state of 0.8 6 − 0.04 + 0.03 for Rb and 0.9 5 − 0.04 + 0.03 for Cs. Our setup overlaps the Raman laser beams used to cool Rb and Cs, reducing hardware requirements by sharing equipment along the same beam path. The cooling protocol is scalable, and we demonstrate cooling of single Rb atoms in an array of four tweezers. After motional ground-state cooling, a 938 nm tweezer is translated to overlap with a 814 nm tweezer so that a single Rb and a single Cs atom can be transferred into a common 1064 nm trap. By minimising the heating during the merging and transfer, we prepare the atoms in the relative motional ground state with an efficiency of 0.8 1 − 0.08 + 0.08 . This is a crucial step towards the formation of single RbCs molecules confined in optical tweezer arrays.

arXiv:2205.09457•New Journal of Physics•Sep 28, 2022•17 citations
We propose a scheme that combines velocity-selective coherent population trapping (CPT) and Raman sideband cooling (RSC) for subrecoil cooling of optically trapped atoms outside the Lamb-Dicke regime. This scheme is based on an inverted Y\mathsf{Y}Y configuration in an alkali-metal atom. It consists of a $\mathrm{\ensuremath{\Lambda}}$ formed by two Raman transitions between the ground hyperfine levels and the DDD transition, allowing RSC along two paths and formation of a CPT dark state. Using the state-dependent difference in vibration frequency of the atom in a circularly polarized trap, we can tune the $\mathrm{\ensuremath{\Lambda}}$ to make only the motional ground state a CPT dark state. We call this scheme motion-selective coherent population trapping (MSCPT). We write the master equations for RSC and MSCPT and solve them numerically for a 87Rb^{87}\mathrm{Rb}87Rb atom in a one-dimensional optical lattice when the Lamb-Dicke parameter is 1. Although MSCPT reaches the steady state slowly compared with RSC, the former consistently produces colder atoms than the latter. The numerical results also show that subrecoil cooling by MSCPT outside the Lamb-Dicke regime is possible under a favorable, yet experimentally feasible, condition. We explain this performance quantitatively by calculating the relative darkness of each motional state. Finally, we discuss the application of the MSCPT scheme to an optically trapped diatomic polar molecule whose Stark shift and vibration frequency exhibit large variations depending on the rotational quantum number.
We present the results of simulations of optical sideband cooling of atomic ions in a trap with a shallow potential well. In such traps, an ion cannot be Doppler cooled near to the Lamb-Dicke regime $\mathrm{[}{\ensuremath{\eta}}^{2}(2\ensuremath{\langle}n\ensuremath{\rangle}+1)\ensuremath{\ll}1]$. Outside the Lamb-Dicke regime, the sideband cooling dynamics are altered by the existence of various Fock states with weak coupling where the cooling becomes very slow. A 40Ca+^{40}\mathrm{Ca}^{+}40Ca+ ion trapped in our Penning trap realizes such a situation; hence single stage cooling is inefficient to prepare the ion in the motional ground state. For these systems, it is necessary to study the cooling dynamics in detail and we show that it is possible to implement an optimized cooling sequence to achieve efficient ground-state cooling. We also present the simulated cooling dynamics of two ions trapped in a Penning trap, where the presence of an additional motional mode requires a complicated cooling sequence in order to cool both axial modes to the ground state simultaneously. Additionally, we demonstrate the dissipative preparation of Fock states outside the Lamb-Dicke regime by sideband heating a single ion in a Penning trap.
Abstract We report simultaneous Raman sideband cooling of a single 87Rb atom and a single 133Cs atom held in separate optical tweezers at 814 nm and 938 nm, respectively. Starting from outside the Lamb-Dicke regime, after 45 ms of cooling we measure probabilities to occupy the three-dimensional motional ground state of 0.8 6 − 0.04 + 0.03 for Rb and 0.9 5 − 0.04 + 0.03 for Cs. Our setup overlaps the Raman laser beams used to cool Rb and Cs, reducing hardware requirements by sharing equipment along the same beam path. The cooling protocol is scalable, and we demonstrate cooling of single Rb atoms in an array of four tweezers. After motional ground-state cooling, a 938 nm tweezer is translated to overlap with a 814 nm tweezer so that a single Rb and a single Cs atom can be transferred into a common 1064 nm trap. By minimising the heating during the merging and transfer, we prepare the atoms in the relative motional ground state with an efficiency of 0.8 1 − 0.08 + 0.08 . This is a crucial step towards the formation of single RbCs molecules confined in optical tweezer arrays.