Challenges
Datasets
Workspaces
Papers
Discussions
Leaderboard
Log inSign up
Challenges
Datasets
Workspaces
Papers
Discussions
Leaderboard
Blog
Job Board
Q3AS

© 2026 Aqora Quantum S.A.S.

TermsPrivacyLegal Notice

arXiv:2006.09014 · Physical Review Letters

Optical Shielding of Destructive Chemical Reactions between Ultracold Ground-State NaRb Molecules

Ting Xie, Maxence Lepers, Romain Véxiau, Andrea Orbán, Olivier Dulieu, Nadia Bouloufa-Maafa

Published Oct 8, 2020• 39 citations
arXivHTMLPDF

Abstract

We propose a method to suppress the chemical reactions between ultracold bosonic ground-state ^{23}Na^{87}Rb molecules based on optical shielding. By applying a laser with a frequency blue-detuned from the transition between the lowest rovibrational level of the electronic ground state X^{1}Σ^{+}(v_{X}=0,j_{X}=0), and the long-lived excited level b^{3}Π_{0}(v_{b}=0,j_{b}=1), the long-range dipole-dipole interaction between the colliding molecules can be engineered, leading to a dramatic suppression of reactive and photoinduced inelastic collisions, for both linear and circular laser polarizations. We demonstrate that the spontaneous emission from b^{3}Π_{0}(v_{b}=0,j_{b}=1) does not deteriorate the shielding process. This opens the possibility for a strong increase of the lifetime of cold molecule traps and for an efficient evaporative cooling. We also anticipate that the proposed mechanism is valid for alkali-metal diatomics with sufficiently large dipole-dipole interactions.

DOI
10.1103/physrevlett.125.153202

Related papers

Optical shielding of destructive chemical reactions between ultracold ground-state NaRb molecules

Andrea Orbán, Ting Xie, Maxence Lepers +3 more

Polar quantum gases represent promising platforms for studying many-body physics and strongly correlated systems with possible applications e.g. in quantum simulation or quantum computation. Due to their large permanent electric dipole moment polar molecules in electric field exhibit strong long-range anisotropic dipole-dipole interactions (DDIs). The creation and trapping of ultracold dipolar diatomic molecules of various species are feasible in many experimental groups nowadays. However long time trapping is still a challenge even in the case of the so called nonreactive molecules which are supposed to be immune against inelastic collisions in their absolute ground state [1] . Various hypothesis have been invoked to explain the possible mechanisms behind the trapping loss, however the check of their pertinence is not trivial since the final products can not be easily detected [2] . To overcome the loss processes we propose the suppression of inelastic collisions between molecules using optical shielding (OS). OS relies on the modification of long-range interactions between ground-state and excited molecules by laser light. The first experimental proof of OS process was demonstrated in case of the collision between identical ultracold alkali-metal atoms [3] .

Conference on Lasers and Electro-Optics Europe & European Quantum Electronics Conference (CLEO/Europe-EQEC)•Jun 21, 2021•1 citation

Optical Shielding of Ultracold 39K-Cs Collision

Ting Xie, Andrea Orbán, Olivier Dulieu +1 more

Research focusing on the formation of ultracold atomic and molecular quantum gases is a continuously expanding field due to its envisioned applications such as quantum-controlled chemistry or quantum simulation. The aim of our theoretical work is to find ways to suppress inelastic or reactive processes between colliding particles in ultracold quantum gases. Using a laser field detuned to the blue of a relevant transition, we propose to couple the initial colliding particle state to a repulsive excited one, thus preventing the particles to come close to each other. This "blueshielding" technique is applied for ultracold quantum gases, close to quantum degeneracy. We investigate the optical shielding in ultracold39K-Cs collision by using close-coupling channel method. As the (3)3Σ+and (2)3Π+molecular states are repulsive in long range[1], one verified effective optical shielding can be realized via driving the transition from the ground α3Σ+state to these excited states in the presence of linear-polarized light. We demonstrate that a strong field with a small blue detuning to the atomic transition is to the benefit of shielding since the Condon point is farther away from the inner region of ground triplet state. The spontaneous emission effect is taken into account by considering excited optical potentials with the modified formula of shielding rate [2]. We expect the shielding efficiency could be improved by using circular-polarized light [3].

Conference on Lasers and Electro-Optics Europe & European Quantum Electronics Conference (CLEO/Europe-EQEC)•Jun 1, 2019•0 citations

Microwave Shielding of Bosonic NaRb Molecules

Junyu Lin, Guanghua Chen, Mucan Jin +7 more

Recent years have witnessed tremendous progress in creating and manipulating ground-state ultracold polar molecules.However, the two-body loss regardless of the chemical reactivities is still a hurdle for many future explorations.Here, we investigate the loss suppression of nonreactive bosonic 23 Na 87 Rb molecules with a circularly polarized microwave blue detuned to the rotational transition.We achieve suppression of the loss by 2 orders of magnitude with the lowest two-body loss rate coefficient reduced to 3 × 10 -12 cm 3 =s.Meanwhile, the elastic collision rate coefficient is increased to the 10 -8 cm 3 =s level.The large good-to-bad collision ratio has allowed us to carry out evaporative cooling of 23 Na 87 Rb with an efficiency of 1.7(2), increasing the phase-space density by a factor of 10.With further improvements, this technique holds great promises for creating a Bose-Einstein condensate of ultracold polar molecules.

arXiv:2304.08312•Physical Review X•Sep 19, 2023•57 citations

Engineering long-range interactions between ultracold atoms with light

Ting Xie, Andrea Orbán, Xiaodong Xing +4 more

Abstract Ultracold temperatures in dilute quantum gases opened the way to an exquisite control of matter at the quantum level. Here we focus on the control of ultracold atomic collisions using a laser to engineer their interactions at large interatomic distances. We show that the entrance channel of two colliding ultracold atoms can be coupled to a repulsive collisional channel by the laser light so that the overall interaction between the two atoms becomes repulsive: this prevents them to come close together and to undergo inelastic processes, thus protecting the atomic gases from unwanted losses. We illustrate such an optical shielding (OS) mechanism with 39 K and 133 Cs atoms colliding at ultracold temperature (<1 μK). The process is described in the framework of the dressed-state picture and we then solve the resulting stationary coupled Schrödinger equations. The role of spontaneous emission and photoinduced inelastic scattering is also investigated as possible limitations of the shielding efficiency. We predict an almost complete suppression of inelastic collisions over a broad range of Rabi frequencies and detunings from the 39 K D2 line of the OS laser, both within the [0, 200 MHz] interval. We found that the polarization of the shielding laser has a minor influence on this efficiency. This proposal could easily be formulated for other bialkali-metal pairs as their long-range interaction are all very similar to each other.

arXiv:2110.15240•Journal of Physics B Atomic Molecular and Optical Physics•Jan 13, 2022•5 citations

Two-photon-assisted collisions in ultracold gases of polar molecules II: Two-photon optical shielding

Gohar Hovhannesyan, Charbel Karam, Romain Véxiau +4 more

We theoretically investigate the collisions between ultracold polar molecules in the presence of two lasers ensuring a Raman resonant transition on individual molecules to suppress photon scattering, taking the example of bosonic Na 23 K 39 molecules. By varying laser detunings and intensities, we enable a repulsive long-range interaction potential between molecules. After solving a set of coupled Schrödinger equations with the Hamiltonian written in the basis of laser-dressed states of the molecule pair at infinite distance, we identify quasiresonant conditions under which elastic collisions are favored over inelastic and reactive ones, by a factor of about 2, thus demonstrating a promising pathway for efficient two-photon optical shielding of ultracold molecular collisions. The results are analyzed in terms of scattering length of the colliding laser-dressed molecules, which exhibit prominent resonances assigned to the interaction of the entrance channel with other specific channels, consistent with the existence of a quasibound level of the long-range molecular pair induced by the lasers.

arXiv:2602.12069•Physical Review Research•Jun 22, 2026•0 citations

Ultracold Polar KRb Molecules in Optical Lattices

Brian Neyenhuis

The creation of a gas of ultracold polar molecules with a high phase space density brings new possibilities beyond experiments with ultracold atomic gases. In particular, long-range, anisotropic, and tunable dipole-dipole interactions open the way for novel quantum gases, with applications including strongly correlated many-body systems, and ultracold chemistry. This thesis will present the final steps to complete control over both internal and external degrees of freedom of the molecule which allows us to control, and even completely suppress, the chemical reactions between molecules. First, the control over internal states has been achieved through coherent state transfer to the ro-vibronic ground state and coherent manipulations of the hyperfine and rotational states with microwave radiation. Second, external degrees of freedom are controlled by loading the gas into an optical lattice. With the molecules loaded into a one-dimensional lattice, the orientation of the molecular collisions is controlled by manipulating both internal (hyperfine states) and external (motional states in the direction of tight confinement) degrees of freedom. Most striking is that by preparing the molecules all in the lowest band of the lattice in the same internal state, the molecular collisions can only occur in a side-by-side" orientation, where the chemical reaction rate is suppressed by the repulsive dipole-dipole interactions. The chemical reaction can be suppressed completely by further constraining the motion in the trap in a strong 3D lattice. Here we see lifetimes longer than 20 s, limited by o-resonant light scattering. Finally, the ac polarizability of the molecules is explored and controlled. The different rotational states of the molecule have different polarizabilities and will experience a different trapping force in both the optical dipole trap or lattice. We show that there is a magic angle" between the quantization axis and the polarization of the trapping laser at which the polarizabilities of two different rotational states can be matched, eliminating dephasing and allowing for coherent manipulations between rotational states.

•Jan 1, 2012•3 citations
We propose a method to suppress the chemical reactions between ultracold bosonic ground-state ^{23}Na^{87}Rb molecules based on optical shielding. By applying a laser with a frequency blue-detuned from the transition between the lowest rovibrational level of the electronic ground state X^{1}Σ^{+}(v_{X}=0,j_{X}=0), and the long-lived excited level b^{3}Π_{0}(v_{b}=0,j_{b}=1), the long-range dipole-dipole interaction between the colliding molecules can be engineered, leading to a dramatic suppression of reactive and photoinduced inelastic collisions, for both linear and circular laser polarizations. We demonstrate that the spontaneous emission from b^{3}Π_{0}(v_{b}=0,j_{b}=1) does not deteriorate the shielding process. This opens the possibility for a strong increase of the lifetime of cold molecule traps and for an efficient evaporative cooling. We also anticipate that the proposed mechanism is valid for alkali-metal diatomics with sufficiently large dipole-dipole interactions.
Polar quantum gases represent promising platforms for studying many-body physics and strongly correlated systems with possible applications e.g. in quantum simulation or quantum computation. Due to their large permanent electric dipole moment polar molecules in electric field exhibit strong long-range anisotropic dipole-dipole interactions (DDIs). The creation and trapping of ultracold dipolar diatomic molecules of various species are feasible in many experimental groups nowadays. However long time trapping is still a challenge even in the case of the so called nonreactive molecules which are supposed to be immune against inelastic collisions in their absolute ground state [1] . Various hypothesis have been invoked to explain the possible mechanisms behind the trapping loss, however the check of their pertinence is not trivial since the final products can not be easily detected [2] . To overcome the loss processes we propose the suppression of inelastic collisions between molecules using optical shielding (OS). OS relies on the modification of long-range interactions between ground-state and excited molecules by laser light. The first experimental proof of OS process was demonstrated in case of the collision between identical ultracold alkali-metal atoms [3] .
Research focusing on the formation of ultracold atomic and molecular quantum gases is a continuously expanding field due to its envisioned applications such as quantum-controlled chemistry or quantum simulation. The aim of our theoretical work is to find ways to suppress inelastic or reactive processes between colliding particles in ultracold quantum gases. Using a laser field detuned to the blue of a relevant transition, we propose to couple the initial colliding particle state to a repulsive excited one, thus preventing the particles to come close to each other. This "blueshielding" technique is applied for ultracold quantum gases, close to quantum degeneracy. We investigate the optical shielding in ultracold39K-Cs collision by using close-coupling channel method. As the (3)3Σ+and (2)3Π+molecular states are repulsive in long range[1], one verified effective optical shielding can be realized via driving the transition from the ground α3Σ+state to these excited states in the presence of linear-polarized light. We demonstrate that a strong field with a small blue detuning to the atomic transition is to the benefit of shielding since the Condon point is farther away from the inner region of ground triplet state. The spontaneous emission effect is taken into account by considering excited optical potentials with the modified formula of shielding rate [2]. We expect the shielding efficiency could be improved by using circular-polarized light [3].
Recent years have witnessed tremendous progress in creating and manipulating ground-state ultracold polar molecules.However, the two-body loss regardless of the chemical reactivities is still a hurdle for many future explorations.Here, we investigate the loss suppression of nonreactive bosonic 23 Na 87 Rb molecules with a circularly polarized microwave blue detuned to the rotational transition.We achieve suppression of the loss by 2 orders of magnitude with the lowest two-body loss rate coefficient reduced to 3 × 10 -12 cm 3 =s.Meanwhile, the elastic collision rate coefficient is increased to the 10 -8 cm 3 =s level.The large good-to-bad collision ratio has allowed us to carry out evaporative cooling of 23 Na 87 Rb with an efficiency of 1.7(2), increasing the phase-space density by a factor of 10.With further improvements, this technique holds great promises for creating a Bose-Einstein condensate of ultracold polar molecules.
Abstract Ultracold temperatures in dilute quantum gases opened the way to an exquisite control of matter at the quantum level. Here we focus on the control of ultracold atomic collisions using a laser to engineer their interactions at large interatomic distances. We show that the entrance channel of two colliding ultracold atoms can be coupled to a repulsive collisional channel by the laser light so that the overall interaction between the two atoms becomes repulsive: this prevents them to come close together and to undergo inelastic processes, thus protecting the atomic gases from unwanted losses. We illustrate such an optical shielding (OS) mechanism with 39 K and 133 Cs atoms colliding at ultracold temperature (<1 μK). The process is described in the framework of the dressed-state picture and we then solve the resulting stationary coupled Schrödinger equations. The role of spontaneous emission and photoinduced inelastic scattering is also investigated as possible limitations of the shielding efficiency. We predict an almost complete suppression of inelastic collisions over a broad range of Rabi frequencies and detunings from the 39 K D2 line of the OS laser, both within the [0, 200 MHz] interval. We found that the polarization of the shielding laser has a minor influence on this efficiency. This proposal could easily be formulated for other bialkali-metal pairs as their long-range interaction are all very similar to each other.
We theoretically investigate the collisions between ultracold polar molecules in the presence of two lasers ensuring a Raman resonant transition on individual molecules to suppress photon scattering, taking the example of bosonic Na 23 K 39 molecules. By varying laser detunings and intensities, we enable a repulsive long-range interaction potential between molecules. After solving a set of coupled Schrödinger equations with the Hamiltonian written in the basis of laser-dressed states of the molecule pair at infinite distance, we identify quasiresonant conditions under which elastic collisions are favored over inelastic and reactive ones, by a factor of about 2, thus demonstrating a promising pathway for efficient two-photon optical shielding of ultracold molecular collisions. The results are analyzed in terms of scattering length of the colliding laser-dressed molecules, which exhibit prominent resonances assigned to the interaction of the entrance channel with other specific channels, consistent with the existence of a quasibound level of the long-range molecular pair induced by the lasers.
The creation of a gas of ultracold polar molecules with a high phase space density brings new possibilities beyond experiments with ultracold atomic gases. In particular, long-range, anisotropic, and tunable dipole-dipole interactions open the way for novel quantum gases, with applications including strongly correlated many-body systems, and ultracold chemistry. This thesis will present the final steps to complete control over both internal and external degrees of freedom of the molecule which allows us to control, and even completely suppress, the chemical reactions between molecules. First, the control over internal states has been achieved through coherent state transfer to the ro-vibronic ground state and coherent manipulations of the hyperfine and rotational states with microwave radiation. Second, external degrees of freedom are controlled by loading the gas into an optical lattice. With the molecules loaded into a one-dimensional lattice, the orientation of the molecular collisions is controlled by manipulating both internal (hyperfine states) and external (motional states in the direction of tight confinement) degrees of freedom. Most striking is that by preparing the molecules all in the lowest band of the lattice in the same internal state, the molecular collisions can only occur in a side-by-side" orientation, where the chemical reaction rate is suppressed by the repulsive dipole-dipole interactions. The chemical reaction can be suppressed completely by further constraining the motion in the trap in a strong 3D lattice. Here we see lifetimes longer than 20 s, limited by o-resonant light scattering. Finally, the ac polarizability of the molecules is explored and controlled. The different rotational states of the molecule have different polarizabilities and will experience a different trapping force in both the optical dipole trap or lattice. We show that there is a magic angle" between the quantization axis and the polarization of the trapping laser at which the polarizabilities of two different rotational states can be matched, eliminating dephasing and allowing for coherent manipulations between rotational states.