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Conference on Lasers and Electro-Optics Europe & European Quantum Electronics Conference (CLEO/Europe-EQEC)

What could THz radiation bring to the field of ultracold gases?

Adrien Devolder, Michèle Desouter-Lecomte, Osman Atabek, Eliane Luc-Koenig, Olivier Dulieu

Published Jun 21, 2021• 0 citations
Publisher

Abstract

The exquisite control of diluted atomic vapors that can be achieved using electromagnetic (em) fields triggered the overwhelming development of researches on ultracold (T<<1millikelvin) quantum gases through laser cooling and trapping, opening ways to amazing applications in quantum technologies. For a composite system like a molecule under such ultracold conditions, the additional control of the internal degrees of freedom has also been recently demonstrated [1] with cw visible, microwave, and radio radiation frequencies for electronic, rotational, and hyperfine transitions, respectively. Vibrational transitions could be addressed with THz transitions, as an attractive path for controlling the interatomic interactions and creating ultracold gases of a wide class of diatomic molecules in their absolute ground state. More specifically, THz radiation can induce a coupling between the bound level of a pair of trapped ultracold ground-state atoms and a loosely-bound vibrational level of the related molecular electronic ground state. This coupling, generated by the intrinsic permanent electric dipole moment of a heteronuclear atomic pair (RbSr in the present work), is related to a specific spectroscopic feature of the atomic pair dressed by the THz field, the Laser Assisted Self-Induced Feshbach Resonance (LASIFR) [2] . In analogy with magnetic Feshbach resonance, the scattering length can be controlled by tuning the THz radiation frequency around a LASIFR (see Fig (a)).

DOI
10.1109/cleo/europe-eqec52157.2021.9541579

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Laser-assisted self-induced Feshbach resonance for controlling heteronuclear quantum gas mixtures

Adrien Devolder, Eliane Luc-Koenig, Osman Atabek +2 more

We propose a type of Feshbach resonance occurring when two different ultracold atoms in their ground state undergo an $s$-wave collision in the presence of a laser. The collisional levels of the atom pair are coupled by the laser to a rovibrational molecular level of the same electronic ground state: We name it a laser-assisted self-induced Feshbach resonance. This mechanism, valid for all heteronuclear quantum gas mixtures, is analyzed on the example of ultracold $^{87}\mathrm{Rb}$ and $^{84}\mathrm{Sr}$ atoms for which the resonant laser frequency falls in the subterahertz range. The interspecies scattering length can be controlled with the laser frequency and intensity without atom loss. Moreover, chirping slowly, the frequency allows for the adiabatic formation of ultracold $^{87}\mathrm{Rb}\phantom{\rule{0.16em}{0ex}}^{84}\mathrm{Sr}$ molecules in a manner very similar to a magnetic Feshbach resonance. A stimulated Raman adiabatic passage follows for stabilizing the molecules in their rovibronic ground state.

arXiv:1902.00323•Physical Review A•Nov 12, 2019•10 citations

Coherent Laser Manipulation of Ultracold Molecules

Elena Kuznetsova, Robin Côté, S. F.

The realization of rovibrationally stable dense samples of ultracold diatomic molecules remains one of the main stepping stones to achieve the next slate of major goals in the field of atomic and molecular physics. Though obtaining diatomic alkali molecules was seen as a logical next step following the optical cooling of atoms, many of the possible applications currently under investigation extend beyond atomic and molecular physics. For example, spectroscopy of ultracold molecules can help in testing extensions of the Standard Model via the search for a permanent electric dipole moment of the electron (1; 2), or the energy difference between enantiomers of chiral molecules (3). Various molecular transitions can be utilized to track the time dependence of fundamental constants, including the fine structure constant and the proton to electron mass ratio (4). They also open the way for cold and ultracold chemistry, where the interacting species and products are in a coherent quantum superposition state (5) and reactions can happen via quantum tunneling. Dipolar ultracold quantum gases promise to show a plethora of new phenomena due to anisotropic long-range dipole-dipole interactions (6). Dipolar molecules in optical lattices can be employed as a quantum simulator of condensed matter systems, and they are predicted to demonstrate new quantum phases such as a dipolar crystal, supersolid, checkerboard and collapse phases (7; 8). Ultracold polar molecules also represent an attractive platform for quantum computation (9). They offer a variety of long-lived states for qubit encoding, including rotational, spin and hyperfine (if electronic and nuclear spins are non-zero), Λ and Ω-doublet states (10) and scalability to a large number of qubits. Polar molecules can be easily controlled by DC electric and magnetic fields, as well as bymicrowave and optical fields, allowing the design of various traps (11; 12). The main appeal of polar molecules for quantum information processing, however, comes from their permanent electric dipole moment, permitting them to interact via a long-range dipole-dipole interaction. The dipole-dipole interaction offers a tool to construct two-qubit gates, required for universal quantum computation (9; 13). Ultracold molecules in their ground vibrational state v = 0 (and even in specific rotational, hyperfine or Zeeman states) are required formany of these applications since they have a large permanent electric dipole moment and are stable with respect to collisions and spontaneous emission. Currently translationally ultracold (100 nK 1 mK) molecules are produced by magneto(14) and photo-association (15) techniques. In a typical photoassociation scheme, 3

InTech eBooks•Nov 14, 2011•0 citations

An ultracold gas of bosonic 23Na39K ground-state molecules

Kai K. Voges

Ultracold bialkali polar molecules play a leading part at the frontline of quantum physics. They recently attract a lot of attention in the field of ultracold quantum chemistry, quantum many-body physics and quantum simulations. The key for their success is the rich internal level structure with rotational and vibrational degrees of freedom and their large electric dipole moments. Still, only a handful of molecular species are available at ultracold temperatures until now, although it is highly desirable to produce new molecular species to further expand the range of applications. Besides direct laser cooling methods for molecules, the assembly of heteronuclear ground-state molecules from ultracold atomic mixtures is the most promising approach for the creation of polar molecules. It includes the formation of weakly bound Feshbach molecules from the diatomic mixture and the subsequent two-photon stimulated Raman adiabatic passage (STIRAP) transfer to the rovibrational ground state. This creation strategy has been successfully demonstrated for the first time in the pioneering experiments at JILA with ultracold 40K87Rb molecules. Since then, only a few more molecular species from different alkali atoms have been created, namely 6Li23Na, 23Na40K, 23Na87Rb and 87Rb133Cs. In this thesis, I report the successful creation of a new species of ultracold polar ground-state molecules: 23Na39K. Starting from an ultracold mixture of bosonic 23Na and 39K atoms, weakly bound molecules are created. For this purpose, a Feshbach resonance in a high angular momentum scattering channel is chosen, experimentally identified and characterized. Close to this resonance the weakly bound Feshbach molecules are formed using resonant radio frequency radiation. For the two-photon ground-state transfer, a unique, highly specialized two-color laser system is designed and realized. It is used for one- and two-photon spectroscopy to identify the relevant transitions for the ground-state transfer. Based on the obtained data, a local model of the singlet-triplet mixed excited state manifolds is developed, with which the hyperfine structure and the magnetic field dependence is predicted with high accuracy. According to these findings, a suitable pathway to a single hyperfine ground state is chosen considering selection rules and experimental conditions such as laser polarization and beam alignment. To precisely determine the two-photon resonance condition for STIRAP, electromagnetically induced transparency measurements are performed. The ground-state transfer is then performed using STIRAP. The experimental findings regarding the STIRAP are successfully supported theoretically by a model based on a five-level master equation. The pure molecular gas shows evidence for two-body dominated loss mechanisms, such as sticky four-body collisions. The molecule-atom mixture of 23Na39K+39K reveals an unexpectedly low loss rate coefficient although sticky three-body collisions are assumed to occur. This behavior demands further investigations regarding different hyperfine collisional chan-nels and magnetic field regions.

•Jan 1, 2020•6 citations

Interacting gases of ultracold polar molecules

Frauke Seeßelberg

Ultracold quantum gases are versatile model systems for exploring quantum physics or for the simulation of solid state materials. Meanwhile, they have been created from various atomic species - from alkali metals over alkaline earths to rare earth elements. The latest addition are quantum gases of different kinds of polar molecules. Expectations for quantum gases of heteronuclear molecules are high: Due to their large electric dipole moments, these molecules can interact with each other via long-range interactions - not just via contact interactions as is the case for most atoms. Additionally, they have vibrational and rotational degrees of freedom, with open up new possibilities for quantum simulation. But the same degrees of freedom also pose some challenges. For example, they make the preparation of the quantum gas more difficult, which is typically produced with a combination of laser cooling and evaporative cooling in the atomic case. Molecules mostly lack closed transitions in their spectra, which are required for laser cooling. Therefore, we create our molecular quantum gas from a mixture of two atomic quantum gases. In this work, such an experimental method was developed for fermionic NaK molecules, which is based on the two-photon process Stimulated Raman Adiabatic Passage (STIRAP). Within STIRAP, the hyperfine structure of the chosen intermediate state plays an important role. Experimentally, and with the help of a theoretical model describing the whole process, we find that we produce the most molecules when we use a large one-photon detuning, if the hyperfine structure of the intermediate state is unresolved. In another project, we explored the rotational level structure of the molecular ground state populated by STIRAP. Rotation is closely linked to the electric dipole moment. The superposition of the ground state with the first excited rotational state, for example, has a transition dipole moment of almost 60% of the permanent electric dipole moment. Unfortunately, coherence times of such superpositions are typically short, as the different polarizabilities of the rotational states lead to dephasing in optical traps. However, using a special polarization angle and a small, dc electric field, we can compensate these differences and realize a spin-decoupled magic trap. With this new technique we obtain record coherence times, at least for small molecular densities. For larger densities we observe first indications for dipolar interactions in a bulk gas of polar molecules, which we also model using the moving-average cluster expansion (MACE).

•Jan 1, 2019•0 citations

Optical control of a magnetic Feshbach resonance in an ultracold Fermi gas

Zhengkun Fu, Pengjun Wang, Lianghui Huang +3 more

We use laser light near resonant with a molecular bound-to-bound transition to control a magnetic Feshbach resonance in ultracold Fermi gases of ${}^{40}$K atoms. The spectrum of excited molecular states is measured by applying a laser field that couples the ground Feshbach molecular state to electronically excited molecular states. Nine strong bound-to-bound resonances are observed below the ${}^{2}{P}_{1/2}+{\phantom{\rule{0.16em}{0ex}}}^{2}{S}_{1/2}$ threshold. We use radio-frequency spectroscopy to characterize the laser-dressed bound state near a specific bound-to-bound resonance and show clearly the shift of the magnetic Feshbach resonance using light. The demonstrated technology could be used to modify interatomic interactions with high spatial and temporal resolutions in the crossover regime from a Bose-Einstein condensate to a Bardeen-Cooper-Schrieffer superfluid.

arXiv:1306.0395•Physical Review A•Oct 9, 2013•36 citations

Focus on Cold and Ultracold Molecules

Lincoln D. Carr, Jun Ye

Cold and ultracold molecules are the next wave of ultracold physics, giving rise to an exciting array of scientific opportunities, including many body physics for novel quantum phase transitions, new states of matter, and quantum information processing. Precision tests of fundamental physical laws benefit from the existence of molecular internal structure with exquisite control. The study of novel collision and reaction dynamics will open a new chapter of quantum chemistry. Cold molecules bring together researchers from a variety of fields, including atomic, molecular, and optical physics, chemistry and chemical physics, quantum information science and quantum simulations, condensed matter physics, nuclear physics, and astrophysics, a truly remarkable synergy of scientific explorations. For the past decade there have been steady advances in direct cooling techniques, from buffer-gas cooling to cold molecular beams to electro- and magneto-molecular decelerators. 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Whether directly or indirectly cooled, heteronuclear polar molecules offer distinct new features in comparison to cold atoms, while sharing all of their advantages (purity, high coherence, controllability, tunable interactions, no disorder, etc). First, they are more easily manipulated because of the strong response of their electric dipole moment to external electric fields, DC or AC. The electric dipole moment also creates the new aspect of long range interactions. Second, they have a rich internal structure, with vibrational and rotational states, fine or hyperfine structure, and Ω- or Λ-doublets. This internal structure allows for wonderful new possibilities in areas such as precision measurement and exquisite control of system dynamics. Therefore, although this focus issue contains a few articles on homonuclear molecules, more complex molecules such as benzene, and even a contribution on atomic chromium, which has a significant magnetic dipole moment, our main focus is on the heteronuclear polar case. This focus issue explores both direct and indirect cooling of mainly polar molecules, and the theory to support and inspire these advances. Thirty-eight research groups have contributed original work, and there are two review articles to complement these advances: the first covers cold and ultracold molecules broadly from few body to many body physics, including foundational theory, the technology to make them, and their scientific applications. The second is on the search for time variation of fundamental constants. The former review, which is comprehensive in nature, concludes with a list of open questions. This sets the tone for the focus issue, namely, openness, innovation, and possibility, an emphasis for which New Journal of Physics , an open-access journal of the highest quality, is especially fitted. Focus on Cold and Ultracold Molecules Contents Cold and ultracold molecules: science, technology and applications Lincoln D Carr, David DeMille, Roman V Krems and Jun Ye Ultracold molecules: new probes on the variation of fundamental constants Cheng Chin, V V Flambaum and M G Kozlov Probing the unitarity limit at low laser intensities Philippe Pellegrini and Robin Côté Single-photon molecular cooling Edvardas Narevicius, S Travis Bannerman and Mark G Raizen Quantum simulations of extended Hubbard models with dipolar crystals M Ortner, A Micheli, G Pupillo and P Zoller Collisional and molecular spectroscopy in an ultracold Bose–Bose mixture G Thalhammer, G Barontini, J Catani, F Rabatti, C Weber, A Simoni, F Minardi and M Inguscio Multi-channel modelling of the formation of vibrationally cold polar KRb molecules Svetlana Kotochigova, Eite Tiesinga and Paul S Julienne Formation of ultracold, highly polar X 1 Σ + NaCs molecules C Haimberger, J Kleinert, P Zabawa, A Wakim and N P Bigelow Quantum polarization spectroscopy of correlations in attractive fermionic gases T Roscilde, M Rodríguez, K Eckert, O Romero-Isart, M Lewenstein, E Polzik and A Sanpera Inelastic semiclassical collisions in cold dipolar gases Michael Cavagnero and Catherine Newell Quasi-universal dipolar scattering in cold and ultracold gases J L Bohn, M Cavagnero and C Ticknor Stark deceleration of lithium hydride molecules S K Tokunaga, J M Dyne, E A Hinds and M R Tarbutt Molecular vibrational cooling by optical pumping with shaped femtosecond pulses D Sofikitis, S Weber, A Fioretti, R Horchani, M Allegrini, B Chatel, D Comparat and P Pillet Deeply bound ultracold molecules in an optical lattice Johann G Danzl, Manfred J Mark, Elmar Haller, Mattias Gustavsson, Russell Hart, Andreas Liem, Holger Zellmer and Hanns-Christoph Nägerl Toward the production of quantum degenerate bosonic polar molecules, 41 K 87 Rb K Aikawa, D Akamatsu, J Kobayashi, M Ueda, T Kishimoto and S Inouye Influence of a Feshbach resonance on the photoassociation of LiCs J Deiglmayr, P Pellegrini, A Grochola, M Repp, R Côté, O Dulieu, R Wester and M Weidemüller The kinematic cooling of molecules with laser-cooled atoms Ken Takase, Larry A Rahn, David W Chandler and Kevin E Strecker Coherent collapses of dipolar Bose–Einstein condensates for different trap geometries J Metz, T Lahaye, B Fröhlich, A Griesmaier, T Pfau, H Saito, Y Kawaguchi and M Ueda High-energy-resolution molecular beams for cold collision studies L P Parazzoli, N Fitch, D S Lobser and H J Lewandowski Collisional effects in the formation of cold guided beams of polar molecules M Motsch, C Sommer, M Zeppenfeld, L D van Buuren, P W H Pinkse and G Rempe Towards sympathetic cooling of large molecules: cold collisions between benzene and rare gas atoms P Barletta, J Tennyson and P F Barker Efficient formation of ground-state ultracold molecules via STIRAP from the continuum at a Feshbach resonance Elena Kuznetsova, Marko Gacesa, Philippe Pellegrini, 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formed by photoassociation J T Kim, D Wang, E E Eyler, P L Gould and W C Stwalley Pumping vortex into a Bose–Einstein condensate of heteronuclear molecules Z F Xu, R Q Wang and L You Intense atomic and molecular beams via neon buffer-gas cooling David Patterson, Julia Rasmussen and John M Doyle Dynamical properties of dipolar Fermi gases T Sogo, L He, T Miyakawa, S Yi, H Lu and H Pu Collisions of bosonic ultracold polar molecules in microwave traps Alexander V Avdeenkov Cold TiO(X 3 Δ)–He collisions Mei-Ju Lu and Jonathan D Weinstein Investigation of dephasing rates in an interacting Rydberg gas U Raitzsch, R Heidemann, H Weimer, B Butscher, P Kollmann, R Löw, H P Büchler and T Pfau Impact of electric fields on highly excited rovibrational states of polar dimers Rosario González-Férez and Peter Schmelcher Phase transition from straight into twisted vortex lines in dipolar Bose–Einstein condensates M Klawunn and L Santos Stimulating the production of deeply bound RbCs molecules with laser pulses: the role of spin–orbit coupling in forming ultracold molecules Subhas Ghosal, Richard J Doyle, Christiane P Koch and Jeremy M Hutson Sensitive measurement of m p / m e variance using vibrational transition frequencies of cold molecules Masatoshi Kajita

New Journal of Physics•May 14, 2009•75 citations
The exquisite control of diluted atomic vapors that can be achieved using electromagnetic (em) fields triggered the overwhelming development of researches on ultracold (T<<1millikelvin) quantum gases through laser cooling and trapping, opening ways to amazing applications in quantum technologies. For a composite system like a molecule under such ultracold conditions, the additional control of the internal degrees of freedom has also been recently demonstrated [1] with cw visible, microwave, and radio radiation frequencies for electronic, rotational, and hyperfine transitions, respectively. Vibrational transitions could be addressed with THz transitions, as an attractive path for controlling the interatomic interactions and creating ultracold gases of a wide class of diatomic molecules in their absolute ground state. More specifically, THz radiation can induce a coupling between the bound level of a pair of trapped ultracold ground-state atoms and a loosely-bound vibrational level of the related molecular electronic ground state. This coupling, generated by the intrinsic permanent electric dipole moment of a heteronuclear atomic pair (RbSr in the present work), is related to a specific spectroscopic feature of the atomic pair dressed by the THz field, the Laser Assisted Self-Induced Feshbach Resonance (LASIFR) [2] . In analogy with magnetic Feshbach resonance, the scattering length can be controlled by tuning the THz radiation frequency around a LASIFR (see Fig (a)).
We propose a type of Feshbach resonance occurring when two different ultracold atoms in their ground state undergo an sss-wave collision in the presence of a laser. The collisional levels of the atom pair are coupled by the laser to a rovibrational molecular level of the same electronic ground state: We name it a laser-assisted self-induced Feshbach resonance. This mechanism, valid for all heteronuclear quantum gas mixtures, is analyzed on the example of ultracold 87Rb^{87}\mathrm{Rb}87Rb and 84Sr^{84}\mathrm{Sr}84Sr atoms for which the resonant laser frequency falls in the subterahertz range. The interspecies scattering length can be controlled with the laser frequency and intensity without atom loss. Moreover, chirping slowly, the frequency allows for the adiabatic formation of ultracold 87Rb84Sr^{87}\mathrm{Rb}\phantom{\rule{0.16em}{0ex}}^{84}\mathrm{Sr}87Rb84Sr molecules in a manner very similar to a magnetic Feshbach resonance. A stimulated Raman adiabatic passage follows for stabilizing the molecules in their rovibronic ground state.
The realization of rovibrationally stable dense samples of ultracold diatomic molecules remains one of the main stepping stones to achieve the next slate of major goals in the field of atomic and molecular physics. Though obtaining diatomic alkali molecules was seen as a logical next step following the optical cooling of atoms, many of the possible applications currently under investigation extend beyond atomic and molecular physics. For example, spectroscopy of ultracold molecules can help in testing extensions of the Standard Model via the search for a permanent electric dipole moment of the electron (1; 2), or the energy difference between enantiomers of chiral molecules (3). Various molecular transitions can be utilized to track the time dependence of fundamental constants, including the fine structure constant and the proton to electron mass ratio (4). They also open the way for cold and ultracold chemistry, where the interacting species and products are in a coherent quantum superposition state (5) and reactions can happen via quantum tunneling. Dipolar ultracold quantum gases promise to show a plethora of new phenomena due to anisotropic long-range dipole-dipole interactions (6). Dipolar molecules in optical lattices can be employed as a quantum simulator of condensed matter systems, and they are predicted to demonstrate new quantum phases such as a dipolar crystal, supersolid, checkerboard and collapse phases (7; 8). Ultracold polar molecules also represent an attractive platform for quantum computation (9). They offer a variety of long-lived states for qubit encoding, including rotational, spin and hyperfine (if electronic and nuclear spins are non-zero), Λ and Ω-doublet states (10) and scalability to a large number of qubits. Polar molecules can be easily controlled by DC electric and magnetic fields, as well as bymicrowave and optical fields, allowing the design of various traps (11; 12). The main appeal of polar molecules for quantum information processing, however, comes from their permanent electric dipole moment, permitting them to interact via a long-range dipole-dipole interaction. The dipole-dipole interaction offers a tool to construct two-qubit gates, required for universal quantum computation (9; 13). Ultracold molecules in their ground vibrational state v = 0 (and even in specific rotational, hyperfine or Zeeman states) are required formany of these applications since they have a large permanent electric dipole moment and are stable with respect to collisions and spontaneous emission. Currently translationally ultracold (100 nK 1 mK) molecules are produced by magneto(14) and photo-association (15) techniques. In a typical photoassociation scheme, 3
Ultracold bialkali polar molecules play a leading part at the frontline of quantum physics. They recently attract a lot of attention in the field of ultracold quantum chemistry, quantum many-body physics and quantum simulations. The key for their success is the rich internal level structure with rotational and vibrational degrees of freedom and their large electric dipole moments. Still, only a handful of molecular species are available at ultracold temperatures until now, although it is highly desirable to produce new molecular species to further expand the range of applications. Besides direct laser cooling methods for molecules, the assembly of heteronuclear ground-state molecules from ultracold atomic mixtures is the most promising approach for the creation of polar molecules. It includes the formation of weakly bound Feshbach molecules from the diatomic mixture and the subsequent two-photon stimulated Raman adiabatic passage (STIRAP) transfer to the rovibrational ground state. This creation strategy has been successfully demonstrated for the first time in the pioneering experiments at JILA with ultracold 40K87Rb molecules. Since then, only a few more molecular species from different alkali atoms have been created, namely 6Li23Na, 23Na40K, 23Na87Rb and 87Rb133Cs. In this thesis, I report the successful creation of a new species of ultracold polar ground-state molecules: 23Na39K. Starting from an ultracold mixture of bosonic 23Na and 39K atoms, weakly bound molecules are created. For this purpose, a Feshbach resonance in a high angular momentum scattering channel is chosen, experimentally identified and characterized. Close to this resonance the weakly bound Feshbach molecules are formed using resonant radio frequency radiation. For the two-photon ground-state transfer, a unique, highly specialized two-color laser system is designed and realized. It is used for one- and two-photon spectroscopy to identify the relevant transitions for the ground-state transfer. Based on the obtained data, a local model of the singlet-triplet mixed excited state manifolds is developed, with which the hyperfine structure and the magnetic field dependence is predicted with high accuracy. According to these findings, a suitable pathway to a single hyperfine ground state is chosen considering selection rules and experimental conditions such as laser polarization and beam alignment. To precisely determine the two-photon resonance condition for STIRAP, electromagnetically induced transparency measurements are performed. The ground-state transfer is then performed using STIRAP. The experimental findings regarding the STIRAP are successfully supported theoretically by a model based on a five-level master equation. The pure molecular gas shows evidence for two-body dominated loss mechanisms, such as sticky four-body collisions. The molecule-atom mixture of 23Na39K+39K reveals an unexpectedly low loss rate coefficient although sticky three-body collisions are assumed to occur. This behavior demands further investigations regarding different hyperfine collisional chan-nels and magnetic field regions.
Ultracold quantum gases are versatile model systems for exploring quantum physics or for the simulation of solid state materials. Meanwhile, they have been created from various atomic species - from alkali metals over alkaline earths to rare earth elements. The latest addition are quantum gases of different kinds of polar molecules. Expectations for quantum gases of heteronuclear molecules are high: Due to their large electric dipole moments, these molecules can interact with each other via long-range interactions - not just via contact interactions as is the case for most atoms. Additionally, they have vibrational and rotational degrees of freedom, with open up new possibilities for quantum simulation. But the same degrees of freedom also pose some challenges. For example, they make the preparation of the quantum gas more difficult, which is typically produced with a combination of laser cooling and evaporative cooling in the atomic case. Molecules mostly lack closed transitions in their spectra, which are required for laser cooling. Therefore, we create our molecular quantum gas from a mixture of two atomic quantum gases. In this work, such an experimental method was developed for fermionic NaK molecules, which is based on the two-photon process Stimulated Raman Adiabatic Passage (STIRAP). Within STIRAP, the hyperfine structure of the chosen intermediate state plays an important role. Experimentally, and with the help of a theoretical model describing the whole process, we find that we produce the most molecules when we use a large one-photon detuning, if the hyperfine structure of the intermediate state is unresolved. In another project, we explored the rotational level structure of the molecular ground state populated by STIRAP. Rotation is closely linked to the electric dipole moment. The superposition of the ground state with the first excited rotational state, for example, has a transition dipole moment of almost 60% of the permanent electric dipole moment. Unfortunately, coherence times of such superpositions are typically short, as the different polarizabilities of the rotational states lead to dephasing in optical traps. However, using a special polarization angle and a small, dc electric field, we can compensate these differences and realize a spin-decoupled magic trap. With this new technique we obtain record coherence times, at least for small molecular densities. For larger densities we observe first indications for dipolar interactions in a bulk gas of polar molecules, which we also model using the moving-average cluster expansion (MACE).
We use laser light near resonant with a molecular bound-to-bound transition to control a magnetic Feshbach resonance in ultracold Fermi gases of 40{}^{40}40K atoms. The spectrum of excited molecular states is measured by applying a laser field that couples the ground Feshbach molecular state to electronically excited molecular states. Nine strong bound-to-bound resonances are observed below the 2P1/2+2S1/2{}^{2}{P}_{1/2}+{\phantom{\rule{0.16em}{0ex}}}^{2}{S}_{1/2}2P1/2​+2S1/2​ threshold. We use radio-frequency spectroscopy to characterize the laser-dressed bound state near a specific bound-to-bound resonance and show clearly the shift of the magnetic Feshbach resonance using light. The demonstrated technology could be used to modify interatomic interactions with high spatial and temporal resolutions in the crossover regime from a Bose-Einstein condensate to a Bardeen-Cooper-Schrieffer superfluid.
Cold and ultracold molecules are the next wave of ultracold physics, giving rise to an exciting array of scientific opportunities, including many body physics for novel quantum phase transitions, new states of matter, and quantum information processing. Precision tests of fundamental physical laws benefit from the existence of molecular internal structure with exquisite control. The study of novel collision and reaction dynamics will open a new chapter of quantum chemistry. Cold molecules bring together researchers from a variety of fields, including atomic, molecular, and optical physics, chemistry and chemical physics, quantum information science and quantum simulations, condensed matter physics, nuclear physics, and astrophysics, a truly remarkable synergy of scientific explorations. For the past decade there have been steady advances in direct cooling techniques, from buffer-gas cooling to cold molecular beams to electro- and magneto-molecular decelerators. These techniques have allowed a large variety of molecules to be cooled for pioneering studies. Recent amazing advances in experimental techniques combining the ultracold and the ultraprecise have furthermore brought molecules to the point of quantum degeneracy. These latter indirect cooling techniques magnetically associate atoms from a Bose–Einstein condensate and/or a quantum degenerate Fermi gas, transferring at 90% efficiency highly excited Fano–Feshbach molecules, which are on the order of 10 000 Bohr radii in size, to absolute ground state molecules just a few Bohr across. It was this latter advance, together with significant breakthroughs in internal state manipulations, which inspired us to coordinate this focus issue now, and is the reason why we say the next wave of ultracold physics has now arrived. Whether directly or indirectly cooled, heteronuclear polar molecules offer distinct new features in comparison to cold atoms, while sharing all of their advantages (purity, high coherence, controllability, tunable interactions, no disorder, etc). First, they are more easily manipulated because of the strong response of their electric dipole moment to external electric fields, DC or AC. The electric dipole moment also creates the new aspect of long range interactions. Second, they have a rich internal structure, with vibrational and rotational states, fine or hyperfine structure, and Ω- or Λ-doublets. This internal structure allows for wonderful new possibilities in areas such as precision measurement and exquisite control of system dynamics. Therefore, although this focus issue contains a few articles on homonuclear molecules, more complex molecules such as benzene, and even a contribution on atomic chromium, which has a significant magnetic dipole moment, our main focus is on the heteronuclear polar case. This focus issue explores both direct and indirect cooling of mainly polar molecules, and the theory to support and inspire these advances. Thirty-eight research groups have contributed original work, and there are two review articles to complement these advances: the first covers cold and ultracold molecules broadly from few body to many body physics, including foundational theory, the technology to make them, and their scientific applications. The second is on the search for time variation of fundamental constants. The former review, which is comprehensive in nature, concludes with a list of open questions. This sets the tone for the focus issue, namely, openness, innovation, and possibility, an emphasis for which New Journal of Physics , an open-access journal of the highest quality, is especially fitted. Focus on Cold and Ultracold Molecules Contents Cold and ultracold molecules: science, technology and applications Lincoln D Carr, David DeMille, Roman V Krems and Jun Ye Ultracold molecules: new probes on the variation of fundamental constants Cheng Chin, V V Flambaum and M G Kozlov Probing the unitarity limit at low laser intensities Philippe Pellegrini and Robin Côté Single-photon molecular cooling Edvardas Narevicius, S Travis Bannerman and Mark G Raizen Quantum simulations of extended Hubbard models with dipolar crystals M Ortner, A Micheli, G Pupillo and P Zoller Collisional and molecular spectroscopy in an ultracold Bose–Bose mixture G Thalhammer, G Barontini, J Catani, F Rabatti, C Weber, A Simoni, F Minardi and M Inguscio Multi-channel modelling of the formation of vibrationally cold polar KRb molecules Svetlana Kotochigova, Eite Tiesinga and Paul S Julienne Formation of ultracold, highly polar X 1 Σ + NaCs molecules C Haimberger, J Kleinert, P Zabawa, A Wakim and N P Bigelow Quantum polarization spectroscopy of correlations in attractive fermionic gases T Roscilde, M Rodríguez, K Eckert, O Romero-Isart, M Lewenstein, E Polzik and A Sanpera Inelastic semiclassical collisions in cold dipolar gases Michael Cavagnero and Catherine Newell Quasi-universal dipolar scattering in cold and ultracold gases J L Bohn, M Cavagnero and C Ticknor Stark deceleration of lithium hydride molecules S K Tokunaga, J M Dyne, E A Hinds and M R Tarbutt Molecular vibrational cooling by optical pumping with shaped femtosecond pulses D Sofikitis, S Weber, A Fioretti, R Horchani, M Allegrini, B Chatel, D Comparat and P Pillet Deeply bound ultracold molecules in an optical lattice Johann G Danzl, Manfred J Mark, Elmar Haller, Mattias Gustavsson, Russell Hart, Andreas Liem, Holger Zellmer and Hanns-Christoph Nägerl Toward the production of quantum degenerate bosonic polar molecules, 41 K 87 Rb K Aikawa, D Akamatsu, J Kobayashi, M Ueda, T Kishimoto and S Inouye Influence of a Feshbach resonance on the photoassociation of LiCs J Deiglmayr, P Pellegrini, A Grochola, M Repp, R Côté, O Dulieu, R Wester and M Weidemüller The kinematic cooling of molecules with laser-cooled atoms Ken Takase, Larry A Rahn, David W Chandler and Kevin E Strecker Coherent collapses of dipolar Bose–Einstein condensates for different trap geometries J Metz, T Lahaye, B Fröhlich, A Griesmaier, T Pfau, H Saito, Y Kawaguchi and M Ueda High-energy-resolution molecular beams for cold collision studies L P Parazzoli, N Fitch, D S Lobser and H J Lewandowski Collisional effects in the formation of cold guided beams of polar molecules M Motsch, C Sommer, M Zeppenfeld, L D van Buuren, P W H Pinkse and G Rempe Towards sympathetic cooling of large molecules: cold collisions between benzene and rare gas atoms P Barletta, J Tennyson and P F Barker Efficient formation of ground-state ultracold molecules via STIRAP from the continuum at a Feshbach resonance Elena Kuznetsova, Marko Gacesa, Philippe Pellegrini, Susanne F Yelin and Robin Côté Emergent timescales in entangled quantum dynamics of ultracold molecules in optical lattices M L Wall and L D Carr Rotational state resolved photodissociation spectroscopy of translationally and vibrationally cold MgH + ions: toward rotational cooling of molecular ions K Højbjerre, A K Hansen, P S Skyt, P F Staanum and M Drewsen Collective transverse cavity cooling of a dense molecular beam Thomas Salzburger and Helmut Ritsch A Stark decelerator on a chip Samuel A Meek, Horst Conrad and Gerard Meijer Deceleration of molecules by dipole force potential: a numerical simulation Susumu Kuma and Takamasa Momose Ultracold molecules: vehicles to scalable quantum information processing Kathy-Anne Brickman Soderberg, Nathan Gemelke and Cheng Chin Magnetic field modification of ultracold molecule–molecule collisions T V Tscherbul, Yu V Suleimanov, V Aquilanti and R V Krems Spectroscopy of 39 K 85 Rb triplet excited states using ultracold a 3 Σ + state molecules formed by photoassociation J T Kim, D Wang, E E Eyler, P L Gould and W C Stwalley Pumping vortex into a Bose–Einstein condensate of heteronuclear molecules Z F Xu, R Q Wang and L You Intense atomic and molecular beams via neon buffer-gas cooling David Patterson, Julia Rasmussen and John M Doyle Dynamical properties of dipolar Fermi gases T Sogo, L He, T Miyakawa, S Yi, H Lu and H Pu Collisions of bosonic ultracold polar molecules in microwave traps Alexander V Avdeenkov Cold TiO(X 3 Δ)–He collisions Mei-Ju Lu and Jonathan D Weinstein Investigation of dephasing rates in an interacting Rydberg gas U Raitzsch, R Heidemann, H Weimer, B Butscher, P Kollmann, R Löw, H P Büchler and T Pfau Impact of electric fields on highly excited rovibrational states of polar dimers Rosario González-Férez and Peter Schmelcher Phase transition from straight into twisted vortex lines in dipolar Bose–Einstein condensates M Klawunn and L Santos Stimulating the production of deeply bound RbCs molecules with laser pulses: the role of spin–orbit coupling in forming ultracold molecules Subhas Ghosal, Richard J Doyle, Christiane P Koch and Jeremy M Hutson Sensitive measurement of m p / m e variance using vibrational transition frequencies of cold molecules Masatoshi Kajita