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:2607.24239 · Nature Chemistry

Evolution of dipole–dipole dynamics in cold ammonia collisions

Yao Chang, André J. A. van Roij, Stach Kuijpers, Sven Herbers, Etienne F. Walraven, Tijs Karman, Sebastiaan Y. T. van de Meerakker

Published Oct 7, 2026• 0 citations
arXivHTMLPDF

Abstract

Cold polar molecules offer fascinating prospects for ultracold chemistry and quantum physics. However, their inherent collision properties remain largely unknown, as it seems fundamentally impossible to reach sufficiently low energies by merging two beams of molecules with substantial dipole moments. Here we report measurements of state-to-state cross-sections for collisions between ammonia isotopologues at energies between 0.3 and 100 cm−1 using an advanced beam-merging protocol. We experimentally observed a local maximum in the cross-sections, which indicates that the dipole moments can switch off at low collision energies. Scattering calculations reproduced this maximum in good agreement and explained the observed scaling with the molecule’s parity splitting energies. Measurements of the correlated energy transfer in both collision partners yielded direct evidence of the suppression of the dipole–dipole interaction at low energies. Our results demonstrate how collisions between an important class of polar molecules evolve from high temperatures towards the ultracold regime in a counterintuitive way, and offer distinctive opportunities to control cold molecular collisions with external fields. Interactions between polar molecules are expected to become increasingly strong at low collision energies through dipole–dipole forces. Now it has been shown that ammonia molecules instead exhibit suppressed dipolar interactions in the cold regime as the dipole moment effectively switches off, as shown by local maxima in the collision cross-sections.

DOI
10.1038/s41557-026-02270-y

Related papers

Quantum state–resolved molecular dipolar collisions over four decades of energy

Guoqiang Tang, Matthieu Besemer, Stach Kuijpers +4 more

Collisions between cold polar molecules represent a fascinating research frontier but have proven hard to probe experimentally. We report measurements of inelastic cross sections for collisions between nitric oxide (NO) and deuterated ammonia (ND 3 ) molecules at energies between 0.1 and 580 centimeter −1 , with full quantum state resolution. At energies below the ~100-centimeter −1 well depth of the interaction potential, we observed backward glories originating from peculiar U-turn trajectories. At energies below 0.2 centimeter −1 , we observed a breakdown of the Langevin capture model, which we interpreted in terms of a suppressed mutual polarization during the collision, effectively switching off the molecular dipole moments. Scattering calculations based on an ab initio NO-ND 3 potential energy surface revealed the crucial role of near-degenerate rotational levels with opposite parity in low-energy dipolar collisions.

arXiv:2302.06866•Science•Mar 10, 2023•36 citations

Cold heteromolecular dipolar collisions

Brian C. Sawyer, Benjamin Stuhl, Mark Yeo +7 more

Cold molecules promise to reveal a rich set of novel collision dynamics in the low-energy regime. By combining for the first time the techniques of Stark deceleration, magnetic trapping, and cryogenic buffer gas cooling, we present the first experimental observation of cold collisions between two different species of state-selected neutral polar molecules. This has enabled an absolute measurement of the total trap loss cross sections between OH and ND(3) at a mean collision energy of 3.6 cm(-1) (5 K). Due to the dipolar interaction, the total cross section increases upon application of an external polarizing electric field. Cross sections computed from ab initio potential energy surfaces are in agreement with the measured value at zero external electric field. The theory presented here represents the first such analysis of collisions between a (2)Π radical and a closed-shell polyatomic molecule.

arXiv:1008.5127•Physical Chemistry Chemical Physics•Jan 1, 2011•95 citations

Ultracold chemistry and dipolar collisions in a quantum gas of polar molecules

Silke Ospelkaus, Amodsen Chotia, Marcio H. G. de Miranda +5 more

Ultracold polar molecular quantum gases promise to open new research directions ranging from the study of ultra-cold chemistry, precision measurements to novel quantum phase transitions. Based on the preparation of high-phase space density gases of polar KRb molecules [1–3], I will discuss the control of dipolar collisions and chemical reactions of polar molecules in a regime where quantum statistics, single scattering partial waves, and quantum threshold laws play a dominant role [4]. In particular, I will point out the crucial role of electric dipole-dipole interactions [5] and external confinement [6] in determining the chemical reaction rate. Finally, I will discuss prospects of reaching quantum degeneracy in bialkali samples of polar molecules and prospects for these systems as novel dipolar quantum many-body systems.

Conference on Lasers and Electro-Optics Europe & European Quantum Electronics Conference (CLEO/Europe-EQEC)•May 1, 2011•0 citations

Cold Polar Molecules for Novel Collision Experiments at Low Energies

Brian C. Sawyer

Research in the field of cold polar molecules is progressing rapidly. An array of interesting\ntopics is being developed including precision measurement and fundamental tests, quantum phase transitions, and ultracold chemistry. In particular, dipolar molecules in well-defined quantum states enable exquisite control of their interactions via applied electric fields. The long-range, anisotropic interaction between dipolar molecules leads to new collision dynamics that could be used for novel collective effects, quantum state engineering, and information processing. The focus of this Thesis is the production of cold samples of neutral OH molecules via Stark deceleration and magnetic trapping for novel collision experiments. This novelty results from our combination of cold external beams and trapped target molecules which facilitates observation of dipolar effects as well as low temperature collision resonances. The large permanent electric dipole moment of OH allows us to precisely tune the lab-frame velocity of the molecular packets from ∼ 500 m/s to rest. We have magnetically trapped OH packets at the terminus of our Stark decelerator at a temperature of 70 mK and density of 106 cm−3. With improved understanding of Stark deceleration, we optimize the decelerator efficiency and its coupling to the magnetic trap. Our latest trap design uses permanent ring magnets to create a three-dimensional magnetic quadrupole field. Use of magnetically trapped OH molecules for collision experiments with external beams allow us the unique opportunity of observing both elastic and inelastic collisions. In addition, the trap confinement yields sensitivity to differential elastic cross sections at low collision energies. This open magnetic trap has allowed measurement of collision cross sections between trapped OH and external supersonic beams of He and D2, the latter of which is of astrophysical interest due to the role of H2-OH collisions in pumping interstellar OH megamasers. The combination of trapped OH molecules and temperature tuned beams of He and D2 has facilitated measurement of the lowest-energy D2-OH collision cross sections yet reported. More recently, we report the first observation of electric-field dependent cross sections between two different species of cold polar molecules - OH and ND3 - thereby demonstrating control over molecular scattering in the cold regime. By combining for the first time the production techniques of Stark deceleration and buffer gas cooling, we increase the molecular interaction time by∼ 105 over traditional crossed-beam experiments to gain enhanced sensitivity at the characteristic densities of cold molecule production.

•Jan 1, 2010•2 citations

A cryofuge for cold-collision experiments with slow polar molecules

Wu, X., Gantner, T., Koller, M. +3 more

Ultracold molecules represent a fascinating research frontier in physics and chemistry, but it has proven challenging to prepare dense samples at low velocities. Here we present a solution to this goal by a non-conventional approach dubbed cryofuge. It employs centrifugal force to bring cryogenically cooled molecules to kinetic energies below $1\,$K$\times k_B$ in the laboratory frame, with corresponding fluxes exceeding $10^{10}$/s at velocities below $20\,$m/s. By attaining densities higher than $10^9$/cm$^3$ and interaction times longer than $25\,$ms in samples of fluoromethane as well as deuterated ammonia, we observe cold dipolar collisions between molecules and determine their collision cross sections.

•Nov 3, 2017•36 citations

Collisional Control of Ground State Polar Molecules and Universal Dipolar Scattering

Christopher Ticknor

We explore the impact of the short-range interaction on the scattering of ground state polar molecules and study the transition from a weak to strong dipolar scattering over an experimentally reasonable range of energies and electric field values. In the strong dipolar limit, the scattering scales with respect to a dimensionless quantity defined by mass, induced dipole moment, and collision energy. The scaling has implications for all quantum mechanical dipolar scattering. Furthermore the universal scattering regime will readily be achieved with polar molecules at ultracold temperatures.

arXiv:0711.4846•Physical Review Letters•Apr 4, 2008•46 citations
Cold polar molecules offer fascinating prospects for ultracold chemistry and quantum physics. However, their inherent collision properties remain largely unknown, as it seems fundamentally impossible to reach sufficiently low energies by merging two beams of molecules with substantial dipole moments. Here we report measurements of state-to-state cross-sections for collisions between ammonia isotopologues at energies between 0.3 and 100 cm−1 using an advanced beam-merging protocol. We experimentally observed a local maximum in the cross-sections, which indicates that the dipole moments can switch off at low collision energies. Scattering calculations reproduced this maximum in good agreement and explained the observed scaling with the molecule’s parity splitting energies. Measurements of the correlated energy transfer in both collision partners yielded direct evidence of the suppression of the dipole–dipole interaction at low energies. Our results demonstrate how collisions between an important class of polar molecules evolve from high temperatures towards the ultracold regime in a counterintuitive way, and offer distinctive opportunities to control cold molecular collisions with external fields. Interactions between polar molecules are expected to become increasingly strong at low collision energies through dipole–dipole forces. Now it has been shown that ammonia molecules instead exhibit suppressed dipolar interactions in the cold regime as the dipole moment effectively switches off, as shown by local maxima in the collision cross-sections.
Collisions between cold polar molecules represent a fascinating research frontier but have proven hard to probe experimentally. We report measurements of inelastic cross sections for collisions between nitric oxide (NO) and deuterated ammonia (ND 3 ) molecules at energies between 0.1 and 580 centimeter −1 , with full quantum state resolution. At energies below the ~100-centimeter −1 well depth of the interaction potential, we observed backward glories originating from peculiar U-turn trajectories. At energies below 0.2 centimeter −1 , we observed a breakdown of the Langevin capture model, which we interpreted in terms of a suppressed mutual polarization during the collision, effectively switching off the molecular dipole moments. Scattering calculations based on an ab initio NO-ND 3 potential energy surface revealed the crucial role of near-degenerate rotational levels with opposite parity in low-energy dipolar collisions.
Cold molecules promise to reveal a rich set of novel collision dynamics in the low-energy regime. By combining for the first time the techniques of Stark deceleration, magnetic trapping, and cryogenic buffer gas cooling, we present the first experimental observation of cold collisions between two different species of state-selected neutral polar molecules. This has enabled an absolute measurement of the total trap loss cross sections between OH and ND(3) at a mean collision energy of 3.6 cm(-1) (5 K). Due to the dipolar interaction, the total cross section increases upon application of an external polarizing electric field. Cross sections computed from ab initio potential energy surfaces are in agreement with the measured value at zero external electric field. The theory presented here represents the first such analysis of collisions between a (2)Π radical and a closed-shell polyatomic molecule.
Ultracold polar molecular quantum gases promise to open new research directions ranging from the study of ultra-cold chemistry, precision measurements to novel quantum phase transitions. Based on the preparation of high-phase space density gases of polar KRb molecules [1–3], I will discuss the control of dipolar collisions and chemical reactions of polar molecules in a regime where quantum statistics, single scattering partial waves, and quantum threshold laws play a dominant role [4]. In particular, I will point out the crucial role of electric dipole-dipole interactions [5] and external confinement [6] in determining the chemical reaction rate. Finally, I will discuss prospects of reaching quantum degeneracy in bialkali samples of polar molecules and prospects for these systems as novel dipolar quantum many-body systems.
Research in the field of cold polar molecules is progressing rapidly. An array of interesting\ntopics is being developed including precision measurement and fundamental tests, quantum phase transitions, and ultracold chemistry. In particular, dipolar molecules in well-defined quantum states enable exquisite control of their interactions via applied electric fields. The long-range, anisotropic interaction between dipolar molecules leads to new collision dynamics that could be used for novel collective effects, quantum state engineering, and information processing. The focus of this Thesis is the production of cold samples of neutral OH molecules via Stark deceleration and magnetic trapping for novel collision experiments. This novelty results from our combination of cold external beams and trapped target molecules which facilitates observation of dipolar effects as well as low temperature collision resonances. The large permanent electric dipole moment of OH allows us to precisely tune the lab-frame velocity of the molecular packets from ∼ 500 m/s to rest. We have magnetically trapped OH packets at the terminus of our Stark decelerator at a temperature of 70 mK and density of 106 cm−3. With improved understanding of Stark deceleration, we optimize the decelerator efficiency and its coupling to the magnetic trap. Our latest trap design uses permanent ring magnets to create a three-dimensional magnetic quadrupole field. Use of magnetically trapped OH molecules for collision experiments with external beams allow us the unique opportunity of observing both elastic and inelastic collisions. In addition, the trap confinement yields sensitivity to differential elastic cross sections at low collision energies. This open magnetic trap has allowed measurement of collision cross sections between trapped OH and external supersonic beams of He and D2, the latter of which is of astrophysical interest due to the role of H2-OH collisions in pumping interstellar OH megamasers. The combination of trapped OH molecules and temperature tuned beams of He and D2 has facilitated measurement of the lowest-energy D2-OH collision cross sections yet reported. More recently, we report the first observation of electric-field dependent cross sections between two different species of cold polar molecules - OH and ND3 - thereby demonstrating control over molecular scattering in the cold regime. By combining for the first time the production techniques of Stark deceleration and buffer gas cooling, we increase the molecular interaction time by∼ 105 over traditional crossed-beam experiments to gain enhanced sensitivity at the characteristic densities of cold molecule production.
Ultracold molecules represent a fascinating research frontier in physics and chemistry, but it has proven challenging to prepare dense samples at low velocities. Here we present a solution to this goal by a non-conventional approach dubbed cryofuge. It employs centrifugal force to bring cryogenically cooled molecules to kinetic energies below 1 1\,1K×kB\times k_B×kB​ in the laboratory frame, with corresponding fluxes exceeding 101010^{10}1010/s at velocities below 20 20\,20m/s. By attaining densities higher than 10910^9109/cm3^33 and interaction times longer than 25 25\,25ms in samples of fluoromethane as well as deuterated ammonia, we observe cold dipolar collisions between molecules and determine their collision cross sections.
We explore the impact of the short-range interaction on the scattering of ground state polar molecules and study the transition from a weak to strong dipolar scattering over an experimentally reasonable range of energies and electric field values. In the strong dipolar limit, the scattering scales with respect to a dimensionless quantity defined by mass, induced dipole moment, and collision energy. The scaling has implications for all quantum mechanical dipolar scattering. Furthermore the universal scattering regime will readily be achieved with polar molecules at ultracold temperatures.