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:1011.5489 · Physical Review Letters

Conical Intersections in an Ultracold Gas

Sebastian Wüster, Alexander Eisfeld, Jan Michael Rost

Published Apr 12, 2011• 50 citations
arXivHTMLPDF

Abstract

We find that energy surfaces of more than two atoms or molecules interacting via transition dipole-dipole potentials generically possess conical intersections (CIs). Typically only few atoms participate strongly in such an intersection. For the fundamental case, a circular trimer, we show how the CI affects adiabatic excitation transport via electronic decoherence or geometric phase interference. These phenomena may be experimentally accessible if the trimer is realized by light alkali atoms in a ring trap, whose interactions are induced by off-resonant dressing with Rydberg states. Such a setup promises a direct probe of the full many-body density dynamics near a CI.

DOI
10.1103/physrevlett.106.153002

Related papers

Exploring the Many-Body Dynamics Near a Conical Intersection with Trapped Rydberg Ions

Filippo Maria Gambetta, Chi Zhang, Markus Hennrich +2 more

Conical intersections between electronic potential energy surfaces are paradigmatic for the study of nonadiabatic processes in the excited states of large molecules. However, since the corresponding dynamics occurs on a femtosecond timescale, their investigation remains challenging and requires ultrafast spectroscopy techniques. We demonstrate that trapped Rydberg ions are a platform to engineer conical intersections and to simulate their ensuing dynamics on larger length scales and timescales of the order of nanometers and microseconds, respectively; all this in a highly controllable system. Here, the shape of the potential energy surfaces and the position of the conical intersection can be tuned thanks to the interplay between the high polarizability and the strong dipolar exchange interactions of Rydberg ions. We study how the presence of a conical intersection affects both the nuclear and electronic dynamics demonstrating, in particular, how it results in the inhibition of the nuclear motion. These effects can be monitored in real time via a direct spectroscopic measurement of the electronic populations in a state-of-the-art experimental setup.

arXiv:2012.01834•Physical Review Letters•Jun 11, 2021•31 citations

Quantum Control of Atom-Ion Charge Exchange via Light-Induced Conical Intersections

Hui Li, Ming Li, Alexander Petrov +2 more

High Resolution Image Download MS PowerPoint Slide Conical intersections are crossing points or lines between two or more adiabatic electronic potential energy surfaces in the multidimensional coordinate space of colliding atoms and molecules. Conical intersections and corresponding nonadiabatic coupling can greatly affect molecular dynamics and chemical properties. In this paper, we predict significant or measurable nonadiabatic effects in an ultracold atom–ion charge-exchange reaction in the presence of laser-induced conical intersections (LICIs). We investigate the fundamental physics of these LICIs on molecular reactivity under unique conditions: those of relatively low laser intensity of 10 8 W/cm 2 and ultracold temperatures below 1 mK. We predict irregular interference effects in the charge-exchange rate coefficients between K and Ca + as functions of the laser frequency. These irregularities occur in our system due to the presence of two LICIs. To further elucidate the role of the LICIs on the reaction dynamics, we compare these rate coefficients with those computed for a system where the CIs have been “removed”. In the laser frequency window, where conical interactions are present, the difference in rate coefficients can be as large as 1 × 10 –9 cm 3 /s.

arXiv:2304.07571•The Journal of Physical Chemistry A•Jul 12, 2023•1 citation

Laser-induced conical intersections in molecular optical lattices

Nimrod Moiseyev, Milan Šindelka, Lorenz S. Cederbaum

Conical intersections of potential energy surfaces widely appear in molecules which consist of more than two atoms. No conical intersections exist in the case of free diatomic molecules. We show here that diatomic molecules interacting with standing laser waves produce periodic arrays of conical intersections. At these laser-induced intersections the non-adiabatic effects are infinitely strong. The translational and rovibrational molecular motions become strongly coupled to each other and energy exchange between the various degrees of freedom influences the dynamics of the system. As an illustrative example, an effect of the laser-induced conical intersections on trapping of ultracold diatomic molecules by light is discussed.

Journal of Physics B Atomic Molecular and Optical Physics•Nov 7, 2008•117 citations

Simulating conical intersections with trapped ions

Jacob Whitlow, Zhubing Jia, Ye Wang +3 more

Conical intersections are common in molecular physics and photochemistry, and are often invoked to explain observed reaction products. A conical intersection can occur when an excited electronic potential energy surface intersects with the ground electronic potential energy surface in the coordinate space of the nuclear positions. Theory predicts that the conical intersection will result in a geometric phase for a wavepacket on the ground potential energy surface. Although conical intersections have been observed experimentally, the geometric phase has not been observed in a molecular system. Here we use a trapped atomic ion system to perform a quantum simulation of a conical intersection. The internal state of a trapped atomic ion serves as the electronic state and the motion of the atomic nuclei are encoded into the normal modes of motion of the ions. The simulated electronic potential is constructed by applying state-dependent forces to the ion with a near-resonant laser. We experimentally observe the geometric phase on the ground-state surface using adiabatic state preparation followed by motional state measurement. Our experiment shows the advantage of combining spin and motion degrees of freedom in a quantum simulator.

arXiv:2211.07319•Nov 14, 2022•7 citations

Switching Exciton Pulses Through Conical Intersections

Karsten Leonhardt, Sebastian Wüster, Jan Michael Rost

Exciton pulses transport excitation and entanglement adiabatically through Rydberg aggregates, assemblies of highly excited light atoms, which are set into directed motion by resonant dipole-dipole interaction. Here, we demonstrate the coherent splitting of such pulses as well as the spatial segregation of electronic excitation and atomic motion. Both mechanisms exploit local nonadiabatic effects at a conical intersection, turning them from a decoherence source into an asset. The intersection provides a sensitive knob controlling the propagation direction and coherence properties of exciton pulses. The fundamental ideas discussed here have general implications for excitons on a dynamic network.

arXiv:1310.6975•Physical Review Letters•Nov 24, 2014•18 citations

Interplay of excitation transport and atomic motion in flexible Rydberg aggregates

Karsten Leonhardt

Strong resonant dipole-dipole interactions in flexible Rydberg aggregates enable the formation of exciton pulses, the interplay of atomic motion and electronic excitation transfer which feature high fidelity entanglement transport. Here, we demonstrate the coherent splitting of such pulses into two modes, which induce strongly different atomic motion, leading to clear signatures of nonadiabatic effects in atomic density profiles. The mechanism exploits local nonadiabatic effects at a conical intersection, turning them from a decoherence source into an asset. The conical intersection is a consequence of the exciton pulses moving along a linear Rydberg chain and approaching an additional linear, perpendicularly aligned Rydberg chain. The intersection provides a sensitive knob controlling the propagation direction and coherence properties of exciton pulses. We demonstrate that this scenario can be exploited as an exciton switch, controlling direction and coherence properties of the joint pulse on the second of the chains. Initially, we demonstrate the pulse splitting on planar aggregates with atomic motion one-dimensionally constrained and employing isotropic interactions. Subsequently, we confirm the splitting mechanism for a fully realistic scenario in which all spatial restrictions are removed and the full anisotropy of the dipole-dipole interactions is taken into account. Our results enable the experimental observation of non-adiabatic electronic dynamics and entanglement transport with Rydberg atoms. The conical intersection crossings are clearly evident, both in atomic mean position information and excited state spectra of the Rydberg system. This suggests flexible Rydberg aggregates as a test-bench for quantum chemical effects in experiments on much-inflated length scales. The fundamental ideas discussed here have general implications for excitons on a dynamic network.

arXiv:1612.07858•Dec 23, 2016•2 citations
We find that energy surfaces of more than two atoms or molecules interacting via transition dipole-dipole potentials generically possess conical intersections (CIs). Typically only few atoms participate strongly in such an intersection. For the fundamental case, a circular trimer, we show how the CI affects adiabatic excitation transport via electronic decoherence or geometric phase interference. These phenomena may be experimentally accessible if the trimer is realized by light alkali atoms in a ring trap, whose interactions are induced by off-resonant dressing with Rydberg states. Such a setup promises a direct probe of the full many-body density dynamics near a CI.
Conical intersections between electronic potential energy surfaces are paradigmatic for the study of nonadiabatic processes in the excited states of large molecules. However, since the corresponding dynamics occurs on a femtosecond timescale, their investigation remains challenging and requires ultrafast spectroscopy techniques. We demonstrate that trapped Rydberg ions are a platform to engineer conical intersections and to simulate their ensuing dynamics on larger length scales and timescales of the order of nanometers and microseconds, respectively; all this in a highly controllable system. Here, the shape of the potential energy surfaces and the position of the conical intersection can be tuned thanks to the interplay between the high polarizability and the strong dipolar exchange interactions of Rydberg ions. We study how the presence of a conical intersection affects both the nuclear and electronic dynamics demonstrating, in particular, how it results in the inhibition of the nuclear motion. These effects can be monitored in real time via a direct spectroscopic measurement of the electronic populations in a state-of-the-art experimental setup.
High Resolution Image Download MS PowerPoint Slide Conical intersections are crossing points or lines between two or more adiabatic electronic potential energy surfaces in the multidimensional coordinate space of colliding atoms and molecules. Conical intersections and corresponding nonadiabatic coupling can greatly affect molecular dynamics and chemical properties. In this paper, we predict significant or measurable nonadiabatic effects in an ultracold atom–ion charge-exchange reaction in the presence of laser-induced conical intersections (LICIs). We investigate the fundamental physics of these LICIs on molecular reactivity under unique conditions: those of relatively low laser intensity of 10 8 W/cm 2 and ultracold temperatures below 1 mK. We predict irregular interference effects in the charge-exchange rate coefficients between K and Ca + as functions of the laser frequency. These irregularities occur in our system due to the presence of two LICIs. To further elucidate the role of the LICIs on the reaction dynamics, we compare these rate coefficients with those computed for a system where the CIs have been “removed”. In the laser frequency window, where conical interactions are present, the difference in rate coefficients can be as large as 1 × 10 –9 cm 3 /s.
Conical intersections of potential energy surfaces widely appear in molecules which consist of more than two atoms. No conical intersections exist in the case of free diatomic molecules. We show here that diatomic molecules interacting with standing laser waves produce periodic arrays of conical intersections. At these laser-induced intersections the non-adiabatic effects are infinitely strong. The translational and rovibrational molecular motions become strongly coupled to each other and energy exchange between the various degrees of freedom influences the dynamics of the system. As an illustrative example, an effect of the laser-induced conical intersections on trapping of ultracold diatomic molecules by light is discussed.
Conical intersections are common in molecular physics and photochemistry, and are often invoked to explain observed reaction products. A conical intersection can occur when an excited electronic potential energy surface intersects with the ground electronic potential energy surface in the coordinate space of the nuclear positions. Theory predicts that the conical intersection will result in a geometric phase for a wavepacket on the ground potential energy surface. Although conical intersections have been observed experimentally, the geometric phase has not been observed in a molecular system. Here we use a trapped atomic ion system to perform a quantum simulation of a conical intersection. The internal state of a trapped atomic ion serves as the electronic state and the motion of the atomic nuclei are encoded into the normal modes of motion of the ions. The simulated electronic potential is constructed by applying state-dependent forces to the ion with a near-resonant laser. We experimentally observe the geometric phase on the ground-state surface using adiabatic state preparation followed by motional state measurement. Our experiment shows the advantage of combining spin and motion degrees of freedom in a quantum simulator.
Exciton pulses transport excitation and entanglement adiabatically through Rydberg aggregates, assemblies of highly excited light atoms, which are set into directed motion by resonant dipole-dipole interaction. Here, we demonstrate the coherent splitting of such pulses as well as the spatial segregation of electronic excitation and atomic motion. Both mechanisms exploit local nonadiabatic effects at a conical intersection, turning them from a decoherence source into an asset. The intersection provides a sensitive knob controlling the propagation direction and coherence properties of exciton pulses. The fundamental ideas discussed here have general implications for excitons on a dynamic network.
Strong resonant dipole-dipole interactions in flexible Rydberg aggregates enable the formation of exciton pulses, the interplay of atomic motion and electronic excitation transfer which feature high fidelity entanglement transport. Here, we demonstrate the coherent splitting of such pulses into two modes, which induce strongly different atomic motion, leading to clear signatures of nonadiabatic effects in atomic density profiles. The mechanism exploits local nonadiabatic effects at a conical intersection, turning them from a decoherence source into an asset. The conical intersection is a consequence of the exciton pulses moving along a linear Rydberg chain and approaching an additional linear, perpendicularly aligned Rydberg chain. The intersection provides a sensitive knob controlling the propagation direction and coherence properties of exciton pulses. We demonstrate that this scenario can be exploited as an exciton switch, controlling direction and coherence properties of the joint pulse on the second of the chains. Initially, we demonstrate the pulse splitting on planar aggregates with atomic motion one-dimensionally constrained and employing isotropic interactions. Subsequently, we confirm the splitting mechanism for a fully realistic scenario in which all spatial restrictions are removed and the full anisotropy of the dipole-dipole interactions is taken into account. Our results enable the experimental observation of non-adiabatic electronic dynamics and entanglement transport with Rydberg atoms. The conical intersection crossings are clearly evident, both in atomic mean position information and excited state spectra of the Rydberg system. This suggests flexible Rydberg aggregates as a test-bench for quantum chemical effects in experiments on much-inflated length scales. The fundamental ideas discussed here have general implications for excitons on a dynamic network.