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$In$ $situ$ observation of non-polar to strongly polar atom-ion collision dynamics
Authors:
Moritz Berngruber,
Daniel J. Bosworth,
Oscar A. Herrera-Sancho,
Viraatt S. V. Anasuri,
Nico Zuber,
Frederic Hummel,
Jennifer Krauter,
Florian Meinert,
Robert Löw,
Peter Schmelcher,
Tilman Pfau
Abstract:
The onset of collision dynamics between an ion and a Rydberg atom is studied in a regime characterized by a multitude of collision channels. These channels arise from coupling between a non-polar Rydberg state and numerous highly polar Stark states. The interaction potentials formed by the polar Stark states show a substantial difference in spatial gradient compared to the non-polar state leading…
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The onset of collision dynamics between an ion and a Rydberg atom is studied in a regime characterized by a multitude of collision channels. These channels arise from coupling between a non-polar Rydberg state and numerous highly polar Stark states. The interaction potentials formed by the polar Stark states show a substantial difference in spatial gradient compared to the non-polar state leading to a separation of collisional timescales, which is observed in situ. For collision energies in the range of $k_\textrm{B}\cdotμ$K to $k_\textrm{B}\cdot$K, the dynamics exhibit a counter-intuitive dependence on temperature, resulting in faster collision dynamics for cold - initially "slow" - systems. Dipole selection rules enable us to prepare the collision pair on the non-polar potential in a highly controlled manner, which determines occupation of the collision channels. The experimental observations are supported by semi-classical simulations, which model the pair state evolution and provide evidence for tunable non-adiabatic dynamics.
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Submitted 22 January, 2024;
originally announced January 2024.
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Observation of vibrational dynamics of orientated Rydberg-atom-ion molecules
Authors:
Yi-Quan Zou,
Moritz Berngruber,
Viraatt S. V. Anasuri,
Nicolas Zuber,
Florian Meinert,
Robert Löw,
Tilman Pfau
Abstract:
Vibrational dynamics in conventional molecules usually takes place on a timescale of picoseconds or shorter. A striking exception are ultralong-range Rydberg molecules, for which dynamics is dramatically slowed down as a consequence of the huge bond length of up to several micrometers. Here, we report on the direct observation of vibrational dynamics of a recently observed Rydberg-atom-ion molecul…
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Vibrational dynamics in conventional molecules usually takes place on a timescale of picoseconds or shorter. A striking exception are ultralong-range Rydberg molecules, for which dynamics is dramatically slowed down as a consequence of the huge bond length of up to several micrometers. Here, we report on the direct observation of vibrational dynamics of a recently observed Rydberg-atom-ion molecule. By applying a weak external electric field of a few mV/cm, we are able to control the orientation of the photoassociated ultralong-range Rydberg molecules and induce vibrational dynamics by quenching the electric field. A high resolution ion microscope allows us to detect the molecule's orientation and its temporal vibrational dynamics in real space. Our study opens the door to the control of molecular dynamics in Rydberg molecules.
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Submitted 16 January, 2023; v1 submitted 16 August, 2022;
originally announced August 2022.
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Spatial imaging of a novel type of molecular ions
Authors:
N. Zuber,
V. S. V. Anasuri,
M. Berngruber,
Y. -Q. Zou,
F. Meinert,
R. Löw,
T. Pfau
Abstract:
Atoms with a highly excited electron, called Rydberg atoms, can form unusual types of molecular bonds. The bond differs from the well known ionic and covalent bonds not only by its binding mechanism, but also by its bond length ranging up to several micrometres. Here, we observe a new type of molecular ion based on the interaction between the ionic charge and a flipping induced dipole of a Rydberg…
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Atoms with a highly excited electron, called Rydberg atoms, can form unusual types of molecular bonds. The bond differs from the well known ionic and covalent bonds not only by its binding mechanism, but also by its bond length ranging up to several micrometres. Here, we observe a new type of molecular ion based on the interaction between the ionic charge and a flipping induced dipole of a Rydberg atom with a bond length of several micrometres. We measure the vibrational spectrum and spatially resolve the bond length and the angular alignment of the molecule using a high-resolution ion microscope. As a consequence of the large bond length, the molecular dynamics is extremely slow. These results pave the way for future studies of spatio-temporal effects in molecular dynamics, e.g., beyond Born-Oppenheimer physics.
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Submitted 4 November, 2021;
originally announced November 2021.
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A pulsed ion microscope to probe quantum gases
Authors:
C. Veit,
N. Zuber,
O. A. Herrera-Sancho,
V. S. V. Anasuri,
T. Schmid,
F. Meinert,
R. Löw,
T. Pfau
Abstract:
The advent of the quantum gas microscope allowed for the in situ probing of ultracold gaseous matter on an unprecedented level of spatial resolution. The study of phenomena on ever smaller length scales as well as the probing of three-dimensional systems is, however, fundamentally limited by the wavelength of the imaging light, for all techniques based on linear optics. Here we report on a high-re…
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The advent of the quantum gas microscope allowed for the in situ probing of ultracold gaseous matter on an unprecedented level of spatial resolution. The study of phenomena on ever smaller length scales as well as the probing of three-dimensional systems is, however, fundamentally limited by the wavelength of the imaging light, for all techniques based on linear optics. Here we report on a high-resolution ion microscope as a versatile and powerful experimental tool to investigate quantum gases. The instrument clearly resolves atoms in an optical lattice with a spacing of $532\,\text{nm}$ over a field of view of 50 sites and offers an extremely large depth of field on the order of at least $70\,μ\text{m}$. With a simple model, we extract an upper limit for the achievable resolution of approximately $200\,\text{nm}$ from our data. We demonstrate a pulsed operation mode which in the future will enable 3D imaging and allow for the study of ionic impurities and Rydberg physics.
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Submitted 19 August, 2020;
originally announced August 2020.
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Observation of Rydberg Blockade Induced by a Single Ion
Authors:
Felix Engel,
Thomas Dieterle,
Thomas Schmid,
Christian Tomschitz,
Christian Veit,
Nicolas Zuber,
Robert Löw,
Tilman Pfau,
Florian Meinert
Abstract:
We study the long-range interaction of a single ion with a highly excited ultracold Rydberg atom and report on the direct observation of ion-induced Rydberg excitation blockade mediated over tens of micrometer distances. Our hybrid ion-atom system is directly produced from an ultracold atomic ensemble via near-threshold photo-ionization of a single Rydberg excitation, employing a two-photon scheme…
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We study the long-range interaction of a single ion with a highly excited ultracold Rydberg atom and report on the direct observation of ion-induced Rydberg excitation blockade mediated over tens of micrometer distances. Our hybrid ion-atom system is directly produced from an ultracold atomic ensemble via near-threshold photo-ionization of a single Rydberg excitation, employing a two-photon scheme which is specifically suited for generating a very low-energy ion. The ion's motion is precisely controlled by small electric fields, which allows us to analyze the blockade mechanism for a range of principal quantum numbers. Finally, we explore the capability of the ion as a high-sensitivity single-atom-based electric field sensor. The observed ion - Rydberg-atom interaction is of current interest for entanglement generation or studies of ultracold chemistry in hybrid ion-atom systems.
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Submitted 4 September, 2018;
originally announced September 2018.
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Rydberg molecules for ion-atom scattering in the ultracold regime
Authors:
T. Schmid,
C. Veit,
N. Zuber,
R. Löw,
T. Pfau,
M. Tarana,
M. Tomza
Abstract:
We propose a novel experimental method to extend the investigation of ion-atom collisions from the so far studied cold, essentially classical regime to the ultracold, quantum regime. Key aspect of this method is the use of Rydberg molecules to initialize the ultracold ion-atom scattering event. We exemplify the proposed method with the lithium ion-atom system, for which we present simulations of h…
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We propose a novel experimental method to extend the investigation of ion-atom collisions from the so far studied cold, essentially classical regime to the ultracold, quantum regime. Key aspect of this method is the use of Rydberg molecules to initialize the ultracold ion-atom scattering event. We exemplify the proposed method with the lithium ion-atom system, for which we present simulations of how the initial Rydberg molecule wavefunction, freed by photoionization, evolves in the presence of the ion-atom scattering potential. We predict bounds for the ion-atom scattering length from ab initio calculations of the interaction potential. We demonstrate that, in the predicted bounds, the scattering length can be experimentally determined from the velocity of the scattered wavepacket in the case of $^\textsf{6}\textsf{Li}^\textsf{+}$ - $^\textsf{6}\textsf{Li}$, and from the molecular ion fraction in the case of $^\textsf{7}\textsf{Li}^\textsf{+}$ - $^\textsf{7}\textsf{Li}$. The proposed method to utilize Rydberg molecules for ultracold ion-atom scattering, here particularized for the lithium ion-atom system, is readily applicable to other ion-atom systems as well.
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Submitted 16 April, 2018; v1 submitted 29 September, 2017;
originally announced September 2017.