Microscopic electronic structure tomography of Rydberg macrodimers
- URL: http://arxiv.org/abs/2010.02144v1
- Date: Mon, 5 Oct 2020 16:48:36 GMT
- Title: Microscopic electronic structure tomography of Rydberg macrodimers
- Authors: Simon Hollerith, Jun Rui, Antonio Rubio-Abadal, Kritsana Srakaew,
David Wei, Johannes Zeiher, Christian Gross and Immanuel Bloch
- Abstract summary: We employ quantum gas microscopy to position and resolve atoms in Rydberg macrodimer states.
We show first photoassociation studies for different molecular symmetries in which the molecular orientation relative to an applied magnetic field is fully controlled.
We additionally observe an orientation-dependent Zeeman shift and reveal a significant influence on it caused by the hyperfine interaction of the macrodimer state.
- Score: 0.0
- License: http://arxiv.org/licenses/nonexclusive-distrib/1.0/
- Abstract: Precise control and study of molecules is challenging due to the variety of
internal degrees of freedom and local coordinates that are typically not
controlled in an experiment. Employing quantum gas microscopy to position and
resolve the atoms in Rydberg macrodimer states solves almost all of these
challenges and enables unique access to the molecular frame. Here, we
demonstrate the power of this approach and present first photoassociation
studies for different molecular symmetries in which the molecular orientation
relative to an applied magnetic field, the polarization of the excitation light
and the initial atomic state are fully controlled. The observed characteristic
dependencies allow for an electronic structure tomography of the molecular
state. We additionally observe an orientation-dependent Zeeman shift and reveal
a significant influence on it caused by the hyperfine interaction of the
macrodimer state. Finally, we demonstrate controlled engineering of the
electrostatic binding potential by opening a gap in the energetic vicinity of
two crossing pair potentials.
Related papers
- Time resolved quantum tomography in molecular spectroscopy by the Maximal Entropy Approach [1.7563879056963012]
A fundamental question emerges: what role, if any, do quantum coherences between molecular electron states play in photochemical reactions?
The Maximal Entropy (MaxEnt) based Quantum State Tomography (QST) approach offers unique advantages in studying molecular dynamics.
We present two methodologies for constructing these operators: one leveraging Molecular Angular Distribution Moments (MADMs) which accurately capture the orientation-dependent vibronic dynamics of molecules.
We achieve a groundbreaking milestone by constructing, for the first time, the entanglement entropy of the electronic subsystem: a metric that was previously inaccessible.
arXiv Detail & Related papers (2024-07-23T16:43:01Z) - Floquet Engineering of a Diatomic Molecule Through a Bichromatic
Radiation Field [0.0]
We report on a theoretical study of a Cs$$ molecule illuminated by two lasers.
We reveal that these interactions facilitate the bypass of the non-crossing rule.
We discuss extensively how the interaction of radiation with matter gives rise to the emergence of potential energy surfaces.
arXiv Detail & Related papers (2023-11-22T21:14:52Z) - Quantum Coherent Control of a Single Molecular-Polariton Rotation [2.2482144023488346]
We present a combined analytical and numerical study for coherent terahertz control of a single molecular polariton.
The presence of a cavity strongly modifies the post-pulse orientation of the polariton, making it difficult to obtain its maximal degree of orientation.
This work offers a new strategy to study rotational dynamics in the strong-coupling regime and provides a method for complete quantum coherent control of a single molecular polariton.
arXiv Detail & Related papers (2022-12-22T12:37:55Z) - Rydberg Macrodimers: Diatomic molecules on the micrometer scale [0.0]
Rydberg macrodimers are bound states between highly excited Rydberg atoms.
They feature bond lengths in the micrometer regime, exceeding those of conventional molecules by orders of magnitude.
This review provides a historic overview and summarizes the recent findings in the field of Rydberg macrodimers.
arXiv Detail & Related papers (2022-12-03T19:09:09Z) - Sensing of magnetic field effects in radical-pair reactions using a
quantum sensor [50.591267188664666]
Magnetic field effects (MFE) in certain chemical reactions have been well established in the last five decades.
We employ elaborate and realistic models of radical-pairs, considering its coupling to the local spin environment and the sensor.
For two model systems, we derive signals of MFE detectable even in the weak coupling regime between radical-pair and NV quantum sensor.
arXiv Detail & Related papers (2022-09-28T12:56:15Z) - High-resolution 'magic'-field spectroscopy on trapped polyatomic
molecules [62.997667081978825]
Rapid progress in cooling and trapping of molecules has enabled first experiments on high resolution spectroscopy of trapped diatomic molecules.
Extending this work to polyatomic molecules provides unique opportunities due to more complex geometries and additional internal degrees of freedom.
arXiv Detail & Related papers (2021-10-21T15:46:17Z) - Relativistic aspects of orbital and magnetic anisotropies in the
chemical bonding and structure of lanthanide molecules [60.17174832243075]
We study the electronic and ro-vibrational states of heavy homonuclear lanthanide Er2 and Tm2 molecules by applying state-of-the-art relativistic methods.
We were able to obtain reliable spin-orbit and correlation-induced splittings between the 91 Er2 and 36 Tm2 electronic potentials dissociating to two ground-state atoms.
arXiv Detail & Related papers (2021-07-06T15:34:00Z) - Molecular Interactions Induced by a Static Electric Field in Quantum
Mechanics and Quantum Electrodynamics [68.98428372162448]
We study the interaction between two neutral atoms or molecules subject to a uniform static electric field.
Our focus is to understand the interplay between leading contributions to field-induced electrostatics/polarization and dispersion interactions.
arXiv Detail & Related papers (2021-03-30T14:45:30Z) - Controlled coherent dynamics of [VO(TPP)], a prototype molecular nuclear
qudit with an electronic ancilla [50.002949299918136]
We show that [VO(TPP)] (vanadyl tetraphenylporphyrinate) is a promising system suitable to implement quantum computation algorithms.
It embeds an electronic spin 1/2 coupled through hyperfine interaction to a nuclear spin 7/2, both characterized by remarkable coherence.
arXiv Detail & Related papers (2021-03-15T21:38:41Z) - Magnetic properties and quench dynamics of two interacting ultracold
molecules in a trap [0.0]
We investigate the magnetic properties and nonequilibrium dynamics of two interacting ultracold polar and paramagnetic molecules in a harmonic trap in external electric and magnetic fields.
The molecules interact via a multichannel two-body contact potential, incorporating the short-range anisotropy of intermolecular interactions.
arXiv Detail & Related papers (2020-10-22T17:35:46Z) - Quantum coherent spin-electric control in a molecular nanomagnet at
clock transitions [57.50861918173065]
Electrical control of spins at the nanoscale offers architectural advantages in spintronics.
Recent demonstrations of electric-field (E-field) sensitivities in molecular spin materials are tantalising.
E-field sensitivities reported so far are rather weak, prompting the question of how to design molecules with stronger spin-electric couplings.
arXiv Detail & Related papers (2020-05-03T09:27:31Z)
This list is automatically generated from the titles and abstracts of the papers in this site.
This site does not guarantee the quality of this site (including all information) and is not responsible for any consequences.