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arXiv:2408.12268 · Optics Express

Observation of electric field induced superradiance slowdown in ultracold Rydberg atomic gases

Yunhui He, Jingxu Bai, Yuechun Jiao, Weibin Li, Jianming Zhao

Published Nov 5, 2024• 0 citations
arXivHTMLPDF

Abstract

Atoms excited to electronically high-lying Rydberg states decay to low-energy states through spontaneous emission processes. We investigate the impact of a static electric field on the superradiant emission process between Rydberg |60 D 5/2 〉 and |61 P 3/2 〉 states in an ultracold Cesium Rydberg atom ensemble. We report experimental observations of a significant slowdown in superradiance upon applying an electric field. To understand the slowing down of superradiance, we employ a master equation in which Stark effects and collective decay are taken into account. We solve the master equation with the discrete truncated Wigner approximation (DTWA) method. Our numerical simulations demonstrate that superradiance decoherence is caused by the Stark shifts of the Rydberg level. Our theoretical simulations qualitatively match the experimental observations. Our work provides new insights into controlling quantum critical behaviors, with implications for quantum many-body dynamics, and the study of quantum phase transitions.

DOI
10.1364/oe.539719

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Atoms excited to electronically high-lying Rydberg states decay to low-energy states through spontaneous emission processes. We investigate the impact of a static electric field on the superradiant emission process between Rydberg |60 D 5/2 〉 and |61 P 3/2 〉 states in an ultracold Cesium Rydberg atom ensemble. We report experimental observations of a significant slowdown in superradiance upon applying an electric field. To understand the slowing down of superradiance, we employ a master equation in which Stark effects and collective decay are taken into account. We solve the master equation with the discrete truncated Wigner approximation (DTWA) method. Our numerical simulations demonstrate that superradiance decoherence is caused by the Stark shifts of the Rydberg level. Our theoretical simulations qualitatively match the experimental observations. Our work provides new insights into controlling quantum critical behaviors, with implications for quantum many-body dynamics, and the study of quantum phase transitions.
Abstract An ensemble of excited atoms can synchronize emission of light collectively in a process known as superradiance when its characteristic size is smaller than the wavelength of emitted photons. The underlying superradiance depends strongly on electromagnetic (photon) fields surrounding the atomic ensemble. High mode densities of microwave photons from 300 K blackbody radiation (BBR) significantly enhance decay rates of Rydberg states to neighbouring states, enabling superradiance that is not possible with bare vacuum induced spontaneous decay. Here we report observations of the superradiance of ultracold Rydberg atoms embedded in a bath of room-temperature photons. The temporal evolution of the Rydberg | nD ⟩ to |( n + 1) P ⟩ superradiant decay of Cs atoms ( n the principal quantum number) is measured directly in free space. Theoretical simulations confirm the BBR enhanced superradiance in large Rydberg ensembles. We demonstrate that the van der Waals interactions between Rydberg atoms change the superradiant dynamics and modify the scaling of the superradiance. In the presence of static electric fields, we find that the superradiance becomes slow, potentially due to many-body interaction induced dephasing. Our study provides insights into many-body dynamics of interacting atoms coupled to thermal BBR, and might open a route to the design of blackbody thermometry at microwave frequencies via collective, dissipative photon-atom interactions.
When atoms are excited to high-lying Rydberg states they interact strongly with dipolar forces. The resulting state-dependent level shifts allow us to study many-body systems displaying intriguing nonequilibrium phenomena, such as constrained spin systems, and are at the heart of numerous technological applications, e.g., in quantum simulation and computation platforms. Here, we show that these interactions also have a significant impact on dissipative effects caused by the inevitable coupling of Rydberg atoms to the surrounding electromagnetic field. We demonstrate that their presence modifies the frequency of the photons emitted from the Rydberg atoms, making it dependent on the local neighborhood of the emitting atom. Interactions among Rydberg atoms thus turn spontaneous emission into a many-body process which manifests, in a thermodynamically consistent Markovian setting, in the emergence of collective jump operators in the quantum master equation governing the dynamics. We discuss how this collective dissipation-stemming from a mechanism different from the much studied superradiance and subradiance-accelerates decoherence and affects dissipative phase transitions in Rydberg ensembles.
The lll-mixing effect and state-transfer induced by an external electric field pulse in ultracold Rydberg gases are observed with cesium atoms excited to nS\mathit{nS}nS states, and measured with a state selective field ionization technique. High-lll states are populated from the initially excited nS\mathit{nS}nS states due to non-adiabatic transitions through avoided crossings that are formed between the nS\mathit{nS}nS state and the ($n\ensuremath{-}4$) manifold. The population of the product state is investigated as a function of the electric field pulse parameters. The coherent property of the transfer is demonstrated using a 2-pulse sequence and the results are consistent with the theoretical calculations. This lll-mixing phenomenon in the electric field may be used to help forming a molecular potential and create Rydberg molecules.
We have studied the decay of Rydberg excitations in a cold Rb gas. A 10 ns, pulsed-dye-amplified diode laser excites Rb atoms at $70\phantom{\rule{0.28em}{0ex}}\ensuremath{\mu}\mathrm{K}$ in a magneto-optical trap to nsnsns or npnpnp Rydberg states with principal quantum numbers $26\ensuremath{\le}n\ensuremath{\le}40$. Time-delayed state-selective field ionization is used to directly monitor the population in the initial and neighboring Rydberg levels. The measured time dependence of the Rydberg population is well described by numerical simulations which consider only spontaneous emission and population transfer by blackbody radiation. No evidence for collective decay is found at atom densities up to $3\ifmmode\times\else\texttimes\fi{}{10}^{9}\phantom{\rule{0.16em}{0ex}}{\mathrm{cm}}^{\ensuremath{-}3}$. This result is in contrast to a previous study [Wang et al., Phys. Rev. A 75, 033802 (2007)], in which superradiant decay was theoretically predicted and experimentally inferred for atom density and laser focal volume conditions very similar to those considered here. Suppression of collective emission is likely due to variations in transition energies within the atom sample, dominated by inhomogeneities in dipole-dipole exchange interactions for initial sss states, or by a combination of dipole-dipole and electric field inhomogeneities for the initial ppp states.
A novel theoretical study of the control of translational motion of atomic and molecular Rydberg states in inhomogeneous static electric fields is presented. Simulations have been carried out demonstrating that, under realistic conditions, the deflection and focusing of Rydberg atoms and molecules should be achievable. Advantage is taken of the high susceptibility of the Rydberg states to external electric fields, allowing the use of much smaller fields than would be necessary for ground state neutrals. The simulations presented are for trajectories of Rydberg states with n = 18-20 in the fields of an electric dipole, quadrupole and hexapole. A deflection of 7 mm is predicted for n = 18 Rydberg states travelling parallel to the dipole after 100 µs time of flight. In the hexapole n = 20 Rydberg states are refocused to a spot size of the order of the laser beam waist (10 µm) after 20 µs. It is demonstrated that the hexapole can also act as a cylindrical lens if its axis is perpendicular to the Rydberg beam direction. Spontaneous emission and black-body decay rates are also calculated, and their variation with the applied field is investigated. The potential applications of this work might include the use of focusing and deflection for controlled low-energy collisions of Rydberg molecules with surfaces.
High resolution laser Stark excitation of np (60<n<85) Rydberg states of ultracold cesium atoms shows an efficient blockade of the excitation attributed to long-range dipole-dipole interaction. The dipole blockade effect is observed as a quenching of the Rydberg excitation depending on the value of the dipole moment induced by the external electric field. Effects of ions which could match the dipole blockade effect are discussed in detail but are ruled out for our experimental conditions. Analytic and Monte Carlo simulations of the excitation of an ensemble of interacting Rydberg atoms agree with the experiments and indicate a major role of the nearest neighboring Rydberg atom.