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arXiv:1604.03005 · Physical Review A

Direct single-shot observation of millimeter-wave superradiance in Rydberg-Rydberg transitions

David Grimes, Stephen L. Coy, Timothy Barnum, Yan Zhou, Susanne F. Yelin, Robert W. Field

Published Apr 12, 2017• 29 citations
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Abstract

We have directly detected millimeter-wave (mm-wave) free-space superradiant emission from Rydberg states (principal quantum number $n\ensuremath{\sim}30$) of barium atoms in single-shot experiments. We trigger the cooperative effects with a weak initial pulse and detect the time-dependent amplitude and phase of the emitted radiation with single-shot sensitivity and 20 ps time resolution. This allows measurement and shot-by-shot analysis of the statistical distribution of decay rates, time delays, and time-dependent frequency shifts. Cooperative line shifts and decay rates are observed that exceed the 250 kHz Doppler width by a factor of 20 and the 50 Hz spontaneous emission rate by a factor of ${10}^{5}$.

DOI
10.1103/physreva.95.043818

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We have directly detected millimeter-wave (mm-wave) free-space superradiant emission from Rydberg states (principal quantum number n\ensuremath∼30n\ensuremath{\sim}30n\ensuremath∼30) of barium atoms in single-shot experiments. We trigger the cooperative effects with a weak initial pulse and detect the time-dependent amplitude and phase of the emitted radiation with single-shot sensitivity and 20 ps time resolution. This allows measurement and shot-by-shot analysis of the statistical distribution of decay rates, time delays, and time-dependent frequency shifts. Cooperative line shifts and decay rates are observed that exceed the 250 kHz Doppler width by a factor of 20 and the 50 Hz spontaneous emission rate by a factor of 105{10}^{5}105.
The 106^{6}6 increase in spectral velocity allowed by the combination of chirped pulse millimeter-wave spectroscopy with a buffer gas cooled molecular beam source qualitatively expands the classes of possible experiments. As an example, it allows for investigation of cooperative radiation effects (such as superradiance and subradiance) in large samples of atoms in Rydberg states in a single shot. However, these same effects can present obstacles to the application of the full increase in spectral velocity to high-resolution spectroscopic experiments through both frequency (chirps, broadenings, and shifts) and intensity effects.
Transitions between Rydberg states of Ca atoms, in a pulsed, supersonic atomic beam, are directly detected by chirped-pulse millimeter-wave spectroscopy. Broadband, high-resolution spectra with accurate relative intensities are recorded instantly. Free induction decay (FID) of atoms, polarized by the chirped pulse, at their Rydberg-Rydberg transition frequencies, is heterodyne detected, averaged in the time domain, and Fourier transformed into the frequency domain. Millimeter-wave transient nutations are observed, and the possibility of FID evolving to superradiance is discussed.
We apply the chirped-pulse millimeter-wave (CPmmW) technique to transitions between Rydberg states in calcium atoms. The unique feature of Rydberg-Rydberg transitions is that they have enormous electric dipole transition moments (~5 kiloDebye at n* ~ 40, where n* is the effective principal quantum number), so they interact strongly with the mm-wave radiation. After polarization by a mm-wave pulse in the 70-84 GHz frequency region, the excited transitions re-radiate free induction decay (FID) at their resonant frequencies, and the FID is heterodyne-detected by the CPmmW spectrometer. Data collection and averaging are performed in the time domain. The spectral resolution is ~100 kHz. Because of the large transition dipole moments, the available mm-wave power is sufficient to polarize the entire bandwidth of the spectrometer (12 GHz) in each pulse, and high-resolution survey spectra may be collected. Both absorptive and emissive transitions are observed, and they are distinguished by the phase of their FID relative to that of the excitation pulse. With the combination of the large transition dipole moments and direct monitoring of transitions, we observe dynamics, such as transient nutations from the interference of the excitation pulse with the polarization that it induces in the sample. Since the waveform produced by the mm-wave source may be precisely controlled, we can populate states with high angular momentum by a sequence of pulses while recording the results of these manipulations in the time domain. We also probe the superradiant decay of the Rydberg sample using photon echoes. The application of the CPmmW technique to transitions between Rydberg states of molecules is discussed.
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.