Ultra strong coupling is studied in a modulation-doped parabolic potential well coupled to an inductance-capacitance resonant circuit. In this system, in accordance to Kohn's theorem, strong reduction of the energy level separation caused by the electron-electron interaction compensates the depolarization shift. As a result, a very large ratio of 27% of the Rabi frequency to the center resonance frequency as well as a polariton gap of width 2π × 670GHz are observed, suggesting parabolic quantum wells as the system of choice in order to explore the ultra-strong coupling regime.

The kinetic analysis of irreversible protein reactions requires an analytical technique that provides access to time-dependent infrared spectra in a single shot. Here, we present a spectrometer based on dual-frequency-comb spectroscopy using mid-infrared frequency combs generated by quantum cascade lasers. Attenuation of the intensity of the combs by molecular vibrational resonances results in absorption spectra covering 55 cm in the fingerprint region. The setup has a native resolution of 0.3 cm, noise levels in the μOD range, and achieves sub-microsecond time resolution. We demonstrate the simultaneous recording of both spectra and transients of the photoactivated proton pump bacteriorhodopsin. More importantly, a single shot, i.e., a single visible light excitation, is sufficient to extract spectral and kinetic characteristics of several intermediates in the bacteriorhodopsin photocycle. This development paves the way for the noninvasive analysis of enzymatic conversions with high time resolution, broad spectral coverage, and minimal sample consumption.

The strong-coupling regime between an electronic transition and the photonic mode of a optical resonator manifests itself in the lifting of the degeneracy between the two modes and the creation of two polariton states with mixed optical and electronic character. This phenomenon has been studied in atoms, excitons in semiconductors and quantum electrodynamics circuits based on Josephson junctions. Recently, there is also strong interest to study similar effects using intersubband transitions in quantum wells in the terahertz, where the ultra strong coupling regime can be reached and new physical effects have been predicted. An other interesting feature of this system is that, in contrast to systems based on superconductors, the ultra strong coupling regime can be maintained up to room temperature. In this work, we demonstrate that parabolic quantum wells coupled to LC circuit resonators in the ultra strong coupling regime can achieve terahertz emission up to room temperature

In the current study, a quantum-cascade-laser-based dual-comb spectrometer (DCS) was used to paint a detailed picture of a 1.0 ms high-temperature reaction between propyne and oxygen. The DCS interfaced with a shock tube to provide pre-ignition conditions of 1225 K, 2.8 atm, and 2% p-C3H4/18% O2/Ar. The spectrometer consisted of two free-running, non-stabilized frequency combs each emitting at 179 wavelengths between 1174 and 1233 cm -1 . A free spectral range, , of 9.86 GHz and a difference in comb spacing, Δ , of 5 MHz, enabled a theoretical time resolution of 0.2 µs but the data was time-integrated to 4 µs to improve SNR. The accuracy of the spectrometer was monitored using a suite of independent laser diagnostics and good agreement observed. Key challenges remain in the fitting of available high-temperature spectroscopic models to the observed spectra of a post-ignition environment.

Strong light-matter coupling at room temperature in the terahertz ͑THz͒ range is demonstrated. The studied system consists of electronic intersubband transitions in Al x Ga 1−x As parabolic quantum wells coupled to an electronic LC microcavity resonator allowing strong subwavelength confinement of the cavity mode. The measured Rabi frequency is 0.48 THz, corresponding to 14% of the center frequency, independent of the temperature of the system in the range 10-300 K.