We calculate the two-photon absorption of squeezed light by rubidium atoms. In the region of large enhancement, Doppler broadening significantly decreases the effectiveness of photon correlations, leading to the prediction of unspectacular fluorescence counts.
We present a theoretical analysis of two-photon absorption of classical and squeezed light valid when one-photon absorption to an intermediate state is either resonant or far-detuned from resonance, and in both the low and high intensity regimes. In this paper we concentrate on continuous-wave excitation, although the approach we develop is more general. We calculate the energy removed from an incident field for typical experimental parameters and consider the limiting cases when the photon pairs are narrowband or broadband compared to the molecular linewidths. We find an enhancement of the two-photon absorption due to resonant contributions from the large squeezed light bandwidth and due to photon bunching in the low intensity regime. However, in both cases, for the parameters we choose, the one-photon absorption is the dominant process in the region of parameter space where a large enhancement of the two-photon absorption is possible.
We consider a single two-level atom in an optical cavity, in which the system is driven by a coherent driving field. In the bad-cavity limit, when the cavity loss rate is taken to be large compared to the atomic decay rate and atom-field coupling, the cavity field can be adiabatically eliminated from the equations of motion for the atomic operators. The main effect of the cavity in this limit is the enhancement of spontaneous emission into the cavity mode. For this model, the second-order intensity correlation function g(2)() has been shown to exhibit photon antibunching, sub-Poissonian photon number distributions, and other nonclassical effects.1 In this paper, analytic results are presented for g(2)() for both the transmitted and fluorescent light fields when broadband squeezed light is injected into the cavity. Effects of the squeezing on nonclassical behavior is examined.
We propose and demonstrate pump-probe spectroscopy of rubidium absorption that reveals the sub-Doppler hyperfine structure of the ${}^{5}{\mathrm{S}}_{1/2}\ensuremath{\leftrightarrow}{}^{5}{\mathrm{P}}_{3/2}$ (D2) transitions. The counterpropagating pump and probe lasers are independently tunable in frequency, with the probe operating at the single-photon level. The two-dimensional spectrum measured as the laser frequencies are scanned shows fluorescence, Doppler-broadened absorption dips, and sub-Doppler features. The detuning between the pump and probe lasers allows compensation of the Doppler shift for all atomic velocities in the room-temperature vapor, meaning we observe sub-Doppler features for all atoms in the beam. We detail a theoretical model of the system that incorporates fluorescence, saturation effects, and optical pumping and compare this with the measured spectrum, finding a mean absolute percentage error of 3.11%. This high level of agreement allows us to extract the number density and temperature of the Rb vapor from the two-dimensional spectrum. In the future this technique could be used as an atomic frequency standard for calibrating and characterising a single-photon or low-light-level source.