We show how temporal or frequency entanglement in a two-photon pure state produced by a three-level cascade source enables the joint excitation of two uncoupled, two-level atoms. Consequences for quantum metrology and information are explored.
Two uncoupled two-level atoms cannot be jointly excited by classical light under general circumstances, due to destructive interference of excitation pathways in two-photon absorption. However, with temporally entangled light, two-atom excitation is shown possible. Photons arising from three-level cascade decay are intrinsically ordered in time of emission. This field correlation induces a joint resonance in the two-atom excitation probability via suppression of one of the time-ordered excitation pathways. The relative gain in two-photon absorption increases with the time-frequency entanglement.
We study the efficiency of different two-photon states of light to induce the simultaneous excitation of two atoms of different kinds when the sum of the energies of the two photons matches the sum of the energies of the two atomic transitions, while no photons are resonant with each individual transition. We find that entangled two-photon states produced by an atomic cascade are indeed capable of enhancing by a large factor the simultaneous excitation probability as compared to uncorrelated photons, as predicted some years ago by Muthukrishnan et al., but that several unentangled, separable, correlated states, produced either by an atomic cascade or parametric down-conversion, or even appropriate combinations of coherent states, have comparable efficiencies. We show that the key ingredient for the increase of simultaneous excitation probability is the presence of strong frequency anticorrelation and neither time correlation nor time-frequency entanglement.
We study in this paper the efficiency of different two-photon states of light to induce the simultaneous excitation of two atoms of different kinds when the sum of the energies of the two photons matches the sum of the energies of the two atomic transitions, while no photons are resonant with each individual transition. We find that entangled two-photon states produced by an atomic cascade are indeed capable of enhancing by a large factor the simultaneous excitation probability as compared to uncorrelated photons, as predicted some years ago by Muthukrishnan et al, but that several non-entangled, separable, correlated states, produced either by an atomic cascade or parametric down conversion, or even appropriate combinations of coher- ent states, have comparable efficiencies. We show that the key ingredient for the increase of simultaneous excitation probability is the presence of strong frequency anti-correlation and not time correlation nor time-frequency entanglement.
We study in this paper the efficiency of different two-photon states of light to induce the simultaneous excitation of two atoms of different kinds when the sum of the energies of the two photons matches the sum of the energies of the two atomic transitions, while no photons are resonant with each individual transition. We find that entangled two-photon states produced by an atomic cascade are indeed capable of enhancing by a large factor the simultaneous excitation probability as compared to uncorrelated photons, as predicted some years ago by Muthukrishnan et al, but that several non-entangled, separable, correlated states, produced either by an atomic cascade or parametric down conversion, or even appropriate combinations of coher- ent states, have comparable efficiencies. We show that the key ingredient for the increase of simultaneous excitation probability is the presence of strong frequency anti-correlation and not time correlation nor time-frequency entanglement.
Inspired by the unique nonclassical character of two-photon interactions induced by entangled photons, we develop a new comprehensive Förster-type formulation for entangled-two-photon resonance energy transfer (E2P-RET) mediated by inhomogeneous, dispersive, and absorptive media with any space-dependent and frequency-dependent dielectric function and with any size of donor/acceptor. In our theoretical framework, two uncoupled particles are jointly excited by the temporally entangled field associated with two virtual photons that are produced by three-level radiative cascade decay in a donor particle. The temporal entanglement leads to frequency anticorrelation in the virtual photon’s field, and vanishing of one of the time-ordered excitation pathways. The underlying mechanism leads to more than 3 orders of magnitude enhancement in the E2P-RET rate compared with the uncorrelated photon case. With the power of our new formulation, we propose a way to characterize E2P-RET through an effective rate coefficient K E2P, introduced here. This coefficient shows how energy transfer can be enhanced or suppressed depending on rate parameters in the radiative cascade, and by varying the donor–acceptor frequency differences.