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Physical Review A

Enhanced vibrational-mode-selective two-step excitation using ultrabroadband frequency-entangled photons

Hisaki Oka

Published Jun 29, 2018• 26 citations
Publisher

Abstract

We theoretically investigate strongly enhanced vibrational-mode-selective two-step excitation by ultrabroadband frequency-entangled photons. A diatomic molecule having three sets of vibronic states is used to evaluate the excitation efficiency of the two-step excitation. We show that the photon entanglement has little influence on the populations of intermediate vibrational modes of intermediate states but selectively increases the population of a single vibrational mode of excited states, resonant with the total energy of the entangled photons. For an ultrashort pulse close to a monocycle with high degree of entanglement, the population of the vibrational mode is enhanced 2500 times more than by uncorrelated photons, and the selectivity nearly reaches unity. Our results indicate that the two-step excitation with ultrabroadband frequency-entangled photons can achieve highly selective and strongly enhanced excitation of a single vibrational mode.

DOI
10.1103/physreva.97.063859

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We theoretically investigate strongly enhanced vibrational-mode-selective two-step excitation by ultrabroadband frequency-entangled photons. A diatomic molecule having three sets of vibronic states is used to evaluate the excitation efficiency of the two-step excitation. We show that the photon entanglement has little influence on the populations of intermediate vibrational modes of intermediate states but selectively increases the population of a single vibrational mode of excited states, resonant with the total energy of the entangled photons. For an ultrashort pulse close to a monocycle with high degree of entanglement, the population of the vibrational mode is enhanced 2500 times more than by uncorrelated photons, and the selectivity nearly reaches unity. Our results indicate that the two-step excitation with ultrabroadband frequency-entangled photons can achieve highly selective and strongly enhanced excitation of a single vibrational mode.
Using second-order perturbation theory in the light-matter interaction, we derive an analytical approximation for the vibronic populations of a diatomic system excited by ultrabroadband frequency-entangled photons and evaluate the population dynamics for different degrees of entanglement between photon pairs. Our analytical approach makes the same predictions as previously derived via numerical solutions of the complete Schrödinger equation [H. Oka, ], with the added advantage of providing clear physical insights into the vibronic selectivity as a function of the degree of photon correlations while requiring significantly reduced computational effort. Specifically, our analytical expression for the probability of vibronic excitation includes a factor which predicts the enhancement of vibrational selectivity as a function of the degree correlation between the entangled photon pairs, the targeted vibrational energy level, and the vibrational molecular structure encoded in the Franck-Condon factors. Our results illustrate the importance of going beyond the usual approximations in second-order perturbation theory to capture the relevance of the vibrational structure of the molecular system of interest in order to gain a deeper understanding of the possible quantum-enhancement provided by the interaction between quantum light and matter.
We theoretically investigate the two-photon excitation of a molecular vibronic state by correlated photons with energy anticorrelation. A Morse oscillator having three sets of vibronic states is used, as an example, to evaluate the selectivity and efficiency of two-photon excitation. We show that a vibrational mode can be selectively excited with high efficiency by the correlated photons, without phase manipulation or pulse-shaping techniques. This can be achieved by controlling the quantum correlation so that the photon pair concurrently has two pulse widths, namely, a temporally narrow width and a spectrally narrow width. Though this concurrence is seemingly contradictory, we can create such a photon pair by tailoring the quantum correlation between two photons.
In this paper, I discuss the selective and efficient vibrational population transfer between electronic states of diatomic molecules by a weak, ultrashort pulse train. The spectrum of each individual pulse in the train is wide enough to simultaneously excite several vibrational levels of the molecule. However, selectivity is achieved by mismatching the frequency comb, associated with the pulse train, to the excited vibrational levels. Efficiency results from the coherent accumulation of population from one pulse in the train to the next.
We theoretically investigate two-photon excitation by spectrally shaped entangled photons with energy anticorrelation in terms of how the real excitation of an intermediate state affects two-photon absorption by entangled photons. Spectral holes are introduced in the entangled photons around the energy levels of an intermediate state so that two-step excitation via the real excitation of the intermediated state can be suppressed. Using a three-level atomic system as an example, we show that the spectral holes well suppress the real excitation of the intermediate state and recover two-photon absorption via a virtual state. Furthermore, for a short pulse close to a monocycle, we show that the excitation efficiency by the spectrally shaped entangled photons can be enhanced a thousand times as large as that by uncorrelated photons.
We theoretically investigate the two-step excitation of a molecular vibronic state using quantum-correlated photons with time delay in order to control the population of the vibronic excited state. A Morse oscillator having three sets of vibronic states, namely, the ground state, intermediate states, and excited states, is used to evaluate the efficiency of the two-step excitation process. We show that we can efficiently and selectively excite only a target state by using correlated photons and can control the excitation population of the target state by adjusting the delay time of the correlated photons. The potential of controlling a chemical reaction using correlated photons is also discussed.
Abstract We present a multi-color ladder excitation scheme that exploits Stark-induced adiabatic Raman passage to selectively populate a highly excited vibrational level of a molecule. We suggest that this multi-color coherent ladder excitation provides a practical way of accessing levels near the vibrational dissociation limit as well as the dissociative continuum, which would allow the generation of an entangled pair of fragments with near-zero relative kinetic energy. Specifically, we consider four- and six-photon coherent excitation of molecular hydrogen to high vibrational levels via intermediate vibrational levels, which are pairwise coupled by two-photon resonant interaction. Using a sequence of three partially overlapping, single-mode, nanosecond laser pulses we show that the sixth vibrational level of H 2 , which is too weakly coupled to be easily accessed by direct two-photon Raman excitation from the ground vibrational level, can be efficiently populated without leaving any population stranded in the intermediate level. Furthermore, we show that the fourteenth vibrational level of H 2 , which is the highest vibrational level in the ground electronic state with a binding energy of 22 meV, can be efficiently and selectively populated using a sequence of four pulses. The present technique offers the unique possibility of preparing entangled quantum states of H atoms without resorting to an ultracold system.