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arXiv:1810.11399 · Journal of Physics B Atomic Molecular and Optical Physics

Quantum model for impulsive stimulated Raman scattering

Filippo Glerean, Stefano Marcantoni, Giorgia Sparapassi, Andrea Blason, Martina Esposito, Fabio Benatti, Daniele Fausti

Published Mar 1, 2019• 22 citations
arXivHTMLPDF

Abstract

Abstract The interaction between ultrashort light pulses and non-absorbing materials is dominated by impulsive stimulated Raman scattering (ISRS). The description of ISRS in the context of pump&probe experiments is based on effective classical models describing the interaction between the phonon and pulsed electromagnetic fields. Here we report a theoretical description of ISRS where we do not make any semi-classical approximation and we treat both photonic and phononic degrees of freedom at the quantum level. The results of the quantum model are compared with semiclassical results and validated by means of spectrally resolved pump&probe measurements on α-quartz.

DOI
10.1088/1361-6455/ab0bdc

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Abstract The interaction between ultrashort light pulses and non-absorbing materials is dominated by impulsive stimulated Raman scattering (ISRS). The description of ISRS in the context of pump&probe experiments is based on effective classical models describing the interaction between the phonon and pulsed electromagnetic fields. Here we report a theoretical description of ISRS where we do not make any semi-classical approximation and we treat both photonic and phononic degrees of freedom at the quantum level. The results of the quantum model are compared with semiclassical results and validated by means of spectrally resolved pump&probe measurements on α-quartz.
We introduce a theoretical framework to describe the interaction of an electromagnetic radiation field and a molecular system, such as a single molecule or a molecular crystal. By knowing in advance which electronic transitions are in resonance with the frequencies of the incident radiation, we propose a procedure to reduce the full problem to a description in terms of an effective Hamiltonian that fully takes into account the vibrational (nuclear) degrees of freedom, but that explicitly involves only those electronic states that meet the resonance condition. The influence of the rest of the electronic states appears as the polarizability of the system. We keep only those terms that give rise to Raman scattering but the scheme allows for a systematic inclusion of higher-order multiphoton processes. The resulting effective Hamiltonian is used to study the interaction of ultrashort laser pulses with a single molecule and with a molecular crystal. As applications, we study the interaction of a single ultrashort nonresonant pulse, and a train of such pulses, with a single molecule; we show that via Raman scattering the pulse impulsively transfers momentum to the molecule leaving it in a vibrational coherent state. We also study the interaction of two crossed laser pulses with a molecular crystal and show that a diffraction grating of lattice vibrations is impulsively created.
We investigated the coherent phonon generation mechanism by irradiation of an ultrashort pulse with a simple two-level model. Our derived formulation shows that both impulsive stimulated Raman scattering (ISRS) and impulsive absorption (IA) simultaneously occur, and phonon wave packets are generated in the electronic ground and excited states by ISRS and IA, respectively. We identify the dominant process from the amplitude of the phonon oscillation. For short pulse widths, ISRS is very small and becomes larger as the pulse width increases. We also show that the initial phase is dependent on the pulse width and the detuning.
We study the stimulated Raman scattering (SRS) of light from an atomic system embedded in a photonic crystal and coherently pumped by a laser field. In our study, the electromagnetic field is treated classically and the atomic system is described quantum mechanically. Considering a decomposition of the pump and Stokes fields into the Bloch modes of the photonic crystals and using a multiscale analysis, we derive the Maxwell-Bloch equations for SRS in photonic crystals. These equations contain effective parameters that characterize the SRS gain, the nonlinear atomic response to the electromagnetic field, and the group velocity and that can be calculated in terms of the Bloch modes of the unperturbed photonic crystal. We show that if the pump laser frequency is tuned near a photonic band edge and the atomic system is carefully chosen such that the Stokes mode matches another photonic band edge, low-threshold, enhanced Raman amplification is possible. Possible physical realizations of SRS in photonic crystals are also discussed.
A theory of quantum beats in a Stokes signal observed in pump-probe experiments upon excitation of four-level atoms with two close upper lying levels by femtosecond laser pulses is developed. Quantum beats arise in the intensity of the Stokes field due to the interference of two atomic wave packets generated by ultrashort pump and probe pulses. An analytical solution of the non-steady-state Maxwell-Bloch equations is obtained, and the dependence of the Stokes radiation intensity on the delay time between two laser pulses is investigated. The theoretical results describe qualitatively well the observed features of quantum beats.