The rotational dynamics of particles subject to external illumination is found to produce light amplification and inelastic scattering at high rotation velocities. Light emission at frequencies shifted with respect to the incident light by twice the rotation frequency dominates over elastic scattering within a wide range of light and rotation frequencies. Remarkably, net amplification of the incident light is produced in this classical linear system via stimulated emission. Large optically-induced acceleration rates are predicted in vacuum accompanied by moderate heating of the particle, thus supporting the possibility of observing these effects under extreme rotation conditions.
We study the scattering problem of photon and polariton in a one-dimensional coupled-cavity system. Analytical approximate analysis and numerical simulation show that a photon can stimulate the photon emission from a polariton through polariton-photon collisions. This observation opens the possibility of photon-stimulated transition from insulating to radiative phase in a coupled-cavity QED system. Inversely, we also find that a polariton can be generated by a two-photon Raman scattering process. This paves the way towards single photon storage by the aid of atom-cavity interaction.
It is known that photon pairs generated from pulse-pumped spontaneous parametric processes can be described by independent temporal modes and form a multi-temporal mode entangled state. However, the exact form of the temporal modes is not known even though the joint spectral intensity of photon pairs can be measured by the method of stimulated emission tomography. In this paper, we describe a feedback-iteration method which, combined with the stimulated emission method, can give rise to the exact forms of the independent temporal modes for the temporally entangled photon pairs.
We characterize both entanglement and quantum coherence in a molecular system by connecting the linear entropy of electronic-nuclear entanglement with Wigner-Yanase skew information measuring vibronic coherence and local quantum uncertainty on electronic energy. Linear entropy of entanglement and quantifiers of quantum coherence are derived for a molecular system described in a bipartite Hilbert space H=Hel x Hvib of finite dimension Nel x Nv, and relations between them are established. For the specific case of the electronic-vibrational entanglement, we find the linear entropy of entanglement as having a more complex informational content than the von Neumann entropy. By keeping the information carried by the vibronic coherences in a molecule, linear entropy seizes vibrational motion in the electronic potentials as entanglement dynamics. We analyze entanglement oscillations in an isolated molecule, and show examples for the control of entanglement dynamics in a molecule through the creation of coherent vibrational wave packets in several electronic potentials by using chirped laser pulses.
We investigate surface plasmon amplification in a silver nanoparticle coupled to an externally driven three-level gain medium, and show that quantum coherence significantly enhances the generation of surface plasmons. Surface plasmon amplification by stimulated emission of radiation is achieved in the absence of population inversion on the spasing transition, which reduces the pump requirements. The coherent drive allows us to control the dynamics, and holds promise for quantum control of nanoplasmonic devices.
Iron-sulfur complexes play an important role in biological processes such as metabolic electron transport. A detailed understanding of the mechanism of long range electron transfer requires knowledge of the electronic structure of the complexes, which has traditionally been challenging to obtain, either by theory or by experiment, but the situation has begun to change with advances in quantum chemical methods and intense free electron laser light sources. We compute the signals from stimulated X-ray Raman spectroscopy (SXRS) and absorption spectroscopy of homovalent and mixed-valence [2Fe-2S] complexes, using the {it ab initio} density matrix renormalization group (DMRG) algorithm. The simulated spectra show clear signatures of the theoretically predicted dense low-lying excited states within the d-d manifold. Furthermore, the difference in signal intensity between the absorption-active and Raman-active states provides a potential mechanism to selectively excite states by a proper tuning of the excitation pump, to access the electronic dynamics within this manifold.
Ana Asenjo-Garcia
,Alejandro Manjavacas
,
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(2011)
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"Stimulated light emission and inelastic scattering by a classical linear system of rotating particles"
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F. Javier Garcia de Abajo
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