اشترك بالحزمة الذهبية واحصل على وصول غير محدود شمرا أكاديميا
تسجيل مستخدم جديدScattering of polarized laser light by an atomic gas in free space: a QSDE approach
233
0
0.0
(
0
)
اسأل ChatGPT حول البحث
ﻻ يوجد ملخص باللغة العربية
We propose a model, based on a quantum stochastic differential equation (QSDE), to describe the scattering of polarized laser light by an atomic gas. The gauge terms in the QSDE account for the direct scattering of the laser light into different field channels. Once the model has been set, we can rigorously derive quantum filtering equations for balanced polarimetry and homodyne detection experiments, study the statistics of output processes and investigate a strong driving, weak coupling limit.
قيم البحث
اقرأ أيضاً
We consider a quantum theory of elastic light scattering from a macroscopic atomic sample existing in the Bose-Einstein condensate (BEC) phase. The dynamics of the optical excitation induced by an incident photon is influenced by the presence of inco
herent scattering channels. For a sample of sufficient length the excitation transports as a polariton wave and the propagation Greens function obeys the scattering equation which we derive. The polariton dynamics could be tracked in the outgoing channel of the scattered photon as we show via numerical solution of the scattering equation for one-dimensional geometry. The results are analyzed and compared with predictions of the conventional macroscopic Maxwell theory for light scattering from a non-degenerate atomic sample of the same density and size.
The coupling of atomic arrays and one-dimensional subwavelength waveguides gives rise to in- teresting photon transport properties, such as recent experimental demonstrations of large Bragg reflection and paves the way for a variety of potential appl
ications in the field of quantum non-linear optics. Here, we present a theoretical analysis for the process of single-photon scattering in this configuration using a full microscopic approach. Based on this formalism, we analyze the spectral dependencies for different scattering channels from either ordered or disordered arrays. The de- veloped approach is entirely applicable for a single-photon scattering from a quasi-one-dimensional array of multilevel atoms with degenerate ground state energy structure. Our approach provides an important framework for including not only Rayleigh but also Raman channels in the microscopic description of the cooperative scattering process.
We show that coherent multiple light scattering, or diffuse light propagation, in a disordered atomic medium, prepared at ultra-low temperatures, can be be effectively delayed in the presence of a strong control field initiating a stimulated Raman pr
ocess. On a relatively short time scale, when the atomic system can preserve its configuration and effects of atomic motion can be ignored, the scattered signal pulse, diffusely propagating via multiple coherent scattering through the medium, can be stored in the spin subsystem through its stimulated Raman-type conversion into spin coherence. We demonstrate how this mechanism, potentially interesting for developing quantum memories, would work for the example of a coherent light pulse propagating through an alkali-metal atomic vapor under typical conditions attainable in experiments with ultracold atoms.
We consider deflection of polarizable molecules by inhomogeneous optical fields, and analyze the role of molecular orientation and rotation in the scattering process. It is shown that molecular rotation induces spectacular rainbow-like features in th
e distribution of the scattering angle. Moreover, by preshaping molecular angular distribution with the help of short and strong femtosecond laser pulses, one may efficiently control the scattering process, manipulate the average deflection angle and its distribution, and reduce substantially the angular dispersion of the deflected molecules. We provide quantum and classical treatment of the deflection process. The effects of strong deflecting field on the scattering of rotating molecules are considered by the means of the adiabatic invariants formalism. This new control scheme opens new ways for many applications involving molecular focusing, guiding and trapping by optical and static fields.
We present a novel approach to engineer the photon correlations emerging from the interference between an input field and the field scattered by a single atom in free space. Nominally, the inefficient atom-light coupling causes the quantum correlatio
ns to be dominated by the input field alone. To overcome this issue, we propose the use of separate pump and probe beams, where the former increases the atomic emission to be comparable to the probe. Examining the second-order correlation function $g^{(2)}(tau)$ of the total field in the probe direction, we find that the addition of the pump formally plays the same role as increasing the coupling efficiency. We show that one can tune the correlation function $g^{(2)}(0)$ from zero (perfect anti-bunching) to infinite (extreme bunching) by a proper choice of pump amplitude. We further elucidate the origin of these correlations in terms of the transient atomic state following the detection of a photon.
سجل دخول لتتمكن من نشر تعليقات
التعليقات
جاري جلب التعليقات
سجل دخول لتتمكن من متابعة معايير البحث التي قمت باختيارها
