اشترك بالحزمة الذهبية واحصل على وصول غير محدود شمرا أكاديميا
تسجيل مستخدم جديدLight mediated non-Gaussian atomic ensemble entanglement
70
0
0.0
(
0
)
اسأل ChatGPT حول البحث
ﻻ يوجد ملخص باللغة العربية
We analyze a similar scheme for producing light-mediated entanglement between atomic ensembles, as first realized by Julsgaard, Kozhekin and Polzik [Nature {bf 413}, 400 (2001)]. In the standard approach to modeling the scheme, a Holstein-Primakoff approximation is made, where the atomic ensembles are treated as bosonic modes, and is only valid for short interaction times. In this paper, we solve the time evolution without this approximation, which extends the region of validity of the interaction time. For short entangling times, we find this produces a state with similar characteristics as a two-mode squeezed state, in agreement with standard predictions. For long entangling times, the state evolves into a non-Gaussian form, and the two-mode squeezed state characteristics start to diminish. This is attributed to more exotic types of entangled states being generated. We characterize the states by examining the Fock state probability distributions, Husimi $Q$ distributions, and non-local entanglement between the ensembles. We compare and connect several quantities obtained using the Holstein-Primakoff approach and our exact time evolution methods.
قيم البحث
اقرأ أيضاً
Quantum light-matter interfaces, based upon ensembles of cold atoms or other quantum emitters, are a vital platform for diverse quantum technologies and the exploration of fundamental quantum phenomena. Most of our understanding and modeling of such
systems are based upon macroscopic theories, wherein the atoms are treated as a smooth, quantum polarizable medium. Although it is known that such approaches ignore a number of microscopic details, such as the granularity of atoms, dipole-dipole interactions and multiple scattering of light, the consequences of such effects in practical settings are usually mixed with background macroscopic effects and difficult to quantify. In this work we demonstrate a time-domain method to measure microscopically-driven optical effects in a background-free fashion, by transiently suppressing the macroscopic dynamics. With the method, we reveal a microscopic dipolar dephasing mechanism that generally limits the lifetime of the optical spin-wave order in a random gas. Theoretically, we show the dephasing effect emerges from the strong resonant dipole interaction between close-by atomic pairs.
We present a fast and Quasideterministic protocol for the production of single ions and electrons from a cloud of laser cooled atoms. The approach is based on a two-step process where first a single Rydberg atom is photo-excited from a dipole-blockad
e configuration and subsequently ionized by an electric field pulse. We theoretically describe these excitation-ionization cycles via dynamical quantum maps and observe a rich behavior of the ionization dynamics as a function of laser Rabi frequency, pulse duration and particle number. Our results show that a fast sequential heralded production of single charged particles is achievable even from an unstructured and fluctuating atomic ensemble.
We demonstrate the ability to load, cool and detect singly-charged calcium ions in a surface electrode trap using only visible and infrared lasers for the trapped-ion control. As opposed to the standard methods of cooling using dipole-allowed transit
ions, we combine power broadening of a quadrupole transition at 729 nm with quenching of the upper level using a dipole allowed transition at 854 nm. By observing the resulting 393 nm fluorescence we are able to perform background-free detection of the ion. We show that this system can be used to smoothly transition between the Doppler cooling and sideband cooling regimes, and verify theoretical predictions throughout this range. We achieve scattering rates which reliably allow recooling after collision events and allow ions to be loaded from a thermal atomic beam. This work is compatible with recent advances in optical waveguides, and thus opens a path in current technologies for large-scale quantum information processing. In situations where dielectric materials are placed close to trapped ions, it carries the additional advantage of using wavelengths which do not lead to significant charging, which should facilitate high rate optical interfaces between remotely held ions.
We present experimental evidence that light storage, i.e. the controlled release of a light pulse by an atomic sample dependent on the past presence of a writing pulse, is not restricted to small group velocity media but can also occur in a negative
group velocity medium. A simple physical picture applicable to both cases and previous light storage experiments is discussed.
A theoretical study is performed for the excitation of a single atom localized in the center of twisted light modes. Here we present the explicit dependence of excitation rates on critical parameters, such as the polarization of light, its orbital an
gular momentum projection, and the orientation of its propagation axis with respect to the atomic quantization axis. The effect of a spatial spread of the atom is also considered in detail. The expressions for transition rates obtained in this work can be used for any atom of arbitrary electronic configuration. For definiteness we apply them to the specific case of $^{2}S_{1/2} (F=0) rightarrow; ^{2}F_{7/2} (F=3, M=0)$ electric octupole (E3) transition in $^{171}$Yb$^{+}$ ion. Our analytical and numerical results are suitable for the analysis and planning of future experiments on the excitation of electric-dipole-forbidden transitions by twisted light modes in optical atomic clocks.
سجل دخول لتتمكن من نشر تعليقات
التعليقات
جاري جلب التعليقات
سجل دخول لتتمكن من متابعة معايير البحث التي قمت باختيارها
