اشترك بالحزمة الذهبية واحصل على وصول غير محدود شمرا أكاديميا
تسجيل مستخدم جديدCavity-induced phase stability to decelerate a fast molecular beam via feedback-controlled time-varying optical pumps
111
0
0.0
(
0
)
اسأل ChatGPT حول البحث
ﻻ يوجد ملخص باللغة العربية
We have identified a novel phase stability mechanism from the intracavity field-induced self-organization of a fast-moving molecular beam into travelling molecular packets in the bad cavity regime, which is then used to decelerate the molecular packets by feedback-controlled time-varying laser pumps to the cavity. We first applied the linear stability analysis to derive an expression for this self-organization in the adiabatic limit and show that the self-organization of the beam leads to the formation of travelling molecular packets, which in turn function as a dynamic Bragg grating, thus modulating periodically the intracavity field by superradiant scattering of the pump photons. The modulation encodes the position information of the molecular packets into the output of the intracavity field instantaneously. We then applied time-varying laser pumps that are automatically switched by the output of the intracavity field to slow down the molecular packets via a feedback mechanism and found that most of the molecules in the molecular packets are decelerated to zero central velocity after tens of stages. Our cavity-based deceleration proposal works well in the bad cavity regime, which is very different from the conventional cavity- based cooling strategies where a good cavity is preferred. Practical issues in realizing the proposal are also discussed.
قيم البحث
اقرأ أيضاً
Cooling the rotation and the vibration of molecules by broadband light sources was possible for trapped molecular ions or ultracold molecules. Because of a low power spectral density, the cooling timescale has never fell below than a few milliseconds
. Here we report on rotational and vibrational cooling of a supersonic beam of barium monofluoride molecules in less than 440 $mu$s. Vibrational cooling was optimized by enhancing the spectral power density of a semiconductor light source at the underlying molecular transitions allowing us to transfer all the populations of $v=1-3$ into the vibrational ground state ($v=0$). Rotational cooling, that requires an efficient vibrational pumping, was then achieved. According to a Boltzmann fit, the rotation temperature was reduced by almost a factor of 10. In this fashion, the population of the lowest rotational levels increased by more than one order of magnitude.
We present an experimental study of cavity assisted Rydberg atom electromagnetically induced transparency (EIT) using a high-finesse optical cavity ($F sim 28000$). Rydberg atoms are excited via a two-photon transition in a ladder-type EIT configurat
ion. A three-peak structure of the cavity transmission spectrum is observed when Rydberg EIT is generated inside the cavity. The two symmetrically spaced side peaks are caused by bright-state polaritons, while the central peak corresponds to a dark-state polariton. Anti-crossing phenomenon and the effects of mirror adsorbate electric fields are studied under different experimental conditions. We determine a lower bound on the coherence time for the system of $7.26 pm 0.06 ,mu$s, most likely limited by laser dephasing. The cavity-Rydberg EIT system can be useful for single photon generation using the Rydberg blockade effect, studying many-body physics, and generating novel quantum states amongst many other applications.
The residual cavity-pulling effect limits further narrowing of linewidth in dual-wavelength (DW) good-bad-cavity active optical clocks (AOCs). In this paper, we for the first time experimentally realize the cavity-length stabilization of the 1064/147
0 nm DW-AOCs by utilizing the phase locking technique of two independent 1064 nm good-cavity lasers. The frequency tracking accuracy between the two main-cavities of DW-AOCs is better than $3 times {10^{ - 16}}$ at 1 s, and can reach $1 times {10^{ - 17}}$ at 1000 s. Each 1470 nm bad-cavity laser achieves a most probable linewidth of 53 Hz, which is about a quarter of that without phase locking. The influence of the asynchronous cavity-lengths variation between two DW laser systems is suppressed.
We propose a method to exploit high finesse optical resonators for light assisted coherent manipulation of atomic ensembles, overcoming the limit imposed by the finite response time of the cavity. The key element of our scheme is to rapidly switch th
e interaction between the atoms and the cavity field with an auxiliary control process as, for example, the light shift induced by an optical beam. The scheme is applicable to many different atomic species, both in trapped and free fall configurations, and can be adopted to control the internal and/or external atomic degrees of freedom. Our method will open new possibilities in cavity-aided atom interferometry and in the preparation of highly non-classical atomic states.
Heavy diatomic molecules have been identified as good candidates for use in electron electric dipole moment (eEDM) searches. Suitable molecular species can be produced in pulsed beams, but with a total flux and/or temporal evolution that varies signi
ficantly from pulse to pulse. These variations can degrade the experimental sensitivity to changes in spin precession phase of an electri- cally polarized state, which is the observable of interest for an eEDM measurement. We present two methods for measurement of the phase that provide immunity to beam temporal variations, and make it possible to reach shot-noise-limited sensitivity. Each method employs rapid projection of the spin state onto both components of an orthonormal basis. We demonstrate both methods using the eEDM-sensitive H state of thorium monoxide (ThO), and use one of them to measure the magnetic moment of this state with increased accuracy relative to previous determinations.
سجل دخول لتتمكن من نشر تعليقات
التعليقات
جاري جلب التعليقات
سجل دخول لتتمكن من متابعة معايير البحث التي قمت باختيارها
