اشترك بالحزمة الذهبية واحصل على وصول غير محدود شمرا أكاديميا
تسجيل مستخدم جديدHyperfine, rotational and Zeeman structure of the lowest vibrational levels of the $^{87}$Rb$_2$ $tripletex$ state
124
0
0.0
(
0
)
اسأل ChatGPT حول البحث
ﻻ يوجد ملخص باللغة العربية
We present the results of an experimental and theoretical study of the electronically excited $tripletex$ state of $^{87}$Rb$_2$ molecules. The vibrational energies are measured for deeply bound states from the bottom up to $v=15$ using laser spectroscopy of ultracold Rb$_2$ Feshbach molecules. The spectrum of each vibrational state is dominated by a 47,GHz splitting into a $cog$ and $clg$ component caused mainly by a strong second order spin-orbit interaction. Our spectroscopy fully resolves the rotational, hyperfine, and Zeeman structure of the spectrum. We are able to describe to first order this structure using a simplified effective Hamiltonian.
قيم البحث
اقرأ أيضاً
Starting from an ultracold sample of ground-state $^{23}$Na$^{87}$Rb molecules, we investigate the lowest ro-vibrational level of the $b^3Pi$ state with high resolution laser spectroscopy. This electronic spin-forbidden $X^1Sigma^+ leftrightarrow b^3
Pi$ transition features a nearly diagonal Franck-Condon factor and has been proposed useful for probing and manipulating the ultracold molecular gas. We measure the transition strength directly by probing the ac Stark shift induced by near resonance light and determine the total excited-state spontaneous emission rate by observing the loss of molecules. From the extracted branching ratio and the theoretical modeling, we find that the leakage to the continuum of the $a^3Sigma^+$ state plays the dominant role in the total transition linewidth. Based on these results, we show that it is feasible to create optical trapping potentials for maximizing the rotational coherence with laser light tuned to near this transition.
We demonstrate coherent control of both the rotational and hyperfine state of ultracold, chemically stable $^{87}$Rb$^{133}$Cs molecules with external microwave fields. We create a sample of ~2000 molecules in the lowest hyperfine level of the rovibr
onic ground state N = 0. We measure the transition frequencies to 8 different hyperfine levels of the N = 1 state at two magnetic fields ~23 G apart. We determine accurate values of rotational and hyperfine coupling constants that agree well with previous calculations. We observe Rabi oscillations on each transition, allowing complete population transfer to a selected hyperfine level of N = 1. Subsequent application of a second microwave pulse allows transfer of molecules back to a different hyperfine level of N = 0.
The fully relativistic theory of the Zeeman splitting of the $(1s)^2 2s$ hyperfine-structure levels in lithiumlike ions with $Z=6 - 32$ is considered for the magnetic field magnitude in the range from 1 to 10 T. The second-order corrections to the Br
eit -- Rabi formula are calculated and discussed including the one-electron contributions as well as the interelectronic-interaction effects of order 1/Z. The 1/Z corrections are evaluated within a rigorous QED approach. These corrections are combined with other interelectronic-interaction, QED, nuclear recoil, and nuclear size corrections to obtain high-precision theoretical values for the Zeeman splitting in Li-like ions with nonzero nuclear spin. The results can be used for a precise determination of nuclear magnetic moments from $g$-factor experiments.
We observe a hyperfine anomaly in the measurement of the hyperfine splitting of the 6S_{1/2} excited level in rubidium. We perform two step spectroscopy using the 5S_{1/2}->5P_{1/2}->6S_{1/2} excitation sequence. We measure the splitting of the 6S1/2
level and obtain for the magnetic dipole constants of ^{85}Rb and ^{87}Rb A = 239.18(4) MHz and A=807.66(8) MHz, respectively. The hyperfine anomaly difference of_{87}delta_{85}=-0.0036(2) comes from the Bohr Weisskopf effect: a correction to the point interaction between the finite nuclear magnetization and the electrons, and agrees with that obtained in the 5S_{1/2} ground state.
Experimental signals of non-linear magneto-optical resonances at D1 excitation of natural rubidium in a vapor cell have been obtained and described with experimental accuracy by a detailed theoretical model based on the optical Bloch equations. The D
1 transition of rubidium is a challenging system to analyze theoretically because it contains transitions that are only partially resolved under Doppler broadening. The theoretical model took into account all nearby transitions, the coherence properties of the exciting laser radiation, and the mixing of magnetic sublevels in an external magnetic field and also included averaging over the Doppler profile. Great care was taken to obtain accurate experimental signals and avoid systematic errors. The experimental signals were reproduced very well at each hyperfine transition and over a wide range of laser power densities, beam diameters, and laser detunings from the exact transition frequency. The bright resonance expected at the F_g=1 --> F_e=2 transition of Rb-87 has been observed. A bright resonance was observed at the F_g=2 --> F_e=3 transition of Rb-85, but displaced from the exact position of the transition due to the influence of the nearby F_g=2 --> F_e=2 transition, which is a dark resonance whose contrast is almost two orders of magnitude larger than the contrast of the bright resonance at the F_g=2 --> F_e=3 transition. Even in this very delicate situation, the theoretical model described in detail the experimental signals at different laser detunings.
سجل دخول لتتمكن من نشر تعليقات
التعليقات
جاري جلب التعليقات
سجل دخول لتتمكن من متابعة معايير البحث التي قمت باختيارها
