ترغب بنشر مسار تعليمي؟ اضغط هنا

Inelastic and elastic collision rates for triplet states of ultracold strontium

48   0   0.0 ( 0 )
 نشر من قبل Thomas Killian
 تاريخ النشر 2009
  مجال البحث فيزياء
والبحث باللغة English




اسأل ChatGPT حول البحث

We report measurement of the inelastic and elastic collision rates for ^{88}Sr atoms in the (5s5p)^3P_0 state in a crossed-beam optical dipole trap. This is the first measurement of ultracold collision properties of a ^3P_0 level in an alkaline-earth atom or atom with similar electronic structure. Since the (5s5p)^3P_0 state is the lowest level of the triplet manifold, large loss rates indicate the importance of principle-quantum-number-changing collisions at short range. We also provide an estimate of the collisional loss rates for the (5s5p){^3P_2} state.

قيم البحث

اقرأ أيضاً

We demonstrate a set of tools for microscopic control of neutral strontium atoms. We report single-atom loading into an array of sub-wavelength scale optical tweezers, light-shift free control of a narrow-linewidth optical transition, three-dimension al ground-state cooling, and high-fidelity nondestructive imaging of single atoms on sub-wavelength spatial scales. Extending the microscopic control currently achievable in single-valence-electron atoms to species with more complex internal structure, like strontium, unlocks a wealth of opportunities in quantum information science, including tweezer-based metrology, new quantum computing architectures, and new paths to low-entropy many-body physics.
Chemical reactions at ultracold temperatures are expected to be dominated by quantum mechanical effects. Although progress towards ultracold chemistry has been made through atomic photoassociation, Feshbach resonances and bimolecular collisions, thes e approaches have been limited by imperfect quantum state selectivity. In particular, attaining complete control of the ground or excited continuum quantum states has remained a challenge. Here we achieve this control using photodissociation, an approach that encodes a wealth of information in the angular distribution of outgoing fragments. By photodissociating ultracold 88Sr2 molecules with full control of the low-energy continuum, we access the quantum regime of ultracold chemistry, observing resonant and nonresonant barrier tunneling, matter-wave interference of reaction products and forbidden reaction pathways. Our results illustrate the failure of the traditional quasiclassical model of photodissociation and instead are accurately described by a quantum mechanical model. The experimental ability to produce well-defined quantum continuum states at low energies will enable high-precision studies of long-range molecular potentials for which accurate quantum chemistry models are unavailable, and may serve as a source of entangled states and coherent matter waves for a wide range of experiments in quantum optics.
We present a combined experimental and theoretical study of the effects of Rydberg interactions on Autler-Townes spectra of ultracold gases of atomic strontium. Realizing two-photon Rydberg excitation via a long-lived triplet state allows us to probe the thus far unexplored regime where Rydberg state decay presents the dominant decoherence mechanism. The effects of Rydberg interactions are observed in shifts, asymmetries, and broadening of the measured atom-loss spectra. The experiment is analyzed within a one-body density matrix approach, accounting for interaction-induced level shifts and dephasing through nonlinear terms that approximately incorporate correlations due to the Rydberg blockade. This description yields good agreement with our experimental observations for short excitation times. For longer excitation times, the loss spectrum is altered qualitatively, suggesting additional dephasing mechanisms beyond the standard blockade mechanism based on pure van der Waals interactions.
We analyse the spectrum on the narrow-line transition arrow at 689 nm in an ultracold gas of $^{88}$Sr via absorption imaging. In the low saturation regime, the Doppler effect dominates in the observed spectrum giving rise to a symmetric Voigt profi le. The atomic temperature and atom number can accurately be deduced from these low-saturation imaging data. At high saturation, the absorption profile becomes asymmetric due to the photon-recoil shift, which is of the same order as the natural line width. The line shape can be described by an extension of the optical Bloch equations including the photon recoil. A lensing effect of the atomic cloud induced by the dispersion of the atoms is also observed at higher atomic densities in both the low and strong saturation regimes.
We demonstrate the interaction-induced blockade effect in an ultracold $^{88}$Sr gas via studying the time dynamics of a two-photon excitation to the triplet Rydberg series $5mathrm{s}nmathrm{s}, ^3textrm{S}_1$ for five different principle quantum nu mbers $n$ ranging from 19 to 37. By using a multi-pulse excitation sequence to increase the detection sensitivity we could identify Rydberg-excitation-induced atom losses as low as $<1%$. Based on an optical Bloch equation formalism, treating the Rydberg-Rydberg interaction on a mean-field level, the van der Waals coefficients are extracted from the observed dynamics, which agree fairly well with emph{ab initio} calculations.
التعليقات
جاري جلب التعليقات جاري جلب التعليقات
سجل دخول لتتمكن من متابعة معايير البحث التي قمت باختيارها
mircosoft-partner

هل ترغب بارسال اشعارات عن اخر التحديثات في شمرا-اكاديميا