ترغب بنشر مسار تعليمي؟ اضغط هنا

A Fermi-degenerate three-dimensional optical lattice clock

128   0   0.0 ( 0 )
 نشر من قبل Sara Campbell
 تاريخ النشر 2017
  مجال البحث فيزياء
والبحث باللغة English




اسأل ChatGPT حول البحث

Strontium optical lattice clocks have the potential to simultaneously interrogate millions of atoms with a high spectroscopic quality factor of $4 times 10^{-17}$. Previously, atomic interactions have forced a compromise between clock stability, which benefits from a large atom number, and accuracy, which suffers from density-dependent frequency shifts. Here, we demonstrate a scalable solution which takes advantage of the high, correlated density of a degenerate Fermi gas in a three-dimensional optical lattice to guard against on-site interaction shifts. We show that contact interactions are resolved so that their contribution to clock shifts is orders of magnitude lower than in previous experiments. A synchronous clock comparison between two regions of the 3D lattice yields a $5 times 10^{-19}$ measurement precision in 1 hour of averaging time.



قيم البحث

اقرأ أيضاً

We report on the realization of a magneto-optical trap (MOT) for metastable strontium operating on the 2.92 $mu$m transition between the energy levels $5s5p~^3mathrm{P}_2$ and $5s4d~^3mathrm{D}_3$. The strontium atoms are initially captured in a MOT operating on the 461 nm transition between the energy levels $5s^2~^1mathrm{S}_0$ and $5s5p~^1mathrm{P}_1$, prior to being transferred into the metastable MOT and cooled to a final temperature of 6 $mu$K. Challenges arising from aligning the mid-infrared and 461 nm light are mitigated by employing the same pyramid reflector to realize both MOTs. Finally, the 2.92 $mu$m transition is used to realize a full cooling sequence for an optical lattice clock, in which cold samples of $^{87}mathrm{Sr}$ are loaded into a magic-wavelength optical lattice and initialized in a spin-polarized state to allow high-precision spectroscopy of the $5s^2~^1mathrm{S}_0$ to $5s5p~^3mathrm{P}_0$ clock transition.
Currently, the most accurate and stable clocks use optical interrogation of either a single ion or an ensemble of neutral atoms confined in an optical lattice. Here, we demonstrate a new optical clock system based on an array of individually trapped neutral atoms with single-atom readout, merging many of the benefits of ion and lattice clocks as well as creating a bridge to recently developed techniques in quantum simulation and computing with neutral atoms. We evaluate single-site resolved frequency shifts and short-term stability via self-comparison. Atom-by-atom feedback control enables direct experimental estimation of laser noise contributions. Results agree well with an ab initio Monte Carlo simulation that incorporates finite temperature, projective read-out, laser noise, and feedback dynamics. Our approach, based on a tweezer array, also suppresses interaction shifts while retaining a short dead time, all in a comparatively simple experimental setup suited for transportable operation. These results establish the foundations for a third optical clock platform and provide a novel starting point for entanglement-enhanced metrology, quantum clock networks, and applications in quantum computing and communication with individual neutral atoms that require optical clock state control.
We experimentally demonstrate a variation on a Sisyphus cooling technique that was proposed for cooling antihydrogen. In our implementation, atoms are selectively excited to an electronic state whose energy is spatially modulated by an optical lattic e, and the ensuing spontaneous decay completes one Sisyphus cooling cycle. We characterize the cooling efficiency of this technique on a continuous beam of Sr, and compare it with radiation pressure based laser cooling. We demonstrate that this technique provides similar atom number for lower end temperatures, provides additional cooling per scattering event and is compatible with other laser cooling methods. This method can be instrumental in bringing new exotic species and molecules to the ultracold regime.
The preparation of large, low-entropy, highly coherent ensembles of identical quantum systems is foundational for many studies in quantum metrology, simulation, and information. Here, we realize these features by leveraging the favorable properties o f tweezer-trapped alkaline-earth atoms while introducing a new, hybrid approach to tailoring optical potentials that balances scalability, high-fidelity state preparation, site-resolved readout, and preservation of atomic coherence. With this approach, we achieve trapping and optical clock excited-state lifetimes exceeding $ 40 $ seconds in ensembles of approximately $ 150 $ atoms. This leads to half-minute-scale atomic coherence on an optical clock transition, corresponding to quality factors well in excess of $10^{16}$. These coherence times and atom numbers reduce the effect of quantum projection noise to a level that is on par with leading atomic systems, yielding a relative fractional frequency stability of $5.2(3)times10^{-17}~(tau/s)^{-1/2}$ for synchronous clock comparisons between sub-ensembles within the tweezer array. When further combined with the microscopic control and readout available in this system, these results pave the way towards long-lived engineered entanglement on an optical clock transition in tailored atom arrays.
Optical frequency comparison of the 40Ca+ clock transition u_{Ca} (2S1/2-2D5/2, 729nm) against the 87Sr optical lattice clock transition u_{Sr}(1S0-3P0, 698nm) has resulted in a frequency ratio u_{Ca} / u_{Sr} = 0.957 631 202 358 049 9(2 3). The rapid nature of optical comparison allowed the statistical uncertainty of frequency ratio u_{Ca} / u_{Sr} to reach 1x10-15 in only 1000s and yielded a value consistent with that calculated from separate absolute frequency measurements of u_{Ca} using the International Atomic Time (TAI) link. The total uncertainty of the frequency ratio using optical comparison (free from microwave link uncertainties) is smaller than that obtained using absolute frequency measurement, demonstrating the advantage of optical frequency evaluation. We report the absolute frequency of ^{40}Ca+ with a systematic uncertainty 14 times smaller than our previous measurement [1].
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