اشترك بالحزمة الذهبية واحصل على وصول غير محدود شمرا أكاديميا
تسجيل مستخدم جديدNumber-resolved imaging of excited-state atoms using a scanning autoionization microscope
57
0
0.0
(
0
)
اسأل ChatGPT حول البحث
ﻻ يوجد ملخص باللغة العربية
We report on a scanning microscopy technique for atom-number-resolved imaging of excited-state atoms. A tightly focused laser beam leads to local autoionization, and the resulting ions are counted electronically. Scanning the beam across the cloud builds up an image of the density distribution of excited atoms, with access to the full counting statistics at each spatial sampling point and an overall detection efficiency of 21 %. We apply this technique to the measurement of a spatially inhomogeneous electric field with a spatial resolution of 50 ?m and a sensitivity to electric field gradients of 0.04 V cm$^{-2}$.
قيم البحث
اقرأ أيضاً
We demonstrate number-resolved detection of individual strontium atoms in a long working distance low numerical aperture (NA = 0.26) tweezer. Using a camera based on single-photon counting technology, we determine the presence of an atom in the tweez
er with a fidelity of 0.989(6) (and loss of 0.13(5)) within a 200 $mu$s imaging time. Adding continuous narrow-line Sisyphus cooling yields similar fidelity, at the expense of much longer imaging times (30 ms). Under these conditions we determine whether the tweezer contains zero, one or two atoms, with a fidelity $>$0.8 in all cases with the high readout speed of the camera enabling real-time monitoring of the number of trapped atoms. Lastly we show that the fidelity can be further improved by using a pulsed cooling/imaging scheme that reduces the effect of camera dark noise.
We successfully demonstrate a quantum gas microscopy using the Faraday effect which has an inherently non-destructive nature. The observed Faraday rotation angle reaches 3.0(2) degrees for a single atom. We reveal the non-destructive feature of this
Faraday imaging method by comparing the detuning dependence of the Faraday signal strength with that of the photon scattering rate. We determine the atom distribution with deconvolution analysis. We also demonstrate the absorption and the dark field Faraday imaging, and reveal the different shapes of the point spread functions for these methods, which are fully explained by theoretical analysis. Our result is an important first step towards an ultimate quantum non-demolition site-resolved imaging and furthermore opens up the possibilities for quantum feedback control of a quantum many-body system with a single-site resolution.
We demonstrate electromagnetic induction imaging with an unshielded, portable radio-frequency atomic magnetometer scanning over the target object. This configuration satisfies standard requirements in typical applications, from security screening to
medical imaging. The ability to scan the magnetometer over the object relies on the miniaturization of the sensor head and on the active compensation of the ambient magnetic field. Additionally, a procedure is implemented to extract high-quality images from the recorded spatial dependent magnetic resonance. The procedure is shown to be effective in suppressing the detrimental effects of the spatial variation of the magnetic environment.
A barrier to realizing the potential of molecules for quantum information science applications is a lack of high-fidelity, single-molecule imaging techniques. Here, we present and theoretically analyze a general scheme for dispersive imaging of elect
ronic ground-state molecules. Our technique relies on the intrinsic anisotropy of excited molecular rotational states to generate optical birefringence, which can be detected through polarization rotation of an off-resonant probe laser beam. Using arb and rbcs as examples, we construct a formalism for choosing the molecular state to be imaged and the excited electronic states involved in off-resonant coupling. Our proposal establishes the relevant parameters for achieving degree-level polarization rotations for bulk molecular gases, thus enabling high-fidelity nondestructive imaging. We additionally outline requirements for the high-fidelity imaging of individually trapped molecules.
We present quantum mechanical calculations of Auger decay rates for two Rubidium Rydberg atoms with weakly overlapping electron clouds. We neglect exchange effects and consider tensor products of independent atom states forming an approximate basis o
f the two-electron state space. We consider large sets of two-atom states with randomly chosen quantum numbers and find that the charge overlap between the two Rydberg electrons allows one to characterise the magnitude of the Auger decay rates. If the electron clouds overlap by more than one percent, the Auger decay rates increase approximately exponentially with the charge overlap. This finding is independent of the energy of the initial state.
سجل دخول لتتمكن من نشر تعليقات
التعليقات
جاري جلب التعليقات
سجل دخول لتتمكن من متابعة معايير البحث التي قمت باختيارها
