We report on the measurement of Stark shifted energy levels of 87 Rb Rydberg atoms in static electric fields by means of electromagnetically induced transparency (EIT). Electric field strengths of up to 500 V cm −1 , ranging beyond the classical ionization threshold, were applied using electrodes inside a glass cell with rubidium vapour. Stark maps for principal quantum numbers n = 35 and n = 70 have been obtained with high signal-to-noise ratio for comparison with results from ab initio calculations following the method described in (Zimmerman et al 1979 Phys. Rev. A 20 2251 ), which was originally only verified for states around n = 15. We also calculate the dipole matrix elements between low-lying states and Stark shifted Rydberg states to give a theoretical estimate of the relative strength of the EIT signal. The present work significantly extends the experimental verification of this numerical method in the range of both high principal quantum numbers and high electric fields with an accuracy of up to 2 MHz.
We report on the measurement of Stark shifted energy levels of 87 Rb Rydberg atoms in static electric fields by means of electromagnetically induced transparency (EIT). Electric field strengths of up to 500 V cm −1 , ranging beyond the classical ionization threshold, were applied using electrodes inside a glass cell with rubidium vapour. Stark maps for principal quantum numbers n = 35 and n = 70 have been obtained with high signal-to-noise ratio for comparison with results from ab initio calculations following the method described in (Zimmerman et al 1979 Phys. Rev. A 20 2251 ), which was originally only verified for states around n = 15. We also calculate the dipole matrix elements between low-lying states and Stark shifted Rydberg states to give a theoretical estimate of the relative strength of the EIT signal. The present work significantly extends the experimental verification of this numerical method in the range of both high principal quantum numbers and high electric fields with an accuracy of up to 2 MHz.
In this work, numerical calculations were implemented based on the diagonalisation of a matrix representation of the Stark Hamiltonian on a subset of the basis given by the zero-field Hamiltonian. Dipole matrix elements between the involved states were calculated, which allow for the prediction of transition strengths to Stark shifted Rydberg states. The applicability of the numerical methods were confirmed experimentally by precision spectroscopy in a rubidium vapour cell with electrodes using electromagnetically induced transparency (EIT). The numerical methods were then extended to predict ionisation rates of Rydberg states in the highly Stark shifted regime beyond the classical ionisation threshold. For this purpose, a complex absorbing potential (CAP) was specifically adjusted to the Stark Hamiltonian. An experiment was conducted, in which cold atoms from a magneto-optical trap (MOT) were excited to Stark shifted Rydberg states and the arising ions were detected. The obtained ionisation spectra agree well with the results from the numerical calculations. Another extension of the numerical methods was implemented for crossed electric and magnetic fields. This was used for approximate calculations of the motional Stark effect (MSE), which acts on atoms moving through static magnetic fields and thereby experiencing a Lorentz electric field. In a precision spectroscopy, once more using EIT in a vapour cell, the MSE was observed in low magnetic fields for the first time in rubidium. The spectral shift, which is caused by the MSE, matches the prediction from the numerical calculations. In a final experiment, the practical use of the knowledge of several properties of Stark shifted Rydberg states was illustrated. The numerical methods including the CAP were used to specifically select states for their optical accessibility, permanent electric dipole moments and ionisation rates. In the experiment, atoms from a MOT were excited to these states to observe different characteristics of the dipole blockade effect. The detection scheme for this experiment was realised by controlled ionisation using only small changes in the external electric field.
We report on the observation and numerical calculation of ionization spectra of highly Stark-shifted Rydberg states of rubidium beyond the classical ionization threshold. In the numerical calculations, a complex absorbing potential (CAP) allows us to predict the energy levels and ionization rates of Rydberg states in this regime. Our approach of adjusting the CAP to the external electric field reduces the number of free parameters from one per resonance to a single one. Furthermore, we have measured the ionization spectra of magneto-optically trapped rubidium atoms which are excited to principal quantum numbers of 43 and 70 at various electric fields. The emerging ions are detected using an ion optics. We find good agreement between the numerically and experimentally obtained spectra.
Rydberg-assisted atomic electrometry with thermal vapors offers a promising approach for detecting external electric fields. However, this technique presents significant challenges for measuring low frequencies due to the effects of metal-alkali atoms adsorbed on the interior surface of the vacuum chamber. In this work, we apply high-contrast Rydberg electromagnetically induced transparency (EIT) spectroscopy to systematically investigate these effects, including the influence of laser power and electric field strength. We demonstrate the ability to measure electric field frequencies ranging from 10 Hz to 1 MHz. Additionally, this study identifies a fundamental limit for data capacity in such measurements. Furthermore, we propose a method for precise Stark shift measurements by locking the coupling laser to Zeeman-split Rydberg EIT peaks. Using the Zeeman shift in a reference cell as a stable frequency reference, we are able to track Stark-induced shifts in a science cell and confirm excellent agreement with theoretical predictions. These results provide valuable insights for future precision measurement techniques and field sensing applications based on Rydberg atom systems.
Rydberg atoms are highly excited atoms with large principal quantum number n, big sizes (~n2) and long lifetimes (~n3). Rydberg atoms are very sensitive to an external field due to the large polarizabilities of Rydberg atoms (~n7). Electromagnetically induced transparency (EIT) of Rydberg atom provides an ideal method to detect Rydberg atoms without destroying atoms, and can be used to measure the external direct current and radio frequency (RF) field. In this paper, we study the EIT effect of a cesium ladder-type three-level atom involving Rydberg state exposed to a weak RF field. The ground state (6S1/2), the excited state (6P3/2) and Rydberg state (48D5/2) constitute the Rydberg three-level system, in which the probe laser couples 6S1/2(F=4)6P3/2(F'=5) transition, whereas the coupling laser scans across the 6P3/248D5/2 Rydberg transition. The coupling laser (510 nm laser, propagating in the z-axis direction and linear polarization in the y-axis direction) and the probe laser (852 nm laser, linear polarization in the y-axis direction) counter-propagate through a 50-mm-long cesium vapor cell at room temperature, yielding Rydberg EIT spectra. Rydberg EIT signal is detected as a function of the detuning of the coupling laser. When a weak RF (80 MHz) electric field polarized in the x-axis direction is applied to a pair of electrode plates located on both sides of the cesium cell, the EIT spectrum of Rydberg 48D5/2 shows the Stark splitting and the even order harmonic sidebands. The experimental results are analyzed by using the Floquet theory. The simulation results accord well with the experimentally measured results. Furthermore, we also investigate the influence of the self-ionization effect of Rydberg atom on the Stark spectrum by changing the RF frequency. We put forward a proposal to avoid the effect of ionization by placing electrode plates in the cesium cell. In the weak RF-field domain, mj=5/2 Stark line crosses mj=1/2, 3/2 sidebands, these cross points provide an antenna-free method of accurately calibrating the RF electric field based on Rydberg atoms.
The interaction between an electric field and the energy levels of Rydberg states results in the Stark effect, which can be used for quantum detection by measuring the frequency shift in electromagnetically induced transparency (EIT) spectra. By using the functional relationship between the frequency shift and the electric field, it is possible to measure the electric field in question. However, the mismatch between the probe laser and the polarization direction of the coupled laser leads to errors in the measurement of the frequency shift, affecting the accurate measurement of the electric field. In this work, the Schrödinger equation is solved by perturbation method to derive the functional relationship between the energy offset and the electric field strength. Then, the functional relationship between the energy offset and the electric field strength is brought into the solution of the density matrix equation, and the influences of the polarization direction of the detected light and coupled light on the EIT-Stark mathematical model are analyzed. Then an internal electrode method is used to prevent shielding effects caused by alkali metal atoms adhering to the surface of the atomic vapor cell, thereby enabling the application of the electric field. The calibration of the Rydberg state polarisation rate is achieved by using a standard source and measuring the frequency shift of the EIT spectrum. Finally, the effects of polarisation mismatch on the measurement results of EIT spectrum and the electric field are verified by modulating the laser polarization direction. The experimental data show that when the polarization directions of the probe laser and coupled laser are parallel to each other, it is the most matched polarization direction for the lasers, the peak value of the EIT spectrum is the largest, and the maximum relative error of the electric field measurement is 1.67%. When the angle between the polarisation directions of the probe light and the coupled light laser is 45°, the laser polarisation mismatch is the most severe, the EIT spectral peak is the lowest and the maximum relative error of the electric field measurement is 10.24%.
The high polarizability of Rydberg atoms enables the multi-parameters measurement of electromagnetic fields. In this paper, we report on an atomic antenna based on Rydberg atoms in a room temperature vapor cell. The EIT is a destructive interference spectroscopy with a narrow linewidth and can be used to detect small electric fields through Autler-Townes splitting or Stark shifts. In our experiments, we employ cascade-type two-photon excitation electromagnetically induced transparency (EIT) spectroscopy to measure the shift of the Rydberg energy level. We introduce a low-frequency electric field (~kHz frequency) using a built-in electrode technique in the cesium cell. The interaction between the Rydberg atom and electric field induces the Stark shifts, where the amplitude of the electric field is converted into corresponding two-photon detuning by the EIT effect. Furthermore, the amplitude of the low-frequency electric field is converted into an intensity signal of EIT probe beam. Under weak field conditions, it is an approximate linear relationship between EIT transmission signal and input electric field amplitude, enabling measurement of waveform, amplitude, and frequency. We have demonstrated optical measurements of low-frequency electric field using Rydberg atoms. By increasing the power of probe beam and coupling beam, the EIT can increase the response bandwidth from ~MHz to hundreds of MHz. This provides a scalable approach for measuring high-frequency electric fields.