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Controlling Rydberg atoms in external electric fields

Jens Grimmel

Published Jan 1, 2018• 0 citations
Publisher

Abstract

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.

DOI
10.15496/publikation-22988

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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.
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.
Rydberg atoms, i.e. atoms with one or more highly excited electrons, show exaggerated properties compared to ground state atoms. For example, their energy levels are very sensitive to external electric fields (Stark effect) and they exhibit strong interatomic interactions, which can lead to a suppression of excitation known as the Rydberg blockade. The latter property makes Rydberg atoms promising candidates for quantum simulation and quantum computing. This work describes the direct observation of the excitation blockade for highly Stark-shifted Rydberg atoms induced by controllable dipole-dipole interactions. We investigate the electric field region around and above the classical ionization threshold, which is typically not considered suitable for blockade experiments. We excite Rydberg atoms in the energy region corresponding to the unperturbed 43S1/2 state at electric fields around 127V/cm out of a magneto-optically trapped cloud of 87Rb atoms with a temperature of 150 μK. We tune the dipole-dipole interaction by the applied electric field thus changing the electric dipole moment of the excited state. The position of the Rydberg atoms is detected by ionization and subsequent ion imaging; the controlled ionization of the atoms is achieved by adiabatic transfer of the Rydberg state to an ionizing state. For the spatially resolved detection of the atoms, a high resolution ion microscope for cold atoms has been developed and experimentally characterized. It features a maximum magnification of 1000 and sub-micrometer spatial resolution. A theoretical treatment of highly Stark-shifted Rydberg states is developed introducing a complex absorbing potential. It is capable of predicting the ionization rates of the Rydberg states for a wide range of electric fields and energies with only one free parameter. Together with the numerical calculations, measurements of the ionization spectra for different Rydberg states are presented. The 43S1/2 state is measured in an electric-field range from 125V/cm to 165V/cm (classical ionization limit 127V/cm), the 70S1/2 state in an electric-field range from 15V/cm to 35V/cm (classical ionization limit 16.1V/cm) and the 100S1/2 state in an electric-field range from 7V/cm to 19V/cm (classical ionization limit 3.7V/cm). Our results show an intricate energy level structure with broad, strongly ionizing states as well as sharp, nearly non-ionizing states. The numerical calculations are also used for the prediction of selective field ionization spectra and the results are used to identify Förster resonances in the Stark spectrum of the 45D5/2 state. Complementary to the spatially resolved measurements in high electric fields, the Rydberg blockade effect is also observed via the excitation number statistics at Förster resonances.
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.
Ultracold Rydberg atoms in a static electric field can exchange energy via the dipole-dipole interaction. The Stark effect shifts the energy levels of the atoms which tunes the energy exchange into resonance at specific values of the electric field (F\"orster resonances). We excite rubidium atoms to Rydberg states by focusing either a 480 nm beam from a tunable dye laser or a pair of diode lasers into a magneto-optical trap. The trap lies at the center of a configuration of electrodes. We scan the electric field by controlling the voltage on the electrodes while measuring the fraction of atoms that interact. Dipole-dipole interaction spectra are presented for initially excited rubidium ndndnd states for n=31n=31n=31 to 46 and for four different pairs of initially excited rubidium nsnsns states. We also present the dipole-dipole interaction spectra for individual rubidium 32ddd (j,mj)(j,\phantom{\rule{0.16em}{0ex}}{m}_{j})(j,mj​) fine structure levels that have been selectively excited. The data are compared to calculated spectra.
Rydberg spectroscopy of rubidium cold atoms trapped in a magneto-optical trap (MOT) was performed in a quartz cell. When electric fields acting on the atoms generated by a plate external to the cell were continuously applied, electric charges on the cell walls were created, as monitored on the Rydberg spectra. Avoiding accumulation of the charges and realizing good control over the applied electric field was instead obtained when the fields were applied only for a short time, typically a few microseconds. In a two-photon excitation via the 62P state to the Rydberg state, the laser resonant with the 52S-62P transition photoionizes the excited state. The photoionization-created ions produce an internal electric field which deforms the excitation spectra, as monitored on the Autler-Townes absorption spectra.