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IEEE Ukrainian Microwave Week (UkrMW)

Laser-Microwave Spectrometer for Studying Mercury Atoms in Rydberg States

Stanislav F. Dyubko, Mykola L. Pogrebnyak, E. A. Alekseev, Michail Perepechaj

Published Sep 21, 2020• 0 citations
Publisher

Abstract

A modification of the laser - microwave spectrometer for studying mercury atoms in Rydberg np and nf states is presented. To test the operability of the performed modification of the laser pump system, the optical excitation spectrum of Rydberg states of mercury atoms was recorded. From the ground 61S0 state to Rydberg np and nf states mercury atoms were excited according to a two-stage scheme: to the intermediate 61D2 with two-photon absorption of the second harmonic radiation from the Rhodamine 560 dye laser, and from the intermediate state to np and nf states by the radiation of a LDS-751 dye laser, which may be tuned in the wavelength range from 751 nm to 790 nm. The performed tests show the operability of the selected scheme for pumping mercury atoms into Rydberg states.

DOI
10.1109/ukrmw49653.2020.9252587

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Acta Physica Sinica•Jan 1, 2017•6 citations
A modification of the laser - microwave spectrometer for studying mercury atoms in Rydberg np and nf states is presented. To test the operability of the performed modification of the laser pump system, the optical excitation spectrum of Rydberg states of mercury atoms was recorded. From the ground 61S0 state to Rydberg np and nf states mercury atoms were excited according to a two-stage scheme: to the intermediate 61D2 with two-photon absorption of the second harmonic radiation from the Rhodamine 560 dye laser, and from the intermediate state to np and nf states by the radiation of a LDS-751 dye laser, which may be tuned in the wavelength range from 751 nm to 790 nm. The performed tests show the operability of the selected scheme for pumping mercury atoms into Rydberg states.
In order to investigate an interaction of an electromagnetic field with Rydberg atoms it is necessary to transfer atoms from ground state to Rydberg state with specified values of quantum numbers. The point is that for each chemical element the way of producing Rydberg atom atoms is strictly individual. In this paper Al atoms are transferred to Rydberg states by nF scheme using a system of lasers and frequency converters on nonlinear crystals. The Au atoms are brought to Rydberg state by three stages of laser excitation.
We present new experimental data on the highly excited levels in mercury using the optogalvanic detection technique in conjunction with a dc discharge cell. The collisionally populated 6s6p 3P2 metastable level has been used as an intermediate level to access the Rydberg states using a frequency-doubled dye laser covering the wavelength region between 370 and 249 nm. The optogalvanic data reveal 6sns 3S1(13≤n≤50), 6snd 2D1(6≤n≤18), 6snp 3D1(6≤n≤14), 6snd 3D2(6≤n≤15), and 6snd 3D3(6≤n≤59) Rydberg series. The 6sns 3S1 and 6snd 3D3 Rydberg series to such a high n value have been reported for the first time. In addition, collisionally induced parity-forbidden transitions 6snp 3P1(44≤n≤50) have been detected.
Isotopically selective resonance ionization of mercury atoms has been accomplished by three-step excitation via the 6 3P1 and 8 1S0 excited states. Three collinear beams, respectively 254, 286, and 532 nm, from two dye lasers and a pulsed neodymium:yttrium aluminum garnet (ND:YAG) pump laser, were passed through a closed mercury vapor cell containing electrodes to which the ions were drawn by an electric field. The ion current and the 254-nm fluorescence radiation were measured as a function of laser wavelengths. Hyperfine structures for the 254- and 286-nm transitions were observed.
A new type of electron/photon coincidence experiment is presented which utilises a laser -electron stepwise excitation technique to prepare atoms in an excited state. An electron collision initially excites an atom from the ground state to an intermediate state. Following this electron excitation process, coherent single mode laser radiation further excites the atom to an upper state, from which the fluorescence is observed. The nature of the laser excitation transfers both amplitude and phase information about the electron excited state to the upper excited state in a coherent way. This information is extracted from the upper state fluorescence by analysis of the fluorescence polarization in coincidence with the electron scattered from the atom for particular polarizations of the laser radiation. The coincidence technique allows an identically prepared sub -ensemble of excited atoms to be selected for measurement. The electron excited state studied was the 61131 state of mercury, excited by a beam of unpolarized electrons at an impact energy of 16 eV. The mercury atomic beam was isotopically selected following electron excitation using the narrow bandwidth of the laser radiation. Excitation from the electron excited 61P1 state was via 579 nm laser radiation to the 61D2 state and fluorescence was monitored from this state to the 63P1 state via a 313 nm transition. Stokes parameters were measured for two different laser polarization angles, since this allowed a complete set of collision parameters to be deduced for a single experimental geometry. Results for three different scattering angles at this energy are presented. The laser excitation process was modelled in both the weak and the strong laser excitation regimes. A perturbation approach developed to model single photon laser excitation allowed the collision parameters to be extracted from the measured coincidence Stokes parameters analytically, whereas a Quantum Electrodynamic model allowed high laser intensity effects on the coincidence signal to be explored theoretically. The Quantum Electrodynamic model indicated that the weak excitation model could be used to extract the collision parameters from the Stokes parameters at the laser intensities used in the experiment. Effects due to variation of the laser intensity were predicted from the Quantum Electrodynamic model and experiments conducted to test these predictions are presented. Collision parameters deduced from the measured stepwise coincidence Stokes parameters following optimization of the experimental conditions are presented. These parameters are compared qualitatively with existing data from heavy atomic systems and with a theoretical model based upon the Distorted Wave Born Approximation. Similarities between the experimental data are found, however significant discrepancies are noted between the parameters obtained here and with the predictions of the theoretical model.
The spectra of Rydberg atoms are of great significance for studying the energy levels of Rydberg atoms and the interaction between neutral atoms, especially, the high-precision spectra of Rydberg atoms can be used to measure the energy level shifts of Rydberg atoms resulting from the dipole-dipole interactions in room-temperature vapor cells. In this paper we report the preparation of cesium Rydberg states based on the cascaded two-photon excitation of 509 nm laser and 852 nm laser in opposite, and the measurements of the fine structure of cesium Rydberg states. In this experiment, the 509 nm laser is generated by the cavity-enhanced second-harmonic generation from 1018 nm laser with a periodically-poled KTP crystal and has a maximum power of about 1 W, and the 852 nm probe laser is provided by an external-cavity diode laser with a maximum output power of 5 mW and a typical linewidth of 1 MHz. By scanning the frequency of 509 nm coupling laser, it is presented that the Doppler-free spectra based on electromagnetically-induced transparency (EIT) of 509 nm coupling laser and 852 nm probe laser. The velocity-selective EIT spectra are used to study the spectral splitting of 6S1/26P3/257S(D) ladder-type system of cesium Rydberg atoms in a room-temperature vapor cell. The powers of 852 nm probe laser and 509 nm coupling laser are 0.3 upW and 200 mW, respectively. Their waist radii are both approximately 50 m. The intervals of hyperfine splitting of the intermediate state 6P3/2(F'=3, 4, 5) and fine splitting of 57D3/2 and 57D5/2 Rydberg states are measured by a frequency calibrating. Concretely, the velocity-selective spectrum with a radio frequency (RF) modulation of 30 MHz is used as a reference to calibrate the Rydberg fine-structure states in the hot vapor cell, where the RF frequency precision is smaller than a hertz on long time scales and the EIT linewidth is smaller than 13 MHz. The experimental value of the fine structure splitting of 57D3/2 and 57D5/2 Rydberg states is (354.72.5) MHz, that is in consistence with the value of 346.8 MHz calculated by Rydberg-Ritz equation and quantum defects of 57D3/2 and 57D5/2 Rydberg states. The experimental values of hyperfine splitting of intermediate state 6P3/2(F'=3, 4, 5) are also coincident with the theoretical calculated values. The dominant discrepancy existing between the experimental and calculated results may arise from the nonlinear correspondence of the PZT while the 509 nm wavelength cavity is scanned, and the measurement accuracy influenced by the spectral linewidth. The velocity-selective spectroscopy technique can also be used to measure the energy level shifts caused by the interactions of Rydberg atoms.