The coupling of the X1Σ+^{1}\Sigma ^{+} and a3Σ+^{3}\Sigma ^{+} states of KRb

A comprehensive study of the electronic states at the 4s+5s asymptote in KRb is presented. Abundant spectroscopic data on the \astate state were collected by Fourier-transform spectroscopy which allow to determine an accurate experimental potential energy curve up to 14.8 \AA . The existing data set (C. Amiot et al. J. Chem. Phys. 112, 7068 (2000)) on the ground state \Xstate was extended by several additional levels lying close to the atomic asymptote. In a coupled channels fitting routine complete molecular potentials for both electronic states were fitted. Along with the line frequencies of the molecular transitions, recently published positions of Feshbach resonances in $^{40}$K and $^{87}$Rb mixtures (F. Ferlaino et al. Phys. Rev. A 74, 039903 (2006)) were included in the fit. This makes the derived potential curves capable for an accurate description of observed cold collision features so far. Predictions of scattering lengths and Feshbach resonances in other isotopic combinations are reported.Comment: 14 pages, 5 figure

The potential of the ground state of NaRb

The X$^{1}\Sigma ^{+}$ state of NaRb was studied by Fourier transform spectroscopy. An accurate potential energy curve was derived from more than 8800 transitions in isotopomers $^{23}$Na$^{85}$Rb and $^{23}$Na$^{87}$Rb. This potential reproduces the experimental observations within their uncertainties of 0.003 \rcm to 0.007 \rcm. The outer classical turning point of the last observed energy level ($v''=76$, $J''=27$) lies at $\approx 12.4$ \AA, leading to a energy of 4.5 \rcm below the ground state asymptote.Comment: 8 pages, 6 figures and 2 table

Morphology Influence on Wettability and Wetting Dynamics of ZnO Nanostructure Arrays

This study has been supported by internal research grant No. 14-95/2021/10 of Daugavpils University “Development of the Nanostructured Metal Oxide Coatings and Their Application in Optical Sensing for Heavy Metal Detection”.Changes in nanostructure morphology and size may result in very different surface wettability. In this research, the impact of different morphological parameters on the wetting dynamics of ZnO nanostructured layers is studied. Six different morphologies are chosen to determine the specific wetting processes of ZnO nanostructures: nanoneedles, small diameter rods, large diameter rods, nanotubes, nanoplates, and plain thin films. Wetting dynamics is investigated using conventional sessile drop technique and a novel approach based on electrochemical impedance spectroscopy. The results show that the surface of nanostructured ZnO thin films exhibits both hydrophilic and hydrophobic wetting behaviour, depending on nanostructure form, size, and orientation. ZnO nanostructure arrays are a promising platform for electrochemical and optical sensing in aqueous solutions. The full and effective use of the sensor working surface can be ensured only under the condition of complete wetting of the nanostructured layer. Therefore, it is important to take into account the peculiarities of the wetting process of a specific morphology of nanostructures. © 2022 V. Gerbreders et al., published by Sciendo.Institute of Solid State Physics, University of Latvia has received funding from the European Union’s Horizon 2020 Framework Programme H2020-WIDESPREAD-01-2016-2017-TeamingPhase2 under grant agreement No. 739508, project CAMART2

Level-crossing spectroscopy of the 7, 9, and 10D_5/2 states of 133Cs and validation of relativistic many-body calculations of the polarizabilities and hyperfine constants

We present an experimental and theoretical investigation of the polarizabilities and hyperfine constants of D_J states in 133Cs for J=3/2 and J=5/2. New experimental values for the hyperfine constant A are obtained from level-crossing signals of the (7,9,10)D_5/2 states of 133Cs and precise calculations of the tensor polarizabilities alpha_2. The results of relativistic many-body calculations for scalar and tensor polarizabilities of the (5-10)D_3/2 and (5-10)D_5/2 states are presented and compared with measured values from the literature. Calculated values of the hyperfine constants A for these states are also presented and checked for consistency with experimental values.Comment: 12 pages, revtex4, 11 figure file

Fourier transform spectroscopy and coupled-channel deperturbation treatment of the A1Sigma+ ~ b3Pi complex of KCs molecule

The laser induced fluorescence (LIF) spectra A1Sigma ~ b3Pi --> X1Sigma+ of KCs dimer were recorded in near infrared region by Fourier Transform Spectrometer with a resolution of 0.03 cm-1. Overall more than 200 LIF spectra were rotationally assigned to 39K133Cs and 41K133Cs isotopomers yielding with the uncertainty of 0.003-0.01 cm-1 more than 3400 rovibronic term values of the strongly mixed singlet A1Sigma+ and triplet b3Pi states. Experimental data massive starts from the lowest vibrational level v_A=0 of the singlet and nonuniformly cover the energy range from 10040 to 13250 cm-1 with rotational quantum numbers J from 7 to 225. Besides of the dominating regular A1Sigma+ ~ b3P Omega=0 interactions the weak and local heterogenous A1S+ ~ b3P Omega=1 perturbations have been discovered and analyzed. Coupled-channel deperturbation analysis of the experimental 39K133Cs e-parity termvalues of the A1S+ ~ b3P complex was accomplished in the framework of the phenomenological 4 x 4 Hamiltonian accounting implicitly for regular interactions with the remote states manifold. The resulting diabatic potential energy curves of the interacting states and relevant spin-orbit coupling matrix elements defined analytically by Expanded Morse Oscillators model reproduce 95% of experimental data field of the 39K133Cs isotopomer with a standard deviation of 0.004 cm-1 which is consistent with the uncertainty of the experiment. Reliability of the derived parameters was additionally confirmed by a good agreement between the predicted and experimental termvalues of 41K133Cs isotopomer. Calculated intensity distributions in the A ~ b --> X LIF progressions are also consistent with their experimental counterparts.Comment: 17 pages, 14 figure

Global analysis of data on the spin-orbit coupled A1Σu+A^{1}\Sigma_{u}^{+} and b3Πub^{3}\Pi_{u} states of Cs2

We present experimentally derived potential curves and spin-orbit interaction functions for the strongly perturbed $A^{1}\Sigma_{u}^{+}$ and $b^{3}\Pi_{u}$ states of the cesium dimer. The results are based on data from several sources. Laser-induced fluorescence Fourier transform spectroscopy (LIF FTS) was used some time ago in the Laboratoire Aim\'{e} Cotton primarily to study the $X ^{1}\Sigma_{g}^{+}$ state. More recent work at Tsinghua University provides information from moderate resolution spectroscopy on the lowest levels of the $b^{3}\Pi_{0u}^{\pm}$ states as well as additional high resolution data. From Innsbruck University, we have precision data obtained with cold Cs$_{2}$ molecules. Recent data from Temple University was obtained using the optical-optical double resonance polarization spectroscopy technique, and finally, a group at the University of Latvia has added additional LIF FTS data. In the Hamiltonian matrix, we have used analytic potentials (the Expanded Morse Oscillator form) with both finite-difference (FD) coupled-channels and discrete variable representation (DVR) calculations of the term values. Fitted diagonal and off-diagonal spin-orbit functions are obtained and compared with {\it ab initio} results from Temple and Moscow State universities

Angular momentum spatial distribution symmetry breaking in Rb by an external magnetic field

Excited state angular momentum alignment -- orientation conversion for atoms with hyperfine structure in presence of an external magnetic field is investigated. Transversal orientation in these conditions is reported for the first time. This phenomenon occurs under Paschen Back conditions at intermediate magnetic field strength. Weak radiation from a linearly polarized diode laser is used to excite Rb atoms in a cell. The laser beam is polarized at an angle of pi/4 with respect to the external magnetic field direction. Ground state hyperfine levels of the 5S_1/2 state are resolved using laser-induced fluorescence spectroscopy under conditions for which all excited 5P_3/2 state hyperfine components are excited simultaneously. Circularly polarized fluorescence is observed to be emitted in the direction perpendicular to both to the direction of the magnetic field B and direction of the light polarization E. The obtained circularity is shown to be in quantitative agreement with theoretical predictions.Comment: Accepted for publication in Phys. Rev.