arXiv subjects

A. V. Stolyarov

Publications and source records attributed to A. V. Stolyarov.

14 recordsLinked to original sources

arXiv2025

A relativistic coupled-cluster treatment of magnetic hyperfine structure of the $X^2Π$ and $A^2Σ^+$ states of OH isotopologues

$\textit{Ab initio}$ calculations of the parallel component of the magnetic dipole hyperfine structure (HFS) constant have been carried out for hydroxyl radical isotopologues ($^{16,17}$OH(D)) over the internuclear distance range $R \in [0.6, 1.8]$ Å. For the ground electronic state $X^2Π$, the HFS functions were evaluated for contributions induced by both oxygen and hydrogen nuclei. In addition, the hydrogen-induced HFS curve was calculated for the excited $A^2Σ^+$ state. The quantum-chemistry study employs a four-component relativistic coupled-cluster (CC) method, including excitations up to the triple level, namely: the contribution of triple-cluster amplitudes was studied both perturbatively (CCSD(T)) and through fully iterative calculations (CCSDT). The resulting oxygen- and hydrogen-induced HFS functions represent the most accurate and reliable theoretical predictions to date exhibiting excellent agreement with semiempirical curve for hydrogen-induced HFS derived from high-resolution spectroscopic data for the lowest vibrational levels ($v\in [0,2]$) of the electronic $X^2Π$ state. Vibrationally averaged $\textit{ab initio}$ values are consistent with experimental values within $1\%$ for all states considered. Furthermore, the internuclear distance range over which the HFS curves are defined has been extended beyond that of previous studies, thereby providing a robust foundation for accurate HFS treatments of higher-lying rovibrational levels of OH isotopologues within both adiabatic and non-adiabatic frameworks.

physics.chem-ph↗

arXiv2023

Fourier-transform spectroscopy and global deperturbation treatment of the $A^1Σ^+_u$ and $b^3Π_u$ states of K$_2$ in the entire bound energy range

Rotationally-resolved Fourier-transform spectra of laser-induced fluorescence (LIF) $A^1Σ^+_u\sim b^3Π_u \rightarrow X^1Σ^+_g$ of K$_2$ molecules were recorded and analyzed yielding 4053 term values of spin-orbit (SO) coupled $A \sim b$ complex of $^{39}$K$_2$ isotopologue with ca 0.01 cm$^{-1}$ accuracy. Their compilation with 1739 term values from previously published sources allowed to cover the energy range [9955, 17436] cm$^{-1}$ from the bottom of the lower-lying $b^3Π_u$ state up to the vicinity of the atomic asymptote $4s\;^2{\rm S}_{1/2}$ + $4p\;^2{\rm P}_{1/2}$, with rotational quantum number $J\in[0,149]$. The experimental data were processed by a direct 6$\times$6 coupled-channel (CC) deperturbation treatment, which accounted explicitly for both SO and electronic-rotational interactions between six states: $A^1Σ^+_u$($0$), $b^3Π_u$(0,1,2), $c^3Σ_u$(1), and $B^1Π_u$(1). The initial parameters of the global deperturbation model have been estimated in the framework of {\it ab initio} electronic structure calculations applying multi-referenced configuration-interaction and coupled-clusters methods. The interatomic potentials analytically defined for $A$ and $b$ states, as well as SO-splitting of the triplet $b$ state and $A\sim b$ SO-coupling functions have been refined to fit 5792 term values of the $^{39}$K$_2$ isotopologue, whereas the rest parameters were fixed on their {\it ab initio} values. The resulting mass-invariant parameters of the CC model reproduced the overall rovibronic term energies of the $A \sim b$ complex of $^{39}$K$_2$ with the accuracy, which is well within the experimental errors. This deperturbation analysis provided the refined dissociation energy $T_{dis}$=17474.569(5) cm$^{-1}$ and the long-range coefficient $C_3^Σ$ = 5.501(4) $\times10^5$cm$^{-1}$ A$^3$ relevant to the non-relativistic atomic limit $4s$+$4p$.

physics.atom-ph↗

arXiv2023

The ground-state potential and dipole moment of carbon monoxide: contributions from electronic correlation, relativistic effects, QED, adiabatic, and non-adiabatic corrections

The ground X1Σ+ state potential energy curve (PEC) and dipole moment curve (DMC) of CO molecule have been revisited within the framework of the relativistic coupled-cluster approach, which incorporates non-perturbative single, double, and triple cluster amplitudes (CCSDT) in conjunction with a finite-field methodology. The generalized relativistic pseudo-potential model was used for the effective introducing the relativity in all-electron correlation treatment and accounting the quantum-electrodynamics (QED) corrections within the model-QED-operator approach. The diagonal Born-Oppenheimer correction to PEC has been evaluated using the CCSD approach. The sensitivity of resulting PEC and DMC to variations in basis set parameters and regular intramolecular perturbations were considered as well. The present ab initio results are in a reasonable agreement with their most accurate semi-empirical counterparts.

physics.chem-ph↗

arXiv2022

Intensities of KCs $E(4)^1Σ^+\to (a^3Σ^+,X^1Σ^+)$ band system up to dissociation threshold: an interplay between spin-orbit, hyperfine and rovibronic coupling effects

The relative intensity distribution in the rotationally resolved laser-induced fluorescence spectra belonging to the $E(4)^1Σ^+\to (a^3Σ^+_1,X^1Σ^+)$ band systems of the KCs molecule was analyzed. The experimental intensities in doublet $P$,$R$ progressions assigned to spin-allowed $E\to X$ and spin-forbidden $E\to a$ transitions up to their common ground dissociation limit were described in the framework of a coupled-channels (CC) deperturbation model applied for the interacting \Xstate\ and \astate\ states. The CC intensity simulation was based solely on fixed electronic structure parameters as functions of the internuclear distance $R$, namely: accurate empirical potential energy curves for all three states, \emph{ab initio} estimates for matrix elements $A(R)$ of the hyperfine structure (HFS) , and transition dipole moments $d_{EX}(R)$ and $d_{Ea}(R)$. A comparison between the measured intensities and their theoretical counterparts demonstrates a strong competition between different intramolecular interactions. A weak spin-orbit coupling of the upper \Estate\ state with the remote $^3Π$ states is responsible for appearance of the $E\to a$ vibrational bands for the intermediate $v_a$-values. In turn, the HFS coupling between \Xstate\ and \astate\ states leads to peculiarities in $E\to (X,a)$ intensities, which are pronounced for high $v_{X/a}$-values in the vicinity of K(4$^2S$)+Cs(6$^2S$) dissociation threshold. Both adiabatic ro-vibrational and non-adiabatic electronic-rotational interactions explain the abrupt deviation of some observed $P/R$ intensity ratios from the expected Hönl-London factors.

physics.atom-ph↗

arXiv2022

The $a^3Σ^+$ state of KCs revisited: hyperfine structure analysis and potential refinement

Laser-induced fluorescence spectra of the $c^3Σ^+(v_{c},J_{c}=N_{c})\rightarrow a^3Σ^+(v_{a},N_{a} = J_{c} \pm 1)$ transitions excited from the ground $X^1Σ^+$ state of $^{39}$K$^{133}$Cs molecule were recorded with Fourier-transform spectrometer IFS125-HR (Bruker) at the highest achievable spectral resolution of 0.0063 cm${}^{-1}$. Systematic study of the hyperfine structure (HFS) of the $a^3Σ^+$ state for levels with $v_{a} \in [0, 27]$ and $N_{a} \in [24, 90]$ shows that the splitting monotonically increases with $v_{a}$. The spectroscopic study was supported by ab initio calculations of the magnetic hyperfine interaction in $X^1Σ^+$ and $a^3Σ^+$ states. The discovered variation of the electronic matrix elements with the internuclear distance $R$ is in a good agreement with the observed $v_{a}$-dependencies of the HFS. Overall set of available experimental data on the $a^3Σ^+$ state was used to improve the potential energy curve particularly near a bottom, providing the refined dissociation energy $D_e$=267.21(1) cm${}^{-1}$. The ab initio HFS matrix elements, combined with the empirical $X^1Σ^+$ and $a^3Σ^+$ PECs in the framework of the invented coupled-channel deperturbation model, reproduce the experimental term values of both ground states within 0.003 cm${}^{-1}$ accuracy up to their common dissociation limit.

physics.atom-ph↗

arXiv2021

ExoMol molecular line lists -- XLIII: Rovibronic molecular line list the low-lying two states of NaO

The sodium monoxide radical (NaO) is observed in night glow in the Earth's mesosphere and likely has astronomical importance. This study concerns the optical transitions within the ground X $^2Π$ state and to the very low-lying ($T_{\textrm e}\approx 2000$ cm$^{-1}$) excited A $^2Σ^+$ state. A line list consisting of rovibronic term values, allowed electric dipole transitions, Einstein coefficients, and partition functions for varying temperature are produced due to a variational solution of the coupled-channel Schrödinger equations using the program \Duo. MRCI \textit{ab initio} calculations characterising the potential energy curves of the both states, spin-orbit and $L$-uncoupling non-adiabatic matrix elements, as well as permanent and transition dipole moments were integral in formation of the final deperturbation model. \textit{Ab initio} potential energy curves are represented in the analytical Extended-Morse-Oscillator form and refined, along with the spin-orbit and $L$-uncoupling functions, by least-squares fitting to the available spectroscopic data. The input experimental data consisted of pure rotational transitions within the fine structure components of the X $^2Π$ state for $v''\in [0,3]$ vibrational levels as well as the rovibronic A $^2Σ^+(v'=0) \leftarrow$ X $^2Π(v''=0)$ transitions, both with limited coverage over rotational excitation. The lack of data detailing the vibrational structure of the X and A states prompts a request for further experimental study of higher excited levels which would provide a robust spectroscopic model. The NaO NaOUCMe line list is available via www.exomol.com and the CDS database.

physics.chem-ph↗

arXiv2019

The Photolysis of Aromatic Hydrocarbons Adsorbed on the Surfaces of Cosmic Dust Grains

The work is devoted to the adaptation of the results of laboratory studies of the laser-induced dissociation of molecules of benzene adsorbed on a quartz substrate to the conditions of the interstellar medium. Adsorption was performed under conditions of low temperature and deep vacuum. The difference between the photolysis of adsorbed molecules and molecules in the gas phase is identified. Significance of process of photolytic desorption in the interstellar conditions is analyzed, in particular, in the conditions of photodissociation regions. It is shown that the efficiency and dissociation channels of photolysis of adsorbed and gas phase benzene differ substantially. It is concluded that the photolysis of aromatic hydrocarbons adsorbed on the interstellar dust grains contributes a negligible fraction to the abundance of small hydrocarbons in the interstellar medium.

astro-ph.GA↗

arXiv2019

Fourier transform spectroscopy, relativistic electronic structure calculation, and coupled-channel deperturbation analysis of the fully mixed $A^1Σ^+_u$ and $b^3Π_u$ states of Cs$_2$

The 4503 rovibronic term values belonging to the mutually perturbed $A^1Σ^+_u$ and $b^3Π_u$ states of Cs$_2$ were extracted from laser induced fluorescence (LIF) $A\sim b\rightarrow X^1Σ^+_g$ Fourier transform spectra with the 0.01 cm$^{-1}$ uncertainty. The experimental term values of the $A^1Σ^+_u\sim b^3Π_u$ complex covering the rotational levels $J\in [4,395]$ in the excitation energy range $[9655,13630]$ cm$^{-1}$ were involved into coupled-channel (CC) deperturbation analysis. The deperturbation model takes explicitly into account spin-orbit coupling of the $A^1Σ^+_u(A0^+_u)$ and $b^3Π^+_{0_u}(b0^+_u)$ states as well as spin-rotational interaction between the $Ω=0$, $1$ and $2$ components of the $b^3Π^+_{Ω_u}$ state. The \emph{ab initio} relativistic calculations on the low-lying electronic states of Cs$_2$ were accomplished in the framework of Fock space relativistic coupled cluster (FSRCC) approach to provide the interatomic potentials of the interacting $A0^+_u$ and $b0^+_u$ states as well as the relevant $A\sim b$ spin-orbit coupling function. To validate the present CC deperturbation analysis solely obtained by energy-based data, the $A\sim b \to X(v^{\prime\prime}_X)$ LIF intensity distributions were measured and compared with their theoretical counterparts obtained by means of the non-adiabatic vibrational wave functions of the $A\sim b$ complex and the FSRCC $A\sim b \to X$ transition dipole moments calculated by the finite-field method.

physics.atom-ph↗

arXiv2019

Energy and radiative properties of the (3)1Π and (5)1Σ+ states of RbCs: Experiment and theory

We combined high-resolution Fourier-transform spectroscopy and large-scale electronic structure calculation to study energy and radiative properties of the high-lying (3)1Π and (5)1Σ+ states of the RbCs molecule. The laser-induced (5)1Σ+(4)1Σ+(3)1Π-A(2)1Σ+ b(1)3Π fluorescence (LIF) spectra were recorded by the Bruker IFS-125(HR) spectrometer in the frequency range ν 5500 to 10000cm-1 with the instrumental resolution of 0.03 cm-1. The rotational assignment of the observed LIF progressions, which exhibit irregular vibrational-rotational spacing due to strong spin-orbit interaction between A1Σ+ and b3(Π) states was based on the coincidences between observed and calculated energy differences. The required rovibronic term values of the strongly perturbed A-b complex have been calculated by a coupled-channels approach for both 85Rb133Cs and 87Rb133Cs isotopologs with accuracy of about 0.01 cm-1, as demonstrated in A. Kruzins et al. [J. Chem. Phys. 141, 184309 (2014)]. The experimental energies of the upper (3)1(Π) and (5)1Σ+ states were involved in a direct-potential-fit analysis performed in the framework of inverted perturbation approach. Quasirelativistic ab initio calculations of the spin-allowed (3)1Π,(5)1Σ+- (1-4)1Σ+(1-3)1Π transition dipole moments were performed. Radiative lifetimes and vibronic branching ratios of radiative transitions from the (3)1Π and (5)1Σ+ states were evaluated. To elucidate the origin of the Λ-doubling effect in the (3)1Π state, the angular coupling (3)1Π-(1-5)1Σ+ electronic matrix elements were calculated and applied for the relevant q-factors estimate. The intensity distributions simulated for the particular (5)1Σ+(3)1Π-A-b LIF progressions have been found to be remarkably close to their experimental counterparts.

physics.atom-ph↗

arXiv2016

The twofold diabatization of the KRb $(1\sim 2)^1Π$ complex in the framework of \emph{ab initio} and deperturbation approaches

We performed a diabatization of the mutually perturbed $1^1Π$ and $2^1Π$ states of KRb based on both electronic structure calculation and direct coupled-channel deperturbation analysis of experimental energies. The potential energy curves (PECs) of the diabatic states and their scalar coupling were constructed from the \textit{ab initio} adiabatic PECs by analytically integrating the radial $\langle ψ_1^{ad}|\partial /\partial R|ψ_2^{ad}\rangle$ matrix element obtained by a finite-difference method. The diabatic potentials and electronic coupling function were refined by the least squares fitting of the rovibronic termvalues of the $1^1Π\sim 2^1Π$ complex. The empirical PECs combined with the coupling function as well as the diabatized spin-orbit coupling and transition dipole matrix elements are useful for further deperturbation treatment of both singlet and triplet states manifold.

physics.chem-ph↗

arXiv2011

Global analysis of data on the spin-orbit coupled $A^{1}Σ_{u}^{+}$ and $b^{3}Π_{u}$ states of Cs2

We present experimentally derived potential curves and spin-orbit interaction functions for the strongly perturbed $A^{1}Σ_{u}^{+}$ and $b^{3}Π_{u}$ 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 Aimé Cotton primarily to study the $X ^{1}Σ_{g}^{+}$ state. More recent work at Tsinghua University provides information from moderate resolution spectroscopy on the lowest levels of the $b^{3}Π_{0u}^{\pm}$ 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.

physics.atom-ph↗

arXiv2010

Identification of Deeply Bound Heteronuclear Molecules Using Pulsed Laser Depletion Spectroscopy

We demonstrate that a near-dissociation photoassociation resonance can be used to create a deeply bound molecular sample of ultracold NaCs. To probe the resulting vibrational distribution of the sample, we use a new technique that can be applied to any ultracold molecular system. We utilize a tunable pulsed dye laser to produce efficient spectroscopic scans ($\sim700$ cm$^{-1}$ at a time) in which we observe the $1^{1} Σ^{+}\rightarrow 2^{1}Σ^{+}-2^{3}Π$ vibrational progression, as well as the dissociation limit to the Cs 6$^{2}$P$_{3/2}$ asymptote. We assign $1^{1} Σ^{+}$$(\emph{v}$ = 4, 5, 6, 11, 19) vibrational levels in our sample.

physics.atom-ph↗

arXiv2010

On Oscillation Theorem for Two-Component Schrodinger Equation

Conventional one-dimensional oscillation theorem is found to be violated for multi-component Schrödinger equations in a general case while for two-component eigenstates coupled by the sign-constant potential operator the following statements are valid: (1) the ground state ($v = 0$) is not degenerate; and (2) the arithmetic mean of nodes $n_1$, $n_2$ for the two-component wavefunction never exceeds the ordering number $v$ of eigenstate: $(n_1 + n_2)/2\leq v$.

physics.atom-ph↗

arXiv2009

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.

physics.atom-ph↗