Aleksander N. Petrov
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Previous Organizations / Institutes
The organizations / institutes from the scholar's other articles in the past ten years
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Research Interests
Aleksander N. Petrov has a total of 215 co-authors. Here are the top co-authors by number of shared publications:
- Anatoly Vladimirovich Titov
Petersburg Nuclear Physics Institute of National Research Center “Kurchatov Institute”, Gatchina, Russia
37 shared publications - Leonid V. Skripnikov
Petersburg Nuclear Physics Institute
34 shared publications - Nikolai Sergeevich Mosyagin
Petersburg Nuclear Physics Institute, Gatchina, Leningrad District 188300, Russia
24 shared publications Svetlana Kotochigova
Department of Physics, Temple University, Philadelphia, Pennsylvania 19122, USA
12 shared publicationsA. V. Titov
National Research Centre "Kurchatov Institute" B.P. Konstantinov Petersburg Nuclear Physics Institute 188300 Gatchina Leningrad district Russia
10 shared publications- Timur A. Isaev
Chemistry Dept M. Lomonosov Moscow State University 119991 Moscow Russia
9 shared publications
Latest Publications
- 28 October 2026
- Published by AIP Publishing in The Journal of Chemical Physics
- Vol. 165 (16)
Dipole moment of the YbOH molecule
The YbOH molecule is a sensitive system to use in searches for fundamental symmetry violations. Its molecular-frame permanent and transition dipole moments are of key importance for preparing and interpreting experiments. We calculate these quantities for the lowest bending vibrational modes of the ground electronic state. A high-level coupled cluster method for electronic structure calculations, together with averaging over vibrational states, was employed to obtain accurate values.
- 28 October 2026
- Published by AIP Publishing in The Journal of Chemical Physics
- Vol. 165 (16)
Dipole moment of the YbOH molecule
The YbOH molecule is a sensitive system to use in searches for fundamental symmetry violations. Its molecular-frame permanent and transition dipole moments are of key importance for preparing and interpreting experiments. We calculate these quantities for the lowest bending vibrational modes of the ground electronic state. A high-level coupled cluster method for electronic structure calculations, together with averaging over vibrational states, was employed to obtain accurate values.
- 13 August 2026
- Published by American Physical Society (APS) in Physical Review A
- Vol. 114 (2) , 022812
Electric-field-dependent g factors of RaOCH 3 molecule
The sensitivity of experiments searching for the electron electric-dipole moment ($e\mathrm{EDM}$) using the symmetric top molecules can be greatly enhanced by laser cooling. A detailed understanding of the Zeeman structure of the $e\mathrm{EDM}$-sensitive levels is crucial for controlling systematic effects. We develop a method for calculating the $g$ factors of $K$-doublet levels in symmetric top molecules and apply it to ${\mathrm{RaOCH}}_{3}$. The electric-field-dependent $g$ factors of the first excited rotational level of ${\mathrm{RaOCH}}_{3}$ are calculated. We find that the $K$ doublet with a total angular momentum projection ${M}_{F}=2$ has a ratio $\mathrm{\ensuremath{\Delta}}g/g\phantom{\rule{0.16em}{0ex}}\ensuremath{\sim}{10}^{\ensuremath{-}6}$ for an electric field in the range from 500 mV/cm to 1 V/cm, where $\mathrm{\ensuremath{\Delta}}g$ is the difference in the $g$ factors for the $K$-doublet components.- 13 August 2026
- Published by American Physical Society (APS) in Physical Review A
- Vol. 114 (2) , 022812
Electric-field-dependent g factors of RaOCH 3 molecule
The sensitivity of experiments searching for the electron electric-dipole moment ($e\mathrm{EDM}$) using the symmetric top molecules can be greatly enhanced by laser cooling. A detailed understanding of the Zeeman structure of the $e\mathrm{EDM}$-sensitive levels is crucial for controlling systematic effects. We develop a method for calculating the $g$ factors of $K$-doublet levels in symmetric top molecules and apply it to ${\mathrm{RaOCH}}_{3}$. The electric-field-dependent $g$ factors of the first excited rotational level of ${\mathrm{RaOCH}}_{3}$ are calculated. We find that the $K$ doublet with a total angular momentum projection ${M}_{F}=2$ has a ratio $\mathrm{\ensuremath{\Delta}}g/g\phantom{\rule{0.16em}{0ex}}\ensuremath{\sim}{10}^{\ensuremath{-}6}$ for an electric field in the range from 500 mV/cm to 1 V/cm, where $\mathrm{\ensuremath{\Delta}}g$ is the difference in the $g$ factors for the $K$-doublet components.- 16 October 2025
- Published by AIP Publishing in The Journal of Chemical Physics
- Vol. 163 (15)
Impact of ligand (OH) deformation on LuOH+ rovibrational spectra
Triatomic cation 175LuOH+, featuring near-degenerate, opposite-parity l-doublets, offers enhanced sensitivity to P- and T-violating interactions. We present ab initio calculations of its electronic structure and rovibrational structure beyond the rigid-ligand approximation by explicitly including OH-ligand deformation together with bending and stretching motions. Potential-energy surfaces are computed at the relativistic coupled cluster level of theory. The nuclear Schrodinger equation in Jacobi coordinates is solved by means of a coupled-channel expansion. Ligand deformation reduces the bending frequency by a few percent and increases the l-doubling constant q, while the stretching frequencies and rotational constants remain largely unchanged. For the first excited bending level, we predict ΔEJ=1 = 2q ≈ 24.9–26.4 MHz. These results establish LuOH+ as a viable platform for precision searches for CP-violating physics via the electron electric dipole moment and the nuclear magnetic quadrupole moment.
- 16 October 2025
- Published by AIP Publishing in The Journal of Chemical Physics
- Vol. 163 (15)
Impact of ligand (OH) deformation on LuOH+ rovibrational spectra
Triatomic cation 175LuOH+, featuring near-degenerate, opposite-parity l-doublets, offers enhanced sensitivity to P- and T-violating interactions. We present ab initio calculations of its electronic structure and rovibrational structure beyond the rigid-ligand approximation by explicitly including OH-ligand deformation together with bending and stretching motions. Potential-energy surfaces are computed at the relativistic coupled cluster level of theory. The nuclear Schrodinger equation in Jacobi coordinates is solved by means of a coupled-channel expansion. Ligand deformation reduces the bending frequency by a few percent and increases the l-doubling constant q, while the stretching frequencies and rotational constants remain largely unchanged. For the first excited bending level, we predict ΔEJ=1 = 2q ≈ 24.9–26.4 MHz. These results establish LuOH+ as a viable platform for precision searches for CP-violating physics via the electron electric dipole moment and the nuclear magnetic quadrupole moment.
- 24 September 2025
- Published by American Physical Society (APS) in Physical Review A
- Vol. 112 (3)
Hyperfine structure and doubling in the molecule- 24 September 2025
- Published by American Physical Society (APS) in Physical Review A
- Vol. 112 (3)
Hyperfine structure and doubling in the molecule- Open Access
Impact of ligand (OH) deformation on LuOH$^+$ rovibrational spectra
Triatomic cation $^{175}$LuOH$^+$, featuring near-degenerate, opposite-parity $l$-doublets, offers enhanced sensitivity to $\mathcal{P}$- and $\mathcal{T}$-violating interactions. We present \emph{ab initio} calculations of its electronic structure and rovibrational structure beyond the rigid-ligand approximation by explicitly including OH-ligand deformation together with bending and stretching motions. Potential-energy surfaces are computed at the relativistic coupled cluster level of theory. The nuclear Schrödinger equation in Jacobi coordinates is solved by means of a coupled-channel expansion. Ligand deformation reduces the bending frequency by a few percent and increases the $l$-doubling constant $q$, while the stretching frequencies and rotational constants remain largely unchanged. For the first excited bending level, we predict $ΔE_{J=1}=2q \approx 24.9$--$26.4$ MHz. These results establish LuOH$^+$ as a viable platform for precision searches for $\mathcal{CP}$-violating physics via the electron electric dipole moment and the nuclear magnetic quadrupole moment.Open AccessImpact of ligand (OH) deformation on LuOH$^+$ rovibrational spectra
Triatomic cation $^{175}$LuOH$^+$, featuring near-degenerate, opposite-parity $l$-doublets, offers enhanced sensitivity to $\mathcal{P}$- and $\mathcal{T}$-violating interactions. We present \emph{ab initio} calculations of its electronic structure and rovibrational structure beyond the rigid-ligand approximation by explicitly including OH-ligand deformation together with bending and stretching motions. Potential-energy surfaces are computed at the relativistic coupled cluster level of theory. The nuclear Schrödinger equation in Jacobi coordinates is solved by means of a coupled-channel expansion. Ligand deformation reduces the bending frequency by a few percent and increases the $l$-doubling constant $q$, while the stretching frequencies and rotational constants remain largely unchanged. For the first excited bending level, we predict $ΔE_{J=1}=2q \approx 24.9$--$26.4$ MHz. These results establish LuOH$^+$ as a viable platform for precision searches for $\mathcal{CP}$-violating physics via the electron electric dipole moment and the nuclear magnetic quadrupole moment. - 24 June 2025
- Published by American Physical Society (APS) in Physical Review A
- Vol. 111 (6)
Electric-field-dependent factors of- 24 June 2025
- Published by American Physical Society (APS) in Physical Review A
- Vol. 111 (6)
Electric-field-dependent factors of- Open Access
Electric field dependent g factors of ThF$^+$
The g-factors for $J = 1$, $F=3/2$, $|M_F|=3/2$ hyperfine levels of the ground electronic state $^3Δ_1$ of the $^{232}$ThF$^+$ cation are calculated as functions of the external electric field. These calculations are necessary for the analysis of systematic effects in the experiment aimed at searching for the electron electric dipole moment.Open AccessElectric field dependent g factors of ThF$^+$
The g-factors for $J = 1$, $F=3/2$, $|M_F|=3/2$ hyperfine levels of the ground electronic state $^3Δ_1$ of the $^{232}$ThF$^+$ cation are calculated as functions of the external electric field. These calculations are necessary for the analysis of systematic effects in the experiment aimed at searching for the electron electric dipole moment. - 24 September 2024
- Published by American Physical Society (APS) in Physical Review A
- Vol. 110 (3) , L030804
Electric-field-dependent factors of a YbOH moleculeThe YbOH molecule is one of the most sensitive systems for the electron electric dipole moment () searches. Zeeman splittings of the sensitive levels have significant implications to control and suppress important systematic effects due to stray magnetic fields in experiments for searches. The electric-field-dependent factors of the lowest rotational level of the first excited bending vibrational mode of are calculated. -doublet levels with a small -factor difference are found and main contributions to the difference are determined.- 24 September 2024
- Published by American Physical Society (APS) in Physical Review A
- Vol. 110 (3) , L030804
Electric-field-dependent factors of a YbOH moleculeThe YbOH molecule is one of the most sensitive systems for the electron electric dipole moment () searches. Zeeman splittings of the sensitive levels have significant implications to control and suppress important systematic effects due to stray magnetic fields in experiments for searches. The electric-field-dependent factors of the lowest rotational level of the first excited bending vibrational mode of are calculated. -doublet levels with a small -factor difference are found and main contributions to the difference are determined.- Top Cited Papers
- 12 July 2024
- Published by IOP Publishing in Reports on Progress in Physics
- Vol. 87 (8) , 084301
Opportunities for fundamental physics research with radioactive molecules
Molecules containing short-lived, radioactive nuclei are uniquely positioned to enable a wide range of scientific discoveries in the areas of fundamental symmetries, astrophysics, nuclear structure, and chemistry. Recent advances in the ability to create, cool, and control complex molecules down to the quantum level, along with recent and upcoming advances in radioactive species production at several facilities around the world, create a compelling opportunity to coordinate and combine these efforts to bring precision measurement and control to molecules containing extreme nuclei. In this manuscript, we review the scientific case for studying radioactive molecules, discuss recent atomic, molecular, nuclear, astrophysical, and chemical advances which provide the foundation for their study, describe the facilities where these species are and will be produced, and provide an outlook for the future of this nascent field.
- 12 July 2024
- Published by IOP Publishing in Reports on Progress in Physics
- Vol. 87 (8) , 084301
Top Cited PapersOpportunities for fundamental physics research with radioactive molecules
Molecules containing short-lived, radioactive nuclei are uniquely positioned to enable a wide range of scientific discoveries in the areas of fundamental symmetries, astrophysics, nuclear structure, and chemistry. Recent advances in the ability to create, cool, and control complex molecules down to the quantum level, along with recent and upcoming advances in radioactive species production at several facilities around the world, create a compelling opportunity to coordinate and combine these efforts to bring precision measurement and control to molecules containing extreme nuclei. In this manuscript, we review the scientific case for studying radioactive molecules, discuss recent atomic, molecular, nuclear, astrophysical, and chemical advances which provide the foundation for their study, describe the facilities where these species are and will be produced, and provide an outlook for the future of this nascent field.
- 26 January 2024
- Published by American Physical Society (APS) in Physical Review A
- Vol. 109 (1) , 012819
Electronic matrix elements for parity doubling in the YbOH molecule
The YbOH molecule is one of the most sensitive systems for electron electric dipole moment (eEDM) searches. The eEDM-induced energy shift is proportional to the polarization of the molecule. Petrov and Zakharova [A. Petrov and A. Zakharov, Phys. Rev. A 105, L050801 (2022)] showed that the value of doubling and spin-rotation splitting directly influence the maximum value of . Recently, Jadbabaie et al. [A. Jadbabaie, Y. Takahashi, N. H. Pilgram, C. J. Conn, Y. Zeng, C. Zhang, and N. R. Hutzler, New J. Phys. 25, 073014 (2023)] determined the corresponding energy levels experimentally. We introduce electronic matrix elements in the Hund's case coupling scheme to reproduce experimental energy levels and calculate as a function of external electric field.- 26 January 2024
- Published by American Physical Society (APS) in Physical Review A
- Vol. 109 (1) , 012819
Electronic matrix elements for parity doubling in the YbOH molecule
The YbOH molecule is one of the most sensitive systems for electron electric dipole moment (eEDM) searches. The eEDM-induced energy shift is proportional to the polarization of the molecule. Petrov and Zakharova [A. Petrov and A. Zakharov, Phys. Rev. A 105, L050801 (2022)] showed that the value of doubling and spin-rotation splitting directly influence the maximum value of . Recently, Jadbabaie et al. [A. Jadbabaie, Y. Takahashi, N. H. Pilgram, C. J. Conn, Y. Zeng, C. Zhang, and N. R. Hutzler, New J. Phys. 25, 073014 (2023)] determined the corresponding energy levels experimentally. We introduce electronic matrix elements in the Hund's case coupling scheme to reproduce experimental energy levels and calculate as a function of external electric field.