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Konstantin Gaul

Publications and source records attributed to Konstantin Gaul.

At least 19 recordsLinked to original sources

A linear rotor trapped and coupled to the vibrational modes of an ion crystal

When molecular ions are trapped together with atomic ions in a Paul trap, their dipole moment couples the molecular rotation to the joint vibrational motion of the particles in the trap. To leverage this coupling for quantum control, a rotational transition in the molecule should be resonant with one of the ion crystal vibrational modes. Focusing on the example of singly charged thorium fluoride molecular ions, cotrapped with two ytterbium ions, we determine the conditions for resonant dipole-phonon coupling, fully accounting for the molecular hyperfine structure. We identify several choices for resonant coupling and discuss its detection using sideband-resolved laser spectroscopy and measurements of decoherence.

quant-ph

Multiply charged uranium monoxide as a versatile probe of fundamental physics

Multiply charged actinide molecules provide a unique platform to study fundamental physics and the chemical bond under extreme conditions. Beyond the inherently large relativistic effects associated with a high proton number $Z$, an increased molecular charge can further enhance the electronic sensitivity to symmetry-violating nuclear effects, including nuclear Schiff moments. Experimental investigations of multiply charged actinide molecules are challenging because the high charges severely destabilize chemical bonds, leading to spontaneous Coulomb explosion. We demonstrate a method to systematically generate and detect molecular ions at the edge of chemical stability. By applying high-fluence laser ablation to a depleted uranium metal foil, we produce atomic uranium ions U$^{z+}$ and uranium monoxide cations UO$^{z+}$ with $z = 1$--4. Among them, we observe UO$^{3+}$ and UO$^{4+}$, which exhibit comparatively simple electronic structures and are therefore promising for precision spectroscopy. The experiments are supported by relativistic density functional theory calculations of equilibrium bond lengths, charge distributions, and binding energies of all observed molecules. Calculations of symmetry-violating properties suggest a pronounced sensitivity of UO$^{3+}$ to hadronic $CP$ violation. This approach opens a pathway for high-precision investigations of fundamental symmetries and the exploration of relativistic actinide chemistry in previously inaccessible regimes.

physics.chem-ph

Enhanced sensitivity to variations of fundamental constants in highly charged molecules from analytic perturbation theory

Quasi-forbidden electronic transitions in atoms and vibronic transitions between quasi-degenerate states in molecules serve as powerful probes of hypothetical temporal variations of fundamental constants. Computation of the sensitivity of a transition to a variation of the fine-structure constant is conventionally performed by numerical variation of the speed of light in sophisticated electronic structure calculations, and therewith several individual calculations have to be performed. An approach is presented herein that obtains sensitivity coefficients as perturbation to the Dirac-Coulomb Hamiltonian and allows, for instance, computation of their leading-order contributions as expectation values of the relativistic kinetic energy and rest-mass operators. These are available in essentially all \emph{ab initio} relativistic electronic structure codes. Additionally, the corresponding operators for two-component Hamiltonians are derived, explicitly for the zeroth order regular approximation Hamiltonian. The approach is applied to demonstrate great sensitivity of highly charged polar molecules that were recently proposed for high-precision spectroscopy in [Zülch \emph{et al.}, arXiv:2203.10333[physics.chem-ph]]. In particular, a high sensitivity of a wealth of quasi-degenerate vibronic transitions in \ce{PaF^3+} and \ce{CeF^2+} to temporal variations of the fine-structure constant and the electron-proton mass ratio is shown.

physics.chem-ph

Rigorous extension of semilocal collinear functionals to noncollinear DFT using $SU(2)$ rotations

In the presence of spin-orbit coupling and in geometrically frustrated materials, a noncollinear treatment the magnetization density is essential. However, in density functional theory most exchange--correlation functional approximations were originally developed for locally collinear magnetization. Many practical approaches to noncollinear DFT have emerged over the past decade. However, a first-principles connection between widely used semilocal collinear functionals and their noncollinear generalizations remains lacking. In this work, a locally exact relation between collinear and noncollinear exchange--correlation functionals is derived at the level of gradient expansions within a $u(2)$ matrix representation of the energy functional. Within this framework, collinear semilocal variables naturally acquire distinct dependencies on transverse and longitudinal magnetization gradient components. The widely used Scalmani--Frisch scheme emerges as a first-order approximation. The transformation of collinear functional derivatives to noncollinear space is implemented through numerically robust $SU(2)$ rotations. A consistent description of local magnetic torques is demonstrated for the prototypical spin-frustrated Cr$_3$ cluster. The approach further extends to fully nonlocal functionals and provides a direct route towards numerically stable relativistic response calculations. The influence on magnetic properties in presence of spin-orbit coupling is illustrated through calculations of hyperfine couplings in the high-spin ground states of uranium and the uranium ion.

physics.chem-ph

Laser fluence-dependent production of molecular thorium ions in different charge states for trapped-ion experiments

Thorium ions and molecules, recognized for their distinctive nuclear and atomic attributes, are central to numerous trapped-ion experiments globally. Our study introduces an effective, compact source of thorium ions produced via laser ablation of microgram-scale, salt-based samples. We thoroughly analyze the variety of ion species and charge states generated at varying laser fluences. Utilizing 10$μ$g of thorium fluoride crystals and laser fluences between $1.00 - 7.00$ J$\cdot$cm$^{-2}$ we produce thorium molecular ions $^{232}$ThF$_x$$^{n+}$ (with $x= 0 - 3$ and charge states up to $n = 3+$), including ThF$^{2+}$ and ThF$^{3+}$. These species are particularly relevant for spectroscopy; ThF$^{3+}$ is valuable for its stable closed-shell configuration, while ThF$^{2+}$, which is isoelectronic to RaF, offers a unique probe for studying nuclear structure and fundamental symmetries due to its simple electronic structure with a single unpaired electron. Density functional theory calculations of the distribution of positive charge in the produced molecular cations and the simplicity of this setup indicate that this method is easily transferable to other actinide systems.

physics.atom-ph

Constraints on new vector boson mediated electron-nucleus interactions from spectroscopy of polar diatomic molecules

A measurement of parity violation in the hyperfine structure of $^{138}$Ba$^{19}$F [E. Altuntaş et al. Phys. Rev. Lett. 120, 142501 (2018)] is reinterpreted with electronic structure calculations in terms of beyond Standard Model vector boson mediated electron-nucleus interactions. Our results set constraints on previously unexplored, new boson mediated axial vector-vector nucleus-electron interactions. Similar bounds are obtained by analyzing the atomic parity violation experiment with $^{133}$Cs. Moreover, we show that future experiments with cold heavy diatomic molecules like $^{225}$RaF can improve the present sensitivity to axial vector-vector nucleus-electron and nucleon-nucleus interactions by up to five orders of magnitudes.

hep-ph

Relativistic and quantum electrodynamics effects on NMR shielding tensors of Tl$X$ ($X$ = H, F, Cl, Br, I, At) molecules

Results of relativistic calculations of nuclear magnetic resonance shielding tensors ($σ$) for the thallium monocation (Tl$^+$), thallium hydride (TlH) and thallium halides (TlF, TlCl, TlBr, TlI, and TlAt) are presented as obtained within a four-component polarization propagator formalism and a two-component linear response approach within the zeroth-order regular approximation. Additionally, some quantum electrodynamical (QED) effects on those NMR shieldings are estimated. A strong dependence of $σ$(Tl) on the bonding partner is found, together with a very weak dependence of QED effects with them. In order to explain the trends observed, the excitation patterns associated with relativistic $ee$ (or paramagnetic-like) and $pp$ (or diamagnetic-like) contributions to $σ$ are analyzed. For this purpose, also the electronic spin-free and spin-dependent contributions are separated within the two-component zeroth-order regular approximation, and the influence of spin-orbit coupling on involved molecular orbitals is studied, which allows for a thorough understanding of the underlying mechanisms.

physics.chem-ph

Towards detection of molecular parity violation via chiral co-sensing: the $^1$H/$^{31}$P model system

Fundamental weak interactions have been shown to violate parity in both nuclear and atomic systems. However, observation of parity violation in a molecular system has proven an elusive target. Nuclear spin dependent contributions of the weak interaction are expected to result in energetic differences between enantiomers manifesting in nuclear magnetic resonance (NMR) spectra as chemical shift differences on the order of $10^{-6}$ Hz to $10^{-3}$ Hz for high-$Z$ nuclei. By employing simultaneous measurements of the diastereomeric splittings for a light and a heavy nucleus in solution-state NMR, residual chemical shift differences persisting in non-chiral environment between enantiomers of chiral compounds smaller than the typical linewidth of high-field NMR may be resolved. Sources of error must be identified and minimized to verify that the observed effect is, in fact, due to parity violation and not systematic effects. This paper presents a detailed analysis of a system incorporating \textsuperscript{31}P and \textsuperscript{1}H NMR to elucidate the systematic effects and to guide experiments with higher-$Z$ nuclei where molecular parity violation may be resolved.

physics.chem-ph

Quantum electrodynamic corrections for molecules: Vacuum polarisation and electron self energy in a two-component relativistic framework

Vacuum polarisation (VP) and electron self energy (SE) are implemented and evaluated as quantum electrodynamic (QED) corrections in a (quasi-relativistic) two-component zeroth order regular approximation (ZORA) framework. For VP, the Uehling potential is considered, and for SE, the effective potentials proposed by Flambaum and Ginges as well as the one proposed by Pyykkö and Zhao. QED contributions to ionisation energies of various atoms and group 2 monofluorides, group 1 and 11 valence orbital energies, $^2\mathrm{P}_{1/2} \leftarrow {}^{2}\mathrm{S}_{1/2}$ and $^{2}\mathrm{P}_{3/2} \leftarrow {}^{2}\mathrm{S}_{1/2}$ transition energies of Li-, Na-, and Cu-like ions of nuclear charge $Z$ = 10, 20, ..., 90 as well as $Π_{1/2}\leftarrow Σ_{1/2}$ and $Π_{3/2}\leftarrowΣ_{1/2}$ transition energies of BaF and RaF are presented. Furthermore, perturbative and self-consistent treatments of QED corrections are compared for Kohn--Sham orbital energies of gold. It is demonstrated, that QED corrections can be obtained in a two-component ZORA framework efficiently and in excellent agreement with corresponding four-component results.

physics.chem-ph

Stopping mass-selected alkaline-earth metal monofluoride beams of high energy via formation of unusually stable anions

Direct laser-coolability and a comparatively simple electronic structure render alkaline-earth metal monofluoride molecules versatile laboratories for precision tests of fundamental physics. In this theoretical work, a route for efficient stopping and cooling of high-energy hot beams of mass-selected alkaline-earth metal monofluorides via their anions is explored to facilitate subsequent precision experiments with trapped molecules. It is shown that these molecular anions possess an unusually strong chemical bond and that RaF$^-$ features properties favourable for efficient pre-cooling, indicating the applicability of direct laser-cooling of the anion.

physics.chem-ph

Global analysis of CP-violation in atoms, molecules and role of medium-heavy systems

Detection of parity (P) and time-reversal (T) symmetry-odd electric dipole moments (EDMs) within currently achievable resolution would evidence physics beyond the Standard Model of particle physics. Via the CPT-theorem, which includes charge conjugation (C), such low-energy searches complement high-energy physics experiments that probe CP-violation up to the TeV scale. Heavy-elemental atoms and molecules are considered to be among the most promising candidates for a first direct detection of P,T-violation due to enhancement effects that increase steeply with increasing nuclear charge number $Z$. However, different P,T-odd sources on the subatomic level can contribute to molecular or atomic EDMs, which are target of measurements, and this complicates obtaining rigorous bounds on P,T-violation on a fundamental level. Consequently, several experiments of complementary sensitivity to these individual P,T-odd sources are required for this purpose. Herein, a simply-applicable qualitative model is developed for global analysis of the P,T-odd parameter space from an electronic-structure theory perspective. Rules of thumb are derived for the choice of atoms and molecules in terms of their angular momenta and nuclear charge number. Contrary to naive expectations from $Z$-scaling laws, it is demonstrated that medium-heavy molecules with $Z\leq54$ can be of great value to tighten global bounds on P,T-violating parameters, in particular, if the number of complementary experiments increases. The model is confirmed by explicit density functional theory calculations of all relevant P,T-odd electronic structure parameters in systems that were used in past experiments or are of current interest for future experiments, respectively: the atoms Xe, Cs, Yb, Hg, Tl, Ra, Fr and the molecules CaOH, SrOH, YO, CdH, BaF, YbF, YbOH, HfF$^+$, WC, TlF, PbO, RaF, ThO, ThF$^+$ and PaF$^{3+}$.

hep-ph

$\mathcal{CP}$-violation sensitivity of closed-shell radium-containing polyatomic molecular ions

Closed-shell atoms and molecules such as Hg or TlF provide some of the best low-energy tests of hadronic $\mathcal{CP}$-violation which is considered to be a necessary ingredient to explain the observed excess of matter over antimatter in our universe. $\mathcal{CP}$-violation is, however, expected to be strongly enhanced in octupole deformed nuclei such as $^{225}$Ra. Recently, closed-shell radium-containing symmetric-top molecular ions were cooled sympathetically in a Coulomb crystal [M. Fan et al., Phys. Rev. Lett. 126, 023002 (2021)] and shown to be well-suited for precision spectroscopy in the search for fundamental physics [P. Yu and N. R. Hutzler, Phys. Rev. Lett. 126, 023003 (2021)]. In closed-shell molecules hadronic $\mathcal{CP}$-violation contributes to a net electric dipole moment (EDM) that violates parity and time-reversal symmetry ($\mathcal{P,T}$), which is the target of measurements. To interpret experiments, it is indispensable to know the electronic structure enhancement parameters for the various sources of $\mathcal{P,T}$-violation which contribute to the net $\mathcal{P,T}$-odd EDM. In this paper we employ relativistic Hartree--Fock and density functional theory calculations to determine relevant parameters for interpretation of possible EDM measurements in RaOCH$_3^+$, RaSH$^+$, RaCH$_3^+$, RaCN$^+$, and RaNC$^+$ and perform accurate relativistic coupled cluster calculations of the Schiff moment enhancement in RaSH$^+$ to gauge the quality of the density functional theory approach. Finally, we project to bounds on various fundamental $\mathcal{P,T}$-odd parameters that could be achievable from an experiment with RaOCH$_3^+$ in the near future and asses the complementarity of this experiment to experiments with Hg and TlF.

physics.atom-ph

Towards detection of molecular parity violation by microwave spectroscopy of CpRe(CH$_{3}$)(CO)(NO)

Parity-violating differences in rotational constants of a chiral 5d transition metal complex, that was previously experimentally well-characterised by broad-band microwave spectroscopy, are predicted with a recently established efficient analytical derivative technique. Relative differences $ΔX/X$ between rotational constants $X=A,B,C$ of enantiomers of the title compound are found to be on the order of $10^{-14}$, which is a favourably large effect. The quality of the theoretical estimates is carefully assessed by computing nuclear electric quadrupole coupling constants that agree well with experiment.

physics.chem-ph

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.

nucl-ex

Quasi-relativistic approach to analytical gradients of parity violating potentials

An analytic gradient approach for the computation of derivatives of parity-violating (PV) potentials with respect to displacements of the nuclei in chiral molecules is described and implemented within a quasirelativistic mean-field framework. Calculated PV potential gradients are utilised for estimating PV frequency splittings between enantiomers in rotational and vibrational spectra of four chiral polyhalomethanes, i.e. CHBrClF, CHClFI, CHBrFI and CHAtFI. Values calculated within the single-mode approximation for the frequency shifts agree well with previously reported theoretical values. The influence of non-separable anharmonic effects (multi-mode effects) on the vibrational frequency shifts, which are readily accessible with the present analytic derivative approach, are estimated for the C--F stretching fundamental of all four molecules and computed for each of the fundamentals in CHBrClF and CHAtFI. Multi-mode effects are found to be significant, in particular for the C--F stretching modes, being for some modes and cases of similar size as the single-mode contribution.

physics.chem-ph

Relativistic and QED corrections to one-bond indirect nulcear spin-spin couplings in X$_2^{2+}$ and X$_3^{2+}$ ions (X = Zn, Cd, Hg)

The indirect nuclear spin-spin coupling tensor, $\mathbf J$, between mercury nuclei in Hg-containing systems can be of the order of few kHz and one of the largest measured. We conduct an analysis of the physics behind the electronic mechanisms that contribute to the one- and two-bond couplings $^n {\mathbf J}_{\mathrm{Hg}-\mathrm{Hg}}$ ($n=1, 2$). We performed calculations for $J$-couplings in X$_2^{2+}$ and $X_3^{2+}$ ions ($X$ = Zn, Cd, Hg), within polarization propagator theory, using the random phase approximation (RPA) and the pure zeroth order approximation (PZOA), with Dirac-Hartree-Fock (DHF) and Dirac-Kohn-Sham (DKS) orbitals, both at four-component and ZORA levels. We show that the "paramagnetic-like" mechanism contribute with more than 99.98\% to the total isotropic component of the coupling tensor. By means of an analysis of the molecular and atomic orbitals involved in the total value of the response function, we find that the $s$-type valence atomic orbitals have a predominant role in the description of the coupling. This fact allows us to develop an effective model from which quantum electrodynamics (QED) effects on $J$-coupling in the aforementioned ions can be estimated. The estimated QED corrections were found in the interval $(0.7; ~ 1.7)$\% of the total relativistic effect on isotropic one-bond $^1 {\mathbf J}$ coupling and from the interval $(-0.2; ~ -0.4)$\%, in Zn-containing ions, to $(-0.8; ~ -1.2)$\%, in Hg-containing ions, of the total isotropic coupling constant in the studied systems. We also show that estimated QED corrections cast a visible dependence on the nuclear charge $Z$ of each atom $X$ in the form of a power-law $\propto Z^5$.

physics.chem-ph

Cool molecular highly charged ions for precision tests of fundamental physics

Molecules and atomic highly charged ions provide powerful low-energy probes of the fundamental laws of physics: Polar molecules possess internal fields suitable to enhance fundamental symmetry violation by several orders of magnitudes, whereas atoms in high charge states can feature large relativistic effects and compressed level structures, ideally posed for high sensitivity to variations of fundamental constants. Polar, highly charged molecules could benefit from both: large internal fields and large relativistic effects. However, a high charge dramatically weakens chemical bonding and drives systems to the edge of Coulomb explosion. Herein, we propose multiply-charged polar molecules, that contain actinides, as promising candidates for precision tests of physics beyond the standard model. Explicitly, we predict PaF$^{3+}$ to be thermodynamically stable, coolable and well-suited for precision spectroscopy. The proposed class of compounds, especially with short-lived actinide isotopes from the territory of pear-shaped nuclei, has potential to advance our understanding of molecules under extreme conditions, to provide a window into unknown properties of atomic nuclei, and to boost developments in molecular precision spectroscopy in various areas, such as optical clocks and searches for new physics.

physics.chem-ph

Parity nonconserving interactions of electrons in chiral molecules with cosmic fields

Pseudoscalar or pseudovector cosmic fields, that serve as a source of parity ($\mathcal{P}$) violation, are invoked in different models for cold dark matter or in the standard model extension that allows for Lorentz invariance violation. A direct detection of the timelike-component of such fields requires a direct measurement of $\mathcal{P}$-odd potentials or their evolution over time. Herein, advantageous properties of chiral molecules, in which $\mathcal{P}$-odd potentials lead to resonance frequency differences between enantiomers, for direct detection of such $\mathcal{P}$-odd cosmic fields are demonstrated. Scaling behavior of electronic structure enhancements of such interactions with respect to nuclear charge number and the fine-structure constant is derived analytically. This allows a simple estimate of the effect sizes for arbitrary molecules. The analytical derivation is supported by quasi-relativistic numerical calculations in the molecules H$_2$X$_2$ and H$_2$XO with X $=$ O, S, Se, Te, Po. Parity violating effects due to cosmic fields on the C--F stretching mode in CHBrClF are compared to electroweak parity violation and influences of non-separable anharmonic vibrational corrections are discussed. On this basis it was estimated from a twenty year old experiment with CHBrClF that bounds on Lorentz invariance violation as characterized by the parameter $|b^\mathrm{e}_0|$ can be pushed down to the order of $10^{-17}\,\mathrm{GeV}$ in modern experiments with suitably selected molecular system, which will be an improvement of the current best limits by at least two orders of magnitude. This serves to highlight the particular opportunities that precision spectroscopy of chiral molecules provides in the search for new physics beyond the standard model.

physics.chem-ph