Four-Dimensional Scaling of Dipole Polarizability in Quantum Systems
- URL: http://arxiv.org/abs/2010.11809v3
- Date: Sun, 23 Jan 2022 17:35:25 GMT
- Title: Four-Dimensional Scaling of Dipole Polarizability in Quantum Systems
- Authors: Peter Szabo, Szabolcs Goger, Jorge Charry, Mohammad Reza Karimpour,
Dmitry V. Fedorov, Alexandre Tkatchenko
- Abstract summary: Polarizability is a key response property of physical and chemical systems.
We show that polarizability follows a universal four-dimensional scaling law.
This formula is also applicable to many-particle systems.
- Score: 55.54838930242243
- License: http://arxiv.org/licenses/nonexclusive-distrib/1.0/
- Abstract: Polarizability is a key response property of physical and chemical systems,
which has an impact on intermolecular interactions, spectroscopic observables,
and vacuum polarization. The calculation of polarizability for quantum systems
involves an infinite sum over all excited (bound and continuum) states,
concealing the physical interpretation of polarization mechanisms and
complicating the derivation of efficient response models. Approximate
expressions for the dipole polarizability, $\alpha$, rely on different scaling
laws $\alpha \propto$ $R^3$, $R^4$, or $R^7$, for various definitions of the
system radius $R$. Here, we consider a range of single-particle quantum systems
of varying spatial dimensionality and having qualitatively different spectra,
demonstrating that their polarizability follows a universal four-dimensional
scaling law $\alpha = C (4 \mu q^2/\hbar^2)L^4$, where $\mu$ and $q$ are the
(effective) particle mass and charge, $C$ is a dimensionless excitation-energy
ratio, and the characteristic length $L$ is defined via the
$\mathcal{L}^2$-norm of the position operator. %The applicability of this
unified formula is demonstrated by accurately predicting the dipole
polarizability of 36 atoms and 1641 small organic~molecules. This unified
formula is also applicable to many-particle systems, as shown by} accurately
predicting the dipole polarizability of 36 atoms, 1641 small organic
\rrr{molecules, and Bloch electrons in periodic systems.
Related papers
- Turning Water to Wine With Polar Impostorons [0.0]
A surprising result from the theory of quantum control is the degree to which the properties of a physical system can be manipulated.
Both atomic and many-body solid state models admit the possibility of creating a 'driven imposter'
Here we apply these techniques to polarons in polar liquids.
arXiv Detail & Related papers (2024-09-09T05:22:04Z) - Symmetry shapes thermodynamics of macroscopic quantum systems [0.0]
We show that the entropy of a system can be described in terms of group-theoretical quantities.
We apply our technique to generic $N$ identical interacting $d$-level quantum systems.
arXiv Detail & Related papers (2024-02-06T18:13:18Z) - Dipolar spin-exchange and entanglement between molecules in an optical
tweezer array [0.0]
Ultracold polar molecules are promising candidate qubits for quantum computing.
Using a molecular optical tweezer array, single molecules can be moved and separately addressed for qubit operations.
We demonstrate a two-qubit gate to generate entanglement deterministically, an essential resource for all quantum information applications.
arXiv Detail & Related papers (2022-11-17T18:53:42Z) - Rydberg ions in coherent motional states: A new method for determining
the polarizability of Rydberg ions [71.05995184390709]
We present a method for measuring the polarizability of Rydberg ions confined in a Paul trap.
The method is easy-to-implement and applicable to different Rydberg states regardless of their principal or angular quantum numbers.
arXiv Detail & Related papers (2022-08-23T17:56:50Z) - Computational Insights into Electronic Excitations, Spin-Orbit Coupling
Effects, and Spin Decoherence in Cr(IV)-based Molecular Qubits [63.18666008322476]
We provide insights into key properties of Cr(IV)-based molecules aimed at assisting chemical design of efficient molecular qubits.
We find that the sign of the uniaxial zero-field splitting (ZFS) parameter is negative for all considered molecules.
We quantify (super)hyperfine coupling to the $53$Cr nuclear spin and to the $13C and $1H nuclear spins.
arXiv Detail & Related papers (2022-05-01T01:23:10Z) - High-resolution 'magic'-field spectroscopy on trapped polyatomic
molecules [62.997667081978825]
Rapid progress in cooling and trapping of molecules has enabled first experiments on high resolution spectroscopy of trapped diatomic molecules.
Extending this work to polyatomic molecules provides unique opportunities due to more complex geometries and additional internal degrees of freedom.
arXiv Detail & Related papers (2021-10-21T15:46:17Z) - The hydrogen atom: consideration of the electron self-field [0.0]
We substantiate the need for account of the proper electromagnetic field of the electron in the canonical problem of hydrogen.
We demonstrate that only particular classes of solutions, "nonlinear" analogues of s- and p-states, can be obtained through decomposition of a solution in a series.
arXiv Detail & Related papers (2021-01-05T21:52:41Z) - $\mathcal{P}$,$\mathcal{T}$-odd effects for RaOH molecule in the excited
vibrational state [77.34726150561087]
Triatomic molecule RaOH combines the advantages of laser-coolability and the spectrum with close opposite-parity doublets.
We obtain the rovibrational wave functions of RaOH in the ground electronic state and excited vibrational state using the close-coupled equations derived from the adiabatic Hamiltonian.
arXiv Detail & Related papers (2020-12-15T17:08:33Z) - Ab initio properties of the NaLi molecule in the $a^3\Sigma^+$
electronic state [0.0]
We calculate the electronic and rovibrational structure of ultracold polar and magnetic molecules with spectroscopic accuracy.
We show that quantum chemistry methods are capable of predicting scattering properties of manyelectron systems.
arXiv Detail & Related papers (2020-03-26T17:39:46Z) - Anisotropy-mediated reentrant localization [62.997667081978825]
We consider a 2d dipolar system, $d=2$, with the generalized dipole-dipole interaction $sim r-a$, and the power $a$ controlled experimentally in trapped-ion or Rydberg-atom systems.
We show that the spatially homogeneous tilt $beta$ of the dipoles giving rise to the anisotropic dipole exchange leads to the non-trivial reentrant localization beyond the locator expansion.
arXiv Detail & Related papers (2020-01-31T19:00:01Z)
This list is automatically generated from the titles and abstracts of the papers in this site.
This site does not guarantee the quality of this site (including all information) and is not responsible for any consequences.