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Horacio Olivares-Pilon

Publications and source records attributed to Horacio Olivares-Pilon.

3 recordsLinked to original sources

Classical-quantum study of confinement in the chaotic $x^{2}y^{2}$ Yang-Mills Hamiltonian

We analyze how quantum mechanics reinstates confinement in Hamiltonian systems that are classically unstable and exhibit chaotic dynamics. Specifically, we consider two paradigmatic models: the Contopoulos Hamiltonian, an isotropic oscillator perturbed by the quartic coupling $α\, x^{2}y^{2}$, and the purely quartic Yang--Mills Hamiltonian $H=\tfrac{1}{2}(p_{x}^{2}+p_{y}^{2})+α\, x^{2}y^{2}$. Classical dynamics, characterized through Poincaré sections, Lyapunov exponents, and periodic orbits, reveals distinct escape mechanisms: in the Contopoulos system, trajectories destabilize along the diagonal valleys $x=\pm y$ for $α<0$, whereas in the Yang--Mills case with $α>0$, escape occurs along the coordinate axes $x=0$ or $y=0$. In sharp contrast, the quantum Yang--Mills Hamiltonian with $α>0$ admits only discrete, normalizable eigenstates. Semiclassical WKB and full two--dimensional analyses further show that these quantum states are localized along the classical escape channels, illustrating how transverse zero--point motion generates an effective confining barrier. Our study combines global Lyapunov--exponent heat maps with high--precision quantum spectra obtained via variational and Lagrange--mesh methods, providing quantitatively controlled results across regimes. In addition, we corroborate the classical predictions through analog electronic simulations based on operational--amplifier circuit models, offering an experimentally inspired validation of the theoretical framework.

nlin.CD↗

The ground electronic state of CS: the potential curve and associated Born-Oppenheimer rovibrational spectrum

Basics of the Born-Oppenheimer (B-O) approximation are reviewed. Assuming the domain of applicability of B-O approximation is limited to 4 significant digits (s.d.) in energy spectrum, where mass, relativistic and QED corrections do NOT contribute, it is shown that for carbon monosulfide ${\rm C}\,{\rm S}$ the potential curve $V(R)$ for the electronic ground state $X^1Σ^+$ can be constructed analytically in the form of two-point Pade approximant $\frac{1}{R}\ P(5,10)(R)$ in the whole range of internuclear distances $R \in [0,\infty)$. Pade approximant is fixed by taking into account the turning points with 4 s.d. accuracy, found by Coxon and Hajigeorgiou (2023), and asymptotics at small and large internuclear distances, By solving two-body radial nuclear Schrödinger equation with the potential $V(R)$ (with standard centrifugal potential included) in the Lagrange Mesh method, the whole B-O rovibrational spectrum for ${}^{12} {\rm C}\,{}^{32} {\rm S}$ diatomic molecule (taken as a particular example) is found: the $\sim 14562$ rovibrational energy states with angular momentum $L_{max}=289$ and vibrational quantum number $ν_{max} \sim 82$ with accuracy $\sim 10^{-4}$ hartree in energy. It is shown that the experimentally observed transition energies are reproduced within 3-5 s.d. Critical analysis of existing theoretical (phenomenological) results on the rovibrational spectrum is carried out and its comparison with present ones is made.

physics.atom-ph↗

Few-electron atomic ions in non-relativistic QED: the Ground state energy

Following detailed analysis of relativistic, QED and mass corrections for helium-like and lithium-like ions with static nuclei for $Z \leq 20$ the domain of applicability of Non-Relativistic QED (NRQED) is localized for ground state energy. It is demonstrated that for both helium-like and lithium-like ions with $Z \leq 20$ the finite nuclear mass effects do not change 4-5 significant digits (s.d.), and the leading relativistic and QED effects leave unchanged 3-4 s.d. in the ground state energy. It is shown that the non-relativistic ground state energy can be interpolated with accuracy not less than 13 s.d. for $Z \leq 12$, and not less than 12 s.d. for $Z \leq 50$ for helium-like as well as for $Z \leq 20$ for lithium-like ions by a compact meromorphic function in $λ=\sqrt{Z-{Z_B}}$ ($Z_B$ is the 2nd critical charge, see {TLO:2016}), $P_9(λ)/Q_5(λ)$. It is found that the Majorana formula - a second degree polynomial in $Z$ with two free parameters - and a fourth degree polynomial in $λ$ (a generalization of the Majorana formula) reproduce the ground state energy of the helium-like and lithium-like ions for $Z \leq 20$ in the domain of applicability of NRQED, thus, at least, 3 s.d. It is noted that $\gtrsim 99.9\%$ of the ground state energy is given by the variational energy for properly optimized trial function of the form of (anti)-symmetrized product of three (six) screened Coulomb orbitals for two-(three) electron system with 3 (7) free parameters for $Z \leq 20$, respectively. It may imply that these trial functions are, in fact, {\it exact} wavefunctions in non-relativistic QED, thus, the NRQED effective potential can be derived. It is shown that the sum of relativistic and QED effects in leading approximation - 3 s.d. - for both 2 and 3 electron systems is interpolated by 4th degree polynomial in $Z$ for $Z \leq 20$.

physics.atom-ph↗