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arXiv:2111.14618

The Hydrogen Atom within a pseudo-complex Quantum Mechanics, involving a minimal length

Peter Oto Hess

Published Nov 24, 2021• 0 citations
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Abstract

The hydrogen atom is investigated, within a pseudo-complex extension of the coordinates and momenta, which introduces a minimal length scale (l) and results into a non-commutative Quantum Mechanics. After resuming the pseudo-complex extension of Quantum Mechanics, the modified energies of the hydrogen atom are deduced, producing corrections of the order of the square of the minimal length scale. Using the Lamb Shift, we obtain an upper boundary for the minimal length scale l, orders of magnitude more restrictive than former estimations.

DOI
10.48550/arxiv.2111.14618

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The hydrogen atom is investigated, within a pseudo-complex extension of the coordinates and momenta, which introduces a minimal length scale (l) and results into a non-commutative Quantum Mechanics. After resuming the pseudo-complex extension of Quantum Mechanics, the modified energies of the hydrogen atom are deduced, producing corrections of the order of the square of the minimal length scale. Using the Lamb Shift, we obtain an upper boundary for the minimal length scale l, orders of magnitude more restrictive than former estimations.
We studied energy spectrum for the hydrogen atom with deformed Heisenberg algebra leading to the minimal length. We developed the correct perturbation theory free of divergences. It gives a possibility to calculate analytically in the three-dimensional case the corrections to sss levels of the hydrogen atom caused by the minimal length. Comparing our results with the experimental data from precision hydrogen spectroscopy an upper bound for the minimal length is obtained.
Abstract The 4‐dimensional space‐time is extended to pseudo‐complex coordinates. Proposing the standard quantization rules in this extended space, the ones for the 4‐dimensional sub‐space acquire, as one solution, the commutation relations with non‐commuting coordinates. This demonstrates that the algebraic extension keeps the simple structure of Quantum Mechanics, while it also introduces an effective quite involved structure in the 4‐dimensional sub‐space. The first steps to pseudo‐complex Quantum Mechanics in 1‐dimension are outlined, awaiting still the interpretation of some new emerging structures. (© 2015 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)
We re-examine the justification for the imposition of regular boundary conditions on the wavefunction at the Coulomb singularity in the treatment of the hydrogen atom in non-relativistic quantum mechanics. We show that the issue of the correct boundary conditions is not independent of the physical structure of the proton. Under the physically reasonable assumption that the finite size and structure of the proton can be represented as a positive correction to the Coulomb potential, we give a justification for the regular boundary condition, which, in contrast to the usual treatments, is physically motivated and mathematically rigorous. We also describe how irregular boundary conditions can be used to model non-positive corrections to the Coulomb potential.
This paper develops an advanced unified description of the hydrogen atom wavefunction across three major theoretical levels: nonrelativistic quantum mechanics, relativistic quantum mechanics, and the Scretching–Schrödinger Equation framework. The study begins with the standard Schrödinger hydrogen wavefunction, where the electron state is represented as a complex probability amplitude labeled by the quantum numbers nnn, lll, mlm_lml, and msm_sms. It then advances to the relativistic Dirac treatment, where the scalar wavefunction is replaced by a four-component spinor labeled by nnn, κ\kappaκ, and mjm_jmj, thereby incorporating spin, relativistic energy corrections, and the natural appearance of fine-structure splitting. The central contribution of the paper is the extension of the hydrogen atom into the Scretching–Schrödinger Equation (SSE) framework, where the ordinary Schrödinger structure is preserved but constrained by a deterministic spectroscopic closure condition from the Scretching Quantum Chain (SQC) and Maxwell–Scretching Chain (MSC). In this formulation, a valid hydrogen wavefunction must not only satisfy the wave equation but must also reproduce the full physical chain ε→f→∣μ∣2→A21→Kν,\varepsilon \rightarrow f \rightarrow |\mu|^2 \rightarrow A_{21} \rightarrow K_{\nu},ε→f→∣μ∣2→A21→Kν, linking molar absorptivity, oscillator strength, transition dipole moment, Einstein spontaneous-emission coefficient, and the SQC invariant. The invariant Kν=2πe2ε0mec3=7.42165600145×10−22 sK_{\nu}=\frac{2\pi e^2}{\varepsilon_0 m_e c^3} =7.42165600145\times 10^{-22}\ \text{s}Kν=ε0mec32πe2=7.42165600145×10−22 s is derived from first principles and treated as the fixed spectroscopic time-scale anchor of the hydrogen SQC closure. The paper verifies the SQC formulation against NIST hydrogen spectral data for the Lyman series (n=2–4)(n=2–4)(n=2–4) and Balmer series (n=3–7)(n=3–7)(n=3–7), obtaining relative errors no larger than 2.7×10−42.7\times 10^{-4}2.7×10−4, with the remaining discrepancy attributed to rounding limits. It also derives the corrected radial transition integral for the 1s→2p1s\rightarrow 2p1s→2p transition, Ir0=1.2902662 a0,I_{r0}=1.2902662\,a_0,Ir0=1.2902662a0, and uses this value to support the deterministic connection between hydrogen wavefunctions, transition moments, oscillator strengths, and Einstein coefficients. The manuscript further develops the hydrogen SSE Hamiltonian in C*-algebraic form, extends the wavefunction treatment to isotope-corrected protium, deuterium, and tritium, and demonstrates that KνK_{\nu}Kν remains invariant under isotope substitution. Fine-structure effects—including Lamb-shift corrections, hyperfine splitting, and Zeeman perturbations—are examined as higher-order refinements within the SSE context rather than violations of the underlying SQC invariant. Finally, the paper maps the full SQC-to-MSC projection, showing how quantum oscillator strength projects upward into macroscopic electromagnetic observables such as absorption, refractive behavior, dielectric response, and radiative transition strength. The result is a deterministic, parameter-free quantum–electromagnetic hydrogen framework in which NRQM, RQM, SSE, SQC, and MSC are treated as connected layers of the same physical closure chain.
The response of a hydrogen atom to a perturbative electric field is presented from a classical viewpoint. We find classical energy shifts in the hydrogen atom in situations that correspond to both the linear and quadratic Stark effects. We then compare these energy shifts to the exact quantum-mechanical values for the Stark effect. We find that the linear Stark effect can be accurately reproduced classically (given the correct initial conditions). In contrast, quantum-mechanical results for the quadratic Stark effect cannot be accurately reproduced classically, except in the correspondence principle limit of large principal quantum numbers n.