We consider a semi-classical model to describe the origin of the spin-orbit interaction in a simple system such as the hydrogen atom. The interaction energy U is calculated in the rest-frame of the nucleus, around which an electron, having linear velocity v and magnetic dipole-moment μ, travels in a circular orbit. The interaction energy U is due to the coupling of the induced electric dipole p=(v/c)×μ with the electric field En of the nucleus. According to quantum mechanics, the radius of the electron’s orbit remains constant during a spin-flip transition. Under such circumstances, our model predicts that the energy of the system changes by ΔE=1/2U, the factor 1/2 emerging naturally as a consequence of equilibrium and the change of the kinetic energy of the electron. The correct 1/2 factor for the spin-orbit coupling energy is thus derived without the need to introduce the well-known Thomas precession in the rest-frame of the electron.
We consider a semi-classical model to describe the origin of the spin-orbit interaction in a simple system such as the hydrogen atom. The interaction energy U is calculated in the rest-frame of the nucleus, around which an electron, having linear velocity v and magnetic dipole-moment μ, travels in a circular orbit. The interaction energy U is due to the coupling of the induced electric dipole p=(v/c)×μ with the electric field En of the nucleus. According to quantum mechanics, the radius of the electron’s orbit remains constant during a spin-flip transition. Under such circumstances, our model predicts that the energy of the system changes by ΔE=1/2U, the factor 1/2 emerging naturally as a consequence of equilibrium and the change of the kinetic energy of the electron. The correct 1/2 factor for the spin-orbit coupling energy is thus derived without the need to introduce the well-known Thomas precession in the rest-frame of the electron.
We consider a semi-classical model to describe the origin of the spin–orbit interaction in a simple system such as the hydrogen atom. The interaction energy is calculated in the rest-frame of the nucleus, around which an electron, having linear velocity and magnetic dipole-moment travels in a circular orbit. The interaction energy is due to the coupling of the induced electric dipole with the electric field of the nucleus. Assuming the radius of the electron's orbit remains constant during a spin-flip transition, our model predicts that the energy of the system changes by the factor emerging naturally as a consequence of equilibrium and the change of the kinetic energy of the electron. The correct factor for the spin–orbit coupling energy is thus derived without the need to invoke the well-known Thomas precession in the rest-frame of the electron.
First, the experimental foundations for the existence of a new dynamical variable, the spin of particles, are presented. The Pauli equation is then derived in detail, two applications are given and the energy levels of a particle with spin in a constant magnetic field are studied. This is the analysis of Landau levels, which can be performed by using the known results on the spectrum of harmonic oscillators. In this chapter we also study in detail the addition of orbital angular momentum and spin, as well as the spin–orbit interaction with the resulting Thomas precession. Stern-Gerlach experiment and electron spin The hypothesis that the electron has an intrinsic magnetic moment and an angular momentum, in short a spin , was first suggested in Uhlenbeck and Goudsmit (1926). They noticed, even before the discovery of quantum mechanics, that a complete description of spectra was not possible unless a magnetic moment and a mechanical moment were ascribed to the electron, and hence the concept of an electron as a point charge was insufficient. First, let us therefore try to understand how a magnetic moment can be associated to an atomic system. For this purpose, consider for simplicity the Bohr model of an hydrogen atom, where the electron moves along a circular orbit and rotates with orbital angular momentum L .
Quantization of spin and orbital angular momenta in standard quantum mechanics is rooted in the fundamental rotational symmetry of space in conjunction with the results of experiments on atomic and subatomic particles conducted with the Stern-Gerlach apparatus. We explain some of the most important features of spin and orbital angular momenta as inescapable consequences of elementary Stern-Gerlach experiments viewed in light of the rotational symmetry of space. The rotation operator is first derived for spin-½ particles, then extended to spin-1 particles by treating the case of a hydrogen atom in its ground state, where the spin of the proton combines with that of the electron to create a spin-1 triplet state. Along the way, we examine the evolution of a particle’s spin state under an applied magnetic field, where the interaction energy arises from the existence of a magnetic dipole moment for each particle in proportion to its spin angular momentum. Whereas a constant magnetic field B0 causes the particle’s magnetic moment to gyrate around the direction of B0, it will be seen that the presence of a small oscillating magnetic field perpendicular to B0 brings about the so-called Rabi oscillations, which involve periodic flippings of the particle’s spin orientation. In the case of a hydrogen atom in its ground state, the interaction between the magnetic dipole moments of the proton and the electron splits the ground state between a lower energy singlet having a net angular momentum of zero (spin-0 state), and a higher energy triplet having a total angular momentum of ħ (spin-1 state). This hyperfine splitting is the source of the well-known 21-cm line observed in the spectrum of the hydrogen atom, which arises from transitions between the atom’s singlet and triplet states. In the final section, we put forward an argument (originally made by Richard Feynman) that ties the rotational symmetry of space to the conservation of angular momentum in quantum mechanics. The argument is, in fact, quite general, enabling one to deduce other conservation laws from various inherent symmetries of quantum mechanical systems.
Even after extensive research in Quantum Mechanics, we are still unable to visualize instant-to-instant motion of an electron in hydrogen atom. That is because in QM treatment, potential energy term has been mistakenly assumed to be time-independent instead of depending on the instant-to-instant varying position of the orbiting electron [1]. This has led to wrong and weird solutions for the electron motion in hydrogen atom. Before the advent of wave mechanics, Sommerfeld model of elliptical electron orbits was able to explain most features of hydrogen spectra, except for the features associated with electron spin and magnetic moment interactions. However, the Sommerfeld elliptical orbits were of kinematic origin and could not provide visualization of instant-to-instant dynamic motion of the orbiting electron. Contrary to the QM perspective, we find that central core of the electron behaves as a classical particle while its electrostatic field behaves as a wave phenomenon. As such an electron under Coulomb force moves strictly in accordance with Newtonian laws of motion. In this paper, we develop dynamic electron orbits in hydrogen atom by using energy and angular momentum conservation principle in central force field. We have shown that during photon emission, angular momentum of the orbiting electron is changed by ħ due to recoil action. This may be the origin of various quantization rules. During emission of a photon, elliptical orbit transitions are also computed and plotted. Orbit transition time is of the order of 10-16 seconds. We have extended this methodology to compute electron orbits in hydrogen molecular bond and computed the H2 bond energy.
Niels Bohr’s model of the hydrogen and hydrogen-like atoms, in which the electron is allowed to revolve in certain circular orbits around the nucleus, was extended by Arnold Sommerfeld to allow for the possibility of elliptical orbits. Each elliptical orbit was constrained by two quantization conditions specified by a positive integer nφ and a non-negative integer nr. If, in the presence of the attractive Coulomb force between the electron and the nucleus, the dynamics of the atom were taken to be governed by the Newtonian laws of motion, the energy Ɛ of the two-particle system was found to be a function of the positive integer n = nr + nφ. The atomic energy levels thus exhibited an n-fold degeneracy, which would be lifted in the presence of external electric or magnetic fields, thus accounting for the fine-structure of the spectral lines emitted by the atom—phenomena observed, respectively, in the Stark effect and the Zeeman effect. Sommerfeld also examined the behavior of his elliptical orbits by allowing the revolving electron to obey Einstein’s relativistic dynamics. In this case, the energy-level degeneracies were lifted (even in the absence of external perturbations), and the elliptical orbits were found to precess around the nucleus—similarly to the precession of, say, the orbit of the planet Mercury around the Sun. What is astonishing about Sommerfeld’s relativistic expression of the energy Ɛ as a function of nφ and nr is that it is precisely the same expression as obtained for hydrogen and hydrogen-like atoms from Dirac’s equation, which came more than a decade later. Recall that the spin of the electron was not yet discovered when Sommerfeld developed his model, and that in Dirac’s fully-relativistic quantum mechanics, the spectral fine-structure arises from the coupling of the electron’s spin to its orbital motion. The present paper provides a streamlined yet detailed account of Sommerfeld’s elliptical orbits in hopes of bringing about a deeper appreciation for the miraculous coincidence of Sommerfeld’s result with that derived from Dirac’s equation.
The behavior of an atom in a nonuniform magnetic field is analyzed, as well as the motion of a classical magnetic dipole (a spinning charged ball) and a rotating charged ring. For the atom it is shown that, while the magnetic field does no work on the electron-orbital contribution to the magnetic moment (the source of translational kinetic energy being the internal energy of the atom), whether or not it does work on the electron-spin contribution to the magnetic moment depends on whether the electron has an intrinsic rotational kinetic energy associated with its spin. A rotational kinetic energy for the electron is shown to be consistent with the Dirac equation. If the electron does have a rotational kinetic energy, the acceleration of a silver atom in a Stern-Gerlach experiment or the emission of a photon from an electron spin flip can be explained without requiring the magnetic field to do work. For a constant magnetic field gradient along the z axis, it is found that the classical objects oscillate in simple harmonic motion along the z axis, the total kinetic energy -- translational plus rotational -- being a constant of the motion. For the charged ball, the change in rotational kinetic energy is associated only with a change in the precession frequency, the rotation rate about the figure axis remaining constant.