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International Journal of Quantum Chemistry

On Ehrenfest's theorem

Viraht Sahni

Published Dec 23, 2003• 3 citations
Publisher

Abstract

Abstract Ehrenfest's theorem for a system of electrons in a time‐dependent external force is the quantal analogue to Newton's second law of motion for interacting classical particles. The theorem is in terms of the averaged force and position of the electrons. Here we draw the quantal analogue to the equation of motion for the individual classical particle and thereby describe the internal forces experienced by each electron and the evolution of these forces with time. This explanation is based on the description of Schrödinger theory in terms of fields and their quantal sources. The quantum mechanical average of the internal fields and their averaged torques, taken over all the electrons, vanish as they must. However, unlike classical physics, the vanishing of the averaged internal fields cannot be attributed solely to Newton's third law but is additionally a consequence of quantum mechanics. The field perspective thus leads to a new derivation of Ehrenfest's theorem. Furthermore, the theorem can be expressed in terms of the response of the electrons to the external field as described by a field representative of the electronic current density. In addition, the vanishing of the averaged torque of the internal fields leads to a quantal torque–angular momentum equation analogous to that of classical physics. The structure of the internal fields is demonstrated for both a ground and an excited state of the analytically solvable Hooke's atom. The concept of the internal field is extended via quantal density functional theory to the S system of noninteracting Fermions with density equivalent to that of the Schrödinger theory of electrons. By invoking Ehrenfest's theorem and the quantal torque–angular momentum relationship, sum rules for the S system are derived. © 2003 Wiley Periodicals, Inc. Int J Quantum Chem, 2004

DOI
10.1002/qua.10824

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Abstract Ehrenfest's theorem for a system of electrons in a time‐dependent external force is the quantal analogue to Newton's second law of motion for interacting classical particles. The theorem is in terms of the averaged force and position of the electrons. Here we draw the quantal analogue to the equation of motion for the individual classical particle and thereby describe the internal forces experienced by each electron and the evolution of these forces with time. This explanation is based on the description of Schrödinger theory in terms of fields and their quantal sources. The quantum mechanical average of the internal fields and their averaged torques, taken over all the electrons, vanish as they must. However, unlike classical physics, the vanishing of the averaged internal fields cannot be attributed solely to Newton's third law but is additionally a consequence of quantum mechanics. The field perspective thus leads to a new derivation of Ehrenfest's theorem. Furthermore, the theorem can be expressed in terms of the response of the electrons to the external field as described by a field representative of the electronic current density. In addition, the vanishing of the averaged torque of the internal fields leads to a quantal torque–angular momentum equation analogous to that of classical physics. The structure of the internal fields is demonstrated for both a ground and an excited state of the analytically solvable Hooke's atom. The concept of the internal field is extended via quantal density functional theory to the S system of noninteracting Fermions with density equivalent to that of the Schrödinger theory of electrons. By invoking Ehrenfest's theorem and the quantal torque–angular momentum relationship, sum rules for the S system are derived. © 2003 Wiley Periodicals, Inc. Int J Quantum Chem, 2004
Abstract The Schrödinger–Pauli (SP) theory of electrons in an electromagnetic field explicitly accounts for the electron spin moment. The many‐electron theory is complemented via a new descriptive perspective namely, that of the individual electron via its equation of motion or “Quantal Newtonian” first law. The law is in terms of ‘classical’ fields whose sources are quantum mechanical expectation values of Hermitian operators taken with respect to the system wave function. The law states that each electron experiences an external and an internal field, the sum of which vanish. The external field is the sum of the binding electrostatic and a Lorentz field. The internal field is a sum of fields representative respectively of electron correlations due to the Pauli principle and Coulomb repulsion; the electron density; kinetic effects; and an internal magnetic field. The energy can be expressed in integral virial form in terms of these fields. The law is elucidated by application to the 23S state of a quantum dot in a magnetic field. It is proved that the Hamiltonian is an exactly known and universal functional of the wave function. This generalizes the SP equation, and reveals that its eigenfunctions and eigenvalues may be determined self‐consistently. A quantal density functional theory (QDFT) of the SP system is developed whereby additional properties are determined. A physical interpretation of Spin‐DFT based on the QDFT mapping is provided. Further generalizations of the present work to the temporal case, and relativistic Dirac theory, are proposed.
A complementary perspective to the Göttingen-Copenhagen interpretation of stationary-state quantum theory of electrons in an electromagnetic field is described. The perspective, derived from Schrödinger-Pauli theory, is that of the individual electron via its equation of motion or 'Quantal Newtonian' First Law. The Law is in terms of 'classical' fields experienced by each electron: the sum of the external and internal fields vanishes. The external field is a sum of the electrostatic and Lorentz fields. The internal field is a sum of fields' representative of Pauli and Coulomb correlations; kinetic effects; electron density; and internal magnetic component. The energy is obtained from these fields. The sources of the fields are expectation values of Hermitian operators. The perspective is elucidated by application to quantum dots in a magnetic field in a ground, excited singlet and triplet states. The relationship of the perspective to Quantal and traditional density functional theories is briefly explained.
Quantum mechanics has a deterministic Schrödinger equation for the wave function. The Göttingen-Copenhagen statistical interpretation is based on the Born Rule that interprets the wave function as a "probability amplitude." A precept of this interpretation is the lack of determinism in quantum mechanics. The Bohm interpretation is that the wave function is a source of a field experienced by the electrons, thereby attributing determinism to quantum theory. In this paper, we present a new perspective on such determinism. The ideas are based on the equations of motion or "Quantal Newtonian" Laws obeyed by each electron. These Laws, derived from the temporal and stationary-state Schrödinger equation, are interpreted in terms of "classical" fields whose sources are quantal expectations of Hermitian operators taken with respect to the wave function. According to the Second Law, each electron experiences an external field-the quantal Coulomb-Lorentz law. It also experiences an internal field representative of properties of the system: correlations due to Coulomb repulsion and Pauli principle; the density; kinetic effects; and an internal magnetic field component. There is a response field. The First Law states that the sum of the external and internal fields experienced by each electron vanishes. These fields are akin to those of classical physics: They pervade all space; their structure is descriptive of the quantum system; the energy of the system is stored in these fields. It is in the classical behavior of these fields, which arise from quantal sources that one may then speak of determinism in quantum mechanics.
The Schrödinger-Pauli (SP) theory of electrons in an electromagnetic field explicitly accounts for the electron spin moment. The many-electron theory is complemented via a new descriptive perspective viz. that of the individual electron via its equation of motion or ‘Quantal Newtonian’ first law. The law is in terms of ‘classical’ fields whose sources are quantum mechanical expectation values of Hermitian operators taken with respect to the system wave function. The law states that each electron experiences an external and an internal field, the sum of which vanish. The external field is the sum of the binding electrostatic and a Lorentz field. The internal field is a sum of fields representative respectively of electron correlations due to the Pauli principle and Coulomb repulsion; the electron density; kinetic effects; and an internal magnetic field. The energy can be expressed in integral virial form in terms of these fields. The law is elucidated by application to the 23S state of a quantum dot in a magnetic field. It is proved that the Hamiltonian is an exactly known and universal functional of the wave function. This generalizes the SP equation, and reveals that its eigenfunctions and eigenvalues may be determined self-consistently. A Quantal density functional theory (QDFT) of the SP system is developed whereby additional properties are determined. A physical interpretation of Spin-DFT based on the QDFT mapping is provided. Further generalizations of the present work to the temporal case, and relativistic Dirac theory, are proposed.
Abstract Ehrenfest theorem is extended to the relativistic quantum theory of charged particles, moving under the influence of a classical electromagnetic field. In order to extend the original Ehrenfest result to the relativistic domain we bypassed the problems with the relativistic position operator by deriving directly Newton’s second law. Our approach is characterized by its universality. The detailed form of the wave equation is not needed. All that is required is the existence of the conserved electric four-current built from the particle wave function. The derivation is based on the conservation laws for the energy and momentum.
Abstract The quantal density functional theory (Q‐DFT) of excited states is the description of the physics of the mapping from any bound nondegenerate excited state of Schrödinger theory to that of the s‐system of noninteracting Fermions with equivalent density ρk(r), energy Ek, and ionization potential Ik. The s‐system may either be in an excited state with the same configuration as in Schrödinger theory or in a ground state with a consequently different configuration. The Q‐DFT description of the s‐system is in terms of a conservative field ℱk(r), whose electron‐interaction ℰee(r) and correlation‐kinetic 𝒵 (r) components are separately representative of electron correlations due to the Pauli exclusion principle and Coulomb repulsion, and correlation‐kinetic effects, respectively. The sources of these fields are expectations of Hermitian operators taken with respect to the system wavefunction. The local electron‐interaction potential vee(r) of the s‐system, representative of all the many‐body correlations, is the work done to move an electron in the force of the field ℱk(r). The electron interaction Eee and correlation‐kinetic Tc components of the total energy Ek may be expressed in integral virial form in terms of their respective fields. The difference between the s‐system in its ground or excited state representation is due entirely to correlation‐kinetic effects. The highest occupied eigenvalue of the s‐system differential equation in either case is minus the ionization potential Ik. In this work we demonstrate the transformation of an excited state of Schrödinger theory, as represented by the first excited singlet state of the exactly solvable Hooke's atom, to that of noninteracting Fermions in their ground state with equivalent excited state density, energy, and ionization potential. To further prove the Fermions are in a ground state, we solve the corresponding singlet s‐system differential equation numerically for the vee(r) determined, and obtain the excited state density from the zero node orbitals generated. The resulting total energy is also the same. In addition, the single eigenvalue determined corresponds to minus the ionization potential of the excited state. © 2001 John Wiley & Sons, Inc. Int J Quantum Chem, 2001