A concept of Kinetic Energy in Quantum Mechanics is analyzed. Kinetic Energy is not zero in many cases where there are no motion and flux. This paradox can be understood, using expansion of the wave function in Fourier integral, that is on the basis of virtual plane waves.
A concept of kinetic energy in quantum mechanics is analyzed. Kinetic energy is a non-zero positive value in many cases of bound states, when a wave function is a real-valued one and there are no visible motion and flux. This can be understood, using expansion of the wave function into Fourier integral, that is, on the basis of virtual plane waves. The ground state energy of a hydrogen atom is calculated in a special way, regarding explicitly all the terms of electrostatic and kinetic energies. The correct values of the ground state energy and the radius of decay are achieved only when the electrostatic energies of the electron and the proton (self-energies) are not taken into account. This proves again that self-action should be excluded in quantum mechanics. A model of a spherical ball with uniformly distributed charge of particles is considered. It is shown that for a neutral ball (with compensated electric charge) the electrostatic energy is a non-zero negative value in this model. This occurs because the self-energy of the constituting particles should be subtracted. So it shown that the energy of the electric field does not have to be of a positive value in any imaginable problem.
Many-body quantum-mechanical stationary states that have real valued wavefunctions are shown to satisfy a classical conservation of energy equation with a kinetic energy function. The terms in the equation depend on the probability distribution, and, in addition, pressure and velocity functions, but these functions also depend on the probability distribution. There are two possible directions of the velocity that satisfy the energy equation. A linear momentum function is defined that integrates to zero, and this property is consistent with the expectation value of the linear momentum for stationary states with real-valued wave functions. The energy equation is integrated to obtain a version of the well known energy equation involving reduced density matrices, where the kinetic energy functional of the one-particle density matrix is replaced by a function of the electron density and a velocity function. Also, the noninteracting kinetic energy functional from the Hohenberg--Kohn theorem is given as an explicit functional of the orbital densities. For the purpose of describing the behavior of particles in a stationary state, a model based on the energy equation is constructed. The model is evaluated for the two different velocity directions using the grounds state of the particle in a one-dimensional box and the hydrogen atom. For one velocity direction, equations of motions with contradictory properties are obtained, and, in the other, an unstable system is found. A discussion is given with suggestions of additional elements that might improve the model.
Abstract Classical mechanics characterizes the kinetic energy of a particle, the energy it holds due to its motion, as consistently positive. By contrast, quantum mechanics describes the motion of particles using wave functions, in which regions of negative local kinetic energy can emerge 1 . This phenomenon occurs when the amplitude of the wave function experiences notable decay, typically associated with quantum tunnelling. Here, we investigate the quantum mechanical motion of particles in a system of two coupled waveguides, in which the population transfer between the waveguides acts as a clock, allowing particle speeds along the waveguide axis to be determined. By applying this scheme to exponentially decaying quantum states at a reflective potential step, we determine an energy–speed relationship for particles with negative local kinetic energy. We find that the smaller the energy of the particles—in other words, the more negative the local kinetic energy—the higher the measured speed inside the potential step. Our findings contribute to the ongoing tunnelling time debate 2–6 and can be viewed as a test of Bohmian trajectories in quantum mechanics 7–9 . Regarding the latter, we find that the measured energy–speed relationship does not align with the particle dynamics postulated by the guiding equation in Bohmian mechanics.
According to both Bohmian and stochastic quantum mechanics, the standard quantum mechanical kinetic energy can be understood as consisting of two hidden-variable components. One component is associated with the current (or Bohmian) velocity, while the other is associated with the osmotic velocity (or quantum potential), and they are identified with the phase and the amplitude, respectively, of the wave function. These two components are experimentally accessible through the real and imaginary parts of the weak value of the momentum postselected in position. In this paper, a kinetic energy equipartition is presented as a signature of quantum thermalization in closed systems. This means that the expectation value of the standard kinetic energy is equally shared between the expectation values of the squares of these two hidden-variable components. Such components cannot be reached from expectation values linked to typical Hermitian operators. To illustrate these concepts, numerical results for the nonequilibrium dynamics of a few-particle harmonic trap under random disorder are presented. Furthermore, the advantages of using the center-of-mass frame of reference for dealing with systems containing many indistinguishable particles are also discussed.
Abstract The kinetic energy, T, of a particle is the energy it possesses on account of its motion. In classical mechanics, the kinetic energy is related to the linear momentum p by T= p2 /2m (and by T=½mv2, where v is the velocity). In quantum mechanics the kinetic energy is proportional to the second derivative of the wavefunction (Box K.1). As the wavefunction becomes more sharply curved, so the kinetic energy of the particle increases. Conversely, a particle with a wavefunction that is almost flat everywhere has almost zero kinetic energy.
The Schrodinger equation has been considered to be a postulate of quantum physics, but it is also perceived and derived heuristically as the quantum equivalent of the classical energy relation. We indicate that the Schrodinger equation cannot be a physical postulate, and we show that the heuristic derivations wrongly consider that the particle kinetic energy is proportional to the square of the momentum operator acting on the wavefunction. The correct term is proportional to the square of the momentum. Analyzing particle interactions, we realize that particles have multiple virtual motions and that each motion is accompanied by a wave that has constant amplitude. Accordingly, we define the wavefunction as the superposition of the virtual waves of the particle. As a result, quantum mechanics becomes a local and global theory, while in the traditional formulation it is a local theory. In several interaction settings we can tell what particle motions arise and explain the outcomes in simple and tangible terms. Most importantly, the mathematical foundation of quantum mechanics becomes clear and justified, and we derive the Schrodinger, Dirac, etc. equations as the conditions the wavefunction must satisfy at each space-time point in order to fulfill the respective total energy equation.