Discrete wave mechanics is formulated for particles in one-dimensional systems by use of a simple finite difference equation. The solutions involve wave vectors (instead of wave functions) as well as a newly defined "wave vector energy." In the limit, as c --> infinity, the treatment reduces to that of Schrödinger's wave mechanics. Specific calculations are made for completely free particles as well as for particles confined to a one-dimensional box. The results exhibit a striking compatibility with relativistic considerations. The wave vectors show properties that can be identified with particles and anti-particles-each possess identical probability distributions with energies that add up to zero.
Discrete wave mechanics is formulated for particles in one-dimensional systems by use of a simple finite difference equation. The solutions involve wave vectors (instead of wave functions) as well as a newly defined "wave vector energy." In the limit, as c --> infinity, the treatment reduces to that of Schrödinger's wave mechanics. Specific calculations are made for completely free particles as well as for particles confined to a one-dimensional box. The results exhibit a striking compatibility with relativistic considerations. The wave vectors show properties that can be identified with particles and anti-particles-each possess identical probability distributions with energies that add up to zero.
The quantum mechanical problem of the hydrogen atom is treated by use of a finite difference equation in place of Schrödinger's differential equation. The exact solution leads to a wave vector energy expression that is readily converted to the Bohr-Rydberg formula. (The calculations here reported are limited to spherically symmetric states.) The wave vectors reduce to the familiar solutions of Schrödinger's equation as c --> infinity. The internal consistency and limiting behavior provide support for the view that the equations employed could well constitute an approach to a relativistic formulation of wave mechanics.
Discrete wave mechanics is pursued further by extending the one-dimensional treatment to two (or more) dimensions in the light of explicit momentum considerations. Cognizance is taken of the effect of particle motion on mass and hence on the interactions between components of motion in different directions. The overall energy parameter turns out to be a product instead of a sum of parameters identified with each of several orthogonal axes. Accordingly, the separation of variables is most directly accomplished by factoring the principal energy parameter in conjunction with factoring the wave vector expression itself. Wave vector energies, on the other hand, remain additive. Finally, group velocity components are discussed for higher-dimensional systems.
The Schrödinger equation assumes that a particle behaves as a wave and yields a solution in terms of wave function and the energy of the particle under consideration. Once the wave function is known, then everything about the particle can be deduced from the wave function. This chapter covers the development of the Schrödinger wave equation and its applications to one-dimensional systems. Time-dependent and time-independent Schrödinger equations, bound and scattering states, probability density, probability current and expectation values, the solution of the time-independent 1D-Schrödinger equation for a free particle, infinite as well as finite potential wells, potential steps, and the finite potential barrier are discussed in detail in the chapter. The phenomenon of tunneling, relevance and the importance of the free particle, potential wells and potential barriers to contemporary fields of physics and chemistry, periodic solids and their band structures, the Kronig-Penney model, confined states in quantum wells, and wires and dots are other topics presented in innovative manners in the chapter. The importance of the topics presented here is demonstrated through carefully chosen solved examples and unsolved exercises from contemporary fields of sciences.
Introduction In this chapter we discuss the basic physical concepts and equations related to the behavior of particles in the nanoworld. We introduce the Schrödinger wave equation for particles and determine the ways to calculate observable physical quantities. We find that, in wave mechanics, the motion of a particle confined to a finite volume is always characterized by discrete values of the energy and standing-wave-like wavefunctions, i.e., such a motion is quantized. While motion in an infinite space (i.e., free motion) is not quantized and is described by propagating waves, the energy of the particle is characterized by a continuous range of values. Keeping in mind the diverse variants of nanostructures, by using wave mechanics we analyze some particular examples, which highlight important quantum properties of particles. Many of the examples analyzed can serve as the simplest models of nanostructures and will be exploited in following chapters to understand the fundamentals of processes in nanoelectronics. The Schrödinger wave equation From the previous chapter, we conclude that nanosize physical systems are quantum-mechanical systems, inasmuch as their sizes are comparable to typical de Broglie wavelengths of the particles composing these systems. In dealing with quantum-mechanical systems, one aims at determining the wavefunction of a single particle or of the whole system. As we will demonstrate in the subsequent discussion, knowledge of the wavefunction in quantum mechanics is sufficient to describe completely a particle or even a system of particles.
Assuming a background in basic classical physics, multivariable calculus, and differential equations, A Concise Introduction to Quantum Mechanics provides a self-contained presentation of the mathematics and physics of quantum mechanics. The relevant aspects of classical mechanics and electrodynamics are reviewed, and the basic concepts of wave-particle duality are developed as a logical outgrowth of experiments involving blackbody radiation, the photoelectric effect, and electron diffraction. The Copenhagen interpretation of the wave function and its relation to the particle probability density is presented in conjunction with Fourier analysis and its generalization to function spaces. These concepts are combined to analyze the system consisting of a particle confined to a box, developing the probabilistic interpretation of observations and their associated expectation values. The Schrödinger equation is then derived by using these results and demanding both Galilean invariance of the probability density and Newtonian energy-momentum relations. The general properties of the Schrödinger equation and its solutions are analyzed, and the theory of observables is developed along with the associated Heisenberg uncertainty principle. Basic applications of wave mechanics are made to free wave packet spreading, barrier penetration, the simple harmonic oscillator, the Hydrogen atom, and an electric charge in a uniform magnetic field. In addition, Dirac notation, elements of Hilbert space theory, operator techniques, and matrix algebra are presented and used to analyze coherent states, the linear potential, two state oscillations, and electron diffraction. Applications are made to photon and electron spin and the addition of angular momentum, and direct product multiparticle states are used to formulate both the Pauli exclusion principle and quantum decoherence. The book concludes with an introduction to the rotation group and the general properties of angular momentum.
A discrete wave mechanical treatment of the hydrogen atom is extended to deal with states involving nonzero angular momentum. Only the radial portions of the wave vectors are covered. It is predicted that there is a nonzero minimum distance between the electron and the nucleus; this threshold distance increases with increasing angular momentum. Appropriate finite difference equations are formulated. The states with angular momentum exhibit the same degeneracy as do corresponding energy levels obtained from solutions of Schrödinger's equation.