Introduction Engineers who design transistors, lasers and other semiconductor components want to understand and control the cause of resistance to current flow so that they may better optimize device performance. A detailed microscopic understanding of electron motion from one part of a semiconductor to another requires the explicit calculation of electron scattering probability. One would like to know how to predict electron scattering from one state to another. In this chapter we will see how to do this using powerful quantummechanical techniques. In addition to understanding electron motion in a semiconductor we also want to understand how to make devices that emit or absorb light. In Chapter 6 it was shown that a superposition of two harmonic oscillator eigenstates could give rise to dipole radiation and emission of a photon. The creation of a photon was only possible if a superposition state existed between a correct pair of eigenstates. This leads directly to the concept of rules determining pairs of eigenstates which can give rise to photon emission. Such selection rules are a useful tool to help us understand the emission and absorption of light by matter. However, the real challenge is to use what we know to make practical devices which operate using emission and absorption of photons. This usually requires imposing some control over atomic-scale physical processes which, of course, can only be understood using quantum mechanics.
Introduction Engineers who design transistors, lasers and other semiconductor components want to understand and control the cause of resistance to current flow so that they may better optimize device performance. A detailed microscopic understanding of electron motion from one part of a semiconductor to another requires the explicit calculation of electron scattering probability. One would like to know how to predict electron scattering from one state to another. In this chapter we will see how to do this using powerful quantummechanical techniques. In addition to understanding electron motion in a semiconductor we also want to understand how to make devices that emit or absorb light. In Chapter 6 it was shown that a superposition of two harmonic oscillator eigenstates could give rise to dipole radiation and emission of a photon. The creation of a photon was only possible if a superposition state existed between a correct pair of eigenstates. This leads directly to the concept of rules determining pairs of eigenstates which can give rise to photon emission. Such selection rules are a useful tool to help us understand the emission and absorption of light by matter. However, the real challenge is to use what we know to make practical devices which operate using emission and absorption of photons. This usually requires imposing some control over atomic-scale physical processes which, of course, can only be understood using quantum mechanics.
Quantum theory has formed a cornerstone for modern physics, engineering, and chemistry since the 1920s. It has found significant modern applications in engineering since the development of the semiconductor diode, transistor, and especially the laser in the 1960s. Not until the 1980s did the fabrication and materials growth technology become sufficiently developed to provide the ability to (1) produce quantum well devices (such as quantum well lasers) and (2) engineer the optical and electrical properties of materials (band-gap engineering). One purpose of this chapter is to summarize a small portion of modern quantum theory. The first few sections of this chapter summarize Lagrange and Hamilton’s approach to classical mechanics. These alternate formulations to Newton’s formulation of classical mechanics allow us to use scalar quantities such as kinetic or potential energy to find the equations of motion. These alternate formulations are so powerful that they can be used to deduce Maxwell’s and other continuous field equations. In fact, the quantum mechanical Hamiltonian comes from the classical one by substituting operators for the classical dynamical variables. The chapter discusses the connection between linear algebra and quantum mechanics and reviews the basic theory. The discussion of the harmonic oscillator introduces the ladder operators and vacuum state, and prepares the way for the harmonic oscillator theory of the electromagnetic field encounter in quantum optics. The chapter includes quantum mechanical representation theory along with the time dependent perturbation theory. The density operator plays a central role in emission and absorption theory.
In this work we shall study the interaction of matter and light. In so doing we shall rely heavily on the description of such processes provided by quantum mechanics. This appears on a number of levels: firstly, a quantum description of matter is indispensable if one wants to understand on the microscopic scale the different kinds of interaction processes that can occur. Secondly, a quantum description of light often turns out to be useful, sometimes necessary, to better understand these processes. We shall study phenomena such as spontaneous emission, which can only be properly treated by a theory taking into account the quantum nature of both light and matter. In the following chapters we shall address, amongst others, the following question: ‘given an atom prepared at a given time in a particular state and subjected from this time onwards to electromagnetic radiation, what is the state of the atom and radiation at any later moment in time?’ In order to be able to answer this question it will be necessary for us to know how to calculate the evolution of a quantum system in a small number of typical situations. These methods we shall demonstrate in the first chapter. The evolution of the coupled atom–light system depends on the temporal dependence of the applied light field, which could, for example, be applied from a given moment and thereafter remain unchanged in intensity, or, perhaps, be appreciable only for a finite period of time (pulsed excitation).
Motivation You may ask why one needs to know about quantum mechanics. Possibly the simplest answer is that we live in a quantum world! Engineers would like to make and control electronic, opto-electronic, and optical devices on an atomic scale. In biology there are molecules and cells we wish to understand and modify on an atomic scale. The same is true in chemistry, where an important goal is the synthesis of both organic and inorganic compounds with precise atomic composition and structure. Quantum mechanics gives the engineer, the biologist, and the chemist the tools with which to study and control objects on an atomic scale. As an example, consider the deoxyribonucleic acid (DNA) molecule shown in Fig. 1.1. The number of atoms in DNA can be so great that it is impossible to track the position and activity of every atom. However, suppose we wish to know the effect a particular site (or neighborhood of an atom) in a single molecule has on a chemical reaction. Making use of quantum mechanics, engineers, biologists, and chemists can work together to solve this problem. In one approach, laser-induced fluorescence of a fluorophore attached to a specific site of a large molecule can be used to study the dynamics of that individual molecule. The light emitted from the fluorophore acts as a small beacon that provides information about the state of the molecule.
Introduction Until now, our discussion of the interaction between radiation and matter has concentrated only on the spectral aspects of radiation. The results could determine the wavelengths for absorption and emission or the selection rules for such transitions, but could not be used to determine the actual extent of emission or absorption. These too are important considerations which are needed to fully quantify radiative energy transfer. Unfortunately, none of the classical theories can predict the extent of emission from an excited medium, or even the extent of absorption. Although the discussion in Section 4.9 (on the propagation of electromagnetic waves through lossy media) touched briefly on the concept of attenuation by absorption, it failed to show the reasons for the spectral properties of the absorption or to accurately predict its extent. We will see later that the classical results are useful only as a benchmark against which the actual absorber is compared. The objective of this chapter is therefore to present an introduction to quantum mechanical processes that control the emission and absorption by microscopic systems consisting of atoms and molecules. The results will then be used to predict the extent of emission by media when excited by an external energy source and to evaluate the absorption of incident radiation. It is now well recognized that all emission or absorption processes are the result of transitions between quantum mechanical energy levels.
Chapter 3 provides a brief review of a few concepts from classical Newtonian physics, and how this fails to explain phenomena at the nanoscopic scale. As is detailed within, the classical mechanical model is able to describe all observed physical phenomena; however, when it comes to the nanoscale this model breaks down, because the properties of the materials change dramatically. At this scale, the surface-to-volume ratio increases, gravitational forces become negligible and random molecular motion becomes more important. This changes the properties of the material and affects the devices that are fabricated at this scale. It is hence necessary to develop a new model that can explain such physical phenomena. This has led to a new branch of physics, i.e. quantum physics (QP) or quantum mechanics, which is able to explain the behavior observed at nanoscale. QP enables us to explain phenomena such as the photoelectric effect, Compton effect. etc. In this chapter, we introduce quantum mechanics and how it evolved in the late 19th and early 20th centuries. Further, light’s behaviour as a particle as well as a wave is described by the photoelectric effect and Young’s double-slit experiment, respectively. Further, the dual nature of the particle is explained using the de Broglie principle. Schrodinger’s equation is then explained, which gives the probability of finding a subatomic-scale particle at a certain position in a quantum well. In addition to the formulation of Schrodinger’s equation, its solution, the concept of a potential well, the characteristics of the wave function and its interpretation and significance, and, finally, the application of Schrodinger’s equation in the structure of an atom form subsequent parts of this chapter. The equation serves as a basis with which to understand band theory. Band theory explains the difference between conductors, insulators and semiconductors. Materials are distinguished according to the differences in their band gaps. Adding impurities or varying temperature changes the band gap in semiconductors, which consequently changes the properties of the semiconductor and its electrical conduction. One more important measure to understand and exploit the properties and behaviour of materials is Fermi–Dirac statistics. It is useful to acquire the probability of electrons at a given energy level at a specific temperature. These concepts can be utilised by physicists and chip makers to make more energy-efficient devices. Hence, this chapter details the fundamentals of quantum physics and how they relate to the electrical properties of nanodevices.
How to deal with time-dependent potentials, what kinds of physical problems having time-dependent potentials can be solved exactly and which are to be solved with the use of perturbation theory, what are different possible forms of time-dependent perturbating fields, and semi-classical treatment of the interaction of fields with matter are the subject matters of this chapter. First order perturbation theory, computation of transition probability, transition rates and Fermi's Golden Rule for harmonic and constant perturbations, absorption, stimulated emission and dipole approximation when electromagnetic fields interact with matter, spontaneous emission and Einstein coefficients, and dipole selection rules are other topics which are dealt with in detail in the chapter. Discussions with properly justified mathematical treatment on time-dependent potentials and on the exactly solvable time-dependent two-state systems are the special foci of this chapter.