Introduction In our treatment of quantum mechanics we discussed the notion of the state of a given system. The state was specified by giving the eigenvalues of a maximal set of mutually commuting observables. This represented the most information we could have about a given system in principle. In practice, of course, we do not really have all of the necessary information about the eigenvalues available. No experimentalist sets out with the primary intention of obtaining results which correspond to a maximal set of mutually compatible observables for any macroscopic system, such as a gas. Even a very small volume of gas contains an enormous number of particles. The quantum mechanical state would require us to know a great deal of information about the internal states of the electrons and nuclei of the gas molecules. The experimentalist may only be concerned with gross properties such as the pressure, internal energy, or specific heat for example. Most of the detailed information about the detailed state of the system is neither observed, nor of direct interest. Instead we must content ourselves with a description of the average, or most likely, behaviour of the system in the probabilistic sense. The usual technique for doing this consists of the introduction of an ensemble, meaning a very large collection of systems whose measured macroscopic properties are the same as those for the system we are interested in, but whose unobserved properties can vary.
Introduction In our treatment of quantum mechanics we discussed the notion of the state of a given system. The state was specified by giving the eigenvalues of a maximal set of mutually commuting observables. This represented the most information we could have about a given system in principle. In practice, of course, we do not really have all of the necessary information about the eigenvalues available. No experimentalist sets out with the primary intention of obtaining results which correspond to a maximal set of mutually compatible observables for any macroscopic system, such as a gas. Even a very small volume of gas contains an enormous number of particles. The quantum mechanical state would require us to know a great deal of information about the internal states of the electrons and nuclei of the gas molecules. The experimentalist may only be concerned with gross properties such as the pressure, internal energy, or specific heat for example. Most of the detailed information about the detailed state of the system is neither observed, nor of direct interest. Instead we must content ourselves with a description of the average, or most likely, behaviour of the system in the probabilistic sense. The usual technique for doing this consists of the introduction of an ensemble, meaning a very large collection of systems whose measured macroscopic properties are the same as those for the system we are interested in, but whose unobserved properties can vary.
Abstract NMR is not performed on a single or a small number of spins, but on a very large number, comparable with the Avogadro number. Even when one is interested in a molecular species with relatively few spins, the sample contains a large number of molecules of that species, all of which are observed simultaneously. What one observes in practice is the average response of the molecules, which is determined by an average over the states of each individual molecule. A common feature of all studies of condensed matter is that in the presence of many identical objects it is impossible to know exactly the state of the whole system, but that this relative ignorance is immaterial in so far as the properties of the system are not very sensitive to its exact state. The approach adapted to macroscopic systems is a statistical one, the correctness and fruitfulness of which is witnessed by the unfailing success of statistical mechanics. When dealing with quantum objects, the statistical approach must be adapted to their quantum character.
For systems which obey quantum mechanics, the formulation of the problem of treating large numbers of particles is, of course, somewhat different than it is for classical systems. The microscopic description of the system is provided by a wave function which (in the absence of spin) is a function of the classical coordinates { q i }. The mathematical model is provided by a Hamiltonian operator H which is often obtained from the corresponding classical Hamiltonian by the replacement p i → ( ħ /i)(∂/∂ q i ). In other cases the form of the Hamiltonian operator is simply postulated. The microscopic dynamics are provided by the Schrödinger equation i ħ (∂Ψ/∂ t ) = H Ψ which requires as initial condition the knowledge of the wave function Ψ({ q i }, t ) at some initial time t 0 . (Boundary conditions on Ψ({ q i }, t ) must be specified as part of the description of the model as well.) The results of experiments in quantum mechanics are characterized by operators, usually obtained, like the Hamiltonian, from their classical forms and termed observables. Operators associated with observables must be Hermitian. In general, the various operators corresponding to observables do not commute with one another. It is possible to find sets of commuting operators whose mutual eigenstates span the Hilbert space in which the wave function is confined by the Schrödinger equation and the boundary conditions. A set of such (time independent) eigenstates, termed ψ ν ( q ), is a basis for the Hilbert space.
Abstract Chapter 9 begins laying a foundation for quantum statistical mechanics with a discussion of relevant topics in quantum mechanics. The fundamental postulates of quantum mechanics are reviewed, beginning with the definition of a quantum state and the introduction of the concept of a state vector in a Hilbert space. The representation of observables as Hermitian operators on Hilbert space vectors is described; it is shown that the eigenvalues of Hermitian operators are real and, therefore, constitute possible outcomes of measurements made on these observables. The notions compatible and non-compatible observables and implication for the measurement problem are presented. The time-dependent Schrödinger equation is introduced as generating the time-evolution of the state vector, and it is shown how to cast the Schrödinger equation into a coordinate basis to yield the wave equation of quantum mechanics. Coordinate and momentum bases and their properties are desribed. Several analytically solvable quantum systems are presented as illustrative examples. The chapter concludes with a discussion of spin and the treatment identical particles
Quantum physics consists of a formal core that is universally agreed upon (basically being a piece of mathematics with suggestive names for concepts matching related concepts of experimental culture) and an interpretational halo (trying to make this relation more precise) that remains highly disputed even after more than 90 years of modern quantum physics. The latter is the subject of the interpretation of quantum mechanics (see Part II), where many interpretations coexist and compete for the attention of those interested in what quantum physics really means. In this chapter, an axiomatic introduction to the undisputed formal core of quantum physics is given. The axioms described present nonrelativistic quantum statistical mechanics in the Schrödinger picture. The relativistic case is outside the scope of these axioms, as it must be treated by quantum field theory; see Chapter 7. As in any axiomatic setting (necessary for a formal discipline), there are a number of different but equivalent sets of axioms or postulates that can be used to define formal quantum physics. Since they are equivalent, their choice is a matter of convenience. The choice presented here is a formulation featuring three aspects: It emphasises the similarity of quantum mechanics and classical mechanics, gives most direct access to statistical mechanics, and is free from allusions to measurement. The reason for the first is that this similarity serves as a guide to meaning. From the axiomatic setting for quantum mechanics presented below, classical mechanics (in the Koopman setting discussed in Section 7.10) is obtained by simply restricting the operators to be diagonal, so that all operations happen pointwise on the diagonal elements. Thus, multiplication is commutative, and one can identify operators and functions. In particular, the density operator degenerates into a probability density. Therefore, the quantum case appears as a generalization of the classical case allowing for noncommutativity, so that both q-observables and the density operator are (usually infinite-dimensional) operators. The reason for the second is that statistical mechanics is the main tool for applications of quantum physics to the macroscopic systems we are familiar with. The reason for the third is that realistic measurements constitute a complex process involving macroscopic detectors, hence should be explained by quantum statistical mechanics rather than be part of the axiomatic foundations themselves. (This is in marked contrast to other foundations, and distinguishes the present system of axioms.)
Ensembles and expectation values Equations of motion provide predictions of time-evolving variables of a dynamical system, and thereby enable us to predict the changing behavior. These equations are characteristic of a particular type of system, say a classical harmonic oscillator or a two-state quantum system. To complete the description of behavior one must specify initial conditions that select, from the many possible solutions to the equations of motion, a particular realization. In the example of a classical point particle the equation is second order in time, and so we need two initial conditions, of position and velocity, to specify a particular solution. These two numbers, taken with the classical equation of motion, provide a complete description of the behavior of a specific harmonic oscillator. Similarly the two-state quantum system requires two initial values to complete its definition. The initial conditions are never defined with infinite precision, even for classical mechanics. More generally we deal with an ensemble, that is, a collection of similar dynamical systems (e.g. oscillators) that differ in their preparation. The individual cases share some common attributes, but not necessarily all. Thus we have only incomplete information about any single system. We might, for example, consider planetary motion in which we know only the mean energy and the orbital plane. The loci of positions of the planets then form ellipses that make up the ensemble. Although it is possible to prepare a single two-state quantum system in which the initial state is known (apart from an overall phase), often one deals with ensembles of such systems, each of which may differ in some uncontrollable property.
From the outset statistical mechanics will be framed in the language of quantum theory. The typical macroscopic system is composed of multiple constituents, and hence described in some many-particle Hilbert space. In general, not much is known about such a system, certainly not the precise preparation of all its microscopic details. Thus, its description requires a more general notion of a quantum state, a so-called mixed state. This chapter begins with a brief review of the basic axioms of quantum theory regarding observables, pure states, measurements, and time evolution. Particular attention is paid to the use of projection operators and to the most elementary quantum system, a two-level system. The chapter then motivates the introduction of mixed states and examines in detail their mathematical representation and properties. It also dwells on the description of composite systems, introducing, in particular, the notions of statistical independence and correlations.