The equation was originally formulated by Ludwig Boltzmann between 1872 and 1875, but later put into its current form by Max Planck in about 1900. To quote Planck, "the logarithmic connection between entropy and probability was first stated by L. Boltzmann in his kinetic theory of gases". The value of was originally intended to be proportional to the Wahrscheinlichkeit of a macroscopic state for some probability distribution of possible microstates—the collection of "ways" the thermodynamic state of a system can be realized by assigning different positions and momenta to the various molecules. Interpreted in this way, Boltzmann's formula is the most general formula for the thermodynamic entropy. However, Boltzmann's paradigm was an ideal gas of identical particles, of which are in the -th microscopic condition of position and momentum. For this case, the probability of each microstate of the system is equal, so it was equivalent for Boltzmann to calculate the number of microstates associated with a macrostate. was historically misinterpreted as literally meaning the number of microstates, and that is what it usually means today. can be counted using the formula for permutations where ranges over all possible molecular conditions and "" denotes factorial. The "correction" in the denominator is due to the fact that identical particles in the same condition are indistinguishable. is sometimes called the "thermodynamic probability" since it is an integergreater than one, while mathematical probabilities are always numbers between zero and one.
Generalization
Boltzmann's formula applies to microstates of the universe as a whole, each possible microstate of which is presumed to be equally probable. But in thermodynamics it is important to be able to make the approximation of dividing the universe into a system of interest, plus its surroundings; and then to be able to identify the entropy of the system with the system entropy in classical thermodynamics. The microstates of such a thermodynamic system are not equally probable—for example, high energy microstates are less probable than low energy microstates for a thermodynamic system kept at a fixed temperature by allowing contact with a heat bath. For thermodynamic systems where microstates of the system may not have equal probabilities, the appropriate generalization, called the Gibbs entropy, is: This reduces to equation if the probabilities pi are all equal. Boltzmann used a formula as early as 1866. He interpreted as a density in phase space—without mentioning probability—but since this satisfies the axiomatic definition of a probability measure we can retrospectively interpret it as a probability anyway. Gibbs gave an explicitly probabilistic interpretation in 1878. Boltzmann himself used an expression equivalent to in his later work and recognized it as more general than equation. That is, equation is a corollary of equation —and not vice versa. In every situation where equation is valid, equation is valid also—and not vice versa.
The term Boltzmann entropy is also sometimes used to indicate entropies calculated based on the approximation that the overall probability can be factored into an identical separate term for each particle—i.e., assuming each particle has an identical independent probability distribution, and ignoring interactions and correlations between the particles. This is exact for an ideal gas of identical particles, and may or may not be a good approximation for other systems. The Boltzmann entropy is obtained if one assumes one can treat all the component particles of a thermodynamic system as statistically independent. The probability distribution of the system as a whole then factorises into the product of N separate identical terms, one term for each particle; and the Gibbs entropy simplifies to the Boltzmann entropy where the summation is taken over each possible state in the 6-dimensional phase space of a single particle. This reflects the original statistical entropy function introduced by Ludwig Boltzmann in 1872. For the special case of an ideal gas it exactly corresponds to the proper thermodynamic entropy. However, for anything but the most dilute of real gases, it leads to increasingly wrong predictions of entropies and physical behaviours, by ignoring the interactions and correlations between different molecules. Instead one must follow Gibbs, and consider the ensemble of states of the system as a whole, rather than single particle states.
