The properties of the ideal Bose gas are calculated from the integral equations for the energy and the number of particles as a function of the temperature and chemical potential. It is shown that the integral equations break down below the Einstein temperature that corresponds to the transition to the low-temperature state. The lowest single-particle energy level must be treated explicitly to get the proper equations. With the inclusion of the lowest single-particle energy level, the low-temperature behavior is calculated. The occupation of the lowest level becomes comparable to the total number of particles in the system below the Einstein temperature, and equal to the total number of particles at zero temperature. A numerical solution to the properties of the Bose gas is discussed, and the detailed calculations are assigned to the problems at the end of the chapter.
The properties of the ideal Bose gas are calculated from the integral equations for the energy and the number of particles as a function of the temperature and chemical potential. It is shown that the integral equations break down below the Einstein temperature that corresponds to the transition to the low-temperature state. The lowest single-particle energy level must be treated explicitly to get the proper equations. With the inclusion of the lowest single-particle energy level, the low-temperature behavior is calculated. The occupation of the lowest level becomes comparable to the total number of particles in the system below the Einstein temperature, and equal to the total number of particles at zero temperature. A numerical solution to the properties of the Bose gas is discussed, and the detailed calculations are assigned to the problems at the end of the chapter.
The topic of Bose–Einstein condensation in a uniform, non-interacting gas of bosons is treated in most textbooks on statistical mechanics. In the present chapter we discuss the properties of a non-interacting Bose gas in a trap. We shall calculate equilibrium properties of systems in a semi-classical approximation, in which the energy spectrum is treated as a continuum. For this approach to be valid the temperature must be large compared with Δ∊/ k , where Δ∊ denotes the separation between neighbouring energy levels. As is well known, at temperatures below the Bose–Einstein condensation temperature, the lowest-energy state is not properly accounted for if one simply replaces sums by integrals, and it must be included explicitly. The statistical distribution function is discussed in Sec. 2.1, as is the single-particle density of states, which is a key ingredient in the calculations of thermodynamic properties. Calculations of the transition temperature and the fraction of particles in the condensate are described in Sec. 2.2. In Sec. 2.3 the semi-classical distribution function is introduced. From this we obtain the density profile and the velocity distribution of particles, and use these to determine the shape of an anisotropic cloud after free expansion. Thermodynamic properties of Bose gases are calculated as functions of the temperature in Sec. 2.4. Finally, Sec. 2.5 treats corrections to the transition temperature due to a finite particle number.
The topic of Bose–Einstein condensation in a uniform, non-interacting gas of bosons is treated in most textbooks on statistical mechanics. In the present chapter we discuss the properties of a non-interacting Bose gas in a trap. We shall calculate equilibrium properties of systems in a semi-classical approximation, in which the energy spectrum is treated as a continuum. For this approach to be valid the temperature must be large compared with Δ∈/ k , where Δ∈ denotes the separation between neighbouring energy levels. As is well known, at temperatures below the Bose–Einstein condensation temperature, the lowest energy state is not properly accounted for if one simply replaces sums by integrals, and it must be included explicitly. The statistical distribution function is discussed in Sec. 2.1, as is the single-particle density of states, which is a key ingredient in the calculations of thermo dynamic properties. Calculations of the transition temperature and the fraction of particles in the condensate are described in Sec. 2.2. In Sec. 2.3 the semi-classical distribution function is introduced, and from this we determine the density profile and the velocity distribution of particles. Thermodynamic properties of Bose gases are calculated as functions of the temperature in Sec. 2.4. The final two sections are devoted to effects not captured by the simplest version of the semi-classical approximation: corrections to the transition temperature due to a finite particle number (Sec. 2.5), and thermodynamic properties of gases in lower dimensions (Sec. 2.6).
In this paper, it has been shown that the usual demonstrations of the phenomenon of Bose-Einstein condensation are invalid. Exact formal solutions have been derived for the partition functions and the mean occupation numbers in classical and Bose statistics, and the theory of fluctuations in the case of Bose statistics has been given. In a second paper, convenient approximations will be derived for the mean occupation numbers in Bose statistics, and it will be shown that for temperatures well above the critical temperature of the supposed Bose-Einstein condensation the well-known result for the mean occupation numbers is valid, whilst for temperatures rather lower than this critical value it will be shown that particles will condense into the lowest available state. The critical temperatureT0is given by where the summation is over all energy levels except the lowest.
In this paper, first of all, we proved if the ideal Bose gas with a finite volume and number of particles has a non-degenerate single-particle energy level n, the chemical potential μ can take the value μn = n and there is a phase transition temperature Tp,n, where n = 0,1,2 Taking 0 ≤ n Tp,n+1. When the temperature T > Tp,n or T ≤ Tp,n+1, μ # n and the most probable occupation number Nn = 0. In the temperature interval Tp,n ≥ T > Tp,n+1, μ = n and 0 ≤ Nn = N - NjsupNn, where Nj is the most probable occupation number in the degenerate level j. Thus, if the finite ideal Bose gas has some non-degenerate single-particle levels, there exists a characteristic temperature Tp = Tp,0. The chemical potential μ is quantized when T ≤ Tp, and this leads to the creation of a macroscopic quantum state (pure state) or Bose-Einstein condensation phase. Tp = Tp,0 is a first-order phase transition point, Tp,n#0 is a zero-order phase transition point. Next, we obtained a new expression of the most probable distribution of the finite ideal Bose gas. In this expression Nj is directly proportional to gj - 1, where gj and Nj are, respectively, the degeneracy and the most probable occupation number in the degenerate level j. This property agrees with what chemical potential can be quantized if there is a non-degenerate level for the finite ideal Bose gas. Finally, using this expression, we defined a micro-partition function M, obtained the statistical expressions of some thermodynamical quantities.
Calculations of chemical potentials for ideal monatomic gases with Bose-Einstein and Fermi-Dirac statistics as functions of temperature, across the temperature region that is typical for the collective quantum degeneracy effect, are presented. Numerical calculations are performed without any additional approximations, and explicit dependences of the chemical potentials on temperature are constructed at a fixed density of gas particles. Approximate polynomial dependences of chemical potentials on temperature are obtained that allow for the results to be used in further studies without re-applying the involved numerical methods. The ease of using the obtained representations is demonstrated on examples of deformation of distribution for a population of energy states at low temperatures, and on the impact of quantum statistics (exchange interaction) on the equations of state for ideal gases and some of the thermodynamic properties thereof. The results of this study essentially unify two opposite limiting cases in an intermediate region that are used to describe the equilibrium states of ideal gases, which are well known from university courses on statistical physics, thus adding value from an educational point of view.
Abstract The Bose-Einstein condensation of a gas is investigated. Starting from the well-known formulae for Bose statistics, the problem has been generalized to include a variety of potential fields in which the particles of the gas move, and the number w of dimensions has not been restricted to three. The energy levels are taken to be εi≡εs1,....,s10=constanth2ms1α−1a12+...+swαaw2(1≤α≤2) the quantum numbers being s1 ,w= 1, 2, ..., and a1, ..., aw being certain characteristic lengths. (For α = 2, the potential field is that of the w-dimensional rectangular box; for α = 1, we obtain the w-dimensional harmonic oscillator field.) A direct rigorous method is used similar to that proposed by Fowler & Jones (1938). It is shown that the number q = w/α determines the appearance of an Einstein transition temperature T0·For q≤ 1 there is no such point, while for q > 1 a transition point exists. For 1 < q≤ 2, the mean energy ϵ- per particle and the specific heat dϵ-/dT are continuous at T = T0· For q > 2, the specific heat is discontinuous at T = T0, giving rise to a A λ-point. A well-defined transition point only appears for a very large (theoretically infinite) number N of particles. T0 is finite only if the quantity v = N/(a1 .... aw)2/ α¯is finite. For a rectangular box, v is equal to the mean density of the gas. If v tends to zero or infinity as N→ ∞, then T0 likewise tends to zero or infinity. In the case q > 1, and at temperatures T < T 0' there is a finite fraction N0 /N of the particles, given by N 0/N = 1-(T/T0)q, in the lowest state. London’s formula (1938 b) for the three-dimensional box is an example of this equation. Some further results are also compared with those given by London’s continuous spectrum approximation.