Quantum Mechanics, Volume 3. Claude Cohen-Tannoudji

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the curve presents no minima, correspond to a normal fluid, whose rotation can slow down because of the viscosity (dissipation of the kinetic energy into heat).

      There is, however, a more general way to address the problem, which shows that our basic conclusions are not limited to the particular case we have studied. It is based on the topological aspects of the wave function phase. When this phase varies by 2lπ as we go around the torus, it expresses a topological property characterized by the winding number l, which is an integer and cannot vary continuously. This is why, as long as the phase is well defined everywhere – i.e. as long as the wave function does not go to zero – we cannot go continuously from l to l ± 1. We already saw this in the particular example of the wave function (63): when the modulus of cl (t) varies in time from 1 to 0, while the modulus of cl′ (t) does the opposite, we necessarily went through a situation where the wave function went to zero through interference, in a plane corresponding to a certain value of φ; but the phase of the wave function is undetermined in this plane, and as we cross it, the phase undergoes a discontinuous jump. Now the canceling of the wave function of a great number of condensed bosons means the density must also be zero at that point, hence larger in other points of space. This spatial density variation introduces an energy increase, due to the finite compressibility of the fluid (as we saw in § 3-b, the energy increase in the high density regions is larger than the energy decrease in low density regions). This means there is an energy barrier opposing the change in the number of turns l of the phase. The height of this barrier must now be compared with the kinetic energy variation. As seen above, there is a drastic change in the flow regime, depending on whether the fluid velocity is smaller or larger than a certain critical velocity vc. In the first case, superfluidity allows a current to flow without dissipation, lasting practically indefinitely. In the second, no energy consideration opposes dissipation, and the rotation slows down progressively, as in an ordinary liquid.

      The essential idea to remember is that superfluidity comes from the repulsive interactions, and for two reasons. First of all, they explain the presence of the energy barrier, responsible for the metastability. The second reason, even more essential, is that the repulsion between bosons constantly tends to put all the fluid particles in the same quantum state – see § 4-c of Complement CXV; thanks to this property, we were able to characterize the intermediate rotational states by a very simple wave function (63). This implies that the quantum fluid can only occupy a very limited number of states, compared to a situation where the particles would be distinguishable. Consequently, it has a hard time dissipating its kinetic energy into heat, as a classical fluid would do, and it therefore maintains its rotation over such long times that a slowing down is practically impossible to observe.

      1 1 It is a “total derivative” term (the derivative describing, in a fluid, the motion of each particle). As the velocity field has a zero curl according to (51), a simple vector analysis calculation shows this term to be equal to m(v · ▽)v; it can therefore be accounted for by replacing on the left-hand side of (57) the partial derivative ∂/∂t by the total derivative d/dt = ∂/∂t + v · ∇.

      2 2 The quantum potential is still present for a single particle, since making g = 0 in (57) does not change this potential. For g = 0, the Gross-Pitaevskii equation simply reduces to the standard Schrödinger equation, valid for a single particle.

      3 3 or not at all, if we suppose the functions ul(r, z) and ul′(r, z) to be equal.

      4 4 When several relaxation channels are present, the one associated with the lowest barrier mainly determines the time evolution.

      Complement EXV Fermion system, Hartree-Fock approximation

      1  1 Foundation of the method 1-a Trial family and Hamiltonian 1-b Energy average value 1-c Optimization of the variational wave function 1-d Equivalent formulation for the average energy stationarity 1-e Variational energy 1-f Hartree-Fock equations

      2  2 Generalization: operator method 2-a Average energy 2-b Optimization of the one-particle density operator 2-c Mean field operator 2-d Hartree-Fock equations for electrons 2-e Discussion

      Introduction

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