Madelung equations

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In theoretical physics, the Madelung equations, or the equations of quantum hydrodynamics, are Erwin Madelung's alternative formulation of the Schrödinger equation for a spinless non relativistic particle, written in terms of hydrodynamical variables, similar to the Navier–Stokes equations of fluid dynamics.Template:Sfn The derivation of the Madelung equations is similar to the de Broglie–Bohm formulation, which represents the Schrödinger equation as a quantum Hamilton–Jacobi equation. In both cases the hydrodynamic interpretations are not equivalent to Schrodinger's equation without the addition of a quantization condition.

History

In the fall of 1926, Erwin Madelung reformulatedTemplate:SfnTemplate:Sfn Schrödinger's quantum equation in a more classical and visualizable form resembling hydrodynamics. His paper was one of numerous early attempts at different approaches to quantum mechanics, including those of Louis de Broglie and Earle Hesse Kennard.Template:Sfn The most influential of these theories was ultimately de Broglie's through the 1952 work of David BohmTemplate:Sfn now called Bohmian mechanics.

In 1994 Timothy C. Wallstrom showed[1] that an additional ad hoc quantization condition must be added to the Madelung equations to reproduce Schrodinger's work. His analysis paralleled earlier work[2] by Takehiko Takabayashi on the hydrodynamic interpretation of Bohmian mechanics. The mathematical foundations of the Madelung equations continue to be a topic of research.[3]

Equations

The Madelung equations are quantum Euler equations:Template:Cn tρm+(ρm𝐯)=0,d𝐯dt=t𝐯+𝐯𝐯=1m(Q+V), where

The Madelung equations answer the question whether 𝐯(𝐱,t) obeys the continuity equations of hydrodynamics and, subsequently, what plays the role of the stress tensor.Template:Sfn

The circulation of the flow velocity field along any closed path obeys the auxiliary quantization condition Γm𝐯d𝐥=2πn for all integers Template:Mvar.Template:SfnTemplate:Sfn

Derivation

The Madelung equations are derived by first writing the wavefunction in polar formTemplate:SfnTemplate:Sfn ψ(𝐱,t)=R(𝐱,t)eiS(𝐱,t)/, with R0 and S both real and ρ(𝐱,t)=ψ(𝐱,t)*ψ(𝐱,t)=R2(𝐱,t), the associated probability density. Substituting this form into the probability current gives: 𝐉=2mi(ψ*ψψψ*)=1mρ(𝐱,t)S(𝐱,t)=ρ(𝐱,t)𝐯(𝐱,t), where the flow velocity is expressed as 𝐯(𝐱,t)=1mS(𝐱,t). However, the interpretation of 𝐯 as a "velocity" should not be taken too literal, because a simultaneous exact measurement of position and velocity would necessarily violate the uncertainty principle.Template:Sfn

Next, substituting the polar form into the Schrödinger equation itψ(𝐱,t)=[22m2+V(𝐱)]ψ(𝐱,t), and performing the appropriate differentiations, dividing the equation by eiS(𝐱,t)/ and separating the real and imaginary parts, one obtains a system of two coupled partial differential equations: tR(𝐱,t)+1mR(𝐱,t)S(𝐱,t)+12mR(𝐱,t)ΔS(𝐱,t)=0,tS(𝐱,t)+12m[S(𝐱,t)]2+V(𝐱)=22mΔR(𝐱,t)R(𝐱,t). The first equation corresponds to the imaginary part of Schrödinger equation and can be interpreted as the continuity equation. The second equation corresponds to the real part and is also referred to as the quantum Hamilton-Jacobi equation.Template:Sfn Multiplying the first equation by 2R and calculating the gradient of the second equation results in the Madelung equations: tρ(𝐱,t)+[ρ(𝐱,t)v(𝐱,t)]=0,ddt𝐯(𝐱,t)=tv(𝐱,t)+[v(𝐱,t)]v(𝐱,t)=1m[V(𝐱)22mΔρ(𝐱,t)ρ(𝐱,t)]=1m[V(𝐱)+Q(𝐱,t)]. with quantum potential Q(𝐱,t)=22mΔρ(𝐱,t)ρ(𝐱,t).

Alternatively, the quantum Hamilton-Jacobi equation can be written in a form similar to the Cauchy momentum equation: ddt𝐯=𝐟1ρm𝐩Q, with an external force defined as 𝐟(𝐱)=1mV(𝐱), and a quantum pressure tensorTemplate:Sfn 𝐩Q=(/2m)2ρmlnρm.

The integral energy stored in the quantum pressure tensor is proportional to the Fisher information, which accounts for the quality of measurements. Thus, according to the Cramér–Rao bound, the Heisenberg uncertainty principle is equivalent to a standard inequality for the efficiency of measurements.Template:SfnTemplate:Sfn

Quantum energies

The thermodynamic definition of the quantum chemical potential μ=Q+V=1ρmH^ρm follows from the hydrostatic force balance above: μ=mρm𝐩Q+V. According to thermodynamics, at equilibrium the chemical potential is constant everywhere, which corresponds straightforwardly to the stationary Schrödinger equation. Therefore, the eigenvalues of the Schrödinger equation are free energies, which differ from the internal energies of the system. The particle internal energy is calculated as ε=μtr(𝐩Q)mρm=28m(lnρm)2+U and is related to the local Carl Friedrich von Weizsäcker correction.Template:Sfn

See also

Notes

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References