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Weakly Interacting Bose Gas Preview

A weakly interacting Bose gas is a dilute gas of bosons whose low-energy two-body collisions are important but whose many-body correlations remain perturbatively small. In three dimensions, the standard control parameter is the gas parameter

γ=nas3≪1,\gamma = n a_s^3 \ll 1,

where n=N/Vn=N/V is the number density and asa_s is the ss-wave scattering length. The phrase weakly interacting does not mean that a dimensional coupling constant is numerically small by itself. It means that the interaction length is much smaller than the mean interparticle spacing:

as≪n−1/3.a_s \ll n^{-1/3}.

Even in this controlled regime, interactions change the infrared physics qualitatively. The ideal condensate has quadratic excitations, zero interaction pressure, divergent compressibility, and no nonzero Landau critical velocity. A weak repulsion produces a finite chemical potential, a healing length, and a linear sound branch. It also depletes the condensate at zero temperature and shifts the ground-state energy beyond mean field.

We connect the dilute-gas equation of state to sound, depletion, and the first correction beyond mean field. The Gross–Pitaevskii equation develops spatial mean fields, while Bogoliubov theory gives the systematic quadratic diagonalization. The point here is to see which physical scale each result predicts and which approximation makes it reliable.

Helpful background. Bose condensation defines the condensate, and field operators explains the Hamiltonian and normalization.

A dilute gas with a matched short-range interaction

Section titled “A dilute gas with a matched short-range interaction”

Unless stated otherwise, consider:

  • one species of spinless bosons;
  • three spatial dimensions;
  • a homogeneous volume VV with periodic boundary conditions;
  • short-range, repulsive interactions;
  • positive scattering length as>0a_s>0;
  • zero temperature, or temperatures low enough that condensate depletion is small;
  • the thermodynamic limit at fixed density;
  • wavelengths long compared with the microscopic interaction range.

A positive scattering length alone does not prove that a microscopic potential is repulsive or that an atomic gas is the absolute ground state: bound molecules may exist. We assume a stable repulsive gas, or a sufficiently long-lived atomic branch whose losses can be neglected on the timescale studied. The low-energy Hamiltonian is

H^=∫d3r ℏ22m∇ψ^†⋅∇ψ^+g2∫d3r ψ^†ψ^†ψ^ψ^,\hat H ={} \int d^3r\, \frac{\hbar^2}{2m} \boldsymbol\nabla\hat\psi^\dagger \boldsymbol\cdot \boldsymbol\nabla\hat\psi + \frac{g}{2} \int d^3r\, \hat\psi^\dagger \hat\psi^\dagger \hat\psi \hat\psi,

with equal-time commutator

[ψ^(r),ψ^†(r′)]=δ(3)(r−r′).[ \hat\psi(\mathbf r), \hat\psi^\dagger(\mathbf r') ] = \delta^{(3)}(\mathbf r-\mathbf r').

At leading order in the low-energy expansion,

g=4πℏ2asm.g = \frac{4\pi\hbar^2 a_s}{m}.

This formula uses the physical, renormalized scattering length. A bare coefficient multiplying a delta function depends on the ultraviolet prescription once loop or zero-point integrals are evaluated. It must not be identified with 4πℏ2as/m4\pi\hbar^2a_s/m at every cutoff without matching.

Let U(r)U(r) be a short-range microscopic two-body potential. At low relative momentum, its ss-wave phase shift obeys the effective-range expansion

kcot⁡δ0(k)=−1as+re2k2+O(k4),k\cot\delta_0(k) = -\frac{1}{a_s} + \frac{r_e}{2}k^2 + O(k^4),

where rer_e is the effective range. The scattering amplitude is

f0(k)=1kcot⁡δ0(k)−ik.f_0(k) = \frac{1}{ k\cot\delta_0(k)-ik }.

Keeping only scattering-length data requires the effective-range term to be small compared with the retained inverse-amplitude terms:

∣re∣k22≪∣−as−1−ik∣.\frac{|r_e|k^2}{2}\ll|-a_s^{-1}-ik|.

One also needs momenta below the inverse microscopic range R−1R^{-1} and below other internal-channel thresholds. In the regime kas≪1k a_s\ll1, a useful sufficient range condition is ∣asre∣k2≪1|a_s r_e|k^2\ll1; the statement k∣re∣≪1k|r_e|\ll1 alone is not the complete matching criterion. An energy-independent leading coupling gg is appropriate on these low-energy scales.

This two-body reduction and the many-body condition nas3≪1na_s^3\ll1 are distinct. For the typical collective momentum k∼ξ−1k\sim\xi^{-1} below, kas∼8πnas3ka_s\sim\sqrt{8\pi na_s^3} becomes small in the dilute limit, but an anomalously large effective range or a nearby channel can introduce another restriction. The contact model is a low-energy representation, not a microscopic point-particle assertion.

For a periodic box,

ψ^(r)=1V∑keik⋅ra^k,\hat\psi(\mathbf r) = \frac{1}{\sqrt V} \sum_{\mathbf k} e^{i\mathbf k\cdot\mathbf r} \hat a_{\mathbf k},

and

ϵk=ℏ2k22m.\epsilon_k = \frac{\hbar^2k^2}{2m}.

The Hamiltonian becomes

H^=∑kϵka^k†a^k+g2V∑k,k′,qa^k+q†a^k′−q†a^k′a^k.\hat H ={} \sum_{\mathbf k} \epsilon_k \hat a_{\mathbf k}^\dagger \hat a_{\mathbf k} + \frac{g}{2V} \sum_{\mathbf k,\mathbf k',\mathbf q} \hat a_{\mathbf k+\mathbf q}^\dagger \hat a_{\mathbf k'-\mathbf q}^\dagger \hat a_{\mathbf k'} \hat a_{\mathbf k}.

The wave-vector transfer q\mathbf q (physical momentum transfer ℏq\hbar\mathbf q) redistributes momentum between two particles while preserving total momentum. Unlike the ideal-gas Hamiltonian, the interaction does not commute with each individual mode occupation. Momentum modes are coupled, and the exact eigenstates are not single occupation-number configurations.

Start with the idealized state in which all NN particles occupy the zero-momentum mode:

∣N0=N⟩=(a^0†)NN!∣0⟩.|N_0=N\rangle = \frac{ (\hat a_{\mathbf0}^\dagger)^N }{\sqrt{N!}} |0\rangle.

Its kinetic energy is zero. The interaction expectation value uses

⟨a^0†a^0†a^0a^0⟩=N(N−1),\left\langle \hat a_{\mathbf0}^\dagger \hat a_{\mathbf0}^\dagger \hat a_{\mathbf0} \hat a_{\mathbf0} \right\rangle = N(N-1),

so

EMF=g2VN(N−1).E_{\mathrm{MF}} = \frac{g}{2V} N(N-1).

In the thermodynamic limit,

EMFV=g2n2.\frac{E_{\mathrm{MF}}}{V} = \frac{g}{2}n^2.

The factor 1/21/2 prevents double counting of particle pairs. This is the leading matched contact-theory mean-field expectation, not an exact microscopic-potential energy. The trial state neglects the pair correlations generated by interactions.

At fixed volume, the mean-field chemical potential is

μMF=(∂EMF∂N)V=gn\mu_{\mathrm{MF}} = \left( \frac{\partial E_{\mathrm{MF}}}{\partial N} \right)_V = gn

in the thermodynamic limit. The pressure is

PMF=−(∂EMF∂V)N=g2n2.P_{\mathrm{MF}} = -\left( \frac{\partial E_{\mathrm{MF}}}{\partial V} \right)_N = \frac{g}{2}n^2.

The isothermal compressibility at zero temperature is

κT=1n(∂n∂P)T=1gn2.\kappa_T = \frac{1}{n} \left( \frac{\partial n}{\partial P} \right)_T = \frac{1}{gn^2}.

Thus an arbitrarily weak positive gg gives the condensate a finite inverse compressibility. In the ideal limit g→0+g\to0^+,

κT→∞.\kappa_T \to \infty.

The Chemical Potential page explains why μ\mu is an addition-energy derivative rather than the energy of a distinguished particle.

Introduce a condensate amplitude Φ(r)\Phi(\mathbf r) normalized by

∫d3r ∣Φ(r)∣2=N.\int d^3r\, |\Phi(\mathbf r)|^2 = N.

At this leading order condensate number is approximated by total number. The corresponding energy functional is

E[Φ]=∫d3r [ℏ22m∣∇Φ∣2+Vext∣Φ∣2+g2∣Φ∣4].E[\Phi] = \int d^3r\, \left[ \frac{\hbar^2}{2m} |\boldsymbol\nabla\Phi|^2 + V_{\mathrm{ext}} |\Phi|^2 + \frac{g}{2} |\Phi|^4 \right].

Stationarity at fixed particle number gives the signpost equation

[−ℏ2∇22m+Vext+g∣Φ∣2]Φ=μΦ.\left[ -\frac{\hbar^2\nabla^2}{2m} + V_{\mathrm{ext}} + g|\Phi|^2 \right] \Phi = \mu\Phi.

For a uniform condensate, Φ=n\Phi=\sqrt n and μ=gn\mu=gn. Gross–Pitaevskii Equation derives this equation carefully, distinguishes stationary and time-dependent formulations, and treats boundary conditions, vortices, and trapped profiles. Here it serves only to show how the uniform equation of state enters a spatially varying condensate.

Replacing an operator by a complex amplitude is a representation of mean-field order, not an exact operator identity. Exact finite-NN states can preserve particle-number symmetry; number-conserving formulations reproduce the leading results without assigning a nonzero expectation value to ψ^\hat\psi.

Three scales organize the weakly interacting gas.

The mean-field energy per added particle is

μ=gn.\mu = gn.

This separates the collective low-energy regime from approximately single-particle behavior.

At zero temperature, hydrodynamics gives

c2=1m∂P∂n.c^2 = \frac{1}{m} \frac{\partial P}{\partial n}.

Using the mean-field pressure,

c=gnm.c = \sqrt{\frac{gn}{m}}.

Equivalently,

mc2=gn.mc^2 = gn.

Balance the kinetic cost of varying the condensate over a distance ξ\xi against the interaction energy:

ℏ22mξ2=gn.\frac{\hbar^2}{2m\xi^2} = gn.

The Gross–Pitaevskii healing-length convention used here is

ξ=ℏ2mgn=18πnas.\xi = \frac{\hbar}{\sqrt{2mgn}} = \frac{1}{\sqrt{8\pi n a_s}}.

It obeys

ξ=ℏ2 mc.\xi = \frac{\hbar}{\sqrt{2}\,mc}.

Different texts sometimes absorb the factor 2\sqrt2 into the definition of a coherence or healing length. Always check the defining balance before comparing formulas.

Parametrically, the dilute limit generates the hierarchy

as≪n−1/3≪ξ,a_s \ll n^{-1/3} \ll \xi,

up to numerical factors. The first inequality suppresses short-range many-body encounters; the second allows collective density variations to involve many particles.

For the ideal gas,

Ek(0)=ϵk=ℏ2k22m.E_k^{(0)} = \epsilon_k = \frac{\hbar^2k^2}{2m}.

The phase velocity tends to zero:

Ek(0)ℏk=ℏk2m⟶0\frac{E_k^{(0)}}{\hbar k} = \frac{\hbar k}{2m} \longrightarrow 0

as k→0k\to0. A fluid with this spectrum has no positive Landau threshold for creating excitations. The same softness appears thermodynamically as infinite compressibility below the ideal-gas condensation temperature.

Interactions cannot be represented merely by adding a constant Hartree shift to every excitation. Particle and hole amplitudes mix, and that mixing is what produces a gapless collective branch.

Work with the grand-canonical operator

K^=H^−μN^.\hat K = \hat H - \mu\hat N.

When the zero-momentum mode is macroscopically occupied, write schematically

a^0≈N0\hat a_{\mathbf0} \approx \sqrt{N_0}

and retain terms through quadratic order in a^k≠0\hat a_{\mathbf k\ne0}. The stationary condensate condition

μ=gn0,n0=N0V,\mu = gn_0, \qquad n_0 = \frac{N_0}{V},

makes the energy stationary under a change of the condensate amplitude. In a uniform expansion restricted to nonzero momenta, translation invariance already forbids linear terms in those modes. The quadratic fluctuation Hamiltonian is

K^2=∑k≠0[(ϵk+gn0)a^k†a^k+gn02(a^k†a^−k†+a^ka^−k)].\hat K_2 ={} \sum_{\mathbf k\ne\mathbf0} \Bigg[ (\epsilon_k+gn_0) \hat a_{\mathbf k}^\dagger \hat a_{\mathbf k} + \frac{gn_0}{2} \left( \hat a_{\mathbf k}^\dagger \hat a_{-\mathbf k}^\dagger + \hat a_{\mathbf k} \hat a_{-\mathbf k} \right) \Bigg].

The anomalous terms exchange opposite-momentum atom pairs with the condensate represented by its amplitude. The underlying Hamiltonian conserves total particle number. Therefore bare particles of momentum k\mathbf k are not the normal modes.

The approximation organizes the Hamiltonian as:

Order in fluctuations Role
no fluctuation operators condensate mean-field energy
one fluctuation operator vanishes when the background is stationary
two fluctuation operators independent quasiparticles after diagonalization
three and four fluctuation operators quasiparticle interactions neglected at leading order

The actual control condition is small depletion and weak quasiparticle interactions, not a formal claim that every higher-power operator is always negligible.

Introduce quasiparticle operators by

a^k=ukb^k−vkb^−k†,\hat a_{\mathbf k} = u_k\hat b_{\mathbf k} - v_k\hat b_{-\mathbf k}^\dagger,

with real coefficients satisfying

uk2−vk2=1.u_k^2-v_k^2 = 1.

This condition preserves the bosonic commutator. For repulsive gg and this minus-sign convention, choose uk,vk≥0u_k,v_k\ge0, with ukvk=gn0/(2Ek)u_kv_k=gn_0/(2E_k). Their squares are

uk2=12(ϵk+gn0Ek+1),u_k^2 = \frac12 \left( \frac{\epsilon_k+gn_0}{E_k} + 1 \right),

and

vk2=12(ϵk+gn0Ek−1).v_k^2 = \frac12 \left( \frac{\epsilon_k+gn_0}{E_k} - 1 \right).

The resulting excitation energy is

Ek=ϵk(ϵk+2gn0).E_k = \sqrt{ \epsilon_k (\epsilon_k+2gn_0) }.

At leading order in the dilute expansion, one may replace n0n_0 by nn inside this spectrum. Their difference is already of relative order nas3\sqrt{na_s^3}.

The quasiparticle vacuum is not the state with every atom in the zero-momentum mode. It is a correlated, pair-squeezed state with nonzero occupation vk2v_k^2 in modes k≠0\mathbf k\ne0.

Bogoliubov Quasiparticles compares this bosonic hyperbolic mixing with fermionic pairing and explains how uku_k and vkv_k enter particle content, conserved quantities, and probe coherence factors.

The equations of motion for the pair

(a^ka^−k†)\begin{pmatrix} \hat a_{\mathbf k} \\ \hat a_{-\mathbf k}^\dagger \end{pmatrix}

involve the matrix

Lk=(ϵk+gn0gn0−gn0−(ϵk+gn0)).\mathcal L_k = \begin{pmatrix} \epsilon_k+gn_0 & gn_0 \\ -gn_0 & -(\epsilon_k+gn_0) \end{pmatrix}.

Its eigenvalues satisfy

λk2=(ϵk+gn0)2−(gn0)2,\lambda_k^2 = (\epsilon_k+gn_0)^2 -(gn_0)^2,

and hence

λk=±Ek.\lambda_k = \pm E_k.

The minus sign in the lower row reflects the bosonic particle–hole metric. This is why diagonalizing the ordinary symmetric coefficient matrix as though it were a one-particle Hamiltonian gives the wrong answer.

Define

q=kξ.q = k\xi.

Because

ϵk=gnq2,\epsilon_k = gnq^2,

the leading spectrum takes the universal dimensionless form

Ekgn=q2(q2+2).\frac{E_k}{gn} = \sqrt{ q^2(q^2+2) }.

Bogoliubov dispersion crossing from a linear sound branch to a particle-like quadratic branch

The Bogoliubov dispersion in units set by gngn and the healing length ξ=ℏ/2mgn\xi=\hbar/\sqrt{2mgn}. For kξ≪1k\xi\ll1, Ek/(gn)≃2 kξE_k/(gn)\simeq\sqrt{2}\,k\xi; for kξ≫1k\xi\gg1, Ek/(gn)≃(kξ)2+1E_k/(gn)\simeq(k\xi)^2+1.

For q≪1q\ll1,

Ek=ℏck[1+(kξ)24+O((kξ)4)].E_k = \hbar ck \left[ 1 + \frac{(k\xi)^2}{4} + O((k\xi)^4) \right].

The excitations are phonons: collective density and phase waves rather than atoms carrying a definite momentum independently of the medium.

For q≫1q\gg1 while the contact description remains valid,

Ek=ϵk+gn−(gn)22ϵk+O(ϵk−2).E_k = \epsilon_k + gn - \frac{(gn)^2}{2\epsilon_k} + O(\epsilon_k^{-2}).

The excitation becomes particle-like, with a leading mean-field shift. This is an intermediate asymptotic statement: at momenta comparable to the inverse interaction range, the contact theory itself must be refined.

The crossover occurs near

kξ∼1,k\xi \sim 1,

or equivalently

ϵk∼gn.\epsilon_k \sim gn.

The healing length is therefore both a spatial recovery scale and the wavelength separating collective from particle-like excitations.

The microscopic Hamiltonian conserves total particle number and is invariant under

ψ^⟼eiαψ^.\hat\psi \longmapsto e^{i\alpha} \hat\psi.

In a thermodynamic symmetry-breaking description, the condensate chooses a phase. Long-wavelength phase variations cost arbitrarily little energy, producing the gapless phonon branch. The simple Bogoliubov spectrum indeed obeys

Ek=0=0.E_{k=0} = 0.

At finite size and fixed NN, one can retain exact number symmetry. The same collective spectrum emerges through number-conserving constructions. A nonzero order-parameter expectation value is a useful thermodynamic representation, not the only logically possible formulation. The broader symmetry logic is introduced in Spontaneous Symmetry Breaking Preview.

At zero temperature, the Bogoliubov quasiparticle vacuum satisfies

⟨b^k†b^k⟩=0,\langle \hat b_{\mathbf k}^\dagger \hat b_{\mathbf k} \rangle = 0,

but the atomic momentum modes have occupation

⟨a^k†a^k⟩=vk2.\langle \hat a_{\mathbf k}^\dagger \hat a_{\mathbf k} \rangle = v_k^2.

Thus the noncondensed density is

nex=∫d3k(2π)3vk2.n_{\mathrm{ex}} = \int \frac{d^3k}{(2\pi)^3} v_k^2.

For the homogeneous three-dimensional dilute gas,

nexn=83πnas3+o(nas3).\frac{n_{\mathrm{ex}}}{n} = \frac{8}{3\sqrt\pi} \sqrt{na_s^3} + o(\sqrt{na_s^3}).

This is quantum depletion: it remains at T=0T=0 and arises from interaction-induced pair correlations. It is distinct from thermal depletion. Small nas3\sqrt{na_s^3} makes the condensate fraction close to one, but never exactly one for a nonzero repulsive interaction in the thermodynamic ground state.

The Bose–Einstein Condensation page defines condensate occupation independently of basis. Here depletion is used as the quantitative diagnostic controlling the weak-correlation expansion.

Beyond Mean Field: Lee–Huang–Yang Term

Section titled “Beyond Mean Field: Lee–Huang–Yang Term”

The quadratic modes have zero-point energy. A naive contact-theory sum is ultraviolet divergent, so the bare coupling must be eliminated in favor of the physical scattering length before a finite result is quoted. After this matching, the ground-state energy density is

EV=gn22[1+12815πnas3+O ⁣(nas3ln⁡(nas3))].\frac{E}{V} = \frac{gn^2}{2} \left[ 1 + \frac{128}{15\sqrt\pi} \sqrt{na_s^3} + O\!\left( na_s^3\ln(na_s^3) \right) \right].

The leading correction is the Lee–Huang–Yang term. Differentiation gives

μ=gn[1+323πnas3+⋯ ].\mu = gn \left[ 1 + \frac{32}{3\sqrt\pi} \sqrt{na_s^3} + \cdots \right].

Several lessons are packed into these formulas:

  1. Mean field is the first term of a controlled expansion, not an exact result.
  2. The first correction is nonanalytic in gg when expressed at fixed density because as∝ga_s\propto g at leading order.
  3. The same parameter nas3\sqrt{na_s^3} controls both depletion and the leading energy correction.
  4. Higher orders eventually depend on additional short-distance data as well as logarithms.

The Lee–Huang–Yang term is a standard established result for the dilute homogeneous three-dimensional gas. Applying a local version of it to mixtures, dipolar gases, low dimensions, or rapidly varying trapped profiles requires a new validity analysis.

For nonzero wave vector, define n^k=∫Vd3r e−ik⋅rψ^†(r)ψ^(r)\hat n_{\mathbf k}=\int_Vd^3r\,e^{-i\mathbf k\cdot\mathbf r}\hat\psi^\dagger(\mathbf r)\hat\psi(\mathbf r) and the fluctuation

δn^k=n^k−⟨n^k⟩.\delta\hat n_{\mathbf k} = \hat n_{\mathbf k} - \langle\hat n_{\mathbf k}\rangle.

With the normalization

S(k)=1N⟨δn^kδn^−k⟩,S(k) = \frac{1}{N} \left\langle \delta\hat n_{\mathbf k} \delta\hat n_{-\mathbf k} \right\rangle,

Bogoliubov theory at zero temperature gives

S(k)=ϵkEk.S(k) = \frac{\epsilon_k}{E_k}.

At long wavelength,

S(k)∼ℏk2mc.S(k) \sim \frac{\hbar k}{2mc}.

The vanishing of S(k)S(k) as k→0k\to0 shows that repulsive interactions suppress long-wavelength density fluctuations. At finite temperature within the quasiparticle approximation,

S(k)=ϵkEkcoth⁡ ⁣(βEk2).S(k) = \frac{\epsilon_k}{E_k} \coth\!\left( \frac{\beta E_k}{2} \right).

Taking k→0k\to0 at fixed positive temperature gives S(k)→kBT/(mc2)S(k)\to k_{\mathrm B}T/(mc^2) at this order, consistent with the compressibility relation nkBTκTn k_{\mathrm B}T\kappa_T. This limit is different from the exactly zero mode: in a fixed-number state, S(0)=Var⁡(N)/N=0S(0)=\operatorname{Var}(N)/N=0. Correlation functions explains the connected density correlator and the order of limits.

Suppose an obstacle moves through the fluid with velocity v\mathbf v. Creating an excitation of momentum p\mathbf p changes the energy in the obstacle frame by

ΔE′=E(p)−v⋅p.\Delta E' = E(\mathbf p) - \mathbf v\boldsymbol\cdot\mathbf p.

Energetic emission is impossible if this is positive for every allowed excitation. The Landau critical velocity is therefore

vL=inf⁡p≠0E(p)∣p∣.v_L = \inf_{\mathbf p\ne\mathbf0} \frac{E(\mathbf p)}{|\mathbf p|}.

For the Bogoliubov branch, p=ℏk\mathbf p=\hbar\mathbf k and

Ek2ℏ2k2=c2+(ℏk2m)2.\frac{E_k^2}{\hbar^2k^2} = c^2 + \left( \frac{\hbar k}{2m} \right)^2.

Hence

vL=c.v_L = c.

This is a striking qualitative change from the ideal gas, for which vL=0v_L=0.

The Landau value is an energetic upper benchmark, not a universal measured critical velocity. In trapped or bounded fluids, vortex nucleation, surfaces, inhomogeneity, finite temperature, disorder, and dissipation can trigger flow decay below cc.

Condensation and superfluidity are related but not identical:

  • condensation concerns an extensive eigenvalue of the one-body density matrix;
  • superfluidity concerns nondissipative response, phase stiffness, metastable flow, and topological defects;
  • a homogeneous three-dimensional weakly interacting gas at low temperature exhibits both;
  • in other dimensions and strongly correlated systems, the relation can be subtler.

Quantum depletion also need not reduce the zero-temperature superfluid mass density. In the translationally invariant Galilean fluid, it equals the total mass density at zero temperature, although the condensate fraction is below one. A lattice or disorder changes the response question.

Take parameters roughly characteristic of a dilute alkali gas:

n=1020 m−3,as=5.3 nm,n = 10^{20}\ \mathrm{m}^{-3}, \qquad a_s = 5.3\ \mathrm{nm},

and

m=1.44×10−25 kg.m = 1.44\times10^{-25}\ \mathrm{kg}.

Then

nas3≈1.5×10−5,na_s^3 \approx 1.5\times10^{-5},

so

nas3≈3.9×10−3.\sqrt{na_s^3} \approx 3.9\times10^{-3}.

The leading quantum depletion is approximately

nexn≈5.8×10−3,\frac{n_{\mathrm{ex}}}{n} \approx 5.8\times10^{-3},

or about 0.6%0.6\%. The mean-field scales are approximately

μkB≈37 nK,\frac{\mu}{k_B} \approx 37\ \mathrm{nK}, c≈1.9 mm s−1,c \approx 1.9\ \mathrm{mm\,s^{-1}},

and

ξ≈0.27 μm.\xi \approx 0.27\ \mu\mathrm m.

These numbers are illustrative, not universal properties of a species. Density, internal state, magnetic field, trap geometry, and scattering length all matter.

As TT approaches the condensation transition, n0n_0 becomes small and long-wavelength critical fluctuations grow. A naive condensate expansion is not uniformly accurate in the critical region. The interaction-induced shift of the transition temperature is a separate finite-temperature many-body problem.

The parameter nas3na_s^3 is specific to three dimensions; low-dimensional gases explains the different control parameters. Couplings have different dimensions in one and two dimensions, long-range order has stronger infrared restrictions, and phase fluctuations can dominate density fluctuations. Three-dimensional depletion and Lee–Huang–Yang coefficients must not be transplanted unchanged.

Near a resonance, asa_s can become comparable to or larger than the interparticle spacing. Then nas3≪1na_s^3\ll1 fails, depletion is not perturbative, and additional few-body scales may enter. Bogoliubov theory is no longer a controlled expansion merely because a condensate remains observable.

For g<0g<0, the mean-field pressure and compressibility indicate instability. Formally,

Ek2=ϵk(ϵk−2∣g∣n),E_k^2 = \epsilon_k (\epsilon_k-2|g|n),

which is negative at sufficiently small kk. A uniform infinite gas therefore has exponentially growing long-wavelength modes. Finite trapped attractive condensates can be metastable below a system-dependent particle-number threshold, but that is a different boundary-value problem.

Dipolar, Coulomb, and other long-range forces produce momentum-dependent interactions and can generate excitation structures absent from the contact model. Replacing them by one scalar asa_s can erase the defining physics.

Use

nex=12π2∫0∞dk k2vk2n_{\mathrm{ex}} = \frac{1}{2\pi^2} \int_0^\infty dk\,k^2v_k^2

to show by rescaling that nex/nn_{\mathrm{ex}}/n is proportional to nas3\sqrt{na_s^3}. You may use

∫0∞dq q22[q2+1q2(q2+2)−1]=132.\int_0^\infty dq\, \frac{q^2}{2} \left[ \frac{q^2+1}{\sqrt{q^2(q^2+2)}} -1 \right] = \frac{1}{3\sqrt2}.
Solution

Set q=kξq=k\xi. Then

vk2=12[q2+1q2(q2+2)−1],v_k^2 = \frac12 \left[ \frac{q^2+1}{\sqrt{q^2(q^2+2)}} -1 \right],

and

nex=12π2ξ3132.n_{\mathrm{ex}} = \frac{1}{2\pi^2\xi^3} \frac{1}{3\sqrt2}.

Using

ξ−3=(8πnas)3/2,\xi^{-3} = (8\pi n a_s)^{3/2},

gives

nex=83πn3/2as3/2.n_{\mathrm{ex}} = \frac{8}{3\sqrt\pi} n^{3/2}a_s^{3/2}.

Dividing by nn yields

nexn=83πnas3.\frac{n_{\mathrm{ex}}}{n} = \frac{8}{3\sqrt\pi} \sqrt{na_s^3}.

The rescaling shows why the square root of the gas parameter, rather than the gas parameter itself, is the first relative correction.

Let g=−∣g∣g=-|g|. Determine the momentum range for which the Bogoliubov frequency is imaginary, and find the fastest growth rate.

Solution

For an attractive interaction,

Ek2=ϵk(ϵk−2∣g∣n).E_k^2 = \epsilon_k (\epsilon_k-2|g|n).

This is negative when

0<ϵk<2∣g∣n.0 < \epsilon_k < 2|g|n.

Since ϵk=ℏ2k2/(2m)\epsilon_k=\hbar^2k^2/(2m), the unstable band is

0<k<2m∣g∣nℏ.0 < k < \frac{2\sqrt{m|g|n}}{\hbar}.

Write Ek=iℏΓkE_k=i\hbar\Gamma_k in this band. Then

Γk=1ℏϵk(2∣g∣n−ϵk).\Gamma_k = \frac{1}{\hbar} \sqrt{ \epsilon_k(2|g|n-\epsilon_k) }.

The product is maximal at

ϵk=∣g∣n,\epsilon_k = |g|n,

giving

Γmax=∣g∣nℏ.\Gamma_{\mathrm{max}} = \frac{|g|n}{\hbar}.

An imaginary frequency signals dynamical collapse of the assumed uniform background, not a stable quasiparticle.

Using the displayed Lee–Huang–Yang chemical potential, find the leading correction to cc at zero temperature and fixed scattering length. Use mc2=n ∂μ/∂nmc^2=n\,\partial\mu/\partial n.

Solution

With γ=nas3\gamma=na_s^3 and A=32/(3π)A=32/(3\sqrt\pi), μ=gn(1+Aγ+⋯ )\mu=gn(1+A\sqrt\gamma+\cdots) gives

mc2=gn[1+16πγ+⋯ ],c=gnm[1+8πγ+⋯ ].mc^2=gn\left[1+\frac{16}{\sqrt\pi}\sqrt\gamma+\cdots\right], \qquad c=\sqrt{\frac{gn}{m}} \left[1+\frac{8}{\sqrt\pi}\sqrt\gamma+\cdots\right].

Differentiating the density-dependent correction is essential. Simply inserting the corrected chemical potential into mc2=μmc^2=\mu, which holds only for the leading linear equation of state, gives the wrong coefficient.

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