Symmetries and Order Parameters

Start out with a system (with properties and dynamics) described by its Hamiltonian H. H is invariant under some group G, which give the symmetries of H.

A system can have states with symmetries lower than the full group of the Hamiltonian, i.e. the state is invariant under some subgroup G. We call those symmetry breaking.

Our state is described by thermodynamic (ensemble) averages of operators ϕα, the ensemble average is then ϕα,ϕ(x) which is not invariant under the full group G.

These averages (⟨Φ⟩) are called order parameters. ϕ is a global order parameter and ϕ(x) is a local order parameter.

We can choose that the global order parameter is zero for high symmetry (always the full group, hence high T).

Symmetries

Discrete symmetries Z2, group 2 integers. Ex. Ising symmetries, uniaxial (anti-)ferromagnetic system. FM: (mz). AFM: mz,Amz,B. Ex: Rb 2 NiF 4, K 2 MnF 4. Order-disorder: Binary-order nAnB [βbrass]. Liquid-gas: nLng.

Dispacive: (Ferroelectric) perouskite nz BaLiO3.

20230130110456-statistical_mechanics.org_20230508_112229.png

Z3 group 3 integers. Graphene/ graphite surface (Krypton occupations on graphene lattice).

20230130110456-statistical_mechanics.org_20230508_112630.png

ZN group N integers.

Continuous Symmetries:

  • Rotations on a plane: O 2/U(1) Phase of a complex number. Examples: Easy plane FM, Easy plane AFM, Bose-Einstein condensation (superfluid), various liquid crystal phases. 20230130110456-statistical_mechanics.org_20230508_113043.png O3 rotations in 3D, Heisenberg FM.

Axioms of Group

Set G with binary operatorion . The group is (G,).

  • a(bc)=a(bc)
  • ai=a
  • aa1=i

Subgroup: Subset H to G, H is a subscrube of G if (H,) is also a group.

Towards Landau/ Landau-Gurburg Theory

F(ϕ(x))=dxf(n(x))

Consider if we have an ideal gas. Subdivide the space into boxes of size ΔV. Then for nj points in the box at position xj we have the density, ρ(xj)=njΔV.

Consider a spatially inhomogenous system. (Ideal gas) with free energy F(T,V,N)=NkT(ln(nλ3)1). Nj=n(xj)Δ(V). fig=F(T,V,N)ΔV=n(xj)kT(ln(n(xj)λ3)1) n(x),F[n]=f(n(x))dx. We integrated out microscopic degrees of freedom and replaced with coarse-grained field. Can calculate any equilibrium property that can be written in terms of n(x). So, what is p(n(x))=?. From before, αpα(H). n(x)p(n(x)) which is governed by the free energy F of the densities. p(n(x))=1Zexp(βF[n(x)]). Driving force (to equilibrium)? μ=FN=F/VN/V=fn. Then μ(x)=δF[n(y)]δn(x)=δδn(x)f(n(y))dy, which is called the variational/ functional derivative. Then, μ(x)=kTln(nλ3).

Considering currents. j=nv, vμx, v=γμx. γ relates to mobility and the negative relates to downhill. So, v=γn(x)kTln(n(x)λ3)x=γn(x)kT1nnx. From the continuituy equation, J+nt=0. Putting this together we get nt=γkT2nx2.

F=dxf(T,ϕ(x))+dx12k(ϕ(x)2). Landau’s theory: ignore the second term. Including the second term is L-G.

So expanding, f(T,ϕ)=f0(T)+f1ϕ+f2ϕ2+f3ϕ3+f4ϕ4+ where the coefficients f can depend on temperature, except:

  1. Highest power of ϕ provides a bounding potential: ϕ2n,f2n>0. So that the order parameter remains finite.
  2. f1: example ϕ=m=MV. F(T,V,M)dF=SdTpdV+BdM FM=fm=B. For high temperature and no field, the magnetization should be zero, hence ϕ=0. Then, fm|m=0=0 since it is a free energy minimum. Therefore, f1=0. Hence: f(T,ϕ)=f0(T)+f2ϕ2+f3ϕ3+f4ϕ4+. f(T,ϕ) Landau free energy density. This is typically written: f=f0(T)+12μ(T)ϕ2+13!f3ϕ3+14!gϕ4 by theorists and partical physics. f=f0(T)+12rϕ2wϕ3+uϕ4. f=f0(T)+12b(T)ϕ2+13c(T)ϕ3+14dϕ4.

Aside: MFT gives qualitative pictures that are pretty accurate to expectation.

Landau Model for Neumatic to Isotropic

Phase transition in liquid crystals.

Isotropic: any orientation of liquid crytals. Neumatic: molecules predominantly align with some axis n^.

Tensor Model - Neumatic to Isotropic Phase Transition in Liquid Crystal

Let n^ be a global unit vector called the Frank director. Let v^α be the unit director for the α molecule’s orientation.

Ordering is a measure of how close v^α is to n^, v^αn^=cosθ. For perfect order, θ=0,π so coskθ with k even.

Want f=f0+f1ϕ+f2ϕ2+f3ϕ3+f4ϕ4.

In the high-temperature phase, f1=0.

Let Q be a tensor. Then, ϕn=Tr{Qn}. In high T phase ϕ(high)=0. So, Tr{Q}=0 for high temperature. So our outer product, vvT. Start with, Qij=αviαvjα. So, Q(s)=1NVαviαvjαδ(xxα). Note the tensor must be symmetric.

Absolute disorder: θ is uniformly distributed, dΩS(θ)=0.

Absolute order, α.vαn^.

Choose a coordinate system such that the first basis vector is n^. So perfect alignment is vα=(100).

In order state, vαTvαTr((100000000)+(1/30001/30001/3))=0.

Tr((S00000000)+(S/3000S/3000S/3))=Tr(2/3S0001/3S0001/3S).

Then, Qij=S(ninj13δij)

dΩS(coskθ)=0=dφdθsinθS(coskθ)=2πdθsinθS(coskθ) with S(coskθ)=1 for θ=0,π. S=12(3(vαn^)z1)=12(3cos2θα1).

Trace: TrQ2=49S2+19S2+19S2=23S2. Trace: TrQ3=827S3127S3127S3=627S3=29S3. Trace: TrQ4=1681S4+181S4+181S4=1881S4=29S4.

f(S)=12rS2wS3+US4.

12r32TrQ2w92(Tr(Q3)+U92Tr(Q4)).

S=12(3cos2θα1)

20230130110456-statistical_mechanics.org_20230512_114256.png

L=dQ, dQ=TdS.

Ising Model Aside

m2m4m4m2m2m2m4.

f=f0f2(T)m2+f4m4 where f4>0. f2(TTC). f2>0 for T>TC and f2<0 for \(T

Can approximate f2 for TTC by a linear approximation, f2a(TTC).

Functional Aside

C.f. Entropy, S=kipilnpi=kdxp(x)lnp(x), Spi=k(lnpi+1)=S[p(x)]=k(lnp(x)+1).

Functional derivatives, for functions f that can be Taylor expanded about x, δF[f(x)]δf(y)=limϵ0F[f(x)+ϵδ(xy)]F[f(x)]ϵ=limϵ0f(x)+ϵδ(xy)dxf(x)dxϵ=limϵ0ϵδ(xy)dxϵ=1. In our case, F[n(x)]=f(n(x))dx. So, δF[n(x)]δn(y)=limϵ0f(n(x)+ϵδ(xy))dxf(n(x))dxϵ=limϵ0(f(n(x))+fn(ϵδ(xy))O(ϵ2))dxf(n(x))dxϵ=limϵ0fn(ϵδ(xy))dxϵ=limϵ0f(n(x))n(x)(δ(xy))dx=f(n(y))n(y).

To Try: F[ϕ(x)]=exp(ϕ(x)f(x)dx), then what is the functional derivative δF[ϕ(x)]δϕ(y)==f(y)F[ϕ(x)].

For one with a gradient: F[n]=f(x,n(x),n(x))dx, δF[n]δn(x)=fnfn.

Aside. For most field theories, we just postulate that p(ϕ(x))=exp(βHIG(ϕ(x)))Z exists but we can show it for a few. Z=(Dϕ)exp(βH(ϕ)).

Multicritical Points

f=12rϕ2+u4ϕ4, u4>0.

When r changes sign you get a continuous phase transition.

Consider the model, f=12rϕ2+u4ϕ4+u6ϕ6, u6>0 and u4 can be either sign. Plotting r versus u4,

Author: Christian Cunningham

Created: 2024-05-30 Thu 21:21

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