Past exam of the phase transitions and collective phenomena course of the University of Cambridge / 2012 / Paper 1 / 3

A coarse-grained scalar order parameter $\varphi (\mathbf{x})$ describes a short-range Ising-like transition with sign symmetry. Write the dimensionless Landau-Ginzburg functional asHere $r=a_{t}t$, with the relevant critical-mass shift understood when fluctuations are included. Higher local powers and gradients are negligible only within a justified long-distance expansion. The partition function is $Z=\int \mathcal{D}\varphi e^{-\mathcal{H}}$ with a microscopic cutoff. The local functional is not already the fluctuation-integrated thermodynamic free energy.

Mean-field theory replaces this integral by its stable uniform saddle, $r{\varphi }_0+u{\varphi }_0^3=h$. At $h=0$,The branch curvature is $r_L=r+3u{\varphi }_0^2$: it is $r$ above and $2|r|$ below. HenceTogether with the finite heat-capacity jump from $f_{\min }$, this yieldsThe equal-$|t|$ susceptibility amplitude ratio is two. Uniform saddles also miss domain walls and spatial texture. For an $n$-component order parameter, symmetry allows a vector generalization; ordered transverse directions additionally carry Goldstone fluctuations.

To include small fluctuations set $\varphi ={\varphi }_0+\delta \varphi$. The Gaussian action is $\frac{1}{2}\int [c(\nabla \delta \varphi {)}^2+r_L(\delta \varphi {)}^2]$, givingThe displayed $G(q)$ is a spectral covariance per Fourier delta, avoiding an extra volume factor. As $r_L\to 0$, a growing correlation length lets increasingly large correlated regions fluctuate. The singular Gaussian heat correction contains $\int d^{d}q/(c{q}^2+r_L{)}^2$, which is infrared singular for $d<4$ and logarithmic at four. This signals failure of a simple saddle expansion; the Gaussian heat exponent obtained by extrapolation is not the exact interacting critical exponent.

The Ginzburg criterion compares the fluctuation of a correlation-volume average with ${\varphi }_0^2$, rather than using all ultraviolet fluctuations at a point. Keeping $q\lesssim {\xi }^{-1}$ below the transition gives, up to finite convention-dependent constants,Dividing by ${\varphi }_0^2=|r|/u$ yieldsFor $d<4$, writing $r=a_{t}t$ gives a nonuniversal Ginzburg reduced-temperature windowInside $|t|\lesssim \mathrm{Gi}$, interacting fluctuations must be treated. For example, in three dimensions $\mathrm{Gi}\sim u^2/(c^3{a}_t)$ in this normalization. Above four dimensions the long-wavelength ratio vanishes at criticality; at four it is marginal and interaction-generated logarithms require further analysis.

The spatial gradient term supplies correlations absent from uniform Landau theory. The Ginzburg test bounds where its mean-field saddle remains self-consistent; it does not compute nonclassical exponents or a universal material-independent window.^[ref]

Renormalization compares the same long-distance physics at different observation scales. The starting object is a microscopic or cutoff statistical Hamiltonian ${\mathcal{H}}_g$ with every symmetry-allowed coupling $g$. Because a critical correlation length is much larger than a lattice spacing, repeatedly eliminating short-distance detail can reveal scale-invariant behavior.

In a real-space transformation choose a normalized blocking kernel $B(S|s)$ for retained variables. DefineSumming over $S$ proves exact preservation of $Z$ before truncation. The transformed Hamiltonian generally gains longer-range and many-body interactions and a field-independent constant. Observables must be blocked consistently. In momentum-shell language split $\varphi ={\varphi }_{<}+{\varphi }_{>}$, integrate $\Lambda /b<|q|<\Lambda$, then use $x^{\prime }=x/b$ and a field rescaling to restore cutoff and kinetic normalization. Coarse-graining, rescaling and tracking generated interactions are distinct steps.

Repeated transformations generate a flow $g^{\prime }=R_b(g)$ with composition $R_b{R}_c=R_{bc}$ when the same exact coarse-graining family is used. Losing degrees of freedom generally makes this a semigroup, despite its conventional group name. A renormalization-group fixed point is invariant after rescaling. At a continuous transition the large-distance theory approaches a critical renormalization-group fixed point; finite correlation length instead eventually flows into an ordinary thermodynamic phase regime.

Linearize in scaling coordinates $u_i$:For increasing observation length, $y_i>0$ is relevant and must be tuned, $y_i<0$ is irrelevant, and $y_i=0$ is marginal and needs nonlinear analysis. Discrete multipliers $b^{y_i}$ must be compared with one, not with zero. The stable manifold forms the critical surface after relevant directions have been set to zero.

After subtracting regular additive contributions, ordinary hyperscaling givesChoosing $b=|t{|}^{-1/y_t}$ or choosing the field as scale yieldsFor a critical two-point function $G(r)\sim r^{-(d-2+\eta )}$, the order parameter scaling dimension is $x_m=(d-2+\eta )/2$, and its conjugate field has $y_h=d-x_m=(d+2-\eta )/2$. This recovers the Q1 identities while distinguishing the gap exponent $\Delta$ from the field's scaling dimension $y_h$.

As a concrete dimensional check, start from a scalar gradient action. Restoring its coefficient uses ${\varphi }^{\prime }(x^{\prime })=b^{(d-2)/2}{\varphi }_{<}(b{x}^{\prime })$, so at the Gaussian fixed pointQuartic interactions are relevant below four dimensions. They can produce an interacting Wilson-Fisher fixed point, whose exponents differ from naive Gaussian counting. Above four, the quartic coupling is irrelevant at the Gaussian fixed point but dangerous for ordered observables: ${\varphi }_0^2=-r/u$ is singular when $u$ is dropped. Thus the simple two-variable hyperscaling formula is not universal above the upper critical dimension.

Different microscopic systems can flow to the same long-distance renormalization-group fixed point, explaining universality of exponents and normalized scaling forms. Critical temperatures, metric factors and regular free energies remain nonuniversal. Dimension, order parameter symmetry, interaction range and additional soft variables constrain the universality class. Truncations, perturbative expansions and numerics approximate the flow; they must not be confused with the exact elimination definition.^[ref]

For a ferromagnetic nearest-neighbour Ising model on a chain let $s_i=\pm 1$, $K=J/(k_{B}T)>0$ and $h=H/(k_{B}T)$. The dimensionless Hamiltonian is $-K{\sum }_i{s}_i{s}_{i+1}-h{\sum }_i{s}_i$. In one dimension, decimating every other spin closes exactly within the nearest-neighbour family, including its additive constant. This is the exact chain building block of the Migdal-Kadanoff approach; bond moving becomes an additional approximation in higher-dimensional lattices.

For exact zero-field Ising-chain decimation, sum over an intermediate spin $\sigma$ between two retained spins:Parallel and antiparallel end spins give $A{e}^{K^{\prime }}=2\cosh 2K$ and $A{e}^{-K^{\prime }}=2$. HenceFor an even periodic chain, $Z_N(K)=A^{N/2}{Z}_{N/2}(K^{\prime })$. Rescaling the lattice spacing $2a$ back to $a$ completes the renormalization step. Decimation of $b$ successive links gives $\tanh K^{\prime }=(\tanh K{)}^b$, as follows by multiplying the transfer matrix $b$ times.

Let $v=\tanh K$. Then $v^{\prime }=v^2$ on $0\le v\le 1$. The infinite-temperature renormalization-group fixed point $v=0$ attracts every $0\le v<1$; the zero-temperature renormalization-group fixed point $v=1$ is unstable to heating, with slope two. There is no intermediate ferromagnetic renormalization-group fixed point. Equivalently $K^{\prime }\simeq K^2$ for small $K$, while $K^{\prime }\simeq K-\frac{1}{2}\log 2$ for large finite $K$. Thus there is no finite-temperature ordered thermodynamic phase in the short-range chain.

The domain-wall scaling coordinate of an Ising chain near $T=0$ is the domain-wall Boltzmann factor $w=e^{-2K}$. Its recursion and the zero-field correlation length areSince $\xi (K^{\prime })/a=[\xi (K)/a]/2$, the recursion has the correct length scaling. Its exponent is one with respect to $w$; it is not a finite power of physical temperature about $T_c=0$. In the thermodynamic limit, a bond is a domain wall with probability $(1-\tanh K)/2\sim e^{-2K}$, giving the same exponentially large length scale. Their finite energy allows entropy to proliferate walls at any positive temperature.

The Ising-chain decimation constant matters for thermodynamics. With dimensionless free energy per spin $f=-\lim N^{-1}\log Z_N$,The second expression follows independently from transfer eigenvalues $2\cosh K$ and $2\sinh K$ and satisfies the recursion. Multiplying it by $k_{B}T$ restores the physical free energy. Dropping $A$ would preserve normalized retained-spin probabilities but lose the eliminated-spin entropy.

Finite-field Ising-chain decimation is also exact. Use the symmetric transfer matrixand read the new couplings fromHere $W_{++}=e^{2K+2h}+e^{-2K}$, $W_{--}=e^{2K-2h}+e^{-2K}$ and $W_{+-}=2\cosh h$. The latter off-diagonal entry, the field convention split between adjacent bonds and the constant must all be tracked consistently. Near the zero-temperature zero-field renormalization-group fixed point $h^{\prime }\simeq 2h$, while at $K=0$ the independent-spin field is unchanged.

In the higher-dimensional Migdal-Kadanoff approximation, moving bonds creates chains that can be decimated. With bond moving first on a $d$-dimensional hypercubic lattice and length factor $b$, the strengthened links have $b^{d-1}K$, giving the conventionFor $d=1$ no transverse bonds move, so this reduces to the exact chain result. In higher dimensions it discards geometric correlations and is generally approximate on the original lattice; moving and decimating in another order yields another approximation, not a contradictory exact chain formula.^[ref]