Use the usual homogeneous, local, analytic Landau-Ginzburg theory; rotational symmetry and Z2 symmetry alone do not specify locality, analyticity, or the signs of the coefficients. The local derivative expansion contains every rotational scalar with an even total number of fields:
The omitted terms include all allowed higher field powers and contracted spatial derivatives. Terms differing by a total derivative are equivalent for bulk behavior with suitable boundary conditions. The displayed gradient energy assumes spatial homogeneity. If only rotations about an origin are imposed, rotationally invariant position-dependent coefficients are also possible.
In the mean-field approximation, take a spatially uniform order parameter and minimize its Landau free energy. For , and with , keeping the quadratic and quartic terms gives
The single minimum splits into two minima as the temperature passes below the critical temperature. Choosing one minimum gives spontaneous symmetry breaking of the Z2 symmetry and a continuous phase transition. The order parameter is the expectation in a selected ordered state; averaging equally over both states gives zero. A Z2 symmetry does not guarantee a continuous phase transition: a negative quartic coefficient stabilized by a positive sextic coefficient can instead give a first-order phase transition.
Relaxing the Z2 symmetry permits odd terms. A nonzero linear source generally rounds this ordinary continuous phase transition. A cubic term can instead give a first-order phase transition: for , and , equal minima occur at
The order parameter jumps from zero to . A continuous phase transition without an exact Z2 symmetry is still possible with additional tuning; odd terms do not logically exclude it.
For the multicritical even Landau potential, set and assume an integer , and . For , all lower even interactions must be absent or tuned to zero to obtain these mean-field critical exponents. The stationary equation is
Its nonzero solutions are minima because . Thus the order-parameter critical exponent is
Substituting into the minimum free energy density gives
The singular heat capacity per unit volume is . Smooth variation of the other coefficients does not change the leading power. Consequently
For , this means a finite heat capacity jump, with ; for , the tricritical point has and . The case would contain only a quadratic potential and would not stabilize an ordered phase.
The Gaussian fluctuation correction near a critical point is more singular than the mean-field approximation contribution when
This is the upper critical dimension of an even scalar interaction. Equivalently, its coupling has engineering dimension , positive below . Dominant fluctuations signal breakdown of the mean-field approximation; the Gaussian expression is not then a calculation of the exact interacting heat-capacity critical exponent. At , equality of the powers allows logarithmic corrections.
Absorb into the free energy, so the statistical weight is . Under the Gaussian fixed point rescaling, invariance of the gradient energy gives the engineering dimension
The engineering dimensions of are respectively . Their coupling eigenvalues are , hence . The quadratic and quartic interactions are relevant operators; the sextic interaction is a marginal operator at this order.
The three steps of the momentum-shell renormalization group are:
  • Split into slow modes and fast modes , and integrate over .
  • Rescale to restore the ultraviolet cutoff to .
  • Rescale the field as to normalize the gradient energy.
Here , so increasing means flowing toward longer distances. At leading order, the fast field has a Gaussian distribution with covariance
This perturbative integration requires on the shell. By the Wick theorem, odd fast-field moments vanish and , . Therefore the first term of the cumulant expansion of a coarse-grained free energy is
This is the quartic interaction generated by a sextic interaction. Including the rescaling, the requested flow is
In spherical coordinates, . In particular, for ,
The same integration shifts the quadratic coefficient by before rescaling and adds an irrelevant constant to the free energy. Thus setting the bare quartic coupling to zero does not place the theory on the tricritical critical surface.
To calculate the sextic renormalization-group beta function to second order, let . The required cumulant expansion is
The subtraction removes disconnected contributions. The term at each vertex supplies the primitive sextic correction. The Wick contractions give
The first term contains three propagators connecting the two vertices; its factor is the number of bijections between the three fields at each vertex. The second contains a local tadpole diagram at each vertex and one connecting propagator. The primitive contribution to the free energy is therefore
Expanding the slow fields about a common point gives a negative local sextic correction proportional to
where restricts a momentum to the shell. This connected Feynman diagram has two independent loop momenta. Other Wick contractions also generate lower interactions and tadpole diagrams; they must be included or subtracted consistently when fixing the tricritical critical surface.
To extract the logarithmic tricritical sextic beta function, use normal ordering to remove local tadpoles and tune the quadratic and quartic relevant operators. The massless three-dimensional propagator is . The same three-line contraction over short separations gives
Its positive coefficient and the negative sign of the second cumulant expansion term establish the sign of the flow. Matching this logarithm to a renormalized coupling, or performing consistent iterated shell integration, gives
The precise normalization of is not needed. In a sharp momentum cutoff scheme, simply forcing all three internal momenta into one infinitesimal shell does not extract this two-loop logarithm: the shell restrictions remove its linear-in- phase space. The finite-shell cumulant and the logarithmic renormalized calculation above are distinct stages of the computation. Field normalization corrections at order enter this renormalization-group beta function only at order .
A positive, stabilizing sextic coupling is marginally irrelevant in three dimensions on the tricritical critical surface. Reversing the convention for reverses the sign of the renormalization-group beta function. A negative sextic coupling without higher stabilizing powers makes the potential unbounded; moreover, the untuned bare choice generally flows away through its generated relevant operator.
Write and assume , as required for quartic stability. In the mean-field approximation, the two-component radial quartic Landau potential is
Set , . At fixed , the quartic term is fixed and the quadratic term is minimized by assigning all of to the component with smaller . Minimizing over then gives
The resulting phase diagram has these regions:
On , the symmetry is enhanced to the orthogonal group , and the minima form the circle
Mixed-component minima occur on this line, rather than in an open coexistence region. Crossing the negative diagonal swaps the selected component discontinuously: this is a first-order phase transition, also called a spin-flop transition. For example, holding fixed and moving across , the derivative jumps from to zero. The angular degeneracy exactly on the line does not remove this discontinuity.
The positive half-axis , is a continuous phase transition, as is , . Their endpoint at is a bicritical point, where the two continuous boundaries meet the first-order negative diagonal. Approaching the origin radially makes the ordered amplitude vanish continuously. The negative half-axes lie inside ordered phases and are not additional transition lines. There are two continuous half-axis boundaries and one first-order negative diagonal, meeting at the origin.
At the Gaussian fixed point, , so all three quartic couplings have engineering dimension . Thus
Take and , as in the perturbative epsilon expansion. Define , , . The renormalization-group fixed point equations become
If , each of is independently or , giving four renormalization-group fixed points. If , subtracting the first two equations gives
The branch forces ; inserting this in the first equation yields a repeated root . Hence every nonzero- solution has . Then , and
has roots and . The complete list of six coupled Ising fixed points near four dimensions, in coordinates , is
The internal symmetries of these renormalization-group fixed points are:
The last point displays the field-rotation equivalence of decoupled Ising theories. With the orthogonal transformation ,
It is the same pair of decoupled Ising models written in fields rotated by , but remains a distinct coordinate solution of the stated renormalization-group beta functions. Here denotes the dihedral group of order eight; an alternative convention calls it . We have described linear internal transformations preserving the gradient energy; free massless sectors also have constant scalar-field shift symmetries. At , the six coordinates coalesce at the Gaussian fixed point.
Assume for stability. With equal quadratic coefficients and , the internal symmetry is the full orthogonal group . In two dimensions at positive temperature, with short-range interactions, the Mermin-Wagner theorem forbids spontaneous symmetry breaking of this continuous symmetry. Thus in both phases in the infinite system; a nonzero average order parameter does not distinguish them.
Instead measure the correlation function
The low-temperature phase has quasi-long-range order and algebraic correlations; the high-temperature phase has a finite correlation length and exponential correlations. More precisely,
A finite order parameter amplitude allows . Its long-distance Goldstone-mode effective free energy is . Restoring the Boltzmann constant and using the renormalized phase stiffness, the thermal phase fluctuations give
The Berezinskii–Kosterlitz–Thouless transition separates vortex-antivortex binding from unbound vortex defects. At the boundary, the universal stiffness jump gives and . The low-temperature phase stiffness is nonzero; it vanishes at long distances in the disordered phase. The exact transition location is fluctuation dependent and cannot be obtained just by setting the bare to zero.

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