Ground states and phase transitions for an aggregation model with fast diffusion on sphere
Razvan C. Fetecau, Hansol Park
TL;DR
This work analyzes an aggregation–diffusion free energy on the unit sphere with fast diffusion (0<m<1) and quadratic nonlocal attraction, identifying how ground states evolve with interaction strength κ for different diffusion regimes. By formulating admissible symmetric minimizers and deriving Euler–Lagrange conditions, the authors classify equilibria as fully supported densities or measure-valued states containing Dirac masses, depending on m and d. They reveal two main phase transitions: a bifurcation from the uniform distribution at κ1 to fully supported equilibria, and a second transition at κ2 where singular measures emerge, with a possible κ3 in certain ranges; numerical experiments corroborate the analytical bifurcation structure and energy ordering. The results extend Onsager-type free energy analyses to fast diffusion on spheres, illuminating when concentration persists despite diffusion and how ground states reorganize across parameter regimes. This has implications for modeling orientation phenomena in polymers and related systems on curved manifolds, and provides a framework for predicting when singular mass concentrations arise as ground states.
Abstract
We consider a free energy on the sphere that contains an entropy associated to nonlinear fast diffusion, and a nonlocal interaction energy. The two components of the free energy compete with each other, as one favours spreading and the other promotes concentration, respectively. The model is a generalization of the Onsager free energy with dipolar potential, used to study polymer orientation. We study the global energy minimizers of the energy functional, and in particular the various phase transitions that occur with respect to the strength of the nonlocal attractive interactions. In the considered regime, diffusion reduces as the density increases, for which reason the global energy minimizers can contain Dirac mass concentrations. We identify various ranges of the fast diffusion exponent and of the interaction strength, which give qualitatively different equilibria and ground states. The theoretical results are supported by numerical illustrations.
