We apply a Wilsonian renormalization group approach to the continuum limit of the attractive t − t ′ Hubbard model, taken when the Fermi level is at the Van Hove singularity of the density of states. We determine the leading instabilities by computing the different response functions up to t ′ = 0.5 t . The phase diagram shows a large boundary between superconducting and charge-density-wave phases, that merge in a triple point with a phase separation instability. The latter is realized down to very low coupling constant, as the Fermi sea degenerates towards a pair of straight lines near t ′ = 0.5 t .
The $t\ensuremath{-}{t}^{\ensuremath{'}}$ Hubbard model for the Fermi level near the van Hove singularity is considered within the renormalization group and parquet approaches. Interplay of ferromagnetic, antiferromagnetic, and superconducting channels is investigated, and the phase diagram of the model is constructed. In comparison with previous approaches, the account of ferromagnetic fluctuations suppresses superconducting pairing and, vice versa, the influence of the Cooper channel decreases the Curie temperature, so that the Stoner criterion is inapplicable even qualitatively.
Controlling the ordered phases of correlated electron systems remains a central challenge in quantum materials design. Divergences in the electronic density of states, known as Van Hove singularities (VHSs), are one obvious route to such control. It is clear from recent work that the exact functional form of these divergences can profoundly affect which phases are realized; a full picture, however, remains elusive. In this work, we use both the hot-spot parquet renormalization group and the truncated-unity functional renormalization group to theoretically study the emergent correlated states of a two-dimensional square-lattice Hubbard model with VHSs at or near the Fermi level. By varying a single hopping parameter,
t3, we are able to change the strength of the VHS divergence in the density of states from logarithmic (for
t3<t3c) to power-law (for
t3=t3c). Further increase of
t3 (
t3>t3c) causes each original Van Hove point to split into two, both of the conventional logarithmic type. We show that which of these regimes we are in strongly influences the predicted ordered states. We also study the dependence on doping, and find that the ferromagnetic state that occurs at Van Hove filling in these models is unstable to very small shifts in the Fermi level, often giving way to distinct ordered states depending on whether the model is electron- or hole-doped. These results highlight the importance of tuning VHS properties to control ordered states in correlated materials, and offer design rules to engineer these phases in novel systems.