Orthorhombic fulleride (CH3NH2)K3C60 close to Mott-Hubbard instability: Ab initio study

We study the electronic structure and magnetic interactions in methylamine-intercalated orthorhombic alkali-doped fullerene (CH3NH2)K3C60 within the density functional theory. As in the simpler ammonia intercalated compound (NH3)K3C60, the orthorhombic crystal-field anisotropy Δlifts the t1u triple degeneracy at the Γpoint and drives the system deep into the Mott-insulating phase. However, the computed Δand conduction electron bandwidth W cannot alone account for the abnormally low experimental Néel temperature, T_N = 11 K of the methylamine compound, compared to the much higher value T_N = 40 K of the ammonia one. Significant interactions between CH3NH2 and C60^{3-} are responsible for the stabilization of particular pseudo-Jahn-Teller fullerene-cage distortions and the ensuing low-spin S = 1/2 state. These interactions also seem to affect the magnetic properties, as interfullerene exchange interactions depend on the relative orientation of pseudo-Jahn-Teller distortions of neighboring C60^{3-} molecules. For the ferro-orientational order of CH3NH2-K^+ groups we find an apparent reduced dimensionality in magnetic exchange interactions, which may explain the suppressed Néel temperature. The disorder in exchange interactions caused by orientational disorder of CH3NH2-K^+ groups could further contribute to this suppression.

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