Weak ferromagnetic order breaking the threefold rotational symmetry of the underlying kagom\'e lattice in CdCu3(OH)6(NO3)2·H2O

Abstract

Novel magnetic phases are expected to occur in highly frustrated spin systems. Here we study the structurally perfect kagom\'e antiferromagnet CdCu3(OH)6(NO3)2·H2O by magnetization, magnetic torque, and heat capacity measurements using single crystals.An antiferromagnetic order accompanied by a small spontaneous magnetization that surprisingly is confined in the kagom\'e plane sets in at TN≈4 K, well below the nearest-neighbor exchange interaction J / kB = 45 K.This suggests that a unique q = 0 type 120 spin structure with "negative" (downward) vector chirality, which breaks the underlying threefold rotational symmetry of the kagom\'e lattice and thus allows a spin canting within the plane, is exceptionally realized in this compound rather than a common one with "positive" (upward) vector chirality. The origin is discussed in terms of the Dzyaloshinskii-Moriya interaction.

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