Abstract
A physical picture of electron spin alignments in organic molecule-based ferrimagnets is given from numerical calculations of magnetic specific heat ( C) and magnetic susceptibility ( χ) as functions of temperature and static magnetic field ( B) in terms of an Ising Hamiltonian for an alternating spin chain. The double-peak structure of specific heat appears for different parameter ratios and different magnetic field B, indicating that one peak originates from the ferromagnetic nature and the other from the antiferromagnetic nature. Meanwhile, we study successively the influence of intermolecular and intramolecular interaction on the magnetic susceptibility, showing that the ferromagnetic spin alignment in the alternating molecular chains of biradicals and monoradicals is equivalent to the ferromagnetic alignment of the effective S=1/2 spins. Our results are consistent with those of the Quantum Monte Carlo simulations and the exact diagonalization method and in qualitative agreement with the experimental ones.
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