Tight Binding Model of Mn12 Single Molecule Magnets: Electronic and Magnetic Structure and Transport Properties
Fatemeh Rostamzadeh Renani, George Kirczenow

TL;DR
This paper develops a comprehensive tight-binding model for Mn12 single molecule magnets, accurately predicting their electronic and magnetic properties, and explores their potential for spintronic transport applications.
Contribution
The model extends Huckel theory to include spin effects and predicts transport properties, providing insights into ligand effects and spin filtering in Mn12 SMMs.
Findings
Model accurately predicts magnetic and electronic properties consistent with experiments.
LUMO orbitals can be ligand-based, enabling potential spintronic applications.
Predicted spin filtering and transport phenomena in Mn12 SMMs.
Abstract
We describe and analyze a tight-binding model of single molecule magnets (SMMs) that captures both the spin and spatial aspects of the SMM electronic structure. The model generalizes extended Huckel theory to include the effects of spin polarization and spin-orbit coupling. For neutral and negatively charged Mn12 SMMs with acetate or benzoate ligands the model yields the total SMM spin, the spins of the individual Mn ions, the magnetic easy axis orientation, the size of the magnetic anisotropy barrier and the size of the HOMO-LUMO gap consistent with experiment. For neutral molecules the predicted spins and spatial locations of the HOMO are consistent with the results of density functional calculations. For the total spin and location of the LUMO density functional theory-based calculations yield varied results while the present model yield results consistent with experiments on…
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