Recent magnetic measurements on tetra-nickel molecular magnets [Ni(hmp)(ROH)Cl]4, where R=CH3, CH2CH3, or (CH2)2C(CH3)3 and hmp− is the monoanion of 2-hydroxymethylpyridine, revealed a strong exchange bias prior to the external magnetic field reversal as well as anomalies in electron paramagnetic resonance peaks at low temperatures. To understand the exchange bias and observed anomalies, we calculate the electronic structure and magnetic properties for the Ni4 molecules with the three different ligands, employing density-functional theory. Considering the optimized structure with possible collinear spin configurations, we determine a total spin of the lowest-energy state to be S=0, which does not agree with experiment. We also calculate magnetic anisotropy barriers for all three types of Ni4 molecules to be in the range of 4-6 K.
@article{arxiv.cond-mat/0409207,
title = {Electronic structure and magnetic anisotropy for nickel-based molecular magnets},
author = {Kyungwha Park and En-Che Yang and David N. Hendrickson},
journal= {arXiv preprint arXiv:cond-mat/0409207},
year = {2009}
}