We present our theoretical results on the electronic state in vanadium spinel oxide AlV₂O₄. The material is a mixed-valent system with the average valence V2.5+, and V cations constitute a frustrated pyrochlore structure. It shows a structural transition at ~ 700 K, leading to the formation of seven V-sites clusters -- heptamers. We study the electronic state of the heptamer by explicitly taking account of orbital degree of freedom as well as electron correlations. We show that the ground state of the heptamer for realistic parameters becomes spin-singlet because of strong σ-type bonding states of t2g orbitals. The temperature dependence of the magnetic susceptibility in experiments is naturally understood by this singlet formation in heptamers. Our results indicate that in AlV₂O₄ orbital physics is relevant to stabilize a cluster-type singlet state instead of a previously proposed charge-ordered state with valence skipping.
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Matsuda et al. (2006) studied this question.
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