Electronic structure and thermodynamics of V2O3 polymorphs

被引:17
作者
Wessel, C. [1 ]
Reimann, C. [2 ]
Mueller, A. [3 ]
Weber, D. [3 ]
Lerch, M. [3 ]
Ressler, T. [3 ]
Bredow, T. [2 ]
Dronskowski, R. [1 ]
机构
[1] Rhein Westfal TH Aachen, Inst Inorgan Chem, D-52056 Aachen, Germany
[2] Univ Bonn, Inst Phys & Theoret Chem, Mulliken Ctr Theoret Chem, D-53115 Bonn, Germany
[3] TU Berlin, Inst Chem, D-10623 Berlin, Germany
基金
日本学术振兴会;
关键词
vanadium sesquioxide; metastable polymorph; density-functional theory; quasiharmonic phonons; BILBAO CRYSTALLOGRAPHIC SERVER; GENERALIZED GRADIENT APPROXIMATION; METAL-INSULATOR-TRANSITION; CRYSTAL-STRUCTURE; EXCHANGE;
D O I
10.1002/jcc.23046
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A metastable bixbyite-type polymorph of vanadium sesquioxide, V2O3, has recently been synthesized, and it transforms to the corundum-type phase at temperatures around 550 degrees C. The possibility of a paramagnetic to canted antiferromagnetic or even spin-glass-like transition has been discussed. Quantum-chemical calculations on the density-functional theory level including explicit electronic correlation confirm the metastability as well as the semiconducting behavior of the material and predict that the bixbyite-type structure is about 0.1 eV less stable than the well-known corundum-type phase. Nonetheless, quasiharmonic phonon calculations manifest that bixbyite-type vanadium sesquioxide is a dynamically stable compound. Other possible V2O3 polymorphs are shown to be even less suitable candidates for the composition V2O3. (c) 2012 Wiley Periodicals, Inc.
引用
收藏
页码:2102 / 2107
页数:6
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