Please use this identifier to cite or link to this item:
http://elar.urfu.ru/handle/10995/101674
Title: | Unusual Mott transition associated with charge-order melting in BiNiO3 under pressure |
Authors: | Leonov, I. Belozerov, A. S. Skornyakov, S. L. |
Issue Date: | 2019 |
Publisher: | American Physical Society |
Citation: | Leonov I. Unusual Mott transition associated with charge-order melting in BiNiO3 under pressure / I. Leonov, A. S. Belozerov, S. L. Skornyakov. — DOI 10.1103/PhysRevB.100.161112 // Physical Review B. — 2019. — Vol. 100. — Iss. 16. — 161112. |
Abstract: | We study the electronic structure, magnetic state, and phase stability of paramagnetic BiNiO3 near a pressure-induced Mott insulator-to-metal transition (MIT) by employing a combination of density functional and dynamical mean-field theory. We obtain that BiNiO3 exhibits an anomalous negative-charge-transfer insulating state, characterized by charge disproportionation of the Bi 6s states, with Ni2+ ions. Upon a compression of the lattice volume by ∼4.8%, BiNiO3 is found to make a Mott MIT, accompanied by the change of crystal structure from triclinic P1 to orthorhombic Pbnm. The pressure-induced MIT is associated with the melting of charge disproportionation of the Bi ions, caused by a charge transfer between the Bi 6s and O 2p states. The Ni sites remain to be Ni2+ across the MIT, which is incompatible with the valence-skipping Ni2+/Ni3+ model. Our results suggest that the pressure-induced change of the crystal structure drives the MIT in BiNiO3. © 2019 American Physical Society. |
URI: | http://elar.urfu.ru/handle/10995/101674 |
Access: | info:eu-repo/semantics/openAccess |
SCOPUS ID: | 85074936555 |
WOS ID: | 000492970400002 |
PURE ID: | 11123324 |
ISSN: | 24699950 |
DOI: | 10.1103/PhysRevB.100.161112 |
Appears in Collections: | Научные публикации ученых УрФУ, проиндексированные в SCOPUS и WoS CC |
Files in This Item:
File | Description | Size | Format | |
---|---|---|---|---|
2-s2.0-85074936555.pdf | 1,58 MB | Adobe PDF | View/Open |
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.