Electronic and magnetic properties of electron-doped and
Abstract
Because of its narrow split-off conduction band, doping of leads to interesting strongly correlated electrons. We study the effects of doping on 's electronic and magnetic properties, either by adding electrons compensated by an artificial homogeneous background, or a virtual crystal approximation (VCA), by changing the atomic number , so as to keep charge neutrality, or by explicitly introducing Na as a dopant. The former two are considered as a way to simulate injected charge by gating, the latter occurs in the vanadium bronze . We also simulate using a virtual crystal approximation by changing the atomic number . The differences in the band structure, which result from how the electrons added to the band are compensated by positive charge in the three models, are compared. The electronic band structures are calculated using the quasiparticle self-consistent method including a lattice polarization correction and the local spin density functional method with Hubbard- corrections (LSDA+ ). For , the half-filling leads to a splitting of the up- and down-spin lowest band. The spins are found to prefer an antiferromagnetic ordering along the chain direction. Other spin configurations are shown to have higher energy and the exchange interactions are extracted and compared with literature. The optical conductivities are calculated and compared with experiment. Similar results are found for simply doping the band compensated by a background or virtual crystal approximation. Yet, the position of the occupied bands depends on the method chosen for compensating the charge. The most realistic way to simulate gating in which the compensating charge is kept away from the layer is the VCA with varying . The splitting between the up- and down-spin bands depends on the filling. Furthermore, we find that below a certain concentration of about 0.88 electrons per V, the FM arrangement becomes preferable over the antiferromagnetic one. The magnetic moments then gradually decrease as we lower the filling of the split-off band.
- Authors:
-
- Case Western Reserve Univ., Cleveland, OH (United States)
- Publication Date:
- Research Org.:
- Case Western Reserve Univ., Cleveland, OH (United States)
- Sponsoring Org.:
- USDOE Office of Science (SC), Basic Energy Sciences (BES); US Air Force Office of Scientific Research (AFOSR)
- OSTI Identifier:
- 1593459
- Alternate Identifier(s):
- OSTI ID: 1221689
- Grant/Contract Number:
- SC0008933; ER-46874-SC0008933
- Resource Type:
- Journal Article: Accepted Manuscript
- Journal Name:
- Physical Review. B, Condensed Matter and Materials Physics
- Additional Journal Information:
- Journal Volume: 92; Journal Issue: 12; Journal ID: ISSN 1098-0121
- Publisher:
- American Physical Society (APS)
- Country of Publication:
- United States
- Language:
- English
- Subject:
- 75 CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND SUPERFLUIDITY; band structure; NaV2O5; antiferromagnetism; doping
Citation Formats
Bhandari, Churna, and Lambrecht, Walter R. L. Electronic and magnetic properties of electron-doped V2O5 and NaV2O5. United States: N. p., 2015.
Web. doi:10.1103/PhysRevB.92.125133.
Bhandari, Churna, & Lambrecht, Walter R. L. Electronic and magnetic properties of electron-doped V2O5 and NaV2O5. United States. https://doi.org/10.1103/PhysRevB.92.125133
Bhandari, Churna, and Lambrecht, Walter R. L. 2015.
"Electronic and magnetic properties of electron-doped V2O5 and NaV2O5". United States. https://doi.org/10.1103/PhysRevB.92.125133. https://www.osti.gov/servlets/purl/1593459.
@article{osti_1593459,
title = {Electronic and magnetic properties of electron-doped V2O5 and NaV2O5},
author = {Bhandari, Churna and Lambrecht, Walter R. L.},
abstractNote = {Because of its narrow split-off conduction band, doping of V2O5 leads to interesting strongly correlated electrons. We study the effects of doping on V2O5's electronic and magnetic properties, either by adding electrons compensated by an artificial homogeneous background, or a virtual crystal approximation (VCA), by changing the atomic number ZV, so as to keep charge neutrality, or by explicitly introducing Na as a dopant. The former two are considered as a way to simulate injected charge by gating, the latter occurs in the vanadium bronze NaV2O5. We also simulate Na1-xV2O5 using a virtual crystal approximation by changing the atomic number 10≤ZNa≤11. The differences in the band structure, which result from how the electrons added to the band are compensated by positive charge in the three models, are compared. The electronic band structures are calculated using the quasiparticle self-consistent QSGW method including a lattice polarization correction and the local spin density functional method with Hubbard-U corrections (LSDA+U). For NaV2O5, the half-filling leads to a splitting of the up- and down-spin lowest dxy band. The spins are found to prefer an antiferromagnetic ordering along the chain direction. Other spin configurations are shown to have higher energy and the exchange interactions are extracted and compared with literature. The optical conductivities are calculated and compared with experiment. Similar results are found for simply doping the band compensated by a background or virtual crystal approximation. Yet, the position of the occupied bands depends on the method chosen for compensating the charge. The most realistic way to simulate gating in which the compensating charge is kept away from the V2O5 layer is the VCA with varying ZNa. The splitting between the up- and down-spin bands depends on the filling. Furthermore, we find that below a certain concentration of about 0.88 electrons per V, the FM arrangement becomes preferable over the antiferromagnetic one. The magnetic moments then gradually decrease as we lower the filling of the split-off band.},
doi = {10.1103/PhysRevB.92.125133},
url = {https://www.osti.gov/biblio/1593459},
journal = {Physical Review. B, Condensed Matter and Materials Physics},
issn = {1098-0121},
number = 12,
volume = 92,
place = {United States},
year = {Thu Sep 17 00:00:00 EDT 2015},
month = {Thu Sep 17 00:00:00 EDT 2015}
}
Web of Science
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