Abstract
Density functional theory calculations indicate that the incorporation of V into Ti lattice positions of rutile TiO2 leads to magnetic V 4 + species, but the extension and sign of the coupling between dopant moments confirm that ferromagnetic order cannot be reached via low-concentration doping in the non-defective oxide. Oxygen vacancies can introduce additional magnetic centres, and we show here that one of the effects of vanadium doping is to reduce the formation energies of these defects. In the presence of both V dopants and O vacancies all the spins tend to align with the same orientation. We conclude that V doping favours the ferromagnetic behaviour of TiO2 not only by introducing spins associated with the dopant centres but also by increasing the concentration of oxygen vacancies with respect to the pure oxide. © 2001 IOP Publishing Ltd.
Original language | English (US) |
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Pages (from-to) | 334216 |
Journal | Journal of Physics: Condensed Matter |
Volume | 23 |
Issue number | 33 |
DOIs | |
State | Published - Aug 3 2011 |
Bibliographical note
KAUST Repository Item: Exported on 2020-10-01Acknowledgements: This work made use of the facilities of HECToR, the UK's national high-performance computing service, via RGC's membership of the UK's HPC Materials Chemistry Consortium, which is funded by EPSRC (EP/F067496).
ASJC Scopus subject areas
- General Materials Science
- Condensed Matter Physics