Quasiparticle and optical properties of rutile and anatase TiO 2
By Wei Kang, M. Hybertsen. 2010
173 citations recorded by the source corpus.
Quasiparticle excitation energies and optical properties of TiO{sub 2} in the rutile and anatase structures are calculated using many-body perturbation-theory methods. Calculations are performed for a frozen crystal lattice; electron-phonon coupling is not explicitly considered. In the GW method, several approximations are compared and it is found that inclusion of the full frequency dependence as well as explicit treatment of the Ti semicore states are essential for accurate calculation of the quasiparticle energy-band gap. The calculated quasiparticle energies are in good agreement with available photoemission and inverse photoemission experiments. The results of the GW calculations, together with the calculated static screened Coulomb interaction, are utilized in the Bethe-Salpeter equation to calculate the dielectric function {epsilon}{sub 2}({omega}) for both the rutile and anatase structures. The results are in good agreement with experimental observations, particularly the onset of the main absorption features around 4 eV. For comparison to low-temperature optical-absorption measurements that resolve individual excitonic transitions in rutile, the low-lying discrete excitonic energy levels are calculated with electronic screening only. The lowest energy exciton found in the energy gap of rutile has a binding energy of 0.13 eV. In agreement with experiment, it is not dipole allowed but the calculated exciton energymore » exceeds that measured in absorption experiments by about 0.22 eV and the scale of the exciton binding energy is also too large. The quasiparticle energy alignment of rutile is calculated for nonpolar (110) surfaces. In the GW approximation, the valence-band maximum is 7.8 eV below the vacuum level, showing a small shift from density-functional theory results.« less
Subfields: Electrical and Electronic Engineering, Materials Chemistry, Renewable Energy, Sustainability and the Environment
View Paper: https://www.semanticscholar.org/paper/4dd4b0d9ecef42fa06338467e30d965fdad86907
How researchers see this paper
The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.
In Electrical and Electronic Engineering
In Materials Chemistry
- Marco Buongiorno Nardelli
- Stefano Curtarolo
- Luis A. Agapito
- Natalio Mingo
- Daniel B. Miracle
- Shidong Wang
- Cormac Toher
In Renewable Energy, Sustainability and the Environment
Citations in the corpus
- Reformulation of DFT + U as a pseudohybrid hubbard density functional for accelerated materials discovery (2015, background): “[68] and X-ray photoelectron spectroscopy (XPS) measurements [69].”