DocumentCode :
3300155
Title :
A DFT+U calculations: Band structural and equation of states for anatase and rutile TiO2
Author :
Mahmood, Tariq ; Cao, Chuanbao ; Saeed, M.A. ; Ahmed, Maqsood ; Hussain, Talib
Author_Institution :
Sch. of Mater. Sci. & Eng., Beijing Inst. of Technol., Beijing, China
fYear :
2012
fDate :
5-7 Jan. 2012
Firstpage :
1
Lastpage :
2
Abstract :
Summary form only given. The band structure of anatase and rutile titanium dioxide has been calculated by using first-principles plane-wave pseudo-potential with CASTEP code, based on density functional and molecular dynamics theories, as incorporated in Accelrys Material studio. Studies presented in this work were performed using the generalized gradient approximation (GGA) method. For exchange-correlation function, we employed Perdow-Burke-Ernzerhof (PBE) by using both GGA and GGA with LDA+U. Localization of the excess electronic charge is encouraged by using +U term. For energy calculations the system is optimized for all values of U for rutile from 0 eV to 8.0 eV and for anatase from 0 eV to 9.5 eV. The optimum values of U for rutile TiO2 is 7.5 eV and for anatase TiO2 is 9.0 eV respectively. Our investigated results of band structure by using GGA-PBE are 2.140eV (fig. 1(a)) and 1.973eV (fig. 2(a)) for anatase and rutile respectively. The calculated band structures by using GGA-PBE with LDA+U term for both structures are 3.350 eV (anatase, fig.1 (b)) and 2.557 eV (rutile, fig. 2(b)). Obtained band gaps for both polymorphs are characterized as direct band gap for rutile (Figs. 2(a, b)) and indirect band gap for anatase (figs. 1(a, b)) TiO2 by using both given methods. Our studies show that GGA underestimates the electronic structure but by introducing LDA+U term with GGA predict comparable to experimentally observed the electronic structure for anatase [1] and rutile [2] TiO2. In addition, to obtain the zero pressure equilibrium volume, bulk modulus and pressure derivative of bulk modulus, the energy volume equation of state calculations were performed. The calculated values for the parameters of equation of state (anatase (V0=141.7 Å, B0=417.4 GPa and B´0 =3.97), rutile (V0=65.68 Å, B0=153.24 GPa and B´0 =3.7)) have good agreement with- experiment [3-5] and DFT [6] studies. Computed results have been compared with experimental and other theoretical predictions. A good agreement is obtained with the experimental measurements.
Keywords :
ab initio calculations; band structure; density functional theory; energy gap; equations of state; molecular dynamics method; pseudopotential methods; titanium compounds; Accelrys Material studio; CASTEP code; DFT+U calculations; Perdow-Burke-Ernzerhof calculation; TiO2; band gap; band structural; band structure; density functional theory; electron volt energy 0 eV to 9.5 eV; electronic charge; energy calculations; equation of states; exchange-correlation function; first-principles plane-wave pseudopotential calculation; generalized gradient approximation; molecular dynamics theory; polymorphs; Discrete Fourier transforms; Equations; Materials; Mathematical model; Nanotechnology; Photonic band gap; Physics; Bandgap; CASTEP; DFT; EOS; TiO2; anatase; rutile;
fLanguage :
English
Publisher :
ieee
Conference_Titel :
Enabling Science and Nanotechnology (ESciNano), 2012 International Conference on
Conference_Location :
Johor Bahru
Print_ISBN :
978-1-4577-0799-5
Type :
conf
DOI :
10.1109/ESciNano.2012.6149648
Filename :
6149648
Link To Document :
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