TY - JOUR
T1 - HLE17
T2 - An Improved Local Exchange-Correlation Functional for Computing Semiconductor Band Gaps and Molecular Excitation Energies
AU - Verma, Pragya
AU - Truhlar, Donald G.
N1 - Publisher Copyright:
© 2017 American Chemical Society.
PY - 2017/4/6
Y1 - 2017/4/6
N2 - The local approximations to exchange-correlation functionals that are widely used in Kohn-Sham density functional theory usually underestimate band gaps and molecular excitation energies, and therefore, it becomes necessary to use more expensive hybrid functionals or more empirical DFT+U functionals for accurate predictions and modeling of these properties. This work presents a meta-generalized gradient approximation (meta-GGA) called High Local Exchange 2017 (HLE17) and illustrates how it can be useful for obtaining accurate semiconductor band gaps and molecular excitation energies. Unlike the conventional way of using the DFT+U method, one does not need to determine new parameters for every property or system studied. The HLE17 functional builds upon our earlier work (HLE16) where we had shown that by increasing the coefficient of local exchange and simultaneously decreasing the coefficient of local correlation with a GGA, the band gaps and excitation energies could be significantly improved without significantly degrading the ground-state molecular energetic properties. However, for almost every database tested in this work, HLE17 shows improvement over HLE16, and the improvement is particularly notable for solid-state lattice constants. This new functional provides a strategy for calculating properties that are otherwise difficult to calculate by a local functional. (Figure Presented).
AB - The local approximations to exchange-correlation functionals that are widely used in Kohn-Sham density functional theory usually underestimate band gaps and molecular excitation energies, and therefore, it becomes necessary to use more expensive hybrid functionals or more empirical DFT+U functionals for accurate predictions and modeling of these properties. This work presents a meta-generalized gradient approximation (meta-GGA) called High Local Exchange 2017 (HLE17) and illustrates how it can be useful for obtaining accurate semiconductor band gaps and molecular excitation energies. Unlike the conventional way of using the DFT+U method, one does not need to determine new parameters for every property or system studied. The HLE17 functional builds upon our earlier work (HLE16) where we had shown that by increasing the coefficient of local exchange and simultaneously decreasing the coefficient of local correlation with a GGA, the band gaps and excitation energies could be significantly improved without significantly degrading the ground-state molecular energetic properties. However, for almost every database tested in this work, HLE17 shows improvement over HLE16, and the improvement is particularly notable for solid-state lattice constants. This new functional provides a strategy for calculating properties that are otherwise difficult to calculate by a local functional. (Figure Presented).
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U2 - 10.1021/acs.jpcc.7b01066
DO - 10.1021/acs.jpcc.7b01066
M3 - Article
AN - SCOPUS:85019760409
SN - 1932-7447
VL - 121
SP - 7144
EP - 7154
JO - Journal of Physical Chemistry C
JF - Journal of Physical Chemistry C
IS - 13
ER -