Efficient and Accurate Double-Hybrid-Meta-GGA Density Functionals-Evaluation with the Extended GMTKN30 Database for General Main Group Thermochemistry, Kinetics, and Noncovalent Interactions

被引:1080
作者
Goerigk, Lars [1 ,2 ]
Grimme, Stefan [1 ]
机构
[1] Univ Munster, Inst Organ Chem, D-48149 Munster, Germany
[2] NRW Grad Sch Chem, D-48149 Munster, Germany
关键词
AUXILIARY BASIS-SETS; PLESSET PERTURBATION-THEORY; CIRCULAR-DICHROISM SPECTRA; POTENTIAL-ENERGY FUNCTIONS; MOLECULAR-ORBITAL THEORY; ZETA VALENCE QUALITY; ELECTRONIC-STRUCTURE; AB-INITIO; HARTREE-FOCK; DISPERSION CORRECTIONS;
D O I
10.1021/ct100466k
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
We present an extended and improved version of our recently published database for general main group thermochemistry, kinetics, and noncovalent interactions [J. Chem. Theory Comput. 2010, 6, 107], which is dubbed GMTKN30. Furthermore, we suggest and investigate two new double-hybrid-meta-GGA density functionals called PTPSS-D3 and PWPB95-D3. PTPSS-D3 is based on reparameterized TPSS exchange and correlation contributions; PWPB95-D3 contains reparameterized PW exchange and B95 parts. Both functionals contain fixed amounts of 50% Fock-exchange. Furthermore, they include a spin-opposite scaled perturbative contribution and are combined with our latest atom-pairwise London-dispersion correction [J. Chem. Phys. 2010, 132, 154104]. When evaluated with the help of the Laplace transformation algorithm, both methods scale as At with system size. The functionals are compared with the double hybrids B2PLYP-D3, B2GPPLYP-D3, DSD-BLYP-D3, and XYG3 for GMTKN30 with a quadruple-zeta basis set. PWPB95-D3 and DSD-BLYP-D3 are the best functionals in our study and turned out to be more robust than B2PLYP-D3 and XYG3. Furthermore, PWPB95-D3 is the least basis set dependent and the best functional at the triple-c level. For the example of transition metal carbonyls, it is shown that, mainly due to the lower amount of Fock-exchange, PWPB95-D3 and PTPSS-D3 are better applicable than the other double hybrids. Finally, we discuss in some detail the XYG3 functional [Proc. Nat. Acad. Sci. U.S.A. 2009, 106, 4963], which makes use of B3LYP orbitals and electron densities. We show that it is basically a highly nonlocal variant of B2PLYP and that its partially good performance is mainly due to a larger effective amount of perturbative correlation compared to other double hybrids. We finally recommend the PWPB95-D3 functional in general chemistry applications.
引用
收藏
页码:291 / 309
页数:19
相关论文
共 136 条
[1]   Exchange functionals with improved long-range behavior and adiabatic connection methods without adjustable parameters:: The mPW and mPW1PW models [J].
Adamo, C ;
Barone, V .
JOURNAL OF CHEMICAL PHYSICS, 1998, 108 (02) :664-675
[2]   ELECTRONIC-STRUCTURE CALCULATIONS ON WORKSTATION COMPUTERS - THE PROGRAM SYSTEM TURBOMOLE [J].
AHLRICHS, R ;
BAR, M ;
HASER, M ;
HORN, H ;
KOLMEL, C .
CHEMICAL PHYSICS LETTERS, 1989, 162 (03) :165-169
[3]  
Ahlrichs R., 2008, Turbomole
[4]   ELIMINATION OF ENERGY DENOMINATORS IN MOLLER-PLESSET PERTURBATION-THEORY BY A LAPLACE TRANSFORM APPROACH [J].
ALMLOF, J .
CHEMICAL PHYSICS LETTERS, 1991, 181 (04) :319-320
[5]   van der Waals forces in density functional theory:: Perturbational long-range electron-interaction corrections -: art. no. 012510 [J].
Angyán, JG ;
Gerber, IC ;
Savin, A ;
Toulouse, J .
PHYSICAL REVIEW A, 2005, 72 (01)
[6]  
[Anonymous], 1989, Density-functional theory of atoms and molecules
[7]  
[Anonymous], MOLPRO, version 2009.1, a package of abinitio program.
[8]  
[Anonymous], 1990, DENSITY FUNCTIONAL T
[9]   Structures and interaction energies of stacked graphene-nucleobase complexes [J].
Antony, Jens ;
Grimme, Stefan .
PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 2008, 10 (19) :2722-2729
[10]   Density-functional thermochemistry .4. A new dynamical correlation functional and implications for exact-exchange mixing [J].
Becke, AD .
JOURNAL OF CHEMICAL PHYSICS, 1996, 104 (03) :1040-1046