%0 Journal Article %1 hlwoodcock:de2005 %A de Jong, G. T. %A Geerke, D. P. %A Diefenbach, A. %A Bickelhaupt, F. M. %D 2005 %J CHEMICAL PHYSICS %K bibtex-import %N 1-3 %P 261--270 %T DFT benchmark study for the oxidative addition of CH4 to Pd. Performance of various density functionals %V 313 %X We have evaluated the performance of 24 popular density functionals for describing the potential energy surface (PES) of the archetypal oxidative addition reaction of the methane C-H bond to the palladium atom by comparing the results with our recent ab initio (CCSD(T) benchmark study of this reaction. The density functionals examined cover the local density approximation (LDA), the generalized gradient approximation (GGA), meta-GGAs as well as hybrid density functional theory. Relativistic effects are accounted for through the zeroth-order regular approximation (ZORA). The basis-set dependence of the density-functional-theory (DFT) results is assessed for the Becke-Lee-Yang-Parr (BLYP) functional using a hierarchical series of Slater-type orbital (STO) basis sets ranging from unpolarized double-zeta (DZ) to quadruply polarized quadruple-zeta quality (QZ4P). Stationary points on the reaction surface have been optimized using various GGA functionals, all of which yield geometries that differ only marginally. Counterpoise-corrected relative energies of stationary points are converged to within a few tenths of a kcal/mol if one uses the doubly polarized triple-zeta (TZ2P) basis set and the basis-set superposition error (BSSE) drops to 0.0 kcal/mol for our largest basis set (QZ4P). Best overall agreement with the ab initio benchmark PES is achieved by functionals of the GGA, meta-GGA, and hybrid-DFT type, with mean absolute errors of 1.3-1.4 kcal/mol and errors in activation energies ranging from +0.8 to1.4 kcal/mol. Interestingly, the well-known BLYP functional compares very reasonably with an only slightly larger mean absolute error of 2.5 kcal/mol and an underestimation by -1.9 kcal/mol of the overall barrier (i.e., the difference in energy between the TS and the separate reactants). For comparison, with B3LYP we arrive at a mean absolute error of 3.8 kcal/mol and an overestimation of the overall barrier by 4.5 kcal/mol. (c) 2005 Elsevier B.V. All rights reserved.

@article{hlwoodcock:de2005, abstract = {We have evaluated the performance of 24 popular density functionals for describing the potential energy surface (PES) of the archetypal oxidative addition reaction of the methane C-H bond to the palladium atom by comparing the results with our recent ab initio (CCSD(T)] benchmark study of this reaction. The density functionals examined cover the local density approximation (LDA), the generalized gradient approximation (GGA), meta-GGAs as well as hybrid density functional theory. Relativistic effects are accounted for through the zeroth-order regular approximation (ZORA). The basis-set dependence of the density-functional-theory (DFT) results is assessed for the Becke-Lee-Yang-Parr (BLYP) functional using a hierarchical series of Slater-type orbital (STO) basis sets ranging from unpolarized double-zeta (DZ) to quadruply polarized quadruple-zeta quality (QZ4P). Stationary points on the reaction surface have been optimized using various GGA functionals, all of which yield geometries that differ only marginally. Counterpoise-corrected relative energies of stationary points are converged to within a few tenths of a kcal/mol if one uses the doubly polarized triple-zeta (TZ2P) basis set and the basis-set superposition error (BSSE) drops to 0.0 kcal/mol for our largest basis set (QZ4P). Best overall agreement with the ab initio benchmark PES is achieved by functionals of the GGA, meta-GGA, and hybrid-DFT type, with mean absolute errors of 1.3-1.4 kcal/mol and errors in activation energies ranging from +0.8 to1.4 kcal/mol. Interestingly, the well-known BLYP functional compares very reasonably with an only slightly larger mean absolute error of 2.5 kcal/mol and an underestimation by -1.9 kcal/mol of the overall barrier (i.e., the difference in energy between the TS and the separate reactants). For comparison, with B3LYP we arrive at a mean absolute error of 3.8 kcal/mol and an overestimation of the overall barrier by 4.5 kcal/mol. (c) 2005 Elsevier B.V. All rights reserved.}, added-at = {2006-06-16T05:03:46.000+0200}, author = {de Jong, G. T. and Geerke, D. P. and Diefenbach, A. and Bickelhaupt, F. M.}, biburl = {https://www.bibsonomy.org/bibtex/2ec2ecfe554df5fb27da63889264a592f/hlwoodcock}, citeulike-article-id = {569691}, interhash = {31c68e50dfbae89f28e70b87565127f0}, intrahash = {ec2ecfe554df5fb27da63889264a592f}, journal = {CHEMICAL PHYSICS}, keywords = {bibtex-import}, number = {1-3}, pages = {261--270}, priority = {2}, timestamp = {2006-06-16T05:03:46.000+0200}, title = {DFT benchmark study for the oxidative addition of CH4 to Pd. Performance of various density functionals}, volume = 313, year = 2005 }