Literature DB >> 21956624

Benchmark results for empirical post-GGA functionals: difficult exchange problems and independent tests.

Narbe Mardirossian1, John A Parkhill, Martin Head-Gordon.   

Abstract

Many of the most promising new density functionals have improved the treatment of non-local exchange effects with the help of semi-empirical information and more sophisticated recipes for combining Hartree-Fock and local exchange approximations. In order to quantify recent advancements and identify directions for improvement, we have examined a broad spectrum of test problems. We evaluate the performance of several new hybrid density functionals (ωB97, ωB97X, ωB97X-D, LRC-ωPBEh, M06, M06-2X, and M06-HF) on a variety of chemical problems, some sensitive to the treatment of exact exchange (which we have hoped to systematically improve) and some which require a balanced treatment of correlation. Since all of the functionals under consideration are parameterized with ground-state thermochemical data, the benchmark aims to determine the applicability of the new density functionals to cases that have not been considered in the optimization of the semi-empirical parameters. The first class of benchmarks includes the excitation energies of 21 molecules (83 states) primarily from a recent benchmark conducted by Tozer and co-workers, with some additional references from data made available from the groups of Thiel and Truhlar. We briefly examine the conformational preferences of a small peptide and complete our study with two recently published sets of data that have shown large, systematic errors in simple alkane thermochemistry. While our results indicate that the more general hybrids currently under development perform well for problems outside of their parameterization and improve over the standard hybrid density functionals in an essentially systematic way, there is still a significant self-interaction error in the more difficult cases. Functionals based on a range-separation of exchange and functionals depending on the kinetic-energy density both perform comparably, and there is evidence for complementary strengths. This journal is © the Owner Societies 2011

Entities:  

Year:  2011        PMID: 21956624     DOI: 10.1039/c1cp21635j

Source DB:  PubMed          Journal:  Phys Chem Chem Phys        ISSN: 1463-9076            Impact factor:   3.676


  6 in total

1.  Benchmarking the Performance of Time-Dependent Density Functional Theory Methods on Biochromophores.

Authors:  Yihan Shao; Ye Mei; Dage Sundholm; Ville R I Kaila
Journal:  J Chem Theory Comput       Date:  2019-12-26       Impact factor: 6.006

2.  Deducing the molecular properties of zwitterionic, protonated, deprotonated, and double-deprotonated forms of L-cysteine from vibrational spectroscopy (IR, Raman, VCD) and quantum chemical calculations.

Authors:  María Mar Quesada-Moreno; Juan Ramón Avilés-Moreno; A A Márquez-García; Juan Jesús López-González
Journal:  J Mol Model       Date:  2014-06-12       Impact factor: 1.810

3.  Benchmarking the Bethe-Salpeter Formalism on a Standard Organic Molecular Set.

Authors:  Denis Jacquemin; Ivan Duchemin; Xavier Blase
Journal:  J Chem Theory Comput       Date:  2015-07-14       Impact factor: 6.006

4.  Conformational properties of 1,4- and 1,5-substituted 1,2,3-triazole amino acids – building units for peptidic foldamers.

Authors:  Nina Kann; Johan R Johansson; Tamás Beke-Somfai
Journal:  Org Biomol Chem       Date:  2015-03-07       Impact factor: 3.876

Review 5.  Photoredox Chemistry with Organic Catalysts: Role of Computational Methods.

Authors:  Kareesa J Kron; Andres Rodriguez-Katakura; Rachelle Elhessen; Shaama Mallikarjun Sharada
Journal:  ACS Omega       Date:  2021-12-03

6.  Benchmark Density Functional Theory Approach for the Calculation of Bond Dissociation Energies of the M-O2 Bond: A Key Step in Water Splitting Reactions.

Authors:  Naveen Kosar; Khurshid Ayub; Mazhar Amjad Gilani; Shabbir Muhammad; Tariq Mahmood
Journal:  ACS Omega       Date:  2022-06-09
  6 in total

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