Literature DB >> 34291643

Time-Dependent Long-Range-Corrected Double-Hybrid Density Functionals with Spin-Component and Spin-Opposite Scaling: A Comprehensive Analysis of Singlet-Singlet and Singlet-Triplet Excitation Energies.

Marcos Casanova-Páez1, Lars Goerigk1.   

Abstract

Following the work on spin-component and spin-opposite scaled (SCS/SOS) global double hybrids for singlet-singlet excitations by Schwabe and Goerigk [ J. Chem. Theory Comput. 2017, 13, 4307-4323] and our own works on new long-range corrected (LC) double hybrids for singlet-singlet and singlet-triplet excitations [ J. Chem. Theory Comput. 2019, 15, 4735-4744 and J. Chem. Phys. 2020, 153, 064106], we present new LC double hybrids with SCS/SOS that demonstrate further improvement over previously published results and methods. We introduce new unscaled and scaled versions of different global and LC double hybrids based on Becke88 or PBE exchange combined with LYP, PBE, or P86 correlation. For singlet-singlet excitations, we cross-validate them on six benchmark sets that cover small to medium-sized chromophores with different excitation types (local-valence, Rydberg, and charge transfer). For singlet-triplet excitations, we perform the cross-validation on three different benchmark sets following the same analysis as in our previous work in 2020. In total, 203 excitations are analyzed. Our results confirm and extend those of Schwabe and Goerigk regarding the superior performance of SCS and SOS variants compared to their unscaled parents by decreasing mean absolute deviations, root-mean-square deviations, or error spans by more than half and bringing absolute mean deviations closer to zero. Our SCS/SOS variants are shown to be highly efficient and robust for the computation of vertical excitation energies, which even outperform specialized double hybrids that also contain an LC in their perturbative part. In particular, our new SCS/SOS-ωPBEPP86 and SCS/SOS-ωB88PP86 functionals are four of the most accurate and robust methods tested in this work, and we fully recommend them for future applications. However, if the relevant SCS and SOS algorithms are not available to the user, we suggest ωPBEPP86 as the best unscaled method in this work.

Entities:  

Year:  2021        PMID: 34291643     DOI: 10.1021/acs.jctc.1c00535

Source DB:  PubMed          Journal:  J Chem Theory Comput        ISSN: 1549-9618            Impact factor:   6.006


  9 in total

1.  Activity-Based Photosensitizers with Optimized Triplet State Characteristics Toward Cancer Cell Selective and Image Guided Photodynamic Therapy.

Authors:  Eda Kilic; Zubeyir Elmazoglu; Toghrul Almammadov; Dilay Kepil; Thibaud Etienne; Antoine Marion; Gorkem Gunbas; Safacan Kolemen
Journal:  ACS Appl Bio Mater       Date:  2022-05-10

2.  Do Double-Hybrid Functionals Benefit from Regularization in the PT2 Term? Observations from an Extensive Benchmark.

Authors:  Golokesh Santra; Jan M L Martin
Journal:  J Phys Chem Lett       Date:  2022-04-13       Impact factor: 6.475

3.  Accurate Spectral Properties within Double-Hybrid Density Functional Theory: A Spin-Scaled Range-Separated Second-Order Algebraic-Diagrammatic Construction-Based Approach.

Authors:  Dávid Mester; Mihály Kállay
Journal:  J Chem Theory Comput       Date:  2022-01-13       Impact factor: 6.006

4.  Accurate predictions of the electronic excited states of BODIPY based dye sensitizers using spin-component-scaled double-hybrid functionals: a TD-DFT benchmark study.

Authors:  Qabas Alkhatib; Wissam Helal; Ali Marashdeh
Journal:  RSC Adv       Date:  2022-01-11       Impact factor: 3.361

5.  Origin of the Failure of Density Functional Theories in Predicting Inverted Singlet-Triplet Gaps.

Authors:  Soumen Ghosh; Kalishankar Bhattacharyya
Journal:  J Phys Chem A       Date:  2022-02-11       Impact factor: 2.781

6.  Charge-Transfer Excitations within Density Functional Theory: How Accurate Are the Most Recommended Approaches?

Authors:  Dávid Mester; Mihály Kállay
Journal:  J Chem Theory Comput       Date:  2022-02-24       Impact factor: 6.006

7.  Noncovalently bound excited-state dimers: a perspective on current time-dependent density functional theory approaches applied to aromatic excimer models.

Authors:  Amy C Hancock; Lars Goerigk
Journal:  RSC Adv       Date:  2022-05-03       Impact factor: 4.036

8.  Benefits of Range-Separated Hybrid and Double-Hybrid Functionals for a Large and Diverse Data Set of Reaction Energies and Barrier Heights.

Authors:  Golokesh Santra; Rivka Calinsky; Jan M L Martin
Journal:  J Phys Chem A       Date:  2022-08-05       Impact factor: 2.944

9.  Theoretical Study of Light-Induced Crosslinking Reaction Between Pyrimidine DNA Bases and Aromatic Amino Acids.

Authors:  Attila Bende; Alex-Adrian Farcaş; Valer Toşa
Journal:  Front Bioeng Biotechnol       Date:  2022-01-17
  9 in total

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