Comparison of Real-Time and Linear-Response Time-Dependent Density Functional Theories for Molecular Chromophores Ranging from Sparse to High Densities of States

被引:103
作者
Tussupbayev, Samat [1 ,2 ]
Govind, Niranjan [3 ]
Lopata, Kenneth [4 ,5 ]
Cramer, Christopher J. [1 ,2 ]
机构
[1] Univ Minnesota, Supercomp Inst, Dept Chem, Minneapolis, MN 55455 USA
[2] Univ Minnesota, Chem Theory Ctr, Minneapolis, MN 55455 USA
[3] Pacific NW Natl Lab, Environm Mol Sci Lab, Richland, WA 99338 USA
[4] Louisiana State Univ, Dept Chem, Baton Rouge, LA 70803 USA
[5] Louisiana State Univ, Ctr Computat & Technol, Baton Rouge, LA 70803 USA
关键词
POLARIZABLE CONTINUUM MODEL; CIRCULAR-DICHROISM SPECTRA; TRANSFER DYNAMICS; HARTREE-FOCK; BASIS-SETS; ABSORPTION; APPROXIMATION; THERMOCHEMISTRY; ACCURACY; FIELD;
D O I
10.1021/ct500763y
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 assess the performance of real-time time-dependent density functional theory (RT-TDDFT) for the calculation of absorption spectra of 12 organic dye molecules relevant to photovoltaics and dye-sensitized solar cells with 8 exchange-correlation functionals (3 traditional, 3 global hybrids, and 2 range-separated hybrids). We compare the calculations with traditional linear-response (LR) TDDFT and experimental spectra. In addition, we demonstrate the efficacy of the RT-TDDFT approach to calculate wide absorption spectra of two large chromophores relevant to photovoltaics and molecular switches. RT-TDDFT generally requires longer simulation times, compared to LR-TDDFT, for absorption spectra of small systems. However, it becomes more effective for the calculation of wide absorption spectra of large molecular complexes and systems with very high densities of states.
引用
收藏
页码:1102 / 1109
页数:8
相关论文
共 68 条
[1]   ENERGY-ADJUSTED ABINITIO PSEUDOPOTENTIALS FOR THE 2ND AND 3RD ROW TRANSITION-ELEMENTS [J].
ANDRAE, D ;
HAUSSERMANN, U ;
DOLG, M ;
STOLL, H ;
PREUSS, H .
THEORETICA CHIMICA ACTA, 1990, 77 (02) :123-141
[2]   Real-time linear response for time-dependent density-functional theory [J].
Baer, R ;
Neuhauser, D .
JOURNAL OF CHEMICAL PHYSICS, 2004, 121 (20) :9803-9807
[3]   A simplified time-dependent density functional theory approach for electronic ultraviolet and circular dichroism spectra of very large molecules [J].
Bannwarth, Christoph ;
Grimme, Stefan .
COMPUTATIONAL AND THEORETICAL CHEMISTRY, 2014, 1040 :45-53
[4]   DENSITY-FUNCTIONAL THERMOCHEMISTRY .3. THE ROLE OF EXACT EXCHANGE [J].
BECKE, AD .
JOURNAL OF CHEMICAL PHYSICS, 1993, 98 (07) :5648-5652
[5]   DENSITY-FUNCTIONAL THERMOCHEMISTRY .3. THE ROLE OF EXACT EXCHANGE [J].
BECKE, AD .
JOURNAL OF CHEMICAL PHYSICS, 1993, 98 (07) :5648-5652
[6]   DENSITY-FUNCTIONAL EXCHANGE-ENERGY APPROXIMATION WITH CORRECT ASYMPTOTIC-BEHAVIOR [J].
BECKE, AD .
PHYSICAL REVIEW A, 1988, 38 (06) :3098-3100
[7]  
Casida ME, 2012, ANNU REV PHYS CHEM, V63, P287, DOI [10.1146/annurev-physchem-032511-143803, 10.1146/annurev-physchem-032511-443803]
[8]   octopus: a tool for the application of time-dependent density functional theory [J].
Castro, Alberto ;
Appel, Heiko ;
Oliveira, Micael ;
Rozzi, Carlo A. ;
Andrade, Xavier ;
Lorenzen, Florian ;
Marques, M. A. L. ;
Gross, E. K. U. ;
Rubio, Angel .
PHYSICA STATUS SOLIDI B-BASIC SOLID STATE PHYSICS, 2006, 243 (11) :2465-2488
[9]   Simulating molecular conductance using real-time density functional theory [J].
Cheng, Chiao-Lun ;
Evans, Jeremy S. ;
Van Voorhis, Troy .
PHYSICAL REVIEW B, 2006, 74 (15)
[10]   Trajectory surface hopping in the time-dependent Kohn-Sham approach for electron-nuclear dynamics [J].
Craig, CF ;
Duncan, WR ;
Prezhdo, OV .
PHYSICAL REVIEW LETTERS, 2005, 95 (16)