An Ab Initio Exciton Model Including Charge-Transfer Excited States

被引:93
作者
Li, Xin [1 ,2 ,3 ]
Parrish, Robert M. [1 ,2 ,3 ]
Liu, Fang [1 ,2 ,3 ]
Schumacher, Sara I. L. Kokkila [1 ,2 ,3 ,4 ]
Martinez, Todd J. [1 ,2 ,3 ]
机构
[1] Stanford Univ, Dept Chem, Stanford, CA 94305 USA
[2] Stanford Univ, PULSE Inst, Stanford, CA 94305 USA
[3] SLAC Natl Accelerator Lab, Menlo Pk, CA 94025 USA
[4] IBM Corp, TJ Watson Res Ctr, Yorktown Hts, NY 10598 USA
基金
美国国家科学基金会;
关键词
DENSITY-FUNCTIONAL THEORY; MOLECULAR-EXCITATION ENERGIES; ELECTRON-TRANSFER; PURPLE BACTERIA; TIME; LIGHT; COMPLEXES; APPROXIMATION; DYNAMICS; EXCHANGE;
D O I
10.1021/acs.jctc.7b00171
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
The Frenkel exciton model is a useful tool for theoretical studies of multichromophore systems. We recently showed that the exciton model could be used to coarse-grain electronic structure in multichromophoric systems, focusing on singly excited exciton states [Acc. Chem. Res. 2014, 47, 2857-2866]. However, our previous implementation excluded charge-transfer excited states, which can play an important role in light-harvesting systems and near-infrared optoelectronic materials. Recent studies have also emphasized the significance of charge-transfer in singlet fission, which mediates the coupling between the locally excited states and the multiexcitonic states. In this work, we report on an ab initio exciton model that incorporates charge-transfer excited states and demonstrate that the model provides correct charge-transfer excitation energies and asymptotic behavior. Comparison with TDDFT and EOM-CC2 calculations shows that our exciton model is robust with respect to system size, screening parameter, and different density functionals. Inclusion of charge-transfer excited states makes the exciton model more useful for studies of singly excited states and provides a starting point for future construction of a model that also includes double-exciton states.
引用
收藏
页码:3493 / 3504
页数:12
相关论文
共 68 条
[1]   Toward reliable density functional methods without adjustable parameters: The PBE0 model [J].
Adamo, C ;
Barone, V .
JOURNAL OF CHEMICAL PHYSICS, 1999, 110 (13) :6158-6170
[2]   2ND-ORDER PERTURBATION-THEORY WITH A CASSCF REFERENCE FUNCTION [J].
ANDERSSON, K ;
MALMQVIST, PA ;
ROOS, BO ;
SADLEJ, AJ ;
WOLINSKI, K .
JOURNAL OF PHYSICAL CHEMISTRY, 1990, 94 (14) :5483-5488
[3]   DENSITY-FUNCTIONAL THERMOCHEMISTRY .3. THE ROLE OF EXACT EXCHANGE [J].
BECKE, AD .
JOURNAL OF CHEMICAL PHYSICS, 1993, 98 (07) :5648-5652
[4]   DENSITY-FUNCTIONAL EXCHANGE-ENERGY APPROXIMATION WITH CORRECT ASYMPTOTIC-BEHAVIOR [J].
BECKE, AD .
PHYSICAL REVIEW A, 1988, 38 (06) :3098-3100
[5]   Microscopic theory of singlet exciton fission. III. Crystalline pentacene [J].
Berkelbach, Timothy C. ;
Hybertsen, Mark S. ;
Reichman, David R. .
JOURNAL OF CHEMICAL PHYSICS, 2014, 141 (07)
[6]   Charge-transfer and energy-transfer processes in π-conjugated oligomers and polymers:: A molecular picture [J].
Brédas, JL ;
Beljonne, D ;
Coropceanu, V ;
Cornil, J .
CHEMICAL REVIEWS, 2004, 104 (11) :4971-5003
[7]   Molecular excitation energies to high-lying bound states from time-dependent density-functional response theory: Characterization and correction of the time-dependent local density approximation ionization threshold [J].
Casida, ME ;
Jamorski, C ;
Casida, KC ;
Salahub, DR .
JOURNAL OF CHEMICAL PHYSICS, 1998, 108 (11) :4439-4449
[8]   THE 2ND-ORDER APPROXIMATE COUPLED-CLUSTER SINGLES AND DOUBLES MODEL CC2 [J].
CHRISTIANSEN, O ;
KOCH, H ;
JORGENSEN, P .
CHEMICAL PHYSICS LETTERS, 1995, 243 (5-6) :409-418
[9]   The structural basis of light-harvesting in purple bacteria [J].
Cogdell, RJ ;
Isaacs, NW ;
Freer, AA ;
Howard, TD ;
Gardiner, AT ;
Prince, SM ;
Papiz, MZ .
FEBS LETTERS, 2003, 555 (01) :35-39
[10]   Insights into current limitations of density functional theory [J].
Cohen, Aron J. ;
Mori-Sanchez, Paula ;
Yang, Weitao .
SCIENCE, 2008, 321 (5890) :792-794