Microscopic theory of singlet exciton fission. I. General formulation

被引:225
作者
Berkelbach, Timothy C. [1 ]
Hybertsen, Mark S. [2 ]
Reichman, David R. [1 ]
机构
[1] Columbia Univ, Dept Chem, New York, NY 10027 USA
[2] Brookhaven Natl Lab, Ctr Funct Nanomat, Upton, NY 11973 USA
关键词
DENSITY-FUNCTIONAL THEORY; DETAILED BALANCE LIMIT; EXCITATION TRANSFER; QUANTUM DYNAMICS; RATE EXPRESSIONS; CHARGE SEPARATION; TRIPLET EXCITONS; TIME EVOLUTION; SOLAR-CELLS; EFFICIENCY;
D O I
10.1063/1.4794425
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
Singlet fission, a spin-allowed energy transfer process generating two triplet excitons from one singlet exciton, has the potential to dramatically increase the efficiency of organic solar cells. However, the dynamical mechanism of this phenomenon is not fully understood and a complete, microscopic theory of singlet fission is lacking. In this work, we assemble the components of a comprehensive microscopic theory of singlet fission that connects excited state quantum chemistry calculations with finite-temperature quantum relaxation theory. We elaborate on the distinction between localized diabatic and delocalized exciton bases for the interpretation of singlet fission experiments in both the time and frequency domains. We discuss various approximations to the exact density matrix dynamics and propose Redfield theory as an ideal compromise between speed and accuracy for the detailed investigation of singlet fission in dimers, clusters, and crystals. Investigations of small model systems based on parameters typical of singlet fission demonstrate the numerical accuracy and practical utility of this approach. (C) 2013 American Institute of Physics. [http://dx.doi.org/10.1063/1.4794425]
引用
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页数:16
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