Multiphonon Relaxation Slows Singlet Fission in Crystalline Hexacene

被引:114
作者
Busby, Erik [1 ,5 ]
Berkelbach, Timothy C. [2 ]
Kumar, Bharat [2 ]
Chernikov, Alexey [3 ,4 ]
Zhong, Yu [2 ]
Hlaing, Htay [3 ]
Zhu, X. -Y. [2 ]
Heinz, Tony F. [3 ,4 ]
Hybertsen, Mark S. [5 ]
Sfeir, Matthew Y. [5 ]
Reichman, David R. [2 ]
Nuckolls, Colin [2 ]
Yaffe, Omer [1 ,5 ]
机构
[1] Columbia Univ, Energy Frontier Res Ctr, New York, NY 10027 USA
[2] Columbia Univ, Dept Chem, New York, NY 10027 USA
[3] Columbia Univ, Dept Phys, New York, NY 10027 USA
[4] Columbia Univ, Dept Elect Engn, New York, NY 10027 USA
[5] Brookhaven Natl Lab, Ctr Funct Nanomat, Upton, NY 11973 USA
关键词
EXCITON-FISSION; TETRACENE; DYNAMICS; PENTACENE; ABSORPTION; ENERGY; STATE;
D O I
10.1021/ja503980c
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Singlet fission, the conversion of a singlet excitation into two triplet excitations, is a viable route to improved solar-cell efficiency. Despite active efforts to understand the singlet fission mechanism, which would aid in the rational design of new materials, a comprehensive understanding of mechanistic principles is still lacking. Here, we present the first study of singlet fission in crystalline hexacene which, together with tetracene and pentacene, enables the elucidation of mechanistic trends. We characterize the static and transient optical absorption and combine our findings with a theoretical analysis of the relevant electronic couplings and rates. We find a singlet fission time scale of 530 fs, which is orders of magnitude faster than tetracene (10-100ps) but significantly slower than pentacene (80-110 fs). We interpret this increased time scale as a multiphonon relaxation effect originating from a large exothermicity and present a microscopic theory that quantitatively reproduces the rates in the acene family.
引用
收藏
页码:10654 / 10660
页数:7
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