Triplet Separation Drives Singlet Fission after Femtosecond Correlated Triplet Pair Production in Rubrene

被引:120
作者
Breen, Ilana [1 ]
Tempelaar, Roel [2 ]
Bizimana, Laurie A. [1 ]
Kloss, Benedikt [2 ]
Reichman, David R. [2 ]
Turner, Daniel B. [1 ]
机构
[1] NYU, Dept Chem, 100 Washington Sq East, New York, NY 10003 USA
[2] Columbia Univ, Dept Chem, 3000 Broadway, New York, NY 10027 USA
基金
美国国家科学基金会;
关键词
EXCITON-FISSION; ELECTRONIC SPECTROSCOPY; ORGANIC SEMICONDUCTORS; TRANSPORT-PROPERTIES; ULTRAFAST DYNAMICS; AMORPHOUS RUBRENE; CHARGE-TRANSPORT; SOLAR-CELLS; THIN-FILM; CRYSTALS;
D O I
10.1021/jacs.7b02621
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Singlet fission, a multistep molecular process in which one photon generates two triplet excitons, holds great technological promise. Here, by applying a combination of transient transmittance and two-dimensional electronic spectroscopy with 5 fs laser pulses, we resolve the full set of fission steps before the onset of spin dephasing. In addition to its role as a viable singlet fission material, single-crystalline rubrene is selected because its energetics and transition dipole alignment uniquely allow for the unambiguous identification of the various fission steps through their contributions to distinct spectroscopic features. The measurements reveal that the neighboring correlated triplet pair achieves its maximum population within 20 fs. Subsequent growth of the triplet signal on picosecond time scales is attributable to spatial separation of the triplets, proceeding nonadiabatically through weakly coupled but near-resonant states. As such, we provide evidence in crystalline rubrene for a singlet fission step that, until now, has not been convincingly observed.
引用
收藏
页码:11745 / 11751
页数:7
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