TY - JOUR
T1 - Triplet Separation Drives Singlet Fission after Femtosecond Correlated Triplet Pair Production in Rubrene
AU - Breen, Ilana
AU - Tempelaar, Roel
AU - Bizimana, Laurie A.
AU - Kloss, Benedikt
AU - Reichman, David R.
AU - Turner, Daniel B.
N1 - Funding Information:
We thank Alejandro Briseño and Gilbert Sloan for assistance with the crystal growth, as well as Alexander Shtukenberg and Jennifer L. Ramirez for help with polarized microscopy and polarized Raman spectroscopy, respectively. The National Science Foundation supported this work through CAREER grant CHE-1552235 to D.B.T., grant CHE-1464802 to D.R.R., and a Graduate Research Fellowship to L.A.B. The Netherlands Organisation for Scientific Research NWO supported this work through a Rubicon grant to R.T. We also thank Ryan Pensack for productive conversations.
Publisher Copyright:
© 2017 American Chemical Society.
PY - 2017/8/30
Y1 - 2017/8/30
N2 - 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.
AB - 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.
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U2 - 10.1021/jacs.7b02621
DO - 10.1021/jacs.7b02621
M3 - Article
AN - SCOPUS:85028676779
SN - 0002-7863
VL - 139
SP - 11745
EP - 11751
JO - Journal of the American Chemical Society
JF - Journal of the American Chemical Society
IS - 34
ER -