Dynamic Evolving Exothermicity Steers Ultrafast Formation of a Correlated Triplet Pair State

Singlet fission (SF) presents an attractive solution to overcome the Shockley-Queisser limit of single-junction solar cells. The conversion from an initial singlet state to final triplet is mediated by the correlated triplet pair state 1(T1T1). Despite significant advancement on 1(T1T1) properties and its role in SF, a comprehensive understanding of the energetic landscape during SF is still unclear. Here, we study an unconventional SF system with excited-state aromaticity, i.e., cyano-substituted dipyrrolonaphtheridinedione derivative (DPND-CN), using time-resolved spectroscopy as a function of the temperature. We demonstrate that the population transfer from S1 to 1(T1T1) is driven by a time-dependent exothermicity resulting from the coherent coupling between electronic and spin degrees of freedom. This is followed by thermal-activated dissociation of 1(T1T1) to yield free triplets. Our results provide some new insight into the SF mechanism, which may guide the development of new efficient and stable SF materials for practical applications.

Automated summary

In this study, an unconventional SF system with excited-state aromaticity was investigated using time-resolved spectroscopy. The authors found that the population transfer occurs by a time-dependent exothermic process driven by coherent coupling between electronic and spin degrees of freedom, leading to the formation of free triplets. These findings provide important insights into the SF mechanism and can guide the development of efficient and stable SF materials for practical applications.