Competitive Triplet Formation and Recombination in Crystalline Films of Perylenediimide Derivatives: Implications for Singlet Fission

• Published in: Journal of physical chemistry. C Vol. 124; no. 21; pp. 11574 - 11585
• Main Authors: Masoomi-Godarzi, Saghar, Hall, Christopher R, Zhang, Bolong, Gregory, Mark A, White, Jonathan M, Wong, Wallace W. H, Ghiggino, Kenneth P, Smith, Trevor A, Jones, David J
• Format: Journal Article
• Language: English
• Published: American Chemical Society 28.05.2020
• ISSN: 1932-7447; 1932-7455
• DOI: 10.1021/acs.jpcc.0c01337

Developing photostable compounds that undergo quantitative singlet fission (SF) is a key challenge. As SF necessitates electron transfer between neighboring molecules, the SF rate is highly sensitive to intermolecular coupling in the solid state. We investigate SF in thin films for a series of perylenediimide (PDI) molecules. By adding different substituents at the imide positions, the packing of the molecules in the solid state can be changed. The relationship between SF parameters and the stacked geometry in PDI films is investigated, with two-electron direct coupling found to be the main SF mechanism. Time-resolved emission and transient absorption data show that all of the PDI films undergo SF although with different rates and yields varying from 35 to 200%. The results show that PDI1 and 2, which are stacked PDI pairs twisted out of alignment along the highest occupied molecular orbital to lowest unoccupied molecular orbital transition, exhibit faster and more efficient SF up to 200% yield. We demonstrate that both triplet formation and decay rates are highly sensitive to the ordering of the molecules within a film. The results of this study will assist in the design of optimized structures with a fast SF rate and low recombination rate that are required for useful light harvesting applications.