Polarity of Ordered Solvent Molecules in 9,9′-Bianthracene Single Crystals Selects between Singlet Fission or Symmetry-Breaking Charge Separation

被引:0
|
作者
Peinkofer, Kathryn R. [1 ,2 ]
Williams, Malik L. [1 ,2 ]
Mantel, Georgia C. [1 ,2 ]
Phelan, Brian T. [1 ,2 ]
Young, Ryan M. [1 ,2 ]
Wasielewski, Michael R. [1 ,2 ]
机构
[1] Northwestern Univ, Dept Chem, Evanston, IL 60208 USA
[2] Northwestern Univ, Paula M Trienens Inst Sustainabil & Energy, Evanston, IL 60208 USA
基金
美国国家科学基金会;
关键词
EXCITED-STATE; MICROSCOPIC SOLVATION; 9,9-BIANTHRYL; ACCEPTOR; DERIVATIVES;
D O I
10.1021/jacs.4c14550
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Singlet exciton fission (SF) and symmetry-breaking charge separation (SB-CS) are both photophysical processes that can occur between two organic chromophores and are both of interest to improve solar energy conversion. Here, we tuned the photophysics of a 9,9 '-bianthracene (BA) single crystal between SF and SB-CS using solvent intercalation to change the electric field within the crystal. Crystals of BA were grown in o-xylene, chlorobenzene, o-dichlorobenzene, and benzonitrile, as well as solvent-free from a melt. The crystals were studied by X-ray diffraction, steady-state optical spectroscopy, and transient absorption microscopy to elucidate the role of the intercalated solvent molecules. The crystals with no solvent in the structure undergo fast SF (<2 ps), while the crystals with intercalated moderately polar solvents o-xylene, chlorobenzene, and o-dichlorobenzene show evidence of charge-transfer-mediated SF. Finally, the crystals containing highly polar benzonitrile undergo SB-CS instead of SF. These results demonstrate that controlling solvation of BA in the crystal structure can tune its photophysics between SF and SB-CS.
引用
收藏
页码:34934 / 34942
页数:9
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