Kathryn R. Peinkofer, Malik L. Williams, Georgia C. Mantel, Brian T. Phelan, Ryan M. Young, Michael R. Wasielewski
{"title":"9,9′-二色系单晶中有序溶剂分子的极性选择:单重态裂变或对称破缺电荷分离","authors":"Kathryn R. Peinkofer, Malik L. Williams, Georgia C. Mantel, Brian T. Phelan, Ryan M. Young, Michael R. Wasielewski","doi":"10.1021/jacs.4c14550","DOIUrl":null,"url":null,"abstract":"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 (<b>BA</b>) single crystal between SF and SB-CS using solvent intercalation to change the electric field within the crystal. Crystals of <b>BA</b> were grown in <i>o</i>-xylene, chlorobenzene, <i>o</i>-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 <i>o</i>-xylene, chlorobenzene, and <i>o</i>-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 <b>BA</b> in the crystal structure can tune its photophysics between SF and SB-CS.","PeriodicalId":49,"journal":{"name":"Journal of the American Chemical Society","volume":"41 1","pages":""},"PeriodicalIF":15.6000,"publicationDate":"2024-12-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Polarity of Ordered Solvent Molecules in 9,9′-Bianthracene Single Crystals Selects between Singlet Fission or Symmetry-Breaking Charge Separation\",\"authors\":\"Kathryn R. Peinkofer, Malik L. Williams, Georgia C. Mantel, Brian T. Phelan, Ryan M. Young, Michael R. Wasielewski\",\"doi\":\"10.1021/jacs.4c14550\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"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 (<b>BA</b>) single crystal between SF and SB-CS using solvent intercalation to change the electric field within the crystal. Crystals of <b>BA</b> were grown in <i>o</i>-xylene, chlorobenzene, <i>o</i>-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 <i>o</i>-xylene, chlorobenzene, and <i>o</i>-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 <b>BA</b> in the crystal structure can tune its photophysics between SF and SB-CS.\",\"PeriodicalId\":49,\"journal\":{\"name\":\"Journal of the American Chemical Society\",\"volume\":\"41 1\",\"pages\":\"\"},\"PeriodicalIF\":15.6000,\"publicationDate\":\"2024-12-10\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of the American Chemical Society\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://doi.org/10.1021/jacs.4c14550\",\"RegionNum\":1,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of the American Chemical Society","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1021/jacs.4c14550","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
Polarity of Ordered Solvent Molecules in 9,9′-Bianthracene Single Crystals Selects between Singlet Fission or Symmetry-Breaking Charge Separation
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.
期刊介绍:
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