Davydov splitting and singlet fission in excitonically coupled pentacene dimers

被引:69
作者
Basel, Bettina Sabine [1 ]
Hetzer, Constantin [2 ]
Zirzlmeier, Johannes [1 ]
Thiel, Dominik [1 ]
Guldi, Rebecca [2 ]
Hampel, Frank [2 ]
Kahnt, Axel [3 ]
Clark, Timothy [4 ]
Guldi, Dirk Michael [1 ]
Tykwinski, Rik R. [5 ]
机构
[1] FAU, Dept Chem & Pharm, ICMM, Egerlandstr 3, D-91058 Erlangen, Germany
[2] FAU, Dept Chem & Pharm, ICMM, Nikolaus Fiebiger Str 10, D-91058 Erlangen, Germany
[3] Leibniz Inst Surface Engn IOM, Permoserstr 15, D-04318 Leipzig, Germany
[4] Friedrich Alexander Univ Erlangen Nurnberg FAU, Dept Chem & Pharm, CCC, Nagelsbachstr 25, D-91052 Erlangen, Germany
[5] Univ Alberta, Dept Chem, Edmonton, AB T6G 2G2, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
CHARGE-TRANSFER STATE; THIN-FILMS; FLUORESCENCE; ACENES; MODEL; INTERMEDIATE; DISSOCIATION; EFFICIENCY; COHERENCES; MECHANISM;
D O I
10.1039/c9sc00384c
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Singlet fission (SF) allows two charges to be generated from the absorption of a single photon and is, therefore, potentially transformative toward improving solar energy conversion. Key to the present study of SF is the design of pentacene dimers featuring a xanthene linker that strictly places two pentacene chromophores in a rigid arrangement and, in turn, enforces efficient, intramolecular pi-overlap that mimics interactions typically found in condensed state (e.g., solids, films, etc.). Inter-chromophore communication ensures Davydov splitting, which plays an unprecedented role toward achieving SF in pentacene dimers. Transient absorption measurements document that intramolecular SF evolves upon excitation into the lower Davydov bands to form a correlated triplet pair at cryogenic temperature. At room temperature, the two spin-correlated triplets, one per pentacene moiety within the dimers, are electronically coupled to an excimer state. The presented results are transferable to a broad range of acene morphologies including aggregates, crystals, and films.
引用
收藏
页码:3854 / 3863
页数:10
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