单重态裂变
并五苯
光化学
材料科学
分子内力
紧身衣
光激发
费斯特共振能量转移
激发态
二聚体
共振(粒子物理)
单重态
超快激光光谱学
化学物理
荧光
化学
原子物理学
光谱学
纳米技术
物理
立体化学
光学
有机化学
薄膜晶体管
量子力学
图层(电子)
作者
Anna‐Sophie Wollny,Giulia Lavarda,Ilias Papadopoulos,Ismael López‐Duarte,Henrik Gotfredsen,Yuxuan Hou,Rik R. Tykwinski,Tomás Torres⊗,Dirk M. Guldi
标识
DOI:10.1002/adom.202300500
摘要
Abstract In the present work, the energy donor 4,4‐difluoro‐4‐bora‐3a,4a‐diaza‐ s ‐indacene (BODIPY) is used for the first time in combination with a pentacene dimer (Pnc 2 ) to provide the conjugate BODIPYPnc 2 that features absorption throughout a large part of the solar spectrum. Upon photoexcitation, the singlet excited state energy of BODIPY is transferred to the pentacene dimer via intramolecular Förster resonance energy transfer (FRET). Subsequently, the pentacene dimer undergoes intramolecular singlet fission. In this process, a singlet correlated triplet pair is generated from the first singlet excited state via coupling to an intermediate state. The results show that solvent polarity has an influence on the system, with the largest FRET rate (i.e., 7.46 × 10 11 s −1 ) being obtained in the most polar solvent (namely, benzonitrile) along with the largest triplet quantum yield (i.e., 207 ± 20%).
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