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Side-chain Engineering of Benzo12-b:45-b’dithiophene Core-structured Small Molecules for High-Performance Organic Solar Cells

机译:苯并12-b:45-b二噻吩核心结构的小分子用于高性能有机太阳能电池的侧链工程

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摘要

Three novel small molecules have been developed by side-chain engineering on benzo[1,2-b:4,5-b’]dithiophene (BDT) core. The typical acceptor-donor-acceptor (A-D-A) structure is adopted with 4,8-functionalized BDT moieties as core, dioctylterthiophene as π bridge and 3-ethylrhodanine as electron-withdrawing end group. Side-chain engineering on BDT core exhibits small but measurable effect on the optoelectronic properties of small molecules. Theoretical simulation and X-ray diffraction study reveal the subtle tuning of interchain distance between conjugated backbones has large effect on the charge transport and thus the photovoltaic performance of these molecules. Bulk-heterojunction solar cells fabricated with a configuration of ITO/PEDOT:PSS/SM:PC71BM/PFN/Al exhibit a highest power conversion efficiency (PCE) of 6.99% after solvent vapor annealing.
机译:通过在苯并[1,2-b:4,5-b']二噻吩(BDT)核上的侧链工程开发了三个新颖的小分子。采用典型的受体-供体-受体(A-D-A)结构,其中4,8-官能化的BDT部分为核,二辛基噻吩为π桥,而3-乙基罗丹宁为吸电子端基。 BDT核心上的侧链工程对小分子的光电性能表现出很小但可测量的影响。理论模拟和X射线衍射研究表明,共轭主链之间链间距离的微调对电荷传输和这些分子的光伏性能有很大影响。 ITO / PEDOT:PSS / SM:PC71BM / PFN / Al构造的体异质结太阳能电池在溶剂蒸汽退火后显示出6.99%的最高功率转换效率(PCE)。

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