CAS Key Laboratory of Bio-based Materials, Qingdao Institute of Bioenergy and Bioprocess Technology, Chinese Academy of Sciences, Qingdao, 266101, P.R. China.
School of Materials Science&Engineering, Wuhan Institute of Technology, Wuhan, 430205, P.R. China.
ChemSusChem. 2018 Jan 23;11(2):360-366. doi: 10.1002/cssc.201701917. Epub 2017 Dec 19.
In recent years, nonfullerene acceptors have attracted much attention, owing to their great potential for use in high-performance polymer solar cells.The ladder-type building block, pyran-bridged indacenodithiophene (PDT), was used for constructing A-D-A nonfullerene acceptors through introduction of oxygen atoms into an indacenodithiophene (IDT) unit. The synthesis of PDT is accomplished by a BBr -mediated tandem cyclization-deprotection reaction to construct the pyran ring. Hence, molecular acceptor PTIC was synthesized and used in a polymer solar cell device. Compared to the IDT-based acceptor, PTIC exhibits higher HOMO levels and wider optical band gap at 550-800 nm. Devices fabricated with poly[(2,6-(4,8-bis(5-(2-ethylhexyl)thiophen-2-yl)benzo[1,2-b:4,5-b']dithiophene)-co-(1,3-di(5-thiophene-2-yl)-5,7-bis(2-ethylhexyl)-benzo[1,2-c:4,5-c']dithiophene-4,8-dione)] (PBDB-T):PTIC as the active layer give a power conversion efficiency (PCE) of 7.66 %.
近年来,由于在高性能聚合物太阳能电池中的巨大应用潜力,非富勒烯受体引起了广泛关注。通过在茚并二噻吩(IDT)单元中引入氧原子, ladder-type 结构单元吡喃桥联的茚并二噻吩(PDT)被用于构建 A-D-A 型非富勒烯受体。PDT 的合成是通过 BBr3 介导的串联环化-脱保护反应来构建吡喃环完成的。因此,合成了分子受体 PTIC 并将其用于聚合物太阳能电池器件中。与基于 IDT 的受体相比,PTIC 具有更高的 HOMO 能级和在 550-800nm 处更宽的光学带隙。以聚[[2,6-(4,8-双(5-(2-乙基己基)噻吩-2-基)苯并[1,2-b:4,5-b']二噻吩)-共-(1,3-二(5-噻吩-2-基)-5,7-双(2-乙基己基)苯并[1,2-c:4,5-c']二噻吩-4,8-二酮)](PBDB-T):PTIC 为活性层的器件获得了 7.66%的功率转换效率(PCE)。