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N-type semiconducting perylene diimide based molecules for organic solar cells

机译:N型半导体基于二酰亚胺的有机太阳能电池分子

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Core substituted perylene diimides (PDIs) are promising candidates as non-fullerene acceptor materials for organic solar cells. The functionalization of PDIs in the bay positions using chemical groups with different electron donating abilities and with steric hindrance is a versatile tool to modify both the optoelectronic properties and the morphology in the solid state. Herein we present two new PDI based molecules having bulky aromatic substituents linked into the bay positions: PDI-SF with spirobifluorene group and PDI-BSF with bithienyl-spirobifluorene moieties. The high steric hindrance of spirobifluorene reduce the tendency to form aggregates that has been identified as a limiting factor for the photovoltaic performances in PDI based solar cells. The PDI molecules were tested as electron acceptors in bulk heterojunction solar cells with P3HT as electron donor. Power conversion efficiencies (PCE) of 1.58% and 1.18% were obtained for PDI-SF and PDI-BSF devices.
机译:核取代的per ine二酰亚胺(PDI)是有机太阳能电池的非富含富烯受体材料的候选者。使用具有不同电子捐赠能力和空间障碍的化学基团的湾位置中PDI的官能化是一种多功能工具,用于改变固态的光电性质和形态。在此,我们提出了两个新的基于PDI的基于芳族取代基的分子,所述芳香取代基连接到海湾位置:PDI-SF,具有螺二芴基和具有二苯基 - 螺氟烯部分的PDI-BSF。螺氟烯烯酮的高空间脉管降低了形成聚集体的倾向,该聚集体已被鉴定为基于PDI的太阳能电池中的光伏性能的限制因子。将PDI分子作为电子受体在散装异质结太阳能电池中用P3HT作为电子给体进行测试。为PDI-SF和PDI-BSF器件获得1.58%和1.18%的功率转换效率(PCE)。

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