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首页> 外文期刊>Chemistry, an Asian journal >Incorporation of Hexa-peri-hexabenzocoronene (HBC) into Carbazole-Benzo-2,1,3-thiadiazole Copolymers to Improve Hole Mobility and Photovoltaic Performance
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Incorporation of Hexa-peri-hexabenzocoronene (HBC) into Carbazole-Benzo-2,1,3-thiadiazole Copolymers to Improve Hole Mobility and Photovoltaic Performance

机译:将六-per-hexabenzobenzoronon(HBC)掺入咔唑-Benzo-2,1,3-噻二唑共聚物中以改善空穴迁移率和光伏性能

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摘要

Hexa-peri-hexabenzocoronene (HBC) is a discotic-shaped conjugated molecule with strong - stacking property, high intrinsic charge mobility, and good self-assembly properties. For a long time, however, organic photovoltaic (OPV) solar cells based on HBC demonstrated low power conversion efficiencies (PCEs). In this study, two conjugated terpolymers, poly[N-9-heptadecanyl-2,7-carbazole-alt-5,5-(4,7-di-2-thienyl-2,1,3-benzothiadiazole)] (PCDTBT)-5HBC and PCDTBT-10HBC, were synthesized by incorporating different amounts of HBC as the third component into poly[N-9-heptadecanyl-2,7-carbazole-alt-5,5-(4,7-di-2-thienyl-2,1,3-benzothiadiazole)] (PCDTBT) through Suzuki coupling polymerization. For comparison, the donor-acceptor (D-A) conjugated dipolymer PCDTBT was also synthesized to investigate the effect of HBC units on conjugated polymers. The HBC-containing polymers exhibited higher thermal stabilities, broader absorption spectra, and lower highest-occupied molecular orbital (HOMO) energy levels. In particular, the field-effect mobilities were enhanced by more than one order of magnitude after the incorporation of HBC into the conjugated polymer backbone on account of increased interchain - stacking interactions. The bulk heterojunction (BHJ) polymer solar cells (PSCs) fabricated with the polymers as donor and PC71BM as acceptor demonstrated gradual improvement of open-circuit voltage (V-OC) and short-circuit current (J(SC)) with the increase in HBC content. As a result, the PCEs were improved from 3.21% for PCDTBT to 3.78% for PCDTBT-5HBC and then to 4.20% for PCDTBT-10HBC.
机译:六面六己苯并六氢呋喃(HBC)是一种盘状共轭分子,具有强堆积特性,高固有电荷迁移率和良好的自组装特性。然而,长期以来,基于HBC的有机光伏(OPV)太阳能电池表现出较低的功率转换效率(PCE)。在这项研究中,两种共轭三元共聚物,聚[N-9-十七烷基-2,7-咔唑-alt-5,5-(4,7-二-2-噻吩基-2,1,3-苯并噻二唑)](PCDTBT )-5HBC和PCDTBT-10HBC,是通过将不同量的HBC作为第三组分掺入聚[N-9-十七烷基-2,7-咔唑-alt-5,5-(4,7-di-2-噻吩-2,1,3-苯并噻二唑)](PCDTBT)通过Suzuki偶联聚合。为了比较,还合成了供体-受体(D-A)共轭二聚物PCDTBT,以研究HBC单元对共轭聚合物的影响。含HBC的聚合物表现出更高的热稳定性,更宽的吸收光谱和更低的最高占据分子轨道(HOMO)能级。特别地,由于链间-堆叠相互作用增加,在将HBC掺入到共轭聚合物主链中之后,场效应迁移率提高了一个数量级以上。以聚合物为施主和PC71BM为受主的体异质结(BHJ)聚合物太阳能电池(PSC)随着开路电压的增加,开路电压(V-OC)和短路电流(J(SC))逐渐提高。 HBC内容。结果,PCE从PCDTBT的3.21%提高到PCDTBT-5HBC的3.78%,再到PCDTBT-10HBC的4.20%。

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