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Compact Bis-Adduct Fullerenes and Additive-Assisted Morphological Optimization for Efficient Organic Photovoltaics

机译:紧凑的双加合物富勒烯和添加剂辅助的形态学优化,用于高效有机光伏

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Bis-adduct fullerenes surrounded by two insulating addends sterically attenuate intermolecular interaction and cause inferior electron transportation. In this research, we have designed and synthesized a new class of bis-adduct fullerene materials, methylphenylmethano-C-60 bis-adduct (MPC(60)BA), methylthienylmethano-C-60 bis-adduct (MTC(60)BA), methylphenylmethano-C-70 bis-adduct (MPC(70)BA), and methylthienylmethano-C-70 bis-adduct (MTC(70)BA), functionalized with two compact phenylmethylmethano and thienylmethylmethano addends via cyclopropyl linkages. These materials with much higher-lying lowest unoccupied molecular orbital (LUMO) energy levels successfully enhanced the V-oc values of the P3HT-based solar cell devices. The compact phenylmethylmethano and thienylmethylmethano addends to promote fullerene intermolecular interactions result in aggregation-induced phase separation as observed by the atomic force microscopy (AFM) and transmission electron microscopy (TEM) images of the poly(3-hexylthiophene-2,5-diyl) (P3HT)/bis-adduct fullerene thin films. The device based on the P3HT/MTC(60)BA blend yielded a V-oc of 0.72 V, a J(sc) of 5.87 mA/cm(2), and a fill factor (FF) of 65.3%, resulting in a power conversion efficiency (PCE) of 2.76%. The unfavorable morphologies can be optimized by introducing a solvent additive to fine-tune the intermolecular interactions. 1-Chloronaphthalene (CN) having better ability to dissolve the bis-adduct fullerenes can homogeneously disperse the fullerene materials into the P3HT matrix. Consequently, the aggregated fullerene domains can be alleviated to reach a favorable morphology. With the assistance of CN additive, the P3HT/MTC(60)BA-based device exhibited enhanced characteristics (a V-oc of 0.78 V, a J(sc) of 9.04 mA/cm(2), and an FF of 69.8%), yielding a much higher PCE of 4.92%. More importantly, the additive-assisted morphological optimization is consistently effective to all four compact bis-adduct fullerenes regardless of the methylphenylmethano or methylthienylmethano scaffolds as well as C-60 or C-70 core structures. Through the extrinsic additive treatment, these bis-adduct fullerene materials with compact architectures show promise for high-performance polymer solar cells.
机译:被两个绝缘加成物包围的双加合物富勒烯在空间上减弱了分子间的相互作用,并导致电子传输的质量降低。在这项研究中,我们设计并合成了新型的双加合物富勒烯材料,甲基苯基甲基-C-60双加合物(MPC(60)BA),甲基噻吩基甲基-C-60双加合物(MTC(60)BA) ,甲基苯基甲基-C-70双加合物(MPC(70)BA)和甲基噻吩基甲基-C-70双加合物(MTC(70)BA),通过环丙基键与两个紧凑的苯基甲基甲基和噻吩甲基甲基加成官能团。这些材料具有更高的最低最低未占据分子轨道(LUMO)能级,成功地提高了基于P3HT的太阳能电池设备的V-oc值。如聚(3-己基噻吩-2,5-二基)的原子力显微镜(AFM)和透射电子显微镜(TEM)图像所观察到的,致密的苯基甲基亚甲基和噻吩基甲基亚甲基会促进富勒烯分子间的相互作用,导致聚集诱导的相分离。 (P3HT)/双加合物富勒烯薄膜。基于P3HT / MTC(60)BA共混物的器件产生的V-oc为0.72 V,J(sc)为5.87 mA / cm(2),填充因子(FF)为65.3%,导致功率转换效率(PCE)为2.76%。不良的形态可通过引入溶剂添加剂来微调分子间的相互作用来优化。具有更好的溶解双加合物富勒烯能力的1-氯萘(CN)可以将富勒烯材料均匀地分散到P3HT基质中。因此,可以减轻聚集的富勒烯结构域以达到良好的形态。在CN添加剂的帮助下,基于P3HT / MTC(60)BA的器件表现出增强的特性(V-oc为0.78 V,J(sc)为9.04 mA / cm(2),FF为69.8% ),产生了4.92%的更高的PCE。更重要的是,无论甲基苯基甲基或甲基噻吩基甲基支架,C-60或C-70核心结构如何,添加剂辅助的形态优化对所有四个紧密的双加合物富勒烯始终有效。通过外部添加剂处理,这些具有紧凑结构的双加合物富勒烯材料显示出对高性能聚合物太阳能电池的希望。

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