首页> 外文期刊>Journal of Materials Chemistry, C. materials for optical and electronic devices >Enhancing the photovoltaic properties of terpolymers containing benzo[1,2-b:4,5-b ']-dithiophene, phenanthro[4,5-abc]phenazine and benzo[c][1,2,5]thiadiazole by changing the substituents
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Enhancing the photovoltaic properties of terpolymers containing benzo[1,2-b:4,5-b ']-dithiophene, phenanthro[4,5-abc]phenazine and benzo[c][1,2,5]thiadiazole by changing the substituents

机译:改变苯并[1,2-b:4,5-b']-二噻吩,菲并[4,5-abc]吩嗪和苯并[c] [1,2,5]噻二唑的三元共聚物的光电性能取代基

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In this study, three novel donor-acceptor (D-A)-type random conjugated terpolymers of PBDTT-PPzBT-H, PBDTT-PPzBT-F and PBDTT-PPzBT-O were synthesized by copolymerizing electron-rich 5,8-dialkylthienyl substituted benzo[1,2-b: 4,5-b']dithiophene (BDTT) and two electron-deficient phenanthro[4,5-abc]phenazine (PPz) and benzo[c][1,2,5]thiadiazole (BT) units. By changing the substituents at the 5,6-positions of BT, the optoelectronic properties of the terpolymers could be rationally adjusted for application as donor materials in polymer solar cells (PSCs). As a result, these terpolymers exhibited different light absorption properties, HOMO energy levels and hole mobilities, which contributed to the optimization of short-circuit current (J(sc)), open-circuit voltage (V-oc) and fill factor (FF) properties, respectively. Interestingly, a maximum power conversion efficiency (PCE) of 6.3% was obtained with an V-oc of 0.75 V, a J(sc) of 13.0 mA cm(-2) and a FF of 64.8% in the PBDTT-PPzBT-O based PSCs using [6,6]-phenyl-C-71-butyric acid methyl ester (PC71BM) as an acceptor, while PBDTT-PPzBT-H and PBDTT-PPzBT-F based devices also demonstrated a PCE of more than 4.5%. To the best of our knowledge, these are the highest recorded maximum PCE, J(sc) and FF values obtained to date compared with previously reported phenazine copolymeric derivatives in BHJ-PSCs. This study illustrates the potential of these random conjugated terpolymers as promising donor materials in the application of PSCs.
机译:在这项研究中,通过共聚富电子的5,8-二烷基噻吩基取代的苯并[3]合成了三种新型的PBDTT-PPzBT-H,PBDTT-PPzBT-F和PBDTT-PPzBT-O供体-受体(DA)型无规共轭三元共聚物。 1,2-b:4,5-b']二噻吩(BDTT)和两个缺电子的菲并[4,5-abc]吩嗪(PPz)和苯并[c] [1,2,5]噻二唑(BT)单位。通过改变BT 5,6-位的取代基,可以合理地调节三元共聚物的光电性能,以用作聚合物太阳能电池(PSC)中的供体材料。结果,这些三元共聚物表现出不同的光吸收特性,HOMO能级和空穴迁移率,这有助于优化短路电流(J(sc)),开路电压(V-oc)和填充系数(FF) )属性。有趣的是,在PBDTT-PPzBT-O中,V-oc为0.75 V,J(sc)为13.0 mA cm(-2)且FF为64.8%时,可获得6.3%的最大功率转换效率(PCE)。 [6,6]-苯基-C-71-丁酸甲酯(PC71BM)作为受体的基于PSC的PSC,而基于PBDTT-PPzBT-H和PBDTT-PPzBT-F的设备也显示PCE超过4.5%。据我们所知,与BHJ-PSC中以前报道的吩嗪共聚衍生物相比,这些是迄今为止获得的最高记录的最大PCE,J(sc)和FF值。这项研究说明了这些无规共轭三元共聚物作为潜在的供体材料在PSC应用中的潜力。

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