首页> 外文期刊>Journal of Materials Chemistry, A. Materials for energy and sustainability >Highly efficient imide functionalized pyrrolo[3,4-c]-pyrrole-1,3-dione-based random copolymer containing thieno[3,4-c]pyrrole-4,6-dione and benzodithiophene for simple structured polymer solar cells
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Highly efficient imide functionalized pyrrolo[3,4-c]-pyrrole-1,3-dione-based random copolymer containing thieno[3,4-c]pyrrole-4,6-dione and benzodithiophene for simple structured polymer solar cells

机译:高效的酰亚胺官能化吡咯并[3,4-c]-吡咯-1,3-二酮基无规共聚物,其中含有噻吩并[3,4-c]吡咯-4,6-二酮和苯并二噻吩,用于结构简单的聚合物太阳能电池

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摘要

As an effort to improve the photovoltaic properties of a highly efficient large band gap (2.11 eV) alternating copolymer, P(BDT-TDPPDT), comprised of electron rich benzodithiophene (BDT) and novel electron accepting pyrrole-based imide functionalized 4,6-bis(thiophen-2-yl)-2,5-dioctylpyrrolo[3,4-c] pyrrole-1,3-dione (TDPPDT) derivatives, we incorporated a relatively strong electron accepting thiophene-based imide functionalized thieno[3,4-c]pyrrole-4,6-dione (TPD) unit in its main chain via random copolymerization between BDT, TDPPDT and TPD units to give polymer P1. The incorporation of a TPD unit resulted in significant improvement in the optoelectrical and photovoltaic properties. P1 exhibits lower optical band gap (1.91 eV) and a deeper lowest unoccupied molecular orbital (LUMO) energy level compared to those of P(BDT-TDPPDT). The hole mobility of P1 was 3.66 x 10(-4) cm(2) V-1 s(-1) and the PSC made with a simple device structure of ITO/PEDOT:PSS/P1:PC70BM(1 : 2.25 wt%) + 3 vol%/Al gave a maximum power conversion efficiency (PCE) of 7.03% with high photovoltaic parameters, such as an open-circuit voltage (V-oc) of 0.87 V, a short-circuit current (J(sc)) of 11.52 mA cm(-2) and a fill factor (FF) of 70%. Interestingly, P1-based PSCs exhibited a high incident photon to current efficiency (IPCE) of a maximum of 78% at 410 nm and a more than 70% response between 370-590 nm. The PCE achieved in this study is the highest value reported thus far among PSCs made with random copolymers.
机译:为了改善高效大带隙(2.11 eV)交替共聚物的光电性能,P(BDT-TDPPDT)由富电子的苯并二噻吩(BDT)和新型的基于电子接受的吡咯基酰亚胺官能化的4,6-苯并二氢噻吩组成双(噻吩-2-基)-2,5-二辛基吡咯并[3,4-c]吡咯-1,3-二酮(TDPPDT)衍生物,我们引入了一种相对强的电子接受噻吩基酰亚胺官能化噻吩并[3,4]通过在BDT,TDPPDT和TPD单元之间进行无规共聚,在主链中形成-c]吡咯-4,6-二酮(TPD)单元,得到聚合物P1。 TPD单元的并入导致光电和光伏特性的显着改善。与P(BDT-TDPPDT)相比,P1具有较低的光学带隙(1.91 eV)和更深的最低未占用分子轨道(LUMO)能级。 P1的空穴迁移率为3.66 x 10(-4)cm(2)V-1 s(-1),PSC由ITO / PEDOT:PSS / P1:PC70BM(1:2.25 wt%)的简单器件结构制成)+ 3 vol%/ Al在高光伏参数(例如0.87 V的开路电压(V-oc),短路电流(J(sc) )为11.52 mA cm(-2),填充系数(FF)为70%。有趣的是,基于P1的PSC的高入射光子电流效率(IPCE)在410 nm处最大为78%,在370-590 nm之间的响应超过70%。在这项研究中获得的PCE是迄今为止用无规共聚物制备的PSC中最高的值。

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