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首页> 外文期刊>Journal of Materials Chemistry, A. Materials for energy and sustainability >Tuning optical and electronic properties of star-shaped conjugated molecules with enlarged π-delocalization for organic solar cell application
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Tuning optical and electronic properties of star-shaped conjugated molecules with enlarged π-delocalization for organic solar cell application

机译:通过扩大π-离域来调节星形共轭分子的光学和电子性质,以用于有机太阳能电池

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摘要

Three structurally related conjugated molecules (BTT-BTD-0, BTT-BTD-1 and BTT-BTD-2) in star shape have been designed and synthesized as donor materials for small molecule based bulk heterojunction (BHJ) solar cells. The structural features of these molecules include a planarized benzo[1,2-b:3,4-ib':5,6-b"]-trithiophene (BTT) with a C_(3h) symmetry as the central core and three conjugated arms incorporating electron deficient benzo[2,1,3]thiadiazole (BTD) units, with arms being linked to the core via different number of thiophene connecting units (e.g., 0, 1, 2 corresponding to BTT-BTD-0, BTT-BTD-1 and BTT-BTD-2, respectively). Comparative analyses of optical and electronic properties indicate that the molecules bearing more thiophene units between the BTT core and the BTD arms possess higher-lying HOMO levels while their LUMO levels remain almost unchanged. The improvement of BHJ device performance, with [6,6]-phenyl-C_(61)-butyric acid methyl ester (PC_(61)BM) as the acceptor, is observed with increasing number of thiophene units between the BTT core and BTD arms, from BTT-BTD-0 to BTT-BTD-1 and BTT-BTD-2. The BTT-BTD-2:PC_(61)BM based BHJ devices show the highest power conversion efficiency (PCE) of 0.74%, with an open-circuit voltage (V_(oc)) of 0.69 V, a short-circuit current density (J_(sc)) of 2.93 mAcm~(-2), and a fill factor (FF) of 0.37 under 1 sun (100 mWcm~(-2)) AM 1.5G simulated solar illumination. The PV performance of BTT-BTD-2 is further improved when [6,6]-phenyI-C71-butyric acid methyl ester (PC_(71)BM) is used as the electron acceptor, yielding the best device performance with J_(sc) of 4.13 mA cm~(-2), V_(oc) of 0.72 V, FF at 0.46 and PCE of 1.36%. The effect of the different number of thiophenes linking the BTT core and the conjugated BTD arms has been clearly demonstrated on regulating optical and electrochemical properties of the three molecules and their BHJ device performances.
机译:设计并合成了三种结构上相关的共轭分子(BTT-BTD-0,BTT-BTD-1和BTT-BTD-2),作为基于小分子的本体异质结(BHJ)太阳能电池的供体材料。这些分子的结构特征包括以C_(3h)对称性为中心的平面化苯并[1,2-b:3,4-ib':5,6-b“]-三噻吩(BTT)和三个共轭包含缺电子的苯并[2,1,3]噻二唑(BTD)单元的臂,臂通过不同数量的噻吩连接单元(例如,与BTT-BTD-0,BTT- BTD-1和BTT-BTD-2)。光学和电子性质的比较分析表明,在BTT核心和BTD臂之间带有更多噻吩单元的分子具有较高的HOMO能级,而它们的LUMO能级几乎保持不变。随着BTT核心和BTD之间噻吩单元数量的增加,观察到以[6,6]-苯基-C_(61)-丁酸甲酯(PC_(61)BM)为受体的BHJ器件性能的提高。从BTT-BTD-0到BTT-BTD-1和BTT-BTD-2的手臂。基于BTT-BTD-2:PC_(61)BM的BHJ器件显示出最高的功率转换效率(PCE) )为0.74%,开路电压(V_(oc))为0.69 V,短路电流密度(J_(sc))为2.93 mAcm〜(-2),填充系数(FF)为在1个太阳(100 mWcm〜(-2))AM 1.5G模拟太阳光照下为0.37。当使用[6,6]-苯基I-C71-丁酸甲酯(PC_(71)BM)作为电子受体时,BTT-BTD-2的PV性能得到了进一步改善,在J_(sc )为4.13 mA cm〜(-2),V_(oc)为0.72 V,FF为0.46,PCE为1.36%。连接BTT核心和共轭BTD臂的不同数目的噻吩对调节这三种分子的光学和电化学性质及其BHJ器件性能的影响已得到明确证明。

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