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首页> 外文期刊>Synthetic Metals >Synthesis and characterization of 2H-benzimidazole- and terthiophene-based polymer for organic photovoltaics
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Synthesis and characterization of 2H-benzimidazole- and terthiophene-based polymer for organic photovoltaics

机译:用于有机光伏的2H-苯并咪唑和对噻吩基聚合物的合成与表征

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摘要

New semiconducting polymer with alkoxy substituted terthiophene, as the electron rich unit, and 2,2-(l,5-pentamethylene)-2H-benzimidazole (PMBI), as the electron deficient unit, was synthesized using Stille polymerization. The advantage of PMBI is higher solubility of the polymer while keeping the coplanarity of the backbone as compared to the benzothiadiazole moiety of PCDTBT. In PMBI, the sulfur at 2-position of BT unit was replaced with the carbon of cyclohexane to make a highly soluble electron deficient moiety while keeping the 1,2-quinoid form of BT unit. The polymer, PTBHOTPMBI, exhibits more red shifted absorption peak as compared to the polymers with benzothiadiazole unit. The PTBHOTPMBI thin film shows two broad absorption bands with peaks at 475 and 755 nm and an absorption onset at 943 nm, corresponding to a band gap of 1.32 eV. The device of PTBHOTPMBI with PC_(71)BM showed an open-circuit voltage (V_(oc)) of 0.25 V, a short-circuit current density (J_(sc)) of 2.30 mA/cm~2, and a fill factor (FF) of 0.30, giving a power conversion efficiency of 0.17%.
机译:使用Stille聚合反应合成了一种新的半导体聚合物,该聚合物以烷氧基取代的噻吩为富电子单元,以2,2-(1,5-五亚甲基)-2H-苯并咪唑(PMBI)为电子不足单元。与PCDTBT的苯并噻二唑部分相比,PMBI的优势在于聚合物的溶解度更高,同时保持了主链的共面性。在PMBI中,将BT单元2位的硫替换为环己烷中的碳,以形成高度可溶的电子缺陷部分,同时保持BT单元的1,2-喹啉形式。与具有苯并噻二唑单元的聚合物相比,PTBHOTPMBI聚合物表现出更多的红移吸收峰。 PTBHOTPMBI薄膜显示两个宽吸收带,在475和755 nm处出现峰,在943 nm处出现吸收开始,对应的带隙为1.32 eV。具有PC_(71)BM的PTBHOTPMBI器件显示的开路电压(V_(oc))为0.25 V,短路电流密度(J_(sc))为2.30 mA / cm〜2,填充系数(FF)为0.30,功率转换效率为0.17%。

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