材料科学
罗丹宁
接受者
聚合物太阳能电池
富勒烯
开路电压
有机太阳能电池
带隙
吸收(声学)
吸收光谱法
光化学
能量转换效率
噻吩
聚合物
光电子学
太阳能电池
分析化学(期刊)
有机化学
光学
化学
电压
复合材料
物理
量子力学
凝聚态物理
作者
María Privado,Virginia Cuesta,Pilar de la Cruz,M. L. Keshtov,Rahul Singhal,Ganesh D. Sharma,Fernando Langa
标识
DOI:10.1021/acsami.6b15717
摘要
Herein we report the synthesis of a novel A-D-A-D-A non-fullerene small-molecule acceptor (NFSMA) bearing a diketopyrrolopyrrole (DPP) acceptor central core coupled to terminal rhodanine acceptors via a thiophene donor linker (denoted as MPU1) for use in non-fullerene polymer solar cells (PSCs). This NFSMA exhibits a narrow optical band gap (1.48 eV), strong absorption in the 600–800 nm wavelength region of the solar spectrum, and a lowest unoccupied energy level of −3.99 eV. When the mixture of a medium band gap D–A copolymer P (1.75 eV) was used as donor and MPU1 as acceptor, the blend film showed a broad absorption profile from 400 to 850 nm, beneficial for light harvesting efficiency of the resulted polymer solar cell. After optimization of the donor-to-acceptor weight ratios and concentration of solvent additive, the P–MPU1-based PSC exhibited a power conversion efficiency of 7.52% (Jsc= 12.37 mA/cm2, Voc = 0.98 V, and fill factor = 0.62), which is much higher than that for a P3HT–MPU1-based device (2.16%) prepared under identical conditions. The higher value for the P–MPU1-based device relative to the P3HT–MPU1-based one is related to the low energy loss and more balanced charge transport in the device based on the P donor. These results indicate that alteration of the absorption spectra and electrochemical energy levels of non-fullerene acceptors, and appropriate selection of the polymer donor with complementary absorption profile, is a promising means to further boost the performance of PSCs.
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