发色团
接受者
偶极子
材料科学
反平行(数学)
有机太阳能电池
菁
太阳能电池
富勒烯
能量转换效率
光化学
超分子化学
结晶学
化学
晶体结构
光电子学
光学
荧光
有机化学
物理
量子力学
磁场
复合材料
凝聚态物理
聚合物
作者
Hannah Bürckstümmer,Elena V. Tulyakova,M. Deppisch,Martin R. Lenze,Nils M. Kronenberg,Marcel Gsänger,Matthias Stolte,Klaus Meerholz,Frank Würthner
标识
DOI:10.1002/anie.201105133
摘要
Abstract A series of dipolar donor–acceptor ( D –A) chromophores with aminothiophene donor and different heterocyclic acceptor units is reported. By modulation of the acceptor strength, absorption bands over the whole visible spectrum are accessible as well as adjustment of the frontier molecular orbital levels. The performance of the chromophores in blends with fullerene acceptors in solution‐processed bulk heterojunction solar cells was studied and related to the molecular properties of the dyes. In particular, the effect of the large ground‐state dipole moments of these dyes was investigated by single crystal X‐ray analysis, which revealed antiparallel dimers, resulting in an annihilation of the dipole moments. This specific feature of supramolecular organization explains the excellent performance of merocyanine dyes in organic solar cells. With blends of HB366 :PC 71 BM, the most efficient solar cell with a V OC of 1.0 V, a J SC of 10.2 mA cm −2 , and a power‐conversion efficiency of 4.5 % was achieved under standard AM1.5, 100 mW cm −2 conditions. Under reduced lighting conditions, even higher efficiencies up to 5.1 % was obtained.
科研通智能强力驱动
Strongly Powered by AbleSci AI