Discotic materials for organic solar cells: Effects of chemical structure on assembly and performance

被引:53
作者
Hesse, Holger Christian [1 ,2 ]
Weickert, Jonas [1 ,2 ]
Al-Hussein, Mahmoud [3 ]
Doessel, Lukas [4 ]
Feng, Xinliang [4 ]
Muellen, Klaus [4 ]
Schmidt-Mende, Lukas [1 ,2 ]
机构
[1] Univ Munich, Dept Phys, D-80799 Munich, Germany
[2] Univ Munich, Ctr NanoSci CeNS, D-80799 Munich, Germany
[3] Univ Jordan, Dept Phys, Amman 11942, Jordan
[4] Max Planck Inst Polymer Res, D-55128 Mainz, Germany
关键词
Organic photovoltaics; Discotic materials; Inverted solar cell; Self-assembly; Transient decay measurements; LIQUID-CRYSTALS; MORPHOLOGY; PHOTOVOLTAICS; TRANSPORT; BLENDS; ENERGY;
D O I
10.1016/j.solmat.2009.11.024
中图分类号
TE [石油、天然气工业]; TK [能源与动力工程];
学科分类号
0807 ; 0820 ;
摘要
Discotic materials have attracted remarkable interest for application in organic solar cells. We analyze a series of phenyl-substituted hexa-peri-hexabenzocoronenes (HBCs) with residue modifications blended with perylenediimide (PDI) as donor material. The effect of differing alkyl chain lengths of 6, 8, 12 and 16 carbon atoms, introduction of a triple bond linker between HBC core and residual phenyl group and a swallow tailed dialkylphenyl chain on the device performance is investigated. Detailed insight to device physics and morphology is gained by analysis of photoluminescence quenching, transient photovoltage and photocurrent decay experiments and atomic force microscopy. Complementary the investigations explain why using short alkyl side chains higher currents and consequently increased device performance can be achieved. We report an external quantum efficiency of over 27% for devices based on discotic molecules. In this work the molecular assembly and its impact on performance in photovoltaic devices is studied. The study also reveals pathways to further increase the quantum yield of small molecule organic solar cells. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:560 / 567
页数:8
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