Optimisation of diketopyrrolopyrrole:fullerene solar cell performance through control of polymer molecular weight and thermal annealing

被引:25
作者
Huang, Zhenggang [1 ]
Fregoso, Elisa Collado [1 ]
Dimitrov, Stoichko [1 ]
Tuladhar, Pabitra Shakya [1 ]
Soon, Ying Woan [1 ]
Bronstein, Hugo [1 ]
Meager, Iain [1 ]
Zhang, Weimin [1 ]
McCulloch, Iain [1 ]
Durrant, James R. [1 ]
机构
[1] Univ London Imperial Coll Sci Technol & Med, Dept Chem, Ctr Plast Electon, London SW7 2AZ, England
基金
英国工程与自然科学研究理事会;
关键词
CHARGE PHOTOGENERATION; SEMICONDUCTING POLYMER; MORPHOLOGY EVOLUTION; EFFICIENCY; CRYSTALLIZATION; MICROSTRUCTURE; PHOTOCURRENT; BLENDS; POLY(3-HEXYLTHIOPHENE); INTERCALATION;
D O I
10.1039/c4ta03589e
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Poly-thieno[3,2b]thiophene-diketopyrrolopyrrole-co-thiophene (DPP-TT-T) is a promising low bandgap donor polymer for organic solar cells. In this study we employ two different approaches to improve the device efficiency via optimisation of the morphology of the active layer: tuning of the molecular weight of the polymer and thermal annealing. In the former case, a higher molecular weight was found to yield a more intermixed morphology, resulting in enhanced exciton dissociation and charge separation, as confirmed by atomic force microscopy, and photoluminescence and transient absorption spectroscopies. In the later case, thermal annealing prior to metal electrode deposition increased the photon conversion efficiency to as high as 6.6%, with this enhanced efficiency being maintained even with prolonged annealing (240 hours at 80 degrees C). This enhancement in performance with thermal annealing was correlated with increased polymer crystallinity.
引用
收藏
页码:19282 / 19289
页数:8
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