Morphology evolution via self-organization and lateral and vertical diffusion in polymer: fullerene solar cell blends

被引:1338
作者
Campoy-Quiles, Mariano [1 ]
Ferenczi, Toby [1 ]
Agostinelli, Tiziano [2 ]
Etchegoin, Pablo G. [3 ]
Kim, Youngkyoo [1 ,4 ]
Anthopoulos, Thomas D. [1 ]
Stavrinou, Paul N. [1 ]
Bradley, Donal D. C. [1 ]
Nelson, Jenny [1 ]
机构
[1] Univ London Imperial Coll Sci Technol & Med, Blackett Lab, Dept Phys, London SW7 2BW, England
[2] Politecn Milan, Dipartimento Elettron & Informaz, I-20133 Milan, Italy
[3] Victoria Univ Wellington, Sch Chem & Phys Sci, MacDiarmid Inst Adv Mat & Nanotechnol, Wellington, New Zealand
[4] Kyungpook Natl Univ, Dept Chem Engn, Organ Nanoelect Lab, Taegu 702701, South Korea
基金
英国工程与自然科学研究理事会;
关键词
D O I
10.1038/nmat2102
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
Control of blend morphology at the microscopic scale is critical for optimizing the power conversion efficiency of plastic solar cells based on blends of conjugated polymer with fullerene derivatives. In the case of bulk heterojunctions of regioregular poly(3-hexylthiophene) (P3HT) and a soluble fullerene derivative ([6,6]-phenyl C-61-butyric acid methyl ester, PCBM), both blend morphology and photovoltaic device performance are influenced by various treatments, including choice of solvent, rate of drying, thermal annealing and vapour annealing. Although the protocols differ significantly, the maximum power conversion efficiency values reported for the various techniques are comparable (4-5%). In this paper, we demonstrate that these techniques all lead to a common arrangement of the components, which consists of a vertically and laterally phase-separated blend of crystalline P3HT and PCBM. We propose a morphology evolution that consists of an initial crystallization of P3HT chains, followed by diffusion of PCBM molecules to nucleation sites, at which aggregates of PCBM then grow.
引用
收藏
页码:158 / 164
页数:7
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