Stabilization of the nanomorphology of polymer-fullerene "bulk heterojunction'' blends using a novel polymerizable fullerene derivative

被引:195
作者
Drees, M
Hoppe, H
Winder, C
Neugebauer, H
Sariciftci, NS
Schwinger, W
Schäffler, F
Topf, C
Scharber, MC
Zhu, ZG
Gaudiana, R
机构
[1] Johannes Kepler Univ Linz, Linz Inst Organ Solar Cells, A-4040 Linz, Austria
[2] Johannes Kepler Univ Linz, Inst Halbleiter & Festkorperphys, A-4040 Linz, Austria
[3] Konarka Austria Forsch & Entwicklungs GmbH, A-4010 Linz, Austria
[4] Konarka Technol Inc, Lowell, MA 01852 USA
关键词
D O I
10.1039/b505361g
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
The morphological stabilization of donor - acceptor blends for bulk heterojunction solar cells can be achieved by cross-linking of the small molecular phase in the polymer matrix using a polymerizable fullerene derivative. In a comparative study the morphology of polymer - fullerene blend films was investigated using poly(3-hexylthiophene) (P3HT) as the polymer and C-61-butyric acid methyl ester (PCBM) or the newly synthesized polymerizable fullerene derivative, C-61-butyric acid glycidol ester, PCBG, as the acceptor molecule, respectively. Changes in the nanomorphology due to heat treatment of the films were studied by means of atomic force microscopy (AFM), transmission electron microscopy (TEM) and photoluminescence (PL) studies. The polymerization process was monitored with infrared absorption studies. As demonstrated by these comparative studies this newly synthesized fullerene gives considerable stabilization of the solid state morphology in these blends. Such prevention of the long term, high temperature instability of bulk heterojunction morphology displays an important route to increase the operational stability of plastic solar cells in future applications.
引用
收藏
页码:5158 / 5163
页数:6
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