Influence of the Ionic Functionalities of Polyfluorene Derivatives as a Cathode Interfacial Layer on Inverted Polymer Solar Cells

被引:68
作者
Kang, Rira [1 ]
Oh, Seung-Hwan [3 ]
Kim, Dong-Yu [1 ,2 ]
机构
[1] Gwangju Inst Sci & Technol, Sch Mat Sci & Engn, HCAM, Kwangju 500712, South Korea
[2] Gwangju Inst Sci & Technol, Dept Nanobio Mat & Elect, Kwangju 500712, South Korea
[3] Korea Atom Energy Res Inst, Radiat Res Div Ind & Environm, Jeongup Si 580185, Jeollabuk Do, South Korea
基金
新加坡国家研究基金会;
关键词
conjugated polyelectrolytes; polyfluorene; dipole layer; work-function modification; interfacial layer; inverted polymer solar cells; LIGHT-EMITTING-DIODES; CONJUGATED POLYELECTROLYTES; ELECTRONIC-PROPERTIES; HIGHLY EFFICIENT; HIGH-PERFORMANCE; WATER; SURFACE;
D O I
10.1021/am500708k
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
In this work, we synthesized water-soluble polyfluorene derivatives (WPFs) with anionic and/or cationic side chains, which were used as an indium tin oxide (ITO) cathode interfacial layer in inverted polymer solar cells. Three WPFs (WPFN+, WPFZW, and WPFS-) were obtained via Suzuki coupling reactions. Their solubility in polar solvents allowed the WPFs to be used as interfacial layers in inverted polymer solar cells (I-PSCs). Among the WPF-modified ITO electrodes, WPFN+ (with ammonium side chains)-modified ITO can be used as a cathode for electron extraction, while WPFS- (with sulfonate side chains)-modified ITO cannot extract electrons in I-PSCs based on poly(3-hexylthiophene): [6,6]-phenyl-C-61-butyric acid methyl ester (P3HT:PC61BM). The electron extraction of WPF-modified ITO can mainly be attributed to the different dipole formations at the WPF/ITO interfaces, based on the types of ionic groups on the side chains of the polyfluorene. In addition, we observed that the extent of ITO work-function modification was not always exactly correlated with the device performance based on the results obtained using a WPFZW (with ammonium and sulfonate side chains)-modified ITO electrode.
引用
收藏
页码:6227 / 6236
页数:10
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