کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
78964 | 49345 | 2012 | 7 صفحه PDF | دانلود رایگان |
Parent or unsubstituted polythiophene (PT) films electrodeposited on hole-extraction-layer-coated ITO electrodes were used as the donor material in bilayer organic photovoltaic (OPV) devices. The electrodeposited PT layers had a porous surface with numerous voids and hollows of nanometer dimensions. The acceptor, [6] and [6]-phenyl-C61-butyric acid methyl ester (PCBM), was deposited on the PT layer by spin-coating from chlorobenzene solutions. Cross-sectional STEM-EDS (scanning transmission electron microscopy combined with energy dispersive X-ray spectroscopy) analysis revealed that some of the PCBM molecules infiltrated into the PT layer to form a PT/PCBM interpenetrating layer 8–9 nm thick between homogeneous PT and PCBM layers. The PT-based OPV devices fabricated with an optimal PT layer thickness (20 nm) showed a power conversion efficiency of 1.5% under AM 1.5 G (100 mW/cm2) illumination, which is higher than that of previously reported OPV devices using electrodeposited polythiophenes in the active layer.
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► Unsubstituted polythiophene films electrodeposited on transparent electrodes were used as the donor material in bilayer organic photovoltaic devices.
► Electrodeposited polythiophene layers had a porous surface with numerous voids and hollows of nanometer dimensions.
► Cross-sectional STEM-EDS analysis revealed that some of the mathanofullerene molecules infiltrated into the polythiophene layer to form a polythiophene/methanofullerene interpenetrating layer.
► Optimized devices showed a power conversion efficiency of 1.5% under AM 1.5G (100 mW/cm2) illumination.
Journal: Solar Energy Materials and Solar Cells - Volume 105, October 2012, Pages 167–173