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R Osterbacka

Publications and source records attributed to R Osterbacka.

4 recordsLinked to original sources

Bimolecular recombination coefficient as a sensitive testing parameter for low-mobility solar-cell materials.

Bimolecular charge carrier recombination has been clarified in bulk-heterojunction solar cells based on a blend of regioregular poly(3-hexylthiophene) and 1-(3-methoxycarbonyl)propyl-1-phenyl-[6,6]-methanofullerene using the time-of-flight method. We show how bimolecular recombination influences the charge carrier transport, how it limits the efficiency of low-mobility solar cells, and how to estimate the bimolecular recombination coefficient. We found that bimolecular recombination in these efficient photovoltaic materials is orders of magnitude slower as compared to Langevin recombination expected for low-mobility materials. This effect is inherent to the nanomorphology of the bicontinuous interpenetrating network creating separate pathways for electrons and holes, and paves the way for the fabrication of bulk-heterojunction solar cells where bimolecular recombination is not the limiting factor.

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Photoinduced quantum interference antiresonances in pi-conjugated polymers.

We observed photoinduced quantum interference antiresonances between several discrete infrared-active vibrations and the lower-polaron continuous absorption band in a series of pi-conjugated polymer films having superior planar orders, where the polaron transition energy is relatively small. The photoinduced Fano-type antiresonances are well explained by extending the amplitude mode model beyond the adiabatic limit. The agreement between the data and the model confirms the presence of a continuous electronic band above the polaron state. We show that high frequency modes are strongly coupled to electrons, with implications for superconductivity.

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Two-dimensional electronic excitations in self-assembled conjugated polymer nanocrystals

Several spectroscopic methods were applied to study the characteristic properties of the electronic excitations in thin films of regioregular and regiorandom polythiophene polymers. In the regioregular polymers, which form two-dimensional lamellar structures, increased interchain coupling strongly influences the traditional one-dimensional electronic properties of the polymer chains. The photogenerated charge excitations (polarons) show two-dimensional delocalization that results in a relatively small polaronic energy, multiple absorption bands in the gap where the lowest energy band becomes dominant, and associated infrared active vibrations with reverse absorption bands caused by electron-vibration interferences. The relatively weak absorption bands of the delocalized polaron in the visible and near-infrared spectral ranges may help to achieve laser action in nanocrystalline polymer devices using current injection.

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