We use photoinduced absorption spectroscopy to measure long-lived photogenerated charge carriers in optically thin donor/acceptor conjugated polymer blend films near plasmon-resonant silver nanoprisms. We measure up to 3 times more charge generation, as judged by the magnitude of the polaron absorption signal, in 35 nm thin blend films of poly(3-hexylthiophene)/phenyl-C(61)-butyric acid methyl ester on top of films of silver nanoprisms (approximately 40-100 nm edge length). We find that the polaron yields increase linearly with the total sample extinction. These excitation enhancements could in principle be used to increase photocurrents in thin organic solar cells.

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We describe bulk heterojunction (BHJ) solar cells containing blends of colloidal PbS nanocrystal quantum dots with several new donor-acceptor conjugated polymers. Using photoinduced absorption spectroscopy we found that blends of PbS quantum dots with one polymer, poly(2,3-didecyl-quinoxaline-5,8-diyl-alt-N-octyldithieno[3,2-b:2',3'-d]pyrrole) (PDTPQx), produce significantly more photoinduced charge than blends of PbS with the other donor-acceptor polymers or with traditionally studied polymers like [2-methoxy-5-(3',7'-dimethyloctyloxy)-para-phenylene vinylene] (MDMO-PPV) and poly(3-hexylthiophene) (P3HT). Photovoltaic devices made with PDTPQx/PbS blends exhibit power conversion efficiencies 10-100 times larger than previously reported BHJ blends made with IR-absorbing quantum dots.

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We use photoluminescence (PL) quenching and photoinduced absorption (PIA) spectroscopy to study charge transfer in bulk heterojunction blends of PbSe quantum dots with the semiconducting polymers poly-3-hexylthiophene (P3HT) and poly[2-methoxy-5-(3',7'-dimethyloctyloxy)-para-phenylene vinylene] (MDMO-PPV). PIA spectra from the PbSe blends are compared to spectra from similar blends of the polymers with phenyl-C(61)-butyric acid methyl ester (PCBM) and blends with CdSe quantum dots. We find that the MDMO-PPV PL is quenched, and the PL lifetime is shortened upon addition of PbSe quantum dots, while the PL of the P3HT is unaffected upon blending. However, for PbSe blends with both polymers, the PIA spectra show very little polaronic signal, suggesting that few, if any, long-lived charges are being produced by photoinduced charge transfer.