We examine the optical and structural properties of polyaniline–silicon nanoparticle capsules — a novel organic/inorganic material. The Si particles absorb UV/blue efficiently and green moderately, while polyaniline (PANI) in its green emeraldine state absorbs UV and red/IR efficiently, effectively providing absorption over a wide range of the solar spectrum. The capsules are produced by miniemulsion of aniline monomers in the presence of Si nanoparticles. Thin films of the capsules were formed on a variety of substrates. We use high resolution transmission electron microscopy (HTEM) and scanning electron microscopy (SEM) to record the structural properties. We also monitor the optical properties of the Si core and the PANI shell using fluorescence microscopy under UV and visible irradiation. Upon on-off cycles of UV irradiation and visible light, the red core switches reversibly between bright and dark states while PANI switches reversibly between emeraldine green and pernigraniline violet states. The results are analyzed in terms of excitonic excitation, charge separation, and transport between the core and the shell, which is useful for photovoltaic applications.

Capabilities of Atomic Force Microscopy in different modes including Electric Force Microscopy and Kelvin Force Microscopy are reviewed and illustrated on several samples including organic photovoltaics (P3HT/PCBM, PEDOT:PSS). Compositional mapping of these blends is enhanced with a combined use of the modes, and variations of local electric properties are detected down to the nanometer scale. The revealed morphology will assist in development of comprehensive models accounting for the structure-property relationship in solar cells and related devices.

An alternating copolymer containing dithienylcyclopentadienone, thiophene and benzothiadiazole was synthesized by palladium (0) catalyzed Stille coupling reaction. Structural characterization of the synthesized alternating copolymer was carried out by NMR and FTIR spectroscopy. This solution processable copolymer shows an excellent thermal stability and has a broad absorption range from 300-800 nm. High LUMO energy level and low band gap of the synthesized copolymers suggest that, this copolymer will be a better donor material for application in organic photovoltaics. Particle size analysis and molecular weight determination of the synthesized copolymer through dynamic light scattering experiment indicates that, high molecular weight copolymer was obtained by this polymerization route. Photovoltaic devices were fabricated from the blend of copolymer and phenyl-C61- butyric acid methyl ester as the active material. Fabricated photovoltaic device results show that this alternating copolymer is a promising candidate for use in organic photovoltaics.

Relatively low efficiency is one of the main obstacles to overcome in the engineering of organic bulk heterojunction (BHJ) solar cells. Reduced graphene oxide (RGO), which has high conductivity, has been proposed to enhance the function of PCBM in the interfacial dissociation of excitons, but incorporating it into the hydrophobic photoactive polymers has proved challenging. Here we describe a novel technique for incorporating Au nanoparticles (AuNp) into the structure of the RGO. The AuNps then interact with the sulfur groups on the photoactive polymer component, while the RGO interacts via π – π stacking with the chemically similar PCBM, thereby anchoring the complex to the polymer interface. Graphene oxide was synthesized and then reduced in the presence of a gold salt. The resulting gold-functionalized RGO (AuRGO) sheets were characterized using TGA, FTIR, and TEM. The AuRGO was not soluble in chlorobenzene; however, in the presence of P3HT, the AuRGO dissolved, suggesting a reaction between the gold and the sulfur of the P3HT via a metal-thiolate bond. At 2 mg/ml, AuRGO increased the solar cell efficiency approximately 50% over the control, but higher concentrations produced large, columnar structures which blocked the electrode from having a uniform contact with the active layer.

We summarize some recent new results probing inter- and intra-chain coupling in aggregated P3HT in isolated nanoparticles and nanofibers. Time-resolved photoluminescence studies show interesting correlations between amplitude and decay constant for different decay components that are tied to both polymer regio-regularity and nanoparticle processing conditions. In the frequency domain, we observe distinct signatures of both H- and J-aggregate type exciton coupling, manifested as different vibronic progressions with different electronic origins, linewidths, and Huang-Rhys factors. We show how the extent of this H/J composite coupling can be tuned to a certain extent by changes in molecular parameters (polymer molecular weight and regioregularity) and by solvent processing conditions. Finally we discuss recent results of near-field optical absorption probes of nanoparticles and nanofibers where optical contrast is afforded by the different absorption cross-section (at 532 nm) for aggregated vs. unaggregated P3HT.