Multilayer polymer films composed of a ruthenium terpyridine complex containing poly(p-phenylenevinylene) (Ru-PPV) and sulfonated polyaniline (SPAN) were prepared by a layer-by-layer electrostatic self-assembly deposition. The deposition process was carried out from SPAN solution in water and Ru-PPV in dimethylformamide (DMF). Optical-quality multilayer thin films were obtained. The film growth process was monitored by quartz crystal microbalance, and the surface morphology of the films was studied by atomic force microscopy. It was found that the properties of the multilayer films were dependent on deposition conditions such as the pH of the SPAN solution, the presence of salt in the polymer solutions, and the post-film-forming thermal annealing process. Cross-section transmission electron microscopic images suggested that there was no stratified structure formed in the multilayer films. Photovoltaic cells were fabricated by sandwiching the multilayer films between indium-tin-oxide and aluminum electrodes. The device performances were examined by illumination with AM 1.5 simulated solar light. The power conversion efficiencies of these devices were on the order of 10(-3)%. The maximum incident photon-to-electron conversion efficiency (IPCE) of the devices was found to be approximately 2% at 510 nm, which is consistent with the absorption maximum of the ruthenium complex. This indicates that the photosensitization process is due to the electronic excitation of the ruthenium complex.
Photovoltaic devices were fabricated by layer-by-layer polyelectrolyte deposition techniques using bisterpyridyl ruthenium(II) complex containing conjugated polymer as the polycation and sulfonated polyaniline as the polyanion. The maximum external quantum efficiencies of the devices were in the range of 1−2%, and the power conversion efficiency was on the order of 10-3% with the fill factor of 0.2.
The use of chlorotricarbonyl rhenium(I) diimine complex as photosensitizing molecule in photovoltaic cells is demonstrated. Unlike other transition-metal-based sensitizers, the complex is sublimable and has low band gap. It also exhibits bipolar charge transport character with relatively high carrier mobilities on the order of 10−3 cm2 V−1 s−1. Multilayer heterojunction and bulk heterojunction devices with fullerene as the electron accepting molecule were prepared. For the bulk heterojunction devices, the fill factor and power conversion efficiency under simulated solar light illumination were 0.56 and 0.48%, respectively. Atomic force microscopic images showed that the complex dispersed evenly with fullerene molecules in solid state.
a b s t r a c tA series of sublimable substituted chlorotricarbonyl bis(phenylimino)acenaphthene rhenium(I) complexes was synthesized and used in the fabrication of photovoltaic devices. The hole and electron carrier mobilities of these complexes are in the order of 10 À3 to 10 À4 cm 2 V À1 s À1 . Heterojunction devices with CuPc/complex/C 60 (CuPc = copper phthalocyanine) as the active layer and bulk heterojunction devices with complex:C 60 as the active layer were fabricated. The rhenium complexes function as photosensitizer in the devices, and exhibit optical absorption in the region between 500 and 550 nm within which other components in the device do not absorb. Other devices with hole transport materials, exciton blocking materials, and different active layer thickness were also fabricated. Variation of substitution groups in the ligand did not show significant difference in device performance. The best power conversion efficiency of the devices was measured to be 1.29% under illumination of AM1.5 simulated solar light.
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