ABSTRACT
The effects of the 4-tert-butylpyridine (TBP) additive in the electrolyte on photovoltaic performance of two push-pull porphyrin sensitizers (YD12 and YD12CN) were examined. Addition of TBP significantly increased the open-circuit voltage (VOC) for YD12 (from 550 to 729 mV) but it was to a lesser extent for YD12CN (from 544 to 636 mV); adding TBP also had the effect of reducing the short-circuit current density (JSC) slightly for YD12 (from 17.65 to 17.19 mA cm(-2)) but it led to a significant reduction for YD12CN (from 16.45 to 9.78 mA cm(-2)). The resulting power conversion efficiencies of the YD12 devices increase from 6.2% to 8.5% whereas those of the YD12CN devices decrease from 5.8% to 4.5%. Based on measurements of temporally resolved photoelectric transients of the devices and femtosecond fluorescence decays of thin-film samples, the poor performance of the YD12CN device in the presence of TBP can be understood as being due to the enhanced charge recombination, decreased electron injection, and a lesser extent of inhibition of the intermolecular energy transfer.
Subject(s)
Electric Power Supplies , Electrons , Porphyrins/chemistry , Pyridines/chemistry , Solar Energy , KineticsABSTRACT
We developed several low-cost catalysts with high catalytic activity, which were used as counter electrodes in dye-sensitized solar cells (DSCs). They showed higher efficiencies than that of Pt. The efficiencies were improved by 18-42% for the DSCs composed of active carbon, niobium dioxide, ordered mesoporous carbon and commercial titanium carbide.
ABSTRACT
Novel porphyrin dimers with broad and strong absorption in the visible and/or near IR regions have been synthesized; the meso-meso-linked porphyrin dimer (YDD1) exhibited the best photovoltaic performance with power conversion efficiency 5.2% under AM 1.5G one solar illumination.
Subject(s)
Coloring Agents/chemistry , Coloring Agents/chemical synthesis , Energy-Generating Resources , Metalloporphyrins/chemistry , Metalloporphyrins/chemical synthesis , Molecular Structure , StereoisomerismABSTRACT
YD12 (eta = 6.7%) is a green sensitizer remarkable for its outstanding cell performance beyond that of N719 (eta = 6.1%) with no added scattering layer; the additional scattering layer assists N719 in promoting the efficiency in the red shoulder of the spectrum, but has only a small effect on the improvement of the cell performance for porphyrins.
ABSTRACT
Myoglobin (Mb), reconstituted zinc protoporphyrin-apomyoglobin (ZnMb), and eosin-modified ZnMb (EoZnMb) were used as photosensitizers to functionalize TiO2 nanocrystalline films for bio-sensitized solar-cell (BSSC) applications. For the Mb-sensitized SC, the poor cell performance was due to a reduction Fe(III) --> Fe(II) that produces a photocurrent density of the device smaller than its unsensitized counterpart. The efficiencies of power conversion of both ZnMb and EoZnMb-sensitized SC were enhanced about ten times due to superior charge separation between TiO2 and the protein, and due to smaller current leakage between TiO2 and the electrolyte. The cell performances of the BSSC devices are discussed in terms of an equivalent-circuit model.
Subject(s)
Myoglobin/chemistry , Photosensitizing Agents/chemistry , Solar Energy , Zinc/chemistry , Animals , Apoproteins/chemistry , Eosine Yellowish-(YS)/chemistry , Horses , Models, Molecular , Nanoparticles/chemistry , Photochemical Processes , Porphyrins/chemistry , Spectrometry, Fluorescence , Titanium/chemistryABSTRACT
Novel meso- or beta-derivatized porphyrins with a carboxyl group have been designed and synthesized for use as sensitizers in dye-sensitized solar cells (DSSCs). The position and nature of a bridge connecting the porphyrin ring and carboxylic acid group show significant influences on the spectral, electrochemical, and photovoltaic properties of these sensitizers. Absorption spectra of porphyrins with a phenylethynyl bridge show that both Soret and Q bands are red-shifted with respect to those of porphyrin 6. This phenomenon is more pronounced for porphyrins 3 and 4, which have a pi-conjugated electron-donating group at the meso position opposite the anchoring group. Upon introduction of an ethynylene group at the meso position, the potential at the first oxidation alters only slightly whereas that for the first reduction is significantly shifted to the positive, thus indicating a decreased HOMO-LUMO gap. Quantum-chemical (DFT) results support the spectroelectrochemical data for a delocalization of charge between the porphyrin ring and the amino group in the first oxidative state of diarylamino-substituted porphyrin 5, which exhibits the best photovoltaic performance among all the porphyrins under investigation. From a comparison of the cell performance based on the same TiO(2) films, the devices made of porphyrin 5 coadsorbed with chenodeoxycholic acid (CDCA) on TiO(2) in ratios [5]/[CDCA] = 1:1 and 1:2 have efficiencies of power conversion similar to that of an N3-based DSSC, which makes this green dye a promising candidate for colorful DSSC applications.
