• Applied Chemistry for Engineering
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• v.16 no.2
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• pp.159-168
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• 2005

Dye-sensitized solar cells (DSCs) have been under investigation for the past decade due to their attractive features such as high energy conversion efficiency and low production costs. The basis for energy conversion is the injection of electrons from a photoexcited state of a dye sensitizer into the conduction band of the nanocrystalline $TiO_2$ semiconductor upon absorption of light. It is believed that the DSC is one of the most promising candidates for renewable energy sources. In this review, the development trends and perspectives of DSCs are investigated.

• Bulletin of the Korean Chemical Society
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• v.34 no.11
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• pp.3183-3184
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• 2013

• Analytical Science and Technology
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• v.11 no.1
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• pp.20-28
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• 1998

Fluorimetric and absorption spectroscopic studies were performed to elucidate the photocurrent decay with time in the conversion process of solar energy into electrical energy using a photoelectrochemical cell containing rose bengal as a sensitizer, and allylthiourea as a supersensitizer. Spectra of dye solution before and after irradiation revealed a new photocatalytic dimerization reaction between sensitizer and supersensitizer. It was also found that the geometrical arrangement of the transition dipoles is oblique in the dimer of dye molecules.

• Analytical Science and Technology
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• v.9 no.1
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• pp.62-71
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• 1996

The enhancement of the solar energy conversion efficiency into the electrical energy by the dye sensitization with a photoelectrochemical cell was studied. The magnitude of the rose bengal sensitized photocurrent containing the supersensitizer, thiourea was five times greater than that in the absence of thiourea. It was observed, however, that the long time span of irradiation causes the decrease in the photocurrent. Spectroscopic analysis of the dye solution showed that the dye molecule was photobleached and the insoluble aggregate which settles down in the solution, was formed as a result of the possible photocatalytic reaction and the disappearance of dye from the solution was the cause of the decreased photocurrent in the sensitization run.

• 한국신재생에너지학회:학술대회논문집
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• 2010.06a
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• pp.89.2-89.2
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• 2010

The dye-sensitized solar cell (DSSC) is a device for the conversion of visible light into electricity, based on the sensitization of wide bandgap semiconductors. The performance of the cell mainly depends on a dye used as sensitizer. The absorption spectrum of the dye and the anchorage of the dye to the surface of $TiO_2$ are important parameters determining the efficiency of the cell. Generally, transition metal coordination compounds(ruthenium polypyridyl complexes) are used as the effective sensitizers, due to their intense charge-transfer absorption in the whole visible range and highly efficient metal-to ligand charge transfer. However, ruthenium polypyridyl complexes contain a heavy metal, which is undesirable from point of view of the environmental aspects. Moreover, the process to synthesize the complexes is complicated and costly. Alternatively, organic dyes can be used for the same purpose with an acceptable efficiency. The advantages of organic dyes include their availability and low cost. We designed and synthesized a series of organic sensitizers containing long wavelength absorption-chromophores for the dye sensitized solar cell. The DSSC composed of Blue-chromophores for the sensitization absorbed long wavelength region which is different also applied into the dye-cocktail (mixing) system. The photovoltaic property of DSSCs organic long wavelength absorption-chromophores were measured and evaluated by comparison with that of individual chromophores.

• 한국신재생에너지학회:학술대회논문집
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• 2011.05a
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• pp.118.1-118.1
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• 2011

The dye-sensitized solar cell (DSSC) is a device for the conversion of visible light into electricity, based on the sensitization of wide bandgap semiconductors. The performance of the cell mainly depends on a dye used as sensitizer. The absorption spectrum of the dye and the anchorage of the dye to the surface of TiO2 are important parameters determining the efficiency of the cell. Generally, transition metal coordination compounds(ruthenium polypyridyl complexes) are used as the effective sensitizers, due to their intense charge-transfer absorption in the whole visible range and highly efficient metal-to ligand charge transfer. However, ruthenium polypyridyl complexes contain a heavy metal, which is undesirable from point of view of the environmental aspects. Moreover, the process to synthesize the complexes is complicated and costly. Alternatively, organic dyes can be used for the same purpose with an acceptable efficiency. The advantages of organic dyes include their availability and low cost. We designed and synthesized a series of organic sensitizers containing long wavelength absorption-chromophores for the dye sensitized solar cell. The DSSC composed of Blue-chromophores for the sensitization absorbed long wavelength region which is different also applied into the dye-cocktail (mixing) system. The photovoltaic property of DSSCs organic long wavelength absorption-chromophores were measured and evaluated by comparison with that of individual chromophores.

• Bulletin of the Korean Chemical Society
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• v.33 no.4
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• pp.1225-1230
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• 2012

A new unsymmetrical zinc phthalocyanine has been designed and synthesized based on the 'push-pull' and extended ${\pi}$-conjugation concept for the dye-sensitized solar cells. Three tert-butoxy groups, which act as electron releasing ('push'), enhance the solubility of phthalocyanine in common organic solvents and reduce the aggregation. Hydroxy substituted 9,10-anthraquinones act as electron acceptors ('pull') for the study of photoinduced electron transfer processes as well as grafting onto nanocrystalline $TiO_2$. The new unsymmetrical zinc phthalocyanine was fully characterized by FTIR, UV-vis, $^1H$ NMR, cyclic voltammetry and differential pulse voltammetry. The new sensitizer was tested in dye-sensitized solar cells, and gave a better performance.

• Proceedings of the Materials Research Society of Korea Conference
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• 2010.05a
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• pp.12.1-12.1
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• 2010

We have developed a facile method to position different dyes (N719 and N749) sequentially in a mesoporous TiO2 layer through selective desorption and adsorption processes. Only upper part of the first adsorbed N719 dye was selectively removed by the desorption solution formulated with polypropylene glycol and tetrabutylammonium hydroxide without any damages of the dye. The desorption depth was controlled by the number of desorption process. Multi-dyed dye-sensitized solar cells (MDSSC) were fabricated by utilizing the method and their photovoltaic properties were investigated. From the incident photon-to-current conversion efficiency (IPCE) measurement, it was found that the MDSSC exhibited the extended spectral response for the solar spectrum while without decrease of maximum IPCE value compare to the DSSCs using one kind of dye (N719 or N749). The highest photocurrent density of 19.3 mA/cm2 was obtained from the MDSSC utilizing $15\;{\mu}m$ N719 / $14\;{\mu}m$ N749 bi-layered mesoporous TiO2 film. The photocurrent density was 25% and 8% higher than that of the DSSC using only N719 and N749 dye as a sensitizer, respectively. The power conversion efficiency of 9.8% was achieved from the MDSSC under the AM 1.5G one sun illumination.

• Proceedings of the Korean Vacuum Society Conference
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• 2010.02a
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• pp.310-310
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• 2010

Electronic and photovoltaic characteristics of two sensitizers (TA-BTD-CA and TA-BTD-St-CA), composed of a different $\pi$-conjugation in the linker group, have been investigated by theoretical and experimental methods. The electronic structure, transition dipole moment and oscillator strengths of two sensitizers have been scrutinized by using density functional theory (DFT) and time-dependent DFT (TD-DFT) method. The LUMO level and the oscillator strength of TA-BTD-St-CA was higher than that of TA-BTD-CA, which may facilitate the electron injection process as well as increase the absorption coefficient. The relative efficiencies of the electron injection from the excited sensitizer to nanocrystalline TiO2 and SnO2 films have also been investigated by nanosecond transient absorption spectroscopy. The relative electron injection efficiency of TA-BTD-St-CA exhibited similar injection efficiency for two different semiconductors. However, in the case of TA-BTD-CA sensitizer, electron injection into SnO2 was approximately three times larger than that into TiO2. This enhancement of electron injection of TA-BTD-CA for the SnO2 is due to the increment of the driving force caused by positive shift of conduction band of semiconductor, which was also confirmed from the investigation for the photovoltaic characteristics according to the electrolyte additive, such as LiI additive.

• Bulletin of the Korean Chemical Society
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• v.35 no.5
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• pp.1433-1439
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• 2014

We report on the influence of water as an electrolyte on the photovoltaic performances. The photovoltaic performance was shown to be quite sensitive to the substituent on the donor group. An optimized efficiency of 4.41% in the presence of 100% water content using $I^-/I{_3}^-$ redox couple was obtained using the D21L6 organic dye.