• The Transactions of The Korean Institute of Electrical Engineers
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• v.61 no.4
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• pp.595-600
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• 2012

In this paper, it is investigated the characteristics of DSSC(Dye Sensitized Solar Cell) with cell area(0.25, 1, 2.25 $cm^2$) and dye absorption time(12, 24, 36 h). Thus, we obtain the following results by using the EIS, UV-VIS, I-V measurement. When the cell area increases, the efficiency decreases to 21~32 percent because of the increase about 40~$60{\Omega}$ of internal impedance regardless of dye absorption time. When the absorption time increases up to 24 hours, the efficiency increases to over 40 percent cause of the reduction of internal impedance regardless of cell area. When the dye absorption time becomes 36 hours, the internal impedance increases and at the same time, in the range of 600~700 nm, as the optical absorption reduces. Therefore, the efficiency decreases to 19~31 percent. When it is absorbed the dye for 24 hours in the smallest cell area which is 0.25 $cm^2$, the DSSC has the best efficiency (7.11 %).

• Bulletin of the Korean Chemical Society
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• v.26 no.11
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• pp.1776-1782
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• 2005

ZnSe/ZnS, UV-blue luminescent core shell quantum dots, were synthesized via a thermal decomposition reaction of organometallic zinc and solvent coordinated Selenium (TOPSe) in a hot solvent mixture. The synthetic conditions of the core (ZnSe) and the shell (ZnS) were independently studied at various reaction temperature conditions. The obtained colloidal nanocrystals at corresponding temperatures were characterized for their optical properties by UV-vis, room temperature solution photoluminescence (PL) spectroscopy, and further obtained powders were characterized by XRD, TEM, and EDXS analyses. The synthetic temperature condition to obtain the best PL emission intensity for the ZnSe core was 300 ${^{\circ}C}$, and for the optimum shell capping, the temperature was 135 ${^{\circ}C}$. At this temperature, solution PL spectrum showed a narrow emission peak at 427 nm with a PL efficiency of 15%. In addition, the measured particle sizes for the ZnSe/ZnS nanocomposite via TEM were in the range of 5 to 12 nm. Furthermore, we have synthesized water-soluble ZnSe/ZnS nanoparticles by capping the ZnSe/ZnS hydrophobic surface with mercaptoacetate (MAA) molecules. For the obtained aqueous colloidal solution, the UV-vis spectrum showed an absorption peak at 250 nm, and the solution PL emission spectrum showed a peak at 425 nm, which is similar to that for hydrophobic quantum dot ZnSe/ZnS. However, the calculated PL efficiency was relatively low (0.1%) due to the luminescence quenching by water and MAA molecules. The capping ligand was also characterized by FT-IR spectroscopy, with the carbonyl stretching peak in the mercaptoacetate molecule appearing at 1575 $cm ^{-1}$. Finally, the particle sizes of the MAA capped ZnSe/ZnS were measured by TEM, showing a range of 12 to 17 nm.

• Polymer(Korea)
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• v.29 no.3
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• pp.308-313
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• 2005

The effects of molecular environments on photoisomerization of an azobenzene group were investigated using In-situ UV/Vis spectroscopy and optical anisotropy measurement technique. The reversible and repeatable photoisomeritation reactions of azobenzene were observed by irradiating the film containing 4-hydroxyazobenzene and by measuring absorption intensities of the characteristic bands of trans and cis isomers simultaneously. When the self-assembled monolayer with azobenzene groups was used as an alignment layer for a liquid crystal cell, the homeotropic alignment was induced due to their compact packing structures of azobenfene groups along the vertical direction of the substrate. By irradiating UV light on this cell, the trans-azobenzene groups change to cis-isomers through the photoisonlerieation and then resulting in the planar alignment of liquid crystal molecules.

• Journal of the Korea Academia-Industrial cooperation Society
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• v.15 no.1
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• pp.39-46
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• 2014

The green tourmalines from Kayah state, Myanmar were investigated by WD X-ray fluorescence, UV-vis, and mid-infrared spectroscopy for comparison to tourmalines of other deposits. The group of tourmaline was calculated and classified by chemical analysis. The samples belonged to the Calcic group and Uvite. The green tourmalines showed a strong absorption band at 415 and 611 nm. The presence of $V^{3+}$ ions is responsible for these absorption bands. Combination of the stretching and bending mode by the vibration between cationic and hydroxyl units (metal-OH) are observed in the 4600 ~ 4200 $cm^{-1}$.

• Asian Pacific Journal of Cancer Prevention
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• v.16 no.16
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• pp.7143-7147
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• 2015

Gold nanoparticles (GNPs) were conjugated with gallic acid (GA) at various concentrations between 30 and $150{\mu}M$ and characterized using transmission electron microscopy (TEM) and UV-Vis spectroscopy (UV-VIS). The anticancer activities of the gallic acid-stabilized gold nanoparticles against well-differentiated (M213) and moderately differentiated (M214) adenocarcinomas were then determined using a neutral red assay. The GA mechanism of action was evaluated using Fourier transform infrared (FTIR) microspectroscopy. Distinctive features of the FTIR spectra between the control and GA-treated cells were confirmed by principal component analysis (PCA). The surface plasmon resonance spectra of the GNPs had a maximum absorption at 520 nm, whereas GNPs-GA shifted the maximum absorption values. In an in vitro study, the complexed GNPs-GA had an increased ability to inhibit the proliferation of cancer cells that was statistically significant (P<0.0001) in both M213 and M214 cells compared to GA alone, indicating that the anticancer activity of GA can be improved by conjugation with GNPs. Moreover, PCA revealed that exposure of the tested cells to GA resulted in significant changes in their cell membrane lipids and fatty acids, which may enhance the efficacy of this anticancer activity regarding apoptosis pathways.

• Polymer(Korea)
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• v.25 no.5
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• pp.671-678
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• 2001

Sodium and zinc salts of poly(ethyaene-co-methacrylic acid) ionomers consist of three phases, i.e. ionic aggregates, amorphous, and crystalline phases. Dye molecules after soaked from the methanol solution are located near the amorphous phase or ionic aggregates within ionomer films. Depending on the location of the molecules in the ionomer film, they are under influence of dispersion forces (ethylene parts), polar forces (acid parts). and ionic dipole (ionic aggregates) interactions. The UV/Vis absorption peak of Nile Red under the dispersion force is found at near 500 nm, for the dye under the polar force effect 525 nm, and 550 and 610 nm for the dyes under $Na^+$ and $Zn^{2+}$ ionization effects, respectively. Since the divalent $Zn^{2+}$ ion has larger ionic dipole than the monovalent $Na^+$ ion, the larger red-shift of the absorption band due to the ionic dipole interaction is observed for $Zn^{2+}$ counter ion.

• Bulletin of the Korean Chemical Society
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• v.31 no.8
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• pp.2170-2174
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• 2010

The surfaces of $TiO_2$ and ZnO nanoparticles have been modified by gold (Au) nanoparticles by a reduction method in solution. Their interfacial electronic structures and optical absorptions have been studied by depth-profiling X-ray photoelectron spectroscopy (XPS) and UV-vis absorption spectroscopy, respectively. Upon Au-modification, UV-vis absorption spectra reveal a broad surface plasmon peak at around 500 nm. For the as-prepared Au-modified $TiO_2$ and ZnO, the Au $4f_{7/2}$ XPS peaks exhibit at 83.7 and 83.9 eV, respectively. These are due to a charge transfer effect from the metal oxide support to the Au. For $TiO_2$, the larger binding energy shift from that (84.0 eV) of bulk Au could indicate that Au-modification site of $TiO_2$ is different from that of ZnO. On the basis of the XPS data with sputtering depth, we conclude that cationic (1+ and 3+) Au species, plausibly $Au(OH)_x$ (x = 1-3), commonly form mainly at the Au-$TiO_2$ and Au-ZnO interfaces. With $Ar^+$ ion sputtering, the oxidation state of Ti dramatically changes from 4+ to 3+ and 2+ while that (2+) of Zn shows no discernible change based on the binding energy position and the full-width at half maximum (FWHM).

• Fashion & Textile Research Journal
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• v.16 no.3
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• pp.492-498
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• 2014

Lotus(Nelumbo nucifera gaertn) is intimate plant to many people that it has clean and noble characteristics despite growth in the mud. Especially Lotus seedpods, byproduct of lotus, are rich in oligometric procyanidins and could be a new source of procyanidins. Procyanidins, also known as condensed tannins, are a class of polyphenols. In other words lotus seedpod contains plenty of tannins. Commonly tannins colorants could increase adsorption and fastness properties in fabric dyeing. This study was made to investigate colorants characteristics of lotus seedpod and various colorfastness properties of dyed silk fabrics. The wavelength of maximum absorption of lotus seedpod solution appeared at 273.5 nm from UV-vis spectrophotometer. From the results of FT-IR spectra measurements, IR absorption band of lotus seedpod colorants appeared at $3415cm^{-1}$, $2900cm^{-1}$ and $1620cm^{-1}$ by tannin structure. And tannin ingredient contents was the highest at pH 9 and flavonoid at pH 11. Lotus seedpod colorants showed relatively good affinity at pH 3 on silk fabrics and optimum dyeing temperature and time for silk was for 50 min, at $80^{\circ}C$. K/s of Light fastness according to different washing method was the highest at process including ironing and ${\Delta}E$ was the lowest. All of fastness(Light rubbing laundering perspiration dry cleaning) showed excellent results over 4 or 4-5 grades.

• Journal of the Korean Applied Science and Technology
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• v.32 no.1
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• pp.16-22
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• 2015

Alkaloids of Vinca minor L. were characterized by HPLC equipped with the photo diode array detector and compared their UV/vis absorption spectra with an index material such as vincamine. UV/vis absorption spectra of more than 9 compounds belong to various classes such as flavonoids were shown and characterized. Extracts with ethanol or hot water were tested against the DPPH (2,2-diphenyl-1-picrylhydrazyl) free-radical to investigate their antioxidant activity. Based on the results, those extracts show about 14-15% of antioxidant activity of quercetine and vitamin C used as standards.

• Analytical Science and Technology
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• v.8 no.3
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• pp.305-311
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• 1995

The stability constant of the complex between salicylic acid($H_2A$) and Fe(III) ion has been determined using UV-Vis absorption spectrometry and pH titration method in O.1M $KNO_3$ aqueous solution at $20^{\circ}C$ and compared with reference value, $logK_f=16.48$. The $pK_{a1}$ and $pK_{a2}$ of $H_2A$ are $2.92{\pm}0.08$ and $12.90{\pm}0.13$, respectively and the $logK_f$ of 1:1 complex Fe(III)-$H_2A$ system is $11.88{\pm}0.12$ at $20^{\circ}C$.