• 한국전기전자재료학회논문지
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• 제23권2호
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• pp.93-97
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• 2010

We have studied the effect of the chemical composition of the ZnO nanorod surface on the optical characteristics. The surface was treated with H- and O-plasma at different surface temperatures. The chemical composition of the surface of the ZnO nanorod, being investigated by Auger Electron Spectroscopy(AES), was related to the Photoluminescence(PL) data reported in our previous results. The AES showed the opposite results for the $H_2$ and $O_2$ plasma treatments. The ratio of Zn to O on the surface of the ZnO nanorod increased in the case of $H_2$ plasma, while the composition rate of O increased after $O_2$ plasma treatment. The AES results seems to be correlated to the shift in PL peaks. The increase in the composition rate of Zn on the surface of ZnO nanorod is considered to cause the blue shift of the UV peak. On the contrary, the relative increase of O is considered to cause the red shift in PL peaks.

• Archives of Pharmacal Research
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• 제26권8호
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• pp.653-658
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• 2003

It has been reported that at low temperature region, poloxamers existed as a monomer. Upon warming, an equilibrium between unimers and micelles was established, and finally micelle aggregates were formed at higher temperature. In this study, the fluorescence spectroscopy was used to study the micelle formation of the poloxamer 407 in aqueous solution. The excitation and emission spectra of pyrene, a fluorescence probe, were measured as a function of the concentration of poloxamer 407 and temperature. A blue shift in the emission spectrum and a red shift in the excitation spectrum were observed as pyrene transferred from an aqueous to a hydrophobic micellar environment. From the $I_1/I_3 and I_{339}/I_{333}$ results, critical micelle concentration (cmc) and critical micelle temperature (cmt) were determined. Also, from the fluorescence spectra of the probe molecules such as 8-anilino-1-naphthalene sulfonic acid and 1-pyrenecarboxaldehyde, the blue shift of the $\lambda_{max}$ was observed. These results suggest a decrease in the polarity of the microenvironment around probe because of micelle formation. The poloxamer 407 above cmc strongly complexed with hydrophobic fluorescent probes and the binding constant of complex increased with increasing the hydrophobicity of the probe.

• Bulletin of the Korean Chemical Society
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• 제6권4호
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• pp.186-191
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• 1985

The effect of pressure and temperature on the stabilities of the charge transfer complexes of hexamethyl benzene with iodine in n-hexane has been investigated by UV-spectrophotometric measurements. In this experiment the absorption spectra of mixed solutions of hexamethyl benzene and iodine in n-hexane were measured at 25, 40 and $60^{\circ}C$ under 1,200, 600, 1200 and 1600 bar. The equilibrium constant of the complex formation was increased with pressure while being decreased with temperature raising. Changes of volume, enthalpy, free energy and entropy for the formation of the complexes were obtained from the equilibrium constants. The red shift at higher pressure, the blue shift at higher temperature and the relation between pressure and oscillator strength were discussed by means of thermodynamic functions. In comparison with the results in the previous studies, it can be seen that the pressure dependence of oscillator strength has a extremum behavior in durene as the variation of ${\Delta}H$ or ${\Delta}S$ with the number of methyl groups of polymethyl benzene near atmospheric pressure in the previous study. The shift or deformation of the potential in the ground state and in the excited state of the complexes formed between polymethyl benzene and iodine was considered from the correlation between the differences of the electron transfer energies and the differences of free energies of the complex formation for the pressure variation.

• Bulletin of the Korean Chemical Society
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• 제26권11호
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• pp.1706-1710
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• 2005

The excited-state intramolecular proton transfer (ESIPT) fluorescence in the 2-(2'-hydroxyphenyl)benzoxazole (HBO) derivatives with different electron donor and acceptor substituents was studied by spectroscopic and theoretical methods. Changes in the electronic transition, energy levels, and orbital diagrams of HBO analogues were investigated by the semi-empirical molecular orbital calculation and were correlated with the experimental spectral position of ESIPT keto emission. It was found that the presence of substituents, regardless of their nature, resulted in the red-shifted absorption relative to HBO. However, the spectral change of the ESIPT fluorescence was differently affected by the nature of substituent: hypsochromic shift with electron donor and bathochromic shift with electron acceptor.

• 한국세라믹학회지
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• 제48권4호
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• pp.278-281
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• 2011

The optical band gap energy for $SrTiO_3$ by reduction at high temperature was 3.15 eV. The reflectivity of reduced $SrTiO_3$ single crystals showed little variation, however, the reflectivity by the reduction condition had no effect. For the phonon mode at about 790 $cm^{-1}$, a blue-shift took place upon $N_2$ reduction and the decreased. However, a red-shift took place upon a $H_2-N_2$ reduction and the increased at the same phonon mode. With decreasing temperature the dielectric constant decreased rapidly. The thermal activation energies were 0.92-1.02 eV.

• 한국전기전자재료학회논문지
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• 제22권3호
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• pp.230-234
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• 2009

Hydrogen and Oxygen plasma treatments have been done on sonochemical grow ZnO nanorods by varying treatment temperature and time, The changes(position and intensity) in ultraviolet(UV) peaks and green peaks of photoluminescence(PL) spectroscopy have been measured, Experimental results showed; i) in the case of hydrogen plasma treatment, the blue shift of UV peak and the increase of PL intensity of the UV peak were observed as the increase of the process time and temperature, ii) in the case of oxygen plasma treatment, the red shift of green peak was observed and the ratio of $I_{Green}/I_{UV}$ was also increased, as the increase of the process time and the temperature.

• Applied Science and Convergence Technology
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• 제25권2호
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• pp.42-45
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• 2016

A two-dimensional metal hole array (2DMHA) structure is fabricated by conventional photo-lithography and electron beam evaporation. The transmittance of the 2DMHA is measured at long wave infrared (LWIR) wavelengths (${\lambda}{\sim}10$ to $24{\mu}m$). The 2DMHA sample shows transmittance of 70 and 67% at $15.4{\mu}m$ due to plasmonic resonance with perforated silver and gold thin films, respectively, under surface normal illumination at LWIR wavelengths. The measured infrared spectrum is separated into two peaks when the size of the hole becomes larger than a half-pitch of the hole array. Six degenerated plasmon modes (1,0) at the metal/Si surface split to three modes at an incident beam angle of $45^{\circ}$ with respect to the surface normal direction, and wavelength shifts of the transmitted spectrum are observed in a red shift and blue shift at the same time.

• 대한화학회지
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• 제11권4호
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• pp.121-125
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• 1967

各種 아민과 할로겐化合物間의 Charge Transfer Complex 形成與否를 檢討하여 보았다. Pyridine Tridthylamine, Piperidine Ethanolamine Triethanolamine, Aniline, Diethylamine 等의 아민類와 四鹽化炭素 또는 클로로폼의 混合溶液을 n-Hexane 溶媒存在下에서 紫外線吸收 스펙트라를 檢査한 結果 장파장쪽의 Shift가 있었으며 特히 Diethylamine과 Triethylamine은 클로로폼 또는 四鹽化炭素와 1:1 Charge Transfer Complex를 形成하였고, Piperidine은 接觸的 Complex를 形成하는 것이 確認되었다. Complex의 形成경향과 아민의 Nucleophilicity와의 關係를 論議하였다.

• Journal of Applied Biological Chemistry
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• 제42권3호
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• pp.151-153
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• 1999

Gromwell (Lithospermum erythrorhizon) pigment solution and Jindo Hongju prepared in the laboratory showed characteristic pH-dependent color changes and a shift in absorption maxima. This phenomenon was not observed in the solution of the artificial food colorant Red No. 2 which was suspected to be used in the manufacture of fake Jindo Hongju. A few fake products could be detected by using the pH-dependent shift in absorption maxima among the Jindo Hongju on market.

• 한국식품과학회지
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• 제33권1호
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• pp.149-152
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• 2001

새로운 천연식용색소원으로서 꽃양배추(Brassica oleracea L. var. acephala)로부터 anthocyanin색소의 추출특성을 조사하였다. 추출된 색소는 $pH\;1{\sim}12$의 범위에서 pH가 높아질수록 ${\lambda}_{max}$가 장파장 쪽으로 이동하는 bathochromic shift 현상을 보였으며 추출용매의 citric acid의 농도가 증가수록 추출속도가 빨라지고 TOD가 증가하였다. 꽃양배추 색소의 추출용매에 $0.8{\sim}1.0%$ citric acid를 첨가하였을 때 최대 TOD값을 나타냈으며 추출용매인 증류수에 10-20% ethanol을 첨가하였을 때 색소의 추출효율이 높게 나타났다. 따라서 citric acid 0.8%를 함유한 10% ethanol 수용액이 꽃양배추 색소를 추출하기 위한 가장 적합한 용매로 결정하였다. 추출 온도가 높을수록 색소추출속도가 증가하였으나 고온에서 추출할 경우 추출시간이 길어지면 색소가 파괴되어 TOD값이 감소하였다. 추출온도 5, 20, 40 및 $60^{\circ}C$에서 TOD값이 2.1에 이르는 시간은 각각 24, 8, 4, 2시간으로 추출온도가 높을수록 추출속도가 증가하여 추출시간이 단축되었다.