• 한국세라믹학회지
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• 제22권4호
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• pp.9-14
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• 1985

The quantum efficiency vs. wavelength curves with different reducing treatments for the 99.99% and 98.5% $TiO_2$ ceramic electrodes have been analyzed according to the Schottky barrier model of the semiconductor-elect-rolyte interface, The model allows the main physical parameters governing the photoelectrochemical properties of the semicon-ductor to be determined. According to these data the impurity ions as three valence state ($Fe^{3+})$ in the $TiO_2$ raw materials have great influence on the photoresponse and the $TiO_2$ ceramic electrodes show much lower quantum efficiency than the $TiO_2$ single crystal due to existence of the recombination centers.

• Journal of Magnetics
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• 제6권1호
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• pp.5-8
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• 2001

Cheju island is composed of volcanic tuff. The soil in Cheju island has principally sprung from basalt and partially made up of trachyte, and andesite. Also ancient relics, plain coarse pottery kilns and pantiles kilns are homogeneously distributed all over the Cheju island. In this study samples of plain coarse pottery and pantiles from five regions of Cheju island have been examined through X-ray fluorescence spectrometer and Mossbauer spectroscopy. It is thought that these samples be partially formed from neutral volcanic rock like trachyte and the valence state of iron is almost $Fe^{3+}$. Also the magnetic hyperfine field of goethite contained in these samples is less than synthetic goethite. This result shows the degradation of magnetic order caused by the partial substitution of diamagnetic positive ion $Fe^{3+}$ by $Al^{3+}$ in the goethite lattice.

• 한국초전도ㆍ저온공학회논문지
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• 제17권4호
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• pp.8-11
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• 2015

We studied on the visible emission of Cu-ion-doped perovskite hafnate $SrHfO_3$ (SHO:Cu) with the photo-excitation energy dependence. The polycrystalline SHO:Cu samples were newly synthesized in the solid state reaction method. From the X-ray diffraction measurement it was found that the crystalline structure of SHO:Cu is nearly identical to that of undoped $SrHfO_3$. Interestingly, the photoluminescence excitation (PLE) spectra change significantly with the emission energy, which is linked to the strong dependence of the visible emission on the photo-excitation energy. This unusual emission behavior is likely to be associated with the mixed valence states of the doped Cu ions, which were revealed by X-ray photoelectron spectroscopy. We compared our finding of tunable visible emission in the SHO:Cu compounds with the cases of similar materials, $SrTiO_3$ and $SrZrO_3$ with Cu-ion-doping.

• Environmental Engineering Research
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• 제11권6호
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• pp.318-324
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• 2006

The higher valence state of iron i.e., Fe(VI) was employed for the oxidation of one of an important toxic ion, cyanide in the aqueous medium. Cyanide was oxidized into cyanate, which is 1,000 times less toxic to cyanide and often accepted for its ultimate disposal. It was to be noted that Fe(VI) is a very powerful oxidizing agent and can oxidize most of the cyanide within few minutes i.e., ca 5 mins of contact. The data was obtained by the UV-Visible measurements for the Fe(VI) decomposition. The UV-Visible data was used to evaluate the overall rate constant for second order redox reaction between ferrate(VI) and cyanide. Also the pseudo first order rate constant was calculated as keeping the cyanide concentration in excess.

• Journal of the Optical Society of Korea
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• 제5권1호
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• pp.1-4
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• 2001

The results of investigating $SiL_{2,3}$/ X-ray emission valence spectra of amorphous silicon films irradiated by excimer laser are presented. It is found that laser annealing leads to crystallization of amorphous silicon films and the crystallinity increases with the laser energy density from 250 to 400 mJ/$\textrm{cm}^2$. The vertical structure of the film is investigated by changing the accelerating voltage on the X-ray tube, and the chemical and structural state of Si$_3$N$_4$ buffer layer is found not to be changed by the excimer laser treatment.

• 한국진공학회:학술대회논문집
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• 한국진공학회 2009년도 제38회 동계학술대회 초록집
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• pp.341-341
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• 2010

Electronic structure of Calix adsorbed on epitaxial graphene (EG) was investigated using high resolution photoemission spectroscopy (HRPES). Increasing the deposition of calix molecule, we found that EG becomes n-type doping using secondary edge measurement (work function change). As we observe bonding nature of O 1s peak, we found that single O 1s peak can be clearly distinguished in the spectra indicating equivalent adsorption state. Finally, we were able to control the band gap of EG using valence band spectra as we change the amount of calix molecule. In this study, we will propose the possibility of band gap modulation of EG using calix molecule.

• Bulletin of the Korean Chemical Society
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• 제16권3호
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• pp.261-264
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• 1995

A series of samples of the Nd1-x(Ba0.40Mg0.60)1+xFeO4-y (x=0.00, 0.10, 0.20, and 0.30) system has been synthesized at 1450 ℃ under an atmospheric air pressure. The x-ray powder diffraction analysis of the solid solutions assigns the structure of all the compositions to orthorhombic system. Mohr salt analysis shows that τ and y values increase with x value and nonstoichiometric chemical formulas of the system can be formulated from the x, τ, and y values. Oxygen vacancies are distributed along c-axis in the perovskite layer. The magnetic ordering temperature remains unchanged with x value. Electrical conductivity and activation energy depend only on the mixed valence state of Fe ion. Conduction mechanism can be suggested as the hopping of electron between eg orbitals of Fe3+ and Fe4+ ions through Fe3+-O-Fe4+ bonds. Magnetic susceptibility and electrical conductivity are discussed with the nonstoichiometric chemical formulas.

• Bulletin of the Korean Chemical Society
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• 제15권10호
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• pp.857-860
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• 1994

We have calculated the ${\pi}$-electron density, atom self-polarizability, and free valence on each atom of N-(2-chlorobenzyl)-pyridinium, N-(benzyl)-2-chloropyridinium, and N-(2-chlorobenzyl)-2-chloropyridinium salts using a simple Huckel method in order to discuss their intramolecular photocyclization reaction in a qualitative method. Our calculation qualitatively predicts that photocyclization occurs through forming radicals as a reaction intermediate by breaking a C-Cl bond after photoexcitation into a triplet state via intersystem crossing from an initially excited singlet state. We noticed that this C-Cl bond breaking is aided by ${\pi}$-complex formation between a chlorine atom and the ${\pi}$ -electrons of the neighboring ring in the triplet state and a stronger ${\pi}$-complex bond makes C-Cl bond breaking, i.e., radical formation, much easier. A chlorine atom will form a stronger ${\pi}$ -complex bond to a benzyl ring of N-(benzyl)-2-chloropyridinium than a pyridinium ring of N-(2-chlorobenzyl)-pyridinium because the former can donate its ${\pi}$-electron more easily than the latter. The chlorine at position 15 of N-(2-chlorobenzyl)-2-chloropyridinium salt in the excited state also provides its ${\pi}$-electron to the benzyl ring. So this ${\pi}$-electron can increase the bond strength of the $\pi-complex.$ Therefore, the strength of ${\pi}$-complex follows the order of N-(2-chlorobenzyl)-2-chloropyridinium, N-(benzyl)-2-chloropyridinium, and N-(2-chlorobenzyl)-pyridinium salts and thus the radical formation rate. This provides us with an intramolecular photocyclization reaction rate of the same order as given above.

• 대한화학회지
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• 제37권11호
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• pp.923-928
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• 1993

$K_2NiF_4$형 구조를 갖는 $Sr_{1+x}Ho_{1-x}FeO_{4-y}$ (x = 0.00, 0.25, 0.50, 0.75 및 1.00) 고용체계를 대기압과 1550$^{\circ}$C에서 제조하였다. 이 시료들의 X-선 회절도는 전 x 영역에서 모든 시료와 결정학적 상이 정방정계임을 나타내고 있다. 격자부피는 $Sr^{2+}$ 이온이 치환되는 양이 증가함에 따라 계속적으로 증가한다. 전체 철이온에 대한$ Fe^{4+}$ 이온의 몰비인${\tau}$값은 시료의 Mohr 염 적정으로 결정하였으며 x값과 ${\tau}$값으로부터 산소비화학량인 y값을 계산하였다. ${\tau}$값과 y값은 x값의 증가에 따라서 증가함을 알 수 있었다. x값, ${\tau}$값 y값을 일반식 $Sr_{1+x}Ho_{1-x}Fe^3_{1-}\;^+_{\tau}Fe_{\tau}^{4+}O_{4-y}$에 대입하여 비화학량론적 화학식을 결정하였다. Mossbauer 스펙트라는 $Fe^{3+}$ 이온과 $Fe^{4+}$ 이온의 혼합원자가 상태와 배위상태를 나타낸다. 각 시료들의 자기적 성질은 상온에서 상자성임을 알 수 있다. 전기전도도는 1.0 ~ 1 ${\times}\;10^{-9}{\Omega}^{-1}cm^{-1}$의 범위의 반도체 영역에서 변한다. 전기전도도의 활성화 에너지는${\tau}$값이 증가함에 따라 감소함을 알 수 있다. 전도성 메카니즘은 $Fe^{3+}$ 와 $Fe^{4+}$ 이온간에 전도성 전자의 건너뜀 모델로 설명되어야 한다.

• 한국자기학회지
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• 제15권3호
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• pp.167-171
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• 2005

다결정질 $La_{1/3}Sr_{2/3}FeO_{2.96}$의 전하불균형(charge disproportionation, CD) 전이현상과 그 전이온도를 전후로 한 자기적 상호작용의 변화양상을 X-선 회절, $M\ddot{o}ssbauer$ 분광계, 그리고 SQUID 자기력계를 이용하여 연구하였다. X선 분석결과, 시료의 결정구조는 공간군 R/3c인 rhombohedral 구조이며, 격자상수는 $a_{R}=5.4874\;\AA,\;a_R=60.07^{\circ}$이었다. $M\ddot{o}ssbauer$ 스펙트럼은 4.2 K에서부터 실온까지의 범위에서 취하였다 분석결과 저온에서는 각각 $Fe^{3+}$와 $Fe^{5+}$에 기인하는 두개의 6-선 스펙트럼이 중첩되어 나타났으며 Fe 이온의 원자가가 두개의 상이한 전하 상태로 분리된 반강자성 혼합원자가 상태임을 알 수 있었다. 반면 고온에서는 $Fe^{3.6+}$에 기인하는 단일 흡수선이 관측되어 상자성의 평균원자가 상태임을 알 수 있었다. 175K부터 200K의 온도 범위에서는 이 두 상태가 혼재되어 나타났으며 이 온도 범위에서 CD전이가 발생함을 알 수 있었다. CD전이의 근원은 열적으로 발생한 전하의 도약현상으로 설명할 수 있었다. 측정된 자기이력곡선의 분석 결과, 자성원자 사이에는 강한 반강자성 상호작용이 존재하며, 온도가 CD 전이온도를 넘어 상승하면서 $Fe^{3+}-Fe^{5+}$간의 상호작용이 한층 더 강한 상호작용으로 대치됨을 알 수 있었다.