• Title/Summary/Keyword: 분광전기화학적 연구

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A Study on Electrochemical Behaviors of Samarium Ions in the Molten LiCl-KCl Eutectic Using Optically Transparent Electrode (LiCl-KCl 용융염에서 광학적으로 투명한 전극을 이용한 사마륨 이온의 전기화학적 거동에 관한 연구)

  • Lee, Ae-Ri;Park, Byung Gi
    • Journal of Nuclear Fuel Cycle and Waste Technology(JNFCWT)
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    • v.15 no.4
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    • pp.313-320
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    • 2017
  • A spectroelectrochemical method has been applied to investigate the electrochemical behaviors and identify the kinds of samarium ions dissolved in high temperature molten LiCl-KCl eutectic. An optically transparent electrode (OTE) fabricated with a tungsten gauze as a working electrode has been used to conduct cyclic voltammetry and potential step chronoabsorptometry. Based on the reversibility of the redox reaction of $Sm^{3+}/Sm^{2+}$, which was determined from the cyclic voltammograms, the formal potential and the diffusion coefficient were calculated to be -1.99 V vs. $Cl_2/Cl^-$ and $2.53{\times}10^{-6}cm^2{\cdot}s^{-1}$, respectively. From the chronoabsorptometry results at the applied potential of -1.5 V vs. Ag/AgCl (1wt%), the characteristic peaks of absorption for samarium ions were determined to be 408.08 nm for $Sm^{3+}$ and 545.62 nm for $Sm^{2+}$. Potential step chronoabsorptometry was conducted using the anodic and the cathodic peak potentials from the voltammograms. Absorbance analysis at 545.63 nm shows that the diffusion coefficient of $Sm^{3+}$ is $2.15{\times}10^{-6}cm^2{\cdot}s^{-1}$, which is comparable to the value determined by cyclic voltammetry at the same temperature.

Spectroelectrochemical Study for Thin Film of Gold Nanoparticles (금 나노입자 박막의 분광전기화학적 연구)

  • Seo, Seong S.;Chambers, James Q.
    • Journal of the Korean Chemical Society
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    • v.50 no.1
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    • pp.32-36
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    • 2006
  • films of gold nanoparticles were formed on indium tin oxide (ITO) by an electrodeposition method from an aminosilicate stabilized gold colloid solution. The thin films were examined by cyclic voltammetry (CV), scanning electron microscopy (SEM), UV-visible, and energy dispersive X-ray spectroscopy (EDXS). The surface coverage of gold nanoparticles on the thin film was estimated to 1.2 nanomole/cm2. An anthraquinone-2, 6-disulfonic acid, disodium salt (AQDS) self-assembled layer was generated by immersing gold thin film into 1mM of AQDS in 0.1M HClO4 solution for over 20 hours. As a result, a new absorbance peak from the multi-layers (AQDS/thin film of gold /ITO) was obtained about at 690 nm. Also, the surface plasmon absorption of multi-layers was measured by UV-Visible spectrometer along with chronoamperometry by applying the various potentials from +0.5V to -0.5V. The maximum surface plasmon absorption band at 550 nm was decreased by applying negative potentials. The change of absorbance was correlated with the surface coverage of the AQDS indicating the pseudo-capacity surface state of the AQDS layer was coupled to the energy level of the plasmonband by applied negative potentials.

MeV 전자빔 조사를 통한 Pt/Graphene 복합 나노구조의 형성

  • Cha, Myeong-Jun;Song, U-Seok;Kim, Yu-Seok;Jeong, Dae-Seong;Kim, Seong-Hwan;Lee, Su-Il;Park, Jong-Yun
    • Proceedings of the Korean Vacuum Society Conference
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    • 2012.02a
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    • pp.570-570
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    • 2012
  • 그래핀(graphene)은 육각형의 탄소원자 한층으로 이루어진 이차원 구조체로써 우수한 물리적, 전기적 특성으로 인해 다양한 분야에서 응요을 위한 연구가 활발히 진행되고 있다. 특히, 그래핀과 금속 나노입자의 복합구조는 수소 저장체, 가스센서, 연료전지, 화학 촉매등의 다양한 분야에서 응용이 가능하다. 현재까지 그래핀/금속나노입자 복합구조의 제작 방법에는 열증발(thermal evaporation), 전기도금법(electrodeposition), 표면 기능화(surface functionalization)를 이용한 방법이 보고되었다. 하지만 이러한 방법은 긴 공정시간이 요구되며, 나노입자의 크기 분포가 넓다는 단점을 지닌다. 본 연구에서는 화학기상증착법을 통해 합성된 그래핀이 전사된 SiO2 (300nm)/Si 기판에 염화기가 포함된 백금 화합물 분산용액을 스핀코팅(spin-coating)하고 MeV 전자빔을 조사하여 Pt/grapheme 복합구조를 형성하였다. 이 방법은 균일한 크기 분포의 나노입자의 형성이 가능하며, 간단하고, 대면적 공정이 가능하며, 다른 방법에 비해 그래핀의 결함형성이 적다는 장점을 지닌다. Pt/grapheme 의 기하학적 구조를 주사전자현미경(scanning electron microscopy)와 투과전자현미경(transimission)을 통해 분석하였고, Pt와 graphene의 일함수(workfunction)의 차이에 의해 야기되는 전하이동에 의한 도핑(doping)현상을 라만 분광기(Raman spectroscopy)와 X-선 광전자 분광기(X-ray photoelectron spectroscopy)를 통해 분석하였다.

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Forward Osmosis Technology for Concentrating the Heavy Water (중수 농축을 위한 정삼투 기술)

  • Chul Ho Park;Seong Bae Cho;Ook Choi
    • Membrane Journal
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    • v.33 no.2
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    • pp.70-76
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    • 2023
  • Heavy water (D2O) can induce various biochemical changes in comparison with light water (H2O). In order to reduce excessive energy consumption, which is a disadvantage of the existing separation process, we conduct the forward osmosis with electrospun polyamide membranes. NaCl and phosphoric acid were used as draw solutions. FT-IR spectroscopy was used to quantify the concentration of heavy water. It was observed that phosphoric acid could concentrate heavy water through a forward osmosis process and its special interaction with hydrogen/deuterium (H/D) was spectrophotometrically confirmed.

Thermodynamic Study on the Solubilization of p-Halogenated Phenol Derivatives in TTAB Solution (TTAB 수용액에서 p-할로겐화 페놀유도체들의 가용화에 대한 열역학적 연구)

  • Lee, Byung-Hwan
    • Applied Chemistry for Engineering
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    • v.25 no.1
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    • pp.20-26
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    • 2014
  • The interaction of p-halogenated phenol derivatives with the micellar system of tetradecyltrimethylammonium bromide (TTAB) was studied by the UV/Vis spectrophotometric method. Effects of substituents, additives, and temperatures on the solubilization of phenol derivatives have been measured. The results show that all the values of ${\Delta}G^o$ and ${\Delta}H^o$ were negative and the values of ${\Delta}S^o$ were positive for all phenol derivatives within the measured temperature range. The calculated thermodynamic parameters depended on the size, the electro-negativity, and the hydrophobic property of halogen substituents. The addition of n-butanol results in the decrement in tthe Ks values and the addition of NaCl caused the increment in the Ks values for all the phenol derivatives. From these changes we can postulate that the solubilization sites of the phenol derivatives in the micelle depend severely on properties of the halogen-substituent.

Ionic Recognition with Quinone-Derivatized Calixarenes in Solution and at Self-Assembled Monlayers

  • Kim Hasuck;Kang Sun Kil;Chung Taek Dong
    • Journal of the Korean Electrochemical Society
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    • v.3 no.2
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    • pp.69-71
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    • 2000
  • Redox-active calix[4]arenes with carboxylic acid and disulfide groups were prepared and spontaneous deposition on silver and gold surfaces was observed. Owing to their unusual structure, the calix[4]arenes exhibit selective affinity fur alkaline earth metal ions in aqueous media. When annular ionophores are immobilized on the surface, voltammetric and spectroscopic studies show the entrapment of metal ions. Furthermore, it was possible to reversibly capture and remove the ions using strong chelating agents such as ethylenediaminetetraacetic acid (EDTA).

Effects of Electron-beam. Patterns on Microstructures of Silicon for Photovoltaic Applications (전자빔패턴에 따른 태양전지용 실리콘의 미세구조)

  • Choi, Sun-Ho;Jang, Bo-Yun;Kim, Joon-Soo;Ahn, Young-Soo
    • Proceedings of the Korean Institute of Electrical and Electronic Material Engineers Conference
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    • 2010.06a
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    • pp.224-224
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    • 2010
  • 야금학적 정련은 태양전지 소재인 실리콘의 저가화를 통한 태양전지의 단가를 낮추는데 유망한 공정이다. 이중에서도 실리콘의 전자빔정련은 고순도의 실리콘 정련에 효과적인 기술이다. 본 연구에서는 전자빔용융법을 이용하여 실리콘 정련을 수행하였으며, 제조된 실리콘의 미세구조 및 분순물농도를 측정하였다. 고진공의 챔버 하부에 수냉동도가니가 위치해있고, 상부에 100 kW출력의 전자총이 설치되었다. 실리콘은 분쇄 및 세척과 같은 전처리 없이 수냉동도가니에 250g 이 장입되었다. 전자빔때턴은 소프트웨어를 통한 헌혈, 나선형의 경로(path)와 원형의 형상(Shape)이 결합하여 원형패턴과 나선형패턴의 형상으로 실리콘에 조사되었다. 전자빔의 출력을 15 kW로 실리콘을 용융하였고 분당 0.5 kW의 속도로 서냉하였다. 제조된 실리콘은 지름 100 mm, 높이 25 mm의 버튼형상이었으며, 횡방향으로 절단하여 미세구조와 불순물거동을 분석하였다. 미세구조는 광학현미경 (OM) 과 전자현미경 (SEM)을 통하여 관찰하였고 불순물거동은 유도결합플라즈마 분광분석기(ICP-AES) 을 통하여 분석하였다. 장입된 실리콘의 초기순도는 99.5 %이고, 전자빔정련 공정 후 99.996 %까지 향상되었다. 전자빔패턴을 이용한 고순도 실리콘의 정련은 태양전지 소재 개발에 유망한 기술로 활용될 것이다.

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Crystallographic and Mossbauer studies of $Ni_{0.65}Zn_{0.35}Cu_{0.1}Fe_{1.9}O_4$ ($Ni_{0.65}Zn_{0.35}Cu_{0.1}Fe_{1.9}O_4$의 결정학적 및 Mossbauer 효과 연구)

  • 김우철;이승화;홍성렬;옥항남;김철성
    • Journal of the Korean Magnetics Society
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    • v.8 no.3
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    • pp.118-124
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    • 1998
  • $Ni_{0.65}Zn_{0.35}Cu_{0.1}Fe{1.9}O_4$ has been studied with Mossbauer spectroscopy and X-ray diffraction. The crystal structure is found to be a cubic spinel with the lattice constant $a_0=8.390{\AA}$. Mossbauer spectra of $Ni_{0.65}Zn_{0.35}Cu_{0.1}Fe{1.9}O_4$ has been taken at various temperatures ranging from 12 K to 705 K. The isomer shift indicates that iron ions are ferric at tetrahedral [A] and octahedral sites [B], respectively. The Neel temperature is determined to be $T_N=705\;K$. As the temperature increases toward $T_N$ a systematic line broadening effect in the Mossbauer spectrum is observed and interpreted to originate from different temperature dependencies of the magnetic hyperfine fields at various iron sites. The quadrupole splitting just on $T_N$ is 0.41 mm/s whereas the quadrupole shift below $T_N$ vanishes. This implies that the orientation of the magnetic hyperfine field with respect to be principal axes of the electric field gradient is random.

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Ionic Liquid Crystal Electrolytes based on Ether Functionalized Ionic Liquid for Lithium Batteries (리튬전지용 에테르가 기능화된 이온성 액체 기반 이온성 액정 전해질의 전기화학적 특성)

  • Kim, Il Jin;Kim, Ki Su;Lee, Jin Hong
    • Applied Chemistry for Engineering
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    • v.31 no.3
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    • pp.305-309
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    • 2020
  • In this study, a series of ionic liquids based electrolytes for lithium batteries were prepared by mixing the anion functionalized ionic liquid, [DMIm][MPEGP] (1,3-dimethylimidazolium (2-methoxy(2-ethoxy(2-ethoxy)))-ethylphosphite), with the lithium salt, LiTf2N (lithium bis(trifluoromethanesulfonyl)imide), and the concentration of lithium salt was varied between 0 and 3.0 molar ratio. We observed the ionic mixtures became opaque and spontaneously aggregated to form a thermotropic ionic liquid crystal. Extensive spectroscopic examinations of the ionic liquid crystals were carried out to investigate their self-organized structures and the ion transport behavior depending on the concentration of lithium salt. An increase in the ionic conductivity was observed for the ionic liquid crystals related to the ability to form ion diffusion pathways along the ordered structures, resulting in improved electrochemical performances of lithium batteries.

Theoritical Studies on Structure of 4H-Pyran-4-one and Its Sulfur Analogues (4H-Pyran-4-one과 그의 황 유도체의 구조에 관한 이론적 연구)

  • Ikchoon Lee;Hyeong Yeoun Park;Young Ki Kim
    • Journal of the Korean Chemical Society
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    • v.30 no.6
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    • pp.495-499
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    • 1986
  • Structures of 4H-pyran-4-one(I), 4H-pyran-4-thione(II), 4H-thiapyran-4-one (III), 4H-thiapyran-4-thione(IV) have been determined by MNDO and MINDO/3 methods. Geometries and physicochemical properties, especially the aromaticity, were found to agree well with the results of microwave experiments. The order of aromaticity was found to be (IV) > (III) > (II) > (I), which demonstrated inhibitory effect of strongly electronegative oxygen atom on the electron delocaligation, and the order of dipole moment, (II) > (IV) > (I) > (III), indicated the dominant contribution of the bond length of carbonyl group (C=O or C=S)

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