• Korean Chemical Engineering Research
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• 제53권2호
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• pp.131-136
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• 2015

본 연구에서는 전극 활물질로서 그래핀-바나듐 산화물 복합체를 pH 1.8 조건에서 0.5M $VOSO_4$ 수용액을 이용하여 전기화학적 전착을 이용해 합성하였다. 전착공정 후 다공성 바나듐 산화물이 작업전극에 생성된 것을 SEM, XRD, XPS를 통해 확인하였으며 생성된 바나듐 산화물은 $V^{5+}$와 $V^{4+}$로 존재한다. 그래핀에 전착된 바나듐 산화물의 직경 약 100 nm의 나노로드로 이루어진 망상 구조는 전극과 전해질과의 접촉을 향상시킨다. 4000 초의 전착공정을 거친 그래핀-바나듐 산화물 복합체를 작업전극으로 하여 3전극 셀에서 전기화학적 특성을 평가한 결과 20 mV/s의 주사속도에서 $854mF/cm^2$의 높은 정전용량을 나타내었고 1000회 충방전 후 초기 용량의 53%가 유지되었다.

• 한국재료학회지
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• 제28권5호
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• pp.261-267
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• 2018

Hydrothermal synthesis of highly crystalline $TiO_2$ nanorods is a well-developed technique and the nanorods have been widely used as the template for growth of various core-shell nanorod structures. Magneli/CdS core-shell nanorod structures are fabricated for the photoelectrochemical cell (PEC) electrode to achieve enhanced carrier transport along the metallic magneli phase nanorod template. However, the long and thin $TiO_2$ nanorods may form a high resistance path to the electrons transferred from the CdS layer. $TiO_2$ nanorods synthesized are reduced to magneli phases, $TixO_{2x-1}$, by heat treatment in a hydrogen environment. Two types of magneli phase nanorods of $Ti_4O_7$ and $Ti_3O_5$ are synthesized. Structural morphology and X-ray diffraction analyses are carried out. CdS nano-films are deposited on the magneli nanorods for the main light absorption layer to form a photoanode, and the PEC performance is measured under simulated sunlight irradiation and compared with the conventional $TiO_2/CdS$ core-shell nanorod electrode. A higher photocurrent is observed from the stand-alone $Ti_3O_5/CdS$ core-shell nanorod structure in which the nanorods are grown on both sides of the seed layer.

• 한국재료학회지
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• 제28권7호
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• pp.371-375
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• 2018

The manganese-, nickel-, and aluminum-doped cobalt ferrite powders, $Mn_{0.2}Co_{0.8}Fe_2O_4$, $Ni_{0.2}Co_{0.8}Fe_2O_4$, and $Al_{0.2}CoFe_{1.8}O_4$, are fabricated by the sol-gel method, and the crystallographic and magnetic properties of the powders are studied in comparison with those of $CoFe_2O_4$. All the ferrite powders are nano-sized and have a single spinel structure with the lattice constant increasing in $Mn_{0.2}Co_{0.8}Fe_2O_4$ but decreasing in $Ni_{0.2}Co_{0.8}Fe_2O_4$ and $Al_{0.2}CoFe_{1.8}O_4$. All the $M{\ddot{o}}ssbauer$ spectra are fitted as a superposition of two Zeeman sextets due to the tetrahedral and octahedral sites of the $Fe^{3+}$ ions. The values of the magnetic hyperfine fields of $Ni_{0.2}Co_{0.8}Fe_2O_4$ are somewhat increased in the A and B sites, while those of $Mn_{0.2}Co_{0.8}Fe_2O_4$ and $Al_{0.2}CoFe_{1.8}O_4$ are decreased. The variation of $M{\ddot{o}}ssbauer$ parameters is explained using the cation distribution equation, superexchange interaction and particle size. The hysteresis curves of the ferrite powders reveal a typical soft ferrite pattern. The variation in the values of saturation magnetization and coercivity are explained in terms of the site distributions, particle sizes and the spin magnetic moments of the doped ions.

• 한국재료학회지
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• 제30권9호
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• pp.447-452
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• 2020

In this work, α-Fe₂O₃ nanocrystals are synthesized by co-precipitation method and used as adsorbent to remove Cr⁶⁺, Cd²⁺, and Pb²⁺ from wastewater at room temperature. The prepared sample is evaluated by XRD, BET surface area, and FESEM for structural and morphological characteristics. XRD patterns confirm the formation of a pure hematite structure of average particle size of ~ 40 nm, which is further supported by the FESEM images of the nanocrystals. The nanocrystals are found to have BET specific surface area of ~ 39.18 m² g^-1. Adsorption experiments are carried out for the different values of pH of the solutions, contact time, and initial concentration of metal ions. High efficiency Cr⁶⁺, Cd²⁺, and Pb²⁺ removal occur at pH 3, 7, and 5.5, respectively. Equilibrium study reveals that the heavy metal ion adsorption of the α-Fe₂O₃ nanocrystals followed Langmuir and Freundlich isotherm models. The Cr⁶⁺, Cd²⁺, and Pb²⁺ adsorption equilibrium data are best fitted to the Langmuir model. The maximum adsorption capacities of α-Fe₂O₃ nanocrystals related to Cr⁶⁺, Cd²⁺, and Pb²⁺ are found to be 15.15, 11.63, and 20 mg g^-1, respectively. These results clearly suggest that the synthesized α-Fe₂O₃ nanocrystals can be considered as potential nano-adsorbents for future environmental and health related applications.

• 폴리머
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• 제30권2호
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• pp.97-107
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• 2006

방향족 강직사슬 폴리이미드는 높은 주사슬 간의 인력으로 인해 유기용제에 용해되지 않고 상전이온도가 분해 온도보다 높아 응용분야에 많은 제한이 되고 있다. 방향족 폴리이미드의 가공성을 향상시키기 위해서 긴 곁사슬을 도입하면 가공성 향상뿐만 아니라 곁사슬과 주사슬 사이에 독특한 구조를 가지게 됨으로써 새로운 응용분야를 개척할 수가 있다. 본 논문에서는 여러 가지 형태의 곁사슬을 가지는 방향족 폴리이미드의 합성과 화학구조에 따른 물성변화에 대해 논의하고 또한 폴리이미드의 액정배향막, 감광재료, 교대 다층박막, 발광재료 등으로의 응용특성에 관해서도 조감한다.

• 한국재료학회지
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• 제24권8호
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• pp.434-442
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• 2014

Serious environmental problems have been caused by the greenhouse effect due to carbon dioxide($CO_2$) or nitrogen oxides($NO_x$) generated by the use of fossil fuels, including oil and liquefied natural gas. Many countries, including our own, the United States, those of the European Union and other developed countries around the world; have shown growing interest in clean energy, and have been concentrating on the development of new energy-saving materials and devices. Typical non-fossil-fuel sources include solar cells, wind power, tidal power, nuclear power, and fuel cells. In particular, organic solar cells(OSCs) have relatively low power-conversion efficiency(PCE) in comparison with inorganic(silicon) based solar cells, compound semiconductor solar cells and the CIGS [$Cu(In_{1-x}Ga_x)Se_2$] thin film solar cells. Recently, organic cell efficiencies greater than 10 % have been obtained by means of the development of new organic semiconducting materials, which feature improvements in crystalline properties, as well as in the quantum-dot nano-structure of the active layers. In this paper, a brief overview of solar cells in general is presented. In particular, the current development status of the next-generation OSCs including their operation principle, device-manufacturing processes, and improvements in the PCE are described.

• 한국자기학회지
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• 제16권1호
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• pp.92-97
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• 2006

C 1s에너지 스캔 방식 광전자회절을 이용하여 Ni(111)$(2\times2)$-O/CO에 공동 흡착된 CO의 흡착구조를 시편의 준비 온도에 따라 연구하였다. 실온근방에서 준비한 시편의 경우 표면진동분광결과와 잘 일치하는 결과인 atop 흡착을 얻었으나, 저온시편의 경우 atop흡착 외에 상당량의 CO가 hollow 흡착으로 해석되었다. 일부분의 hollow 흡착 CO는 미리 흡착된 산소의 precoverage가 적거나 없는 곳에 흡착된 곳으로 해석된다. 유사한 결과가 C 1s와 O 1s를 통행 얻은 고 분해능 XPS에서 얻은 흡착위치에서도 확인되었다.

• 한국분말재료학회지
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• 제25권1호
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• pp.12-18
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• 2018

Cost-effective functional phosphor nanoparticles are prepared by introducing low-cost $SiO_2$ spheres to rare-earth phosphor ($YVO_4:Eu^{3+}$, $YVO_4:Er^{3+}$, and $YVO_4:Nd^{3+}$) shells using a sol-gel synthetic method. These functional nanoparticles are characterized by X-ray diffraction, X-ray photoelectron spectroscopy, transmission electron microscopy, and general photoluminescence spectra. The $SiO_2$ sphere occupying the interior of the conventional phosphor is advantageous in significantly reducing the cost of expensive rare-earth phosphor nanoparticles. The sol-gel process facilitates the core-shell structure formation; the rare-earth shell phosphor has strong interactions with chelating agents on the surfaces of $SiO_2$ nanoparticles and thus forms layers of several nanometers in thickness. The photoluminescence wavelength is simply tuned by replacing the active materials of $Eu^{3+}$, $Er^{3+}$, and $Nd^{3+}$. Moreover, the photoluminescent properties of the core-shell nanoparticles can be optimized by manipulating the specific contents of active materials in the phosphors. Our simple approach substitutes low-cost $SiO_2$ for expensive rare-earth-based phosphor materials to realize cost-effective phosphor nanoparticles for various applications.

• 한국표면공학회:학술대회논문집
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• 한국표면공학회 2016년도 추계학술대회 논문집
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• pp.152-152
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• 2016

Anodizing is a technology to generate thicker and high-quality films than natural oxide films by treating metals via electrochemical methods. It is a technique to develop metals for various uses, and extensive research on the commercial use has been performed for a long time. Aluminum anodic oxide (AAO) is generate oxide films, whose sizes and characteristics depending on the types of electrolytes, voltages, temperatures and time. Electrochemical manufacturing method of nano structure is an efficient technology in terms of cost reduction, high productivity and complicated shapes, which receives the spotlight in diverse areas. The sulfuric acid was used as an anodizing electrolyte, controlling its temperature to $10^{\circ}C$. The anode was 5083 Al alloy with dimension of $5(t){\times}20{\times}20mm$ while the cathode was the platinum. The distance between the anode and the cathode was maintained at 3 cm. Agitation was introduced by magnetic stirrer at 300 rpm to prevent localized temperature rise that hinders stable growth of oxide layer. In order to observe surface characteristics with applied current density, the electrolyte temperature, concentration was maintained at constant condition for $10^{\circ}C$, 10 vol.%, respectively. To prevent hindrance of stable growth of oxide layer due to local temperature increase during the experiment, stirring was maintained at constant rate. In addition, using galvanostatic method, it was maintained at current density of $10{\sim}30mA/cm^2$ for 40 minutes. The cavitation experiment was carried out with an ultrasonic vibratory apparatus using piezo-electric effect with modified ASTM-G32. The peak-to-peak amplitude was $30{\mu}m$ and the distance between the horn tip and specimen was 1 mm. The specimen after the experiment was cleaned in an ultrasonic, dried in a vacuum oven for more than 24 hours, and weighed with an electric balance. The surface damage morphology was observed with 3D analysis microscope. As a result of the investigation, differences were observed surface hardness and anti-cavitation characteristics depending on the development of oxide film with applied current density.

• 마이크로전자및패키징학회지
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• 제12권2호
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• pp.149-154
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• 2005

궁극적으로 게이트를 저저항 복합 실리사이드로 대체하는 가능성을 확인하기 위해 70 nm 두께의 폴리실리콘 위에 각 20nm의 Ni, Co를 열증착기로 적층순서를 달리하여 poly/Ni/Co, poly/Co/Ni구조를 만들었다. 쾌속열처리기를 이용하여 실리사이드화 열처리를 40초간 $700{\~}1100^{\circ}C$ 범위에서 실시하였다. 복합 실리사이드의 온도별 전기저항변화, 두께변화, 표면조도변화를 각각 사점전기저항측정기와 광발산주사전자현미경, 주사탐침현미경으로 확인하였다. 적층순서와 관계없이 폴리실리콘으로부터 제조된 복합실리사이드는 $800^{\circ}C$ 이상부터 급격한 고저항을 보이고, 두께도 급격히 얇아졌다. 두께의 감소는 기존의 단결정에서는 없던 현상으로 폴리실리콘의 두께가 한정된 경우 금속성분의 inversion 현상이 커서 폴리실리콘이 오히려 실리사이드 상부에 위치하여 제거되기 때문이라고 생각되었고 $1000^{\circ}C$ 이상에서는 실리사이드가 형성되지 못하였다. 이러한 결과는 나노급 두께의 게이트를 저저항 실리사이드로 만 들기 위해서는 inversion과 두께감소를 고려하여야 함을 의미하였다.