• Proceedings of the Korean Vacuum Society Conference
• /
• 2011.08a
• /
• pp.354-354
• /
• 2011

ZnO 나노와이어는 밴드 갭이 3.37 ev로 큰 밴드 갭을 갖는 물질이며 엑시톤 결합에너지가 60 meV로 GaN(25 meV)같은 다른 반도체보다 매우 크다. 또한 밴드갭 에너지가 큰 GaN, SiC와 같은 반도체에 비해서 화학적, 열적 안정성이 크며 낮은 온도에서 성장이 가능하다는 장점이 있다. 본 연구에서는 pre-heating process를 이용하여 1차원 구조인 ZnO nanowire를 수열합성법으로 합성하였다. 실험방법으로는 E2K glass 기판위에 AZO40 nm를 증착후, 시드층으로 이용하여 ZnO nanowire를 성장하였다. precusor 전구체에는 ZN(NO3)2 ${\cdot}$ 6H2O와 Capping agent으로의 역할을 위해 PEI와 OH-source 공급을 위한 Ammonium chloride를 첨가하여 합성하였고, 그에 따른 ZnO nanowire의 morphology 및 aspect ratio를 조절하고자 하였다. 마지막으로 ZnO 나노와이어의 구조적, 광학적 특성 평가를 하기위해 XRD, FE-SEM, PL 등을 이용하여 측정 하였고, 향후 나노발전기, 태양전지 등 여러 광학기기 등에 전극재료로서 응용 가능성에 대해 알아보고자 하였다.

• Journal of the Korean Vacuum Society
• /
• v.18 no.3
• /
• pp.229-235
• /
• 2009

Millimeter-scale aligned arrays of thin-multiwalled carbon nanotube (t-MWCNT) on layered Si substrates have been synthesized by oxygen-assisted microwave plasma chemical vapor deposition (MPCVD). We have succeeded in growth of vertically aligned MWCNTs up to 2.7 mm in height for 150 min. The effect of $O_2$ and water vapour on growth rate was systematically investigated. In the case of $O_2$ gas, the growth rate was ${\sim}22{\mu}m/min$, which is outstanding growth rate comparing with those of conventional thermal CVD (TCVD). Scanning electron microscope (SEM), energy-dispersive spectroscopy (EDS), and Raman spectroscopy were used to analyze the CNT morphology, composition and growth mechanism. The role of $O_2$ gas during the CNT growth was discussed on.

• Proceedings of the Korean Vacuum Society Conference
• /
• 2010.02a
• /
• pp.189-189
• /
• 2010

ZnO nanorods 구조는 광소자 및 태양광 소자의 성능을 향상시키기 위해서 무반사계수, 광추출효율, 전기적, 열적 전도도를 개선시킬 수 있어, 매우 큰 관심을 가지고 왔다. 또한 Ag 나노입자는 표면 플라즈몬 효과를 이용하여 LED나 태양전지에 응용하여 소자의 성능이 향상됨을 이론적, 실험적으로 증명되어 왔으며, 현재에도 활발한 연구가 진행되고 있다. 이러한 ZnO nanorods 특성과 Ag 나노입자의 표면 플라즈몬 효과를 이용하기 위해서, 본 연구에서는 Ag 나노 입자를 형성된 ZnO seed층에 ZnO nanorods를 성장시켰다. 시료를 제작을 위해서 비교적 성장이 간단하고 저온성장이 가능한 화학적 합성방법을 이용하였다. Ag 나노입자가 형성된 ZnO seed층 제작을 위해서 먼저 Si 기판위에 RF magnetron 스퍼터를 이용하여 고진공, $N_2$ 분위기에서 일정한 두께로 증착을 하였으며, 이후 Ag 박막을 thermal evaporator로 10 nm 두께로 증착하였다. 그 다음, 크기가 다른 Ag 나노입자를 형성을 위해서 rapid thermal annealing (RTA)을 여러 가지 온도에서 수행하였다. 그리고 이러한 시료들를 이용하여, ZnO nanorods를 성장하기 위하여, $90-95^{\circ}$의 온도에서 zinc nitrate $Zn(NO_3)_2{\cdot}6H_2O$과 hexamethylentetramines (HMT)으로 혼합된 용액에 담가두어 ZnO nanorods를 성장시켰다. Ag 나노입자의 크기에 따라 ZnO nanorods의 구조와 형태에 대하여 어떠한 영향을 주는지를 관찰하기 위해 field emission scanning electron microscopy (FE-SEM)을 이용하여 측정하였으며, Ag와 ZnO의 성분분석과 결정성을 조사하기 위해 X-ray diffraction (XRD)을 이용하여 분석하였다. 그리고 표면 플라즈몬에 의한 영향에 대하여 조사하기 위해, ZnO nanorods와 Ag 나노입자가 형성된 ZnO nanorods를 UV-Vis-NIR spectrophotometer을 이용하여 흡수계수와 반사계수를 비교하여 측정하였으며. 태양전지의 성능향상을 수 있음을 이론적으로 계산하였다. 그리고 또한 photoluminescence (PL) 분석을 수행하여 ZnO nanorods의 구조에 대하여 Ag 나노입자의 영향에 대한 광특성을 측정하였다.

• Polymer(Korea)
• /
• v.29 no.3
• /
• pp.266-270
• /
• 2005

Iron oxide nanoparticles were prepared by the thermal decomposition of iron pentacarbonyl (Fe(CO)$_5$) Poly(vinylpyrrolidone) (PVP) was used as surface-modifying agent to control the size of the iron oxide nanoparticles. The crystalline structure of PVP coated iron oxide nanoparticles was determined by XRD. The size of PVP coated iron oxide nanoparticles was determined by TEM and ELS. The particle sizes of PVP coated iron oxide nanoparticles were controlled by adjusting the molar ratio of PVP/Fe (CO)$_5$, solvent and molecular weight of PVP Particle sizes increased with increasing PVP content. Spherical $50\~100$ nm sized iron oxide nanoclusters were produced when dimethylformamide was used as a solvent. And well-defined 10 nm iron oxide nanoparticles were produced in Carbitol. The prepared PVP coated iron oxide nanoparticles exhibited a well-dispersed property in water. The results obtained in this study confirmed the feasibility of the PVP-coated iron oxide nanoparticles as a biomaterial for MRI contrast agent.

• Journal of the Korean Chemical Society
• /
• v.60 no.1
• /
• pp.34-38
• /
• 2016

In this paper, zinc oxide nanoparticles (ZnO NPs) were synthesized using the sonochemical method, where equimolar amounts of zinc acetate dehydrate and sodium hydroxide were separately dissolved in deionized water, and then mixed for 30 min under magnetic stirring. The resultant white gel was sonicated for 60, 120, 180, 240, and 360 min with magnetic stirring. The obtained precipitates were centrifuged, repeatedly washed with ethanol to remove ionic impurities, and dried at 50 ℃ for 24 h. The formation of pure NPs was confirmed by X-ray diffraction, and their crystallinity and crystal phases were analyzed as well. Structural investigation was carried out by field-emission scanning electron microscopy (FE-SEM). The photocatalysis behavior of the ZnO NPs was investigated in a dark room under UV irradiation, using Rhodamine B. Spherical, rod, and flower-like ZnO NPs could be obtained by adjusting the sonication time, as observed by FE-SEM. The flower-like ZnO NPs exhibited excellent photocatalytic activity.

• Journal of the Korean Vacuum Society
• /
• v.17 no.1
• /
• pp.67-72
• /
• 2008

We have studied the effect of heat treatment of multi-walled carbon nanotubes (MWNTs) as a counter electrode on the electro-chemical properties of dye-snsitized solar cells. MWNTs on the p-type Si substrate were synthesized by thermal chemical vapor deposition (CVD) using Fe catalysts. We prepared the two types of MWNTs samples with the different diameters. The rapid thermal annealing (RTA) treatment for the MWNTs was carried out at the growth temperature ($900^{\circ}C$) for 1 minute with $N_2$ gas atmosphere. The structural, electrical and electrochemical properties of MWNTs were investigated by field-emission scanning electron microscopy (FE-SEM), Raman spectroscopy, 2-point probe station and electrochemical impedance spectroscopy (EIS). The I(D)/I(G) ratio of heat-treated MWNTs in Raman spectra was considerably decreased. It was also found that the heat-treated MWNTs showed better redox reaction of iodide at the interface between MWNTs surface and electrolyte than that of as-grown MWNTs. The redox resistance value of heat-treated electrodes was measured to be much lower than that of as-grown electrode at the interface. As a result, the counter electrode using the heat-treated MWNTs showed better electrochemical properties.

• Polymer(Korea)
• /
• v.36 no.5
• /
• pp.656-661
• /
• 2012

The palladium nanoparticles were self-assembled to make Pd-POSS using POSS-$NH_3{^+}$ (polyhedral oligomeric silsesquioxane) as a crosslinker. Graphene oxide (GO) was produced by the reaction of graphite under a strong acid and oxidizer and poly(acrylic acid) (PAA) was covalently grafted on the surface of graphene to make PAA-grafted graphene through the radical polymerization of acrylic acid and GO along with a reduction process under $NaBH_4$. The nanocomposites of Pd-POSS and PAA-grafted graphene were fabricated via ionic interactions between positively charged Pd-POSS and negatively charged PAA-grafted graphene. Pd-POSS nanoparticles were attached to the surface of PAA-grafted graphene through ionic interactions. The thermal stability of Pd-POSS/PAA-grafted graphene was higher than that of PAA and PAA-grafted graphene. The composition, structure, surface morphology, and thermal stability of the Pd-POSS/PAA-grafted graphene were studied by FE-SEM, AFM, TEM, FTIR, and TGA.

• Journal of Powder Materials
• /
• v.14 no.1 s.60
• /
• pp.19-25
• /
• 2007

This study was focused on the optimization of low-pressure ultrasonic spraying process for synthesis of pure ${\gamma}-Fe_2O_3$ nanoparticles. As process variables, pressure in the reactor, precursor concentration, and reaction temperature were changed in order to control the chemical and microstructural properties of iron oxide nanoparticles including crystal phase, mean particle size and particle size distribution. X-ray diffraction (XRD) and transmission electron microscopy (TEM) studies revealed that pure ${\gamma}-Fe_2O_3$ nanoparticles with narrow particle size distribution of 5-15 nm were successfully synthesized from iron pentacarbonyl ($Fe(CO)_{5}$) in hexane under 30 mbar with precursor concentrations of 0.1M and 0.2M, at temperatures over $800^{\circ}C$. Also magnetic properties, coercivity ($H_c$) and saturation magnetization ($M_s$) were reported in terms of the microstructure of particles based on the results from vibration sampling magnetometer (VSM).

• Korean Chemical Engineering Research
• /
• v.60 no.3
• /
• pp.446-451
• /
• 2022

In this study, to improve capacity and cycle stability, the pitch coated nano silicon sheets/CNT composites were prepared through electrostatic bonding of nano silicon sheets and CNT. Silica sheets were synthesized by hydrolyzing TEOS on the crystal planes of NaCl, and then nano silicon sheets were prepared by using magnesiothermic reduction method. To fabricate the nano silicon sheets/CNT composites, the negatively charged CNT after the acid treatment was used to assemble the positively charged nano silicon sheets modified with APTES. THF as a solvent was used in the coating process of PFO pitch. The physical properties of the prepared anode composites were analysed by FE-SEM, XRD and EDS. The electrochemical performances of the synthesized anode composites were performed by current charge/discharge, rate performances, differential capacity and EIS tests in the electrolyte LiPF₆ dissolve solvent (EC:DMC:EMC = 1:1:1 vol%). It was found that the anode material with high capacity and stability could be synthesized when high composition of silicon and conductivity of CNT were used. The pitch coated nano silicon sheets/CNT anode composites showed initial discharge capacity of 2344.9 mAh/g and the capacity retention ratio of 81% after 50 cycles. The electrochemical property of pitch coated anode material was more improved than that of the nano silicon sheets/CNT composites.

• Journal of the Mineralogical Society of Korea
• /
• v.22 no.1
• /
• pp.63-72
• /
• 2009

Carbon-coated lithium iron phosphate ($LiFePO_4/C$) composites are synthesized by the modified mechanical activation method (modified MA process) and studied by the Rietveld structural refinement. Rietveld indices of $LiFePO_4/C$ indicate good fitting with $R_p=8.14%,\;R_{wp}=11.1%,\;R_{exp}=9.09%,\;R_B=3.88%$, and S (GofF, Goodness of fit) = 1.2, respectively. $LiFePO_4/C$ with a space group Pnma shows a = 10.3229(3)${\AA}$, b = 6.0052(2) ${\AA}$, c = 4.6939(1) ${\AA}$, and V = 290.98(1) ${\AA}^3$ in dimension, indicating good agreements with those of previous works. Synthetic powders are nano-sized ($65{\sim}90nm$) homogeneous particles with high purity. Thus the modified MA method will be an efficient process to get a high quality cathode material for commercial lithium batteries.