• 한국세라믹학회지
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• 제38권10호
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• pp.867-870
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• 2001

지지촉매로 Ni-graphite를 사용하고 ${C_2}{H_2}$를 이용한 열화학기상증착법에 의하여 탄소나노소재를 합성하였다. 합성된 시편은 SEM, TEM, 라만 분광법으로 분석하였으며, 수소저장특성은 전기화학적인 방법에 의하여 평가하였다. 탄소나노소재 합성시 메카노케미컬 처리과정을 거친 시편이 거치지 않은 시편에 비하여 탄소나노튜브의 순도가 우수하였다. 한편, 탄소나노소재를 정제함에 따라 수소저장특성이 크게 향상되었다.

• 한국세라믹학회지
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• 제39권1호
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• pp.68-73
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• 2002

$La_2O_3-Al_2O_3$(LAO)와 $La_2O_3-Al(OH)_3$(LAH)의 물질을 메카노케미칼 방법으로 분쇄하여 $LaAlO_3$세라믹스의 합성과 유전특성에 대하여 비교.조사하였다. $LaAlO_3$단일상을 얻기 위한 열처리온도는 LAO분말에서 $1300^{\circ}C$, LAH 분말은 $1000^{\circ}C$였다. 하소분말 중에 미 반응한 $La_2O_3$가 존재하면, 공기 중의 습기로 인하여 $La_2O_3$에서 $La(OH)_3$로 변하고,소결체의 밀도는 나빠진다. $1500^{\circ}C$에서 4시간 소결한 LAO 시료는 이론밀도의 97.3%이고, $1400^{\circ}C$에서 4시간 소결한 LAH시료는 98.3%였다. LAO시료는 입자의 크기가 불 균일하고 평균 입경은 4-5${mu}m$이며, LAH시료는 입자가 균일하고 크기가 $0.75{\mu}m$ 정도로 아주 작았다. 비유전율은 LAO와 LAH시료가 비슷하였고, 그 값은 약 22를 나타내었다. 그러나 LAH시료(0.0003)의 유전손실은 LAO시료 (0.001)보다 작았는데 이는 입자의 크기에 기인된다.

• 한국전기전자재료학회논문지
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• 제26권12호
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• pp.909-914
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• 2013

CIGS is one of thin film solar cell and has been studied so much, because of the possibility of low price and high efficiency. Until now, co-evaporation and sputtering were typical method to prepare CIGS absorption layer, and a few company commercialized solar cell by these method. However, non-vacuum process which has been studied for long time has not been progressed, though the merit of low price. Especially, aerosol deposition method has not been reported, because it is difficult to prepare a large quantity of various CIGS powder. In this study, CIGS powder was synthesized by mechanochemical method and CIGS absorption layer was deposited by aerosol deposition method. The thickness of the CIGS layer was controlled by the number of deposition and the surface roughness of it was affected by the amount of flow gas. And, also, I-V curve of it appeared metallic property in the case of 'as deposition'. After heat treatment in Se-rich atmosphere, the electrical property of it changed to a semiconductor. CdS and transparent conduction layer were formed by a typical method on it for solar cell. The efficiency of cell was appeared 0.19%. Though the efficiency was low because of the disharmony in the after-process, it was conformed that CIGS solar cell could be prepared by aerosol deposition.

• 한국결정성장학회지
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• 제18권6호
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• pp.248-252
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• 2008

전기전도성이 우수하면서 입자 크기가 작은 $LiFePO_4$ 분말을 얻기 위해서, 이종원소(Cr+B 또는 Cr+Al) 도핑이 $LiFePO_4$의 전기전도도에 미치는 영향과 열처리 조건이 입자 크기에 미치는 영향에 대해서 조사하였다. 조성이 $LiFe_{0.965}Cr_{0.03}B_{0.005}PO_4$ and $LiFe_{0.065}Cr_{0.03}Al_{0.005}PO_4$인 두 종류의 분말을 기계화학적 밀링법으로 혼합 후 $675{\sim}759^{\circ}C$에서 $5{\sim}10$시간 열처리하여 합성하였다. 이종원소 도핑은 입자성장을 촉진하였고 전기전도도를 높이는 효과가 있었다. $LiFe_{0.065}Cr_{0.03}Al_{0.005}PO_4$의 전기전도도는 $1{\times}10^{-8}S/cm$로 도핑하지 않은 것의 $5{\times}10^{-10}S/cm$보다 높았다.

• Bulletin of the Korean Chemical Society
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• 제32권3호
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• pp.921-926
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• 2011

This study investigates a root cause of the improved rate performance of $LiFePO_4$ after metal doping to Fesites. This is because the metal doped $LiFePO_4$/C maintains its initial capacity at higher C-rates than undoped one. Using $LiFePO_4$/C and doped $LiFe_{0.97}M_{0.03}PO_4$/C (M=$Al^{3+}$, $Cr^{3+}$, $Zr^{4+}$), which are synthesized by a mechanochemical process followed by one-step heat treatment, the Li content before and after chemical delithiation in the $LiFePO_4$/C and the binding energy are compared using atomic absorption spectroscopy (AAS) and X-ray photoelectron spectroscopy (XPS). The results from AAS and XPS indicate that the low Li content of the metal doped $LiFePO_4$/C after chemical delithiation is attributed to the low binding energy induced by weak Li-O interactions. The improved capacity retention of the doped $LiFePO_4$/C at high discharge rates is, therefore, achieved by relatively low binding energy between Li and O ions, which leads to fast Li diffusivity.

• Journal of Electrochemical Science and Technology
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• 제12권1호
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• pp.112-125
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• 2021

The new emerging "High entropy materials" attract the attention of the scientific society because of their simpler structure and spectacular applications in many fields. A novel nanocrystalline high entropy (Be,Mg,Ca,Sr,Zn,Ni)3O4 oxide has been successfully synthesized through mechanochemical treatment followed by sintering and air quenching. The present research work focuses on the possibility of single-phase formation in the aforementioned high entropy oxide despite the great difference in the atomic sizes of reactant alkaline earth and 3d transition metal oxides. Structural properties of (Be,Mg,Ca,Sr,Zn,Ni)3O4 high entropy oxide were explored by confirmation of its single-phase Fd-3m spinel structure by x-ray diffraction (XRD). Further, nanocrystalline nature and morphology were analyzed by scanning electron microscopy (SEM). Among thermal properties, thermogravimetric analysis (TGA) revealed that the (Be,Mg,Ca,Sr,Zn,Ni)3O4 high entropy oxide is thermally stable up to a temperature of 1200℃. Whereas phase evolution in (Be,Mg,Ca,Sr,Zn,Ni)3O4 high entropy oxide before and after sintering was analyzed through differential scanning calorimetry (DSC). Electrochemical studies of (Be,Mg,Ca,Sr,Zn,Ni)3O4 high entropy oxide consists of a comparison of thermodynamic and kinetic parameters of water and hydrazine hydrate oxidation. Values of activation energy for water oxidation (9.31 kJ mol-1) and hydrazine hydrate oxidation (13.93 kJ mol-1) reveal that (Be,Mg,Ca,Sr,Zn,Ni)3O4 high entropy oxide is catalytically more active towards water oxidation as compared to that of hydrazine hydrate oxidation. Electrochemical impedance spectroscopy is also performed to get insight into the kinetics of both types of reactions.

• 한국지하수토양환경학회지:지하수토양환경
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• 제28권1호
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• pp.15-24
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• 2023

A persulfate(PS)/sulfidated microscale zero-valent iron(S-mZVI) system was tested for treating a soil contaminated with phenol. Sulfidation of bare mZVI was conducted using a mechanochemical process utilizing a ball mill in order to improve persulfate activation capacity and stability of unmodified mZVI. The synthesized S-mZVI performed markedly better than the bare mZVI in activating PS. The optimum molar ratio of sulfur to mZVI was around 0.12. In the soil slurry experiments, a very rapid and complete removal of phenol was observed at the optimum molar ratios of PS to S-mZVI of 2:1 and PS to phenol of 16:1. The phenol removal efficiencies decreased as the water content of the slurries decreased. This was believed to be due to increased soil oxidant demand as the amount of soil was increased as relative to the water content. To evaluate the field applicability of the process, slurry experiments adopting high soil contents were carried out that simulated in-situ soil mixing conditions. These experiments resulted in substantially compromised degradation efficiencies of 54.3% and 43.8% within 4 hours. The current study generally shows that the PS/S-mZVI process has a potential to be developed into a remediation technology for soils contaminated with organics.

• 한국결정성장학회지
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• 제20권3호
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• pp.141-146
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• 2010

크롬이 도핑된 $LiFePO_4$ 분말이 도핑되지 않은 것보다 이차전지용 양극활물질로서 우수한 전기화학적 특성을 나타내었다. 이러한 향상은 도핑에 의해서 양극활물질의 전자전도도가 높아지기 때문인 것으로 생각되고 있다. 크롬과 또 하나의 전형원소가 도핑된 $LiFe_{0.965}Cr_{0.03}B_{0.005}PO_4$와 $LiFe_{0.965}Cr_{0.03}Al_{0.005}PO_4$의 전기전도도를 30에서 $80^{\circ}C$ 범위에서 측정하였다. 도핑된 분말은 유성밀에 의한 기계화학적 혼합을 한 후 675~$750^{\circ}C$에서 5~10시간 열처리하여 합성하였다. 이러한 도핑은 분말의 전기전도도를 높이고 입자 성장을 촉진시켰다. 크롬과 알루미늄이 도핑된 $LiFe_{0.965}Cr_{0.03}Al_{0.005}PO_4$ 분말의 $30^{\circ}C$에서의 전기전도도는 $1{\times}10^{-8}S/cm$이었으며, 이 값은 도핑하지 않은 것보다 두 자릿수 높은 값 이었다.