• 전기학회논문지
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• 제67권12호
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• pp.1626-1632
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• 2018

In this paper, we describe the fabrication and characterization of a hydrogen peroxide ($H_2O_2$) sensor based on palladium and copper (PdCu) electroplated laser induced graphene (LIG) electrodes. $CO_2$ laser was used to form LIG electrodes on a PI film. This fabrication method allows simple control of the LIG electrode size and shape. The PdCu was electrochemically deposited on the LIG electrodes to improve the electrocatalytic reaction with $H_2O_2$. The electrochemical performance of this sensor was evaluated in terms of selectivity, sensitivity, and linearity. The physical characterization of this sensor was conducted using scanning electron microscopy (SEM) and energy-dispersive X-ray spectroscopy (EDS), which confirmed that PdCu was formed on the laser induced graphene electrode. In order to increase the sensor sensitivity, the Pd:Cu ratio of the electroplated PdCu was varied to five different values and the condition of highest amperometric current at an identical of $H_2O_2$ concentration was chosen among them. The resulting amperometric current was highest when the ratio of Pd:Cu was 7:3 and this Pd;Cu ratio was employed in the sensor fabrication. The fabricated PdCu/LIG electrode based $H_2O_2$ sensor exhibited a sensitivity of $139.4{\mu}A/mM{\cdot}cm^2$, a broad linear range between 0 mM and 16 mM of $H_2O_2$ concentrations at applied potential of -0.15 V, and high reproducibility (RSD = 2.6%). The selectivity of the fabricated sensors was also evaluated by applying ascorbic acid, glucose, and lactose separately onto the sensor in order to see if the sensor ourput is affected by one of them and the sensor output was not affected. In conclusion, the proposed PdCu/LIG electrode based $H_2O_2$ sensor seems to be suitable $H_2O_2$ sensor in various applications.

• 분석과학
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• 제19권4호
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• pp.309-315
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• 2006

Two piperazine-templated metal sulfate complexes, $(C_4N_2H_{12})[Ni(H_2O)_6](SO_4)_2$, I and ($C_4N_2H_{12}$) $[Co(H_2O)_6](SO_4)_2$, II, have been synthesized by hydro/solvothermal reactions and their crystal structures analyzed by single crystal X-ray diffraction methods. Complex I crystallizes in the monoclinic system, $P2_1/n$ space group, a=12.920(3), b=10.616(2), $c=13.303(2){\AA}$, ${\beta}=114.09(1)^{\circ}$, Z=4, $R_1=0.030$ for 3683 reflections; II: monoclinic $P2_1/n$, a=12.906(3), b=10.711(2), $c=13.303(2){\AA}$, ${\beta}=114.10(2)^{\circ}$, Z=4, $R_1=0.032$ for 4010 reflections. The crystal structures of the piperazine-templated metal(II) sulfates demonstrate zero-dimensional compound constituted by diprotonated piperazine cations, metal(II) cations and sulfate anions. The structures of complex I and II are substantially isostructural to that of the previously reported our piperazine-templated copper(II) sulfate complex $(C_4N_2H_{12})[Cu(H_2O)_6](SO_4)_2$. The central metal(II) atoms are coordinated by six water molecules in the octahedral geometry. The crystal structures are stabilized by three-dimensional networks of the $O_{water}-H{\cdots}O_{sulfate}$ and $N_{pip}-H{\cdots}O_{sulfate}$ hydrogen bonds between the water molecules and sulfate anions and protonated piperazine cations. Based on the results of thermal analysis, the thermal decomposition reactions of the complex I was analyzed to have three distinctive stages whereas the complex II proceed through several stages.

• Journal of Magnetics
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• 제9권1호
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• pp.17-22
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• 2004

We studied the magnetotransport properties of tunnel junctions with AlO and AlN barriers fabricated using microwave-excited plasma. The plasma nitridation process provided wider controllability than the plasma oxidization for the formation of MTJs with ultra-thin insulating layer, because of the slow nitriding rate of metal Al layers, comparing with the oxidizing rate of them. High tunnel magnetoresistance (TMR) ratios of 49 and 44% with respective resistance-area product $(R{\times}A) of 3 {\times} 10^4 and 6 {\times} 10^3 {\Omega}{\mu}m^2$ were obtained in the Co-Fe/Al-N/Co-Fe MTJs. We conclude that AlN is a hopeful barrier material to realize MTJs with high TMR ratio and low $R{\times}A$ for high performance MRAM cells. In addition, in order to clarify the annealing temperature dependence of TMR, the local transport properties were measured for Ta $50{\AA} /Cu 200 {\AA}/Ta 50 {\AA}/Ni_{76}Fe_{24} 20 {\AA}/Cu 50 {\AA}/Mn_{75}Ir_{25} 100 {\AA}/Co_{71}Fe_{29} 40 {\AA}/Al-O$ junction with $d_{Al}= 8 {\AA} and P_{O2}{\times}t_{0X}/ = 8.4 {\times} 10^4$ at various temperatures. The current histogram statistically calculated from the electrical current image was well in accord with the fitting result considering the Gaussian distribution and Fowler-Nordheim equation. After annealing at $340^{\circ}C$, where the TMR ratio of the corresponding MTJ had the maximum value of 44%, the average barrier height increased to 1.12 eV and its standard deviation decreased to 0.1 eV. The increase of TMR ratio after annealing could be well explained by the enhancement of the average barrier height and the reduction of its fluctuation.

• 한국전기전자재료학회논문지
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• 제29권8호
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• pp.489-493
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• 2016

In this study, the effect of vanadium oxide ($V_2O_5$) content and pre-sintering atmosphere on sealing property of glass frit that consisted of $V_2O_5-BaO-ZnO-P_2O_5-TeO_2-CuO-Fe_2O_3-SeO_2$ was investigated by XPS (X-ray photoelectron spectroscopy). The content of V2O5 was changed to 15, 30, and 45 mol%, and the pre-sintering was carried out in air and $N_2$ condition, respectively. XPS analysis conducted before and after laser irradiation with identical sample. Before laser treatment, glass frits that were pre-sintered at air condition showed both $V^{4+}$ and $V^{5+}$, but the valence state was changed to $V^{5+}$ after laser irradiation when the glass frits contained 30 and 45 mol% $V_2O_5$; this change led to non-adhesive property. On the other hand, glass frits that were pre-sintered at $N_2$ condition exhibited only $V^{4+}$ and it showed fine adhesion irrespective of the $V_2O_5$ content. As a result, the existence of $V^{4+}$ seems to be a major factor for controlling the adhesive property of glass frit for laser sealing.

• 한국자기학회지
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• 제7권1호
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• pp.13-18
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• 1997

기본 조성 N $i_{0.18}$Z $n_{0.68}$C $u_{0.14}$F $e_{2}$ $O_{4}$와 N $i_{0.14}$Z $n_{0.64}$C $u_{0.22}$F $e_{2}$ $O_{4}$ 및 N $i_{0.24}$Z $n_{0.64}$C $u_{0.12}$F $e_{2}$ $O_{4}$에 입계의 고저항층을 형성하고 소결을 촉진시키기 위해서 0.1 mol %의 Ca $Co_{3}$와 입자의 성장을 촉진시키고 높은 투자율을 얻을 목적으로 $V_{2}$ $O_{5}$를 0.04 mol% 첨가하였다. 이들 원료들을 혼합한 후 950 .deg. C에서 3시간 하소 과정을 거친후 ball mill해서 toroid 시편을 만들고 1030 .deg. C, 1050 .deg. C 및 1070 .deg. C 에서 2시간 동안 공기중에서 소결 시켰다. Raw material의 조성비 변화 및 소결 온도 변화에 따른 여러 가지 물리적 특성들을 조사하였다. X-선 회절 분석 결과 이들 시편들이 spinel 구조를 이루고 있음을 확인하였고 금속현미경으로 측정한 결정 입자의 크기는 6 .mu. m ~ 16 .mu. m 이었다. 초투자율, 자기 유도는 소결 온도가 1030 .deg. C에서 1050 .deg. C로 증가함에 따라 증가하였고 Q factor와 보자력은 감소하였다. 보자력과 큐리온도는 각각 0.17 Oe 및 220 .deg. C 근처로 모든 시편들에서 거의 비슷하였다. 본 시편의 사용 주파수 범위는 0.4 ~ 20 MHz로 확인되었으며, 소결 온도 1050 .deg.C와 기본 조성 N $i_{0.14}$Z $n_{0.64}$C $u_{0.22}$F $e_{2}$ $O_{4}$ 에서 다른 사람들 보다 더욱 더 우수한 자기유도값(B, $B_{m}$ )을 얻을 수 있었다.

• 한국진공학회:학술대회논문집
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• 한국진공학회 2012년도 제42회 동계 정기 학술대회 초록집
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• pp.377-377
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• 2012

Microprocessor technology now relies on copper for most of its electrical interconnections. Because of the high diffusivity of copper, Atomic layer deposition (ALD) $TaN_x$ is used as a diffusion barrier to prevent copper diffusion into the Si or $SiO_2$. Another problem with copper is that it has weak adhesion to most materials. Strong adhesion to copper is an essential characteristic for the new barrier layer because copper films prepared by electroplating peel off easily in the damascene process. Thus adhesion-enhancing layer of cobalt is placed between the $TaN_x$ and the copper. Because, cobalt has strong adhesion to the copper layer and possible seedless electro-plating of copper. Until now, metal film has generally been deposited by physical vapor deposition. However, one draw-back of this method is poor step coverage in applications of ultralarge-scale integration metallization technology. Metal organic chemical vapor deposition (MOCVD) is a good approach to address this problem. In addition, the MOCVD method has several advantages, such as conformal coverage, uniform deposition over large substrate areas and less substrate damage. For this reasons, cobalt films have been studied using MOCVD and various metal-organic precursors. In this study, we used $C_{12}H_{10}O_6(Co)_2$ (dicobalt hexacarbonyl tert-butylacetylene, CCTBA) as a cobalt precursor because of its high vapor pressure and volatility, a liquid state and its excellent thermal stability under normal conditions. Furthermore, the cobalt film was also deposited at various $H_2/NH_3$ gas ratio(1, 1:1,2,6,8) producing pure cobalt thin films with excellent conformality. Compared to MOCVD cobalt using $H_2$ gas as a reactant, the cobalt thin film deposited by MOCVD using $H_2$ with $NH_3$ showed a low roughness, a low resistivity, and a low carbon impurity. It was found that Co/$TaN_x$ film can achieve a low resistivity of $90{\mu}{\Omega}-cm$, a low root-mean-square roughness of 0.97 nm at a growth temperature of $150^{\circ}C$ and a low carbon impurity of 4~6% carbon concentration.

• 헤리티지:역사와 과학
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• 제45권3호
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• pp.212-223
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• 2012

고대부터 회화 장신구 장식품 무기 일상용품 등에 사용된 안료는 시대 제작기법 문화이동을 확인할 수 있는 중요한 물질로, 우리나라에서는 1963년부터 분석을 통해 안료의 성분을 확인하였으며 최근에는 휴대용형광X선분석기를 사용하여 안료에 손상을 주지 않고 성분분석을 실시하여 고대 안료 물질을 밝히는 연구가 활발히 진행 중에 있다. 그러나 이러한 단편적인 연구로는 시대별, 지역별 안료의 쓰임 및 사용시기를 파악할 수 없기 때문에 안료에 대한 종합적이고 체계적인 연구가 필요한 실정이다. 따라서 이 연구는 조성시기가 전해지는 불국사 대웅전 석가모니후불탱화의 안료를 과학적으로 분석하여 사용안료를 밝히는 한편, 시대와 지역이 비슷한 조선시대 불화 안료와 비교 분석하고자 하였다. 성분분석 결과와 기존의 연구자료를 종합해본 결과, 불국사 대웅전 석가모니후불탱화는 연백을 이용해 배채하였으며, 채색안료로는 연백, 주사, 연단, 구리 화합물인 석록(혹은 동록, 녹염동광), 철산화물인 석간주 및 금분 등을 이용하여 색을 표현한 것으로 판단된다. 불국사 대웅전 석가모니후불탱화에 사용된 안료들은 전통안료를 혼합하여 사용된 것으로 추정되나 모든 안료에 대해 결정구조를 분석한 것이 아니므로 명확히 판단하기는 어렵다. 이러한 결과를 통해 향후 회화 안료의 성분 및 제작특성, 특히 조선시대 불화의 안료에 대한 기초자료로 활용될 것으로 판단된다.

• 자원환경지질
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• 제47권4호
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• pp.335-349
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• 2014

선캄브리아기 경기육괴의 북서부에 위치한 포천 스카른 광상은 명성산 화강암과 선캄브리아기 변성퇴적암류에 협재된 탄산염암의 접촉대를 중심으로 산출되며, N-S방향 전단대를 따라 배태되고 있다. 포천 스카른대 분포와 함께 광물학적 특성은 구조 규제와 암층 규제에 따라 유도되었다. 포천 스카른은 스카른 광물조합에 따라 백운암을 교대한 Na-Ca계열과 Mg계열 스카른 및 석회암을 교대한 Ca계열 스카른으로 구분된다. 철광화작용은 주로 Na-Ca계열 스카른대를 따라 배태되고 있으며, 후퇴 스카른 단계에 일부 동 광화작용이 중첩된다. Na-Ca계열 스카른은 주로 추휘석, 투휘석, 조장석, 석류석, 자철석, 매그헤마이트, 경석고, 인회석, 스핀의 공생관계를 보이며, 후퇴 스카른에서는 투각섬석, 금운모, 녹렴석, 견운모, 석고, 녹니석, 석영, 방해석, 황화광물로 구성된다. 한편 Mg계열 스카른은 주로 감람석과 투휘석의 단순한 광물조합을 보이며, 투휘석과 감람석은 투각섬석과 함께 소량 금운모, 사문석, 녹니석으로 교대된다. 반면에 Ca계열 스카른은 전진 스카른 단계에서 주로 단사휘석, 석류석, 규회석이 정출되며, 후퇴 스카른에서 녹렴석, 베수비아나이트, 각섬석, 흑운모, 녹니석, 자철석, 석영, 방해석, 황화광물이 수반된다. 전자현미분석 결과에 의하면 포천 스카른광물은 대부분 Na-Mg 성분이 부화되었으며, 높은 $Fe^{3+}/Fe^{2+}$비, $Mg^{2+}/Fe^{2+}$비, $Al^{3+}/Fe^{2+}$비의 조성 특징을 보인다. 즉 단사휘석은 추휘석과 투휘석 조성이 부화되어 있는 반면, 석류석은 상대적으로 그로슐라 조성이 부화된 경향을 보인다. 또한 각섬석은 투각섬석, 파가사이트, Mg-헤이스팅사이트로 조성변화를 보인다. 한편 전진 스카른 단계의 주요 광물조합은 약 0.5 kbar와 $X(CO_2)=0.10$ 조건에서 $400^{\circ}{\sim}500^{\circ}C$ 온도와 높은 산화 환경($fO_2=10^{-23}{\sim}10^{-26}$)을 지시하고 있다. 후퇴 스카른 단계에서는 물-암석반응이 증가됨에 따라 녹렴석, 베수비아나이트, 각섬석, 녹니석, 석영, 방해석은 $X(CO_2)=0.10$ 조건에서 $250^{\circ}{\sim}400^{\circ}C$ 온도 범위에서 정출되었다.

• Ocean and Polar Research
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• 제26권2호
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• pp.231-243
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• 2004

Sequential extraction was carried out on twenty two subsamples of three ferromanganese crusts from three seamounts (Lemkein, Lomilik, and Litakpooki) near the Marshall Islands in the western Pacific. The extraction was designed to fractionate Fe-Mn crust forming elements into low defined groups: (1) exchangeable and carbornate, (2) Mn-oxide, (3) Fe-oxyhyd.oxide, and (4) residual fraction. X-ray diffraction result shows that target material were well removed by each extraction step except for CFA in phosphatized crusts generation. According to chemical analysis of each leachate, most of elements in the Fe-Mn crusts are bound with two major phases. Mn, Ba, Co, Ni, Zn, (Fe, Sr, Cu, and V) are strongly bounded with Mn-oxide $({\delta}-MnO_2)$ phase, whereas Fe, Ti, Zr, Mo, Pb, Al, Cu,(V, P, and Zn) show chemical affinity with Fe-oxyhydroxide phase. This result indicates that significant amount of Al, Ti, and Zr can not be explained by detrital origin. Ca, Mg, K, and Sr mainly occur as exchangeable elements and/or carbonate phase. Outermost layer 1 and inner layer 2 which are both young crusts generations are similar in chemical speciations of elements. However, some of Fe-oxyhydroxide bounded elements (Pb, Y, Mo, Ba, Al, and V) in phosphatized innermost layer 3 are released during phosphatization and incorporated into phosphate (Pb, Y, Mo, and Ba) or Mn-oxide phase (Al and V). Our sequential extraction results reveal that chemical speciations of elements in the hydrogenetic crusts are more or less different from interelemental relationship calculated by statistical method based on bulk chemistry.

• Asian Journal of Atmospheric Environment
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• 제6권2호
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• pp.83-95
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• 2012

China has been a top producer and exporter of refined lead products in the world since the year 2000. After the phasing-out of leaded gasoline in the late 1990s, non-ferrous metallurgy and coal combustion have been identified as potential major sources of aerosol lead in China. This paper presents the single particle analytical results of ambient aerosol particles collected near a lead smelter using a scanning electron microscopy- energy dispersive x-ray spectroscopy (SEM-EDX). Aerosol particle samples were collected over a 24-hour period, starting from 8 pm on 31 May 2002, using a high volume TSP sampler. For this near source sample, 73 particles among 377 particles analyzed (accounting for 19.4%) were lead-containing particles mixed with other species (S, Cl, K, Ca, and/or C), which probably appeared to be from a nearby lead smelter. Lead-containing particles of less than $2{\mu}m$ size in the near source sample were most frequently encountered with the relative abundances of 42%. SEM-EDX analysis of individual standard particles, such as PbO, PbS, $PbSO_4$, $PbCl_2$, and $PbCO_3$, was also performed to assist in the clear identification of lead-containing aerosol particles. Lead-containing particles were frequently associated with arsenic and zinc, indicating that the smelter had emitted those species during the non-ferrous metallurgical process. The frequently encountered particles following the lead-containing particles were mineral dust particles, such as aluminosilicates (denoted as AlSi), $SiO_2$, and $CaCO_3$. Nitrate- and sulfate-containing particles were encountered frequently in $2-4{\mu}m$ size range, and existed mostly in the forms of $Ca(NO_3,SO_4)/C$, $(Mg,Ca)SO_4/C$, and $AlSi+(NO_3,SO_4)$. Particles containing metals (e.g., Fe, Cu, and As) in this near source sample had relative abundances of approximately 10%. Although the airborne particles collected near the lead smelter contained elevated levels of lead, other types of particles, such as $CaCO_3$-containing, carbonaceous, metal-containing, nitrates, sulfates, and fly-ash particles, showed the unique signatures of samples influenced by emissions from the lead smelter.