• 한국진공학회지
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• 제16권4호
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• pp.286-290
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• 2007

실리콘 기판위에 성장된 ZnO 나노막대에 NiO를 코팅하여 core-shell 형태의 나노막대를 제작하였다. 이렇게 제작된 나노막대를 수소 분위기에서 열처리한 결과 ZnO 나노막대 표면에 Ni 나노점들이 형성됨을 확인하였다. 이러한 여러 종류의 나노막대의 저온(5K)에서 광발광 (photoluminescence) 특성을 연구하였는데 $ZnO{\rightarrow}NiO-ZnO{\rightarrow}Ni$ 나노점-ZnO 순서로 시료가 변화함에 따라 속박된 exciton들의 전이 에너지와 진폭이 변화함을 확인하였다. ZnO에 비하여 NiO-ZnO 시료의 경우 받개에 속박된 exciton ($A^0X$) 전이가 크게 감소함을 보이나 Ni 나노점-ZnO 시료의 경우 $A^0X$ 전이가 가장 우세함을 보인다. 이러한 현상은 수소화 과정에서 침투한 Ni과 수소 이온이 주개로 작용하였기 때문이다.

• 한국세라믹학회지
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• 제28권4호
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• pp.305-314
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• 1991

This study was conducted to research the formation and the color development of NiO-ZnO-Fe2O3-TiO2-SnO2 system for the purpose of synthesizing the spinel pigments which are stable at high temperature. After preparing ZnO-Fe2O3 as a basic composition, {{{{ chi }}NiO.(l-{{{{ chi }})ZnO.Fe2O3 system, {{{{ chi }}NiO.(l-{{{{ chi }})ZnO.TiO2 system, and {{{{ chi }}NiO.(l-{{{{ chi }})ZnO.SnO2 system were prepared with {{{{ chi }}=0, 0.2, 0.5, 0.7, 1 mole ratio respectively. The manufacturing was carried out at 128$0^{\circ}C$ for 30 minutes. The reflectance measurement and the X-ray analysis of these specimens were carried out and the results were summarized as follows. 1. In the specimens which included NiO, it was difficult for the spinel structure to be formed. 2. As increasing the contents of NiO and Fe2O3, all the groups which were yellow or green colored changed to brown. 3. NiO-ZnO-Fe2O3 system and NiO-ZnO-TiO2 system formed the spinel structure and the illmenite structure appeared in NiO-TiO2 system.

• 한국세라믹학회지
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• 제14권3호
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• pp.187-192
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• 1977

For the purpose researching to the influence of tetrahedral and octahedral preference of cations of $Ni^{2+}$, $Ti^{4+}$ upon the formation and the color development of the $ZnO-SnO_2$ spinel containing $Ni^{2+}$ and $Ti^{4+}$ ions, the gradual substitution of $Ni^{2+}$ ions for $Zn^{2+}$ ions and of $Ti^{4+}$ ions for $Sn^{4+}$ ions of the spinel in NiO-ZnO-$SnO_2$-$TiO_2$ system was carried out. On samples prepared by calcining the oxide and basic cabonate mixtures at $1300^{\circ}C$ for 2 hours, the X-ray analysis, measurement of reflectance and the test of their stabilaity as a glaze pigment were also carried out. The results are summarized as follows 1) Single spinel was formed completely to x=1 in the $xNiO\cdot(2-x)ZnO\cdot{SnO}_2$system, and gave brilliant lightgreen hue. Moreover, $NiO\cdot{ZnO}\cdot{SnO}_2$ formed easily spinel than $NiO\cdot{MgO}\cdot{SnO}_2$ because Zn^{2+}$ ions had more strong tetrahedral preference than $Mg^{2+}$ ions. 2) As the gradual substitution of $Ti^{4+}$ ions for $Sn^{4+}$ ions in $NiO\cdot{MgO}\cdot{SnO}_2$ system, the spinels formed well and was nearly not changed in the hue. 3) The results of glaze test. (1) As the gradual substitution of $Ni^{2+}$ ions for $Zn^{2+}$ ions, the color changed from dull white to graish broun gradually in calcium-zinc glaze and calcium glaze, and from white to beige in tile glaze. (2) As the gradual substitution of $Ti^{4+}$ ions for $Sn^{4+}$ ions in $NiO-ZnO-SnO_2-TiO_2$ system, the color was become dull generally and was not change in tile glaze.

• 한국재료학회지
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• 제23권4호
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• pp.211-214
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• 2013

The effects of a Ni coating on the sensing properties of nano ZnO:Ni based gas sensors were studied for $CH_4$ and $CH_3CH_2CH_3$ gases. Nano ZnO sensing materials were prepared by the hydrothermal reaction method. The Ni coatings on the nano ZnO surface were deposited by the hydrolysis of zinc chloride with $NH_4OH$. The weight % of Ni coating on the ZnO surface ranged from 0 to 10 %. The nano ZnO:Ni gas sensors were fabricated by a screen printing method on alumina substrates. The structural and morphological properties of the nano ZnO : Ni sensing materials were investigated by XRD, EDS, and SEM. The XRD patterns showed that nano ZnO : Ni powders with a wurtzite structure were grown with (1 0 0), (0 0 2), and (1 0 1) dominant peaks. The particle size of nano ZnO powders was about 250 nm. The sensitivity of nano ZnO:Ni based sensors for 5 ppm $CH_4$ gas and $CH_3CH_2CH_3$ gas was measured at room temperature by comparing the resistance in air with that in target gases. The highest sensitivity of the ZnO:Ni sensor to $CH_4$ gas and $CH_3CH_2CH_3$ gas was observed at Ni 4 wt%. The response and recovery times of 4 wt% Ni coated ZnO:Ni gas sensors were 14 s and 15 s, respectively.

• E2M - 전기 전자와 첨단 소재
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• 제9권6호
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• pp.542-550
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• 1996

ZnO-based ceramic varistors containing NiO range 0.5 mol% to 4.0 mol% were fabricated by standard ceramic techniques. The influence of NiO on the microstructure and electrical behavior of ZnO varistor was investigated. As the content of NiO additive increases, average grain size decreased from 16.5.mu.m to 13.2.mu.m, and the amount of NiO existing in the grain interior and grain boundary region was approximately equal. NiO acted as an acceptor which decreases donor concentration due to the increase of Zn vacancy in the grain, and as a driver which migrates Zn interstitial in the depletion region toward the interface of grain boundary, which resulted in the decrease of interface state density. As a result, increasing the content of NiO additive, barrier height, nonlinear exponent, and varistor voltage decreased, and leakage current increased. Wholly, the physical and electrical properties of the ZnO varistor can be said to be affected by the NiO additive.

• 한국자기학회지
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• 제5권3호
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• pp.191-196
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• 1995

고상반응법에 의해 NiCuZn ferrite를 제조하였으며 소결온도 $900^{\circ}C$에서의 조성 및 공정변화에 따른 특성을 검토하였다. NiCuZn ferrite에서 Cu 치환 첨가량과 (Ni+Cu)/Zn의 조성비를 변화시킨 결과 ${(Ni_{0.2}Cu_{0.2}Zn_{0.6}O)}_{1.02}{(Fe_{2}O_{3})}_{0.98}$의 조성을 가질 때 초기투자율이 가장 높게 나타났다. NiCuZn ferrite의 Curie 온도 ($T_{c}$)는 Cu의 치환 첨가량이 증가함에 따라 점차 감소하였으며, Cu의 함량을 고정하고 Ni의 함량을 변화시킬 경우, (Ni+Cu)/Zn의 조성비가 증가할 수록 현저하게 증가하였다. ${(Ni_{0.2}Cu_{0.2}Zn_{0.6}O)}_{1-w}{(Fe_{2}O_{3})}_{1+w}$의 조성에서 분쇄시간을 20~80시간으로 변화시켰을 경우 $Fe_{2}O_{3}$ 결핍량(w)이 -0.015일 때 초기투자율이 가장 높았으며, Curie 온도 ($T_{c}$)는 $Fe_{2}O_{3}$ 결핍량(w)이 0에서 -0.025로 증가할 수록 점차 감소하였다.

• 청정기술
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• 제21권1호
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• pp.39-44
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• 2015

본 연구에서는 다섯 종의 씨앗(춘채, 아욱, 양배추, 배추, 당근)을 이용하여 금속산화물 나노입자(CuO, NiO, Fe₂O₃, Co₃O₄, TiO₂, ZnO)들이 씨앗발아와 발아지수에 미치는 영향을 조사하였다. CuO, ZnO, NiO 나노입자는 씨앗 활성에 뚜렷한 독성 영향을 나타내었으며, 나노입자종류에 따라 상이한 민감도를 나타내었다. 각 나노입자에 대한 독성순서(EC₅₀ 범위)는 다음과 같다: CuO 6~27 mg/L > ZnO 16~86 mg/L > NiO 48~112 mg/L. 나머지 조사 대상 나노입자인 Co₃O₄, TiO₂, Fe₂O₃은 최대 1,000 mg/L 높은 농도 노출에도 뚜렷한 영향을 나타내지 않았다. 씨앗별 상이한 민감도를 나타내었으며, 가장 민감한 종인 아욱의 씨앗발아 EC₅₀은 CuO 5.5 mg/L ZnO 16.4 mg/L, NiO 53.4 mg/L로 조사되었다. 씨앗별 나노입자에 대한 독성 영향은 CuO > ZnO > NiO > Fe₂O₃ ≈ Co₃O₄ ≈ TiO₂ 나타났으나, 당근씨앗은 NiO [EC₅₀ 80.4(71.41~90.54) mg/L]와 ZnO [EC₅₀ 85.8(69.31~106.29) mg/L]가 유사한 독성을 나타내었다.

• 한국자기학회지
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• 제5권1호
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• pp.15-20
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• 1995

연자성재료인 Mn-Zn 페라이트에 미량의 첨가물로 CaO(0.1 mol%), NiO(0.0~6.0 mol%) 그리고 CoO(0.0~0.8 mol%) 첨가하여 20 종류의 시료를 공침법으로 제조하여, 첨가물의 첨가량에 따른 Mn-Zn 페라이트의 자기적 성질을 연구하였다. NiO, CoO의 첨가량이 증가함에 따라 초기투자율은 감소하고, 반면 Curie 온도는 증가하였다. 보자력$(H_{c})$, 포화자화$(B_{s})$ 및 자기이력손실$(W_{h})$은 NiO의 첨가량이 증가함에 따라 증가하는 것으로 나타났다.

• 한국자기학회지
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• 제7권1호
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• pp.19-24
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• 1997

적층형 chip inductor 소재인 NiCuZn ferrite의 제조 공정 조건 및 조성을 선정하였다. NiCuZn ferrite의 NiO 함량이 증가할 수록 저온 소결에 필요한 Fe$_{2}$O$_{3}$ 결핍량은 점차 증가하였고, NiO 함량과 Co$_{3}$O$_{4}$ 첨가량을 변화하여 투자율을 12 ~ 562 범위에서 제어할 수 있었다. NiCuZn ferrite의 투자율이 562에서 60으로 변화함에 따라서 Q$_{max}$ 주파수는 3 MHz에서 50 MHz 범위로 제어할 수 있었다. 이때 Q$_{max}$ 주파수(Y)와 투자율(X)은 log Y = 4.2-1.4 log X의 상관관계를 나타내었다.

• 한국세라믹학회지
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• 제34권10호
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• pp.1074-1082
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• 1997

Microstructure and permeability as a function of sintering temperature and composition were studied on the Ni$\delta$Cu0.4-$\delta$Zn0.6Fe2O4 ($\delta$=0, 0.1, 0.2, 0.3, 0.4) which was prepared by Cu2+ substitution for Ni2+ in Ni.0.4Zn0.6Fe2O4, then followed by 8 wt% CuO and 1wt% Bi2O3 as sintering aids. It was found that NiCuZn ferrite in which Cu2+ is substituted for Ni2+ is more effective in reduction of sintering temperature than Ni.0.4Zn0.6Fe2O4, containing CuO as a sintering aid. The specimen $\delta$=0.2 sintered at 90$0^{\circ}C$ for 2hr exhibited the highest initial permeability value ($\mu$o=280 at 1Mhz), but the real permeability decreased at the frequency under 10 MHz. EPMA analysis showed that Ni$\delta$Cu0.4-$\delta$Zn0.6Fe2O4 ($\delta$=0.4), sintered at 95$0^{\circ}C$ for 2hrs consisted of three phase regions of Ni.0.3Cu0.1Zn0.6Fe2O4 region, Cu and Bi liquid existed at the 3-point boundary, although the stabilization energy of Ni2+ is higher than that of Cu2+ in B site.