• 한국세라믹학회지
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• 제43권1호
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• pp.10-15
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• 2006

Photoluminescence (PL) and crystal structures of the $(l-x)CaWO_4-xLi_2WO_4$ binary system added with $Eu_2O_3$ activator have been characterized. The $CaWO_4\;and\;Li_2WO_4$ have the scheelite and phenakite structures respectively. The $CaWO_4-Li_2WO_4-Eu_2O_3$ phosphors show the red luminescence of 613 nm peak wavelength. The wavelength range of excitation spectral band is $380\~470$ nm with the peak wavelength of 397 nm. The $0.88(0.5CaWO_4-0.5Li_2WO_4)-0.12Eu_2O_3$ showed the most superior luminescence characteristics. The effect of co-doping elements such as $Al_2O_3$ and rare-earth oxides on PL has been characterized. The co-doping elements deteriorated the luminescence intensity except the $Al_2O_3$ and $Gd_2O_3$. The PL characteristics of $CaWO_4-Li_2WO_4-Eu_2O_3$ phosphors have been compared to those of the alkali europium double molybdates (tungstates) of scheelite-related structure such as $LiEu(MoO_4)_2$ and $CsEu(MoO_4)_2$. The crystal structures of $(l-y)[(l-x)CaWO_4-xLi_2WO_4]-yEu_2O_3$ phosphors have been characterized using XRD data and rietveld refinement.

• 한국전기전자재료학회:학술대회논문집
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• 한국전기전자재료학회 2003년도 하계학술대회 논문집 Vol.4 No.1
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• pp.131-134
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• 2003

[ $ZnWO_4$ ] shows excellent frequency selectivity due to its high quality factor($Q{\times}f$) at microwave frequencies. However, in order to use $ZnWO_4$ as multilayered wireless communication components, its other properties such as sintering temperature($1050^{\circ}C$), ${\tau}_f$ ($-70ppm/^{\circ}C$) and ${\varepsilon}_r(15.5)$ should be modified. In present study, $TiO_2$ and LiF were used to improve the microwave dielectric and sintering properties of $ZnWO_4$. $TiO_2$ additions to $ZnWO_4$ changed ${\tau}_f$ from negative to positive value, and also increased ${\varepsilon}_r$ due to its high ${\tau}_f$ ($+400ppm/^{\circ}C$) and ${\varepsilon}_r$(100). At 20 mol% $TiO_2$ addition, ${\tau}_f$ was controlled to near zero $ppm/^{\circ}C$ with ${\varepsilon}_r=19.4$ and $Q{\times}f=50000GHz$. However, the sintering temperature was still high to $1100^{\circ}C$. LiF addition to the $ZnWO_4+TiO_2$ mixture was greatly reduced the sintering temperature from $1100^{\circ}C$ to $850^{\circ}C$ due to liquid phase formation. Also LiF addition decreased the ${\tau}_f$ value due to its high negative ${\tau}_f$ value. Therefore, by controlling the $TiO_2$ and LiF amount, temperature stable LTCC material in the $ZnWO_4$-TiO_2-LiF$ system could be fabricated.

• 한국산학기술학회논문지
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• 제4권4호
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• pp.341-345
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• 2003

ZnWO₄는 높은 품질계수에 의해 주파수 선택성이 뛰어나지만 다층형태의 고주파 무선부품으로의 응용을 위해서는 높은 소결온도(1100℃), 큰 음의 공진주파수 온도계수(-70ppm/℃), 낮은 유전율(15.5) 등에 대한 보정이 필요하다. 본 연구에서는 ZnWO₄에 TiO₂및 LiF를 첨가하여 ZnWO₄의 저손실특성을 유지하면서 주파수 온도안정성 및 저온소결성을 부여하고자 하였다. 큰 양의 공진주파수 온도계수(＋400ppm/℃) 및 유전율(100)을 갖는 TiO₂의 첨가는 공진주파수 온도계수를 음의 값에서 양의 값으로 변화시켰으며 유전율의 증가를 가져왔다. TiO₂를 20 mol％ 첨가한 경우 공진주파수 온도계수가 0에 가깝고 유전율 19.4에 품질계수 50000㎓의 특성을 얻을 수 있었으나 소결온도는 1100℃로 높은 소결온도를 보였다. ZnWO₄에 TiO₂가 첨가된 혼합체에 LiF의 첨가는 액상형성에 의해 소결온도를 1100℃에서 850℃로 크게 저하시킬 수 있었다. LiF는 첨가는 LiF 자체의 큰 공진주파수 온도계수에 의해 온도계수를 음의 값으로 변화시켰다. 따라서 TiO₂및 LiF의 적당량의 첨가는 온도 안정성을 갖는 저손실 ZnWO₄-TiO₂-LiF 계 LTCC(Low Temperature Confined Ceramics) 소재를 제조할 수 있었다.

• 마이크로전자및패키징학회지
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• 제10권2호
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• pp.13-17
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• 2003

본 연구에서는 $ZnWO_4-LiF$계를 이용하여 RF모듈 구현을 위한 새로운 조성의 LTCC 소재를 개발하고자 하였다. 순수 $ZnWO_4$의 경우 98% 이상의 상대밀도를 얻기 위해서는 $1050^{\circ}C$이상의 소결온도가 필요하였고 소결체의 고주파유전특성은 유전율($\epsilon_r$) 15.5, 품질계수($Q{\times}f0$) 74000 GHz, 공진주파수 온도계수$(\tau_f)-70ppm/^{\circ}C$이었다. $ZnWO_4$에 LiF의 첨가는 상호 반응에 의해 $810^{\circ}C$ 부근에서 액상을 형성하였고 따라서 0.5에서 1.5 wt%의 LiF의 첨가로 $ZnWO_4$를 $820^{\circ}C$에서 치밀화를 얻을 수 있었다. 주어진 LiF의 첨가범위에서 소결 수축률은 LiF 량의 증가와 함께 증가하였다. LiF의 첨가는 LiF 자체의 낮은 유전율에 의해 유전율을 15.5에서 14.2∼15의 범위로 감소시켰으며 품질계수($Q{\times}f0$)도 LiF와 $ZnWO_4$의 반응 및 미세구조의 불균일화로 LiF의 첨가량의 증가와 함께 낮아지는 경향을 보였다.

• 한국재료학회지
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• 제17권8호
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• pp.442-446
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• 2007

Microwave dielectric properties of $0.85CaWO_4-0.15LnNbO_4$ (Ln = La, Sm) ceramics were investigated as a function of the sintering temperature and $Li_2WO_4$ content from 0.8 wt.% to 1.5 wt.%. A single phase with tetragonal scheelite structure was obtained at a given composition ranges. For the specimens with $Li_2WO_4$, the sintering temperature could be effectively reduced from $1150^{\circ}C$ to $900^{\circ}C$ due to the enhancement of sinterability. Dielectric constant (K) of the specimens with $LaNbO_4$ and $SmNbO_4$ was increased with the increase of sintering temperature and/or $Li_2WO_4$ content. However, K of the specimens with $LaNbO_4$ was higher than that of $SmNbO_4$ due to the larger dielectric polarizability $(\alpha)$ of $LaNbO_4$ ($18.08{\AA}$) than that of $SmNbO_4$ ($16.75{\AA}$). With an increase of $Li_2WO_4$ content, Qf value of the specimens with $SmNbO_4$ was decreased, while that of the specimens with $LaNbO_4$ was increased. Temperature coefficient of resonant frequency (TCF) was increased with the increase of $Li_2WO_4$ content.

• 한국전기전자재료학회:학술대회논문집
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• 한국전기전자재료학회 2002년도 하계학술대회 논문집 Vol.3 No.2
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• pp.541-544
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• 2002

In this study, a new LTCC material using $ZnWO_4$-LiF system was attempted with respect to use as a capacitor layer in Front-End Module. Pure $ZnWO_4$ must be sintered above $1050^{\circ}C$ in order to obtain up to 98% of full density. It's measured dielectric constant, quality factor, and temperature coefficient of resonant frequency were 15.5, 74380GHz, and $-70ppm/^{\circ}C$, respectively. LiF addition resulted in an liquid phase formation at $810^{\circ}C$ due to interaction between $ZnWO_4$ and LiF. Therefore $ZnWO_4$ with 0.5~1.5wt% LiF could be densified at $850^{\circ}C$. Addition of LiF slightly lowered the dielectric constant from 15.5 to 14.2~15. In the given LiF addition range, the sintering shrinkage increased with increasing LiF content. $Q{\times}fo$ value, however, decreased with increasing LiF content(or increasing densification). This is originated from the interaction between the liquid phase and $ZnWO_4$ and inhomogeneity of grain morphology.

• 한국결정성장학회지
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• 제23권3호
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• pp.142-145
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• 2013

The upconversion (UC) luminescence of $Li^+/Er^{3+}/Yb^{3+}$ co-doped $CaWO_4$ phosphors and effects of $Yb^{3+}$ concentration are investigated in detail. Single crystallized $CaWO_4$ : $Li^+/Er^{3+}/Yb^{3+}$ phosphor can be obtained, co-doped up to 35.0/5.0/30.0 mol% ($Li^+/Er^{3+}/Yb^{3+}$) by solid-state reaction. Under 980 nm excitation, $CaWO_4$ : $Li^+/Er^{3+}/Yb^{3+}$ phosphor exhibited strong green UC emissions visible to the naked eye at 530 and 550 nm induced by the intra 4f transitions of $Er^{3+}$ ($^4H_{11/2}$, $^4S_{3/2}{\rightarrow}^4I_{15/2}$). The optimum doping concentrations of $Yb^{3+}$ that would result in the highest UC luminescence were determined, and a possible UC mechanism that depends on the pumping power is discussed in detail.

• 한국세라믹학회지
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• 제22권3호
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• pp.72-76
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• 1985

Single crystals of the compound MeI $(LiMoO_4)$ and $Me^I(LiWO_4)$ ($Me^I=K$, Rb, Cs) were synthesized by slow evaporation from aqueous solution and bycooling from melt. The compounds of potassium or rubidium are hygroscopic and they form easily hydrated crystals $Me^I LiMoO_4$.$H_2O$ or $Me^ILiMoO_4$.$H_2O$ or $Me^ILiWO_4$.$H_2O$ from aqueous solution. The structures of these hydrated crystals are each other isotypic and they are built up of distorted layers of $(LiMoO_5)$ or $(LiWO_5)$. There exist two types of tetrahedral framework structures in this group of anhydrous molybdates and tung-states ; tridymite-type and cristobalite-type. $KLiMoO_4$ and $KLiWO_4$ have two types of polymorphic structures where as only the cristobalite-type is found in the Rb-and Cs-compounds. The system $KLiSO_4-KLiMoO_4$ was studied. Two components are almost immiscible but there eixst a narrow area of solid solution on the side of sulfate in the system.

• 한국재료학회:학술대회논문집
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• 한국재료학회 2006년도 춘계학술발표대회 및 제10회 신소재 심포지엄 논문개요집
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• pp.33.2-33.2
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• 2006

• 한국재료학회지
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• 제3권6호
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• pp.632-637
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• 1993

3000$\AA$~6000$\AA$의 두께로 진공 증착한 $WO_3$ 박막의 광특성 및 일렉트로크로미즘에 대하여 연구하였다. 증착된 $WO_3$ 박막은 모두 무색 투명 하였으며 X-선회절 분석결과 비정질 상태로 밝혀졌으며, 비정질 $WO_3$ 박막의 굴절율은 가시광선 영격에서 1.9-2.1로, 광에너지 gap은 3.25eV로 나타났다. ITO투명전극/$WO_3$박막/$LiCIO_4$ ~propylene carbonate/백금 대향전극 구조를 갖는 일렉트로크로믹소자를 구성하여 일렉트로크로믹 특성을 조사하였다. $WO_3$ 박막의 coloration/과 bleaching현상은 $LiCIO_{4}$~propylene carbonate유기전해질과 ITO투명전극으로 부터 $Li^{+}$이온과 전자의 이중주입에 의하여 청색으로 나타났으며, 가역적으로 전기 화학적인 산화반응에 의하여 bleaching현상이 일어났다. Coloration과 bleaching현상, 광학밀도, 구동전압 및 응답속도 등의 일렉트로크로믹 특성은 $WO_3$ 박막의 증착조건, 전해액 농도, 투명전극의 sheet resistance 인가전압에 크게 의존하는 것으로 밝혀졌다.