• Title/Summary/Keyword: $LiTaO_3$

Search Result 154, Processing Time 0.024 seconds

A Study on Electrooptic Guided-Wave TE-TM Mode Converter (전기광학효과를 이용한 광도파로형 TE-TM 모드 변환기에 관한 연구)

  • Hong Sik Jung
    • Journal of the Korean Institute of Telematics and Electronics A
    • /
    • v.30A no.2
    • /
    • pp.29-35
    • /
    • 1993
  • A guided-wave TE to TM mode converter was demonstrated by using of the off-diagonal electrooptic coefficients in LiTaO$_{3}$. The input mode is coupled to the other orthogonal mode by the electrooptically induced off-diagonal polarizability. Compared with LiNbO$_{3}$, LiTaO$_{3}$ provides a smaller birefringence and thus a larger phase match period and larger optical bnadwidth. A novel electrode structure allowed a first-order Bragg-coupling phase matching. TE/TM mode conversion efficiency of 90% at 25 [V] was demonstrated with ${\lambda}$=0.63$\mu$m He-Ne laser.

  • PDF

Strain characteristics and electrical properties of [Li0.055(K0.5Na0.5)0.945](Nb1-xTax)O3 ceramics

  • Lee, Jong-Kyu;Cho, Jeng-Ho;Kim, Byung-Ik;Kim, Eung Soo
    • Journal of Ceramic Processing Research
    • /
    • v.13 no.spc2
    • /
    • pp.341-345
    • /
    • 2012
  • [Li0.055(K0.5Na0.5)0.945](Nb1-xTax)O3 (0.05 ≤ x ≤ 0.25) ceramics were prepared by the partial sol-gel (PSG) method to improve the microstructure homogeneity of Ta5+ ion and were compared to those prepared by the conventional mixed oxide (CMO) method. For the PSG method, Ta(OC2H5)5 was directly reacted with calcined [Li0.055(K0.5Na0.5)0.945]NbO3 powders and the specimens sintered at 1100 ℃ for 5 hrs showed a single phase with a perovskite structure. Compared to the specimens prepared by conventional mixed oxide powders, the relative ratio of tetragonal phase to orthorhombic phase of the sintered specimens prepared by Ta(OC2H5)5 was larger than that of the sintered specimens prepared by Ta2O5. The electromechanical coupling factor (kp), piezoelectric constant (d33) and dielectric constant (εr) of the sintered specimens were increased with Ta5+ content. These results could be attributed to the decrease of the orthorhombic-tetragonal polymorphic phase transition temperature (To-t), which could be evaluated by oxygen octahedral distortion. Strain of the sintered specimens prepared by the PSG method was higher than that of specimens prepared by the CMO method due to the increase of relative density. The effects of crystal structure on the strain characteristics of the specimens were also discussed.

Enhanced Piezoelectric Properties of (1-x)[0.675BiFeO3-0.325BaTiO3]-xLiTaO3 Ternary System by Air-Quenching

  • Akram, Fazli;Malik, Rizwan Ahmed;Lee, Soonil;Pasha, Riffat Asim;Kim, Myong Ho
    • Korean Journal of Materials Research
    • /
    • v.28 no.9
    • /
    • pp.489-494
    • /
    • 2018
  • Lead free $(1-x)(0.675BiFeO_3-0.325BaTiO_3)-xLiTaO_3$ (BFBTLT, x = 0, 0.01, 0.02, and 0.03, with 0.6 mol% $MnO_2$ and 0.4 mol% CuO) were prepared by a solid state reaction method, followed by air quenching and their crystalline phase, morphology, dielectric, ferroelectric and piezoelectric properties were explored. An X-ray diffraction study indicates that lithium (Li) and tantalum (Ta) were fully incorporated in the BFBT materials with the absence of any secondary phases. Dense ceramic samples (> 92 %) with a wide range of grain sizes from $3.70{\mu}m$ to $1.82{\mu}m$ were obtained in the selected compositions ($0{\leq}x{\leq}0.03$) of BFBTLT system. The maximum temperatures ($T_{max}$) were mostly higher than $420^{\circ}C$ in the studied composition range. The maximum values of maximum polarization ($P_{max}{\approx}31.01{\mu}C/cm^2$), remnant polarization ($P_{rem}{\approx}22.82{\mu}C/cm^2$) and static piezoelectric constant ($d_{33}{\approx}145pC/N$) were obtained at BFBT-0.01LT composition with 0.6 mol% $MnO_2$ and 0.4 mol% CuO. This study demonstrates that the high $T_{max}$ and $d_{33}$ for BFBTLT ceramics are favorable for industrial applications.

Dynamic Pyroelectric Properties and Their Frequency Dependences of $LiTaO_3$ Crystal ($LiTaO_3$ crystal의 dynamic 초전특성과 그 주파수의 의존성)

  • Lee, Won-Jae;Kang, Seong-Jun;Joung, Yang-Hee;Yoon, Yung-Sup
    • Journal of the Institute of Electronics Engineers of Korea SD
    • /
    • v.37 no.8
    • /
    • pp.35-41
    • /
    • 2000
  • The frequency dependence of the pyroelectric characteristics of $LiTaO_3$ have been investigated by using the dynamic method. In the frequency range between 2 and 1000 Hz, they are measured in both the regimes of pyroelectric current ($R_L=1M{\Omega}$) and pyrelectric voltage ($R_L=17.3G{\Omega}$), which can be selected by adjusting the value of the load resistance. Pyroelectric coefficient depending on the voltage response in the regime of pyroelectric current shows the maximum value of $1.56{\times}10^{-8}C/cm^2{\cdot}K$ at 40 Hz. The maximum values of figures of merits for the voltage response and for the detectivity are measured as $10.8{\times}10^{-11}C{\cdot}cm/J$ and $13{\times}10^{-7}C{\cdot}cm/J$, respectively. The voltage responsivity depending on the voltage response in the regime of pyroelectrci voltage shows the maximum value of 488 V/W at 2 Hz. Noise equivalent power and detectivity shows the minimum value of $3.95{\times}10^{-10}W/{\sqrt}Hz$ and maximum value of $5.6{\times}10^8cm{\cdot}{\sqrt}Hz/W$ at 40 Hz, respectively.

  • PDF

Electrical Properties of lead free (Na,K,Li)(Nb,Sb,Ta)O3 Ceramics with MnO2 Addition (MnO2 첨가량에 따른 비납계 (Na,K,Li)(Nb,Sb,Ta)O3 세라믹스의 전기적특성)

  • Lee, Seung-Hwan;Nam, Sung-Pill;Lee, Dong-Hyun;Lee, Sung-Gap;Lee, Sang-Chul;Lee, Young-Hie
    • The Transactions of The Korean Institute of Electrical Engineers
    • /
    • v.60 no.4
    • /
    • pp.801-804
    • /
    • 2011
  • Electrical properties and microstructure were investigated on the effects of $MnO_2$ and the lead-free $(Na_{0.44}K_{0.52}Li_{0.04})(Nb_{0.83}Sb_{0.07}Ta_{0.1})O_3$ ceramics with the addition of $MnO_2$ were fabricated by a conventional mixed oxide method. A gradual change in the crystal and microstructure was observed with the increase of $MnO_2$ addition. For the NKN-LST-xmol%$MnO_2$ sintered at $1100^{\circ}C$, bulk density increased with the addition of $MnO_2$ and showed maximum value at addition 1.0mol% of $MnO_2$. Curie temperature of the NKN-LST ceramics slightly decreased with adding $MnO_2$. The dielectric constant, piezoelectric constant ($d_{33}$) and electromechanical coupling factor ($k_p$) increased below 0.25mol% of $MnO_2$ addition, which might be due to the increase in density. The high piezoelectric properties = 145 pC/N, electromechanical coupling factor = 0.421 and dielectric constant = 2883 were obtained for the NKN-LST-0.25mol%$MnO_2$ sintered at $1100^{\circ}C$ for 4h.

Dielectric and Piezoelectric Properties of [Li0.04(Na0.5K0.5)0.96](Nb0.86Ta0.10Sb0.04)O3 Ceramics Doped with SrO (SrO의 첨가에 따른 [Li0.04(Na0.5K0.5)0.96](Nb0.86Ta0.10Sb0.04)O3세라믹스의 유전 및 압전 특성)

  • Park, Min-Ho;Yoo, Ju-Hyun
    • Journal of the Korean Institute of Electrical and Electronic Material Engineers
    • /
    • v.25 no.3
    • /
    • pp.198-203
    • /
    • 2012
  • In this study, $[Li_{0.04}(Na_{0.5}K_{0.5})_{0.96}](Nb_{0.86}Ta_{0.10}Sb_{0.04})O_3+xSrO$ (x=0, 0.0025, 0.005, 0.0075) ceramics were synthesized by the conventional mixed oxide method. The X-ray diffraction patterns demonstrated that ceramics possessed single perovskite structure. The SEM images indicate that microstructure can be obviously affected by a small amount of added SrO. The phase transition temperature tetragonal-cubic($T_c$) and orthorhombic-tetragonal($T_{o-t}$) shifts downward and upward with the increase of Sr addition, respectively. The excellent piezoelectric properties of $d_{33}=170[pC/N]$, $k_p=0.37$, $Q_m=64.12$, $T_{o-t}=153^{\circ}C$ and $T_c=370^{\circ}C$ were obtained from the 0.25 mol% Sr added ceramics sintered at $1,120^{\circ}C$ for 1 h.

Fractionation and Rare-Element Mineralization of Kenticha Pegmatite, Southern Ethiopia (에티오피아 남부 켄티차 페그마타이트의 분화양상과 희유원소 광화작용)

  • Kim, Eui-Jun;Kim, Soo-Young;Moon, Dong-Hyeok;Koh, Sang-Mo
    • Economic and Environmental Geology
    • /
    • v.46 no.5
    • /
    • pp.375-390
    • /
    • 2013
  • The Kenticha rare-element (Ta-Li-Nb-Be) mineralized zone is located in ophiolitic fold and thrust complex of southern Ethiopia and was firstly discovered by joint exploration program of Ethiopia-Soviet in 1980s. It includes Dermidama, Kilkele, Shuni Hill, Kenticha, and Bupo pegmatites from south to north. The Kenticha pegmatite intruded parallel to NS-striking serpentinite and talc-chlorite schist, and is exposed approximately 2 km length and 400-700 m width. The Kenticha pegmatite is internally zoned and subdivided into lower quartz-muscovite-albite granite, intermediate muscovite-quartz-albite-microcline pegmatite, and upper spodumene-quartz-albite pegmatite, based on their mineral assemblage. The major, trace elements (e.g., Rb, Li, Nb, Ta, and Ga), and element ratios (e.g., K/Rb, Nb/Ta, Mg/Li, and Al/Ga) suggest that the fractionation and solidification of pegmatite have progressed from the lower towards upper pegmatite. In contrast, unlike general magmatic fractionation, Mg/Li ratios of the Kenticha pegmatite tend to be increased towards the upper pegmatite. It may result from post-magmatic hydrothermal alteration and/or interaction with upper ultramafic rock. Rare-element mineralization in Kenticha pegmatite concentrates on the upper pegmatite, which contains up to 3.0 wt % $Li_2O$, 3,780 ppm Rb, 111 ppm Cs, 1,320 ppm Ta, and 332 ppm Nb. Ore minerals in Kenticha pegmatite mostly include tantalite, spodumene, and lepidolite, and tantalite has an association with coarser quartz-spodumene and relatively fine sacchroidal albite. The tantalite is classified into Mn-tantalite as a function of $Mn^*[Mn/(Mn+Fe)]$ and $Ta^*[Ta/(Ta+Nb)]$ values. Its compositions ($Mn^*$, $Ta^*$, and Nb/Ta) between coarse and fine tantalites are different and the former is strongly enriched in Ta and depleted in Nb compared to latter one. In conclusion, rare-element mineralization in the Kenticha pegmatite may has occurred in the latest stage of magmatic fractionation.

Electrical properties of lead free (Na,K,Li)(Nb,Sb,Ta)$O_3$ ceramics with $MnO_2$ addition ($MnO_2$ 첨가량에 따른 비납계 (Na,K,Li)(Nb,Sb,Ta)$O_3$ 세라믹스의 전기적특성)

  • Lee, Seung-Hwan;Nam, Sung-Pill;Lee, Sung-Gap;Shin, Dong-Jin;Lee, Young-Hie
    • Proceedings of the KIEE Conference
    • /
    • 2011.07a
    • /
    • pp.1487-1488
    • /
    • 2011
  • Electrical properties and microstructure were investigated on the effects of $MnO_2$ and the lead-free $(Na_{0.44}K_{0.52}Li_{0.04})(Nb_{0.83}Sb_{0.07}Ta_{0.1})O_3$ ceramics with the addition of $MnO_2$ were fabricated by a conventional mixed oxide method. A gradual change in the crystal and microstructure was observed with the increase of $MnO_2$ addition. For the NKN-LST-xmol%$MnO_2$ sintered at $1100^{\circ}C$, bulk density increased with the addition of $MnO_2$ and showed maximum value at addition 1.0mol% of $MnO_2$. Curie temperature of the NKN-LST ceramics slightly decreased with adding $MnO_2$. The dielectric constant, piezoelectric constant ($d_{33}$) and electromechanical coupling factor ($k_p$) increased below 0.25mol% of $MnO_2$ addition, which might be due to the increase in density. The high piezoelectric properties = 145 pC/N, electromechanical coupling factor = 0.421 and dielectric constant = 2883 were obtained for the NKN-LST-0.25mol%$MnO_2$ sintered at $1100^{\circ}C$ for 4h.

  • PDF

Dielectric and Piezoelectric Properties of Environmantal Friendly(Li0.04(Na0.56K0.44)0.96(Nb0.9Ta0.10)0.998Zn0.005O3 Ceramics for Energy Harvesting Devices (에너지수확소자용 친환경 (Li0.04(Na0.56K0.44)0.96(Nb0.9Ta0.10)0.998Zn0.005O3 세라믹스의 유전 및 압전 특성)

  • Sin, Sang-Hoon;Yoo, Ju-Hyun
    • Journal of the Korean Institute of Electrical and Electronic Material Engineers
    • /
    • v.26 no.5
    • /
    • pp.355-359
    • /
    • 2013
  • In this paper, the $0.995(Li_{0.04}(Na_{0.56}K_{0.44})_{0.96}(Nb_{0.90}Ta_{0.10})_{0.998}Zn_{0.005}O_3+0.005KNbO_3+xwt%\;TeO_2$ lead-free piezoelectric ceramics for energy harvesting devices were fabricated by the conventional mixed oxide method. The microstructure, dielectric, and piezoelectric properties were investigated as a function of the $TeO_2$ addition. All the specimens showed an orthorhombic phase structure. At the composition ceramics doped with 0.1 wt%$TeO_2$, the optimum values of $d_{33}$= 212 pC/N, $d_{33}{\cdot}g_{33}=9.54pm^2/N$, and kp=0.448 were obtained, respectively. The results indicate that the composition ceramics is a promising candidate for energy harvesting devices applications.

Preparation and Characterization of Ta-substituted Li7La3Zr2-xO12 Garnet Solid Electrolyte by Sol-Gel Processing

  • Yoon, Sang A;Oh, Nu Ri;Yoo, Ae Ri;Lee, Hee Gyun;Lee, Hee Chul
    • Journal of the Korean Ceramic Society
    • /
    • v.54 no.4
    • /
    • pp.278-284
    • /
    • 2017
  • In this work, Ta-substituted $Li_7La_3Zr_{2-x}O_{12}$ (LLZTO) powder and pellets with garnet cubic structure were fabricated and characterized by modified and optimized sol-gel synthesis. Ta-substituted LLZO powder with the smallest grain size and pure cubic structure with little pyrochlore phase was obtained by synthesis method in which Li and La sources in propanol solvent were mixed together with Zr and Ta sources in 2-methoxy ethanol. The LLZTO pellets made with the prepared powder showed cubic garnet structure for all conditions when the amount of Li addition was varied from 6.2 to 7.4 mol. All the X-ray peaks of the pyrochlore phase disappeared when the Li addition was increased above 7.0 mol. When the final sintering temperature was varied, the LLZTO pellet had a pyrochlore-mixed cubic phase above $1000^{\circ}C$. However, the surface morphology became much denser when the final sintering temperature was increased. The sol-gel-driven LLZTO pellet with a sintering temperature of $1100^{\circ}C$ showed a lithium ionic conductivity of 0.21 mS/cm when Au was adopted as electrode material for the blocking capacitor. The results of this study suggest that modified sol-gel synthesis is the optimum method to obtain cubic phase of LLZTO powder for highly dense and conductive solid electrolyte ceramics.