• Bulletin of the Korean Chemical Society
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• 제18권9호
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• pp.972-976
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• 1997

Single phase ruthenium oxides with perovskite (ATi1-xRuxO3 (A=Ca, Sr)) and pyrochlore structure (Bi2Ru2O7, Pb2Ru2O6.5) have been prepared reproducibly by solid state reaction methods and their electrocatalytic activities for oxygen evolution have been examined by Tafel plots. Tafel slopes vary from a low value of 42 mV/decade up to 222 mV/decade at room temperature. The high exchange current densities and high Tafel slopes compared with those obtained from the RuO2 DSA electrode at the crystalline single phase metal oxide electrodes suggest that they are better electrocatalysts at low overpotentials. A favorable change in the Tafel slope for the oxygen evolution reaction occurs as the ruthenium content increases. Substitution of Ti for Ru in the perovskite solid solutions enhanced their chemical stability by losing marginal electrochemical activity.

• 대한화학회지
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• 제40권9호
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• pp.607-614
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• 1996

$ABO_3$계 perovskite 구조에서 A자리의 $Pb^{2+}$ 이온이 $Na^+La^{3+}$혼합 이온 으로 0-50mol.%치환된 $Pb_{1-x}(Na_12/La_12)_x(Mg_13/Nb_23/)O_3$ 화합물의 구조변화와 유전 성질을 X-선 회절법, 작외선과 라만 분광법, LCR meter등으로 연구하였다. $Na^+La^{3+}$혼합 이온의 치환량과 소결 온도가 증가함에 따라 perovskite 상의 양이 증가하였다. 치환량이 증가할 때 1:1 질서화에 의한 초격자선을 X-선 회절법으로 발견할수 없었지만, 라만 분광법과 이완성 매개변수의 증가로부터 A자리 양이온의 크기감소가 질서화에 영향을 미침을 알 수 있었다. Pb_{1-x}(Na_12/La_12)_x(Mg_13/Nb_23/)O_3$의 유전 성질은 perovskite 상의 양과 낟알 크기 및 밀도에 의해 영향을 받았고, 치환량이 증가할 때 상전이는 확산되었으며 상전이 온도는 감소하였다.

• 한국진공학회지
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• 제7권1호
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• pp.17-23
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• 1998

RF magnetron co-sputtering법으로 PFN[$Pb(Fe_{0.5}Nb_{0.5}O_3(PFN)$]박막을 제조한 후 급속 열처리(rapid thermal annealing, RTA)하여 XRD(s-ray diffractometer)를 통한 박막의 상변 태 및 전기적 특성에 대하여 연구하였다. $SiO_2$/Si, ITO/glass, 및 Pt/Ti/$SiO_2$/Si기판에 PFN 박막을 증착시켰다. 기판의 변화에 따른 증착된 PFN박막의 조성변화는 관찰할 수 없었다. ITO/glass기판을 사용한 경우와 $SiO_2$/Si기판을 사용하여 증착시킨 PFN박막의 결정구조를 분석한 결과 ITO/glass기판에 증착한 시편이 perovskite상으로의 결정화가 더욱 우세하였다. 이는$SiO_2$기판의 경우 Pb의 확산에 의해 결정화가 잘 되지 못하기 때문이다. Pt/Ti/$SiO_2$/Si 기판 위에 증착시킨 PFN박막의 경우 perovskite상과 pyrochlore상이 공존하였다. Perovskite 상으로의 상변태에 대한 중요한 변수로는 열처리 온도와 Pb의 함량인 것이 확인되었으며, Pb의 함량이 화학양론적 조성비에 비해 5-10%정도 과량일수록 perovskite상으로의 상변태 온도가 낮아지고 상전이 정도가 향상되는 것으로 나타났으며, 급속 열처리 후 XRD를 이용 한 결정성 분석결과를 통해 결정한 perovskite상으로의 상전이 최저온도는 $500^{\circ}C$였다. Pb/(Fe+Nb)의 조성비가 1.17인 경우의 박막을 질소 분위기 하에서 $600^{\circ}C$로 30초간 급속열 처리 하였을 때 낮은 누설 전류 값과 1kHz에서 88의 유전 상수 값, 2.0$\mu$C/$\textrm{cm}^2$의 잔류 분극 값과 144kV/cm의 항전계 값을 얻었다.

• 한국전기전자재료학회:학술대회논문집
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• 한국전기전자재료학회 1998년도 추계학술대회 논문집
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• pp.271-274
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• 1998

Metallic ferromagnet LA$_{1-x}$ Sr$_{x}$MnO$_3$ has received considerable attentions because of its metallic conductivity and giant magnetic resistivity. It is generally believed that layered perovskite SrO(LA$_{1-x}$ Sr$_{x}$MnO$_3$)$_{n}$ phase is insulating and shows no metallic transition. But recent report revealed that some single crystal SrO(LA$_{1-x}$ Sr$_{x}$MnO$_3$)$_{n}$ phase showed MR effect. In this study, layered perovskite SrO(LA$_{1-x}$ Sr$_{x}$MnO$_3$)$_2$ Phases were synthesized by solid state reaction at 140$0^{\circ}C$ in air atmosphere, for wide range of x and their phases were confirmed by X-ray diffraction. Electrical and magnetic properties were measured down to 10K and the possibility of MR effects was investigated.as investigated.

• 한국광물학회지
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• 제16권2호
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• pp.161-169
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• 2003

한성 비정질 투휘석$(Ca,Mg)SiO_3$에 대한 상변이 연구를 압력은 다이아몬드앤빌기기를 이용하여 ∼30 GPa까지, 온도는 약(YAG) 레이저 가열기기를 이용하여 ∼$1000^{\circ}C$에서 조사(scanning)하여 시행하였다. 비정질 투휘석은 고온-고압 하에서 곧바로 등축정계에 속하는 단상의 $(Ca,Mg)SiO_3$페롭스카이트 결정구조로 상변이 하였다. 이러한 결과는 고온-고압 하에서 사방정계에 속하는 $MgSiO_3$페롭스카이트 상과 등축정계에 속하는 $CaSiO_3$페롭스카이트 상으로 분리되는 상변이를 하는 결정질 투휘석의 상변이 계통과는 큰 차이를 보이고 있다. 이러한 차이는 출발시료의 차이점이나 특히 온도가 상변이에 큰 영향인자로 작용하여 기인한 것으로 판단된다. 이러한 강변이 관계는 맨틀의 온도, 압력 및 산소분압 차이 등에 의해 맨틀전이대나 하부맨틀을 구성하는 광물상의 조합에 영향을 줄 수 있다.

• 한국세라믹학회지
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• 제45권5호
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• pp.290-296
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• 2008

$AB'_{0.5}B"_{0.5}O_3$ type complex perovskite structures which have been reported as proton conductors over $600^{\circ}C$ were studied. The $AB'_{0.5}B"_{0.5}O_3$ type complex perovskite structure is known to be more easily synthesized and has better stability than normal $ABO_3$ perovskite structure. And it is stable at about $800^{\circ}C$ in the $CO_2$ atmosphere, whereas the $BaCeO_3$ perovskite is easily decomposed into carbonate. In addition, this $AB'_{0.5}B"_{0.5}O_3$ type complex perovskite structure could simply produce oxygen vacancies within their structure not by introducing additional doping oxides but by just controling the molar ratio of $B'^{+3}$ and $B"^{+5}$ metal ions in the B site. Hence it is easy to design the structure which shows highly sensitive electrical conductivity to humidity. In this study, the single phase boundary of $BaR_{0.5+x}Ta_{0.5-x}O_{3-{\delta}}$(R = rare earth) complex perovskite structures and it's phase stability were investigated with changes in composition, x. And the humidity dependance of electrical conductivity at different $P_{H2O}$ conditions was investigated.

• Bulletin of the Korean Chemical Society
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• 제34권7호
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• pp.2041-2043
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• 2013

A layered perovskite of Dion-Jacobson phase, $RbLaTa_2O_7$, was successfully exfoliated into colloidal suspension via successive ion-exchange and intercalation reaction. The pristine perovskite $RbLaTa_2O_7$ was synthesized by conventional solid-state reaction, and then, it was ion-exchanged with hydrochloric acid to obtain a protonic form of perovskite. The resulting proton-exchanged perovskite was reacted with ethylamine to increase interlayer spaces for further intercalation reaction. Finally, the ethylamine-intercalated form was exfoliated into nanosheets via an intercalation of bulky organic cations (tetrabutylammonium). According to X-ray diffraction (XRD) analysis, the TBA-intercalated form showed remarkably increased interlayer spacing (${\Delta}d$ = 1.67 nm) in comparison with that of the pristine material. Transmission electron microscopic image of exfoliated perovskite clearly revealed that the present exfoliated perovskite were composed of very thin layers. This exfoliated perovskite nanosheets could be applicable as building blocks for fabricating functional nanocomposites.

• 한국진공학회:학술대회논문집
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• 한국진공학회 2016년도 제50회 동계 정기학술대회 초록집
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• pp.427-427
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• 2016

Organic-inorganic hybrid perovskite have attracted significant attention as a new revolutionary light absorber for photovoltaic device due to its remarkable characteristics such as long charge diffusion lengths (100-1000nm), low recombination rate, and high extinction coefficient. Recently, power conversion efficiency of perovskite solar cell is above 20% that is approached to crystalline silicon solar cells. Planar heterojunction perovskite solar cells have simple device structure and can be fabricated low temperature process due to absence of mesoporous scaffold that should be annealed over 500 oC. However, in the planar structure, controlling perovskite film qualities such as crystallinity and coverage is important for high performances. Those controlling methods in one-step deposition have been reported such as adding additive, solvent-engineering, using anti-solvent, for pin-hole free perovskite layer to reduce shunting paths connecting between electron transport layer and hole transport layer. Here, we studied the effect of alkali metal halide to control the fabrication process of perovskite film. During the morphology determination step, alkali metal halides can affect film morphologies by intercalating with PbI2 layer and reducing $CH3NH3PbI3{\cdot}DMF$ intermediate phase resulting in needle shape morphology. As types of alkali metal ions, the diverse grain sizes of film were observed due to different crystallization rate depending on the size of alkali metal ions. The pin-hole free perovskite film was obtained with this method, and the resulting perovskite solar cells showed higher performance as > 10% of power conversion efficiency in large size perovskite solar cell as $5{\times}5cm$. X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), and inductively coupled plasma optical emission spectrometry (ICP-OES) are analyzed to prove the mechanism of perovskite film formation with alkali metal halides.

• 한국전기전자재료학회논문지
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• 제32권1호
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• pp.64-69
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• 2019

Methylammonium lead triiodide ($MAPbI_3$)-based perovskite solar cells potentially have potential advantages such as high efficiency and low-cost manufacturing procedures. However, $MAPbI_3$ is structurally unstable and has low phase-change temperatures ($30^{\circ}C$ and $130^{\circ}C$); it is necessary to solve these problems. We investigated the crystal structure and phase separation using real-time temperature-change X-ray diffraction, transmission electron microscopy, and electron energy loss spectroscopy. $MAPbI_3$ has a tetragonal structure, and at about $35^{\circ}C$ the c-axis contracts, transforming $MAPbI_3$ into the related cubic crystal structure. In addition, at $130^{\circ}C$, phase separation occurs in which $CH_3NH_2$ and HI at the center of the unit cell of the perovskite structure are extracted by gas, leavingand only $PbI_2$ of the three-component structure, is produced as the final solid product.

• 한국결정성장학회지
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• 제15권2호
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• pp.86-91
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• 2005

층상 구조의 유기-무기 페로브스카이트 복합 소재 $(C_nH_{2n+1}NH_3)_2CuC1_4$ (n=6, 8, 10, 12)을 합성하였다. $(C_nH_{2n+1}NH_3)_2CuC1_4$ 화합물에서 긴 사슬의 양성자화된 알킬 암모늄 이온은 기울어진 이중층의 구조로 $CuCl_6$ 팔면체의 구석을 공유하고 있는 페로브스카이트형의 층들 사이에의 삽입되었다. 페로브스카이트 층상 화합물에서의 3개의 고체상을 HT-XRD와 DSC를 사용하여 조사하였다. $(C_nH_{2n+1}NH_3)_2CuC1_4$ 화합물은 단계적인 층간거리의 증가와 함께 고체-고체 상전이 현상을 보여준다 3개의 다른 구조는 긴 사슬의 양성자화된 알킬 암모늄 이온의 형태 변화로 설명하였다.