• Journal of the Korean Physical Society
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• 제73권11호
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• pp.1716-1724
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• 2018

Single crystal of organic lead halide ($CH_3NH_3PbX_3$; $CH_3NH^+_3$ = methylammonium (MA), $X=Cl^-$, $Br^-$, $I^-$) is the best candidate for material intrinsic property studies due to no grain boundary and high crystal quality than the film having a lot of grain boundary and surface defects. The representative crystallization methods are inverse temperature crystallization (ITC) and anti-solvent vapor assisted crystallization (AVC). Herein, we report bandgap modulated organic lead halide single crystals having a bandgap ranging from ~ 2.1 eV to ~ 3 eV with ITC and AVC methods. The bandgap modulation was achieved by controlling the solvents and chloride-to-bromide ratio. Structural, optical and compositional properties of prepared crystals were characterized. The results show that the crystals synthesized by the two crystallization methods have similar properties, but the halide ratios in the crystals synthesized by the AVC method are controlled more quantitatively than the crystals synthesized by ITC.

• 한국재료학회지
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• 제31권9호
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• pp.496-501
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• 2021

Metal halide perovskite nanocrystals, due to their high absorption coefficient, high diffusion length, and photoluminescence quantum yield, have received significant attention in the fields of optoelectronic applications such as highly efficient photovoltaic cells and narrow-line-width light emitting diodes. Their energy band structure can be controlled via chemical exchange of the halide anion or monovalent cations in the perovskite nanocrystals. Recently, it has been demonstrated that chemical exfoliation of the halide perovskite crystal structure can be achieved by addition of organic ligands such as n-octylamine during the synthetic process. In this study, we systematically investigated the quantum confinement effect of methylammonium lead bromide (CH₃NH₃PbBr₃, MAPbBr₃) nanocrystals by precise control of the crystal thickness via chemical exfoliation using n-octylammonium bromide (OABr). We found that the crystalline thickness consistently decreases with increasing amounts of OABr, which has a larger ionic radius than that of CH₃NH₃⁺ ions. In particular, a significant quantum confinement effect is observed when the amounts of OABr are higher than 60 %, which exhibited a blue-shifted PL emission (~ 100 nm) as well as an increase of energy bandgap (~ 1.53 eV).

• EDISON SW 활용 경진대회 논문집
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• 제4회(2015년)
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• pp.378-381
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• 2015

To produce low cost and efficient photovoltaic cells, inorganic-organic lead halide perovskite materials appear promising for most suitable solar cells owing to their high power conversion efficiency. Most recent research showes that formamidinium lead iodide ($FAPbI_3$) with methylammonium lead bromide ($MAPbBr_3$) improves the power conversion efficiency of the solar cell to more than 18 per cent under a standard illumination because incorporated $MAPbBr_3$ makes $FAPbI_3$-relatively unstable but comparatively narrow band gap-more stable composition. In respect to first principle study, we investigated band gap of $MAPbI_3$, $FAPbI_3$, $MAPbBr_3$, $(FAPbI_3)_{0.89}-(MAPbBr_3)_{0.11}$ and 0.615(eV), 0.466, 1.197, 0.518 respectively through EDISON DFT software. These results emphasize enhancing structure stability is important factor as well as finding narrow band gap.

• Advances in nano research
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• 제13권2호
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• pp.187-197
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• 2022

The synthesis of organic and hybrid organic-inorganic perovskites directly from solution improves the cost- and energy-efficiency of processing. To date, numerous research efforts have been devoted to investigating the influence of the various solvent parameters for the synthesis of lead halide perovskites, focused on the effects of different single solvents on the efficiency of the resulting perovskites. In this work, we investigated the effect of solvent blends for the first time on the structure and phase of perovskites produced via the Lewis base vapor diffusion method to develop a new synthetic approach for water-stable CsPbBr₃ particles with nanometer-sized dimensions. Solvent blends prepared with DMF and water-miscible solvents with different Gutmann's donor numbers (D_N) affect the Pb ions differently, resulting in a variety of lead bromide species with various colors. The use of a DMF/isopropanol solvent mixture was found to induce the formation of the Ruddlesden-Popper perovskite based on lead bromide. This perovskite undergoes a blue color shift in the solvated state owing to the separation of nanoplatelets. In contrast, the replacement of isopropanol with DMSO, which has a high DN, induces the formation of spherical CsPbBr₃ perovskite nanoparticles that exhibit green emission. Finally, the integration of acetone in the solvent system leads to the formation of lead bromide complexes with a yellow-orange color and the perovskite CsPbBr₃.

• Electronic Materials Letters
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• 제14권6호
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• pp.657-668
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• 2018

Organic-inorganic hybrid lead halide perovskites have been extensively investigated for various optoelectronic applications. Particularly, owing to their ability to form highly crystalline and homogeneous films utilizing low-temperature solution processes (< $150^{\circ}C$), perovskites have become promising photoactive materials for realizing high-performance flexible solar cells. However, the current use of mesoporous $TiO_2$ scaff olds, which require high-temperature sintering processes (> $400^{\circ}C$), has limited the fabrication of perovskite solar cells on flexible substrates. Therefore, the development of a low-temperature processable charge-transporting layer has emerged as an urgent task for achieving flexible perovskite solar cells. This review summarizes the recent progress in low-temperature processable electron- and hole-transporting layer materials, which contribute to improved device performance in flexible perovskite solar cells.

• Bulletin of the Korean Chemical Society
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• 제11권2호
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• pp.109-114
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• 1990

The anionic transition metal hydrides $(HW(CO)_4P(OMe)_3\;^-,\;HW(CO)_5\;^-,\;HCr(CO)_5\;^-,\;HFe(CO)_4\;^-)$ react with transition metal alkyl $(CpMo(CO)_3(CH_3)$ to yield $CH_4\;and\;CH_3CHO$ in addition to the inorganic products $(CpMo(Co)_3\;^-$, etc.). The reaction of these anionic metal hydrides with CpMo(CO)3{CH2CH(CH2)2} may lead to an elucidation of the reaction mechanisms involved; the organic product distributions are among $CH_4,\;CH_2\;=\;CHCH_2CH_3$, and $CH_3CH(CH_2)_2$, depending upon the anionic metal hydride used. These anionic metal hydrides also are reported to undergo a hydride-halide exchange reaction with organic halides; therefore, these similar reactions have been compared in terms of leaving group ability $(CpMo(CO)_3\;^-\;vs.\;Br^-)$ and the mechanistic pathways.

• 한국표면공학회지
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• 제52권2호
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• pp.90-95
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• 2019

Methylammonium lead bromide ($MAPbBr_3$) has attracted a lot of attention due to their excellent optoelectronic properties such as the compositional flexibility relevant to photoluminescence (PL) and UV-Vis absorbance spectrum, high diffusion length, and photoluminescence quantum yield (PLQY). Despite such advantages of organic-inorganic perovskite materials, more systematic study on manipulation of their optoelectronic properties in homo- or heterovalent metal ions doped halide perovskite nanocrystals is lacking. In this study, we systematically investigated the optical properties of colloidal $CH_3NH_3Pb_{1-x}Sn_xCl_{2x}Br_{3-2x}$ particles by addition of $SnCl_2$ into the typical methylammonium lead tribromide ($CH_3NH_3PbBr_3$) precursor solution. We found that only 1% addition of $SnCl_2$ shows a significant blue-shift from 540 nm to 420 nm in UV-Vis absorbance spectrum due to the strong quantum confinement effect. Furthermore, continuous blue-shift in photoluminescence spectra was observed as the amount of Cl increases. These experimental results provide new insights into the replacement of Pb within $MAPbBr_3$, required for the broadening of their application.

• 한국환경농학회지
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• 제10권1호
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• pp.1-10
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• 1991

자동차(自動車) 배기(排氣)가수에 포함(包含)된 연화합물(鉛化合物)의 배출(排出)에 의하여 오염(汚染)이 되었을 것으로 예상(豫想)되는 대구직할시(大邱直轄市)를 중심(中心)으로 경상북도(慶尙北道) 내(內)의 고속도로(高速道路) 및 주요국도변(主要國道邊)에 인접(隣接)한 18개(個) 지점(地點)을 선정(選定)하여 도로(道路)로부터 거리(距離)에 따른 답토양(畓土壤)에서 연오염도(鉛汚染度) 및 토양중(土壤中) 연화합물(鉛化合物)을 $KNO_3$침출성(浸出性)(치환태(置換態)), $Na_4P_2O_7$ 침출성(浸出性)(유기태(有機態)), EDTA 침출성(浸出性)(탄산태(炭酸態)) $NHO_3$ 침출성(浸出性)(황산태(黃酸態)), 비침출성(非浸出性)(부용태(不溶態))로 형태별(形態別) 분포(分布)를 조사(調査)한 결과(結果)는 다음과 같다. 1. 답토양중(畓土壤中) 평균(平均) 연함량(鉛含量)은 청도(淸道)에서 30.0 ppm으로 가장 높았고 고령(高靈)에서 14.8 ppm으로 가장 낮았으며 평균(平均) 21.9 ppm 으로 나타났으며, 교통량(交通量)과 관련(關聯)하여 토양중(土壤中) 연함량(鉛含量)은 차이(差異)를 발견(發見)할 수 없었으나 도로(道路)의 개통년도(開通年度)에 따라 약간의 차이(差異)를 나타났다. 2. 도로(道路)로부터의 거리(距離)에 따른 연함량(鉛含量)은 10m 이내(以內)에서 22.2 ppm, 10∼30m에서 22.1 ppm, 30∼50m에서 22.2 ppm, 50m 이상(以上) 지역(地域)에서 21.3 ppm으로 도로(道路)로부터 거리(距離)에 따른 답토양중(畓土壤中)의 연오염도(鉛汚染度)는 크게 차이(差異) 나지 않았다. 3. 토양중(土壤中) 연화합물(鉛化合物)을 형태별(形態別)로 분별(分別) 추출(抽出)한 결과(結果) 여러 가지 토양특성(土壤特性)에 따라 차이(差異)가 심(深)하나 18개(個) 지점(地點)에서 평균(平均)한 연화합물(鉛化合物)의 화학적(化學的) 형태별(形態別) 분포비(分布比)는 유기태(有機態) 33.6%, 탄산태(炭酸態) 29.8%, 황산태(黃酸態) 21.5%, 치환태(置換態) 8.6% 및 부용태(不溶態) 6.7%의 순(順)으로 나타났다. 4. 토양중(土壤中) 유기물함량(有機物含量)이 증가(增加)할수록 유기태(有機態) 연(鉛)의 분포비(分布比)는 증가(增加)하는 경향(傾向)을 나타낸 반면 치환태(置換態) 연(鉛)의 분포비(分布比)는 감소(減少)하는 경향(傾向)을 나타내었다. 5. CEC가 증가(增加)할수록 유기태(有機態)의 연(鉛)의 분포비(分布比)는 증가(增加)하는 경향(傾向)을 나타낸 반면 치환태(置換態) 연의(鉛) 분포비(分布比)는 감소(減少)하는 경향(傾向)을 나타내었으며, CEC에 의(依)한 토양중(土壤中) 연화합물(鉛化合物)의 화학적(化學的) 형태별(形態別) 분포비(分布比)는 유기물(有機物)에 의(依)한 분포비(分布比)와 비슷한 경향(傾向)을 나타내었다.