Organic-inorganic hybrid coating films have been used to increase the transmittance and enhance the physical properties of plastic substrates. Sol-gel organic-inorganic thin films were fabricated on polymethylmethacrylate (PMMA) substrates using a dip coater. Metal alkoxide precursor tetraethylsilicate (TEOS) and alkoxy silanes including decyltrimethoxysilane (DTMS), 3-glycidoxypropyltrimethoxysilane (GPTMS), phenyltrimethoxysilane (PTMS), 3-(trimethoxysilyl)propyl methacrylate (TMSPM) and vinyltrimethoxysilane (VTMS) were used to synthesize sol-gel hybrid coating solutions. Sol-gel synthesis was confirmed by the results of FT-IR. Cross-linking of the Si-O-Si network during synthesis of the sol-gel reaction was confirmed. The effects of each alkoxy silane on the coating film properties were investigated. All of the organicinorganic hybrid coatings showed improved transmittance of over 90 %. The surface hardness of all coating films on the PMMA substrate was measured to be 4H or higher and the average thickness of the coating films was measured to be about 500 nm. Notably, the TEOS/DTMS coating film showed excellent hydrophobic properties, of about 97°.

Various types of solidifying materials are used to stabilize and solidify low and intermediatelevel radioactive dispersible waste. Portland cement is generally used to solidify various radioactive wastes because its facilities and processes are simple, less dangerous, and it has excellent compressive strength after curing compared to other materials. However, it is difficult to use Portland cement in radioactive waste containing highly water-soluble harmful substances such as sodium fluoride because it is prone to leaching harmful ingredients in immersion tests due to its low water resistance. In this study, solidification was achieved using an organic-inorganic hybrid solidifying binders consisting of inorganic binders such as Portland cement, blast furnace slag powder, silica fume, and organic binders such as epoxy resin. This material was then compared with a solidification material made of Portland cement alone. The mixing ratio of inorganic binders, water, and organic binders to simulated waste is 35%, 20%, and 25%, respectively. The mixing ratio of inorganic binders and water when using only Portland cement for simulated waste is 100% and 80%, respectively. The mixed paste was poured into a cylinder mold (Φ 5 × 10 cm) to seal the upper part, cured at room temperature for 28 days to produce a solidification specimen, and then subjected to various tests were performed, including compressive strength, immersion compressive strength, hydration peak temperature, length change, and immersion weight change. The compressive strength of the organic-inorganic hybrid solidification test was 13-17 MPa, the immersion compressive strength was 15-18 MPa, the hydration peak temperature was 33-36°C, the length change rate was -0.086%, and the immersion weight change rate was –2.359%. The compressive strength of the Inorganic solidification test using only Portland cement was 16-18 MPa, the immersion compressive strength was 20-21 MPa, the hydration peak temperature was 23-25°C, the length change rate was -0.150%, and the immersion weight change rate was -5.213%. The compressive strength and immersion compressive strength of the organic-inorganic hybrid solidification materials were slightly lower compared to those of Portland cement solidification materials, they still met the compressive strength standard of 7-12 MPa, taking into consideration the strength reduce and economic feasibility of the core drill process. Furthermore, it indicates that the rates of change in length and immersion weight decreased to about 1% and 5%, suggesting an improvement in water resistance. The above results suggest that applying the organic-inorganic hybrid solidification method to radioactive waste treatment can effectively improve water resistance and help secure long-term stability.

휘어지며 투명한 전자기기의 개발을 위해서 최근 유기반도체, 탄소기반 나노소재, 금속산화물 반도체등의 다양한 신소재 반도체 개발에 대한 연구가 관심을 받으며 지속적으로 발전하고 있다. 그러나, 이러한 신소재 반도체 기술의 꾸준하고 지속적인 발전에도 불구하고 트랜지스터를 구성하는 주요 소재중 하나인 유전체에 대한 연구는 반도체의 개발속도에 크게 미치지 못하여, 기계적인 휘어짐의 특성을 갖추고, 높은 캐패시턴스와 좋은 누전전류 특성을 갖는 새로운 유전체 개발에 대한 요구가 지속적으로 커지고 있다. 이에 본 연구는 저전압에서 구동 가능한 박막트랜지스터를 위한 유기-무기 하이브리드소재 박막을 개발하며 이를 저전압 구동이 가능한 유기박막트랜지스터에 적용하였다. 상대적으로 높은 유전상수를 갖는 염화하프늄 (HfO2)과 소수성기를 갖고 있으며 금속산화물과 공유결합이 가능한 실란산 기반의 유기물 (octadecyltrimethoxysilane)을 혼합한 전구체 용액을 합성하며 상대적으로 낮은 온도에서 열처리를 통해 얻을 수 있었다. 제조된 하이브리드 게이트 유전체 박막은 우수한 절연 및 유전체 특성과 함께 소수성 표면 특성을 가질 수 있었고 펜타센 유기박막트랜지스터로 응용하여 저전압에서 구동이 되며 우수한 트랜지스터 성능을 갖는 소자를 개발하였다.

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 noctylamine 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).

Using UV nanoimprint lithography(UV-NIL), 1-dimensional(1-D) pattern structures were fabricated on a hybrid mixture thin film of lanthanum oxide and a UV-curable resin. 1-D pattern on a wafer fabricated by the laser interference lithography was transferred to polydimethylsiloxane and this is used as a mold of UV-NIL process. Conducting an X-ray photoelectron spectroscopy, C 1s and La 3d spectra were analyzed, and it was confirmed that hybrid thin film was successfully deposited on glass substrate. Also, transferred pattern structure was observed by using an atomic force microscopy. Through this, it was revealed that agglomerations between 1-D pattern were increased as UV irradiation time increased and this phenomenon disrupted the quality of NIL process. Additionally, liquid crystal(LC) cells with patterned hybrid thin films were fabricated and LC alignment performances were investigated. Using the polarizing optical microscopy and the crystal rotation method, LC alignment state and pretilt angles were observed. Consequently, the uniform homogeneous LC alignment was achieved at UV irradiation time of 1min and 3min where high resolution pattern transfer was observed.

Organic-inorganic hybrid perovskite nanocrystals have attracted a lot of attention owing to their excellent optical properties such as high absorption coefficient, high diffusion length, and photoluminescence quantum yield in optoelectronic applications. Despite the many advantages of optoelectronic materials, understanding on how these materials interact with their environments is still lacking. In this study, the fluorescence properties of methylammonium lead bromide (CH3NH3PbBr3, MAPbBr3) nanoparticles are investigated for the detection of volatile organic compounds (VOCs) and aliphatic amines (monoethylamine, diethylamine, and trimethylamine). In particular, colloidal MAPbBr3 nanoparticles demonstrate a high selectivity in response to diethylamine, in which a significant photoluminescence (PL) quenching (~ 100%) is observed at a concentration of 100 ppm. This selectivity to the aliphatic amines may originate from the relative size of the amine molecules that must be accommodated in the perovskite crystals structure with a narrow range of tolerance factor. Sensitive PL response of MAPbBr3 nanocrystals suggests a simple and effective strategy for colorimetric and fluorescence sensing of aliphatic amines in organic solution phase.

PURPOSES: This study aims to evaluate the resistance to chemical attack of combined organic and inorganic hybrid mortars as the repair materials (i.e., HRM mortar) used for concrete road facilities through a comparison with mortars made from cement repair materials (i.e., IRM mortar). METHODS: Inorganic materials used as a binder and two mineral fillers were adopted to produce HRM mortars. The ratio of the main resin versus the hardener was fixed at 2:1. For comparison, IRM mortars made of cement repair materials were also manufactured. The mortars were exposed to chemical solutions, such as NaCl, MgSO4, Na2SO4, and H2SO4, with the same concentration of 5% after 7 days of curing. The compressive strength, compressive strength loss, mass ratio, and relative bulk density of the mortar samples exposed to the chemical solutions were measured at predetermined periods. In addition, a scanning electron microscope observation was performed to evaluate the microstructures and the products formed by the chemical reaction of the mortar samples. RESULTS : As a result, the resistance to chemical attack of the HRM mortars was found to be much better than that of the IRM mortars, regardless of the types of attacking sources. This finding implies that HRM is a highly promising and versatile material because of its excellent resistance to chemical attack. CONCLUSIONS: The application of the combined organic and inorganic hybrid mortars is a possible option for repair of concrete road facilities exposed to aggressive environments.

Titanium dioxide (TiO2) is a typical inorganic material that has an excellent photocatalytic property and a high refractive index. It is used in water/air purifiers, solar cells, white pigments, refractory materials, semiconductors, etc.; its demand is continuously increasing. In this study, anatase and rutile phase titanium dioxide is prepared using hydroxyl and carboxyl; the titanium complex and its mechanism are investigated. As a result of analyzing the phase transition characteristics by a heat treatment temperature using a titanium complex having a hydroxyl group and a carboxyl group, it is confirmed that the material properties were different from each other and that the anatase and rutile phase contents can be controlled. The titanium complexes prepared in this study show different characteristics from the titania-formation temperatures of the known anatase and rutile phases. It is inferred that this is due to the change of electrostatic adsorption behavior due to the complexing function of the oxygen sharing point, which crystals of the TiO6 structure share.

PURPOSES: The objective of this study is to evaluate the durable performance of combined organic and inorganic hybrid mortar as repair material (HRM mortar) for concrete road facilities via comparison with that of cement repair materials (IRM mortar). METHODS : To produce HRM mortars, inorganic materials as binder and 2 mineral fillers were adopted. The ratio of main resin versus hardener was fixed at 1:2. For comparison, IRM mortars made with cement repair materials were also manufactured. Compressive, flexural, and bonding strengths were measured at predetermined periods. For durability assessment, the scaling resistance, freezing & thawing resistance, rapid chloride penetration resistance, and acid attack resistance of those mortars were experimentally monitored. RESULTS: The durability performances of HRM mortars, especially with respect to freezing & thawing, rapid chloride penetration and acid attack, were identified to be much better than those of IRM mortars. This result implies that HRM is a highly promising and versatile material because of its excellent durability. CONCLUSIONS: It is concluded that the application of the combined organic and inorganic hybrid mortars is possibly an option for the repair of concrete road facilities exposed to aggressive environments.

A flexible piezoelectric energy harvester(f-PEH) that converts tiny mechanical and vibrational energy resources into electric signals without any restraints is drawing attention as a self-powered source to operate flexible electronic systems. In particular, the nanocomposites-based f-PEHs fabricated by a simple and low-cost spin-coating method show a mechanically stable and high output performance compared to only piezoelectric polymers or perovskite thin films. Here, the non-piezoelectric polymer matrix of the nanocomposite-based f-PEH is replaced by a P(VDF-TrFE) piezoelectric polymer to improve the output performance generated from the f-PEH. The piezoelectric hybrid nanocomposite is produced by distributing the perovskite PZT nanoparticles inside the piezoelectric elastomer; subsequently, the piezoelectric hybrid material is spin-coated onto a thin metal substrate to achieve a nanocomposite-based f-PEH. A fabricated energy device after a two-step poling process shows a maximum output voltage of 9.4 V and a current of 160 nA under repeated mechanical bending. Finite element analysis(FEA) simulation results support the experimental results.

To abate the problem of odor from restaurants, a hybrid adsorbent consisting of organic and inorganic materials was developed and evaluated using acetaldehyde as a model compound was deveioped and evaluated. Powders of activated carbon, bentonite, and calcium hydroxide were mixed and calcinated to form adsorbent structure. The surface area of the hybrid adsorbent was smaller than that of high-quality activated carbon, but its microscopic image showed that contours and pores were developed on its surface. To determine its adsorption capacity, both batch isotherm and continuous flow column experiments were performed, and these results were compared with those using commercially available activated carbon. The isotherm tests showed that the hybrid adsorbent had a capacity 40 times higher than that of the activated carbon. In addition, the column experiments revealed that breakthrough time of the hybrid adsorbent was 2.5 times longer than that of the activated carbon. These experimental results were fitted to numerical simulations by using a homogeneous surface diffusion model (HSDM); the model estimated that the hybrid adsorbent might be able to remove acetaldehyde at a concentration of 40 ppm for a 5-month period. Since various odor compounds are commonly emitted as a mixture when meat is barbecued, it is necessary to conduct a series of experiments and HSDM simulations under various conditions to obtain design parameters for a full-scale device using the hybrid adsorbent.

PURPOSES : The objective of this study is to evaluate the performance of combined organic and inorganic hybrid mortar used as repair materials (UM mortar) for concrete road facilities by comparison with cement repair materials (RM mortar). METHODS: In order to produce UM mortar, four different levels of inorganic materials were adopted and the ratio of main resin to hardener was fixed at 1:2. For comparison, RM mortar made with cement repair materials was also produced. Fluidity, strength characteristics, length change, and freezing-thawing resistance of the mortars were measured at the predetermined periods. In addition, the microstructures of the mortars was performed on the 28-day mortar samples to examine the properties of the interfacial transition zone (ITZ). RESULTS : It was observed that the mechanical properties, except for compressive strength, and freezing-thawing resistance of UM mortars were much better than those of RM mortar. Furthermore, showing a densified ITZ properties on the UM mortars from the microstructural observation, the usage of UM mortars exhibited a beneficial effect on the enhancement of mortar properties. CONCLUSIONS: It is concluded that the application of combined organic and inorganic hybrid mortars is a possible option for the repair of deteriorated concrete road facilities.

최근 우수한 유연성과 화학적 안정성 등을 가진 고분자 수지와 우수한 기계적 성질 등을 나타내는 무기 재료로 이루어진 나노 복합 시스템으로써 유-무기 하이브리드 코팅 필름에 관한 연구가 활발히 진행되고 있다. 아크릴레이트 단량체로써 사용된 o-phenylphenoxyethyl acrylate (OPPEA)는 1.576의 높은 굴절률을 나타내고, Bisphenol A ethoxylate diacrylate (BAEDA)는 굴절률은 낮지만 경화된 고분자의 경도를 향상시킨다. 또한, 무기 소재로써 사용된 지르코니아는 산화지르코늄으로써 우수한 내구성과 광학특성 등을 나타낸다. 본 연구에서는 광학 특성을 향상시키기 위한 목적으로 아크릴레이트 단량체 중 BAEDA의 함량을 조절하여 필름을 제조한 뒤 연필 경도계와 아베굴절계를 이용하여 광학 특성 변화를 확인하였고, UV-vis spectrophotometer을 이용해 투과도를 비교하여 최적의 조건을 확립하였다. 그리고 실란 커플링제인 γ-methacryloxypropyltrimethoxysilane (MPS)를 사용하여 지르코니아를 소수화 처리하여 아크릴레이트 단량체에 대한 분산성을 향상시키고, 개질 전후의 물에 대한 분산성 변화를 조사하여 물에 대한 친화력이 감소하였음을 확인하였고, FT-IR ATR spectrophotometer를 통해 MPS에 의해 도입된 1716 cm-1에서의 에스터 C=O 결합 peak의 존재를 통해 MPS에 의한 지르코니아 표면의 개질 반응이 진행되었음을 확인하였다. 또한, 지르코니아의 표면에 도입된 규소 원자의 존재는 X 선 형광법을 이용하여 확인하였다. 그리고 화학적으로 개질된 지르코니아를 아크릴레이트 단량체에 도입하여 광경화 필름을 제조하였을 때, 굴절률은 아크릴레이트 자체 필름보다 1.2% 향상되었음을 확인하였고, SEM/EDS mapping 분석을 통해 PET 필름에 코팅된 개질 후 지르코니아가 아크릴레이트 코팅층에 균일하게 분포되어 있음을 알 수 있었다.

백색을 띄고 물리적·화학적으로 안정한 지르코니아는 열전도도가 낮고 강도와 인성, 내식성이 우수하여 단열재, 내화물과 같은 고온 재료와 각종 산업용 구조세라믹스에 사용되고 있다. 이러한 지르 코니아를 낮은 경도 및 굴절률 등과 같은 단점을 가진 고분자 코팅제에 도입하게 되면 화학적, 전기적, 광학적인 특성이 향상된다. 이와 같이 유기 소재에 무기 소재를 혼합하여 사용하는 유-무기 하이브리드 코팅을 목적으로 본 연구에서는 지르코니아 표면에 trimethylchlorosilane(TMCS)과 hexamethyldisilazane(HMDZ)을 사용하여 실릴화반응을 통한 -CH3기를 도입하여 소수성을 나노지르코 니아 표면에 도입하였다. 소수화된 지르코니아 표면에서의 TMCS와 HMDZ에 의해 도입된 Si-CH3의 존재는 FT-IR ATR spectroscopy를 통해 확인하였고, silicon 원소의 존재를 FE-SEM/EDS와 ICP-AES 를 통해 확인하였다. 또한, 개질 전후의 지르코니아를 아크릴레이트 단량체에 분산하여 침강속도를 확인 하여 분산성이 향상되는 것을 확인하였다. 지르코니아 입자의 크기 및 분포는 입도 분석기를 통해 확인 하였으며, BET 분석을 통해 개질 반응 전후의 비표면적은 18 m2/g 정도로 큰 변화가 없었다.

Transparent organic-inorganic hybrid hard coating films were prepared by the addition of SiO2 or ZrO2, as an inorganic filler to improve the hardness property, filler was highly dispersed in the acrylic resin. To improve the compatibility in the acrylic resin, SiO2 or ZrO2 is surface-modified using various silanes with variation of the modification time and silane content. Depending on the content and kind of the modified inorganic oxide, transparent modified inorganic sols were formulated in acryl resin. Then, the sols were bar coated and cured on PET films to investigate the optical and mechanical properties. The optimized film, which has a modified ZrO2 content of 4 wt% markedly improved in terms of the hardness, haze, and transparency as compared to neat acrylate resin and acrylate resin containing modified SiO2 content of 8 wt%. Meanwhile, the low transparency and high haze of these films slowly appeared at SiO2 content above 10 wt% and ZrO2 content of 5 wt%, but the hardness values were maintained at 2H and 3H, respectively, in comparison with the HB of neat acrylate resin.