Seawater evaporation and purification powered by solar energy are considered as a promising approach to alleviate the global freshwater crisis, and the development of photothermal materials with high efficiency is imminent. In this study, cellulose nanofiber (CNF)/MXene/Ni chain (CMN) aerogels were successfully synthesized by electrostatic force and hydrogen bond interaction force. CMN10 achieved a favorable evaporation rate as high as 1.85 kg m− 2 h− 1 in pure water, and the corresponding evaporation efficiency could be up to 96.04%. Even if it is applied to seawater with multiple interference factors, its evaporation rate can still be 1.81 kg m− 2 h− 1. The superior seawater evaporation activity origins from the promoted separation of photoexcited charges and photothermal conversion by the synergy of Ni chain and MXene, as well as the water transport channel supported by the 3D structure frame of CNF. Most importantly, CMN aerogel can maintain water vapor evaporation rates above 1.73 kg m− 2 h− 1 under extreme conditions such as acidic (pH 2) and alkaline (pH 12) conditions. In addition, various major ions, heavy metals and organic pollutants in seawater can be rejected by CMN10 during desalination, and the rejection rates can reach more than 99.69%, ensuring the purity of water resources after treatment. This work shows the great potential of CMN aerogel as a high-efficiency solar evaporator and low-cost photothermal conversion material. Cellulose nanofiber (CNF)/MXene/Ni chain (CMN) aerogels demonstrated high evaporation of water from sea water.

본 논문에서는 ~1.5 μm의 기공 크기를 가지는 고투과도 알파 알루미나 지지체 위에 도포된 서스펜션의 증발유도 자기조립 현상을 이용하여 중간층을 형성하는 새로운 코팅 방식을 소개한다. 새로운 코팅 방법으로 만들어진 중간층은 일반 적으로 사용되는 담지법으로 코팅된 중간층과 비교하여 표면거칠기와 불균일도가 낮아 코팅에 적합하였다. 복합막 지지체로 서의 평가를 위해 제조된 지지체는 감마 알루미나 복합막 제조에 사용되었다. 메조 기공을 가지는 감마 알루미나 복합막은 반복코팅 없이도 매크로 기공 크기의 결함이 존재하지 않았으며 일반적으로 널리 사용되는 100~200 nm의 기공 크기를 가지 는 지지체로부터 만들어진 같은 두께의 복합막과 비교하여 2.3배 이상의 높은 질소투과도를 보였다.

Vitamin A is essential for growth and differentiation of a number of cells and tissues, as result the precursor, a carotenoid β-carotene remains their essential source of vitamin A. However, the major problem this carotenoid face, is its susceptible to photodegradation and chemical oxidation, those properties make it difficult to use as an ingredient as functional food product and reduce its bioavailability. This study presents a novel approach to prepare a one-step inclusion complex using amylose microparticles as host molecule using amylosucrase from Deinococcus geothermalis (DGAS) and β-carotene nanoparticles, which were added into the DGAS enzyme reaction solution to entrap them during the synthesis of amylose chains. HRFE-SEM showing a spherical shape and average diameter of 4-8 μm; XRD and DSC showed an amorphous structure as well as less energy required to start the gelatinization process, due to the complexation of amylose chains with the β-carotene nano dispersion. Last but not least Raman spectroscopy was performed in order to confirmed the complex formation between β-carotene and amylose microparticles, showing the characteristic peaks of both compound. The stability test in this study showed the high stability of the complexed microparticles against environmental stresses such as, photodegradation and chemical oxidation. We expect this study contributes to the development of functional food materials to enhance the stability and bioavailability of active compounds.

Resveratrol was incorporated into various combinations of single- and double-layer nanoemulsions, prepared by selfassembly emulsification and complex coacervation with chitosan, alginate, and β-cyclodextrin, respectively. Resveratrol nanoemulsions were composed of medium-chain trigacylglycerols (MCTs), Tween ® 80, water, chitosan, alginate, and β-cyclodextrin. The corresponding mixtures were formulated for the purpose of being used as a nutraceutical delivery system. Resveratrol nanoemulsions were obtained with particle sizes of 10-800 nm, with the size variation dependent on the emulsification parameters including the ratio of aqueous phase and surfactant ratio. Resveratrol nanoemulsions were characterized by evaluating particle size, zeta-potential value, stability, and release rate. There were no significant changes in particle size and zeta-potential value of resveratrol nanoemulsions during storage for 28 days at 25°C. The stability of resveratrol in the double-layer nanoemulsions complexed with chitosan or β-cyclodextrin was higher, compared with the single-layer nanoemulsions.

Starch is an abundant, renewable, and low cost material that has been extensively studied for its role in crystallization. The aim of this study is to develop a convenient and green approach to synthesize starch nanoparticles (StNPs). Short glucan chains were successfully prepared by using pullulanase that could debranch the amylopectin obtained from waxy maize starch. StNPs were prepared via the self-association of short glucan chains, of which the crystallinity structure changed from A-type (native starch) to B-type (starch nanoparticles) through the enzymatic hydrolysis and reassembly process at 4°C. Scanning electron microscopy (SEM), X-ray diffraction (XRD), dynamic light scattering (DLS) and differential scanning calorimetry (DSC) were used to characterize the morphology and crystalline structure of StNPs. The results showed that the diameter of StNPs ranged from 300 nm to 1.5 μm, depending on the initial concentration of short glucan chains and self-assembly time. The developed approach could produce well-defined and uniform starch nanoparticles that could readily be employed to encapsulate various functional guest molecules in biocompatible starch based nanoparticles in food industry.

Self-assembled monolayers(SAM) of microspheres such as silica and polystyrene(PS) beads have found widespread application in photonic crystals, sensors, and lithographic masks or templates. From a practical viewpoint, setting up a highthroughput process to form a SAM over large areas in a controllable manner is a key challenging issue. Various methods have been suggested including drop casting, spin coating, Langmuir Blodgett, and convective self-assembly(CSA) techniques. Among these, the CSA method has recently attracted attention due to its potential scalability to an automated high-throughput process. By controlling various parameters, this process can be precisely tuned to achieve well-ordered arrays of microspheres. In this study, using a restricted meniscus CSA method, we systematically investigate the effect of the processing parameters on the formation of large area self-assembled monolayers of PS beads. A way to provide hydrophilicity, a prerequisite for a CSA, to the surface of a hydrophobic photoresist layer, is presented in order to apply the SAM of the PS beads as a mask for photonic nanojet lithography.

(PDDA/SiO2) thin films that consisted of positively charged poly (diallyldimethylammonium chloride) (PDDA) and negatively charged SiO2 nanoparticles were fabricated on a glass substrate by an applying voltage layer-by-layer (LBL) self-assembly method. In this study, the microstructure and optical properties of the (PDDA/SiO2) thin films coated on glass substrate were measured as a function of the applied voltage on the Pt electrodes. When 1.0 V was applied to a Pt electrode in a PDDA and SiO2 solution, the thickness of the (PDDA/SiO2)10 thin film increased from 79 nm to 166 nm. The surface roughness also increased from 15.21 nm to 33.25 nm because the adsorption volume of the oppositely charged PDDA and SiO2 solution increased. Especially, when the voltage was applied to the Pt electrode in the SiO2 solution, the thickness increase of the (PDDA/SiO2) thin film was larger than that obtained when using the PDDA solution. The refractive index of the fabricated (PDDA/SiO2) thin film was ca. n = 1.31~1.32. The transmittance of the glass substrate coated by (PDDA/SiO2)6 thin film with a thickness of 106 nm increased from ca. 91.37 to 95.74% in the visible range.

화장료의 UV 차단과 은폐효과를 갖는 이산화티탄을 사용하여 자기조직체 형성공법을 적용한 하이브리드 이산화티탄을 제조하고 형태, 성질, 공정의 최적조건과 자외선차단 개선을 확인하였다. 하이브리드 이산화티탄은 마이크로 이산화티탄(250~300nm)의 표면에 나노 이산화티탄(20~30nm)을 자기조직체 형성공법을 이용해 결합시킨, 이산화티탄 대 이산화티탄의 결합체를 말한다. 하이브리드 이산화티탄 제조의 최적조건을 알아내기 위해 (-)을 띄는 마이크로 이산화티탄의 표면에 양이온의 링크로써 AlCl3 를 농도별로 조정하고, 그에 따른 마이크로와 나노 이산화티탄의 투입비율을 달리하여 각각의 조건에서 만들어진 시료를 광학분석, 입도분석, 전위차분석 등을 이용해 확인하고 최적의 제조 조건을 알 수 있었다. 최적의 제조 조건에서 만들어진 하이브리드 이산화티탄의 자외선차단 상승효과를 확인하기 위하여 하이브리드 이산화티탄이 첨가된 화장료와 사용된 하이브리드 이산화티탄과 같은 비율의 마이크로와 나노 이산화티탄을 첨가한 화장료의 SPF in-vitro 를 측정하였고, 15%내지 30%의 자외선차단 상승 효과를 확인하였다.

이 연구는 경표피흡수를 위하여 큐빅액정의 자기조직체의 형성에 관한 것이다. 복수 수산기 (-OH)를 가지는 친수부에 4개의 메칠 그룹을 가지는 양친매성지질인 diglyceryl phytylacetate (DGPA) 를 합성하여 다양한 성능평가를 수행하였다. DGPA의 유화력은 1%의 적은 농도에서도 고 내상의 물을 함유하는 안정한 W/O water-in-oil)에멀젼이 유지되었다. DGPA, dimethicone (2CS), water의 3성분 계의 특정영역에서, 안정한 큐빅상의 액정이 형성되었다. 3상 구조도 작성을 통하여 큐빅 액정영역, 헥 사고날 영역, 물과 헥사고날이 혼제된 영역, 역미셀 영역을 확인하였고, SAXS (small angled x-ray scattering)분석을 통하여 그 구조를 증명하였다. 화장품의 응용으로, 큐보좀 (cubosome)에 10%의 마그 네슘아스코르빌포스페이트, 5％의 피리독신트리헥사데카노에이트를 봉입하여 캡슐화하였다. 큐보좀의 occlusive 효과는 역미셀(reverse micelle)보다 1.7배 우수한 효과를 가졌다. 큐보좀을 분산제인 poloxamer를 사용하여 W/O 에멀젼을 만든 것으로부터 큐빅구조의 액정상으로 회복되는 것을 새롭게 발견하였다. 따라서, DGPA의 양친매성지질의 특성을 이용하여, 큐빅상의 액정을 형성하는 기재로써 화 장품 산업과 의약품분야에서 경표피흡수제로써 응용이 가능할 것으로 기대된다.

Controlling the stick and slip motions of the contact lines in a confined geometry comprised of a spherical lens with a flat substrate is useful for manufacturing polymer ring patterns. We used a sphere on a flat geometry, by which we could control the interfaces of the solution, vapor and substrate. By this method, hundreds of concentric ring-pattern formations of a linear conjugated polymer, poly [2-methoxy-5-(2-thylhexyloxy)-1,4-phenylenevinylene] (MEH-PPV), were generated with excellent regularity over large areas after complete solvent evaporation. Subsequently, the MEH-PPV ring patterns played a role as a directed template to organize highly regular concentric rings of single-walled carbon nanotubes(SWCNTs); when a droplet of the SWCNT suspension in water was casted onto the prepared substrate, hydrophobic polymer patterns confined the water dispersed SWCNTs in between the hydrophilicized SiO2/Si substrate. As the solvent evaporated, SWCNT-rings were formed in between MEH-PPV rings with controlled density. Finally, we used a lift-off process to produce SWCNT patterns by the removal of a sacrificial polymer template with organic solvent. We also fabricated a field effect transistor using self-assembled SWCNT networks on a SiO2/Si substrate.

Hexagonal barium ferrite () nano-particles have been successfully fabricated by spraypylorysis process. precursor solutions were synthesized by self-assembly method. Diethyleneamine (DEA) surfactant was used to fabricate the micelle structure of Ba-DEA complex under various DEA concentrations. powders were synthesized with addition of Fe ions to Ba-DEA complex and then fabricated powders by spray-pyrolysis process at the temperature range of . The molar ratio of Ba/DEA and heat-treatment temperatures significantly affected the magnetic properties and morphology of powders. powders synthesized with Ba/DEA molar ratio of 1 and heat-treated at showed the coercive forces (iHc) of 4.2 kOe with average crystal size of about 100 nm.

Surface modification of silica nanoparticles was investigated using an aerosol self assembly. Stearic acid was used as surface treating agent. A two-fluid jet nozzle was employed to generate an aerosol of the colloidal suspension, which contained 20 nm of silica nanoparticles, surface modifier, and ethyl alcohol. Powder properties such as morphology, specific surface area and pore size distribution were analyzed by SEM, BET and BJH methods, respectively. Surface properties of the silica power were analyzed by FT-IR. The OH bond of the SiO2 surface was converted to a C-H bond. It was revealed that the hydrophilic surface changed to a hydrophobic one due to the aerosol self assembly. Morphology of the surface treated powder was nanostructured with lots of pores having an average diameter of around 2 μm. Depending on the stearic acid concentration (0.25 to 1.0 wt%), the pore size distribution of the particles and the degree of hydrophobicity ranged from 1.5 nm to 180 nm and 29.6% to 50.2%, respectively.

Hexagonal barium ferrite () nano-particles have been successfully synthesised using selfassembly method. Diethyleneamine (DEA) surfactant was used to fabricate the micelle structure of Ba-DEA complex under various DEA concentrations. powders were synthesized with addition Fe ions to Ba-DEA complex and then heat treated at temperature range of 800-1000. The molar ratio of Ba/DEA and heat-treatment temperature significantly affected the magnetic properties and morphology of powders. powders synthesized with Ba/DEA molar ratio of 1 and heat-treated at 1000 for 1 hour showed the coercive forces (iHc) of 4.84 kOe with average crystal size of about 200 nm.

Vapor phase polymerization of a conductive polymer on a SiO2 surface can offer an easy and convenient means to depositing pure and conductive polymer thin films. However, the vapor phase deposition is generally associated with very poor adhesion as well as difficulty when patterning the polymer thin film onto an oxide dielectric substrate. For a significant improvement of the patternability and adhesion of Poly(3-hexylthiophene) (P3HT) thin film to a SiO2 surface, the substrate was pre-patterned with n-octadecyltrichlorosilane (OTS) molecules using a μ-contact printing method. The negative patterns were then backfilled with each of three amino-functionalized silane self-assembled monolayers (SAMs) of (3-aminopropyl) trimethoxysilane (APS), N-(2-aminoethyl)-aminopropyltrimethoxysilane (EDA), and (3- trimethoxysilylpropyl)diethylenetriamine (DET). The quality and electrical properties of the patterned P3HT thin films were investigated with optical and atomic force microscopy and a four-point probe. The results exhibited excellent selective deposition and significantly improved adhesion of P3HT films to a SiO2 surface. In addition, the conductivity of polymeric thin films was relatively high (~13.51 S/cm).

본 연구에서는 수용액상에서 자기조립 나노입자를 형성할 수 있는 레티노익산이 접목된 양친성 폴리아미 노산 유도체를 합성하였다. 합성한 양친성 폴리아미노산은 레티노익산의 접목도가 각각 5, 10, 30 mol%가 되도 록 조절하였다. 수용액 상에서 양친성 폴리아미노산은 소수성 레티노익산의 분자 결합에 의해 안정한 자기조립 나노입자를 형성하였다. 자기조립 나노입자는 레티노익산의 접목도가 증가할수록 크기는 작아지고 형태는 구형 에서 이중층 구조로 전이되었다. 또한 접목도가 10%일 때, 자기조립 입자의 구조 붕괴 없이 레티놀의 포집 및 전달이 가장 효과적인 것을 확인하였다. 접목도가 제어된 자기조립입자는 레티놀을 안정적으로 포집할 수 있기 때문에 주름개선제 및 다양한 기능성 화장품 전달체로 활용될 수 있다