• 한국재료학회지
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• 제20권1호
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• pp.25-30
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• 2010

Si nanowire/multiwalled carbon nanotube nanocomposite arrays were synthesized. Vertically aligned Si nanowire arrays were fabricated by Ag nanodendrite-assisted wet chemical etching of n-type wafers using $HF/AgNO_3$ solution. The composite structure was synthesized by formation of a sheath of carbon multilayers on a Si nanowire template surface through a thermal CVD process under various conditions. The results of Raman spectroscopy, scanning electron microscopy, and high resolution transmission electron microcopy demonstrate that the obtained nanocomposite has a Si nanowire core/carbon nanotube shell structure. The remarkable feature of the proposed method is that the vertically aligned Si nanowire was encapsulated with a multiwalled carbon nanotube without metal catalysts, which is important for nanodevice fabrication. It can be expected that the introduction of Si nanowires into multiwalled carbon nanotubes may significantly alter their electronic and mechanical properties, and may even result in some unexpected material properties. The proposed method possesses great potential for fabricating other semiconductor/CNT nanocomposites.

• 한국진공학회:학술대회논문집
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• 한국진공학회 2011년도 제41회 하계 정기 학술대회 초록집
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• pp.199-199
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• 2011

The addition of a carbanion to ${\yen}{\acute{a}}{\yen}{\hat{a}}$-unsaturated carbonyl compounds is of importance in the C-C bond formation reactions for modern pharmaceuticals and organic synthesis. Recently, heterogeneous asymmetric catalysis became more attractive area of research because of the easy recovery and separation of the catalyst from the reaction system. Most of synthetic methods for heterogeneous catalysts were grafting or immobilization of homogeneous catalyst onto the solid supports. Trans-1,2-Diaminocyclohexane(DACH) and L-proline ligands have been enormously used as chiral ligands in several catalytic transformation under homogenous conditions. Our group prepared l-proline functionalized mesoporous silica was synthesized under acidic condition using a poly(ethylene oxide)-poly(propylene oxide)-poly(ethylene oxide) triblock copolymer template (EO20PO70EO20, Pluronic P-123, BASF). Furthermore, we successfully directly synthesized trans-1,2 diaminocyclohexane functionalized mesoporous silica by using microwave method. The direct functionalization of chiral ligand into the framework of mesoporous materials is expected to be useful for the heterogeneous asymmetric catalysis. So, we adopt the direct synthesis of chiral ligand functionalized mesoporous silica by using thermal and microwave irradiation. Then, chiral ligand functionalized mesoporous silicas were applied to enantioselective asymmetric catalytic reactions.

• 대한화학회지
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• 제33권5호
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• pp.510-515
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• 1989

테트라에틸렌펜타아민과 포름알데히드의 주형축합반응으로부터 새로운 펜타아자 거대두고리 리간드인 1,3,6,9,12-펜타아자비시클로[10,2,1]펜타데칸(D)의 니켈(II) 및 구리(II) 착화합물 $[Ni(D)]^{2+},\;[Cu(d)]6{2+}\;그리고\;[Cu(D)Cl]^+$를 합성하였다. 거대두고리 리간드인 D에는 한 개의 이미다졸리딘 고리가 있다. $[Ni(D)]^{2+}와 [Cu(D)]^{2+}$는 5-5-5-6 킬레이트고리 배열로 된 평면사각형 구조를 이루며, 5-배위 착이온인 $[Cu(D)Cl]^+$의 구조는 그의 전자스펙트럼으로 볼 때 사각피라미드일 것으로 보인다. 이들 니켈(II) 및 구리(II) 착화합물의 합성과 확인 그리고 분광학적인 특성과 화학적인 특성이 논의된다.

• 대한화학회지
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• 제54권4호
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• pp.395-401
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• 2010

[M(L/L')$(NO_3)_n$].$mH_2O$ 및 [VO(L/L')($SO_4)$].$2H_2O$ (여기서 L/L'는 Schiff 염기로 thiocarbohydrazide (TCH), benzilmonohydrazone (BMH)/diacetylmonohydrazone (DMH) 및 carbon disulphide에서 유도된 "3,4,10,11-tetraphenyl/tetramethyl-1,2,5,6,8,9,12,13-octaazacyclotetradeca-2,4,9,11-tetraene-7,14-dithione")의 분자식을 갖는 일련의 거대고리 착물을 (M = $UO_2$(VI), Th(IV) and ZrO(IV), n = 2, 4, m = 2, 3)을 금속이온 주형법으로 합성하였다. 이들 착물의 특성을 원소분석, 열분석, 몰 전기전도도, 자기모멘트 그리고 전자, 적외선 및 $^1H$-NMR로 조사하였다. 바나딜 착물의 경우 ESR 및 순환 전압전류법을 사용하였다. 그 결과, VO(IV) 이온은 5배위의 상자기성 착물을 이루며, $UO_2$(VI) 및 ZrO(IV)는 6배위 그리고 Th(IV)는 8배위를 가지나 공통적으로 위의 조성을 갖는 반자기성임을 알았다.

• 한국재료학회지
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• 제33권10호
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• pp.377-384
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• 2023

Exploring earth-abundant, highly effective and stable electrocatalysts for electrochemical water splitting is urgent and essential to the development of hydrogen (H₂) energy technology. Iron-cobalt layered double hydroxide (FeCo-LDH) has been widely used as an electrocatalystfor OER due to its facile synthesis, tunable components, and low cost. However, LDH synthesized by the traditional hydrothermal method tends to easily agglomerate, resulting in an unstable structure that can change or dissolve in an alkaline solution. Therefore, studying the real active phase is highly significant in the design of electrochemical electrode materials. Here, metal-organic frameworks (MOFs) are used as template precursors to derive FeCo-LDH from different iron sources. Iron salts with different anions have a significant impact on the morphology and charge transfer properties of the resulting materials. FeCo-LDH synthesized from iron sulfate solution (FeCo-LDH-SO₄) exhibits a hybrid structure of nanosheets and nanowires, quite different from other electrocatalysts that were synthesized from iron chloride and iron nitrate solutions. The final FeCo-LDH-SO₄ had an overpotential of 247 mV with a low Tafel-slope of 60.6 mV dec^-1 at a current density of 10 mA cm^-2 and delivered a long-term stability of 40 h for the OER. This work provides an innovative and feasible strategy to construct efficient electrocatalysts.

• 접착 및 계면
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• 제24권4호
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• pp.136-142
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• 2023

본 연구에서는 실리카원으로 Tetraethyl orthosilicate (TEOS)를 사용하고 주형으로 트리블럭 공중합체(P123)를 사용하여 산성 조건에서 자기조립 방법과 수열합성 과정을 거쳐서 잘 배열된 육방체 구조의 메조세공 배열구조를 가지는 다공성 실리카 물질(Surfactant-extracted SBA-15)을 합성하였다. Surfactant-extracted SBA-15는 약 980 nm의 크기를 가지는 짧은 로드의 입자 모양을 보여주었다. 그리고 표면적과 세공 직경은 각각 730 m²g^-1와 70.8 Å이었다. 한편, 포스트-합성방법(post-synthesis method)을 이용하여 메조세공 내에 아미노실란(3-aminopropyltriethoxysilane, APTES)을 그래프팅(grafting) 하였다. 아미노실란으로 개질된 메조다공성 실리카(APTES-SBA-15)는 잘 배열된 세공구조(p6mm)를 가지고 짧은 로드의 입자모양을 잘 유지 하였다. APTES-SBA-15의 표면적과 세공 직경은 각각 350 m²g^-1와 60.7 Å으로 감소하였다. APTES가 개질된 메조 다공성 실리카에 희토류 금속이온(Eu³⁺, Tb³⁺) 용액을 처리하여 메조세공 내에 희토류 금속 착물이 도입된 메조다공성 실리카 물질을 합성하였다. (Eu/APTES-SBA-15, Tb/APTES- SBA-15) 이들 물질은 λ_ex=250 nm 광에 의해 특징적인 광발광 스펙트라를 나타내었다. (Tb/APTES-SBA-15를 위하여 ⁵D₄→⁷F₅ (543.5 nm), ⁵D₄→⁷F₄ (583.5 nm), ⁵D₄→⁷F₃ (620.2 nm) 전이; Eu/APTES-SBA-15를 위하여 ⁵D0→⁷F₀ (577.7 nm), ⁵D0→⁷F₁ (592.0 nm), ⁵D0→⁷F₂ (614.9 nm), ⁵D₀→⁷F₃ (650.3 nm) and ⁵D₀→⁷F₄ (698.5 nm) 전이)

• 한국분말재료학회지
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• 제28권2호
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• pp.127-133
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• 2021

One-dimensional (1D) piezoelectric nanostructures are attractive candidates for energy generation because of their excellent piezoelectric properties attributed to their high aspect ratios and large surface areas. Vertically grown BaTiO₃ nanotube (NT) arrays on conducting substrates are intensively studied because they can be easily synthesized with excellent uniformity and anisotropic orientation. In this study, we demonstrate the synthesis of 1D BaTiO₃ NT arrays on a conductive Ti substrate by electrochemical anodization and sequential hydrothermal reactions. Subsequently, we explore the effect of hydrothermal reaction conditions on the piezoelectric energy conversion efficiency of the BaTiO₃ NT arrays. Vertically aligned TiO₂ NT arrays, which act as the initial template, are converted into BaTiO₃ NT arrays using hydrothermal reaction with various concentrations of the Ba source and reaction times. To validate the electrical output performance of the BaTiO₃ NT arrays, we measure the electricity generated from each NT array packaged with a conductive metal foil and epoxy under mechanical pushings. The generated output voltage signals from the BaTiO₃ NT arrays increase with increasing concentration of the Ba source and reaction time. These results provide a new strategy for fabricating advanced 1D piezoelectric nanostructures by demonstrating the correlation between hydrothermal reaction conditions and piezoelectric output performance.

• 청정기술
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• 제30권2호
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• pp.123-133
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• 2024

대기 중에 존재하는 저농도 CH₄을 제거를 위한 흡착제 개발을 위해서 Zeolite Template Carbon (ZTC)을 합성하였다. 탄소 전구체가 ZTC 합성에 미치는 영향을 알아보기 위해서, CH₄와 C₂H₂를 탄소 전구체로 사용하여 ZTC를 합성하였으며, 또한 이온 교환에 사용된 금속의 영향을 알아보기 위해서 CaCl₂와 LiCl을 사용하여 이온교환한 Y Zeolite을 Template로 사용하여 ZTC를 합성하였다. 탄소 전구체 간의 비교에서는 C₂H₂가 CH₄ 보다 더 높은 탄소 수율을 보였으며, 또한 미세기공이 발달한 ZTC를 합성하였다. 이는 C₂H₂의 분자 동역학적 크기(Kinetic Diameter) (3.3 Å)가 CH₄의 분자 동역학적 크기(Kinetic Diameter) (3.8 Å)보다 더 작기 때문에, 제올라이트 템플릿의 미세 기공 내부의 깊숙한 곳에서부터 탄소 침착을 가능하였기 때문인 것으로 판단된다. 이온 교환에 사용된 금속 전구체 간의 비교에서는 CaCl₂ 기반의 ZTC가 LiCl을 기반의 ZTC보다 미세 기공이 발달한 것을 확인하였는데, 이온 교환된 Ca가 탄소 전구체에 의한 Pore Blocking을 억제해서 기공 내부로 탄소 전구체가 들어 갈 수 있게 한 덕분으로 판단된다. 합성된 ZTC를 이용하여, 298 K에서의 N₂와 CH₄의 흡착 등온선을 측정하였는데, 전체적으로 CH₄의 흡착량이 N₂보다는 높다는 것을 확인하였다. 또한 CaY 기반으로 C₂H₂를 이용하여 합성한 ZTC 샘플이 N₂와 CH₄ 흡착량이 가장 높았지만, 흡착 공정 설계의 중요한 인자인 CH₄와 N₂의 흡착 비율 기준으론 CH₄으로 합성한 샘플이 가장 높게 나왔다. 이는 N₂ 흡착과 관련 깊은 초미세기공이 덜 발달하여, N₂의 흡착량을 줄임으로서 오히려 CH₄/N₂ 분리도를 높게 해 주었기 때문으로 판단된다.

• 한국진공학회:학술대회논문집
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• 한국진공학회 2011년도 제40회 동계학술대회 초록집
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• pp.17-18
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• 2011

Plasma in liquid phase has attracted great attention in the last few years by the wide domain of applications in material processing, decomposition of organic and inorganic chemical compounds and sterilization of water. The plasma in liquid is characterized by three main regions which interact each - other during the plasma operation: the liquid phase, which supply the plasma gas phase with various chemical compounds and ions, the plasma in the gas phase at atmospheric pressure and the interface between these two regions. The most complex region, but extremely interesting from the fundamental, chemical and physical processes which occur here, is the boundary between the liquid phase and the plasma gas phase. In our laboratory, plasma in liquid which behaves as a glow discharge type, is generated by using a bipolar pulsed power supply, with variable pulse width, in the range of 0.5~10 ${\mu}s$ and 10 to 30 kHz repetition rate. Plasma in water and other different solutions was characterized by electrical and optical measurements. Strong emissions of OH and H radicals dominate the optical spectra. Generally water with 500 ${\mu}S/cm$ conductivity has a breakdown voltage around 2 kV, depending on the pulse width and the repetition rate of the power supply. The characteristics of the plasma initiated in ultrapure water between pairs of different materials used for electrodes (W and Ta) were investigated by the time-resolved optical emission and the broad-band absorption spectroscopy. The deexcitation processes of the reactive species formed in the water plasma depend on the electrode material, but have been independent on the polarity of the applied voltage pulses. Recently, Coherent anti-Stokes Raman Spectroscopy method was employed to investigate the chemistry in the liquid phase and at the interface between the gas and the liquid phases of the solution plasma system. The use of the solution plasma allows rapid fabrication of the metal nanoparticles without being necessary the addition of different reducing agents, because plasma in the liquid phase provides a reaction field with a highly excited energy radicals. We successfully synthesized gold nanoparticles using a glow discharge in aqueous solution. Nanoparticles with an average size of less than 10 nm were obtained using chlorauric acid solutions as the metal source. Carbon/Pt hybrid nanostructures have been obtained by treating carbon balls, synthesized in a CVD chamber, with hexachloro- platinum acid in a solution plasma system. The solution plasma was successfully used to remove the template remained after the mesoporous silica synthesis. Surface functionalization of the carbon structures and the silica surface with different chemical groups and nanoparticles, was also performed by processing these materials in the liquid plasma.