• Title/Summary/Keyword: $TiO_2$ shell

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Synthesis and Characterization of Au/TiO2 Nanoparticles with Core-shell Structure (Core-shell 구조의 Au/TiO2 나노 미립자의 합성 및 특성 평가)

  • ;Paul Mulvaney
    • Journal of the Korean Ceramic Society
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    • v.40 no.9
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    • pp.902-908
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    • 2003
  • Au/TiO$_2$ core-shell structure nanoparticles were synthesised by sol-gel process, and the morphology and crystallinity of TiO$_2$ shell were investigated by TEM and UV-Vis. absorption spectrometer. Au/TiO$_2$ core-shell structure nanoparticles could be prepared by the hydrolysis of TOAA (Titanium Oxide Acethylacetonate) in Au colloid ethanol solution with $H_2O$. The thickness of TiO$_2$ shell on the surface of Au particles was about 1 nm. To investigate the crystallinity of TiO$_2$ shell, UV light with 254 nm and radioactive lay of $^{60}$ CO were irradiated on the TiO$_2$ coated Au colloid ethanol solution. The surface plasmon phenomenon of Au nanoparticles appeared only when the radioactive lay was irradiated on the TiO$_2$ coated Au colloid ethanol solution. From these results, it was found that the TiO$_2$ shell was amorphous and the MUA (Mercaptoundecanoic Acid) layer on the Au particle for its dispersion didn't act as an obstacle to disturb the movement of electron onto the surface of Au particle.

Synthesis of Au/TiO2 Core-Shell Nanoparticles by Using TTIP/TEOA Mixed Solution (TTIP/TEOA 혼합용액을 이용한 Au/TiO2 Core-Shell 구조 나노입자 합성)

  • Kwon, Hyun-Woo;Lim, Young-Min;Yu, Yeon-Tae
    • Korean Journal of Materials Research
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    • v.16 no.8
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    • pp.524-528
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    • 2006
  • On the synthesis of Au/$TiO_2$ core-shell structure nanoparticle, the effect of concentration of $Ti^{4+}$ and reaction temperature on the morphology and optical property of Au/$TiO_2$ core-shell nanoparticles is examined. A gold colloid was prepared by $HAuCl_4{\cdot}4H_2O\;and\;C_6H_5Na_3{\cdot}2H_2O$. Titanium stock solution was prepared by mixing solution of titanium(IV) isopropoxide (TTIP) and triethanolamine (TEOA). The concentrations of $Ti^{4+}$ stock solution were adjusted to $10.01{\sim}0.3$ mM, and then the gold colloid is added to the $Ti^{4+}$ stock solution. Au/$TiO_2$ core-shell structure nanoparticles could be prepared by the hydrolysis of the $Ti^{4+}$ stock solution at $80^{\circ}C$. The size of synthesized Au nanoparticles was 15 nm. The thickness of $TiO_2$ shell on the surface of gold particles was about 10 nm. The absorption peak of synthesized Au/$TiO_2$ core-shell nanoparticles shifted towards the red end of the spectrum by about 3 nm because of the formation of $TiO_2$ shell on the surface of gold particles. The good $TiO_2$ shell is produced when $Ti^{4+}$ concentration is varied between 0.01 and 0.05 mM, and reaction temperature is maintained at $80^{\circ}C$. The crystal structure of $TiO_2$ shell was amorphous.

Sol-gel 법을 이용한 ZnO-$TiO_2$ Core-shell 나노입자의 합성

  • Yang, Hui-Su;Nam, Sang-Hun;Jo, Sang-Jin;Jeong, Won-Seok;Bu, Jin-Hyo
    • Proceedings of the Korean Vacuum Society Conference
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    • 2011.08a
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    • pp.366-366
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    • 2011
  • 이성분 산화물인 ZnO/$TiO_2$ core-shell 나노입자는 core-shell 구조의 특성과 이성분 산화물의 상호작용에 의해서 염료감응형 태양전지의 효율향상을 기대할 수 있다. Znic acetate($Zn_2(CH_3COO)$)와 Titanium(IV) butoxide($Ti(OBu)_4$)를 이용하여 ZnO 나노입자를 수열합성하고 그 주의에 $TiO_2$을 가수분해 반응을 이용하여 둘러싸는 core-shell형태의 물질을 합성하였다. 그 이후 결정성 및 유기물 제거를 위해서 4시간 동안 고온에서 소성하였다. SEM 결과에 따르면 소성 온도를 600도까지 증가시키면 ZnO의 경우 나노입자의 크기가 증가하는 경향을 확인하였다. 하지만 core-shell의 경우는 ZnO의 뭉침현상을 $TiO_2$이 방해하여 초기합성된 크기와 동일한 크기를 유지하는 것을 확인하였다. 또한 XRD 결과에 따르면 주변에 형성된 $TiO_2$ 이외에 $Zn_2TiO_4$의 spinel 구조를 가지는 물질이 합성되는 것을 확인할 수 있었다. 합성된 core-shell 구조의 나노입자는 약 40~50 nm의 크기를 가지고 600도에서 소성된 입자의 경우 산소 정공이 거의 없는 약 3 eV의 밴드갭을 가지는 물질로 합성이 되었다. Core-shell 나노입자의 경우 염료 감응형 태양전지의 반도체 물질로 응용 가능할 것으로 판단된다.

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Synthesis of Metallic Gold Colored α-Al2O3 Nanoplate-TiO2 Core-Shell Pigments with Robust and Photo-Stable Smooth TiO2 Shell

  • Lee, Su Jin;You, Myoung Sang;Park, Jin Kyoung;Park, Bum Jun;Im, Sang Hyuk
    • Applied Chemistry for Engineering
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    • v.31 no.4
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    • pp.390-397
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    • 2020
  • To synthesize non-corrosive metallic gold colored α-Al2O3 nanoplate-TiO2 core-shell pigments with controlled roughness, we systematically checked the morphological variation of the TiO2 shell with the mole ratio of TiCl4 and NaOH from 1 : 1 to 1 : 1.5, 1 : 2, 1 : 2.5, 1 : 3, 1 : 3.5, and 1 : 4. The more increased mole ratio of TiCl4 and NaOH resulted in the smoother TiO2 shell due to the promoted formation of anatase TiO2 than that of the rutile one. By the heat-treatment of pigments at 500 ℃, we could improve the adhesiveness between TiO2 shell and α-Al2O3 nanoplates without changing their topology and roughness. In addition, the α-Al2O3 nanoplate with the robust TiO2 by heat-treatment exhibited comparable photo-stability against photo-catalytic degradation by UV exposure compared with the commercially available α-Al2O3/TiO2 lustering pigment.

Synthesis of CeO2/TiO2 core-shell Nanoparticles (CeO2/TiO2 코어-쉘 나노입자의 합성)

  • Mun, Young Gil;Park, Chang Woo;Kim, Sang Hern
    • Journal of the Korean Applied Science and Technology
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    • v.34 no.4
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    • pp.746-755
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    • 2017
  • In this study, $CeO_2/TiO_2$ nanoparticle with structure of core and shell was synthesized by growing $TiO_2$ onto the surface of $CeO_2$ according to hydrolysis of $Ti(SO_4)_2$. Reaction time, temperature, concentration of $CeO_2$ slurry, pH control of $Ti(SO_4)_2$ were optimized about synthesis of $CeO_2/TiO_2$ core-shell nanoparticle. It was found that optimal mole ratio range of $CeO_2:TiO_2$ was 1:0.2~1.1, the optimal concentration of $CeO_2$ slurry was 1 %, and the optimal reaction temperature was $50^{\circ}C$. The optimal concentration of $CeO_2$ slurry could be increased up to 10 % by adjusting the pH of $Ti(SO_4)_2$ to 1 using $NH_4OH$ and adding to $CeO_2$ slurry. If reaction was carried at $80^{\circ}C$ or higher, the separated $TiO_2$ particles were obtained instead of $CeO_2/TiO_2$ core-shell nanoparticles. The optimal reaction temperature was $50^{\circ}C$ at which good shaped core-shell structure of $CeO_2/TiO_2$ was obtained.

Synthesis of Fe-Doped TiO2/α-Fe2O3 Core-Shell Nanowires Using Co-Electrospinning and Their Magnetic Property (복합 전기방사법을 이용한 Fe-doped TiO2/α-Fe2O3 이중구조 나노와이어의 합성 및 자성 특성)

  • Koo, Bon-Ryul;Ahn, Hyo-Jin
    • Korean Journal of Materials Research
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    • v.24 no.8
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    • pp.423-428
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    • 2014
  • We synthesized Fe-doped $TiO_2/{\alpha}-Fe_2O_3$ core-shell nanowires(NWs) by means of a co-electrospinning method and demonstrated their magnetic properties. To investigate the structural, morphological, chemical, and magnetic properties of the samples, X-ray diffraction, scanning electron microscopy, transmission electron microscopy, and X-ray photoelectron spectroscopy were used, as was a vibrating sample magnetometer. The morphology of the nanostructures obtained after calcination at $500^{\circ}C$ exhibited core/shell NWs consisting of $TiO_2$ in the core region and ${\alpha}-Fe_2O_3$ in the shell region. In addition, the XPS results confirmed the formation of Fe-doped $TiO_2$ by the doping effect of $Fe^{3+}$ ions into the $TiO_2$ lattice, which can affect the ferromagnetic properties in the core region. For comparison, pure ${\alpha}-Fe_2O_3$ NWs were also fabricated using an electrospinning method. With regard to the magnetic properties, the Fe-doped $TiO_2/{\alpha}-Fe_2O_3$ core-shell NWs exhibited improved saturation magnetization(Ms) of approximately ~2.96 emu/g, which is approximately 6.1 times larger than that of pure ${\alpha}-Fe_2O_3$ NWs. The performance enhancement can be explained by three main mechanisms: the doping effect of Fe ions into the $TiO_2$ lattice, the size effect of the $Fe_2O3_$ nanoparticles, and the structural effect of the core-shell nanostructures.

Synthesis of Au@TiO2 Core-shell Nanoparticle-decorated rGO Nanocomposite and its NO2 Sensing Properties

  • Kumar Naik, Gautam;Yu, Yeon Tae
    • Journal of Sensor Science and Technology
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    • v.28 no.4
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    • pp.225-230
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    • 2019
  • $Au@TiO_2$ core-shell decorated rGO nanocomposite (NC) was prepared using a simple solvothermal method followed by heat treatment for gas sensor application. The crystal structure and morphology of the composites were characterized by X-ray powder diffraction and transmission electron microscopy, respectively. The $NO_2$ sensing response of the $Au@TiO_2/rGO$ NC was tested at operating temperatures from $250^{\circ}C$ to $500^{\circ}C$, and was compared with those of the bare rGO and $Au@TiO_2$ core-shell NPs. The $Au@TiO_2/rGO$ NC-based sensor showed a far higher response than the rGO or $Au@TiO_2$ core-shell based sensors, with the maximum response detected when the operating temperature was $400^{\circ}C$. This improved response was due to the high rGO gas absorption capability for $NO_2$ gas and the catalytic effect of $Au@TiO_2$ core-shell NPs in oxidizing $NO_2$ to $NO_3$.

Synthesis of Ag/TiO2 Core/Shell Nanoparticles with Antibacterial Properties

  • Lin, Yue;Qiqiang, Wang;Xiaoming, Zhang;Zhouping, Wang;Wenshui, Xia;Yuming, Dong
    • Bulletin of the Korean Chemical Society
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    • v.32 no.8
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    • pp.2607-2610
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    • 2011
  • Monodispersed Ag/$TiO_2$ core/shell nanoparticles were synthesized in solution via colloid-seeded deposition process using Ag nanoparticles as colloid seeds and $Ti(SO_4)_2$ as Ti-source respectively. Silver nitrate was reduced to Ag nanoparticles with $N_2H_4{\cdot}H_2O$ in the presence of CTAB as stabilizing agent. The titania sols hydrolyzed by the $Ti(SO_4)_2$ solution deposited on the surface of Ag nanoparticles to form the Ag/$TiO_2$ core/shell nanoparticles. Inductively coupled plasma atomic emission spectrometry (ICP-AES) showed low amount of Ag ion leaching from the Ag/$TiO_2$ core/shell nanoparticles. The Ag/$TiO_2$ core/shell nanoparticles indicated excellent antibacterial effects against Escherichia coli and maintained long-term antibacterial property.

CO Oxidation Activities of Ni and Pd-TiO2@SiO2 Core-Shell Nanostructures

  • Do, Yeji;Cho, Insu;Park, Yohan;Pradhan, Debabrata;Sohn, Youngku
    • Bulletin of the Korean Chemical Society
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    • v.34 no.12
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    • pp.3635-3640
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    • 2013
  • We prepared Ni and Pd-modified $TiO_2@SiO_2$ core-shell nanostructures and then analyzed them by scanning electron microscopy, optical microscopy, X-ray diffraction crystallography, FT-IR and UV-Visible absorption spectroscopy. In addition, their CO oxidation performance was tested by temperature-programmed mass spectrometry. The CO oxidation activity showed an order of Ni-$TiO_2@SiO_2$ ($900^{\circ}C$) < Ni-$TiO_2@SiO_2$ ($90^{\circ}C$) < Ni-$TiO_2@SiO_2$ ($450^{\circ}C$) in the first CO oxidation run, and greatly improved activity in the same order in the second run. The $T_{10%}$ (the temperature at 10% CO conversion) corresponds to the CO oxidation rate of $2.8{\times}10^{-5}$ molCO $g{_{cat}}^{-1}s^{-1}$. For Ni-$TiO_2@SiO_2$ ($450^{\circ}C$), the $T_{10%}$ was observed at $365^{\circ}C$ in the first run and at $335^{\circ}C$ in the second run. For the Pd-$TiO_2@SiO_2$ ($450^{\circ}C$), the $T_{10%}$ was observed at a much lower temperature of $263^{\circ}C$ in the first CO oxidation run, and at $247^{\circ}C$ in the second run. The CO oxidation activities of transition metal modified $TiO_2@SiO_2$ core-shell nanostructures presented herein provide new insights that will be useful in developing catalysts for various environments.