• 제목/요약/키워드: Surface chemistry

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Surface Potential Change Depending on Molecular Orientation of Hexadecanethiol Self-Assembled Monolayers on Au(111)

  • Ito, Eisuke;Arai, Takayuki;Hara, Masahiko;Noh, Jaegeun
    • Bulletin of the Korean Chemical Society
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    • 제30권6호
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    • pp.1309-1312
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    • 2009
  • Surface potential and growth processes of hexadecanethiol (HDT) self-assembled monolayers (SAMs) on Au(111) surfaces were examined by Kelvin probe method and scanning tunneling microscopy. It was found that surface potential strongly depends on surface structure of HDT SAMs. The surface potential shift for the striped phase of HDT SAMs chemisorbed on Au(111) surface was +0.45 eV, which was nearly the same as that of the flat-lying hexadecane layer physisorbed on Au(111) surface. This result indicates that the interfacial dipole layer induced by adsorption of alkyl chains is a main contributor to the surface potential change. In the densely-packed HDT monolayer, further change of the surface potential was observed, suggesting that the dipole moment of the alkanethiol molecules is an origin of the surface potential change. These results indicate that the work function of a metal electrode can be modified by controlling the molecular orientation of an adsorbed molecule.

Orientation Control of Polyoxometalate Nanoparticles in Organic- Inorganic Hybrid LB Films

  • Lee, Burm-Jong;Kim, Hee-Sang;Park, Dong-Ho;Nam, Sang-Hee;Yunghee Oh
    • KIEE International Transactions on Electrophysics and Applications
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    • 제4C권1호
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    • pp.26-30
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    • 2004
  • Orientation control of a polyoxometalate (POM) nanoparticle in its two-dimensional arrangement was attempted by Langmuir-Blodgett (LB) technique. For their uniorientation, two carboxyl groups were introduced on one side of the POM particle, and hydrophobic long chains were attached by esterification with the carboxyl groups (C18-POM). The C18-POM layer spread on water surface showed stability against surface pressure up to 60 mN/m. The pattern of the C18-POM isotherm was quite different from stearyl alcohol (C18-OH), while the POM itself did not show any development of surface pressure on water surface. The AFM images of C18-POM LB films showed some microcrystalline structures that were noticed as dot structures by Brewster angle microscopy. The microimages for C18-POM did not completely spread out as a monolayer on the water surface. The XPS spectra indicated the presence of POM structures and stearyl ester bonds formed from about 65% of the total carboxyls. The XRD spectra showed that the unioriented POMs were not positioned with the same lattice distance but rather in a wavy surface state.

Surface-enhanced Raman Spectroscopy of Quinomethionate Adsorbed on Silver Colloids

  • Kim, Mak-Soon;Kang, Jae-Soo;Park, Si-Bum;Lee, Mu-Sang
    • Bulletin of the Korean Chemical Society
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    • 제24권5호
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    • pp.633-637
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    • 2003
  • We have studied the surface-enhanced Raman spectroscopy (SERS) spectrum of quinomethionate (6-methyl-1,3-dithiolo[4,5-b]quinoxalin-2-one), which is an insecticide or fungicide used on vegetables and wheat. We observed no signals in the ordinary Raman spectra of solid-state quinomethionate, but when it was adsorbed on a colloidal silver surface, strong vibrational signals were obtained at a very low concentration. The SERS spectra were obtained by silver colloids prepared by the Creighton et al. method. The influence of pH and the aggregation inductors ($Cl^-,\;Br^-,\;I^-,\;F^-$) on the adsorption mechanism was investigated. Two different adsorption mechanisms were deduced, depending on the experimental conditions: The one N atom or two N atoms are chemisorbed on an Ag surface. An important contribution of the chemical mechanism was inferred when the one N atom was perpendicularly adsorbed on a surface. It is possible that quinomethionate can be detected to about $10^{-5}$ M.

Feasibility of icephobicity induced by self-propelling condensed water droplets

  • Lee, Hyung-Seok;Lee, Kyu Hwan;Park, Hyun Sun;Claessond, Per M.;Yun, Sang H.
    • 한국표면공학회:학술대회논문집
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    • 한국표면공학회 2015년도 추계학술대회 논문집
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    • pp.199-200
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    • 2015
  • 실리콘 기판위에 Gecko의 피부를 모사한 다층의 나노, 마이크로 구조표면에서 일어나는 응결된 water vapor droplets의 coalescence에 기인하는 surface energy의 kinetic energy의 변환을 통하여 발생하는 water droplets의 self-propelling을 이용한 빙점하에서 dynamic wetting 성질의 관찰을 통해서 얼음 방지, 지연, 또는 얼음 부착성 최소화 표면의 구현 가능성을 보여준다.

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펨토몰 농도의 옥시토신 검출을 위한 항체 기능성 UiO-66-(COOH)2 증폭형 표면 플라즈몬 공명 분석법 개발 (Antibody Functionalized UiO-66-(COOH)2 Amplified Surface Plasmon Resonance Analysis Method for fM Oxytocin)

  • 이명섭;남하영;박수연;정성화;이혜진
    • 공업화학
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    • 제35권4호
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    • pp.335-340
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    • 2024
  • 본 논문에서는 UIO-66에 항체 기능성을 도입한 유무기 하이브리드 소재를 합성하고 이를 표면 플라즈몬 공명(surface plasmon resonance, SPR) 분석법에 접목하여 옥시토신과 같은 작은 분자를 검출하는 감도를 향상시키고자 하였다. 옥시토신은 암, 알츠하이머, 심부전증 진단에 중요한 생물학적 표지 펩타이드 분자로 알려져 있으며, 이를 수 펨토몰(femtomole, fM) 농도 수준까지 검출하기 위해 다공성이며 표면적이 우수한 metal organic frameworks 중 하나인 UiO-66-(COOH)2 소재를 신호증폭용으로 활용하면서 옥시토신에 특이적인 항체 페어를 이용하는 표면 샌드위치 분석법을 개발함으로써 선택성을 향상시키고자 하였다. 이를 위해 먼저 선정한 각 옥시토신 특이적 항체가 옥시토신에 대해 강하게 결합하는지 그리고 각 항체가 옥시토신의 서로 다른 결합사이트에 결합하는지를 실시간 SPR 분석법으로 확인하였다. 선정한 항체 중 한 개(예: anti-OXT [OTI5G4])를 SPR용 금 박막 칩 표면에 고정하고, 옥시토신을 흘려준 후, UiO-66-(COOH)2에 컨쥬게이션된 다른 항체(예: anti-OXT[4G11])를 순차적으로 흘려주어 표면에 샌드위치 복합체(anti-OXT[OTI5G4]/옥시토신/UiO-66-(COOH)2-anti-OXT[4G11])를 형성하였을 때 옥시토신 농도에 따라 SPR 신호가 변화하는 것을 실시간으로 모니터링하였다. 그 결과, UiO-66-(COOH)2를 사용하지 않았을 때 대비 약 백만 배 이상 감도를 증폭시켜 약 10 fM까지 검출 가능함을 보여주었다.

Bioanalytical Application of SERS Immunoassay for Detection of Prostate-Specific Antigen

  • Yoon, Kyung-Jin;Seo, Hyeong-Kuyn;Hwang, Hoon;Pyo, Dong-Jin;Eom, In-Yong;Hahn, Jong-Hoon;Jung, Young-Mee
    • Bulletin of the Korean Chemical Society
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    • 제31권5호
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    • pp.1215-1218
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    • 2010
  • We demonstrate the possible application of the sandwich type surface-enhanced Raman scattering (SERS) immunoassay using antigen-antibody binding for detection of prostate-specific antigen (PSA) in cancer cells. In this sandwich type of SERS immunoassay, to capture antigens onto the immobilized layer of antibodies on the gold substrate we prepared the monolayer of gold nanoparticles on the APTMS-derivatized surface of a glass slide by using the SAM technique. This sandwich type of SERS immunoassay in which antigens on the substrate specifically capture antibodies on a Raman reporter (DSNB coated gold nanoparticles with R6G) could successfully detect PSA at low levels. A strong SERS spectrum of Raman reporter was observed only with a substrate in which PSA is present.

Quantum Chemical Molecular Dynamics and Kinetic Monte Carlo Approach to the Design of MgO Protecting Layer in Plasma Display Panel

  • Kubo, Momoji;Kikuchi, Hiromi;Tsuboi, Hideyuki;Koyama, Michihisa;Endou, Akira;Carpio, Carlos A. Del;Kajiyama, Hiroshi;Miyamoto, Akira
    • 한국정보디스플레이학회:학술대회논문집
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    • 한국정보디스플레이학회 2006년도 6th International Meeting on Information Display
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    • pp.371-374
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    • 2006
  • We developed new quantum chemical molecular dynamics and kinetic Monte Carlo programs to simulate the destruction processes of MgO protecting layer in plasma display panel. Our simulation results proposed that MgO(111) surface with nano-dot structures covered by (001) facets has the highest stability, which is against the previous knowledge. The formation of nano-dot structures on the MgO(111) surface covered by (001) facets was found to be the reason for the high stability of the MgO(111) surface. Furthermore, the effect of grain boundary on the stability of MgO surfaces was also clarified.

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N-Dodecanoyl, N-Methyl Glucamine(GL 12)과 음이온 계면활성제 혼합물의 Dynamic Surface Tension에 관한 연구 (Studies on the Dynamic Surface Tension of GL12 and Anionic Mixtures)

  • 안호정;최규석
    • 공업화학
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    • 제7권1호
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    • pp.101-108
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    • 1996
  • 본 연구에서는 수용액 내에서 생분해도가 우수하고 인체에 mild한 비이온성 계면활성제 GL12와 범용 음이온성 계면활성제인 linear laurylbenzene sulfonate(LAS) 또는 sodium polyoxyethylene(3) glycol lauryl ether sulfate(SLES) 각각 용액의 dynamic surface tension과 이들 계면활성제 혼합용액의 dynamic surface tension이 혼합비에 따라 어떻게 변화되는지 maximum bubble pressure method를 이용하여 조사하였다. 또한 salting-cut 효과가 있는 NaCl, CsCl과 salting-in 효과가 있는 요소를 계면활성제 용액에 첨가하여 이들 염들이 용액의 dynamic surface tension에 미치는 영향에 대하여도 연구하였다. 비이온성 계면활성제인 GL12의 dynamic surface tension은 염의 존재에 영향을 크게 받지 않았으나 음이온성인 SLES와 LAS는 크게 영향을 받았다. 또한 GL12/SLES와 GL12/LAS 혼합계에서도 GL12의 함량이 많을수륵 용액의 dynamic surface tension에 대한 염의 영향이 감소하였으나 LAS 또는 SLES의 함량이 증가할수록 염의 영향은 증가하였다.

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Hydrogenation of Phenylacetylene to Styrene on Pre-CxHy- and C-Covered Cu(111) Single Crystal Catalysts

  • Sohn, Young-Ku;Wei, Wei;White, John M.
    • Bulletin of the Korean Chemical Society
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    • 제32권5호
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    • pp.1559-1563
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    • 2011
  • Thermal hydrogenation of phenylacetylene (PA, $C_8H_6$) to styrene ($C_8H_8$) on pre-$C_xH_y$- and C-covered Cu(111) single crystal substrates has been studied using temperature-programmed desorption (TPD) mass spectrometry. Chemisorbed PA with an acetylene group has been proved to be associated with hydrogen of pre-adsorbed $C_xH_y$ to form styrene (104 amu) on Cu surface. For the parent (PA) mass (102 amu) TPD profile, the TPD peaks at 360 K and 410 K are assigned to chemisorbed vertically aligned PA and flat-lying cross-bridged PA, respectively (J. Phys. Chem. C 2007, 111, 5101). The relative $I_{360K}/I_{410K}$ TPD ratio dramatically increases with increasing pre-adsorbed $C_xH_y$ before dosing PA, while the ratio does not increase for pre-C-covered surface. For PA on pre-$C_xH_y$-covered Cu(111) surface, styrene desorption is enhanced relative to the parent PA desorption, while styrene formation is dramatically quenched on pre-C-covered (lack of adsorbed hydrogen nearby) surface. It appears that only cross-bridged PA associates with adsorbed hydrogen to form styrene that promptly desorbs at 410 K, while vertically aligned PA is less likely to participate in forming styrene.