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Sample records for adsorbed organic films

  1. Computer simulations of adsorbed liquid crystal films

    Science.gov (United States)

    Wall, Greg D.; Cleaver, Douglas J.

    2003-01-01

    The structures adopted by adsorbed thin films of Gay-Berne particles in the presence of a coexisting vapour phase are investigated by molecular dynamics simulation. The films are adsorbed at a flat substrate which favours planar anchoring, whereas the nematic-vapour interface favours normal alignment. On cooling, a system with a high molecule-substrate interaction strength exhibits substrate-induced planar orientational ordering and considerable stratification is observed in the density profiles. In contrast, a system with weak molecule-substrate coupling adopts a director orientation orthogonal to the substrate plane, owing to the increased influence of the nematic-vapour interface. There are significant differences between the structures adopted at the two interfaces, in contrast with the predictions of density functional treatments of such systems.

  2. Hydrophobic Porous Material Adsorbs Small Organic Molecules

    Science.gov (United States)

    Sharma, Pramod K.; Hickey, Gregory S.

    1994-01-01

    Composite molecular-sieve material has pore structure designed specifically for preferential adsorption of organic molecules for sizes ranging from 3 to 6 angstrom. Design based on principle that contaminant molecules become strongly bound to surface of adsorbent when size of contaminant molecules is nearly same as that of pores in adsorbent. Material used to remove small organic contaminant molecules from vacuum systems or from enclosed gaseous environments like closed-loop life-support systems.

  3. Size selective hydrophobic adsorbent for organic molecules

    Science.gov (United States)

    Sharma, Pramod K. (Inventor); Hickey, Gregory S. (Inventor)

    1997-01-01

    The present invention relates to an adsorbent formed by the pyrolysis of a hydrophobic silica with a pore size greater than 5 .ANG., such as SILICALITE.TM., with a molecular sieving polymer precursor such as polyfurfuryl alcohol, polyacrylonitrile, polyvinylidene chloride, phenol-formaldehyde resin, polyvinylidene difluoride and mixtures thereof. Polyfurfuryl alcohol is the most preferred. The adsorbent produced by the pyrolysis has a silicon to carbon mole ratio of between about 10:1 and 1:3, and preferably about 2:1 to 1:2, most preferably 1:1. The pyrolysis is performed as a ramped temperature program between about 100.degree. and 800.degree. C., and preferably between about 100.degree. and 600.degree. C. The present invention also relates to a method for selectively adsorbing organic molecules having a molecular size (mean molecular diameter) of between about 3 and 6 .ANG. comprising contacting a vapor containing the small organic molecules to be adsorbed with the adsorbent composition of the present invention.

  4. Structure and properties of water film adsorbed on mica surfaces

    Science.gov (United States)

    Zhao, Gutian; Tan, Qiyan; Xiang, Li; Cai, Di; Zeng, Hongbo; Yi, Hong; Ni, Zhonghua; Chen, Yunfei

    2015-09-01

    The structure profiles and physical properties of the adsorbed water film on a mica surface under conditions with different degrees of relative humidity are investigated by a surface force apparatus. The first layer of the adsorbed water film shows ice-like properties, including a lattice constant similar with ice crystal, a high bearing capacity that can support normal pressure as high as 4 MPa, a creep behavior under the action of even a small normal load, and a character of hydrogen bond. Adjacent to the first layer of the adsorbed water film, the water molecules in the outer layer are liquid-like that can flow freely under the action of external loads. Experimental results demonstrate that the adsorbed water layer makes the mica surface change from hydrophilic to weak hydrophobic. The weak hydrophobic surface may induce the latter adsorbed water molecules to form water islands on a mica sheet.

  5. Structure and properties of water film adsorbed on mica surfaces.

    Science.gov (United States)

    Zhao, Gutian; Tan, Qiyan; Xiang, Li; Cai, Di; Zeng, Hongbo; Yi, Hong; Ni, Zhonghua; Chen, Yunfei

    2015-09-14

    The structure profiles and physical properties of the adsorbed water film on a mica surface under conditions with different degrees of relative humidity are investigated by a surface force apparatus. The first layer of the adsorbed water film shows ice-like properties, including a lattice constant similar with ice crystal, a high bearing capacity that can support normal pressure as high as 4 MPa, a creep behavior under the action of even a small normal load, and a character of hydrogen bond. Adjacent to the first layer of the adsorbed water film, the water molecules in the outer layer are liquid-like that can flow freely under the action of external loads. Experimental results demonstrate that the adsorbed water layer makes the mica surface change from hydrophilic to weak hydrophobic. The weak hydrophobic surface may induce the latter adsorbed water molecules to form water islands on a mica sheet.

  6. Interactions of organic contaminants with mineral-adsorbed surfactants

    Science.gov (United States)

    Zhu, L.; Chen, B.; Tao, S.; Chiou, C.T.

    2003-01-01

    Sorption of organic contaminants (phenol, p-nitrophenol, and naphthalene) to natural solids (soils and bentonite) with and without myristylpyridinium bromide (MPB) cationic surfactant was studied to provide novel insight to interactions of contaminants with the mineral-adsorbed surfactant. Contaminant sorption coefficients with mineral-adsorbed surfactants, Kss, show a strong dependence on surfactant loading in the solid. At low surfactant levels, the Kss values increased with increasing sorbed surfactant mass, reached a maximum, and then decreased with increasing surfactant loading. The Kss values for contaminants were always higher than respective partition coefficients with surfactant micelles (Kmc) and natural organic matter (Koc). At examined MPB concentrations in water the three organic contaminants showed little solubility enhancement by MPB. At low sorbed-surfactant levels, the resulting mineral-adsorbed surfactant via the cation-exchange process appears to form a thin organic film, which effectively "adsorbs" the contaminants, resulting in very high Kss values. At high surfactant levels, the sorbed surfactant on minerals appears to form a bulklike medium that behaves essentially as a partition phase (rather than an adsorptive surface), with the resulting Kss being significantly decreased and less dependent on the MPB loading. The results provide a reference to the use of surfactants for remediation of contaminated soils/sediments or groundwater in engineered surfactant-enhanced washing.

  7. Ordered molecular layer structure of lubricating oil adsorbed films

    Institute of Scientific and Technical Information of China (English)

    2001-01-01

    Low-angle X-ray diffraction has been applied to analyze the structure of stearic acid LB films and self-grown surface adsorbed films of aluminium product metalworking lubricants. The results show that LB films exhibit a good layer-like ordered structure in the normal direction of film-carrying surface, while in the tangential direction, they do not show a cyclically ordered molecular arrangement; as for the self-grown surface adsorbed films of aluminium sheet and strip metalworking lubricants, their molecules are orderly arranged to certain degree in both the tangential and the normal directions of film-carrying surface, and they have a short-range ordered structure. Moreover, the better the orientation of normal molecules is, the higher the oil film strength is, and the smaller the friction factor is.

  8. AQUATIC PHOTOLYSIS OF OXY-ORGANIC COMPOUNDS ADSORBED ON GOETHITE.

    Science.gov (United States)

    Goldberg, Marvin C.

    1985-01-01

    Organic materials that will not absorb light at wavelengths longer than 295 nanometers (the solar wavelength cutoff) may nevertheless, undergo electron transfer reactions initiated by light. These reactions occur when the organic materials are adsorbed as ligand complexes to the surface of iron oxy-hydroxide (goethite). The adsorbed materials can be either inner or outer coordination sphere complexes. Goethite was chosen as the iron oxyhydroxide surface because it has the highest thermodynamic stability of any of the oxyhydroxides in water and it can be synthesized easily, with high purity.

  9. Preconcentration in gas or liquid phases using adsorbent thin films

    Directory of Open Access Journals (Sweden)

    Antonio Pereira Nascimento Filho

    2006-03-01

    Full Text Available The possibility of preconcentration on microchannels for organic compounds in gas or liquid phases was evaluated. Microstructures with different geometries were mechanically machined using poly(methyl methacrylate - PMMA as substrates and some cavities were covered with cellulose. The surfaces of the microchannels were modified by plasma deposition of hydrophilic or hydrophobic films using 2-propanol and hexamethyldisilazane (HMDS, respectively. Double layers of HMDS + 2-propanol were also used. Adsorption characterization was made by Quartz Crystal Measurements (QCM technique using reactants in a large polarity range that showed the adsorption ability of the structures depends more on the films used than on the capillary phenomena. Cellulose modified by double layer film showed a high retention capacity for all gaseous compounds tested. However, structures without plasma deposition showed low retention capacity. Microchannels modified with double layers or 2-propanol plasma films showed higher retention than non-modified ones on gas or liquid phase.

  10. Organobentonites as multifunctional adsorbents of organic and inorganic water pollutants

    Directory of Open Access Journals (Sweden)

    Jović-Jovičić Natаša

    2014-01-01

    Full Text Available The aim of this study was to find a low cost, easy to synthesize and efficient adsorbent for the simultaneous adsorption of both organic and inorganic pollutants (including textile dyes, toxic metals etc.. The starting material, domestic bentonite clay from Bogovina was modified with amounts of hexadecyltrimethylammonium cations corresponding to 0.5 and 1.0 times of the value of the cation exchange capacity value. The organobentonites were tested as adsorbents in a three-dye-containing solution, a three-component solution of Pb2+, Cd2+ and Ni2+ and a hexa- component solution containing all investigated dyes and toxic metal cations. The used adsorbents showed the highest affinity toward Acid Yellow 99 and Ni2+ ions. Dye adsorption was enhanced in the presence of toxic metal cations, while the adsorption of all toxic cations from the hexa-component solution was lower than from the three-component solution containing only toxic cations. The synthesized hexadecyltrimethylammonium bentonite could be regarded as an efficient multifunctional adsorbent for the investigated type of water pollutants.

  11. Mechanism of melting in submonolayer films of nitrogen molecules adsorbed on the basal planes of graphite

    DEFF Research Database (Denmark)

    Hansen, Flemming Yssing; Bruch, Ludwig Walter; Taub, H.

    1995-01-01

    The melting mechanism in submonolayer films of N-2 molecules adsorbed on the basal planes of graphite is studied using molecular-dynamics simulations. The melting is strongly correlated with the formation of vacancies in the films. As the temperature increases, the edges of the submonolayer patch...

  12. Interactions between adsorbed macromolecules : measurements on emulsions and liquid films

    NARCIS (Netherlands)

    Vliet, van T.

    1977-01-01

    The aim of this study was to gain more insight into the factors, determining the inter- and intramolecular interactions between adsorbed macromolecules. To that end several experimental and theoretical approaches were followed, using well-defined systems. It was shown that these interactions could c

  13. Organic adsorbates on metal surfaces. PTCDA and NTCDA on AG(110)

    Energy Technology Data Exchange (ETDEWEB)

    Abbasi, Afshin

    2010-02-22

    Polyaromatic molecules functionalized with carboxylic groups have served as model systems for the growth of organic semiconducting films on a large variety of substrates. Most non-reactive substrates allow for a growth mode compatible with the bulk phase of the molecular crystal with two molecules in the unit cell, but some more reactive substrates including Ag(111) and Ag(110) can induce substantial changes in the first monolayer (ML). In the specific case of Ag(110), the adsorbate unit cell of both NTCDA and PTCDA resembles a brickwall structure, with a single molecule in the unit cell. From this finding, it can be concluded that the adsorbate-substrate interaction is stronger than typical inter-molecular binding energies in the respective bulk phases. In the present work, the interactions between small Ag(110) clusters and a single NTCDA or PTCDA molecule are investigated with different ab initio techniques. Four major ingredients contribute to the binding between adsorbate and substrate: Directional bonds between Ag atoms in the topmost layer and the oxygen atoms of the molecule, Pauli repulsion between filled orbitals of molecule and substrate, an attractive van-der-Waals interaction, and a negative net charge on the molecule inducing positive image charges in the substrate, resulting therefore in an attractive Coulomb interaction between these opposite charges. As both Hartree-Fock theory and density functional theory with typical gradient-corrected density functional do not contain any long range correlation energy required for dispersion interactions, we compare these approaches with the fastest numerical technique where the leading term of the van-der-Waals interaction is included, i.e. second order Moeller-Plesset theory (MP2). Both Hartree-Fock and density functional theory result in bended optimized geometries where the adsorbate is interacting mainly via the oxygen atoms, with the core of the molecule repelled from the substrate. Only at the MP2 level

  14. Fluorescence of dyes adsorbed on highly organized nanostructured gold surfaces

    NARCIS (Netherlands)

    Levi, Stefano A.; Mourran, Ahmed; Spatz, Joachim P.; Veggel, van Frank C.J.M.; Reinhoudt, David N.; Möller, M.

    2002-01-01

    It is shown that fluorescent dyes can be adsorbed selectively on gold nanoparticles which are immobilized on a glass substrate and that the fluorescence originating from the adsorbed dyes exhibits significantly less quenching when compared to dyes adsorbed on bulk gold. Self-assembled monolayers of

  15. Heat capacity measurements of atoms and molecules adsorbed on evaporated metal films

    Energy Technology Data Exchange (ETDEWEB)

    Kenny, T.W.

    1989-05-01

    Investigations of the properties of absorbed monolayers have received great experimental and theoretical attention recently, both because of the importance of surface processes in practical applications such as catalysis, and the importance of such systems to the understanding of the fundamentals of thermodynamics in two dimensions. We have adapted the composite bolometer technology to the construction of microcalorimeters. For these calorimeters, the adsorption substrate is an evaporated film deposited on one surface of an optically polished sapphire wafer. This approach has allowed us to make the first measurements of the heat capacity of submonolayer films of /sup 4/He adsorbed on metallic films. In contrast to measurements of /sup 4/He adsorbed on all other insulating substrates, we have shown that /sup 4/He on silver films occupies a two-dimensional gas phase over a broad range of coverages and temperatures. Our apparatus has been used to study the heat capacity of Indium flakes. CO multilayers, /sup 4/He adsorbed on sapphire and on Ag films and H/sub 2/ adsorbed on Ag films. The results are compared with appropriate theories. 68 refs., 19 figs.

  16. Heat capacity measurements of atoms and molecules adsorbed on evaporated metal films

    International Nuclear Information System (INIS)

    Investigations of the properties of absorbed monolayers have received great experimental and theoretical attention recently, both because of the importance of surface processes in practical applications such as catalysis, and the importance of such systems to the understanding of the fundamentals of thermodynamics in two dimensions. We have adapted the composite bolometer technology to the construction of microcalorimeters. For these calorimeters, the adsorption substrate is an evaporated film deposited on one surface of an optically polished sapphire wafer. This approach has allowed us to make the first measurements of the heat capacity of submonolayer films of 4He adsorbed on metallic films. In contrast to measurements of 4He adsorbed on all other insulating substrates, we have shown that 4He on silver films occupies a two-dimensional gas phase over a broad range of coverages and temperatures. Our apparatus has been used to study the heat capacity of Indium flakes. CO multilayers, 4He adsorbed on sapphire and on Ag films and H2 adsorbed on Ag films. The results are compared with appropriate theories. 68 refs., 19 figs

  17. Wetting transitions of simple liquid films adsorbed on selfassembled monolayer substrates: an ellipsometric study

    Science.gov (United States)

    Batchelder, D. N.; Cheng, Y. L.; Evans, S. D.; Henderson, J. R.

    We report on an ellipsometric experimental study designed to explore the relevance of the wetting phase diagram predicted by liquid state physics of basic models, to the wide class of simple organic liquid films that adsorb from saturated vapour onto planar substrates at room temperature. The wetting properties are explored by measuring adsorption isotherms in the approach to saturation, in particular, for adsorption of n -hexane on a variety of specially constructed substrates (self-assembled monolayers) spanning a wide range of surface energy, and by carrying out the microscopic equivalent of contact angle experiments at saturation. We locate a wetting transition, which in our case is continuous, and then study its properties in detail. The general prediction of the wetting phase diagram, that wetting transitions should be ubiquitous in nature and readily located via control over the substrate field, is supported by our data, but the quantitative nature of the thick film adsorption regime is not in agreement with Lifshitz theory. This conclusion supports the work of a variety of earlier related studies, but contrasts with recent results for adsorption onto the surface of water. In addition, the correlation length determined from our complete wetting adsorption isotherms is mesoscopic, suggesting that equilibrium statistical mechanics of simple models of inhomogeneous fluids cannot explain the data.

  18. Heterogeneous and Photochemical Reactions Involving Surface Adsorbed Organics: Common Lignin Pyrolysis Products With Nitrogen Dioxide.

    Science.gov (United States)

    Hinrichs, R. Z.; Nichols, B. R.; Rapa, C.; Costa, V.

    2009-05-01

    Solid-air interfaces, such as airborne particulate matter and ground level surfaces, provide unique supports for tropospheric heterogeneous chemistry. These interfaces commonly contain surface adsorbed organics, such as lignin pyrolysis products, that can significantly alter their physical and chemical properties. Attenuated total reflectance infrared spectroscopy (ATR-FTIR) provides an ideal tool for monitoring chemical changes in thin organic films during heterogeneous and photochemical reactions. Phenolic compounds, with and without co- adsorbed photosensitizers, were exposed to NO2 concentrations in the parts-per-billion range at 300 K and 20% relative humidity. Catechol, when mixed with benzophenone or dicyclohexylketone, formed 4- nitrocatechol as the dominant product under dark conditions. Deuterating the catechol alcohol groups caused the initial rate of reaction to decrease by a factor of 3.3±0.5, consistent with formation of the ortho- semiquinone radical as the rate determining step. The rate of 4-nitrocatechol formation did not increase under illuminated conditions, even with the presence of benzophenone a well known photosensitizer. UV-A/visible radiation did, however, initiate a photochemical reaction between benzophenone and 4-nitrocatechol, likely forming high molecular weight polymerization products. In contrast, 2-ethoxyphenol displayed no reactivity with NO2, even under illuminated conditions with a photosensitizer. Implications for the fate of lignin pyrolysis products, which are prevalent in biomass combustion smoke, will be discussed.

  19. Preparation and characterization of a novel adsorbent for removing lipophilic organic from water

    Institute of Scientific and Technical Information of China (English)

    LIU; Huijuan; DAI; Ruihua; QU; Jiuhui; RU; Jia

    2005-01-01

    A novel composite adsorbent containing a kind of lipid-triolein is studied. The adsorbent is prepared by embedding triolein into cellulose acetate (CA) sphere. The preparation method, the physical-chemical properties of the adsorbent and the removal efficiency of two organochlorinated pesticides are studied. The adsorbent is stable in water and no triolein leaks into water for 465 h soaking. The adsorbent has high adsorption capacity for organochlorinated pesticides such as dieldrin and aldrin. The results suggest that triolein-containing adsorbent could serve as a good adsorbent for lipophilic organic pollutants. The adsorption rate for lipophilic pollutants is very fast and has relation with the logKow of the compounds.

  20. Role of structure and glycosylation of adsorbed protein films in biolubrication.

    Directory of Open Access Journals (Sweden)

    Deepak H Veeregowda

    Full Text Available Water forms the basis of lubrication in the human body, but is unable to provide sufficient lubrication without additives. The importance of biolubrication becomes evident upon aging and disease, particularly under conditions that affect secretion or composition of body fluids. Insufficient biolubrication, may impede proper speech, mastication and swallowing, underlie excessive friction and wear of articulating cartilage surfaces in hips and knees, cause vaginal dryness, and result in dry, irritated eyes. Currently, our understanding of biolubrication is insufficient to design effective therapeutics to restore biolubrication. Aim of this study was to establish the role of structure and glycosylation of adsorbed protein films in biolubrication, taking the oral cavity as a model and making use of its dynamics with daily perturbations due to different glandular secretions, speech, drinking and eating, and tooth brushing. Using different surface analytical techniques (a quartz crystal microbalance with dissipation monitoring, colloidal probe atomic force microscopy, contact angle measurements and X-ray photo-electron spectroscopy, we demonstrated that adsorbed salivary conditioning films in vitro are more lubricious when their hydrophilicity and degree of glycosylation increase, meanwhile decreasing their structural softness. High-molecular-weight, glycosylated proteins adsorbing in loops and trains, are described as necessary scaffolds impeding removal of water during loading of articulating surfaces. Comparing in vitro and in vivo water contact angles measured intra-orally, these findings were extrapolated to the in vivo situation. Accordingly, lubricating properties of teeth, as perceived in 20 volunteers comprising of equal numbers of male and female subjects, could be related with structural softness and glycosylation of adsorbed protein films on tooth surfaces. Summarizing, biolubrication is due to a combination of structure and glycosylation

  1. Anomalous conformational transitions in cytochrome C adsorbing to Langmuir-Blodgett films

    Science.gov (United States)

    Sankaranarayanan, Kamatchi; Nair, B. U.; Dhathathreyan, A.

    2013-05-01

    Helix to beta conformational transitions in proteins has attracted much attention due to their relevance to fibril formation which is implicated in many neurological diseases. This study reports on unusual conformational transition of cytochrome C adsorbing to hydrophilic surface containing pure cationic lipid and mixed Langmuir-Blodgett films (LB films) of cationic and neutral lipids. Evidence for conformational changes of the protein from its native helical state to beta sheet comes from Circular dichroic spectroscopy (CD spectroscopy). Analysis of these samples using High resolution TEM (HRTEM) shows a typical fibrillar pattern with each strand spacing of about 0.41 nm across which can be attributed to the repeat distance of interdigitated neighboring hydrogen-bonded ribbons in a beta sheet. Changes in contact angles of protein adsorbing to the LB films together with the increased mass uptake of water using quartz crystal microbalance (QCM) confirm the role of positive charges in the conformational transition. Dehydration of the protein resulting from the excess water entrainment in the polar planes of the cationic lipid in hydrophilic surface seems to trigger the refolding of the protein to beta sheet while it retains its native conformation in hydrophobic films. The results suggest that drastic conformational changes in CytC adsorbing to cationic lipids may be of significance in its role as a peripheral membrane protein.

  2. Unusual Morphologies of Poly(vinyl alcohol) Thin Films Adsorbed on Poly(dimethylsiloxane) Substrates.

    Science.gov (United States)

    Karki, Akchheta; Nguyen, Lien; Sharma, Bhanushee; Yan, Yan; Chen, Wei

    2016-04-01

    Adsorption of poly(vinyl alcohol) (PVOH), 99% and 88% hydrolyzed poly(vinyl acetate), to poly(dimethylsiloxane) (PDMS) substrates was studied. The substrates were prepared by covalently attaching linear PDMS polymers of 2, 9, 17, 49, and 116 kDa onto silicon wafers. As the PDMS molecular weight/thickness increases, the adsorbed PVOH thin films progressively transition from continuous to discontinuous morphologies, including honeycomb and fractal/droplet. The structures are the result of thin film dewetting that occurs upon exposure to air. The PVOH film thickness does not vary significantly on these PDMS substrates, implicating the PDMS thickness as the cause for the morphology differences. The adsorbed PVOH thin films are less stable and have a stronger tendency to dewet on thicker, more liquid-like PDMS layers. When PVOH(99%) and PVOH(88%) thin films are compared, fractal and droplet morphologies are observed on high molecular weight PDMS substrates, respectively. The formation of the unique fractal features in the PVOH(99%) thin films as well as other crystalline and semicrystalline thin films is most likely driven by crystallization during the dehydration process in a diffusion-limited aggregation fashion. The only significant enhancement in hydrophilicity via PVOH adsorption was obtained on PDMS(2k), which is completely covered with a PVOH thin film. To mimic the lower receding contact angle and less liquid-like character of the PDMS(2k) substrate, light plasma treatment of the higher molecular weight PDMS substrates was carried out. On the treated PDMS substrates, the adsorbed PVOH thin films are in the more continuous honeycomb morphology, giving rise to significantly enhanced wettability. Furthermore, hydrophobic recovery of the hydrophilized PDMS substrates was not observed during a 1 week period. Thus, light plasma oxidation and subsequent PVOH adsorption can be utilized as a means to effectively hydrophilize conventional PDMS substrates. This study

  3. Competition between the superfluidity and the slippage of 4He films adsorbed on porous gold

    International Nuclear Information System (INIS)

    We have carried out QCM measurements for 4He films adsorbed on porous gold in the crossover region between the superfluidity and slippage. In relative low areal densities, the resonance frequency increases gradually below TS due to the slippage of solid film, while the superfluid onset is observed in high areal densities. In the crossover region, we observed a peculiar behavior: The increase in the resonance frequency below TS is suddenly suppressed at a certain temperature TD. From these observations, it is concluded that the superfluidity and the slippage of 4He competes with each other.

  4. Competition between the superfluidity and the slippage of {sup 4}He films adsorbed on porous gold

    Energy Technology Data Exchange (ETDEWEB)

    Ideura, K; Kobayashi, H; Taniguchi, J; Suzuki, M [Department of Applied Physics and Chimistry, University of Eletro-Communications, Chofu, Tokyo 182-8585 (Japan); Hosomi, N [Department of Physics, Aichi University of Education, Kariya, Aichi 448-8542 (Japan)], E-mail: ide@phys.uec.ac.jp

    2009-02-01

    We have carried out QCM measurements for {sup 4}He films adsorbed on porous gold in the crossover region between the superfluidity and slippage. In relative low areal densities, the resonance frequency increases gradually below T{sub S} due to the slippage of solid film, while the superfluid onset is observed in high areal densities. In the crossover region, we observed a peculiar behavior: The increase in the resonance frequency below T{sub S} is suddenly suppressed at a certain temperature T{sub D}. From these observations, it is concluded that the superfluidity and the slippage of {sup 4}He competes with each other.

  5. Heat capacity of quantum adsorbates: Hydrogen and helium on evaporated gold films

    Energy Technology Data Exchange (ETDEWEB)

    Birmingham, J.T. [Univ. of California, Berkeley, CA (United States). Dept. of Physics]|[Lawrence Berkeley National Lab., CA (United States). Materials Sciences Div.

    1996-06-01

    The author has constructed an apparatus to make specific heat measurements of quantum gases adsorbed on metallic films at temperatures between 0.3 and 4 K. He has used this apparatus to study quench-condensed hydrogen films between 4 and 923 layers thick with J = 1 concentrations between 0.28 and 0.75 deposited on an evaporated gold surface. He has observed that the orientational ordering of the J = 1 molecules depends on the substrate temperature during deposition of the hydrogen film. He has inferred that the density of the films condensed at the lowest temperatures is 25% higher than in bulk H{sub 2} crystals and have observed that the structure of those films is affected by annealing at 3.4 K. The author has measured the J = 1 to J = 0 conversion rate to be comparable to that of the bulk for thick films; however, he found evidence that the gold surface catalyzes conversion in the first two to four layers. He has also used this apparatus to study films of {sup 4}He less than one layer thick adsorbed on an evaporated gold surface. He shows that the phase diagram of the system is similar to that for {sup 4}He/graphite although not as rich in structure, and the phase boundaries occur at different coverages and temperatures. At coverages below about half a layer and at sufficiently high temperatures, the {sup 4}He behaves like a two-dimensional noninteracting Bose gas. At lower temperatures and higher coverages, liquidlike and solidlike behavior is observed. The Appendix shows measurements of the far-infrared absorptivity of the high-{Tc} superconductor La{sub 1.87}Sr{sub 0.13}CuO{sub 4}.

  6. Organic photovoltaic films

    Directory of Open Access Journals (Sweden)

    Jenny Nelson

    2002-05-01

    The last two years have seen an unprecedented growth of interest in solar cells made from organic electronic materials. This is partly due to the rapid growth of the photovoltaic market1, which has stimulated research into longer term, more innovative photovoltaic technologies, and partly to the development of organic electronic materials for display applications. The rapid progress in optoelectronic molecular materials has introduced a range of potential new photovoltaic materials, as well as an improved understanding of the capabilities of such materials and confidence in their application2.

  7. Scandium-Triflate/Metal-Organic Frameworks: Remarkable Adsorbents for Desulfurization and Denitrogenation.

    Science.gov (United States)

    Khan, Nazmul Abedin; Jhung, Sung Hwa

    2015-12-01

    Scandium-triflate (Sc(OTf)3) was introduced for the first time on metal-organic frameworks (MOFs), to utilize acidic Sc(OTf)3 for adsorptive desulfurization and denitrogenation of fuel containing benzothiophene (BT), dibenzothiophene (DBT), quinoline (QUI), and indole (IND). A remarkable improvement in the adsorption capacity (about 65% based on the weight of adsorbents; 90% based on the surface area of the adsorbents) was observed with the Sc(OTf)3/MOFs as compared to the virgin MOFs for the adsorption of BT from liquid fuel. The basic QUI was also adsorbed preferentially onto the acidic Sc(OTf)3/MOFs. However, nonsupported Sc(OTf)3 showed negligible adsorption capacities. The improved adsorptive performance for BT, DBT, and QUI might be derived from acid-base interactions between the acidic Sc(OTf)3 and basic adsorbates. On the other hand, the Sc(OTf)3, loaded on MOFs, reduced the adsorption capacity for neutral IND due to lack of interaction between the neutral adsorbate and acidic adsorbent and the reduced porosities of the modified adsorbents. The reusability of the adsorbents was found satisfactory up to the fourth run. On the basis of the result, it is suggested that metal-triflates, such as Sc(OTf)3, can be prospective materials for adsorptive desulfurization/denitrogenation of fuels when supported on porous materials such as MOFs. PMID:26575418

  8. Photoconductivity of thin organic films

    International Nuclear Information System (INIS)

    Thin organic films were deposited on silicon oxide surfaces with golden interdigitated electrodes (interelectrode gap was 2 μm), and the film resistivities were measured in dark and under white light illumination. The compounds selected for the measurements include molecules widely used in solar cell applications, such as polythiophene (PHT), fullerene (C60), pyrelene tetracarboxylic diimide (PTCDI) and copper phthalocyanine (CuPc), as well as molecules potentially interesting for photovoltaic applications, e.g. porphyrin-fullerene dyads. The films were deposited using thermal evaporation (e.g. for C60 and CuPc films), spin coating for PHT, and Langmuir-Schaeffer for the layer-by-layer deposition of porphyrin-fullerene dyads. The most conducting materials in the series are films of PHT and CuPc with resistivities 1.2 x 103 Ω m and 3 x 104 Ω m, respectively. Under light illumination resistivity of all films decreases, with the strongest light effect observed for PTCDI, for which resistivity decreases by 100 times, from 3.2 x 108 Ω m in dark to 3.1 x 106 Ω m under the light.

  9. A novel aminated polymeric adsorbent for removing refractory dissolved organic matter from landfill leachate treatment plant

    Institute of Scientific and Technical Information of China (English)

    ZHANG Long; LI Aimin; WANG Jinnan; LU Yufei; ZHOU Youdong

    2009-01-01

    Refractory dissolved organic matter (DOM) from landfill leachate treatment plant was with high dissolved organic carbon (DOC) content.An aminated polymeric adsorbent NDA-8 with tertiary amino groups and sufficient mesopore was synthesized, which exhibited high adsorption capacity to the DOM (raw water after coagulation).Resin NDA-8 performed better in the uptake of the DOM than resin DAX-8 and A100.Electrostatic attraction was considered as the decisive interaction between the adsorbent and adsorbate.Special attention was paid to the correlation between porous structure and adsorption capacity.The mesopore of NDA-8 played a crucial role during uptake of the DOM.In general, resin in chloride form performed a higher removal rate of DOC.According to the column adsorption test, total adsorption capacity of NDA-8 was calculated to 52.28 mg DOC/mL wet resin.0.2 mol/L sodium hydroxide solution could regenerate the adsorbent efficiently.

  10. Comparative study of normal and branched alkane monolayer films adsorbed on a solid surface. II. Dynamics

    DEFF Research Database (Denmark)

    Enevoldsen, Ann Dorrit; Hansen, Flemming Yssing; Diama, A.;

    2007-01-01

    The dynamics of monolayer films of the n-alkane tetracosane (n-C24H52) and the branched alkane squalane (C30H62) adsorbed on graphite have been studied by quasielastic and inelastic neutron scattering and molecular dynamics (MD) simulations. Both molecules have 24 carbon atoms along their carbon...... on very different time scales: 1-40 ps (DCS) and 0.1-4 ns (HFBS). The MD simulations were done on corresponding time scales and were used to interpret the neutron spectra. The authors found that the dynamics of the two monolayers are qualitatively similar on the respective time scales...

  11. Comparative study of normal and branched alkane monolayer films adsorbed on a solid surface. I. Structure

    DEFF Research Database (Denmark)

    Enevoldsen, Ann Dorrit; Hansen, Flemming Yssing; Diama, A.;

    2007-01-01

    The structure of a monolayer film of the branched alkane squalane (C30H62) adsorbed on graphite has been studied by neutron diffraction and molecular dynamics (MD) simulations and compared with a similar study of the n-alkane tetracosane (n-C24H52). Both molecules have 24 carbon atoms along...... their backbone and squalane has, in addition, six methyl side groups. Upon adsorption, there are significant differences as well as similarities in the behavior of these molecular films. Both molecules form ordered structures at low temperatures; however, while the melting point of the two-dimensional (2D...... temperature. The neutron diffraction data show that the translational order in the squalane monolayer is significantly less than in the tetracosane monolayer. The authors' MD simulations suggest that this is caused by a distortion of the squalane molecules upon adsorption on the graphite surface. When...

  12. Molecular separations with breathing metal-organic frameworks: modelling packed bed adsorbers.

    Science.gov (United States)

    Van Assche, Tom R C; Baron, Gino V; Denayer, Joeri F M

    2016-03-14

    Various metal-organic framework (MOFs) adsorbents show peculiar adsorption behaviour as they can adopt different crystal phases, each phase with its own adsorption characteristics. Besides external stimuli such as temperature or light, different species of guest adsorbate can trigger a transition (breathing) of the host structure at a different pressure. Such phase transitions also occur during dynamic separations on a packed bed of adsorbent, where the concentrations of the adsorbates vary throughout axial column distance and time. This work presents a general strategy to model the adsorption behavior of such phase changing adsorbents during column separations and focuses on remarkable model predictions for pure components and binary mixtures in diluted and non-diluted conditions. During binary breakthrough experiments, the behaviour of flexible adsorbents is quite complex. A succession of complete or even partial phase transformations (resulting in phase coexistence) can occur during the adsorption process. A variety of unusual breakthrough profiles is observed for diluted binary mixtures. Simulations reveal at least five types of breakthrough profiles to emerge. The occurrence of these cases can be rationalized by the hodograph technique, combined with the phase diagram of the adsorbent. The remarkable experimental breakthrough profiles observed for ortho-xylene/ethylbenzene (diluted) and CO2/CH4 (non-diluted) separation on the flexible MIL-53 framework can be rationalized by application of the proposed model strategy. PMID:26885972

  13. Organic thin-film photovoltaics

    OpenAIRE

    Liu, Miaoyin

    2010-01-01

    Zusammenfassung Zur Verbesserung der Leistungsumwandlung in organischen Solarzellen sind neue Materialien von zentraler Bedeutung, die sämtliche Erfordernisse für organische Photovoltaik-Elemente erfüllen. In der vorliegenden Arbeit „Organic thin-film photovoltaics“ wurden im Hinblick auf ein besseres Verständnis der Zusammenhänge zwischen molekularer Struktur und der Leistungsfähigkeit neue Materialien in „bulk-heterojunction“ Solarzellen und in Festphasen-Farbstoffsensibilisierten ...

  14. Nanotribological properties of water films adsorbing atop, and absorbing below, graphene layers supported by metal substrates

    Science.gov (United States)

    Liu, Zijian; Curtis, C. K.; Stine, R.; Sheehan, P.; Krim, J.

    The tribological properties of graphite, a common lubricant with known sensitivity to the presence of water, have been studied extensively at the macroscopic and microscopic scales. Although far less attention has been devoted to the tribological properties of graphene, it has been established that the tribological response to the presence of water is dissimilar from that of graphite. We report here a quartz crystal microbalance study of the nanotribological properties of water films adsorbed/absorbed on graphene layers prepared by either chemical decomposition on nickel(111) substrates or transfer of freestanding graphene layers to aluminum substrates. Sliding friction levels of the water films were also measured for metal surfaces in the absence of a graphene layer. We observe very high friction levels for water adsorbed atop graphene on Ni(111) and very low levels for water on aluminum. For the case of graphene/aluminum, the data indicate that the water is absorbing between the graphene layer and the aluminum. Dissipation levels moreover indicate the presence of an interstitial water increases sliding friction between the graphene and the aluminum substrate Work supported by NSF and NRL.

  15. The onset of superfluidity in thin films of 4He adsorbed on ordered and disordered substrates

    International Nuclear Information System (INIS)

    The authors have completed a systematic study of the superfluid density of 4He films adsorbed on two substrates: exfoliated basal-plane graphite and 91% porosity aerogel glass. The authors measurements demonstrate a dramatic difference in the coverage-dependence of the superfluid density in these two systems. The onset of superfluidity in the aerogel system is similar to that observed in the case of other disordered substrates such as Vycor glass and mylar. The superfluid density at zero temperature is nearly proportional to coverage once the critical coverage for superfluidity is exceeded. The superfluid density for films adsorbed on graphite does not evolve in this simple fashion. The onset of superfluidity appears to occur near two layers, but the superfluid density increases very rapidly between 2.5 and 3 layers. This coverage regime is also characterized by a dramatic sharpening density and transition temperature remain essentially unchanged as the coverage is increased. We will discuss in the context of recent theoretical work on the onset of superfluidity in model Bose systems

  16. Effect of γ-ray irradiation on adsorbents used in organic waste treatment

    International Nuclear Information System (INIS)

    Radioactive organic liquids (ROLs) are waste that require specific treatment. The Arvia process, developed by Arvia Technology Ltd., combines adsorption of organic material with electrochemical oxidation. This work focuses on the effect of γ-rays on the performance of adsorbents used in the Arvia process. Adsorbents used in this experimental study were provided by Arvia Technology Ltd. Specifically, Nyex 1000, a flake like carbon-based adsorbent, and Nyex 2105, a carbon-based adsorbent with a granular morphology. The γ-ray irradiation experiments were carried out using a Co-60 irradiator. The impact of irradiation on the microstructure, the adsorption capacity and the leaching of the 2 adsorbents were studied. The results show that no significant changes were detected in terms of structure, adsorption capacity and leaching of ions. The results of this paper are promising for the use of Nyex 1000 and Nyex 2105 as adsorbents in electrochemical waste treatment processes which involve high levels of γ-rays. The article is followed by the slides of the presentation

  17. Covalent organic frameworks: Potential adsorbent for carbon dioxide adsorption

    Science.gov (United States)

    Xie, Yinhuan

    A series of covalent organic frameworks (COFs) based on propeller shaped hexaphenylbenzene derivatives were obtained under solvothermal conditions via Schiff base reaction. The relationship between the geometry parameters of monomers and gas absorption behaviors of planar COFs was investigated. The FT-IR spectroscopy confirms the formation of imine double bond in the obtained COFs by showing a peak around 1620 cm-1. The resulting frameworks have high BET surface areas approaching 700 m2/g and CO2 uptake up to 14% at 273 K and 1 bar, which are better than most of the 2-D porous aromatic frameworks. The thermogravimetric analysis shows those frameworks are stable until 773 K, allowing for the practical application of the post-combustion CO2 technology. Moreover, a novel synthetic strategy for the trigonal pyramidal hydrozide monomers was established. It provides an efficient way to synthesize the hydrozide monomers at multi-gram scale, promising for the synthesis of hydrozane porous organic cages.

  18. Graphene nanosheets and graphite oxide as promising adsorbents for removal of organic contaminants from aqueous solution.

    Science.gov (United States)

    Ji, Liangliang; Chen, Wei; Xu, Zhaoyi; Zheng, Shourong; Zhu, Dongqiang

    2013-01-01

    Graphenes are an emerging class of carbon nanomaterials whose adsorption properties toward organic compounds have not been well understood. In the present study, graphene nanosheets were prepared by reoxidation and abrupt heating of graphite oxide, which was prepared by sequential chemical oxidation of commercial nonporous graphite powder. Adsorption properties of three aromatic compounds (naphthalene, 2-naphthol, and 1-naphthylamine) and one pharmaceutical compound (tylosin) on graphene nanosheets and graphite oxide were examined to explore the potential of these two adsorbents for the removal of organic contaminants from aqueous solutions. Compared with the literature data of adsorption on carbon nanotubes, adsorption of bulky, flexible tylosin on graphene nanosheets exhibited markedly faster adsorption kinetics, which can be attributed to their opened-up layer structure. Graphene nanosheets and graphite oxide showed similar sequences of adsorption affinity: 1-naphthylamine > 2-naphthol > tylosin > naphthalene (with much larger differences observed on graphite oxide). It was proposed that the strong adsorption of the three aromatic compounds was mainly due to π-π electron donor-acceptor interactions with the graphitic surfaces of adsorbents. Additionally, Lewis acid-base interaction was likely an important factor contributing to the strong adsorption of 1-naphthylamine and tylosin, especially for the O-functionality-abundant graphite oxide. After being normalized on the basis of adsorbent surface area, adsorption affinities of all four tested adsorbates on graphene nanosheets were very close to those on nonporous graphite powder, reflecting complete accessibility of the adsorbent surface area in adsorption.

  19. Comparative study of normal and branched alkane monolayer films adsorbed on a solid surface. I. Structure

    Science.gov (United States)

    Enevoldsen, A. D.; Hansen, F. Y.; Diama, A.; Criswell, L.; Taub, H.

    2007-03-01

    The structure of a monolayer film of the branched alkane squalane (C30H62) adsorbed on graphite has been studied by neutron diffraction and molecular dynamics (MD) simulations and compared with a similar study of the n-alkane tetracosane (n-C24H52). Both molecules have 24 carbon atoms along their backbone and squalane has, in addition, six methyl side groups. Upon adsorption, there are significant differences as well as similarities in the behavior of these molecular films. Both molecules form ordered structures at low temperatures; however, while the melting point of the two-dimensional (2D) tetracosane film is roughly the same as the bulk melting point, the surface strongly stabilizes the 2D squalane film such that its melting point is 91K above its value in bulk. Therefore, squalane, like tetracosane, will be a poor lubricant in those nanoscale devices that require a fluid lubricant at room temperature. The neutron diffraction data show that the translational order in the squalane monolayer is significantly less than in the tetracosane monolayer. The authors' MD simulations suggest that this is caused by a distortion of the squalane molecules upon adsorption on the graphite surface. When the molecules are allowed to relax on the surface, they distort such that all six methyl groups point away from the surface. This results in a reduction in the monolayer's translational order characterized by a decrease in its coherence length and hence a broadening of the diffraction peaks. The MD simulations also show that the melting mechanism in the squalane monolayer is the same footprint reduction mechanism found in the tetracosane monolayer, where a chain melting drives the lattice melting.

  20. Atomic force microscopy measurements of topography and friction on dotriacontane films adsorbed on a SiO2 surface

    DEFF Research Database (Denmark)

    Trogisch, S.; Simpson, M.J.; Taub, H.;

    2005-01-01

    We report comprehensive atomic force microscopy (AFM) measurements at room temperature of the nanoscale topography and lateral friction on the surface of thin solid films of an intermediate-length normal alkane, dotriacontane (n-C32H66), adsorbed onto a SiO2 surface. Our topographic and frictional...

  1. The Use of Amberlite Adsorbents for Green Chromatography Determination of Volatile Organic Compounds in Air

    Directory of Open Access Journals (Sweden)

    Luis Juan-Peiró

    2012-01-01

    Full Text Available Passive samplers have been widely used for volatile organic compounds determination. Following the green chemistry tendency of the direct determination of adsorbed compounds in membrane-based devices through using head space direct chromatography analysis, this work has evaluated the use of Amberlite XAD-2, XAD-4, and XAD-16 adsorbents as a filling material for passive samplers. Direct analysis of the membranes by HS-GC-MS involves a solvent-free method avoiding any sample treatment. For exposed membranes, recoveries ranged from 10% to 203%, depending on the compound and adsorbent used. The limit of the detection values ranged from 1 to 140 ng per sampler. Acceptable precision and sensitivity levels were obtained for the XAD resins assayed.

  2. Low cost adsorbents for the removal of organic pollutants from wastewater.

    Science.gov (United States)

    Ali, Imran; Asim, Mohd; Khan, Tabrez A

    2012-12-30

    Water pollution due to organic contaminants is a serious issue because of acute toxicities and carcinogenic nature of the pollutants. Among various water treatment methods, adsorption is supposed as the best one due to its inexpensiveness, universal nature and ease of operation. Many waste materials used include fruit wastes, coconut shell, scrap tyres, bark and other tannin-rich materials, sawdust and other wood type materials, rice husk, petroleum wastes, fertilizer wastes, fly ash, sugar industry wastes blast furnace slag, chitosan and seafood processing wastes, seaweed and algae, peat moss, clays, red mud, zeolites, sediment and soil, ore minerals etc. These adsorbents have been found to remove various organic pollutants ranging from 80 to 99.9%. The present article describes the conversion of waste products into effective adsorbents and their application for water treatment. The possible mechanism of adsorption on these adsorbents has also been included in this article. Besides, attempts have been made to discuss the future perspectives of low cost adsorbents in water treatment. PMID:23023039

  3. DNA adsorption measured with ultra-thin film organic field effect transistors

    NARCIS (Netherlands)

    Stoliar, P.; Bystrenova, E.; Quiroga, S.D.; Annibale, P.; Facchini, M.; Spijkman, M.; Setayesh, S.; Leeuw, D. de; Biscarini, F.

    2009-01-01

    Organic ultra-thin film field effect transistors (FET) are operated as label-free sensors of deoxyribonucleic acid (DNA) adsorption. Linearized plasmid DNA molecules (4361 base pairs) are deposited froma solution on two monolayers thick pentacene FET. The amount of adsorbed DNA is measured by AFM an

  4. Microcrystalline organic thin-film solar cells.

    Science.gov (United States)

    Verreet, Bregt; Heremans, Paul; Stesmans, Andre; Rand, Barry P

    2013-10-11

    Microcrystalline organic films with tunable thickness are produced directly on an indium-tin-oxide substrate, by crystallizing a thin amorphous rubrene film followed by its use as a template for subsequent homoepitaxial growth. These films, with exciton diffusion lengths exceeding 200 nm, produce solar cells with increasing photocurrents at thicknesses up to 400 nm with a fill factor >65%, demonstrating significant potential for microcrystalline organic electronic devices. PMID:23939936

  5. Organic and Inorganic Dyes in Polyelectrolyte Multilayer Films

    Directory of Open Access Journals (Sweden)

    Vincent Ball

    2012-12-01

    Full Text Available Polyelectrolyte multilayer films are a versatile functionalization method of surfaces and rely on the alternated adsorption of oppositely charged species. Among such species, charged dyes can also be alternated with oppositely charged polymers, which is challenging from a fundamental point of view, because polyelectrolytes require a minimal number of charges, whereas even monovalent dyes can be incorporated during the alternated adsorption process. We will not only focus on organic dyes but also on their inorganic counterparts and on metal complexes. Such films offer plenty of possible applications in dye sensitized solar cells. In addition, dyes are massively used in the textile industry and in histology to stain textile fibers or tissues. However, the excess of non bound dyes poses serious environmental problems. It is hence of the highest interest to design materials able to adsorb such dyes in an almost irreversible manner. Polyelectrolyte multilayer films, owing to their ion exchange behavior can be useful for such a task allowing for impressive overconcentration of dyes with respect to the dye in solution. The actual state of knowledge of the interactions between charged dyes and adsorbed polyelectrolytes is the focus of this review article.

  6. Adsorbed films of three-patch colloids: Continuous and discontinuous transitions between thick and thin films

    Science.gov (United States)

    Dias, C. S.; Araújo, N. A. M.; Telo da Gama, M. M.

    2014-09-01

    We investigate numerically the role of spatial arrangement of the patches on the irreversible adsorption of patchy colloids on a substrate. We consider spherical three-patch colloids and study the dependence of the kinetics on the opening angle between patches. We show that growth is suppressed below and above minimum and maximum opening angles, revealing two absorbing phase transitions between thick and thin film regimes. While the transition at the minimum angle is continuous, in the directed percolation class, that at the maximum angle is clearly discontinuous. For intermediate values of the opening angle, a rough colloidal network in the Kardar-Parisi-Zhang universality class grows indefinitely. The nature of the transitions was analyzed in detail by considering bond flexibility, defined as the dispersion of the angle between the bond and the center of the patch. For the range of flexibilities considered we always observe two phase transitions. However, the range of opening angles where growth is sustained increases with flexibility. At a tricritical flexibility, the discontinuous transition becomes continuous. The practical implications of our findings and the relation to other nonequilibrium transitions are discussed.

  7. Relaxation of surface stress induced by an organic adsorbate: PTCDA on vicinal Ag(111)

    Energy Technology Data Exchange (ETDEWEB)

    Pollinger, Florian; Vrdoljak, Pavo; Fertig, Dominik; Schmitt, Stefan; Kumpf, Christian; Schoell, Achim; Umbach, Eberhard [Universitaet Wuerzburg, Experimentelle Physik II, Am Hubland, 97074 Wuerzburg (Germany); Tian, Zhen; Sander, Dirk; Kirschner, Juergen [Max-Planck-Institut fuer Mikrostrukturphysik, Weinberg 2, 06120 Halle (Germany)

    2007-07-01

    Self-organization of metallic surfaces on large scales can be induced by the adsorption of organic molecules and has been observed in several experiments. One example is the growth of 3,4,9,10-perylenetetracarboxylic-acid dianhydride (PTCDA) on stepped (8.5 -vicinal) Ag(111) surfaces. At elevated temperatures, the adsorbate molecules lead to a bunching of substrate steps, which agglomerate to facets of critical sizes. The facets arrange in a coverage-dependent grating-like pattern on a mesoscopic length scale. The resulting order requires a long-range interaction which is mediated by the substrate. It can be explained by a change of surface stress induced by the adsorbate layer. Experimentally, such a change is directly accessible by an optical cantilever bending technique. We monitored the bending of a faceting thin Ag(10 8 7) crystal with this method in order to quantify the occurring relaxation of surface stress.

  8. Solid waste from leather industry as adsorbent of organic dyes in aqueous-medium

    Energy Technology Data Exchange (ETDEWEB)

    Oliveira, Luiz C.A. [Universidade Federal de Lavras, Depto. de Quimica, Caixa Postal 37, CEP 37200.000, Lavras-MG (Brazil)]. E-mail: luizoliveira@ufla.br; Goncalves, Maraisa [Universidade Federal de Lavras, Depto. de Quimica, Caixa Postal 37, CEP 37200.000, Lavras-MG (Brazil); Oliveira, Diana Q.L. [Universidade Federal de Lavras, Depto. de Quimica, Caixa Postal 37, CEP 37200.000, Lavras-MG (Brazil); Guerreiro, Mario C. [Universidade Federal de Lavras, Depto. de Quimica, Caixa Postal 37, CEP 37200.000, Lavras-MG (Brazil); Guilherme, Luiz R.G. [Universidade Federal de Lavras, Depto. de Ciencia do solo, CEP 37200.000, Lavras-MG (Brazil); Dallago, Rogerio M. [URI-Campus Erechim, Av. 7 Setembro 1621, Centro, CEP 99700-000, Depto de Quimica, Erechim-RS (Brazil)

    2007-03-06

    The industrial tanning of leather usually produces considerable amounts of chromium-containing solid waste and liquid effluents and raises many concerns on its environmental effect as well as on escalating landfill costs. Actually, these shortcomings are becoming increasingly a limiting factor to this industrial activity that claims for alternative methods of residue disposals. In this work, it is proposed a novel alternative destination of the solid waste, based on the removal of organic contaminants from the out coming aqueous-residue. The adsorption isotherm pattern for the wet blue leather from the Aurea tanning industry in Erechim-RS (Brazil) showed that these materials present high activity on adsorbing the reactive red textile dye as well as other compounds. The adsorbent materials were characterized by IR spectroscopy and SEM and tested for the dye adsorption (reactive textile and methylene blue dyes). The concentrations of dyes were measured by UV-vis spectrophotometry and the chromium extraction from leather waste was realized by basic hydrolysis and determined by atomic absorption. As a low cost abundant adsorbent material with high adsorption ability on removing dye methylene blue (80 mg g{sup -1}) and textile dye reactive red (163 mg g{sup -1}), the leather waste is revealed to be a interesting alternative relatively to more costly adsorbent materials.

  9. Solid waste from leather industry as adsorbent of organic dyes in aqueous-medium

    International Nuclear Information System (INIS)

    The industrial tanning of leather usually produces considerable amounts of chromium-containing solid waste and liquid effluents and raises many concerns on its environmental effect as well as on escalating landfill costs. Actually, these shortcomings are becoming increasingly a limiting factor to this industrial activity that claims for alternative methods of residue disposals. In this work, it is proposed a novel alternative destination of the solid waste, based on the removal of organic contaminants from the out coming aqueous-residue. The adsorption isotherm pattern for the wet blue leather from the Aurea tanning industry in Erechim-RS (Brazil) showed that these materials present high activity on adsorbing the reactive red textile dye as well as other compounds. The adsorbent materials were characterized by IR spectroscopy and SEM and tested for the dye adsorption (reactive textile and methylene blue dyes). The concentrations of dyes were measured by UV-vis spectrophotometry and the chromium extraction from leather waste was realized by basic hydrolysis and determined by atomic absorption. As a low cost abundant adsorbent material with high adsorption ability on removing dye methylene blue (80 mg g-1) and textile dye reactive red (163 mg g-1), the leather waste is revealed to be a interesting alternative relatively to more costly adsorbent materials

  10. Experimental study of two-dimensional helium mixture films adsorbed on graphite

    CERN Document Server

    Patel, H

    2002-01-01

    sup 3 He- sup 4 He mixture films adsorbed on graphite were studied down to temperatures below 1 mK using heat capacity and nuclear magnetic resonance (NMR) to probe the system. This work represents the first measurements in this temperature range of the various systems studied. The work focused on two types of mixtures, sup 3 He- sup 4 He mixtures within the second layer, and sup 3 He floating on three layers of sup 4 He. For mixtures within the layer, a homogeneous mixed phase was observed, followed by a phase interpreted as a Fermi liquid of sup 3 He quasiparticle excitations tunneling within a solid sup 4 He lattice. For the second type of mixture, the expected occupancy of the first excited surface normal state was observed. This is accompanied by anomalous behaviour at low temperatures (T < 10 mK) which arises due to a low concentration of sup 3 He atoms being pushed into the third superfluid sup 4 He layer. An NMR spectrometer utilising a cooled differential preamplifier operating at 4 K was develope...

  11. Efficient adsorbents of nanoporous aluminosilicate monoliths for organic dyes from aqueous solution.

    Science.gov (United States)

    El-Safty, Sherif A; Shahat, Ahmed; Awual, Md Rabiul

    2011-07-01

    Growing public awareness on the potential risk to humans of toxic chemicals in the environment has generated demand for new and improved methods for toxicity assessment and removal, rational means for health risk estimation. With the aim of controlling nanoscale adsorbents for functionality in molecular sieving of organic pollutants, we fabricated cubic Im3m mesocages with uniform entrance and large cavity pores of aluminosilicates as highly promising candidates for the colorimetric monitoring of organic dyes in an aqueous solution. However, a feasible control over engineering of three-dimensional (3D) mesopore cage structures with uniform entrance (~5 nm) and large cavity (~10 nm) allowed the development of nanoadsorbent membranes as a powerful tool for large-quantity and high-speed (in minutes) adsorption/removal of bulk molecules such as organic dyes. Incorporation of high aluminum contents (Si/Al=1) into 3D cubic Im3m cage mesoporous silica monoliths resulted in small, easy-to-use optical adsorbent strips. In such adsorption systems, natural surfaces of active acid sites of aluminosilicate strips strongly induced both physical adsorption of chemically responsive dyes and intraparticle diffusion into cubic Im3m mesocage monoliths. Results likewise indicated that although aluminosilicate strips with low Si/Al ratios exhibit distortion in pore ordering and decrease in surface area and pore volume, enhancement of both molecular converges and intraparticle diffusion onto the network surfaces and into the pore architectures of adsorbent membranes was achieved. Moreover, 3D mesopore cage adsorbents are reversible, offering potential for multiple adsorption assays.

  12. Validation of thermodesorption method for analysis of semi-volatile organic compounds adsorbed on wafer surface.

    Science.gov (United States)

    Hayeck, Nathalie; Gligorovski, Sasho; Poulet, Irène; Wortham, Henri

    2014-05-01

    To prevent the degradation of the device characteristics it is important to detect the organic contaminants adsorbed on the wafers. In this respect, a reliable qualitative and quantitative analytical method for analysis of semi-volatile organic compounds which can adsorb on wafer surfaces is of paramount importance. Here, we present a new analytical method based on Wafer Outgassing System (WOS) coupled to Automated Thermal Desorber-Gas chromatography-Mass spectrometry (ATD-GC-MS) to identify and quantify volatile and semi-volatile organic compounds from 6", 8" and 12" wafers. WOS technique allows the desorption of organic compounds from one side of the wafers. This method was tested on three important airborne contaminants in cleanroom i.e. tris-(2-chloroethyl) phosphate (TCEP), tris-(2-chloroisopropyl) phosphate (TCPP) and diethyl phthalate (DEP). In addition, we validated this method for the analysis and quantification of DEP, TCEP and TCPP and we estimated the backside organic contamination which may contribute to the front side of the contaminated wafers. We are demonstrating that WOS/ATD-GC-MS is a suitable and highly efficient technique for desorption and quantitative analysis of organophosphorous compounds and phthalate ester which could be found on the wafer surface.

  13. Development of adsorbent for the simultaneous removal of organic and inorganic contaminants from aqueous solution.

    Science.gov (United States)

    Choi, J W; Chung, S G; Hong, S W; Kim, D J; Lee, S H

    2011-01-01

    In this study, a modified adsorbent, alginate complex beads, was prepared and applied to the removal of mixed contaminants from wastewater. The alginate complex beads were generated by the immobilization of powdered activated carbon and synthetic zeolites onto alginate gel beads, which were then dried at 110 °C for 20 h until the diameter had been reduced to 1 mm. This dry technique increased the hardness of the adsorbent to assure its durability and application. The adsorption onto the alginate complex beads of organic and inorganic compounds, as target contaminants, was investigated by performing both equilibrium and kinetic batch experiments. From the adsorption isotherms, according to the Langmuir equation, the alginate complex bead was capable of effectively removing benzene, toluene, zinc and cadmium. From kinetic batch experiments, the removal efficiencies of benzene, toluene, zinc and cadmium were found to be 66.5, 92.4, 74.1 and 76.7%, respectively, for initial solution concentrations of 100 mg L(-1). The results indicated that the adsorbent developed in this study has the potential to be a promising material for the removal of mixed pollutants from industrial wastewater or contaminated groundwater. PMID:22020474

  14. Comparative study of normal and branched alkane monolayer films adsorbed on a solid surface. II. Dynamics

    Science.gov (United States)

    Enevoldsen, A. D.; Hansen, F. Y.; Diama, A.; Taub, H.; Dimeo, R. M.; Neumann, D. A.; Copley, J. R. D.

    2007-03-01

    The dynamics of monolayer films of the n-alkane tetracosane (n-C24H52) and the branched alkane squalane (C30H62) adsorbed on graphite have been studied by quasielastic and inelastic neutron scattering and molecular dynamics (MD) simulations. Both molecules have 24 carbon atoms along their carbon backbone, and squalane has an additional six methyl side groups symmetrically placed along its length. The authors' principal objective has been to determine the influence of the side groups on the dynamics of the squalane monolayer and thereby assess its potential as a nanoscale lubricant. To investigate the dynamics of these monolayers they used both the disk chopper spectrometer (DCS) and the high flux backscattering spectrometer (HFBS) at the National Institute of Standards and Technology. These instruments made it possible to study dynamical processes such as molecular diffusive motions and vibrations on very different time scales: 1-40ps (DCS) and 0.1-4ns (HFBS). The MD simulations were done on corresponding time scales and were used to interpret the neutron spectra. The authors found that the dynamics of the two monolayers are qualitatively similar on the respective time scales and that there are only small quantitative differences that can be understood in terms of the different masses and moments of inertia of the two molecules. In the course of this study, the authors developed a procedure to separate out the low-frequency vibrational modes in the spectra, thereby facilitating an analysis of the quasielastic scattering. They conclude that there are no major differences in the monolayer dynamics caused by intramolecular branching. It remains to be seen whether this similarity in monolayer dynamics also holds for the lubricating properties of these molecules in confined geometries.

  15. Properties of Organic Films on Aqueous Subphases

    Science.gov (United States)

    Gilman, J.; Vaida, V.

    2003-12-01

    Recently, it has been determined that organics represent a significant percentage of the composition of certain atmospheric aerosols. The air/aqueous interface of such an aerosol has the ability to act as a concentrator and selector of organic surfactants. Amphiphilic organics, such as fatty acids and alcohols, have been found to partition to the interface of aerosols thus creating a hydrophobic organic coating on an aqueous core. The selectivity of the interface was studied by monitoring the composition of various films, via GC-MS, as a function of exposure time. A Langmuir-Blodgett trough was used to contain and collect the self-assembled films that were produced from the addition of binary solutions of surfactants to the surface of an aqueous subphase. Surfactants with differing carbon number and head group functionalities were studied. The stability of the films was examined by varying the thickness of the organic films and the pH of the subphase. For a multilayer film containing equimolar stearic acid and lauric acid on a distilled water subphase, it was found that the acid with the longer hydrocarbon tail (stearic acid) remained at the interface much longer that the shorter acid. Films containing 1-octadecanol and stearic acid, both of which have identical carbon numbers, showed similar lifetimes at the air/water interface. Octadecane was found to have a longer lifetime at the interface when dissolved in equimolar stearic acid than when in a homogeneous film. Multilayer films and films formed on acidic subphases were found to be the most stable for both fatty acids studied. The relevance of these findings as they relate to organic aerosol content and structure as well as atmospheric processing and transport will be discussed.

  16. The effects of adsorbing organic pollutants from super heavy oil wastewater by lignite activated coke.

    Science.gov (United States)

    Tong, Kun; Lin, Aiguo; Ji, Guodong; Wang, Dong; Wang, Xinghui

    2016-05-01

    The adsorption of organic pollutants from super heavy oil wastewater (SHOW) by lignite activated coke (LAC) was investigated. Specifically, the effects of LAC adsorption on pH, BOD5/COD(Cr)(B/C), and the main pollutants before and after adsorption were examined. The removed organic pollutants were characterized by Fourier transform infrared spectroscopy (FTIR), Boehm titrations, gas chromatography-mass spectrometry (GC-MS), and liquid chromatography with organic carbon detection (LC-OCD). FTIR spectra indicated that organic pollutants containing -COOH and -NH2 functional groups were adsorbed from the SHOW. Boehm titrations further demonstrated that carboxyl, phenolic hydroxyl, and lactonic groups on the surface of the LAC increased. GC-MS showed that the removed main organic compounds are difficult to be degraded or extremely toxics to aquatic organisms. According to the results of LC-OCD, 30.37 mg/L of dissolved organic carbons were removed by LAC adsorption. Among these, hydrophobic organic contaminants accounted for 25.03 mg/L. Furthermore, LAC adsorption was found to increase pH and B/C ratio of the SHOW. The mechanisms of adsorption were found to involve between the hydrogen bonding and the functional groups of carboxylic, phenolic, and lactonic on the LAC surface. In summary, all these results demonstrated that LAC adsorption can remove bio-refractory DOCs, which is beneficial for biodegradation. PMID:26808249

  17. Adsorption and oxidation of formaldehyde on a polycrystalline Pt film electrode: An in situ IR spectroscopy search for adsorbed reaction intermediates.

    Science.gov (United States)

    Jusys, Zenonas; Behm, R Jürgen

    2014-01-01

    As part of a mechanistic study of the electrooxidation of C1 molecules we have systematically investigated the dissociative adsorption/oxidation of formaldehyde on a polycrystalline Pt film electrode under experimental conditions optimizing the chance for detecting weakly adsorbed reaction intermediates. Employing in situ IR spectroscopy in an attenuated total reflection configuration (ATR-FTIRS) with p-polarized IR radiation to further improve the signal-to-noise ratio, and using low reaction temperatures (3 °C) and deuterium substitution to slow down the reaction kinetics and to stabilize weakly adsorbed reaction intermediates, we could detect an IR absorption band at 1660 cm(-1) characteristic for adsorbed formyl intermediates. This assignment is supported by an isotope shift in wave number. Effects of temperature, potential and deuterium substitution on the formation and disappearance of different adsorbed species (COad, adsorbed formate, adsorbed formyl), are monitored and quantified. Consequences on the mechanism for dissociative adsorption and oxidation of formaldehyde are discussed.

  18. Advanced Structural Characterization of Organic Thin Films

    DEFF Research Database (Denmark)

    Gu, Yun

    In this thesis, the structural characterizations of three organic film systems are described. Several X-ray based techniques have been utilized for the characterizations for different research goals. The structures of N,N',N-trioctyltriazatriangulenium (Oct3-TATA+) salts have been investigated...... by optical, surface and X-ray method. We describe the production of Langmuir-Blodgett film and how the absorption spectroscopy is a powerful tool to identify layer of monomer and dimer. X-ray refelctometry has been applied as a method for the study of the multilayer film and interface structure. A separation...... of small molecule and polymer layers is indicated by Flory- Huggins theory for the triisopropylsilylethynl pentacene (TIPS-PEN) and polystyrene blend films. In order to investigate the phase separated layers in the ink-jet printed films, we propose a method to measure diraction Bragg peaks by X...

  19. Structure and friction of stearic acid and oleic acid films adsorbed on iron oxide surfaces in squalane.

    Science.gov (United States)

    Doig, Michael; Warrens, Chris P; Camp, Philip J

    2014-01-14

    The structure and friction of fatty acid surfactant films adsorbed on iron oxide surfaces lubricated by squalane are examined using large-scale molecular dynamics simulations. The structures of stearic acid and oleic acid films under static and shear conditions, and at various surface coverages, are described in detail, and the effects of unsaturation in the tail group are highlighted. At high surface coverage, the measured properties of stearic acid and oleic acid films are seen to be very similar. At low and intermediate surface coverages, the presence of a double bond, as in oleic acid, is seen to give rise to less penetration of lubricant in to the surfactant film and less layering of the lubricant near to the film. The kinetic friction coefficient is measured as a function of shear rate within the hydrodynamic (high shear rate) lubrication regime. Lubricant penetration and layering are observed to be correlated with friction coefficient. The friction coefficient with oleic acid depends only weakly on surface coverage, while stearic acid admits more lubricant penetration, and its friction coefficient increases significantly with decreasing surface coverage. Connections between film structure and friction are discussed.

  20. Injection currents in thin disordered organic films

    International Nuclear Information System (INIS)

    Analytic model of barrier-limited injection of charge carriers from metal electrodes into organic film, which was introduced by Arkhipov and co-workers, is modified, considering effects of multiple image charges and injection from both electrodes. Limits of applicability of Arkhipov's model are discussed. Variations from Arkhipov's model are important, if film thickness is comparable with Onsager length

  1. Ellipsometry of functional organic surfaces and films

    CERN Document Server

    Hinrichs, Karsten

    2013-01-01

    Ellipsometry is the method of choice to determin the properties of surfaces and thin films. It provides comprehensive and sensitive characterization in a contactless and non-invasive measurements. This book gives a state-of-the-art survey of ellipsometric investigations of organic films and surfaces, from laboratory to synchrotron applications, with a special focus on in-situ use in processing environments and at solid-liquid interfaces.

  2. Performance of non-coconut base adsorbers in removal of iodine and organic iodides

    International Nuclear Information System (INIS)

    Systems for the removal of radioactive iodine and organic iodides have used impregnated coconut shell activated carbons almost exclusively. Coconut shell carbons have some disadvantages: their geographical origin determines their trace chemical content; pore structures and impregnant effectiveness are highly dependent on activation and impregnation techniques. The authors report laboratory performance of a group of iodine-organic iodide adsorbers using bases other than coconut shell carbon. These have been evaluated in conformity with USAEC Regulatory Guide 1.52 and RDT M16 1T. Performance with regard to 131I2 and CH3131I penetration and high-temperature elution have equaled or exceeded both the requirements of Guide 1.52 and results on typical coconut-shell carbons. Some performance outside Guide 1.52 ranges is included. Experimental problems in simulated LOCA testing are discussed. (U.S.)

  3. Adsorption of metal adatoms on FeO(111) and MgO(111) monolayers: Effects of charge state of adsorbate on rumpling of supported oxide film

    Science.gov (United States)

    Goniakowski, Jacek; Noguera, Claudine; Giordano, Livia; Pacchioni, Gianfranco

    2009-09-01

    We present a theoretical density-functional theory study on the deposition of metal atoms (Ir, Pd, Pt, Ag, and Au) on FeO(111) and MgO(111) monolayers supported on Pt(111). We show the existence of a strong coupling between the charge state of the adsorbed adatom and the local polaroniclike distortion of the oxide film, and we identify two qualitatively different adsorption modes in which the distortion either reinforces the rumpling of the supported oxide film (positively charged adsorbates) or reduces or even reverses the cation-anion stacking (negatively charged adsorbates). Thus, the adsorption mode is a response to the charge state of the adsorbate and is driven mainly by the capacity of adatoms to exchange electrons with the support.

  4. Control of volatile organic chemical emissions by adsorption onto hydrophobic and organophilic adsorbents

    Science.gov (United States)

    Yee, Lee Lai

    With the advent of the Environmental Protection Act 1990, the control of volatile organic chemical (VOC) emissions has become necessary. Complying with regulations may result in additional costs, but these may be alleviated if solvent recovery by means of low pressure drop monoliths is considered. Monoliths, in comparison with traditional packed beds, have a very low pressure drop and high surface areas. The principal aims of the research were to determine the effectiveness of high silica zeolites as adsorbents for the recovery of VOCs and to utilise the zeolites in the monolithic configuration. Silicalite and ZSM-5 were selected as the adsorbents and propane, ethanol and methylene chloride were selected as representative VOCs. The project was divided into two phases. The first was concerned with optimising the chemical formulation of pastes containing a high percentage of silicalite such that they can be extruded to form monolith structures. The second phase of the project involved comparing the equilibrium and kinetic performances of the manufactured monoliths with the performance of an equivalent packed bed containing commercially available silicalite pellets. Multichannel monoliths containing up to 90 % silicalite and with cell densities up to 29 cells/cm and adsorbent wall thicknesses down to 0.6 mm were produced. A square channel monolith having a channel size of 1.0 mm, a wall thickness of 1.0 mm and a cell density of 25 cells/cm was selected for further study due to its relatively high mechanical strength, ease of fabrication, and to the fact that its overall dimensions were comparable with those of an equivalent packed bed. The single component adsorption of VOCs onto high silica zeolites is highly favourable and isotherms of rectangular shape were obtained. The equilibrium capacities for the VOCs were found to be broadly similar for the two adsorbent forms whilst, in their favour for air pollution control applications, the manufactured monoliths were

  5. Evaluation of adsorbent sampling tube materials and Tenax-TA for analysis of volatile biogenic organic compounds

    Science.gov (United States)

    Arnts, Robert R.

    2010-04-01

    Adsorbent tube materials, bed retainers and Tenax-TA were evaluated for their respective roles in adsorbing biogenic volatile organic compounds from air and their tendencies to cause chemical transformation of analytes upon thermal desorption. Stainless steel, Silcosteel ® and Sulfinert ® treated stainless steel tubes exhibited varying degrees of adsorption and reactivity towards some analytes. However, the typical short exposure of the sample stream to wall material before entering an adsorbent bed, minimizes the effect of these properties. Three forms of silica wool (untreated glass wool and siloxane-treated glass and fused silica wool), often used as adsorbent bed retainers, were evaluated and found to function as an adsorbent bed especially for oxygenated monoterpenes and sesquiterpenes. Tenax-TA was evaluated in stainless steel tubes (untreated and treated) with a 2 μm mesh woven wire disk (also untreated and treated) to circumvent the effects of using a silica wool bed retainer. Tenax-TA adsorbent in stainless steel, Silcosteel and Sulfinert tubes yielded equivalent results when compared with direct (cryogenic) pre-concentration analysis of a multi-component mixture of n-alkanes and selected biogenic VOC. Tenax-TA tubes that had been used for 15-20 bake out-sample-desorption cycles (field and laboratory sampling) were compared with freshly packed tubes and found to give equivalent results.

  6. Low concentration CO2 capture using physical adsorbents: Are Metal-Organic Frameworks becoming the new benchmark materials?

    KAUST Repository

    Belmabkhout, Youssef

    2016-03-30

    The capture and separation of traces and concentrated CO2 from important commodities such as CH4, H2, O2 and N2, is becoming important in many areas related to energy security and environmental sustainability. While trace CO2 concentration removal applications have been modestly studied for decades, the spike in interest in the capture of concentrated CO2 was motivated by the need for new energy vectors to replace highly concentrated carbon fuels and the necessity to reduce emissions from fossil fuel-fired power plants. CO2 capture from various gas streams, at different concentrations, using physical adsorbents, such as activated carbon, zeolites, and metal-organic frameworks (MOFs), is attractive. However, the adsorbents must be designed with consideration of many parameters including CO2 affinity, kinetics, energetics, stability, capture mechanism, in addition to cost. Here, we perform a systematic analysis regarding the key technical parameters that are required for the best CO2 capture performance using physical adsorbents. We also experimentally demonstrate a suitable material model of Metal Organic Framework as advanced adsorbents with unprecedented properties for CO2 capture in a wide range of CO2 concentration. These recently developed class of MOF adsorbents represent a breakthrough finding in the removal of traces CO2 using physical adsorption. This platform shows colossal tuning potential for more efficient separation agents.

  7. Activated carbon prepared from coffee pulp: potential adsorbent of organic contaminants in aqueous solution.

    Science.gov (United States)

    Gonçalves, Maraisa; Guerreiro, Mário César; Ramos, Paulize Honorato; de Oliveira, Luiz Carlos Alves; Sapag, Karim

    2013-01-01

    The processing of coffee beans generates large amounts of solid and liquid residues. The solid residues (pulp, husk and parchment) represent a serious environmental problem and do not have an adequate disposal mechanism. In this work, activated carbons (ACs) for adsorption of organic compounds were prepared from coffee pulp by controlled temperature at different pulp/Na2HPO4 ratios (4:1, 2:1, 5:4 and 1:1). The N2 adsorption/desorption isotherms showed ACs with high quantities of mesopores and micropores and specific surface areas of 140, 150, 450 and 440 m(2)g(-1) for AC 4:1, AC 2:1, AC 5:4 and AC 1:1, respectively. The prepared material AC 5:4 showed a higher removal capacity of the organic contaminants methylene blue (MB), direct red (DR) and phenol than did a Merck AC. The maximum capacities for this AC are approximately 150, 120 and 120 mg g(-1) for MB, DR and phenol, respectively. Thus, a good adsorbent was obtained from coffee pulp, an abundant Brazilian residue.

  8. The inter-adsorbate interaction mediated by Shockley-type surface state electrons and dipole moment: Cs and Ba atoms absorbed on Ag (1 1 1) films

    Energy Technology Data Exchange (ETDEWEB)

    Zhang, Shuyuan [College of Physical Science and Technology, Sichuan University, Chengdu 610065 (China); Zhang, Hong, E-mail: hongzhang@scu.edu.cn [College of Physical Science and Technology, Sichuan University, Chengdu 610065 (China); Key Laboratory of High Energy Density Physics and Technology of Ministry of Education, Sichuan University, Chengdu 610064 (China); Miyamoto, Yoshiyuki [Nanosystem Research Institute, National Institute of Advanced Industrial Science and Technology (AIST), Central 2, 1-1-1 Umezono, Tsukuba 305-8568 (Japan)

    2014-01-15

    Through first-principles investigation, we display the formation process of Shockley-type surface states which emerges on silver thin films along Ag (1 1 1) orientation with increasing thicknesses from 6 to 21 layers. We look at the surface state band for various adatoms adsorbed on 6, 12, 18 layers strained Ag (1 1 1) films with different coverage, and discuss the long range interaction mediated by surface state electrons. We discovered that film's thickness can modulate the surface state mediated interaction drastically, but the dipole–dipole repulsive interaction is not affected by slab thickness. This factor had never been discussed in detail. Therefore, adatoms adsorbed on thin films have strong attractive interaction which leads to small adsorption separation and the tendency of island formation. For different coverage or different adsorbate types, both surface states and dipole moment are modulated. The three factors, film's thickness, adsorbate coverage and adatoms types, could help us learn more about the interactions between adatoms and exploit advanced ways to control surface geometry structures of self-assembly.

  9. Investigation on the Morphology of Adsorbed Benzotriazole Film on Copper Surface by Scanning Tunneling Microcopy

    Institute of Scientific and Technical Information of China (English)

    XUChunchun; Win-yanNG; 等

    2002-01-01

    It is observed by scanning tunneling microscopy (STM) that the adsorbed Benzotriazole (BTA) on copper is long in shape and has an irregular rectangle.The growth of BTA on copper is in the from of polymeric chain and mainly in one dimension rather than two dimensions.The copper surface covered by BTA becomes flatter,smoother and the roughness was smaller than that of bare copper,so the corrosion is largely decreased.However,many grooves can be seen between BTA polymeric chains in which corrosion may exist to a degrees.

  10. Preface: Thin films of molecular organic materials

    Science.gov (United States)

    Fraxedas, J.

    2008-03-01

    This special issue is devoted to thin films of molecular organic materials and its aim is to assemble numerous different aspects of this topic in order to reach a wide scientific audience. Under the term 'thin films', structures with thicknesses spanning from one monolayer or less up to several micrometers are included. In order to narrow down this relaxed definition (how thin is thin?) I suggest joining the stream that makes a distinction according to the length scale involved, separating nanometer-thick films from micrometer-thick films. While the physical properties of micrometer-thick films tend to mimic those of bulk materials, in the low nanometer regime new structures (e.g., crystallographic and substrate-induced phases) and properties are found. However, one has to bear in mind that some properties of micrometer-thick films are really confined to the film/substrate interface (e.g. charge injection), and are thus of nanometer nature. Supported in this dimensionality framework, this issue covers the most ideal and model 0D case, a single molecule on a surface, through to the more application-oriented 3D case, placing special emphasis on the fascinating 2D domain that is monolayer assembly. Thus, many aspects will be reviewed, such as single molecules, self-organization, monolayer regime, chirality, growth, physical properties and applications. This issue has been intentionally restricted to small molecules, thus leaving out polymers and biomolecules, because for small molecules it is easier to establish structure--property relationships. Traditionally, the preparation of thin films of molecular organic materials has been considered as a secondary, lower-ranked part of the more general field of this class of materials. The coating of diverse surfaces such as silicon, inorganic and organic single crystals, chemically modified substrates, polymers, etc., with interesting molecules was driven by the potential applications of such molecular materials

  11. Direct electrochemistry and electroanalysis of hemoglobin adsorbed in self-assembled films of gold nanoshells.

    Science.gov (United States)

    Wang, Yi; Qian, Weiping; Tan, Yong; Ding, Shaohua; Zhang, Haiqian

    2007-05-15

    Gold nanoshells (GNSs), consisting of a silica core and a thin gold shell, were self-assembled on the surface of 3-aminopropyltrimethoxysilane (APTES) modified indium tin oxide (ITO) electrode. The resulting novel GNSs-coated ITO (GNSs/APTES/ITO) electrode could provide a biocompatible surface for the adsorption of hemoglobin (Hb). The UV-visible (UV-vis) spectra indicated that Hb adsorbed on the GNSs interface retained the native structure. Electrochemical impedance spectra and cyclic voltammetric techniques were employed to evaluate the electrochemical behaviors of Hb, the results demonstrated that GNSs could act as electron tunnels to facilitate electron transfer between Hb and the electrode. Based on the activity of Hb adsorbed on the GNSs/APTES/ITO electrode toward the reduction of hydrogen peroxide, a mediator-free H(2)O(2) biosensor was constructed, which showed a broad linear range from 5muM to 1mM with a detection limit of 3.4muM (S/N=3). The apparent Michaelis-Menten constant was calculated to be 180muM, suggesting a high affinity.

  12. Adsorption of HSA, IgG and laminin-1 on model titania surfaces--effects of glow discharge treatment on competitively adsorbed film composition.

    Science.gov (United States)

    Santos, Olga; Svendsen, Ida E; Lindh, Liselott; Arnebrant, Thomas

    2011-10-01

    This study investigated the effect of glow discharge treatment of titania surfaces on plasma protein adsorption, by means of ellipsometry and mechanically assisted SDS elution. The adsorption and film elution of three plasma proteins, viz. human serum albumin (HSA), human immunoglobulin G (IgG) and laminin-1, as well as competitive adsorption from a mixture of the three proteins, showed that the adsorbed amount of the individual proteins after 1 h increased in the order HSA Film elutability showed that 30 min of SDS interaction resulted in almost complete removal of adsorbed films. No difference in the total adsorbed amounts of individual proteins, or from the mixture, was observed between untreated and glow discharge treated titania surfaces. However, the composition of the adsorbed films from the mixture differed between the untreated and glow discharge treated substrata. On glow discharge-treated titania the fraction of HSA increased, the fraction of laminin-1 decreased and the fraction of IgG was unchanged compared to the adsorption on the untreated titania, which was attributed to protein-protein interactions and competitive/associative adsorption behaviour.

  13. Surface morphology and thickness of a multilayer film composed of strong and weak polyelectrolytes: Effect of the number of adsorbed layers, concentration and type of salts

    International Nuclear Information System (INIS)

    Self-assembled multilayered films were prepared by alternate deposition of a strong cationic polyelectrolyte, poly(trimethylammonium ethyl methacrylate chloride) and a pH-dependant anionic polyelectrolyte, poly(acrylic acid). The layer-by-layer adsorption was followed in-situ by optical fixed-angle reflectometry and after drying by ellipsometry. A recently developed 'substrate thickness method' was applied to calculate the adsorbed amount of polymer from the reflectometric signal. Surface film morphology was imaged before and after drying with atomic force microscopy (AFM). Influence of the number of adsorbed layers, concentration and type of salts on the multilayer growth was examined. The number of adsorbed layers produced a specific effect on the reflectometric signal which is linked to the refractive index of the film. Adjustment of the adsorbed amount of polyelectrolytes was done by changing sodium chloride salt concentration within a range of 10-3 to 10-1 M. AFM observations showed a significant evolution in surface morphology and a maximum of surface roughness for films built-up at 10-2 M. Experiments were then carried out at 10-3 M in either barium chloride or zinc chloride salts. In the presence of Ba2+ and Zn2+ ions, adsorption of 5 bilayers is completely modified and the surface morphology was smoother than the multilayers obtained using sodium chloride salt

  14. Organic silicon compounds anf hydrogen sulfide removal from biogas by mineral and adsorbent

    Science.gov (United States)

    Choi, J.

    2015-12-01

    Biogas utilized for energy production needs to be free from organic silicon compounds and hydrogen sulfide , as their burning has damaging effects on utilities and humans; organic silicon compounds and hydrogen sulfide can be found in biogas produced from biomass wastes, due to their massive industrial use in synthetic product,such as cosmetics, detergents and paints.Siloxanes and hydrogen sulfide removal from biogas can be carried out by various methods (Ajhar et al., 2010); aim of the present work is to find a single practical andeconomic way to drastically and simultaneously reduce both hydrogen sulfide and the siloxanes concentration to less than 1 ppm. Some commercial activated carbons previously selected (Monteleoneet al., 2011) as being effective in hydrogen sulfide up taking have been tested in an adsorption measurement apparatus, by flowing both hydrogen sulphide and volatile siloxane (Decamethycyclopentasiloxane or D5) in a nitrogen stream,typically 25-300 ppm D5 over N2, through an clay minerals, Fe oxides and Silica; the adsorption process was analyzed by varying some experimental parameters (concentration, grain size, bed height). The best silica shows an adsorption capacity of 0.2 g D5 per gram of silica. The next thermo gravimetric analysis (TGA) confirms the capacity data obtained experimentally by the breakthrough curve tests.The capacity results depend on D5 and hydrogen sulphide concentrations. A regenerative silica process is then carried out byheating the silica bed up to 200 ° C and flushing out the adsorbed D5 and hydrogen sulphide samples in a nitrogen stream in athree step heating procedure up to 200 ° C. The adsorption capacity is observed to degrade after cyclingthe samples through several adsorption-desorption cycles.

  15. Novel magnetic Fe3O4-C nanoparticles as adsorbents for removal of organic dyes from aqueous solution

    International Nuclear Information System (INIS)

    Highlights: → In this work, novel magnetic Fe3O4-C nanoparticles have been synthesized and employed as high efficient adsorbent for removal cationic dyes from polluted water. → While up to now, little study is done on adsorption of dyes by the Fe3O4-C nanoparticles. → Hence, here we provide a simply and environment friendly method for removal of cationic dyes or other pollutants from water. - Abstract: The magnetic Fe3O4/C core-shell nanoparticles have been synthesized by a simple strategy and used as adsorbents for removal of organic dyes from aqueous solution. The resulting products are characterized by scanning electron microscope (SEM), energy dispersive X-ray spectrometry (EDX), X-ray photoelectron spectroscopy (XPS), X-ray diffraction (XRD), Raman spectra and Fourier transform infrared spectra (FTIR). Adsorption performances of the nanomaterial adsorbents are tested with removal of methylene blue (MB) and cresol red (CR) from aqueous solution. The effects of solution pH value, adsorption time and capacity of the nanocomposites have been fully investigated. The results reveal that the nanospheres can be easily manipulated by an external magnetic field with high separation efficiency. In addition, the process is clean and safe for purifying water pollution. The prepared Fe3O4/C complex nanomaterials could thus be used as promising adsorbents for the remove organic dyes, especially, cationic dye, from polluted water.

  16. Methyl red removal from water by iron based metal-organic frameworks loaded onto iron oxide nanoparticle adsorbent

    Energy Technology Data Exchange (ETDEWEB)

    Dadfarnia, S., E-mail: sdadfarnia@yazd.ac.ir [Department of Chemistry, Faculty of Science, Yazd University, Yazd 89195-741 (Iran, Islamic Republic of); Haji Shabani, A.M.; Moradi, S.E. [Department of Chemistry, Faculty of Science, Yazd University, Yazd 89195-741 (Iran, Islamic Republic of); Emami, S. [Department of Medicinal Chemistry and Pharmaceutical Sciences Research Center, Faculty of Pharmacy, Mazandaran University of Medical Sciences, Sari (Iran, Islamic Republic of)

    2015-03-01

    Highlights: • Synthesis and characterization of (Fe{sub 3}O{sub 4}@MIL-100(Fe)). • Studying the capability of (Fe{sub 3}O{sub 4}@MIL-100(Fe)) for the removal of methyl red. • Studying the adsorption kinetic of MR on (Fe{sub 3}O{sub 4}@MIL-100(Fe)). • Studying the adsorption thermodynamic of MR on (Fe{sub 3}O{sub 4}@MIL-100(Fe)). • Introduction of a sorbent with high capacity for MR removal. - Abstract: The objective followed by this research is the synthesis of iron based metal organic framework loaded on iron oxide nanoparticles (Fe{sub 3}O{sub 4}@MIL-100(Fe)) and the study of its capability for the removal of methyl red. Effective parameters in the selection of a new adsorbent, i.e. adsorption capacity, thermodynamics, and kinetics were investigated. All the studies were carried out in batch experiments. Removal of methyl red from aqueous solutions varied with the amount of adsorbent, methyl red contact time, initial concentration of dye, adsorbent dosage, and solution pH. The capability of the synthesized adsorbent in the removal of methyl red was compared with the metal organic framework (MIL-100(Fe)) and iron oxide nanoparticles. The results show that Fe{sub 3}O{sub 4}@MIL-100(Fe) nanocomposite exhibits an enhanced adsorption capacity.

  17. Low concentration volatile organic pollutants removal in combined adsorber-desorber-catalytic reactor system

    Directory of Open Access Journals (Sweden)

    Arsenijević Zorana

    2008-01-01

    Full Text Available The removal of volatile organic compounds (VOCs from numerous emission sources is of crucial importance due to more rigorous demands on air quality. Different technologies can be used to treat the VOCs from effluent gases: absorption, physical adsorption, open flame combustion, thermal and catalytic incineration. Their appropriateness for the specific process depends on several factors such as efficiency, energy consumption, secondary pollution, capital investments etc. The distinctive features of the catalytic combustion are high efficiency and selectivity toward be­nign products, low energy consumption and absence of secondary polluti­on. The supported noble catalysts are widely used for catalytic incineration due to their low ignition temperatures and high thermal and chemical stability. In our combined system adsorption and desorption are applied in the spouted bed with draft tube (SBDT unit. The annular zone, loaded with sorbent, was divided in adsorption and desorption section. Draft tube enabled sorbent recirculation between sections. Combustion of desorbed gases to CO2 and water vapor are realized in additive catalytic reactor. This integrated device provided low concentrations VOCs removal with reduced energy consumption. Experiments were conducted on a pilot unit of 220 m3/h nominal capacity. The sorbent was activated carbon, type K81/B - Trayal Corporation, Krusevac. A sphere shaped commercial Pt/Al2O3 catalyst with "egg-shell" macro-distribution was used for the investigation of xylene deep oxidation. Within this paper the investigations of removal of xylene vapors, a typical pollutant in production of liquid pesticides, in combined adsorber/desorber/catalytic reactor system is presented.

  18. Structure and dynamics of monolayer films of squalane molecules adsorbed on a solid surface

    Science.gov (United States)

    D. T Enevoldsen, A.; Hansen, F. Y.; Diama, A.; Taub, H.

    2003-03-01

    Squalane is a branched alkane (C_30H_62). It consists of a straight chain with 24 carbon atoms, as in tetracosane (C_24H_50), and has six methyl side groups. Branched polymers such as squalane are thought to be better lubricants than n-alkanes. At low temperature, our molecular dynamics (MD) simulations show that the molecules form an ordered monolayer which melts at approximately 325 K compared to the tetracosane monolayer melting point of ˜ 340 K. Our MD simulations indicate the same melting mechanism in the squalane monolayer that was found previously for tetracosane (F. Y. Hansen and H. Taub, Phys. Rev. Lett. 69, 652 (1992).) They also show that the adsorbed molecules are distorted from an all-trans carbon backbone in contrast to what was found for tetracosane. This may explain why the Bragg diffraction peaks were observed to be broader for the squalane monolayer than for tetracosane (D. Fuhrmann, A. P. Graham, L. Criswell, H. Mo, B. Matthies, K. W. Herwig, and H. Taub, Surf. Sci. 482-485, 77 (2001).). The diffusive motion in a squalane monolayer has been investigated by both quasielastic neutron scattering and MD simulations and compared to the dynamics in tetracosane monolayers. Focus will be on differences in the dynamics.

  19. Neutron scattering study of 36 Ar monolayer films adsorbed on graphite

    DEFF Research Database (Denmark)

    Taub, H.; da Costa Carneiro, Kim; Kjems, Jørgen;

    1977-01-01

    surfaces at low temperatures) are observed to decrease smoothly above 40 K, falling from 100 to 15 Å at 80 K. Little if any positional order remains at temperatures where the nearest-neighbor distance in the monolayer matches that of a registered √3×√3 phase. The spectrum of neutrons inelastically......Diffraction of neutrons from 36 Ar monolayers adsorbed on graphite basal planes indicates that an ordered, two-dimensional (2D) triangular lattice is formed at low temperature. The lattice constant is found to be slightly larger than that of the bulk 3D solid but significantly smaller than...... that of a registered √3×√3 overlayer. Thermal expansion of the monolayer is anomalously large; up to 60 K the linear expansion is 4.5 times greater than in the 3D solid. There is no evidence of a sharp melting transition. Instead, the positional correlations (which extend to the full dimensions of the crystallite...

  20. Adsorption and oxidation of formaldehyde on a polycrystalline Pt film electrode: An in situ IR spectroscopy search for adsorbed reaction intermediates

    Directory of Open Access Journals (Sweden)

    Zenonas Jusys

    2014-05-01

    Full Text Available As part of a mechanistic study of the electrooxidation of C1 molecules we have systematically investigated the dissociative adsorption/oxidation of formaldehyde on a polycrystalline Pt film electrode under experimental conditions optimizing the chance for detecting weakly adsorbed reaction intermediates. Employing in situ IR spectroscopy in an attenuated total reflection configuration (ATR-FTIRS with p-polarized IR radiation to further improve the signal-to-noise ratio, and using low reaction temperatures (3 °C and deuterium substitution to slow down the reaction kinetics and to stabilize weakly adsorbed reaction intermediates, we could detect an IR absorption band at 1660 cm−1 characteristic for adsorbed formyl intermediates. This assignment is supported by an isotope shift in wave number. Effects of temperature, potential and deuterium substitution on the formation and disappearance of different adsorbed species (COad, adsorbed formate, adsorbed formyl, are monitored and quantified. Consequences on the mechanism for dissociative adsorption and oxidation of formaldehyde are discussed.

  1. Use of Low-cost Adsorbents to Chlorophenols and Organic Matter Removal of Petrochemical Wastewater

    Directory of Open Access Journals (Sweden)

    Aretha Moreira de Oliveira

    2013-11-01

    Full Text Available The removal of 2,4 diclorophenol (2,4-DCF and 2,4,6 trichlorophenol (2,4,6 TCF present in  petrochemical wastewater was evaluated using low-cost adsorbents, such as chitin, chitosan and coconut shells. Batch studies showed that the absorption efficiency for 2,4 DCF and 2,4,6 TCF follow the order: chitosan > chitin > coconut shells. Langmuir and Freundlich models have been applied to experimental isotherms data, to better understand the adsorption mechanisms. Petrochemical wastewater treatment with fixed bed column system using chitinous adsorbents showed a removal of COD (75% , TOG (90% and turbidity (74-89%.

  2. Adsorption of organic layers over electrodeposited magnetite (Fe3O4) thin films

    International Nuclear Information System (INIS)

    Research highlights: → Adherent low roughness magnetite films ranging from 80 nm to 3.75 μm-thick were electrodeposited on Au/glass substrates under galvanostatic control. → X-ray diffraction and magnetic measurements corroborates the purity of the electrodeposited magnetite. → Both dodecanethiol and oleic acid are shown to adsorb on the magnetite prepared at low temperature, significantly inducing the hydrophobicity of the surface. → Contact angle and voltammetric measurements, as well as XPS confirm the monolayers formation. - Abstract: The formation of monolayers of two organic compounds (oleic acid and dodecanethiol) over magnetite films was studied. Magnetite films ranging from 80 nm to 3.75 μm-thick were electrodeposited on Au on glass substrates under galvanostatic control, with deposition parameters optimized for minimum surface roughness. Films were characterised by SEM and AFM, showing granular deposits with a low rms roughness of 5-40 nm measured over an area of 1 μm2. The growth rate was estimated by measuring cross-sections of the thin films. Pure magnetite with an fcc structure is observed in XRD diffractograms. The adsorption of both oleic acid and dodecanethiol on the magnetite films was tested by immersing them in ethanol solutions containing the organic molecules, for different deposition time, temperature and cleaning procedure. Monolayer formation in both cases was studied by contact angle and voltammetric measurements, as well as XPS.

  3. Neutron diffraction and quasielastic neutron scattering studies of films of intermediate-length alkanes adsorbed on a graphite surface

    Science.gov (United States)

    Diama, Armand

    Over the past several years, we have conducted a variety of elastic neutron diffraction and quasielastic neutron scattering experiments to study the structure and the dynamics of films of two intermediate-length alkane molecules (C nH2n+2), adsorbed on a graphite basal-plane surface. The two molecules are the normal alkane n-tetracosane [n-CH 3(CH2)22CH3] and the branched alkane squalane (C30H62 or 2, 6, 10, 15, 19, 23-hexamethyltetracosane) whose carbon backbone is the same length as teteracosane. The temperature dependence of the monolayer structure of tetracosane and squalane was investigated using elastic neutron diffraction and evidence of two phase transitions was observed. Both the low-coverage tetracosane (C 24H50) and squalane (C30H62) monolayers have crystalline-to-"smectic" and "smectic"-to-isotropic fluid phase transitions upon heating. The diffusive motion in the tetracosane and squalane monolayers has been investigated by quasielastic neutron scattering. Two different quasielastic neutron scattering spectrometers at the Center for Neutron Research, National Institute of Standards and Technology (NIST) have been used. The spectrometers differ in both their dynamic range and energy resolution allowing molecular motions to be investigated on time scales in the range 10-13--10 -9 s. On these time scales, we observe evidence of translational, rotational, and intermolecular diffusive motions in the tetracosane and squalane monolayers. We conclude that the molecular diffusive motion in the two monolayers is qualitatively similar. Thus, despite the three methyl sidegroups at each end of the squalane molecule, its monolayer structure, phase transitions, and dynamics are qualitatively similar to that of a monolayer of the unbranched tetracosane molecules. With the higher resolution spectrometer at NIST, we have also investigated the molecular diffusive motion in multilayer tetracosane films. The analysis of our measurements indicates slower diffusive motion in

  4. Inorganic-organic phase arrangement as a factor affecting gas-phase desulfurization on catalytic carbonaceous adsorbents.

    Science.gov (United States)

    Ansari, Adil; Bandosz, Teresa J

    2005-08-15

    Dried sewage sludge was physically mixed with waste paper (paper-to-sludge ratios from 25% to 75%). To increase the catalytic activity, from 1% to 6% calcium hydroxide was added to the mixtures. Then the precursors were carbonized at 950 degrees C. The performance of materials as H2S adsorbents was tested using a home-developed dynamic breakthrough test. The samples, before and after the adsorption process, were characterized by adsorption of nitrogen, potentiometric titration, thermal analysis, XRF, and SEM. Differences in the performance were linked to the surface properties. Itwas found that mixing paper with sludge increases the amount of H2S adsorbed/oxidized in comparison with that adsorbed/oxidized by the adsorbents obtained from pure precursors (sludge or waste paper) and the capacity is comparable to those of the best activated carbons existing on the market. Although both sewage sludge and waste paper provide the catalytic centers for hydrogen sulfide oxidation, the dispersion of the catalyst and its location within accessible pores is an important factor. The presence of cellulose in the precursor mixture leads to the formation of a light macroporous char whose particles physically separate the inorganic catalytic phase of the sewage sludge origin, decreasing the density of the adsorbent and thus providing more space for storage of oxidation products. This, along with calcium, contributes to a significant increase in the capacity of the materials as hydrogen sulfide adsorbents. On their surface about 30 wt % H2S can be adsorbed, mainly as elemental sulfur or sulfates. The results demonstrate the importance of the composition and arrangement of inorganic/ organic phases for the removal of hydrogen sulfide. The interesting finding is that although some microporosity is necessary to increase the storage area for oxidation products, the carbonaceous phase does not need to be highly microporous. It is important that it provides space for deposition of sulfur

  5. David Adler Lectureship Award Talk: Friction and energy dissipation mechanisms in adsorbed molecules and molecularly thin films

    Science.gov (United States)

    Krim, Jacqueline

    2015-03-01

    Studies of the fundamental origins of friction have undergone rapid progress in recent years, with the development of new experimental and computational techniques for measuring and simulating friction at atomic length and time scales. The increased interest has sparked a variety of discussions and debates concerning the nature of the atomic-scale and quantum mechanisms that dominate the dissipative process by which mechanical energy is transformed into heat. Measurements of the sliding friction of physisorbed monolayers and bilayers can provide information on the relative contributions of these various dissipative mechanisms. Adsorbed films, whether intentionally applied or present as trace levels of physisorbed contaminants, moreover are ubiquitous at virtually all surfaces. As such, they impact a wide range of applications whose progress depends on precise control and/or knowledge of surface diffusion processes. Examples include nanoscale assembly, directed transport of Brownian particles, material flow through restricted geometries such as graphene membranes and molecular sieves, passivation and edge effects in carbon-based lubricants, and the stability of granular materials associated with frictional and frictionless contacts. Work supported by NSFDMR1310456.

  6. Two-Factor Model of Soil Suction from Capillarity, Shrinkage, Adsorbed Film, and Intra-aggregate Structure

    CERN Document Server

    Chertkov, V Y

    2014-01-01

    The objective of this work is to derive the soil water retention from the soil structure without curve-fitting and only using the physical parameters found irrespective of an experimental retention curve. Two key points underlie the work: (i) the soil suction at drying coincides with that of the soil intra-aggregate matrix and contributive clay; and (ii) both the soil suction and volume shrinkage at drying depend on the same soil water content. In addition the two following results are used: (i) the available two-factor (capillarity and shrinkage) model of clay suction enables one to connect a clay suction and clay water content using the clay matrix structure; and (ii) the recent reference shrinkage curve model based on the concepts of intra-aggregate soil structure permits one to connect the soil water content at shrinkage with the water content of the contributive clay. With that the available two-factor model was essentially modified and, in particular, the effect of adsorbed water film was taken into acc...

  7. Tribochemical synthesis of nano-lubricant films from adsorbed molecules at sliding solid interface: Tribo-polymers from α-pinene, pinane, and n-decane

    Science.gov (United States)

    He, Xin; Barthel, Anthony J.; Kim, Seong H.

    2016-06-01

    The mechanochemical reactions of adsorbed molecules at sliding interfaces were studied for α-pinene (C10H16), pinane (C10H18), and n-decane (C10H22) on a stainless steel substrate surface. During vapor phase lubrication, molecules adsorbed at the sliding interface could be activated by mechanical shear. Under the equilibrium adsorption condition of these molecules, the friction coefficient of sliding steel surfaces was about 0.2 and a polymeric film was tribochemically produced. The synthesis yield of α-pinene tribo-polymers was about twice as much as pinane tribo-polymers. In contrast to these strained bicyclic hydrocarbons, n-decane showed much weaker activity for tribo-polymerization at the same mechanical shear condition. These results suggested that the mechanical shear at tribological interfaces could induce the opening of the strained ring structure of α-pinene and pinane, which leads to polymerization of adsorbed molecules at the sliding track. On a stainless steel surface, such polymerization reactions of adsorbed molecules do not occur under typical surface reaction conditions. The mechanical properties and boundary lubrication efficiency of the produced tribo-polymer films are discussed.

  8. Organic thin films and surfaces directions for the nineties

    CERN Document Server

    Ulman, Abraham

    1995-01-01

    Physics of Thin Films has been one of the longest running continuing series in thin film science consisting of 20 volumes since 1963. The series contains some of the highest quality studies of the properties ofvarious thin films materials and systems.In order to be able to reflect the development of todays science and to cover all modern aspects of thin films, the series, beginning with Volume 20, will move beyond the basic physics of thin films. It will address the most important aspects of both inorganic and organic thin films, in both their theoretical as well as technological aspects. Ther

  9. Scanning tunneling microscopy studies of organic monolayers adsorbed on the rhodium(111) crystal surface

    Energy Technology Data Exchange (ETDEWEB)

    Cernota, Paul D.

    1999-08-01

    Scanning Tunneling Microscopy studies were carried out on ordered overlayers on the (111) surface of rhodium. These adsorbates include carbon monoxide (CO), cyclohexane, cyclohexene, 1,4-cyclohexadiene, para-xylene, and meta-xylene. Coadsorbate systems included: CO with ethylidyne, CO with para- and meta-xylene, and para-xylene with meta-xylene. In the case of CO, the structure of the low coverage (2x2) overlayer has been observed. The symmetry of the unit cell in this layer suggests that the CO is adsorbed in the 3-fold hollow sites. There were also two higher coverage surface structures with ({radical}7x{radical}7) unit cells. One of these is composed of trimers of CO and has three CO molecules in each unit cell. The other structure has an additional CO molecule, making a total of four. This extra CO sits on a top site.

  10. The development of composite adsorbent for organic waste decomposion treatment and chemical recovery

    Energy Technology Data Exchange (ETDEWEB)

    Gun, Shul Yong; Jung, Kyeong Taek; Kim, Hyung Tae; Kim, Ki Wook; Kim, Hyun Jong [Yonsei University, Seoul (Korea); Kim, Jong [Konyang University, Nonsan (Korea)

    1999-01-01

    Up to now inorganic adsorbents has been known to effective for treatment of radioactive waste containing metal ions due to their high selectivity toward the specific ions(Cs{sup +}, Sr{sup 2+}, Co{sup 2+}, Ag{sup +} ...). The draw back of this adsorption system is in the operation difficulties such as separation of fine solids (adsorbents) and pressure drop ({delta}p) problem. To come over these problems, preparation of composite adsorbents has been attempted. In our study, PAN-inorganic ion exchanger(Ni{sub 2}Fe(Cn){sub 6}, K{sub 2}Ti{sub 4}O{sub 9}) composite beads were prepared in the range of 0.5 {approx} 3.5mm in size. The selectivity for Ag{sup +}, Sr{sup 2+}, Cs{sup +} and Co{sup 2+} ions in binary and tertiary systems in composite beads was Sr{sup 2+}>Ag{sup +}, Ag{sup +}>Co{sup 2+}, Co{sup 2+}>Sr{sup 2+} and Sr{sup 2+}>Co{sup 2+}>Ag{sup +} respectively. As an selective Cs{sup +} adsorbent, 1,3-Dipropyloxycalix(4)arene crown ether (CCE1) and 1,3-Dipropyl-oxycalix(4)arene dibenzo crown ethers(CCE2) were also successfully synthesized in the fixed 1,3-alternate conformation with good yields by the reaction of corresponding 1,3-Dipropyloxy-calix(4)arenes 3 with pentaethylene glycol ditosylate and dibenzodimesylate 7, respectively in acetonitrile in the presence of cesium carbonate as a base. Solvent extraction of cesium picrates and cesium nitrate from aqueous solutions into chloroform were investigated. (author). 37 refs., 60 figs., 7 tabs.

  11. Ultrathin organic semiconductor films--soft matter effect.

    Science.gov (United States)

    Wang, Tong; Yan, Donghang

    2014-05-01

    The growth of organic semiconductor thin films has been a crucial issue in organic electronics, especially the growth at the early stages. The thin-film phase has been found to be a common phenomenon in many organic semiconductor thin films, which is closely related with the weak van der Waals interaction between organic molecules, the long-range interaction between organic molecules and the substrate, as well as the soft matter characteristics of ultrathin films. The growth behavior and soft matter characteristics of the thin-film phase have great effects on thin film morphology and structure, for example, the formation and coalescence of grain boundaries, which further influences the performance of organic electronic devices. The understanding of thin-film phase and its intrinsic quality is necessary for fabricating large-size, highly ordered, continuous and defect-free ultrathin films. This review will focus on the growth behavior of organic ultrathin films, i.e., the level of the first several molecular layers, and provide an overview of the soft matter characteristics. PMID:24548597

  12. Effects of molecule-insulator interaction on geometric property of a single phthalocyanine molecule adsorbed on an ultrathin NaCl film

    Science.gov (United States)

    Miwa, Kuniyuki; Imada, Hiroshi; Kawahara, Shota; Kim, Yousoo

    2016-04-01

    The adsorption structure and orientation of a metal-free phthalocyanine (H2Pc ) and a magnesium phthalocyanine (MgPc) on a bilayer of NaCl films were investigated both theoretically and experimentally by means of first-principles calculations based on density functional theory and by scanning tunneling microscopy. H2Pc is adsorbed with its center over the sodium cation, and H-N bonds in the molecule are aligned with the [100] or [010] surface direction of a bilayer (001)-terminated NaCl film. The most stable structures of MgPc on the NaCl film show two kinds of orientations corresponding to the molecule rotated by ±7∘ relative to the [110] surface direction, with the Mg cation positioned over the chlorine anion in both cases. The energetic barrier for switching between these orientations is as low as 9.0 meV, and during an STM measurement, an orientational change of MgPc can be observed. The interaction between the adsorbed molecule and the NaCl film were analyzed in terms of dispersion interaction, Mg-Cl chemical bonding, and electrostatic interaction. It is found that the small electrostatic interaction between the molecule and the film gives a dominant contribution to determining the molecular orientation. Our detailed and comprehensive studies of the molecule-insulator interaction will provide knowledge to understand and control the properties of molecules on an insulating material.

  13. A New Experimental Method to Determine the Henry’s Law Constant of a Volatile Organic Compound Adsorbed in Soil

    OpenAIRE

    2015-01-01

    This paper presents a new mechanical method to determine Henry’s law constant (HLC) of a volatile organic compound (VOC). This method is an extension of the one proposed by Ouoba et al. (2010) to determine the water activity in porous media. This work focuses on TCE and aims at characterizing its liquid-vapor equilibrium in various cases in the form of a pure liquid phase or dissolved in an aqueous solution, adsorbed or not in a natural soil. A liquid phase is disposed in a closed chamber who...

  14. Magnetic niobia as adsorbent of organic contaminants in aqueous medium: effect of temperature and pH

    International Nuclear Information System (INIS)

    This work describes novel materials based on pure iron oxide and iron oxide/niobia composite to produce a magnetic adsorbent. These materials were prepared with synthetic iron oxide and characterized by powder XRD, SEM, FTIR, TPR and Moessbauer spectroscopy. Results showed that the main iron oxides formed were goethite (α FeOOH) and maghemite (γFe2O3) with small particle size. The iron oxide and iron oxide/niobia composite showed high adsorption ability for organic compounds. The positive enthalpy indicated an endothermic adsorption process suggesting physical adsorption. (author)

  15. Multilayer bonding using a conformal adsorbate film (CAF) for the fabrication of 3D monolithic microfluidic devices in photopolymer

    International Nuclear Information System (INIS)

    Reliable microfabrication processes and materials compatible with complementary metal-oxide semiconductor (CMOS) technology are required by industry for the mass production of complex and highly miniaturized lab-on-a-chip systems. Photopolymers are commonly used in the semiconductor industry, and are suitable for the integration of multilayer structures onto CMOS substrates. This paper describes a novel photopolymer bonding process compatible with CMOS technology for the fabrication of three-dimensional monolithic microfluidic devices. The process consists of the formation of a conformal adsorbate film (CAF) approximately 15 nm thick on a patterned photopolymer layer (KMPR), thereby increasing the number of open polymer chains at the bonding interface and acting as an ultra-thin adhesive layer. This thin adhesive layer is made of the same photopolymer as the microfluidic structures, but has a substantially lower crosslinking density so it will be able to make better bonds during a thermocompressive bonding step. This CAF treatment substantially improves the bonding yield between two patterned and previously crosslinked photopolymer layers because both optimum structure strength (to resist deformation during bonding) and bonding strength from epoxy crosslinking can be achieved. We demonstrate high bonding yields of up to 99% of the useful area of the substrate after three successive bonding steps. With this technique, up to six layers have been bonded in a single device. Unlike previously reported methods the quality of bonding is mostly decoupled from soft-bake parameters and crosslinking level of the previously patterned layers. Three differentbonding processes were characterized to describe the bonding mechanism and the differences between the presented method and the partial-crosslinking bonding method. Capillary filling experiments were performed in microchannels of multilayer structures built with the CAF technique, without any observable leakage between

  16. Uenbinding'' an adsorbed organic molecule: K plus PTCDA on Ag(110)

    Energy Technology Data Exchange (ETDEWEB)

    Bauer, Oliver; Schmitz, Christoph H.; Fiedler, Benjamin; Sokolowski, Moritz [Institut fuer Physikalische und Theoretische Chemie, Universitaet Bonn (Germany); Mercurio, Giuseppe; Subach, Sergey; Tautz, Frank Stefan [Institut fuer Bio- und Nanosysteme 3, Forschungszentrum Juelich (Germany)

    2010-07-01

    We have doped the well-known brick-wall structure of pristine PTCDA which is present in the monolayer on the Ag(110) surface with potassium (K) and investigated the induced structural and electronic changes at the interface. SPA-LEED measurements reveal that the structural order of the PTCDA molecules is strongly altered upon K dosing: A variety of co-existing binary phases is observed within the monolayer. In addition we have conducted XPS and NIXSW measurements on K+PTCDA/Ag(110). The photoemission experiments indicate that the K atoms preferentially interact with the carboxylic groups of the co-adsorbed PTCDA molecules. This interpretation is further supported by the NIXSW results: The adsorption geometries of the carboxylic and the anhydride oxygen (O) atoms are highly influenced by the presence of K on the surface, the bonding distances are extended. The adsorption height of the perylene core is also increased by K doping. Hence we conclude that the local Ag-O bonds at the interface are partially lifted by the co-adsorbed K and that K and Ag atoms compete for the interaction with the carboxylic groups of PTCDA while the bonding across the interface is weakened.

  17. Fluorescent thin gel films using organic dyes and pigments

    Science.gov (United States)

    Nakazumi, Hiroyuki; Takashi, Tarao; Taniguchi, Shin-ichi; Nanto, Hidehito

    1997-10-01

    New organic-inorganic fluorescent thin gel films included with laser dyes or fluorescent organic pigments have been prepared for display application. The florescent dyes (benzoxazolium, pyrromethene, and rhodamine dyes) and super-fine particles of fluorescent pigments (coumarin and perylene) were successfully incorporated into thin silicate gel films prepared from tetraethoxysilane (TEOS), methyltriethoxysilane (MTES), and methoxysilane oligomer (MTSO) under acid catalyzed hydrolysis. The blue, green, and red luminescence were observed from these thin films (thickness: 100 - 400 nm), respectively. Fluorescence spectra, fluorescent quantum yield and lifetime of thin gel films are examined. Fluorescent peaks for most of dyes and pigments used in gel films were similar to those in solution, and fluorescent lifetime for dyes and pigments used in gel films were 2.9 - 4.5 ns. Photostability of fluorescent gel films is dependent on fluorescent organic dyes and pigments used and/or silicate gel matrixes. Coumarin and perylene pigments have higher fluorescent quantum yield in gel film prepared from MTSO. The large Stokes shift was observed in fluorescent gel film using coumarin and benzoxazolium dyes. The coumarin and perylene pigments are significantly photo- stable in gel film prepared from MTSO, and photodegradation of perylene red after irradiation of 500 W Xi-lamp for 30 min is below 20%.

  18. Linear and nonlinear surface spectroscopy of supported size selected metal clusters and organic adsorbates

    Energy Technology Data Exchange (ETDEWEB)

    Thaemer, Martin Georg

    2012-03-08

    The spectroscopic investigation of supported size selected metal clusters over a wide wavelength range plays an important role for understanding their outstanding catalytic properties. The challenge which must be overcome to perform such measurements is the difficult detection of the weak spectroscopic signals from these samples. As a consequence, highly sensitive spectroscopic methods are applied, such as surface Cavity Ringdown Spectroscopy and surface Second Harmonic Generation Spectroscopy. The spectroscopic apparatus developed is shown to have a sensitivity which is high enough to detect sub-monolayer coverages of adsorbates on surfaces. In the measured spectra of small supported silver clusters of the sizes Ag{sub 4}2, Ag{sub 2}1, Ag{sub 9}, and Ag atoms a stepwise transition from particles with purely metallic character to particles with molecule-like properties can be observed within this size range.

  19. Zirconium-based metal organic frameworks: Highly selective adsorbents for removal of phosphate from water and urine

    International Nuclear Information System (INIS)

    Phosphate is one of the most concerning compounds in wastewater streams and a main nutrient that causes eutrophication. To eliminate the phosphate pollution, Metal Organic Frameworks (MOFs) are proposed in this study as adsorbents to remove phosphate from water. The zirconium-based MOF, UiO-66, was selected as representative MOF given its exceptional stability in water. To investigate the effect of an amine functional group, UiO-66-NH2 was also prepared using an amine-substituted ligand. The adsorption kinetics and isotherm reveal that UiO-66-NH2 exhibited higher adsorption capacities than UiO-66 possibly due to the amine group. However, the interaction between phosphate and zirconium sites of UiO MOFs might be the primary factor accounting for the phosphate adsorption to UiO MOFs. UiO MOFs also exhibited a high selectivity towards phosphate over other anions such as bromate, nitrite and nitrate. Furthermore, UiO MOFs were found to adsorb phosphate and to completely remove diluted phosphate in urine. We also found that UiO MOFs could be easily regenerated and re-used for phosphate adsorption. These findings suggest that UiO MOFs can be effective and selective adsorbents to remove phosphate from water as well as urine. - Highlights: • UiO-66 as the first type of MOFs was used to remove phosphate from water and urine. • The amine group in UiO MOFs was found to enhance the phosphate adsorption. • UiO-66 exhibited a high adsorption selectivity towards phosphate over other anions. • UiO-66 could be easily regenerated and re-used with 85% regeneration efficiency

  20. Influence of molecular structure and adsorbent properties on sorption of organic compounds to a temperature series of wood chars.

    Science.gov (United States)

    Lattao, Charisma; Cao, Xiaoyan; Mao, Jingdong; Schmidt-Rohr, Klaus; Pignatello, Joseph J

    2014-05-01

    Chars from wildfires and soil amendments (biochars) are strong adsorbents that can impact the fate of organic compounds in soil, yet the effects of solute and adsorbent properties on sorption are poorly understood. We studied sorption of benzene, naphthalene, and 1,4-dinitrobenzene from water to a series of wood chars made anaerobically at different heat treatment temperatures (HTT) from 300 to 700 °C, and to graphite as a nonporous, unfunctionalized reference adsorbent. Peak suppression in the NMR spectrum by sorption of the paramagnetic relaxation probe TEMPO indicated that only a small fraction of char C atoms lie near sorption sites. Sorption intensity for all solutes maximized with the 500 °C char, but failed to trend regularly with N2 or CO2 surface area, micropore volume, mesopore volume, H/C ratio, O/C ratio, aromatic fused ring size, or HTT. A model relating sorption intensity to a weighted sum of microporosity and mesoporosity was more successful. Sorption isotherm linearity declined progressively with carbonization of the char. Application of a thermodynamic model incorporating solvent-water and char-graphite partition coefficients permitted for the first time quantification of steric (size exclusion in pores) and π-π electron donor-acceptor (EDA) free energy contributions, relative to benzene. Steric hindrance for naphthalene increases exponentially from 9 to 16 kJ/mol (∼ 1.6-2.9 log units of sorption coefficient) with the fraction of porosity in small micropores. π-π EDA interactions of dinitrobenzene contribute -17 to -19 kJ/mol (3-3.4 log units of sorption coefficient) to sorption on graphite, but less on chars. π-π EDA interaction of naphthalene on graphite is small (-2 to 2 kJ/mol). The results show that sorption is a complex function of char properties and solute molecular structure, and not very predictable on the basis of readily determined char properties.

  1. Electrochemical Behavior of Organic Film With Nano Silica

    Institute of Scientific and Technical Information of China (English)

    GONG Li; LU Tan-ping

    2004-01-01

    Organic-inorganic composite films were prepared by adding different amount of nano-SiO2into water soluble acrylic resin (AC) on hot-dip galvanized steel sheet. The electrochemical behavior of nano SiO2 modified acrylic resin films in 5 % NaCl solution were studied by electrochemical measurement techniques. Results indicate when there are 8% ~ 12% SiO2 in organic film, it can shows an analogous passivation propertyin anodic polarization curves, increase anodic polarization function of galvanized coating, retarde lectrode reaction more efficiently. The reason is that either SiO2 in organic film occur chemical reaction with Zn, produce stable zinc silicate compound; or as aresult of dissolve-redeposit of SiO2 in the film.

  2. Fabrication and characterization of advanced Organic Thin Film Transistors

    OpenAIRE

    Scaldaferri, Rossana

    2009-01-01

    The thesis aims to the development of Organic Thin Film Transistors and more complex devices based on organic materials. The experimental work demonstrates the possibility to manufacture transistors and more complex circuits with innovative polymers and technologies, leading to an experimental validation of the possibility to realize all-organic devices.

  3. Characterization of interfaces between metals and organic thin films by electron and ion spectroscopies

    Energy Technology Data Exchange (ETDEWEB)

    Schmid, Martin

    2012-01-18

    In this thesis, interfaces between metals and organic thin films have been characterized with photoelectron and ion-scattering spectroscopies. Two different classes of metal/organic interfaces were examined in detail. First, interfaces which can be mainly characterized by relatively weak coordinative interactions between substrate and adsorbate. Second, interfaces which are mostly determined, or even created, by chemical reactions between different adsorbates or between adsorbates and substrate. Typical examples from the first class are metalated tetrapyrrole monolayers on Ag(111) and Au(111) single-crystal substrates. In this study, a focus was set to the interaction between iron and cobalt tetrapyrroles with Ag(111) or Au(111) substrates. A detailed examination of the corresponding photoelectron spectra revealed that the adsorbatesubstrate interaction is associated with a charge transfer from the metallic substrate to the Fe(II) or Co(II) ions within the tetrapyrrole units. The examination of cobalt(II) phthalocyanine monolayers further led to the conclusion that the magnetic moment, as present in unperturbed CoPc molecules, is efficiently quenched by the contact to the Ag(111) surface and the associated charge transfer. Similar investigations on Au(111) substrates gave evidence for possible adsorption site effects, further complicating the adsorbate/substrate interaction. Furthermore the formation of two-dimensional structures of poly(p-phenylene-terephthalamide) (PPTA, trademark Kevlar) on Ag(111) was closely examined. The Ag(111) surface does not only provide the geometrical boundary for the formation of the 2D covalent structures, but, moreover, actively participates in the reaction; after the adsorption of TPC molecules, a scission of the C-Cl bond, in particular at temperatures above 120 K, was evident. The resulting radical fragments appear stable and can act as reaction partners for the co-adsorbed PPD units. The chlorine atoms reside on the surface even

  4. Preparation of magnetic metal organic frameworks adsorbent modified with mercapto groups for the extraction and analysis of lead in food samples by flame atomic absorption spectrometry.

    Science.gov (United States)

    Wang, Yang; Chen, Huanhuan; Tang, Jie; Ye, Guiqin; Ge, Huali; Hu, Xiaoya

    2015-08-15

    A novel magnetic metal organic frameworks adsorbent modified with mercapto groups was synthesized and developed for extraction and spectrophotometric determination of trace lead. The adsorbent was characterized by Fourier transforms infrared spectrometer, X-ray diffraction, scanning electron microscopy and vibrating sample magnetometry. The results indicated the adsorbents exhibited high adsorption capacities for lead due to the chelation mechanism between metal cations and mercapto groups. Meanwhile, the lead sorption onto the adsorbents could be easily separated from aqueous solution using a magnetic separation method. Under the optimal conditions, a linear calibration curve in the range from 1 to 20 μg L(-1) was achieved with an enrichment factor of 100. The limits of detection and quantitation for lead were found to be 0.29 and 0.97 μg L(-1), respectively. The developed method was successfully applied to the determination of trace amounts of lead in food samples and certified reference material with satisfactory results.

  5. A Neutron-Diffraction Study of the Solid Layers at the Liquid Solid Boundary in 4He-Films Adsorbed on Graphite

    DEFF Research Database (Denmark)

    da Costa Carneiro, Kim; Passell, L.; Thomlinson, W.;

    1981-01-01

    A neutron scattering study of the structure of 4He films adsorbed on graphite is reported. Diffraction from helium monolayers at a temperature of 1.2K shows the formation of an incommensurate, triangular-lattice solid of high density. As the coverage is increased above two layers, the diffraction...... pattern changes indicating solidification of a second layer. The observed two-layer patterns can be indexed with either a pair of incommensurate, triangular-lattice solid layers of different densities or a close-packed bilayer; the experimental information available is not sufficient to make a more...

  6. Thin-film organic photonics molecular layer deposition and applications

    CERN Document Server

    Yoshimura, Tetsuzo

    2011-01-01

    Among the many atomic/molecular assembling techniques used to develop artificial materials, molecular layer deposition (MLD) continues to receive special attention as the next-generation growth technique for organic thin-film materials used in photonics and electronics. Thin-Film Organic Photonics: Molecular Layer Deposition and Applications describes how photonic/electronic properties of thin films can be improved through MLD, which enables precise control of atomic and molecular arrangements to construct a wire network that achieves ""three-dimensional growth"". MLD facilitates dot-by-dot--o

  7. Organic nanostructured thin film devices and coatings for clean energy

    CERN Document Server

    Zhang, Sam

    2010-01-01

    Authored by leading experts from around the world, the three-volume Handbook of Nanostructured Thin Films and Coatings gives scientific researchers and product engineers a resource as dynamic and flexible as the field itself. The first two volumes cover the latest research and application of the mechanical and functional properties of thin films and coatings, while the third volume explores the cutting-edge organic nanostructured devices used to produce clean energy. This third volume, Organic Nanostructured Thin Film Devices and Coatings for Clean Energy, addresses various aspects of the proc

  8. Removal of hexenuronic acid by xylanase to reduce adsorbable organic halides formation in chlorine dioxide bleaching of bagasse pulp.

    Science.gov (United States)

    Nie, Shuangxi; Wang, Shuangfei; Qin, Chengrong; Yao, Shuangquan; Ebonka, Johnbull Friday; Song, Xueping; Li, Kecheng

    2015-11-01

    Xylanase-aided chlorine dioxide bleaching of bagasse pulp was investigated. The pulp was pretreated with xylanase and followed a chlorine dioxide bleaching stage. The ATR-FTIR and XPS were employed to determine the surface chemistry of the control pulp, xylanase treated and chlorine dioxide treated pulps. The hexenuronic acid (HexA) could obviously be reduced after xylanase pretreatment, and the adsorbable organic halides (AOX) were reduced after chlorine dioxide bleaching. Compared to the control pulp, AOX could be reduced by 21.4-26.6% with xylanase treatment. Chlorine dioxide demand could be reduced by 12.5-22% to achieve the same brightness. The ATR-FTIR and XPS results showed that lignin and hemicellulose (mainly HexA) were the main source for AOX formation. Xylanase pretreatment could remove HexA and expose more lignin, which decreased the chlorine dioxide demand and thus reduced formation of AOX. PMID:26263004

  9. Biogas from MSW landfill: Composition and determination of chlorine content with the AOX (adsorbable organically bound halogens) technique

    International Nuclear Information System (INIS)

    An exhaustive characterization of the biogas from some waste disposal facilities has been carried out. The analysis includes the main components (methane, carbon dioxide, nitrogen and oxygen) as well as trace components such as hydrogen sulphide, ammonia and VOCs (volatile organic compounds) including siloxanes and halogenated compounds. VOCs were measured by GC/MS (Gas Chromatography/Mass Spectrometry) using two different procedures: thermal desorption of the Tenax TA and Carbotrap 349 tubes and SPME (Solid Phase Micro-Extraction). A method has been established to measure the total halogen content of the biogas with the AOX (adsorbable organically bound halogens) technique. The equipment used to analyze the samples was a Total Organic Halogen Analyzer (TOX-100). Similar results were obtained when comparing the TOX (Total Organic Halogen) values with those obtained by GC/MS. The halogen content in all the samples was under 22 mg Cl/Nm3 which is below the limit of 150 mg/Nm3 proposed in the Spanish Regulations for any use of the biogas. The low chlorine content in the biogas studied, as well as the low content of other trace compounds, makes it suitable for use as a fuel for electricity generating engines

  10. On the nucleation and initial film growth of rod-like organic molecules

    Science.gov (United States)

    Winkler, Adolf

    2016-10-01

    In this article, some fundamental topics related to the initial steps of organic film growth are reviewed. General conclusions will be drawn based on experimental results obtained for the film formation of oligophenylene and pentacene molecules on gold and mica substrates. Thin films were prepared via physical vapor deposition under ultrahigh-vacuum conditions and characterized in-situ mainly by thermal desorption spectroscopy, and ex-situ by X-ray diffraction and atomic force microscopy. In this short review article the following topics will be discussed: What are the necessary conditions to form island-like films which are either composed of flat-lying or of standing molecules? Does a wetting layer exist below and in between the islands? What is the reason behind the occasionally observed bimodal island size distribution? Can one describe the nucleation process with the diffusion-limited aggregation model? Do the impinging molecules directly adsorb on the surface or rather via a hot-precursor state? Finally, it will be described how the critical island size can be determined by an independent measurement of the deposition rate dependence of the island density and the capture-zone distribution via a universal relationship.

  11. Prediction of capacity factors for aqueous organic solutes adsorbed on a porous acrylic resin

    Science.gov (United States)

    Thurman, E.M.

    1978-01-01

    The capacity factors of 20 aromatic, allphatic, and allcycllc organic solutes with carboxyl, hydroxyl, amine, and methyl functional groups were determined on Amberlite XAD-8, a porous acrylic resin. The logarithm of the capacity factor, k???, correlated inversely with the logarithm of the aqueous molar solubility with significance of less than 0.001. The log k???-log solubility relationship may be used to predict the capacity of any organic solute for XAD-8 using only the solubility of the solute. The prediction is useful as a guide for determining the proper ratio of sample to column size In the preconcentration of organic solutes from water. The inverse relationship of solubility and capacity is due to the unfavorable entropy of solution of organic solutes which affects both solubility and sorption.

  12. TiO{sub 2} films organofunctionalized with 2-aminothiazole ligand and adsorbed Pd(II) ions applied in the photocatalytic degradation of phenol in an aqueous medium

    Energy Technology Data Exchange (ETDEWEB)

    Cristante, Valtair M. [Instituto de Quimica, Departamento de Quimica Analitica/UNESP, P.O. box-355, 14800-900, Araraquara, SP (Brazil); Jorge, Sonia M.A. [Instituto de Biociencias, Departamento de Quimica e Bioquimica/UNESP, P.O. box-510, 18618-000, Botucatu, SP (Brazil); Valente, Jose P.S. [Instituto de Biociencias, Departamento de Quimica e Bioquimica/UNESP, P.O. box-510, 18618-000, Botucatu, SP (Brazil); Saeki, Margarida J. [Faculdade de Ciencias de Bauru, Departamento de Quimica, P.O. box-473, 17033360, Bauru, SP, Brasil (Brazil); Florentino, Ariovaldo O. [Instituto de Biociencias, Departamento de Quimica e Bioquimica/UNESP, P.O. box-510, 18618-000, Botucatu, SP (Brazil); Padilha, Pedro M. [Instituto de Biociencias, Departamento de Quimica e Bioquimica/UNESP, P.O. box-510, 18618-000, Botucatu, SP (Brazil)]. E-mail: padilha@ibb.unesp.br

    2007-05-07

    This paper describes the preparation of thin titanium films via sol-gel route and their subsequent chemical modification by anchoring with 2-aminothiazole ligand and Pd(II) ion sorption, aiming to maximize the photocatalytic activity. The material was characterized by diffuse reflectance infrared Fourier transform spectroscopy, ultraviolet and visible spectrometry, X-ray diffractometry, and scanning electronic microscopy. The amount of palladium adsorbed on the film's surface, determined by graphite furnace atomic absorption spectrometry, showed a value of 2.69 x 10{sup 16} atoms cm{sup -2}. The photocatalytic tests indicated that the functionalization with 2-aminothiazole and the adsorption of palladium (II) were determinants in the semiconductor's enhanced photocatalytic activity.

  13. ADSORPTION DYNAMICS OF MACROPOROUS POL YMERIC ADSORBENT Ⅱ.The Studies on the FIlm DIffusion Mass—Transfer Process

    Institute of Scientific and Technical Information of China (English)

    WANGChunhong; XUMingcheng; 等

    2000-01-01

    The film diffusion mass-transfer process of adsorption of phenol on macroporous polystyrene resin was investigated in detail.In order to revise the Boyd film diffusion kinetics equation,the out-surface structure of the macroporous resin and that of gel-type ion-exchange resin was compared and the new film diffusion equation was also suggested.These results showed that the film diffusion was influenced by porosity of the macroporous resin greatly,which differed from the film diffustion behavior of ion-exchange resin obviously.

  14. Tunneling spectroscopy of highly ordered organic thin films

    OpenAIRE

    Törker, Michael

    2003-01-01

    In this work, a Au(100) single crystal was used as substrate for organic molecular beam epitaxy. Highly ordered organic thin films of the molecules 3,4,9,10-perylenetetracarboxylic-3,4,9,10-dianhydrid (PTCDA) and hexa-peri-hexabenzo-coronene (HBC) as well as organic-organic heterostructures on reconstructed Au(100) were prepared. The molecular arrangement was characterized in Scanning Tunneling Microscopy and Low Energy Electron Diffraction investigations. Scanning Tunneling Spectroscopy data...

  15. AMBIENT LEVEL VOLATILE ORGANIC COMPOUND (VOC) MONITORING USING SOLID ADSORBANTS - RECENT U.S. EPA STUDIES

    Science.gov (United States)

    Ambient air spiked with 1-10 ppbv concentrations of 41 toxic volatile organic compounds (VOCs) listed in U.S. Environmental Protection Agency (EPA) Compendium Method TO-14A was monitored using solid sorbents for sample collection and a Varian Saturn 2000 ion trap mass spectrome...

  16. The role of dissolved organic matter in adsorbing heavy metals in clay-rich soils

    NARCIS (Netherlands)

    Y. Refaey; B. Jansen; A.H. El-Shater; A.A. El-Haddad; K. Kalbitz

    2014-01-01

    Adsorption of tested heavy metals on Egyptian soils was large in all situations tested and follows the order: Cu >> Ni ≈ Zn. Copper was influenced by the timing of dissolved organic matter addition more than Ni and Zn. Specific binding mechanisms (inner-sphere complexes) dominated the affinity of Cu

  17. Method for analyzing structural changes of flexible metal-organic frameworks induced by adsorbates

    NARCIS (Netherlands)

    D. Dubbeldam; R. Krishna; R.Q. Snurr

    2009-01-01

    Metal−organic frameworks (MOFs) have crystal structures that exhibit unusual flexibility. An extreme example is that of the "breathing MOF" MIL-53 that expands or shrinks to admit guest molecules like CO2 and water. We present a powerful simulation tool to quickly calculate unit cell shape and size

  18. Polymeric Thin Films for Organic Electronics: Properties and Adaptive Structures

    Directory of Open Access Journals (Sweden)

    Bruno Pignataro

    2013-03-01

    Full Text Available This review deals with the correlation between morphology, structure and performance of organic electronic devices including thin film transistors and solar cells. In particular, we report on solution processed devices going into the role of the 3D supramolecular organization in determining their electronic properties. A selection of case studies from recent literature are reviewed, relying on solution methods for organic thin-film deposition which allow fine control of the supramolecular aggregation of polymers confined at surfaces in nanoscopic layers. A special focus is given to issues exploiting morphological structures stemming from the intrinsic polymeric dynamic adaptation under non-equilibrium conditions.

  19. Fundamentals of laser-assisted fabrication of inorganic and organic films

    DEFF Research Database (Denmark)

    Schou, Jørgen

    2008-01-01

    The standard method for producing films by laser-assisted methods, Pulsed Laser Deposition (PLD) will be reviewed. The films considered are usually inorganic films, but also films of organic materials have been produced. Also the deposition of organic films by MAPLE (Matrix Assisted Pulsed Laser...

  20. Thin films by metal-organic precursor plasma spray

    International Nuclear Information System (INIS)

    While most plasma spray routes to coatings utilize solids as the precursor feedstock, metal-organic precursor plasma spray (MOPPS) is an area that the authors have investigated recently as a novel route to thin film materials. Very thin films are possible via MOPPS and the technology offers the possibility of forming graded structures by metering the liquid feed. The current work employs metal-organic compounds that are liquids at standard temperature-pressure conditions. In addition, these complexes contain chemical functionality that allows straightforward thermolytic transformation to targeted phases of interest. Toward that end, aluminum 3,5-heptanedionate (Al(hd)3), triethylsilane (HSi(C2H5)3 or HSiEt3), and titanium tetrakisdiethylamide (Ti(N(C2H5)2)4 or Ti(NEt2)4) were employed as precursors to aluminum oxide, silicon carbide, and titanium nitride, respectively. In all instances, the liquids contain metal-heteroatom bonds envisioned to provide atomic concentrations of the appropriate reagents at the film growth surface, thus promoting phase formation (e.g., Si-C bond in triethylsilane, Ti-N bond in titanium amide, etc.). Films were deposited using a Sulzer Metco TriplexPro-200 plasma spray system under various experimental conditions using design of experiment principles. Film compositions were analyzed by glazing incidence x-ray diffraction and elemental determination by x-ray spectroscopy. MOPPS films from HSiEt3 showed the formation of SiC phase but Al(hd)3-derived films were amorphous. The Ti(NEt2)4 precursor gave MOPPS films that appear to consist of nanosized splats of TiOCN with spheres of TiO2 anatase. While all films in this study suffered from poor adhesion, it is anticipated that the use of heated substrates will aid in the formation of dense, adherent films.

  1. High-resolution ellipsometric study of an n-alkane film, dotriacontane, adsorbed on a SiO2 surface

    DEFF Research Database (Denmark)

    Volkmann, U.G.; Pino, M.; Altamirano, L.A.;

    2002-01-01

    alkane/SiO2 interfacial region differs qualitatively from that which occurs in the surface freezing effect at the bulk alkane fluid/vapor interface. In that case, there is again a perpendicular film phase adjacent to the air interface but no parallel film phase intervenes between it and the bulk alkane...... present at higher coverages. In addition, we have performed high-resolution ellipsometry and stray-light measurements on dotriacontane films deposited from solution onto highly oriented pyrolytic graphite substrates. After film deposition, these substrates proved to be less stable in air than SiO2....

  2. Langmuir-Blodgett films of molecular organic materials

    Energy Technology Data Exchange (ETDEWEB)

    Talham, Daniel R; Yamamoto, Takashi [Department of Chemistry, University of Florida, Gainesville, FL 32611-7200 (United States); Meisel, Mark W [Department of Physics, Center for Condensed Matter Science, University of Florida, Gainesville, FL 32611-8440 (United States)], E-mail: talham@chem.ufl.edu

    2008-05-07

    Langmuir-Blodgett methods are perhaps the original approach for achieving controlled deposition of organic thin films. Molecules are first organized into a monolayer array on the surface of water before transfer as a monolayer onto solid supports. Molecular monolayers, multilayers, and multilayered heterostructures can be achieved. The capability of exercising such control over thin film assemblies has attracted materials chemists and physicists to develop Langmuir-Blodgett films for studies on organic conductors, magnets, non-linear optics, rectifiers, and intermolecular electron transfer. This article reviews objectives in each of these areas and selects some specific examples from the literature to highlight the state of the art, mostly from the point of view of the chemical systems that are studied. Mixed organic/inorganic hybrid films represent a new direction for Langmuir-Blodgett films in materials science, combining conventional inorganic solid-state phenomena with the properties of the organic networks, and recent examples, taken principally from the authors' work, are highlighted.

  3. Cathode liminescence properties of organic lengmuir-blodgett films

    CERN Document Server

    Voronkina, N I; L'vov, A N; Skibin, V I

    2001-01-01

    Some investigation results of the beta-sensitivity of organic Langmuir-Blodgett (LB) films irradiated with an electron beam are described. The dependences of the integral luminescence (DELTA lambda=380-450nm) on the electron energy (0.2...6kV) with a constant density (0.05...4.0 mu A/cm sup 2) are represented. The possible spheres of LB films application as scintillator detectors of ionizing radiation are discussed.

  4. Liquid crystals for organic thin-film transistors

    OpenAIRE

    Iino, Hiroaki; Usui, Takayuki; Hanna, Jun-ichi

    2015-01-01

    Crystalline thin films of organic semiconductors are a good candidate for field effect transistor (FET) materials in printed electronics. However, there are currently two main problems, which are associated with inhomogeneity and poor thermal durability of these films. Here we report that liquid crystalline materials exhibiting a highly ordered liquid crystal phase of smectic E (SmE) can solve both these problems. We design a SmE liquid crystalline material, 2-decyl-7-phenyl-[1]benzothieno[3,...

  5. Organic photo detectors for an integrated thin-film spectrometer

    Science.gov (United States)

    Peters, Sabine; Sui, Yunwu; Glöckler, Felix; Lemmer, Uli; Gerken, Martina

    2007-09-01

    We introduce a thin-film spectrometer that is based on the superprism effect in photonic crystals. While the reliable fabrication of two and three dimensional photonic crystals is still a challenge, the realization of one-dimensional photonic crystals as thin-film stacks is a relatively easy and inexpensive approach. Additionally, dispersive thin-film stacks offer the possibility to custom-design the dispersion profile according to the application. The thin-film stack is designed such that light incident at an angle experiences a wavelength-dependent spatial beam shift at the output surface. We propose the monolithic integration of organic photo detectors to register the spatial beam position and thus determine the beam wavelength. This thin-film spectrometer has a size of approximately 5 mm2. We demonstrate that the output position of a laser beam is determined with a resolution of at least 20 μm by the fabricated organic photo detectors. Depending on the design of the thin-film filter the wavelength resolution of the proposed spectrometer is at least 1 nm. Possible applications for the proposed thin-film spectrometer are in the field of absorption spectroscopy, e.g., for gas analysis or biomedical applications.

  6. Reduction of ferrihydrite with adsorbed and coprecipitated organic matter: microbial reduction by Geobacter bremensis vs. abiotic reduction by Na-dithionite

    Science.gov (United States)

    Eusterhues, K.; Hädrich, A.; Neidhardt, J.; Küsel, K.; Keller, T. F.; Jandt, K. D.; Totsche, K. U.

    2014-09-01

    Ferrihydrite is a widespread poorly crystalline Fe oxide which becomes easily coated by natural organic matter in the environment. This mineral-bound organic matter entirely changes the mineral surface properties and therefore the reactivity of the original mineral. Here, we investigated 2-line ferrihydrite, ferrihydrite with adsorbed organic matter, and ferrihydrite coprecipitated with organic matter for microbial and abiotic reduction of Fe(III). Ferrihydrite-organic matter associations with different organic matter loadings were reduced either by Geobacter bremensis or abiotically by Na-dithionite. Both types of experiments showed decreasing initial Fe-reduction rates and decreasing degrees of reduction with increasing amounts of mineral-bound organic matter. At similar organic matter loadings, coprecipitated ferrihydrites were more reactive than ferrihydrites with adsorbed organic matter. The difference can be explained by the smaller crystal size and poor crystallinity of such coprecipitates. At small organic matter loadings the poor crystallinity of coprecipitates led to even faster Fe-reduction rates than found for pure ferrihydrite. The amount of mineral-bound organic matter also affected the formation of secondary minerals: goethite was only found after reduction of organic matter-free ferrihydrite and siderite was only detected when ferrihydrites with relatively low amounts of mineral-bound organic matter were reduced. We conclude that direct contact of G. bremensis to the Fe oxide mineral surface was inhibited by attached organic matter. Consequently, mineral-bound organic matter shall be taken into account as a factor in slowing down reductive dissolution.

  7. Thin film Encapsulations of Flexible Organic Light Emitting Diodes

    Directory of Open Access Journals (Sweden)

    Tsai Fa-Ta

    2016-01-01

    Full Text Available Various encapsulated films for flexible organic light emitting diodes (OLEDs were studied in this work, where gas barrier layers including inorganic Al2O3 thin films prepared by atomic layer deposition, organic Parylene C thin films prepared by chemical vapor deposition, and their combination were considered. The transmittance and water vapor transmission rate of the various organic and inorgabic encapsulated films were tested. The effects of the encapsulated films on the luminance and current density of the OLEDs were discussed, and the life time experiments of the OLEDs with these encapsulated films were also conducted. The results showed that the transmittance are acceptable even the PET substrate were coated two Al2O3 and Parylene C layers. The results also indicated the WVTR of the PET substrate improved by coating the barrier layers. In the encapsulation performance, it indicates the OLED with Al2O3 /PET, 1 pair/PET, and 2 pairs/PET presents similarly higher luminance than the other two cases. Although the 1 pair/PET encapsulation behaves a litter better luminance than the 2 pairs/PET encapsulation, the 2 pairs/PET encapsulation has much better life time. The OLED with 2 pairs/PET encapsulation behaves near double life time to the 1 pair encapsulation, and four times to none encapsulation.

  8. Chemical Annealing of Zinc Tetraphenylporphyrin Films: Effects on Film Morphology and Organic Photovoltaic Performance

    KAUST Repository

    Trinh, Cong

    2012-07-10

    We present a chemical annealing process for organic thin films. In this process, a thin film of a molecular material, such as zinc tetraphenylporphyrin (ZnTPP), is exposed to a vapor of nitrogen-based ligand (e.g., pyrazine, pz, and triazine, tz), forming a film composed of the metal-ligand complex. Fast and quantitative formation of the complex leads to marked changes in the morphology and optical properties of the film. X-ray diffraction studies show that the chemical annealing process converts amorphous ZnTPP films to crystalline ZnTPP•ligand films, whose porphryin planes lie nearly parallel to the substrate (average deviation is 8° for the ZnTPP•pz film). Organic solar cells were prepared with ZnTPP donor and C 60 acceptor layers. Devices were prepared with and without chemical annealing of the ZnTPP layer with a pyrazine ligand. The devices with chemically annealed ZnTPP donor layer show an increase in short-circuit current (J SC) and fill factor (FF) relative to analogous unannealed devices, presumably because of enhanced exciton diffusion length and improved charge conductivity. The open circuit voltages (V OC) of the chemically annealed devices are lower than their unannealed counterpart because of enhanced polaron pair recombination at the donor/acceptor heterojunction. A net improvement of 5-20% in efficiency has been achieved, after chemical annealing of ZnTPP films with pyrazine. © 2012 American Chemical Society.

  9. Organic Thin-Film Transistor (OTFT-Based Sensors

    Directory of Open Access Journals (Sweden)

    Daniel Elkington

    2014-04-01

    Full Text Available Organic thin film transistors have been a popular research topic in recent decades and have found applications from flexible displays to disposable sensors. In this review, we present an overview of some notable articles reporting sensing applications for organic transistors with a focus on the most recent publications. In particular, we concentrate on three main types of organic transistor-based sensors: biosensors, pressure sensors and “e-nose”/vapour sensors.

  10. Organic Thin-Film Transistor (OTFT)-Based Sensors

    OpenAIRE

    Daniel Elkington; Nathan Cooling; Warwick Belcher; Paul C. Dastoor; Xiaojing Zhou

    2014-01-01

    Organic thin film transistors have been a popular research topic in recent decades and have found applications from flexible displays to disposable sensors. In this review, we present an overview of some notable articles reporting sensing applications for organic transistors with a focus on the most recent publications. In particular, we concentrate on three main types of organic transistor-based sensors: biosensors, pressure sensors and “e-nose”/vapour sensors.

  11. A Water-Stable Cationic Metal-Organic Framework as a Dual Adsorbent of Oxoanion Pollutants.

    Science.gov (United States)

    Desai, Aamod V; Manna, Biplab; Karmakar, Avishek; Sahu, Amit; Ghosh, Sujit K

    2016-06-27

    A three-dimensional water-stable cationic metal-organic framework (MOF) pillared by a neutral ligand and with Ni(II)  metal nodes has been synthesized employing a rational design approach. Owing to the ordered arrangement of the uncoordinated tetrahedral sulfate (SO4 (2-) ) ions in the channels, the compound has been employed for aqueous-phase ion-exchange applications. The compound exhibits rapid and colorimetric aqueous-phase capture of environmentally toxic oxoanions (with similar geometries) in a selective manner. This system is the first example of a MOF-based system which absorbs both dichromate (Cr2 O7 (2-) ) and permanganate (MnO4 (-) ) ions, with the latter acting as a model for the radioactive contaminant pertechnetate (TcO4 (-) ). PMID:26855323

  12. Aluminium fumarate metal-organic framework: A super adsorbent for fluoride from water.

    Science.gov (United States)

    Karmakar, Sankha; Dechnik, Janina; Janiak, Christoph; De, Sirshendu

    2016-02-13

    Potential of aluminium fumarate metal organic framework (MOF) for fluoride removal from groundwater has been explored in this work. The laboratory produced MOF exhibited characteristics similar to the commercial version. MOF was found to be micro-porous with surface area of 1156 m(2)/g and average pore size 17Å. Scanning electron micrograph of the AlFu MOF showed minute pores and texture was completely different from either of the parent materials. Change in the composition of AlFu MOF after fluoride adsorption was evident from powder X-ray diffraction analysis. Thermal stability of the AlFu MOF up to 700K was established by thermo-gravimetric analysis. Incorporation of fluoride phase after adsorption was confirmed by X-ray fluorescence analysis. As observed from FTIR study, hydroxyl ions in AlFu MOF were substituted by fluoride. 0.75 g/l AlFu MOF was good enough for complete removal of 30 mg/l fluoride concentration in feed solution. The maximum adsorption capacity for fluoride was 600, 550, 504 and 431 mg/g, respectively, at 293, 303, 313 and 333K. PMID:26513559

  13. Pulsed laser deposition of organic semiconductor rubrene thin films

    Science.gov (United States)

    Grochowska, K.; Majumdar, S.; Laukkanen, P.; Majumdar, H. S.; Sawczak, M.; Śliwiński, G.

    2015-01-01

    Pulsed Laser Deposition (PLD) technique is applied to produce organic semiconductor (OS) rubrene thin film for spintronics applications. The use of organic material for spintronics is motivated by the advantages such as long spin diffusion length due to low spin-orbit and hyperfine coupling1,2, chemical tuning of electronic functionality, easy structural modifications, ability of self-assembly and mechanical flexibility3 etc. However, a major drawback of OS is its low mobility compared to inorganic semiconductors. The PLD growth of rubrene aims on fabricating OS films under more controlled environment to achieve higher crystalline order to improve its mobility and spin coherence length. Among organic materials, rubrene reveals the highest hole mobility - up to 40 cm2/(V•s) and can be exploited in organic light-emitting diodes (OLEDs) or field-effect transistors (OFETs) 4. In this work the rubrene thin films are produced from hardened pellets in vacuum using Nd:YAG pulsed laser operated at 1064 nm, 2 Hz and energy fluence around 0.2 J/cm2. For the reference rubrene samples on SiO2 glass the AFM data reveal continuous 5-7 nm thick films. The amorphous structures are confirmed by XRD measurements and also Raman spectra which show signatures of both tetracene and phenyl bands and a broadband at 1373 cm-1. The obtained results indicate that continuous, defect-free rubrene films can be prepared by means of PLD for investigation of the spin polarization properties of organic-inorganic hybrids. Further studies are on the way to improve crystalline qualities of the rubrene films for less grain boundary related defects and improved mobility and spin diffusion length.

  14. Preparation and characterization of humic acid-carbon hybrid materials as adsorbents for organic micro-pollutants.

    Science.gov (United States)

    Radwan, Emad K; Abdel Ghafar, Hany H; Moursy, Ahmed S; Langford, Cooper H; Bedair, Ahmed H; Achari, Gopal

    2015-08-01

    The present work involves the preparation of novel adsorbent materials by the insolubilization and hybridization of humic acid (HA) with carbon. The prepared materials were characterized by N2 adsorption, elemental analysis, Fourier transform infrared spectroscopy, scanning electron microscopy, transmission electron microscopy, solid-state (13)C cross polarization magic angle spinning nuclear magnetic resonance, and low-field nuclear magnetic resonance (NMR) relaxometry on wetted samples. The water solubility of these materials and the lack of effect of oxidants were also confirmed. With this background, the adsorption capacities toward phenol, 2,4,6-tricholrophenol, and atrazine were evaluated, using these as model compounds for organic micropollutants of concern in water. Experimental results show that the prepared materials are mesoporous and have a higher surface area than humic acid and even than the porous carbon in the case of carbon coating. They retain the basic features of the starting materials with lowered functional group content. Moreover, there are interesting new features. NMR relaxometry shows that equilibration of water uptake is very fast, making use in water simple. They have higher adsorption capacities than the pure materials, and they can be applied under a wide range of environmental conditions. PMID:25874433

  15. Preparation and characterization of humic acid-carbon hybrid materials as adsorbents for organic micro-pollutants.

    Science.gov (United States)

    Radwan, Emad K; Abdel Ghafar, Hany H; Moursy, Ahmed S; Langford, Cooper H; Bedair, Ahmed H; Achari, Gopal

    2015-08-01

    The present work involves the preparation of novel adsorbent materials by the insolubilization and hybridization of humic acid (HA) with carbon. The prepared materials were characterized by N2 adsorption, elemental analysis, Fourier transform infrared spectroscopy, scanning electron microscopy, transmission electron microscopy, solid-state (13)C cross polarization magic angle spinning nuclear magnetic resonance, and low-field nuclear magnetic resonance (NMR) relaxometry on wetted samples. The water solubility of these materials and the lack of effect of oxidants were also confirmed. With this background, the adsorption capacities toward phenol, 2,4,6-tricholrophenol, and atrazine were evaluated, using these as model compounds for organic micropollutants of concern in water. Experimental results show that the prepared materials are mesoporous and have a higher surface area than humic acid and even than the porous carbon in the case of carbon coating. They retain the basic features of the starting materials with lowered functional group content. Moreover, there are interesting new features. NMR relaxometry shows that equilibration of water uptake is very fast, making use in water simple. They have higher adsorption capacities than the pure materials, and they can be applied under a wide range of environmental conditions.

  16. Mechanism of formation of humus coatings on mineral surfaces 3. Composition of adsorbed organic acids from compost leachate on alumina by solid-state 13C NMR

    Science.gov (United States)

    Wershaw, R. L.; Llaguno, E.C.; Leenheer, J.A.

    1996-01-01

    The adsorption of compost leachate DOC on alumina is used as a model for elucidation of the mechanism of formation of natural organic coatings on hydrous metal oxide surfaces in soils and sediments. Compost leachate DOC is composed mainly of organic acid molecules. The solid-state 13C NMR spectra of these organic acids indicate that they are very similar in composition to aquatic humic substances. Changes in the solid-state 13C NMR spectra of compost leachate DOC fractions adsorbed on alumina indicate that the DOC molecules are most likely adsorbed on metal oxide surfaces through a combination of polar and hydrophobic interaction mechanisms. This combination of polar and hydrophobic mechanism leads to the formation of bilayer coatings of the leachate molecules on the oxide surfaces.

  17. Study of neural cells on organic semiconductor ultra thin films

    Energy Technology Data Exchange (ETDEWEB)

    Bystrenova, Eva; Tonazzini, Ilaria; Stoliar, Pablo; Greco, Pierpaolo; Lazar, Adina; Dutta, Soumya; Dionigi, Chiara; Cacace, Marcello; Biscarini, Fabio [ISMN-CNR, Bologna (Italy); Jelitai, Marta; Madarasz, Emilia [IEM- HAS, Budapest (Hungary); Huth, Martin; Nickel, Bert [LMU, Munich (Germany); Martini, Claudia [Dept. PNPB, Univ. of Pisa (Italy)

    2008-07-01

    Many technological advances are currently being developed for nano-fabrication, offering the ability to create and control patterns of soft materials. We report the deposition of cells on organic semiconductor ultra-thin films. This is a first step towards the development of active bio/non bio systems for electrical transduction. Thin films of pentacene, whose thickness was systematically varied, were grown by high vacuum sublimation. We report adhesion, growth, and differentiation of human astroglial cells and mouse neural stem cells on an organic semiconductor. Viability of astroglial cells in time was measured as a function of the roughness and the characteristic morphology of ultra thin organic film, as well as the features of the patterned molecules. Optical fluorescence microscope coupled to atomic force microscope was used to monitor the presence, density and shape of deposited cells. Neural stem cells remain viable, differentiate by retinoic acid and form dense neuronal networks. We have shown the possibility to integrate living neural cells on organic semiconductor thin films.

  18. Morphology of polymer-based films for organic photovoltaics

    OpenAIRE

    Ruderer, Matthias A.

    2012-01-01

    In this thesis, polymer-based films are examined for applications in organic photovoltaics. Polymer-fullerene, polymer-polymer and diblock copolymer systems are characterized as active layer materials. The focus is on experimental parameters influencing the morphology formation of the active layer in organic solar cells. Scattering and imaging techniques provide a complete understanding of the internal structure on different length scales which is compared to spectroscopic and photovoltaic pr...

  19. Removal of methylene blue from aqueous solutions by an adsorbent based on metal-organic framework and polyoxometalate

    Energy Technology Data Exchange (ETDEWEB)

    Liu, Xiaoxia; Luo, Jing; Zhu, Yating; Yang, Yun; Yang, Shuijin, E-mail: yangshuijin@163.com

    2015-11-05

    A metal-organic framework (Cu{sub 3}(BTC){sub 2}, BTC = 1,3,5-benzenetricarboxylate) composite based on polyoxometalate (H{sub 6}P{sub 2}W{sub 18}O{sub 62}) was synthesized by a simple one-pot solvent-thermal method and applied as an adsorbent to remove methylene blue (MB) from aqueous solution. The chemical structure, morphology and thermostability of the composite were characterized by Fourier Transform Infrared Spectroscopy (FTIR), X-ray diffraction (XRD), Scanning Electron Microscope (SEM), Thermogravimetric Analysis (TG) and N{sub 2} adsorption–desorption isotherms. The removal rate of the composite H{sub 6}P{sub 2}W{sub 18}O{sub 62}@Cu{sub 3}(BTC){sub 2} was greater than that of the pure Cu{sub 3}(BTC){sub 2}, especially at higher initial concentrations, showing that the adsorption performance of porous Cu{sub 3}(BTC){sub 2} can be improved through the modification of H{sub 6}P{sub 2}W{sub 18}O{sub 62}. The effect factors containing the initial concentration, contact time, initial solution pH and temperature of MB adsorption onto the composite were systematically explored. The experimental isotherm data was found to fit the Freundlich model well and the process of MB adsorption onto H{sub 6}P{sub 2}W{sub 18}O{sub 62}@Cu{sub 3}(BTC){sub 2} was controlled by the pseudo-second-order kinetic model. The thermodynamic parameters illustrated that the adsorption was spontaneous and exothermic process. These results show that designing a metal-organic framework composite is a quite promising strategy to achieve extreme application for metal-organic framework. - Graphical abstract: Comparison of removal rate for MB in pure Cu{sub 3}(BTC){sub 2} and H{sub 6}P{sub 2}W{sub 18}O{sub 62}@Cu{sub 3}(BTC){sub 2} at different initial concentration. - Highlights: • Metal-organic framework (MOF) composite in the adsorption application was proposed. • The adsorption rate of MOF was improved by introducing polyoxometalates. • The adsorption isotherm and kinetic was used to

  20. Self-standing chitosan films as dielectrics in organic thin-film transistors

    Directory of Open Access Journals (Sweden)

    J. Morgado

    2013-12-01

    Full Text Available Organic thin film transistors, using self-standing 50 µm thick chitosan films as dielectric, are fabricated using sublimed pentacene or two conjugated polymers deposited by spin coating as semiconductors. Field-effect mobilities are found to be similar to values obtained with other dielectrics and, in the case of pentacene, a value (0.13 cm2/(V•s comparable to high performing transistors was determined. In spite of the low On/Off ratios (a maximum value of 600 was obtained for the pentacene-based transistors, these are promising results for the area of sustainable organic electronics in general and for biocompatible electronics in particular.

  1. Self-assembly of organic films on a liquid metal

    Science.gov (United States)

    Magnussen, Olaf M.; Ocko, Benjamin M.; Deutsch, Moshe; Regan, Michael J.; Pershan, Peter S.; Abernathy, Douglas; Grübel, Gerhard; Legrand, Jean-François

    1996-11-01

    THE structure and phase behaviour of organic thin films result from the subtle interplay of intermolecular Van der Waals interactions, which promote self-assembly and long-ranged order, and the more complex interactions between the end groups of the organic chains and the substrate. The structure of molecular films of amphiphiles has been extensively studied on subphases of dielectric liquids, notably water (Langmuir mono-layers) and on solid surfaces (self-assembled monolayers, SAMs)1-4. Here we report structural studies, by synchrotron X-ray scattering, of an intermediate case: densely packed alka-nethiol films on the surface of liquid mercury. While, like SAMs, these films form strong chemical bonds to the subphase, this subphase is smooth and unstructured, as in the case of Langmuir monolayers. But unlike either of these1,2,5-7, our films have no in-plane long-range order. We suggest that the strong interaction of the thiol group with the underlying disordered liquid dominates here over the order-promoting interactions of the alkyl chains.

  2. Crystalline-to-plastic phase transitions in molecularly thin n-dotriacontane films adsorbed on solid surfaces

    DEFF Research Database (Denmark)

    Cisternas, Edgardo; Corrales, T. P.; del Campo, V.;

    2009-01-01

    Crystalline-to-rotator phase transitions have been widely studied in bulk hydrocarbons, in particular in normal alkanes. But few studies of these transitions deal with molecularly thin films of pure n-alkanes on solid substrates. In this work, we were able to grow dotriacontane (n-C32H66) films...... identify with a solid-solid phase transition. At higher coverages, we observed additional steps in the ellipsometric signal that we identify with a solid-solid phase transition in multilayer islands (similar to 333 K) and with the transition to the rotator phase in bulk crystallites (similar to 337 K...

  3. Fabrication of a room-temperature NO2 gas sensor based on WO3 films and WO3/MWCNT nanocomposite films by combining polyol process with metal organic decomposition method

    International Nuclear Information System (INIS)

    Research highlights: → In this study, we fabricated a room-temperature NO2 gas sensor based on WO3/MWCNT nanocomposite film by combining polyol process with metal organic decomposition method. → The response of the WO3/MWCNT nanocomposite film to NO2 gas increased dramatically when a few MWCNTs were added to the WO3 film. → New electrical paths and depletion layers formed in the WO3/MWCNT nanocomposite film were used to explain the high sensitivity of WO3/MWCNT nanocomposite film. - Abstract: Polyol process was combined with metal organic decomposition (MOD) method to fabricate a room-temperature NO2 gas sensor based on a tungsten oxide (WO3) film and another a nanocomposite film of WO3/multi-walled carbon nanotubes (WO3/MWCNTs). X-ray diffractometry (XRD), scanning electron microscopy (SEM) and atomic force microscopy (AFM) were used to analyze the structure and morphology of the fabricated films. Comparative gas sensing results indicated that the sensor that was based on the WO3/MWCNT nanocomposite film exhibited a much higher sensitivity than that based on a WO3 film in detecting NO2 gas at room temperature. Microstructural observations revealed that MWCNTs were embedded in the WO3 matrix. Therefore, a model of potential barriers to electronic conduction in the composite material was used to suggest that the high sensitivity is associated with the stretching of the two depletion layers at the surface of the WO3 film and at the interface of the WO3 film and the MWCNTs when detected gases are adsorbed at room temperature. The sensor that is based on a nanocomposite film of WO3/MWCNT exhibited a strong response in detecting very low concentrations of NO2 gas at room temperature and is practical because of the ease of its fabrication.

  4. Thin films by metal-organic precursor plasma spray

    Energy Technology Data Exchange (ETDEWEB)

    Schulz, Douglas L.; Sailer, Robert A.; Payne, Scott; Leach, James; Molz, Ronald J. [North Dakota State University, Fargo, North Dakota 58108-6050 (United States); Sulzer Metco (United States) Inc., Westbury, New York 11590-2724 (United States)

    2009-07-15

    While most plasma spray routes to coatings utilize solids as the precursor feedstock, metal-organic precursor plasma spray (MOPPS) is an area that the authors have investigated recently as a novel route to thin film materials. Very thin films are possible via MOPPS and the technology offers the possibility of forming graded structures by metering the liquid feed. The current work employs metal-organic compounds that are liquids at standard temperature-pressure conditions. In addition, these complexes contain chemical functionality that allows straightforward thermolytic transformation to targeted phases of interest. Toward that end, aluminum 3,5-heptanedionate (Al(hd){sub 3}), triethylsilane (HSi(C{sub 2}H{sub 5}){sub 3} or HSiEt{sub 3}), and titanium tetrakisdiethylamide (Ti(N(C{sub 2}H{sub 5}){sub 2}){sub 4} or Ti(NEt{sub 2}){sub 4}) were employed as precursors to aluminum oxide, silicon carbide, and titanium nitride, respectively. In all instances, the liquids contain metal-heteroatom bonds envisioned to provide atomic concentrations of the appropriate reagents at the film growth surface, thus promoting phase formation (e.g., Si-C bond in triethylsilane, Ti-N bond in titanium amide, etc.). Films were deposited using a Sulzer Metco TriplexPro-200 plasma spray system under various experimental conditions using design of experiment principles. Film compositions were analyzed by glazing incidence x-ray diffraction and elemental determination by x-ray spectroscopy. MOPPS films from HSiEt{sub 3} showed the formation of SiC phase but Al(hd){sub 3}-derived films were amorphous. The Ti(NEt{sub 2}){sub 4} precursor gave MOPPS films that appear to consist of nanosized splats of TiOCN with spheres of TiO{sub 2} anatase. While all films in this study suffered from poor adhesion, it is anticipated that the use of heated substrates will aid in the formation of dense, adherent films.

  5. Organic Thin Film Electroluminescent Passive Matrix Display

    Institute of Scientific and Technical Information of China (English)

    2001-01-01

    Long life green-emitting matrix display based on organic light-emitting diode is reported. The pixel number is 96×60, equivalent pixel size 0.4×0.4 mm2, and the pixel gap 0.1 mm. An image with no crosstalk between pixels is obtained. The average luminance of these pixels at duty cycle of 1/64 is 100 cd/m2, and the power consumption is 0.6 W. The dark room contrast of 1:100 is achieved without using a polarization filter.

  6. Exploration of exciton delocalization in organic crystalline thin films

    Science.gov (United States)

    Hua, Kim; Manning, Lane; Rawat, Naveen; Ainsworth, Victoria; Furis, Madalina

    The electronic properties of organic semiconductors play a crucial role in designing new materials for specific applications. Our group recently found evidence for a rotation of molecular planes in phthalocyanines that is responsible for the disappearance of a delocalized exciton in these systems for T >150K.................()().......1 In this study, we attempt to tune the exciton delocalization of small organic molecules using strain effects and alloying different molecules in the same family. The exciton behavior is monitored using time- and polarization resolved photolumniscence (PL) spectroscopy as a function of temperature. Specifically, organic crystalline thin films of octabutoxy phthalocyanine (H2OBPc), octyloxy phthalocyanines and H-bonded semiconductors such as the quinacridone and indigo derivatives are deposited on flexible substrates (i.e. Kapton and PEN) using an in-house developed pen-writing method.........2 that results in crystalline films with macroscopic long range order. The room temperature PL studies show redshift and changes in polarization upon bending of the film. Crystalline thin films of alloyed H2OBPc and octabutoxy naphthalocyanine with ratios ranging from 1:1 to 100:1 fabricated on both sapphire and flexible substrates are also explored using the same PL spectroscopy to elucidate the behaviors of delocalized excitons. .1N. Rawat, et al., J Phys Chem Lett 6, 1834 (2015). 2R. L. Headrick, et al., Applied Physics Letters 92, 063302 (2008). NSF DMR-1056589, NSF DMR-1062966.

  7. Pentacene Organic-Thin-Film Field-Effect Transistors

    Institute of Scientific and Technical Information of China (English)

    张素梅; 石家纬; 刘明大; 李靖; 郭树旭; 王伟

    2004-01-01

    We have fabricated organic thin-film transistors using the small-molecule polycyclic aromatic hydrocarbon pentacene as an active material. Devices were fabricated on glass substrates by using rf-magnetron sputtered amorphous aluminium as the gate electrode, and gelatinized polyimide as the gate dielectric with physical vapour grown pentacene thin films pasted on it as the active layer, then using rf-magnetron sputtered amorphous aluminium as the source and drain contacts. Field effect mobility and threshold voltage is 0.092 cm2 /Vs and 14.5 V,respectively. On-off current ratio is nearly 103.

  8. Self-organized structures in soft confined thin films

    Indian Academy of Sciences (India)

    Ashutosh Sharma

    2005-10-01

    We present a mini-review of our recent work on spontaneous, self-organized creation of mesostructures in soft materials like thin films of polymeric liquids and elastic solids. These very small scale, highly confined systems are inherently unstable and thus self-organize into ordered structures which can be exploited for MEMS, sensors, opto-electronic devices and a host of other nanotechnology applications. In particular, mesomechanics requires incorporation of intermolecular interactions and surface tension forces, which are usually inconsequential in classical macroscale mechanics. We point to some experiments and quasi-continuum simulations of self-organized structures in thin soft films which are germane not only to nanotechnology, but also to a spectrum of classical issues such as adhesion/debonding, wetting, coatings, tribology and membranes.

  9. Change in surface states of Ag(111) thin films upon adsorption of a monolayer of PTCDA organic molecules

    International Nuclear Information System (INIS)

    The change in the electronic structure of silver thin films of different thicknesses with the Ag( 111) orientation due to the interaction with an adsorbed monolayer of ordered organic molecules of 3,4,9,10-perylene-tetracarboxylic acid dianhydride (PTCDA) has been investigated in terms of density functional theory. It has been shown that one of the two surface states of the pure films transforms into an unocc upied interface state due to the interaction so that all the main features of the initial state are retained. The relation of the resulting state to the unoccupied state experimentally observed in the PTCDA/Ag( 111 ) system by scanning tunneling and two-photon photoemission spectroscopy has been discussed.

  10. Direct observation of epitaxial organic film growth: temperature-dependent growth mechanisms and metastability.

    Science.gov (United States)

    Marchetto, Helder; Schmidt, Thomas; Groh, Ullrich; Maier, Florian C; Lévesque, Pierre L; Fink, Rainer H; Freund, Hans-Joachim; Umbach, Eberhard

    2015-11-21

    The growth of the first ten layers of organic thin films on a smooth metallic substrate has been investigated in real-time using the model system PTCDA on Ag(111). The complex behaviour is comprehensively studied by electron microscopy, spectroscopy and diffraction in a combined PEEM/LEEM instrument revealing several new phenomena and yielding a consistent picture of this layer growth. PTCDA grows above room temperature in a Stranski-Krastanov mode, forming three-dimensional islands on a stable bi-layer, in competition with metastable 3rd and 4th layers. Around room temperature this growth mode changes into a quasi layer-by-layer growth, while at temperatures below about 250 K a Vollmer-Weber-like behaviour is observed. By means of laterally resolved soft X-ray absorption spectroscopy the orientation of all adsorbed molecules is found to be homogeneously flat lying on the surface, even during the growth process. The films grow epitaxially, showing long-range order with rotational domains. For the monolayer these domains could be directly analysed, showing an average size of several micrometers extending over substrate steps. PMID:26462749

  11. Formation of Organized Protein Thin Films with External Electric Field.

    Science.gov (United States)

    Ferreira, Cecília Fabiana da G; Camargo, Paulo C; Benelli, Elaine M

    2015-10-01

    The effect of an external electric field on the formation of protein GlnB-Hs films and on its buffer solution on siliconized glass slides has been analyzed by current versus electric field curves and atomic force microscopy (AFM). The Herbaspirillum seropedicae GlnB protein (GlnB-Hs) is a globular, soluble homotrimer (36 kDa) with its 3-D structure previously determined. Concentrations of 10 nM native denatured GlnB-Hs protein were deposited on siliconized glass slides under ambient conditions. Immediately after solution deposition a maximum electric field of 30 kV/m was applied with rates of 3 V/s. The measured currents were surface currents and were analyzed as transport current. Electric current started to flow only after a minimum electric field (critical value) for the systems analyzed. The AFM images showed films with a high degree of directional organization only when the proteins were present in the solution. These results showed that the applied electric field favored directional organization of the protein GlnB-Hs films and may contribute to understand the formation of protein films under applied electric fields.

  12. Temperature and layer thickness dependent in situ investigations on epindolidione organic thin-film transistors

    Science.gov (United States)

    Lassnig, R.; Striedinger, B.; Jones, A.O.F.; Scherwitzl, B.; Fian, A.; Głowacl, E.D.; Stadlober, B.; Winkler, A.

    2016-01-01

    We report on in situ performance evaluations as a function of layer thickness and substrate temperature for bottom-gate, bottom-gold contact epindolidione organic thin-film transistors on various gate dielectrics. Experiments were carried out under ultra-high vacuum conditions, enabling quasi-simultaneous electrical and surface analysis. Auger electron spectroscopy and thermal desorption spectroscopy (TDS) were applied to characterize the quality of the substrate surface and the thermal stability of the organic films. Ex situ atomic force microscopy (AFM) was used to gain additional information on the layer formation and surface morphology of the hydrogen-bonded organic pigment. The examined gate dielectrics included SiO2, in its untreated and sputtered forms, as well as the spin-coated organic capping layers poly(vinyl-cinnamate) (PVCi) and poly((±)endo,exo-bicyclo[2.2.1]hept-5-ene-2,3-dicarboxylic acid, diphenylester) (PNDPE, from the class of polynorbornenes). TDS and AFM revealed Volmer-Weber island growth dominated film formation with no evidence of a subjacent wetting layer. This growth mode is responsible for the comparably high coverage required for transistor behavior at 90–95% of a monolayer composed of standing molecules. Surface sputtering and an increased sample temperature during epindolidione deposition augmented the surface diffusion of adsorbing molecules and therefore led to a lower number of better-ordered islands. Consequently, while the onset of charge transport was delayed, higher saturation mobility was obtained. The highest, bottom-contact configuration, mobilities of approximately 2.5 × 10−3cm2/Vs were found for high coverages (50 nm) on sputtered samples. The coverage dependence of the mobility showed very different characteristics for the different gate dielectrics, while the change of the threshold voltage with coverage was approximately the same for all systems. An apparent decrease of the mobility with increasing coverage on the

  13. Multilevel organization in hybrid thin films for optoelectronic applications.

    Science.gov (United States)

    Vohra, Varun; Bolognesi, Alberto; Calzaferri, Gion; Botta, Chiara

    2009-10-20

    In this work we report two simple approaches to prepare hybrid thin films displaying a high concentration of zeolite crystals that could be used as active layers in optoelectronic devices. In the first approach, in order to organize nanodimensional zeolite crystals of 40 nm diameter in an electroactive environment, we chemically modify their external surface and play on the hydrophilic/hydrophobic forces. We obtain inorganic nanocrystals that self-organize in honeycomb electroluminescent polymer structures obtained by breath figure formation. The different functionalizations of the zeolite surface result in different organizations inside the cavities of the polymeric structure. The second approach involving soft-litography techniques allows one to arrange single dye-loaded zeolite L crystals of 800 nm of length by mechanical loading into the nanocavities of a conjugated polymer. Both techniques result in the formation of thin hybrid films displaying three levels of organization: organization of the dye molecules inside the zeolite nanochannels, organization of the zeolite crystals inside the polymer cavities, and micro- or nanostructuration of the polymer.

  14. Magnetic field effect in organic films and devices

    Science.gov (United States)

    Gautam, Bhoj Raj

    In this work, we focused on the magnetic field effect in organic films and devices, including organic light emitting diodes (OLEDs) and organic photovoltaic (OPV) cells. We measured magnetic field effect (MFE) such as magnetoconductance (MC) and magneto-electroluminescence (MEL) in OLEDs based on several pi- conjugated polymers and small molecules for fields |B|˜2mT. Magnetic field effect (MFE) measured on three isotopes of Poly (dioctyloxy) phenylenevinylene (DOO-PPV) showed that both regular and ultra-small effects are isotope dependent. This indicates that MFE response in OLED is mainly due to the hyperfine interaction (HFI). We also performed spectroscopy of the MFE including magneto-photoinduced absorption (MPA) and magneto-photoluminescence (MPL) at steady state conditions in several systems. This includes pristine Poly[2-methoxy-5-(2-ethylhexyl-oxy)-1,4-phenylene-vinylene] (MEH-PPV) films, MEH-PPV films subjected to prolonged illumination, and MEH-PPV/[6,6]-Phenyl C61 butyric acid methyl ester (PCBM) blend, as well as annealed and pristine C60 thin films. For comparison, we also measured MC and MEL in organic diodes based on the same materials. By directly comparing the MPA and MPL responses in films to MC and MEL in organic diodes based on the same active layers, we are able to relate the MFE in organic diodes to the spin densities of the excitations formed in the device, regardless of whether they are formed by photon absorption or carrier injection from the electrodes. We also studied magneto-photocurrent (MPC) and power conversion efficiency (PCE) of a 'standard' Poly (3-hexylthiophene)/PCBM device at various Galvinoxyl radical wt%. We found that the MPC reduction with Galvinoxyl wt% follows the same trend as that of the PCE enhancement. In addition, we also measured the MPC response of a series of OPV cells. We attribute the observed broad MPC to short-lived charge transfer complex species, where spin mixing is caused by the difference, Deltag of the

  15. Remediation of organic and inorganic arsenic contaminated groundwater using a nanocrystalline TiO{sub 2}-based adsorbent

    Energy Technology Data Exchange (ETDEWEB)

    Jing Chuanyong, E-mail: cyjing@rcees.ac.c [State Key Laboratory of Environmental Chemistry and Ecotoxicology, Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, 18 Shuangqing Road, Beijing 100085 (China); Center for Environmental Systems, Stevens Institute of Technology, Hoboken, NJ 07030 (United States); Meng Xiaoguang; Calvache, Edwin [Center for Environmental Systems, Stevens Institute of Technology, Hoboken, NJ 07030 (United States); Jiang Guibin [State Key Laboratory of Environmental Chemistry and Ecotoxicology, Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, 18 Shuangqing Road, Beijing 100085 (China)

    2009-08-15

    A nanocrystalline TiO{sub 2}-based adsorbent was evaluated for the simultaneous removal of As(V), As(III), monomethylarsonic acid (MMA), and dimethylarsinic acid (DMA) in contaminated groundwater. Batch experimental results show that As adsorption followed pseudo-second order rate kinetics. The competitive adsorption was described with the charge distribution multi-site surface complexation model (CD-MUSIC). The groundwater containing an average of 329 mug L{sup -1} As(III), 246 mug L{sup -1} As(V), 151 mug L{sup -1} MMA, and 202 mug L{sup -1} DMA was continuously passed through a TiO{sub 2} filter at an empty bed contact time of 6 min for 4 months. Approximately 11 000, 14 000, and 9900 bed volumes of water had been treated before the As(III), As(V), and MMA concentration in the effluent increased to 10 mug L{sup -1}. However, very little DMA was removed. The EXAFS results demonstrate the existence of a bidentate binuclear As(V) surface complex on spent adsorbent, indicating the oxidation of adsorbed As(III). - A nanocrystalline TiO{sub 2}-based adsorbent could be used for the simultaneous removal of As(V), As(III), MMA, and DMA in contaminated groundwater.

  16. Printed organic thin-film transistor-based integrated circuits

    International Nuclear Information System (INIS)

    Organic electronics is moving ahead on its journey towards reality. However, this technology will only be possible when it is able to meet specific criteria including flexibility, transparency, disposability and low cost. Printing is one of the conventional techniques to deposit thin films from solution-based ink. It is used worldwide for visual modes of information, and it is now poised to enter into the manufacturing processes of various consumer electronics. The continuous progress made in the field of functional organic semiconductors has achieved high solubility in common solvents as well as high charge carrier mobility, which offers ample opportunity for organic-based printed integrated circuits. In this paper, we present a comprehensive review of all-printed organic thin-film transistor-based integrated circuits, mainly ring oscillators. First, the necessity of all-printed organic integrated circuits is discussed; we consider how the gap between printed electronics and real applications can be bridged. Next, various materials for printed organic integrated circuits are discussed. The features of these circuits and their suitability for electronics using different printing and coating techniques follow. Interconnection technology is equally important to make this product industrially viable; much attention in this review is placed here. For high-frequency operation, channel length should be sufficiently small; this could be achievable with a combination of surface treatment-assisted printing or laser writing. Registration is also an important issue related to printing; the printed gate should be perfectly aligned with the source and drain to minimize parasitic capacitances. All-printed organic inverters and ring oscillators are discussed here, along with their importance. Finally, future applications of all-printed organic integrated circuits are highlighted. (paper)

  17. Film stresses and electrode buckling in organic solar cells

    KAUST Repository

    Brand, Vitali

    2012-08-01

    We investigate the film stresses that develop in the polymer films and metal electrodes of poly(3-hexyl thiophene) (P3HT) and [6,6]-phenyl C61-butyric acid methyl ester (PCBM) bulk heterojunction (BHJ) organic solar cells. A compressive biaxial stress of ∼-36 MPa was measured in PEDOT:PSS while a tensile stress of ∼6 MPa was measured in the BHJ layer. We then analyze the effect of electrode deposition rate on the film stresses in the Al electrode. Compressive stresses of ∼-100 to -145 MPa in the Al electrode lead to a buckling instability resulting in undulating electrode surface topography. The BHJ layer was found to have the lowest cohesion (∼1.5-1.8 J/m 2) among the layers of the solar cell and dependent on the Al electrode deposition rate. The cohesive failure path in the BHJ layer exhibited the same periodicity and orientation of the Al electrode buckling topography. We discuss the implications of the film stresses on damage processes during device fabrication and operation. © 2012 Elsevier B.V. All rights reserved.

  18. Oriented Thin Films of a Benzodithiophene Covalent Organic Framework

    Science.gov (United States)

    2014-01-01

    A mesoporous electron-donor covalent organic framework based on a benzodithiophene core, BDT-COF, was obtained through condensation of a benzodithiophene-containing diboronic acid and hexahydroxytriphenylene (HHTP). BDT-COF is a highly porous, crystalline, and thermally stable material, which can be handled in air. Highly porous, crystalline oriented thin BDT-COF films were synthesized from solution on different polycrystalline surfaces, indicating the generality of the synthetic strategy. The favorable orientation, crystallinity, porosity, and the growth mode of the thin BDT-COF films were studied by means of X-ray diffraction (XRD), 2D grazing incidence diffraction (GID), transmission and scanning electron microscopy (TEM, SEM), and krypton sorption. The highly porous thin BDT-COF films were infiltrated with soluble fullerene derivatives, such as [6,6]-phenyl C61 butyric acid methyl ester (PCBM), to obtain an interpenetrated electron-donor/acceptor host–guest system. Light-induced charge transfer from the BDT-framework to PCBM acceptor molecules was indicated by efficient photoluminescence quenching. Moreover, we monitored the dynamics of photogenerated hole-polarons via transient absorption spectroscopy. This work represents a combined study of the structural and optical properties of highly oriented mesoporous thin COF films serving as host for the generation of periodic interpenetrated electron-donor and electron-acceptor systems. PMID:24559375

  19. Cellulose nanocrystals as organic nanofillers for transparent polycarbonate films

    Energy Technology Data Exchange (ETDEWEB)

    Xu Weinan; Qin Zongyi, E-mail: phqin@dhu.edu.cn; Yu Houyong; Liu Yannan; Liu Na; Zhou Zhe; Chen Long, E-mail: happyjack@dhu.edu.cn [College of Materials Science and Engineering, Donghua University, State Key Laboratory for Modification of Chemical Fibers and Polymer Materials (China)

    2013-04-15

    Cellulose nanocrystals (CNCs) produced by sulfuric acid hydrolysis as organic nanofillers were dispersed into polycarbonate (PC) in organic solution through a solvent exchange procedure, and their influence on the optical, mechanical, and thermal properties of the resulting composite films were studied. It is demonstrated that due to the good dispersion of the nanofillers in the polymeric matrix, the formation of strong hydrogen bonds between carbonyl groups of PC and hydroxyl groups of the CNCs can be achieved, leading to a simultaneous reinforcement effect on mechanical and thermal properties of the composite films. Moreover, it was further found that the existence of nanofillers in the composite efficiently hindered the main thermal degradation pathways of PC involving the chain scission at carbonate linkage and rearrangement of carbonate groups. Compared with neat PC, the composite film with 3 wt% CNCs has an increase of about 30.6 % in tensile strength, 27.3 % in Young's modulus, and 3.3 % in maximum decomposition temperature, but still remain quite transparent.

  20. Two-Dimensional Organic-Inorganic Hybrid Perovskite Photonic Films.

    Science.gov (United States)

    Meng, Ke; Gao, Shanshan; Wu, Longlong; Wang, Geng; Liu, Xin; Chen, Gang; Liu, Zhou; Chen, Gang

    2016-07-13

    Organic-inorganic hybrid perovskites have created enormous expectations for low-cost and high-performance optoelectronic devices. In prospect, future advancements may derive from reaping novel electrical and optical properties beyond pristine perovskites through microscopic structure design and engineering. Herein, we report the successful preparation of two-dimensional inverse-opal perovskite (IOP) photonic films, featuring unique nanostructures and vivid colors. Further compositional and structural managements promise optical property and energy level tunability of the IOP films. They are further functionalized in solar cells, resulting in colorful devices with respectable power conversion efficiency. Such concept has not been previously applied for perovskite-based solar cells, which could open a route for more versatile optoelectronic devices. PMID:27267266

  1. Electrocatalytic Organic-Inorganic Hybrid Films and Their Applications in Chemical Sensors and Biosensors

    Institute of Scientific and Technical Information of China (English)

    LI; XiaoYuan

    2001-01-01

    In this report, we will present the organic-inorganic hybrid molecular films prepared in our group and their applications in chemical sensors and biosensors.Many types of multi-layered films have been prepared in an alternatively assembled organic-inorganic and layer-by-layer manner. We will focus on the alternatively organized organic surfactant and metal-complex films and their conversion into electrocatalytically active films. Especially, we will demonstrate the preparation of bifunctional films for the detection of two different but correlated species, such as nitric oxide and oxygen, in biomedia.  ……

  2. Adsorptive Removal of Pharmaceuticals and Personal Care Products from Water with Functionalized Metal-organic Frameworks: Remarkable Adsorbents with Hydrogen-bonding Abilities

    Science.gov (United States)

    Seo, Pill Won; Bhadra, Biswa Nath; Ahmed, Imteaz; Khan, Nazmul Abedin; Jhung, Sung Hwa

    2016-01-01

    Adsorption of typical pharmaceuticals and personal care products (PPCPs) (such as naproxen, ibuprofen and oxybenzone) from aqueous solutions was studied by using the highly porous metal-organic framework (MOF) MIL-101 with and without functionalization. Adsorption results showed that MIL-101s with H-donor functional groups such as –OH and –NH2 were very effective for naproxen adsorption, despite a decrease in porosity, probably because of H-bonding between O atoms on naproxen and H atoms on the adsorbent. For this reason, MIL-101 with two functional groups capable of H-bonding (MIL-101-(OH)2) exhibited remarkable adsorption capacity based on adsorbent surface area. The favorable contributions of –OH and –(OH)2 on MIL-101 in the increased adsorption of ibuprofen and oxybenzone (especially based on porosity) confirmed again the importance of H-bonding mechanism. The adsorbent with the highest adsorption capacity, MIL-101-OH, was very competitive when compared with carbonaceous materials, mesoporous materials, and pristine MIL-101. Moreover, the MIL-101-OH could be recycled several times by simply washing with ethanol, suggesting potential application in the adsorptive removal of PPCPs from water. PMID:27695005

  3. Controlling Listeria monocytogenes on Pork Meat with Combinations of Lyophilized Cell-adsorbed Bacteriocin of Lactobacillus curvatus CWBI-B28 and Organic Acids or Salts

    Directory of Open Access Journals (Sweden)

    Privat Kouakou

    2016-06-01

    Full Text Available The main aim of this study was to see if the antilisterial action of lyophilized cell-adsorbed bacteriocin from Lactobacillus curvatus CWBI-B28 might be reinforced by simultaneous treatment with an organic acid or salt. Slices of raw pork (lean bacon inoculated with Listeria monocytogenes (at 102 cfu/g meat were either vacuum packaged directly and stored at 4°C or treated prior to packaging with a solution containing either lyophilized cell-adsorbed bacteriocin from Lactobacillus curvatus CWBI-B28 (at 1 g/100 mL, an organic acid or salt, or both. The organic acids/salts used were acetic acid, lactic acid, sodium acetate, sodium diacetate, potassium sorbate, and potassium benzoate and the concentrations of the corresponding solutions were calculated so as to treat each slice with approximately 0.1, 0.3, or 0.5 mg acid/salt. Of the antimicrobials used alone, LCaB had the strongest inhibitory effect (a 1-Log reduction in the Listeria cfu count after two weeks, followed by an increase. In combination with LCaB, three antimicrobials had a much more drastic effect: acetic acid, sodium diacetate, and potassium benzoate. At the highest acid/salt concentration tested in such combinations, Listeria became undetectable after one or two weeks and remained so until the end of the 6-week experiment.

  4. Controlled Growth of Ultrathin Film of Organic Semiconductors by Balancing the Competitive Processes in Dip-Coating for Organic Transistors.

    Science.gov (United States)

    Wu, Kunjie; Li, Hongwei; Li, Liqiang; Zhang, Suna; Chen, Xiaosong; Xu, Zeyang; Zhang, Xi; Hu, Wenping; Chi, Lifeng; Gao, Xike; Meng, Yancheng

    2016-06-28

    Ultrathin film with thickness below 15 nm of organic semiconductors provides excellent platform for some fundamental research and practical applications in the field of organic electronics. However, it is quite challenging to develop a general principle for the growth of uniform and continuous ultrathin film over large area. Dip-coating is a useful technique to prepare diverse structures of organic semiconductors, but the assembly of organic semiconductors in dip-coating is quite complicated, and there are no reports about the core rules for the growth of ultrathin film via dip-coating until now. In this work, we develop a general strategy for the growth of ultrathin film of organic semiconductor via dip-coating, which provides a relatively facile model to analyze the growth behavior. The balance between the three direct factors (nucleation rate, assembly rate, and recession rate) is the key to determine the growth of ultrathin film. Under the direction of this rule, ultrathin films of four organic semiconductors are obtained. The field-effect transistors constructed on the ultrathin film show good field-effect property. This work provides a general principle and systematic guideline to prepare ultrathin film of organic semiconductors via dip-coating, which would be highly meaningful for organic electronics as well as for the assembly of other materials via solution processes. PMID:27267545

  5. Controlled Growth of Ultrathin Film of Organic Semiconductors by Balancing the Competitive Processes in Dip-Coating for Organic Transistors.

    Science.gov (United States)

    Wu, Kunjie; Li, Hongwei; Li, Liqiang; Zhang, Suna; Chen, Xiaosong; Xu, Zeyang; Zhang, Xi; Hu, Wenping; Chi, Lifeng; Gao, Xike; Meng, Yancheng

    2016-06-28

    Ultrathin film with thickness below 15 nm of organic semiconductors provides excellent platform for some fundamental research and practical applications in the field of organic electronics. However, it is quite challenging to develop a general principle for the growth of uniform and continuous ultrathin film over large area. Dip-coating is a useful technique to prepare diverse structures of organic semiconductors, but the assembly of organic semiconductors in dip-coating is quite complicated, and there are no reports about the core rules for the growth of ultrathin film via dip-coating until now. In this work, we develop a general strategy for the growth of ultrathin film of organic semiconductor via dip-coating, which provides a relatively facile model to analyze the growth behavior. The balance between the three direct factors (nucleation rate, assembly rate, and recession rate) is the key to determine the growth of ultrathin film. Under the direction of this rule, ultrathin films of four organic semiconductors are obtained. The field-effect transistors constructed on the ultrathin film show good field-effect property. This work provides a general principle and systematic guideline to prepare ultrathin film of organic semiconductors via dip-coating, which would be highly meaningful for organic electronics as well as for the assembly of other materials via solution processes.

  6. Adsorption energy and geometry of adsorbed organic molecules on Au(111) probed by surface-state photoemission

    Energy Technology Data Exchange (ETDEWEB)

    Ziroff, Johannes; Forster, Frank [Universitaet Wuerzburg, Experimentelle Physik II, D-97074 Wuerzburg (Germany); Reinert, Friedrich [Universitaet Wuerzburg, Experimentelle Physik II, D-97074 Wuerzburg (Germany); Forschungszentrum Karlsruhe, Gemeinschaftslabor fuer Nanoanalytik, D-76021 Karlsruhe (Germany)

    2009-07-01

    The modification of the Au(111) surface states by an adsorbed monolayer of large {pi}-conjugated molecules (PTCDA, NTCDA, CuPc) was investigated by high-resolution angle-resolved photoelectron spectroscopy. We determined binding energy, band mass, and Rashba-splitting and discuss the results in the context of rare-gas adsorption on noble metals. This comparison allows the determination of the bonding strength of the adsorbates, found to be physisorptive with derived binding energies per molecule of 2.0 eV for PTCDA and 1.5 eV for NTCDA. We will also present a superstructure model for the NTCDA/Au(111) system, deduced from low energy electron diffraction images in combination with band-backfolding of the Tamm and Shockley states. The coverage dependent evolution of the surface states was also investigated for the three molecules, giving evidence for a dilute-phase growth of the CuPc molecule on the Au(111) surface.

  7. Development of adsorbents from used tire rubber. Their use in the adsorption of organic and inorganic solutes in aqueous solution

    Energy Technology Data Exchange (ETDEWEB)

    Troca-Torrado, Cesar; Alexandre-Franco, Maria; Fernandez-Gonzalez, Carmen; Gomez-Serrano, Vicente [Extremadura Univ., Badajoz (Spain). Dept. de Quimica Organica e Inorganica; Alfaro-Dominguez, Manuel [Extremadura Univ., Badajoz (Spain). Dept. de Ingenieria Mecanica, Energetica y de los Materiales

    2011-02-15

    Using used tire rubber (UTR), carbonaceous adsorbents (CAs) were prepared by chemical treatment of the material with HCl, HNO{sub 3} and NaOH aqueous solutions and by heat treatment at 900 C for 2 h in N{sub 2} atmosphere (H900). UTR and the UTR-derived products were first characterized in terms of texture by N{sub 2} adsorption at - 196 C and of oxygen surface groups by FT-IR spectroscopy and pH of the point of zero charge (pH{sub pzc}). Then, the products were tested as adsorbents of phenol, p-aminophenol, p-nitrophenol, and p-chlorophenol and of chromium, cadmium, mercury and lead in aqueous solution. The development of porosity is very poor in UTR and in the chemically treated products. H900 is the only CA with a better developed porosity, mainly in the regions of meso and macropores. pH{sub pzc} is close to 7.0 for most of the CAs. As an exception to the rule, pH{sub pzc} is 8.4 for H900. For this CA, the adsorption of all the adsorptives is greater. Usually, adsorption kinetics are fast. This is so in particular for p-nitrophenol and p-chlorophenol, on the one side, and for mercury and lead, on the other side. Adsorption is much higher for mercury and lead than for the remaining adsorptives. (author)

  8. Graphene nanosheets as novel adsorbents in adsorption, preconcentration and removal of gases, organic compounds and metal ions

    Energy Technology Data Exchange (ETDEWEB)

    Yu, Jin-Gang, E-mail: yujg@csu.edu.cn [College of Chemistry and Chemical Engineering, Central South University, Changsha, Hunan 410083 (China); College of Chemistry and Chemical Engineering, Hunan University, Changsha, Hunan 410082 (China); Yu, Lin-Yan; Yang, Hua; Liu, Qi [College of Chemistry and Chemical Engineering, Central South University, Changsha, Hunan 410083 (China); Chen, Xiao-Hong [Collaborative Innovation Center of Resource-conserving and Environment-friendly Society and Ecological Civilization, Changsha, Hunan 410083 (China); Jiang, Xin-Yu [College of Chemistry and Chemical Engineering, Central South University, Changsha, Hunan 410083 (China); Chen, Xiao-Qing, E-mail: xqchen@csu.edu.cn [College of Chemistry and Chemical Engineering, Central South University, Changsha, Hunan 410083 (China); Jiao, Fei-Peng, E-mail: jiaofp@163.com [College of Chemistry and Chemical Engineering, Central South University, Changsha, Hunan 410083 (China)

    2015-01-01

    Due to their high adsorption capacities, carbon-based nanomaterials such as carbon nanotubes, activated carbons, fullerene and graphene are widely used as the currently most promising functional materials. Since its discovery in 2004, graphene has exhibited great potential in many technological fields, such as energy storage materials, supercapacitors, resonators, quantum dots, solar cells, electronics, and sensors. The large theoretical specific surface area of graphene nanosheets (2630 m{sup 2}·g{sup −1}) makes them excellent candidates for adsorption technologies. Further, graphene nanosheets could be used as substrates for decorating the surfaces of nanoparticles, and the corresponding nanocomposites could be applied as novel adsorbents for the removal of low concentrated contaminants from aqueous solutions. Therefore, graphene nanosheets will challenge the current existing adsorbents, including other types of carbon-based nanomaterials. - Highlights: • The recent progress of application of graphene in adsorption was presented. • The design and practical application of graphene based composites was discussed. • The future trends and prospects of graphene were analyzed and proposed.

  9. Graphene nanosheets as novel adsorbents in adsorption, preconcentration and removal of gases, organic compounds and metal ions

    International Nuclear Information System (INIS)

    Due to their high adsorption capacities, carbon-based nanomaterials such as carbon nanotubes, activated carbons, fullerene and graphene are widely used as the currently most promising functional materials. Since its discovery in 2004, graphene has exhibited great potential in many technological fields, such as energy storage materials, supercapacitors, resonators, quantum dots, solar cells, electronics, and sensors. The large theoretical specific surface area of graphene nanosheets (2630 m2·g−1) makes them excellent candidates for adsorption technologies. Further, graphene nanosheets could be used as substrates for decorating the surfaces of nanoparticles, and the corresponding nanocomposites could be applied as novel adsorbents for the removal of low concentrated contaminants from aqueous solutions. Therefore, graphene nanosheets will challenge the current existing adsorbents, including other types of carbon-based nanomaterials. - Highlights: • The recent progress of application of graphene in adsorption was presented. • The design and practical application of graphene based composites was discussed. • The future trends and prospects of graphene were analyzed and proposed

  10. Stabilization of organic thin film transistors by ion implantation

    Energy Technology Data Exchange (ETDEWEB)

    Fraboni, B., E-mail: beatrice.fraboni@unibo.it [CNISM and Dipartimento di Fisica, Universita di Bologna, viale Berti Pichat 6/2, 40127 Bologna (Italy); Cosseddu, P. [Dipartimento di Ingegneria Elettrica ed Elettronica, Universita di Cagliari, piazza d' Armi, 09123 Cagliari, Italy and CNR-INFM S3 via Campi 213/a 41100 Modena (Italy); Wang, Y.Q.; Schulze, R.K. [Los Alamos National Laboratory MS-K771 Los Alamos NM 87545 (United States); Cavallini, A. [CNISM and Dipartimento di Fisica, Universita di Bologna, viale Berti Pichat 6/2, 40127 Bologna (Italy); Nastasi, M. [Los Alamos National Laboratory MS-K771 Los Alamos NM 87545 (United States); Bonfiglio, A. [Dipartimento di Ingegneria Elettrica ed Elettronica, Universita di Cagliari, piazza d' Armi, 09123 Cagliari, Italy and CNR-INFM S3 via Campi 213/a 41100 Modena (Italy)

    2012-08-01

    We report on the effects of low energy ion implantation (N and Ne) in the reduction and control of the degradation of pentacene organic thin film transistors (OTFTs) due to the exposure to atmosphere (i.e. oxygen and water). We have observed that a controlled damage depth distribution preserves the functionality of the devices, even if ion implantation induces significant molecular structure modifications, in particular a combination of dehydrogenation and carbonification effects. No relevant changes in the pentacene thin film thickness have been observed. The two major transport parameters that characterize OTFT performance are the carrier mobility and the threshold voltage. We have monitored the effectiveness of this process in stabilizing the device by monitoring the carrier mobility and the threshold voltage over a long time (over 2000 h). Finally, we have assessed by depth resolved X-ray Photoemission Spectroscopy analyses that, by selectively implanting with ions that can react with the hydrocarbon matrix (e.g. N{sup +}), it is possible to locally modify the charge distribution within the organic layer.

  11. Orbital tomography for highly symmetric adsorbate systems

    Science.gov (United States)

    Stadtmüller, B.; Willenbockel, M.; Reinisch, E. M.; Ules, T.; Bocquet, F. C.; Soubatch, S.; Puschnig, P.; Koller, G.; Ramsey, M. G.; Tautz, F. S.; Kumpf, C.

    2012-10-01

    Orbital tomography is a new and very powerful tool to analyze the angular distribution of a photoemission spectroscopy experiment. It was successfully used for organic adsorbate systems to identify (and consequently deconvolute) the contributions of specific molecular orbitals to the photoemission data. The technique was so far limited to surfaces with low symmetry like fcc(110) oriented surfaces, owing to the small number of rotational domains that occur on such surfaces. In this letter we overcome this limitation and present an orbital tomography study of a 3,4,9,10-perylene-tetra-carboxylic-dianhydride (PTCDA) monolayer film adsorbed on Ag(111). Although this system exhibits twelve differently oriented molecules, the angular resolved photoemission data still allow a meaningful analysis of the different local density of states and reveal different electronic structures for symmetrically inequivalent molecules. We also discuss the precision of the orbital tomography technique in terms of counting statistics and linear regression fitting algorithm. Our results demonstrate that orbital tomography is not limited to low-symmetry surfaces, a finding which makes a broad field of complex adsorbate systems accessible to this powerful technique.

  12. Quantification of LEED measurements. II. Application to epitaxial organic films

    Energy Technology Data Exchange (ETDEWEB)

    Meissner, Matthias; Sojka, Falko; Gruenewald, Marco; Forker, Roman; Fritz, Torsten [University of Jena, Institute of Solid State Physics, Max-Wien-Platz 1, 07743 Jena (Germany)

    2012-07-01

    Low energy electron diffraction (LEED) on epitaxial layers is a powerful tool to examine long-range ordering at the interface. However, due to limitations like distortion of the LEED images, often additional efforts have to be made in order to derive precise epitaxial relations. Based on LEED images corrected for their distortion and calibrated by means of a Si(111)-7 x 7 diffraction pattern, a home-made algorithm finds the LEED spots belonging to a certain structure and fits a lattice to all those spots simultaneously. This provides us with absolute lattice parameters within a small error margin. Additionally, in the case of organic-inorganic epitaxy, measurements at higher energies can be used to relate the adsorbate lattice to the substrate lattice and derive the epitaxy matrix. The precision of this procedure will be evaluated on the basis of two systems: (a) 3,4,9,10-perylenetetracarboxylic dianhydride (PTCDA) on epitaxial graphene, featuring two different PTCDA phases, one known, the other not; (b) Tin-phthalocyanine (SnPc) on Au(111), not being described in literature yet.

  13. Significant Improvement of Organic Thin-Film Transistor Mobility Utilizing an Organic Heterojunction Buffer Layer

    Institute of Scientific and Technical Information of China (English)

    PAN Feng; QIAN Xian-Rui; HUANG Li-Zhen; WANG Hai-Bo; YAN Dong-Hang

    2011-01-01

    High-mobility vanadyl phthalocyanine (VOPc)/5,5″′-bis(4-fluorophenyl)-2,2′:5′,2″:5″,2″′-quaterthiophene (F2-P4T) thin-film transistors are demonstrated by employing a copper hexadecafluorophthalocyanine (F16 CuPc)/copper phthalocyanine (CuPc) heterojunction unit,which are fabricated at different substrate temperatures,as a buffer layer. The highest mobility of 4.08cm2/Vs is achieved using a F16CuPc/CuPc organic heterojunction buffer layer fabricated at high substrate temperature.Compared with the random small grain-like morphology of the room-temperature buffer layer,the high-temperature organic heterojunction presents a large-sized fiber-like film morphology,resulting in an enhanced conductivity.Thus the contact resistance of the transistor is significantly reduced and an obvious improvement in device mobility is obtained.

  14. A rapid microwave-assisted synthesis of a sodium-cadmium metal-organic framework having improved performance as a CO2 adsorbent for CCS.

    Science.gov (United States)

    Palomino Cabello, Carlos; Arean, Carlos Otero; Parra, José B; Ania, Conchi O; Rumori, P; Turnes Palomino, G

    2015-06-01

    We report on a facile and rapid microwave-assisted method for preparing a sodium-cadmium metal-organic framework (having coordinatively unsaturated sodium ions) that considerably shortens the conventional synthesis time from 5 days to 1 hour. The obtained (Na,Cd)-MOF showed an excellent volumetric CO2 adsorption capacity (5.2 mmol cm(-3) at 298 K and 1 bar) and better CO2 adsorption properties than those shown by the same metal-organic framework when synthesized following a more conventional procedure. Moreover, the newly prepared material was found to display high selectivity for adsorption of carbon dioxide over nitrogen, and good regenerability and stability during repeated CO2 adsorption-desorption cycles, which are the required properties for any adsorbent intended for carbon dioxide capture and sequestration (CSS) from the post-combustion flue gas of fossil fuelled power stations. PMID:25939594

  15. Study on Preparation of High-k Organic-Inorganic Thin Film for Organic-Inorganic Thin Film Transistor Gate Dielectric Application

    Science.gov (United States)

    Lee, Wen-Hsi; Liu, Chao-Te; Lee, Ying-Chieh

    2012-06-01

    A simple solution-based deposition technique combined with spin-coating is a plausible way to prepare ultra-thin organic-inorganic nanocomposite films. In this study, we describe the spin-coating deposition of a colloidal nanoparticle suspension to obtain an ultra-thin organic-inorganic composite film as a gate insulator for organic thin film transistor (O-TFT) application. To obtain a homogenous organic-inorganic composite film, well-dispersed TiO2 nanoparticles in γ-butyrolactone and polyimide are important; therefore, several dispersants were assessed on the basis of the measurement of the rheological behavior of slurries. The thickness of the organic-inorganic composite film is mainly determined by the speed of spin-coating and viscosity of slurries. An approximately 4000-Å-thick nanocomposite film with homogeneous distribution of TiO2 nanoparticles in polyimide and low roughness was obtained after curing at 200 °C, resulting in a low leakage current density of the nano-composite film, when less than 2 vol % TiO2 nanoparticles were well dispersed in polyimide slurry. The dielectric constant of the organic-inorganic nanocomposite increases with increasing TiO2 content in polyimide, being situated in the range between 4 and 5.

  16. Use of chloroflurocarbons as internal standards for the measurement of atmospheric non-methane volatile organic compounds sampled onto solid adsorbent cartridges.

    Science.gov (United States)

    Karbiwnyk, Christine M; Mills, Craig S; Helmig, Detlev; Birks, John W

    2003-03-01

    Solid adsorbents have proven useful for determining the vertical profiles of volatile organic compounds (VOCs) using sampling platforms such as balloons, kites, and light aircraft, and those profiles provide valuable information about the sources, sinks, transformations, and transport of atmospheric VOCs. One of the largest contributions to error in VOC concentrations is the estimation of the volume of air sampled on the adsorbent cartridge. These errors arise from different sources, such as variations in pumping flow rates from changes in ambient temperature and pressure with altitude, and decrease in the sampling pump battery power. Another significant source for sampling rate variations are differences in the flow resistance of individual sampling cartridges. To improve the accuracy and precision of VOC measurements, the use of ambient chlorofluorocarbons (CFCs) as internal standards was investigated. A multibed solid adsorbent, AirToxic (Supelco), was chosen for its wide sampling range (C3-C12). Analysis was accomplished by thermal desorption and dual detection GC/FID/ECD, resulting in sensitive and selective detection of both VOCs and CFCs in the same sample. Long-lived chlorinated compounds (CFC-11, CFC-12, CFC-113, CCl4 and CH3CCl3) banned by the Montreal Protocol and subsequent amendments were studied for their ability to predict sample volumes using both ground-based and vertical profiling platforms through the boundary layer and free troposphere. Of these compounds, CFC-113 and CCl4 were found to yield the greatest accuracy and precision for sampling volume determination. Use of ambient CFC-113 and CCl4 as internal standards resulted in accuracy and precision of generally better than 10% for the prediction of sample volumes in ground-, balloon-, and aircraft-based measurements. Consequently, use of CFCs as reference compounds can yield a significant improvement of accuracy and precision for ambient VOC measurements in situations where accurate flow

  17. Organic and inorganic-organic thin film structures by molecular layer deposition: A review.

    Science.gov (United States)

    Sundberg, Pia; Karppinen, Maarit

    2014-01-01

    The possibility to deposit purely organic and hybrid inorganic-organic materials in a way parallel to the state-of-the-art gas-phase deposition method of inorganic thin films, i.e., atomic layer deposition (ALD), is currently experiencing a strongly growing interest. Like ALD in case of the inorganics, the emerging molecular layer deposition (MLD) technique for organic constituents can be employed to fabricate high-quality thin films and coatings with thickness and composition control on the molecular scale, even on complex three-dimensional structures. Moreover, by combining the two techniques, ALD and MLD, fundamentally new types of inorganic-organic hybrid materials can be produced. In this review article, we first describe the basic concepts regarding the MLD and ALD/MLD processes, followed by a comprehensive review of the various precursors and precursor pairs so far employed in these processes. Finally, we discuss the first proof-of-concept experiments in which the newly developed MLD and ALD/MLD processes are exploited to fabricate novel multilayer and nanostructure architectures by combining different inorganic, organic and hybrid material layers into on-demand designed mixtures, superlattices and nanolaminates, and employing new innovative nanotemplates or post-deposition treatments to, e.g., selectively decompose parts of the structure. Such layer-engineered and/or nanostructured hybrid materials with exciting combinations of functional properties hold great promise for high-end technological applications. PMID:25161845

  18. Organic and inorganic–organic thin film structures by molecular layer deposition: A review

    Directory of Open Access Journals (Sweden)

    Pia Sundberg

    2014-07-01

    Full Text Available The possibility to deposit purely organic and hybrid inorganic–organic materials in a way parallel to the state-of-the-art gas-phase deposition method of inorganic thin films, i.e., atomic layer deposition (ALD, is currently experiencing a strongly growing interest. Like ALD in case of the inorganics, the emerging molecular layer deposition (MLD technique for organic constituents can be employed to fabricate high-quality thin films and coatings with thickness and composition control on the molecular scale, even on complex three-dimensional structures. Moreover, by combining the two techniques, ALD and MLD, fundamentally new types of inorganic–organic hybrid materials can be produced. In this review article, we first describe the basic concepts regarding the MLD and ALD/MLD processes, followed by a comprehensive review of the various precursors and precursor pairs so far employed in these processes. Finally, we discuss the first proof-of-concept experiments in which the newly developed MLD and ALD/MLD processes are exploited to fabricate novel multilayer and nanostructure architectures by combining different inorganic, organic and hybrid material layers into on-demand designed mixtures, superlattices and nanolaminates, and employing new innovative nanotemplates or post-deposition treatments to, e.g., selectively decompose parts of the structure. Such layer-engineered and/or nanostructured hybrid materials with exciting combinations of functional properties hold great promise for high-end technological applications.

  19. Preparation of organic thin-film field effect transistor

    Institute of Scientific and Technical Information of China (English)

    2002-01-01

    The organic thin-film field effect transistor was prepared through vacuum deposition by using teflon as di-electric material. Indium-tin-oxide acted as the source and drain electrodes. Copper phthalocyanine and teflon were used as the semiconductor layer and dielectric layer, respectively. The gate electrode was made of Ag. The channel length between the source and drain was 50 μm. After preparing the source and drain electrodes by lithography, the copper phthalocyanine layer, teflon layer and Ag layerwere prepared by vacuum deposition sequentially. The field effect electron mobility of the device reached 1.1×10ˉ6 cm2/(V@s), and the on/off current ratio reached 500.

  20. Organically Modified Nanoclay-Reinforced Rigid Polyurethane Films

    Science.gov (United States)

    Park, Yong Tae; Qian, Yuqiang; Lindsay, Chris; Stein, Andreas; Macosko, Christopher

    2012-02-01

    The nanodispersion of vermiculite in polyurethanes was investigated to produce organoclay-reinforced rigid gas barrier films. Reducing gas transport can improve the insulation performance of closed cell polyurethane foam. In a previous study, the dispersion of vermiculite in polyurethanes without organic modification was not sufficient due to the non-uniform dispersion morphology. When vermiculite was modified by cation exchange with long-chain quaternary ammonium cations, the dispersion in methylene diphenyl diisocyanate (MDI) was significantly improved. Dispersion was improved by combining high intensity dispersive mixing with efficient distributive mixing. Polymerization conditions were also optimized in order to provide a high state of nanodispersion in the polyurethane nanocomposite. The dispersions were characterized using rheological, microscopic and scattering/diffraction techniques. The final nanocomposites showed enhancement of mechanical properties and reduction in permeability to carbon dioxide at low clay concentration (around 2 wt percent).

  1. Organic Thin Film Devices for Displays and Lighting

    Science.gov (United States)

    Weiss, Oliver J.; Krause, Ralf; Paetzold, Ralph

    Organic materials can be used for fabrication of, e.g., electronic circuits, solar cells, light sensors, memory cells and light emitting diodes. Especially organic light emitting diodes (OLEDs) are increasingly attractive because of their huge market potential. The feasibility of efficient OLEDs was first shown in 1987 [3]. Only about ten years later the first product, a display for car radios, entered the market. Today monochrome and full colour OLED-displays can be found in many applications replacing established flat panel display technologies like TFT-LCDs. This substitution is a consequence of the outstanding attributes of OLED technology: Organic light emitting displays are self-emissive, thin, video capable and in addition they show a wide temperature operation range and allow a viewing angle of nearly 180 degree in conjunction with a low power consumption. As performance has steadily increased over the last years, today OLEDs are also under investigation as next generation light source. In contrast to inorganic LEDs, they can be built as flat 2-dimensional light sources that are lightweight, colour tunable, and potentially cheap. This will open up new degrees of freedom in design leading also to completely new applications. In this contribution we will have a brief view on the history of organic electroluminescent materials before we introduce the basic principles of OLEDs with a focus on the physical processes leading to light generation in thin organic films. Along with an overview of different concepts and technologies used to build OLEDs, the current status of OLED development will be illustrated. The last part focuses on the challenges that have to be overcome to enable a sustainable success in the display and lighting markets.

  2. Quantitation of persistent organic pollutants adsorbed on plastic debris from the Northern Pacific Gyre's "eastern garbage patch".

    Science.gov (United States)

    Rios, Lorena M; Jones, Patrick R; Moore, Charles; Narayan, Urja V

    2010-12-01

    Floating marine plastic debris was found to function as solid-phase extraction media, adsorbing and concentrating pollutants out of the water column. Plastic debris was collected in the North Pacific Gyre, extracted, and analyzed for 36 individual PCB congeners, 17 organochlorine pesticides, and 16 EPA priority PAHs. Over 50% contained PCBs, 40% contained pesticides, and nearly 80% contained PAHs. The PAHs included 2, 3 and 4 ring congeners. The PCBs were primarily CB-11, 28, 44, 52, 66, and 101. The pesticides detected were primarily p,p-DDTs and its metabolite, o,p-DDD, as well as BHC (a,b,g and d). The concentrations of pollutants found ranged from a few ppb to thousands of ppb. The types of PCBs and PAHs found were similar to those found in marine sediments. However, these plastic particles were mostly polyethylene which is resistant to degradation and although functioning similarly to sediments in accumulating pollutants, these had remained on or near the ocean surface. Particles collected included intact plastic items as well as many pieces less than 5 mm in size. PMID:21042605

  3. Efficacy of mineral and organic adsorbent in alleviating harmful effects of zearalenone on pig blood serum protein status

    Directory of Open Access Journals (Sweden)

    Nešić Ksenija

    2008-01-01

    Full Text Available The influence of zearalenone on blood serum protein status and the feasibility of utilizing a modified clinoptilolite and esterified glucomannan to alleviate its harmful effects was examined in two trials, 31 and 29 days long, conducted on a total of 64 pigs (32 each 60 days old, divided into four groups, each containing 8 pigs. Control groups (K received noncontaminated feed, while experimental groups received feed supplemented with 3.84 mg/kg in the first trial and 5.12 mg/kg of zearalenone in the second trial. Pigs in the first experimental groups (O-I were given feed with toxin only. Modified clinoptilolite in the amount of 0.2% and esterified glucomannan in the amount of 0.1% were introduced in contaminated feed of the second (O-II and the third experimental groups (O-III of both trials. With the use of contaminated feed, a declining trend of the A/G ratio was observed: decrease of albumin content and increase of globulin content on account of the _ globulin fraction. A decrease of the _ globulin fraction was detected at the same time. Total protein concentration was also lower. The application of adsorbents successfully alleviated harmful effects of the F-2 toxin on the affected biochemical parameters in blood serum.

  4. Optical properties of organic films, multilayers and plasmonic metal-organic waveguides fabricated by organic molecular beam deposition

    Science.gov (United States)

    Wickremasinghe, Niranjala D.

    In this thesis, the optical properties of tris (8-hydroxyquinoline) aluminum (Alq3) and 3,5,9,10-perylentetracarboxylic dianhydride (PTCDA) organic films, PTCDA/ Alq3 multilayers and plasmonic Alq3 -metal waveguides are investigated. The organic films and heterostructures used for this work were fabricated by organic molecular beam deposition (OMBD). We investigated the quenching of the light emission in Alq3 films grown on a Si substrate as a function of cw laser excitation intensity at varying temperatures from 15 to 300 K. The saturation of the singlet-singlet annihilation coefficient was measured with spectrally-integrated (SI) photoluminescence (PL) using a photodiode. The bimolecular quenching coefficient was further studied with time-resolved (TR) PL as a function of 100 fs pulse fluences. The PL quenching is attributed to the annihilation of trapped excitons at Alq3 nanocrystal grain boundaries. The saturation is explained by the limited density of available trapping states at the grain boundaries. Our interpretation is supported by structural investigations of ultrathin Alq3 films with atomic force microscopy (AFM), scanning electron microscopy (SEM) and by comparing the experimental data with calculations using a coupled rate equation model. The wavelength dispersion of the refractive indices of PTCDA and Alq 3 layers and of PTCDA/Alq3 multilayer waveguides grown on Pyrex substrates was investigated. The m-line technique, an evanescent prism coupling technique, was used to determine the layers' thickness and the in-plane (TE modes) and normal (TM modes) refractive indices. The potential for controlling the refractive index dispersion and anisotropy by tailored organic multilayer waveguides is discussed.

  5. Structure of the Buried Metal-Molecule Interface in Organic Thin Film Devices

    DEFF Research Database (Denmark)

    Hansen, Christian Rein; Sørensen, Thomas Just; Glyvradal, Magni;

    2009-01-01

    . By comparison of XR data for the five-layer Pb2+ arachidate LB film before and after vapor deposition of the Ti/Al top electrode, a detailed account of the structural damage to the organic film at the buried metal-molecule interface is obtained. We find that the organized structure of the two topmost LB layers...

  6. Organic thin film devices with stabilized threshold voltage and mobility, and method for preparing the devices

    Science.gov (United States)

    Nastasi, Michael Anthony; Wang, Yongqiang; Fraboni, Beatrice; Cosseddu, Piero; Bonfiglio, Annalisa

    2013-06-11

    Organic thin film devices that included an organic thin film subjected to a selected dose of a selected energy of ions exhibited a stabilized mobility (.mu.) and threshold voltage (VT), a decrease in contact resistance R.sub.C, and an extended operational lifetime that did not degrade after 2000 hours of operation in the air.

  7. Electro-optical Properties of Ultra-Thin Organic Films

    OpenAIRE

    Hodges, Ping Y.

    2001-01-01

    Electro-optical properties of thin film are of great interest owing to the perpetual demand for miniaturization and higher speed devices for communication, electronic, and biomedical applications. The thickness of polymer films developed for these applications has decreased dramatically making interfacial effects significant. It is well documented that, in submicron thickness range, both film/substrate & film/air interface are critical. In this study, we probe the dynamics of electro-optic...

  8. Mutagenicity of organic pollutants adsorbed on suspended particulate matter in the center of Wrocław (Poland)

    Science.gov (United States)

    Bełcik, Maciej; Trusz-Zdybek, Agnieszka; Galas, Ewa; Piekarska, Katarzyna

    2014-10-01

    Mutagenicity of pollutants adsorbed on suspended dust of the PM10 fraction, collected in winter and summer season alike over the Wrocław city centre (Poland) was studied using the standard Salmonella assay (plate-incorporation) and the Kado modified assay (microsuspension method). The dust was collected using Staplex high volume air sampler. Further on it was extracted with dichloromethane in a Soxhlet apparatus. PAH content in extracts was determined by the high performance liquid chromatography technique using fluorescence detection, whereas the nitro-PAH content- by the gas chromatography using mass detection. Two Salmonella typhimurium strains, TA98 and YG1041, were used in the assays. The assays were conducted with and without a metabolic activation. Investigated air pollution extracts differed against each other with regard to a total content as well as to a percentage of individual compounds, depending on the sampling season. Both the total PAH content and the nitro-PAH content in the tested samples, and their spectrum as well, were found the highest in winter season. Higher mutagenic effect was noted for the dust extract from samples collected in wintertime than from those collected in summer. Pollutants directly affecting the genetic material and those showing such indirect action were present in the examined samples. The YG1041 strain turned out to be the most sensitive, which was the sign that large amounts of nitro-aromatic compounds were present in the tested samples. Obtained results proved that the Kado modified Salmonella assay would be useful for the atmospheric air pollution monitoring in urban agglomerations. Mutagenic effect in assays conducted according to the Kado procedure was obtained by using in the assays lower concentrations of tested extracts, compared to the classical assay.

  9. Nanoporous carbon derived from a metal organic framework as a new kind of adsorbent for dispersive solid phase extraction of benzoylurea insecticides

    International Nuclear Information System (INIS)

    We describe the preparation of nanoporous carbon using a metal-organic framework (MOF) as a template and furfuryl alcohol as the source for carbon. The MOF consists of a zeolitic framework (ZIF-8) that was obtained from 2-methylimidazole and Zn(II) ions. ZIF-8 was soaked with furfuryl alcohol which then was carbonized at 900 °C. The resulting nanoporous carbon (MOF-C) exhibits a high specific surface area and a large pore volume. It was used as a dispersive solid-phase adsorbent for the preconcentration of the benzoylurea insecticides diflubenzuron, triflumuron, hexaflumuron and teflubenzuron from water and tangerine samples. Under optimized conditions, the methods exhibits excellent extraction performance. The insecticides can be quantified via HPLC with UV detection in the 0.5 to 100 ng mL−1 concentration range in case of spiked tap water, and in the 2.0 to 200 ng g−1 concentration range in case of tangerines. The limits of detection range from 0.10 to 0.23 ng mL−1 in case of water samples, and from 0.34 to 0.71 ng g−1 for tangerine sample (at an S/N ratio of 3). Mean recoveries range from 91.7 to 107.9 %, with relative standard deviations of <7.1 %. The results indicate that the method was efficient for the preconcentration of trace levels of benzoylurea insecticides from water and tangerine samples. Conceivably, this new adsorbent has a large potential with respect to the enrichment of other organic pollutants from various kinds of samples. (author)

  10. Clean graphene electrodes on organic thin-film devices via orthogonal fluorinated chemistry.

    Science.gov (United States)

    Beck, Jonathan H; Barton, Robert A; Cox, Marshall P; Alexandrou, Konstantinos; Petrone, Nicholas; Olivieri, Giorgia; Yang, Shyuan; Hone, James; Kymissis, Ioannis

    2015-04-01

    Graphene is a promising flexible, highly transparent, and elementally abundant electrode for organic electronics. Typical methods utilized to transfer large-area films of graphene synthesized by chemical vapor deposition on metal catalysts are not compatible with organic thin-films, limiting the integration of graphene into organic optoelectronic devices. This article describes a graphene transfer process onto chemically sensitive organic semiconductor thin-films. The process incorporates an elastomeric stamp with a fluorinated polymer release layer that can be removed, post-transfer, via a fluorinated solvent; neither fluorinated material adversely affects the organic semiconductor materials. We used Raman spectroscopy, atomic force microscopy, and scanning electron microscopy to show that chemical vapor deposition graphene can be successfully transferred without inducing defects in the graphene film. To demonstrate our transfer method's compatibility with organic semiconductors, we fabricate three classes of organic thin-film devices: graphene field effect transistors without additional cleaning processes, transparent organic light-emitting diodes, and transparent small-molecule organic photovoltaic devices. These experiments demonstrate the potential of hybrid graphene/organic devices in which graphene is deposited directly onto underlying organic thin-film structures.

  11. QSAR models for removal rates of organic pollutants adsorbed by in situ formed manganese dioxide under acid condition.

    Science.gov (United States)

    Su, Pingru; Zhu, Huicen; Shen, Zhemin

    2016-02-01

    Manganese dioxide formed in oxidation process by potassium permanganate exhibits promising adsorptive capacity which can be utilized to remove organic pollutants in wastewater. However, the structure variances of organic molecules lead to wide difference of adsorption efficiency. Therefore, it is of great significance to find a general relationship between removal rate of organic compounds and their quantum parameters. This study focused on building up quantitative structure activity relationship (QSAR) models based on experimental removal rate (r(exp)) of 25 organic compounds and 17 quantum parameters of each organic compounds computed by Gaussian 09 and Material Studio 6.1. The recommended model is rpre = -0.502-7.742 f(+)x + 0.107 E HOMO + 0.959 q(H(+)) + 1.388 BOx. Both internal and external validations of the recommended model are satisfied, suggesting optimum stability and predictive ability. The definition of applicability domain and the Y-randomization test indicate all the prediction is reliable and no possibility of chance correlation. The recommended model contains four variables, which are closely related to adsorption mechanism. f(+)x reveals the degree of affinity for nucleophilic attack. E HOMO represents the difficulty of electron loss. q(H(+)) reflect the distribution of partial charge between carbon and hydrogen atom. BO x shows the stability of a molecule. PMID:26490942

  12. Influence of organic acids on kinetic release of chromium in soil contaminated with leather factory waste in the presence of some adsorbents.

    Science.gov (United States)

    Taghipour, Marzieh; Jalali, Mohsen

    2016-07-01

    In this study, batch experiments were conducted to investigate the effects of nanoparticles (NPs) (MgO, ZnO, TiO2) and clay minerals (bentonite, zeolite) on the release of chromium (Cr) from leather factory waste (LFW) and LFW treated soil using organic acids. Chromium release from all treatments was studied in the presence of citric acid, oxalic acid and CaCl2 solutions. The results showed that, in all treatments, organic acids released more Cr than inorganic salt (CaCl2). The release of Cr by citric acid was higher than that by oxalic acid. In LFW treated soil and LFW, the release of Cr from the all treatments with NPs was less than that from the clay mineral treatments. On the other hand, in the presence of organic acids, Cr release by NPs and clay minerals decreased. Two kinetic models including pseudo-first- and pseudo-second-order model were tested to describe the time dependent Cr release data. Among the kinetic models used, the pseudo-second-order model generally gave the best fits to experimental data. Before and after release experiments, Cr in LFW, treated LFW, control soil and LFW treated soils were fractionated. In all treatments, the greatest amounts of Cr were found in the residual fraction (RES). The organic acids were effective in reducing the exchangeable (EXC), bound to organic matter (OM) and bound to carbonate (CAR) fractions of Cr in all treatments, whereas, after release of Cr from treated soils, Cr remained mainly in the RES fraction. The application of NPs and clay minerals in soil led to a significant transformation of Cr from mobile fractions to the RES fraction. Therefore, organic ligands played a dominant role in mobility and bioavailability of Cr and the removal of Cr by adsorbents.

  13. Influence of organic acids on kinetic release of chromium in soil contaminated with leather factory waste in the presence of some adsorbents.

    Science.gov (United States)

    Taghipour, Marzieh; Jalali, Mohsen

    2016-07-01

    In this study, batch experiments were conducted to investigate the effects of nanoparticles (NPs) (MgO, ZnO, TiO2) and clay minerals (bentonite, zeolite) on the release of chromium (Cr) from leather factory waste (LFW) and LFW treated soil using organic acids. Chromium release from all treatments was studied in the presence of citric acid, oxalic acid and CaCl2 solutions. The results showed that, in all treatments, organic acids released more Cr than inorganic salt (CaCl2). The release of Cr by citric acid was higher than that by oxalic acid. In LFW treated soil and LFW, the release of Cr from the all treatments with NPs was less than that from the clay mineral treatments. On the other hand, in the presence of organic acids, Cr release by NPs and clay minerals decreased. Two kinetic models including pseudo-first- and pseudo-second-order model were tested to describe the time dependent Cr release data. Among the kinetic models used, the pseudo-second-order model generally gave the best fits to experimental data. Before and after release experiments, Cr in LFW, treated LFW, control soil and LFW treated soils were fractionated. In all treatments, the greatest amounts of Cr were found in the residual fraction (RES). The organic acids were effective in reducing the exchangeable (EXC), bound to organic matter (OM) and bound to carbonate (CAR) fractions of Cr in all treatments, whereas, after release of Cr from treated soils, Cr remained mainly in the RES fraction. The application of NPs and clay minerals in soil led to a significant transformation of Cr from mobile fractions to the RES fraction. Therefore, organic ligands played a dominant role in mobility and bioavailability of Cr and the removal of Cr by adsorbents. PMID:27139119

  14. Electromagnetic Scattering from Rough Sea Surface with PM Spectrum Covered by an Organic Film

    Institute of Scientific and Technical Information of China (English)

    WANG Rui; GUO Li-Xin; WANG An-Qi; WU Zhen-Sen

    2011-01-01

    The rough sea surface covered by an organic film will cause attenuation of capillarity waves, which implies that the organic films play an important role in rough sea surface processes. We focus on a one-dimensional(1D)rough sea surface with the Pierson-Moskowitz(PM)spectrum distributed to the homogeneous insoluble organic slicks. First, the impact of the organic film on the PM surface spectrum is presented, as well as that of the correlation length, the rms height and slope of the rough sea surface. The damping effect of the organic film changes the physical parameters of the rough sea surface. For example, the organic film will reduce the rms height and slopee of the rough sea surface, which results in the attenuation of the high-frequency components of the PM spectrum leading to modification of the surface PM spectrum. Then, the influence of the organic film on the electromagnetic(EM) scattering coefficients from PM rough sea surface covered by the organic film is investigated and discussed in detail, compared with the clean PM rough sea surface through the method of moments.

  15. Simultaneous removal of multiple pesticides from water: effect of organically modified clays as coagulant aid and adsorbent in coagulation-flocculation process.

    Science.gov (United States)

    Shabeer, T P Ahammed; Saha, Ajoy; Gajbhiye, V T; Gupta, Suman; Manjaiah, K M; Varghese, Eldho

    2014-01-01

    Contamination of drinking water sources with agrochemical residues became a major concern in the twenty-first century. Coagulation-flocculation is the most widely used water-treatment process, but the efficiency to remove pesticides and other organic pollutants are limited compared to adsorption process. Thus, simultaneous action of adsorption on normal bentonite or organo-modified montmorillonite clays [modified with octadecylamine (ODA-M) and octadecylamine + amino-propyltriethoxysilane (ODAAPS-M)] followed by coagulation-flocculation by alum and poly aluminium chloride has been evaluated for removal of 10 different pesticides, namely atrazine, lindane, metribuzin, aldrin, chlorpyriphos, pendimethalin, alpha-endosulphan, beta-endosulphan, p,p'-DDT, cypermethrin and two of its metabolites, endosulphan sulphate and p,p'-DDE, from water. The coagulation without integration of adsorption was less effective (removal % varies from 12 to 49) than the adsorption-coagulation integrated system (removal % varies from 71 to 100). Further, coagulation integrated with adsorption was more effective when organically modified montmorillonite was used as adsorbent compared to normal bentonite. The removal efficiency of organic clay depends upon the concentration of pesticides, doses of clay minerals, and efficiency was more for ODAAPS-M as compared to ODA-M. The combination of ODAAPS-M-clay with coagulants was also used efficiently for the removal of pesticides from natural and fortified natural water collected and the results exhibit the usefulness of this remediation technique for application in water decontamination and in treatment of industrial and agricultural waste waters.

  16. Photo-Induced Magnetic Anisotropy of Polymer Film Containing Azobenzene Organic Free Radical Group

    Institute of Scientific and Technical Information of China (English)

    徐则达; 张勇; 陈小芳; 范星河; 宛新华; 周其凤

    2003-01-01

    The forward degenerate four-wave mixing geometry was employed to induce microstructure in an organic free radical azobenzene polymer film. Before irradiated with Ar+ laser beams (λ = 514.5 nm), the azobenzene organic free radical polymer exhibits magnetic isotropic measured by superconducting quantum interference device. After photo-induced microstructure, the polymer film becomes magnetic anisotropy. When the applied magnetic field H = 50 Gauss, the magnetization along the normal direction of the polymer film is Mz = 5.5 × 10-5 emu/g,which is larger than Mx = 4.1 × 10-5 emu/g in the direction parallel to the polymer film.

  17. The structure of deuterated benzene films adsorbed on the graphite (0001) basal plane: what happens below and above the monolayer coverage?

    OpenAIRE

    Bahn, Emanuel; Hedgeland, Holly; Jardine, Andrew P.; Henry, Paul F.; Hansen, Thomas C.; Fouquet, Peter

    2014-01-01

    An exact description of the interactions in aromatic carbon systems is a key condition for the design of carbon based nanomaterials. In this paper we investigate the binding and adsorbate structure of the simplest prototype system in this class – the single aromatic ring molecule benzene on graphite. We have collected neutron diffraction data of the ordered phase of deuterated benzene, C6D6, adsorbed on the graphite (0001) basal plane surface. We examined relative coverages from 0.15 up to 1....

  18. Reduction of ferrihydrite with adsorbed and coprecipitated organic matter: microbial reduction by Geobacter bremensis vs. abiotic reduction by Na-dithionite

    Directory of Open Access Journals (Sweden)

    K. Eusterhues

    2014-04-01

    Full Text Available Ferrihydrite (Fh is a widespread poorly crystalline Fe oxide which becomes easily coated by natural organic matter (OM in the environment. This mineral-bound OM entirely changes the mineral surface properties and therefore the reactivity of the original mineral. Here, we investigated the reactivity of 2-line Fh, Fh with adsorbed OM and Fh coprecipitated with OM towards microbial and abiotic reduction of Fe(III. As a surrogate for dissolved soil OM we used a water extract of a Podzol forest floor. Fh-OM associations with different OM-loadings were reduced either by Geobacter bremensis or abiotically by Na-dithionite. Both types of experiments showed decreasing initial Fe reduction rates and decreasing degrees of reduction with increasing amounts of mineral-bound OM. At similar OM-loadings, coprecipitated Fhs were more reactive than Fhs with adsorbed OM. The difference can be explained by the smaller crystal size and poor crystallinity of such coprecipitates. At small OM loadings this led to even faster Fe reduction rates than found for pure Fh. The amount of mineral-bound OM also affected the formation of secondary minerals: goethite was only found after reduction of OM-free Fh and siderite was only detected when Fhs with relatively low amounts of mineral-bound OM were reduced. We conclude that direct contact of G. bremensis to the Fe oxide mineral surface was inhibited when blocked by OM. Consequently, mineral-bound OM shall be taken into account besides Fe(II accumulation as a further widespread mechanism to slow down reductive dissolution.

  19. Metal–organic coordinated multilayer film formation: Quantitative analysis of composition and structure

    Energy Technology Data Exchange (ETDEWEB)

    Benson, Alexandra S.; Elinski, Meagan B.; Ohnsorg, Monica L.; Beaudoin, Christopher K.; Alexander, Kyle A.; Peaslee, Graham F.; DeYoung, Paul A.; Anderson, Mary E., E-mail: meanderson@hope.edu

    2015-09-01

    Metal–organic coordinated multilayers are self-assembled thin films fabricated by alternating solution–phase deposition of bifunctional organic molecules and metal ions. The multilayer film composed of α,ω-mercaptoalkanoic acid and Cu (II) has been the focus of fundamental and applied research with its robust reproducibility and seemingly simple hierarchical architecture. However, internal structure and composition have not been unambiguously established. The composition of films up to thirty layers thick was investigated using Rutherford backscattering spectrometry and particle induced X-ray emission. Findings show these films are copper enriched, elucidating a 2:1 ratio for the ion to molecule complexation at the metal–organic interface. Results also reveal that these films have an average layer density similar to literature values established for a self-assembled monolayer, indicating a robust and stable structure. The surface structures of multilayer films have been characterized by contact angle goniometry, ellipsometry, and scanning probe microscopy. A morphological transition is observed as film thickness increases from the first few foundational layers to films containing five or more layers. Surface roughness analysis quantifies this evolution as the film initially increases in roughness before obtaining a lower roughness comparable to the underlying gold substrate. Quantitative analysis of topographical structure and internal composition for metal–organic coordinated multilayers as a function of number of deposited layers has implications for their incorporation in the fields of photonics and nanolithography. - Highlights: • Layer-by-layer deposition is examined by scanning probe microscopy and ion beam analysis. • Film growth undergoes morphological evolution during foundational layer deposition. • Image analysis quantified surface features such as roughness, grain size, and coverage. • Molecular density of each film layer is found to

  20. The structure of organic langmuir films on liquid metal surfaces

    International Nuclear Information System (INIS)

    Langmuir films (LFs) on water have long been studied for their interest for basic science and their numerous applications in chemistry, physics, materials science and biology. We present here A-resolution synchrotron X-ray studies of the structure of stearic acid LFs on a liquid mercury surface. At low coverage, ≥110 A2/mol, a 2D gas phase of flat-lying molecules is observed. At high coverage, ≤23 A2/mol, two different hexatic phases of standing-up molecules are observed. At intermediate coverage, 52≤A≤110 A2/mol, novel single- and double-layered phases of flat-lying molecular dimers are found, exhibiting a 1D in-layer order. Such flat-lying phases were not hitherto observed in any LF. Measurements on LFs of fatty acids of other chain lengths indicate that this structure is generic to chain molecules on mercury, although the existence of some of the flat-lying phases, and the observed phase sequence, depend on the chain length. Organic LFs on Hg, and in particular the new flat-lying phases, should provide a broader nano-structural tunability range for molecular electronic device construction than most solid-supported self-assembled monolayers used at present

  1. The Self-Assembly of Nano-Objects Code: Applications to supramolecular organic monolayers adsorbed on metal surfaces

    CERN Document Server

    Roussel, Thomas

    2012-01-01

    The Self-Assembly of Nano-Objects (SANO) code we implemented demonstrates the ability to predict the molecular self-assembly of different structural motifs by tuning the molecular building blocks as well as the metallic substrate. It consists in a two-dimensional Grand Canonical Monte-Carlo (GCMC) approach developed to perform atomistic simulations of thousands of large organic molecules self-assembling on metal surfaces. Computing adsorption isotherms at room temperature and spanning over the characteristic sub-micrometric scales, we confront the robustness of the approach with three different well-known systems: ZnPcCl8 on Ag(111), CuPcF16 on Au(111) and PTBC on Ag(111). We retrieve respectively their square, oblique and hexagonal supramolecular tilling. The code incorporates generalized force fields to describe the molecular interactions, which provides transferability and versatility to many organic building blocks and metal surfaces.

  2. The Self-Assembly of Nano-Objects Code: Applications to supramolecular organic monolayers adsorbed on metal surfaces

    OpenAIRE

    Roussel, Thomas; Vega, Lourdes F.

    2012-01-01

    The Self-Assembly of Nano-Objects (SANO) code we implemented demonstrates the ability to predict the molecular self-assembly of different structural motifs by tuning the molecular building blocks as well as the metallic substrate. It consists in a two-dimensional Grand Canonical Monte-Carlo (GCMC) approach developed to perform atomistic simulations of thousands of large organic molecules self-assembling on metal surfaces. Computing adsorption isotherms at room temperature and spanning over th...

  3. Biogas from MSW landfill: Composition and determination of chlorine content with the AOX (adsorbable organically bound halogens) technique

    OpenAIRE

    Rey Martínez, María Dolores; Font Montesinos, Rafael; Aracil, Ignacio

    2013-01-01

    An exhaustive characterization of the biogas from some waste disposal facilities has been carried out. The analysis includes the main components (methane, carbon dioxide, nitrogen and oxygen) as well as trace components such as hydrogen sulphide, ammonia and VOCs (volatile organic compounds) including siloxanes and halogenated compounds. VOCs were measured by GC/MS (Gas Chromatography/Mass Spectrometry) using two different procedures: thermal desorption of the Tenax TA and Carbotrap 349 tubes...

  4. Organic nanodielectrics for low voltage carbon nanotube thin film transistors and complementary logic gates.

    Science.gov (United States)

    Hur, Seung-Hyun; Yoon, Myung-Han; Gaur, Anshu; Shim, Moonsub; Facchetti, Antonio; Marks, Tobin J; Rogers, John A

    2005-10-12

    We report the implementation of three dimensionally cross-linked, organic nanodielectric multilayers as ultrathin gate dielectrics for a type of thin film transistor device that uses networks of single-walled carbon nanotubes as effective semiconductor thin films. Unipolar n- and p-channel devices are demonstrated by use of polymer coatings to control the behavior of the networks. Monolithically integrating these devices yields complementary logic gates. The organic multilayers provide exceptionally good gate dielectrics for these systems and allow for low voltage, low hysteresis operation. The excellent performance characteristics suggest that organic dielectrics of this general type could provide a promising path to SWNT-based thin film electronics.

  5. Organic ultrathin film adhesion on compliant substrate using scratch test technique

    OpenAIRE

    Boddaert, Xavier; Covarel, Grégory; Ben Saïd, Bassem; Mattei, Mylene; Benaben, Patrick; Bois, Jérôme

    2012-01-01

    International audience Many adhesion test techniques have been developed to measure the adhesion energy of thin films but they are hard to implement in the case of submicron organic thin films deposited on a flexible substrate. Recently the feasibility and repeatability of the scratch test technique as a tool for testing the adhesion and the damage behaviour of ultra-thin films on polymer substrates has been demonstrated. However, direct comparison of the critical load between samples was ...

  6. Deposition of metal oxide films and nanostructures by methods derived from photochemical metal organic deposition

    OpenAIRE

    Xin ZHANG

    2009-01-01

    In this research, methods for the deposition of patterned films and nanostructures were developed from photochemical metal organic deposition (PMOD). Positive lithographic PMOD was demonstrated with films of titanium (IV) di-n-butoxide bis(2-ethylhexanoate) (Ti(OBun)2(eh)2), titanium (IV) diisopropoxide bis(2,4-pentanedionate), and zirconium (IV) di-n-butoxide bis(2,4-pentanedionate). The photochemistry of these complexes in films was studied by FTIR, AES, and XRD. Photo-induced reactivity an...

  7. Morphology of quaterthiophene thin films in organic field effect transistors

    NARCIS (Netherlands)

    Schoonveld, W.A; Stok, R.W; Weijtmans, J.W; Vrijmoeth, J; Wildeman, J.; Klapwijk, T.M

    1997-01-01

    The morphology of vacuum evaporated unsubstituted quaterthiophene films is studied as a function of the evaporation parameters. X-ray diffraction and AFM studies show that the thin film has a layered structure. Upon increasing the substrate temperature an increase in size of the single crystallites

  8. Self-organizing nanochannel networks in periodically perforated semiconductor films

    NARCIS (Netherlands)

    Annabattula, R. K.; Onck, P. R.

    2011-01-01

    In this paper we theoretically analyze the mechanism of nanochannel formation by an evolutionary etching process in periodically perforated semiconductor films. The compressive stresses due to lattice mismatch of the epitaxially grown nanoscale films are gradually relaxed; leading to an evolutionary

  9. Molecular beam deposition and characterization of thin organic films on metals for applications in organic electronics

    Energy Technology Data Exchange (ETDEWEB)

    Witte, G.; Woell, C. [Physikalische Chemie I, Ruhr-Universitaet Bochum, 44780 Bochum (Germany)

    2008-03-15

    The deposition of organic thin films on metal substrates using molecular beam deposition will be reviewed with a special emphasis on molecules which exhibit high charge carrier mobilities and are thus suited to be used as organic semiconductors (OSCs), namely pentacene, rubrene and perylene. Special emphasis will be on aspects of organic molecular beam deposition (OMBD) relevant for the device performance in organic field effect transistors (OFETs), in particular with regard to avoiding or minimizing structural defects at support/OSC interfaces. In addition, another aspect governing - and often limiting - charge injection at electrodes into an OSC, electronic level alignment at molecule/metal interfaces, are discussed in the context of recent accurate ab-initio electronic structure calculations. Finally, we present a novel experimental approach to determine charge transport properties of defect-free, nm-sized OSCs where extrinsic contributions to e.g. charge carrier mobilities can be strictly excluded, thus opening the way towards the determination of true intrinsic OSC properties. (copyright 2008 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim) (orig.)

  10. Rewritable organic films for near-field recording

    Science.gov (United States)

    Lee, Hyo Won; Kim, Young Mi; Jeon, Dong Ju; Kim, Eunkyoung; Kim, Jeongyong; Park, Kangho

    2003-01-01

    Photochromic thin films were prepared for near-field recording. Acetyl substituted diarylethene were synthesized from 1,2-bis(2-methylbenzo[ b]thiophene-3-yl)hexafluorocyclopentene in one step. Transparent and homogeneous thin films were coated on a substrate by vacuum deposition method. A colorless vacuum deposited diarylethene film turned to deep red hue upon exposure to a UV light. Near-field scanning optical microscopy (NSOM) was used to characterize nanoscale color change of the films. NSOM images showed distinct recording mark by 514 nm laser with mark speed of 30 ms. The records were completely erased upon excitation with a UV light, and rewritable with visible light (514 nm) on a UV activated colored film.

  11. Erbium-doped yttria thin films prepared by metal organic decomposition for up-conversion

    Energy Technology Data Exchange (ETDEWEB)

    Andriamiadamanana, Christian, E-mail: chriast@yahoo.fr [LCMCP UMR7574 CNRS/UPMC/Chimie Paristech, 11 Rue Pierre et Marie Curie, F-75235 Paris (France); IRDEP, UMR 7174 CNRS/EDF/Chimie ParisTech, 6 Quai Watier, F-78401 Chatou (France); Ibanez, Alain [Institut Néel, UPR2940, CNRS/Université Joseph Fourier, 25 rue des Martyrs, BP166, F-38042, Grenoble Cedex 9 (France); Ferrier, Alban [LCMCP UMR7574 CNRS/UPMC/Chimie Paristech, 11 Rue Pierre et Marie Curie, F-75235 Paris (France); Joudrier, Anne-Laure [LCMCP UMR7574 CNRS/UPMC/Chimie Paristech, 11 Rue Pierre et Marie Curie, F-75235 Paris (France); IRDEP, UMR 7174 CNRS/EDF/Chimie ParisTech, 6 Quai Watier, F-78401 Chatou (France); Lombez, Laurent [IRDEP, UMR 7174 CNRS/EDF/Chimie ParisTech, 6 Quai Watier, F-78401 Chatou (France); Liotaud, Marine [Institut Néel, UPR2940, CNRS/Université Joseph Fourier, 25 rue des Martyrs, BP166, F-38042, Grenoble Cedex 9 (France); Guillemoles, Jean-François [IRDEP, UMR 7174 CNRS/EDF/Chimie ParisTech, 6 Quai Watier, F-78401 Chatou (France); Pellé, Fabienne [LCMCP UMR7574 CNRS/UPMC/Chimie Paristech, 11 Rue Pierre et Marie Curie, F-75235 Paris (France)

    2013-06-30

    Er:Y{sub 2}O{sub 3} thin films have been obtained by spin coating process. Precursor solutions were prepared using nitrates as metal precursors and water as solvent. Citric, malic, and lactic acids were used as complexant. Investigations on resin compositions and on their coating parameters have been made, leading to crack-free thin films with citric and malic acids after direct deposition under standard room conditions (temperature, pressure and atmosphere). The films are homogeneous with a low root mean square roughness, less than 2.5 nm. We demonstrated that the nature of the carboxylic acid is the key point to obtain high quality thin films on silicon substrates from 20 nm up to 230 nm thick, while the film porosity is related to the number of carbon in the acid molecule. All films exhibit up-conversion luminescence in the near infrared and in the visible range, under 1.54 μm laser excitation. Furthermore, the up-conversion luminescence intensity increases with the applied annealing temperature on the films, due to an improvement of their crystallinity and to the total decomposition of organics. - Highlights: • We deposit films by spin-coating, using aqueous precursor solutions. • No special control of atmosphere is needed during all the process. • The organics are the key parameter for controlling the quality of films. • Multilayer have been obtained with all carboxylic acids we have studied. • All films exhibit an up-conversion property.

  12. Erbium-doped yttria thin films prepared by metal organic decomposition for up-conversion

    International Nuclear Information System (INIS)

    Er:Y2O3 thin films have been obtained by spin coating process. Precursor solutions were prepared using nitrates as metal precursors and water as solvent. Citric, malic, and lactic acids were used as complexant. Investigations on resin compositions and on their coating parameters have been made, leading to crack-free thin films with citric and malic acids after direct deposition under standard room conditions (temperature, pressure and atmosphere). The films are homogeneous with a low root mean square roughness, less than 2.5 nm. We demonstrated that the nature of the carboxylic acid is the key point to obtain high quality thin films on silicon substrates from 20 nm up to 230 nm thick, while the film porosity is related to the number of carbon in the acid molecule. All films exhibit up-conversion luminescence in the near infrared and in the visible range, under 1.54 μm laser excitation. Furthermore, the up-conversion luminescence intensity increases with the applied annealing temperature on the films, due to an improvement of their crystallinity and to the total decomposition of organics. - Highlights: • We deposit films by spin-coating, using aqueous precursor solutions. • No special control of atmosphere is needed during all the process. • The organics are the key parameter for controlling the quality of films. • Multilayer have been obtained with all carboxylic acids we have studied. • All films exhibit an up-conversion property

  13. Heterogeneous Reactions of Surface-Adsorbed Catechol: A Comparison of Tropospheric Aerosol Surrogates

    Science.gov (United States)

    Hinrichs, R. Z.; Woodill, L. A.

    2009-12-01

    Surface-adsorbed organics can alter the chemistry of tropospheric solid-air interfaces, such as aerosol and ground level surfaces, thereby impacting photochemical cycles and altering aerosol properties. The nature of the surface can also influence the chemistry of the surface-adsorbed organic. We employed diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS) to monitor the adsorption of gaseous catechol on several tropospheric aerosol surrogates and to investigate the subsequent reactivity of adsorbed-catechol with nitrogen dioxide and, in separate preliminary experiments, ozone. Graphite, kaolinite, and sodium halide (NaF, NaCl, NaBr) powders served as carbonaceous, mineral and sea salt aerosol surrogates, respectively. Broad OH stretching bands for adsorbed catechol shifted to lower wavenumber with peak frequencies following the trend NaBr > NaCl > NaF ≈ kaolinite, consistent with the increasing basicity of the halide anions and basic Brønsted sites on kaolinite. The dark heterogeneous reaction of NO2 with NaCl-adsorbed catechol at relative humidity (RH) 4-nitrocatechol and oxidation forming 1,2-benzoquinone and the ring cleavage product muconic acid, with product yields of 88%, 8%, and 4%, respectively. 4-Nitrocatechol was the dominant product for catechol adsorbed on NaF and kaolinite, while NaBr-adsorbed catechol produced less 4-nitrocatechol and more 1,2-benzoquinone and muconic acid. For all three sodium halides, the reactions of NO2 with adsorbed catechol were orders of magnitude faster than between NO2 and each NaX substrate. 4-Nitrocatechol rates and product yields were consistent with the relative ability of each substrate to enhance the deprotonated nature of adsorbed-catechol. Increasing the relative humidity caused the rate of each product channel to decrease and also altered the product branching ratios. Most notably, 1,2-benzoquinone formation decreased significantly even at 13% RH. The dramatic reactivity of surface-adsorbed

  14. Influence of surface chemistry on the structural organization of monomolecular protein layers adsorbed to functionalized aqueous interfaces

    DEFF Research Database (Denmark)

    Lösche, M.; Piepenstock, M.; Diederich, A.;

    1993-01-01

    The molecular organization of streptavidin (SA) bound to aqueous surface monolayers of biotin-functionalized lipids and binary lipid mixtures has been investigated with neutron reflectivity and electron and fluorescence microscopy. The substitution of deuterons (2H) for protons (1H), both...... in subphase water molecules and in the alkyl chains of the lipid surface monolayer, was utilized to determine the interface structure on the molecular length scale. In all cases studied, the protein forms monomolecular layers underneath the interface with thickness values of apprx 40 ANG . A systematic...... dependence of the structural properties of such self-assembled SA monolayers on the surface chemistry was observed: the lateral protein density depends on the length of the spacer connecting the biotin moiety and its hydrophobic anchor. The hydration of the lipid head groups in the protein-bound state...

  15. Highly Crystalline Films of Organic Small Molecules with Alkyl Chains Fabricated by Weak Epitaxy Growth.

    Science.gov (United States)

    Zhu, Yangjie; Chen, Weiping; Wang, Tong; Wang, Haibo; Wang, Yue; Yan, Donghang

    2016-05-12

    Because side-chain engineering of organic conjugated molecules has been widely utilized to tune organic solid-state optoelectronic properties, the achievement of their high-quality films is important for realizing high-performance devices. Here, highly crystalline films of an organic molecule with short alkyl chains, 5,8,15,18-tetrabutyl-5,8,15,18-tetrahydroindolo[3,2-a]indole[30,20:5,6]quinacridone (C4-IDQA), are fabricated by weak epitaxy growth, and highly oriented, large-area, and continuous films are obtained. Because of the soft matter properties, the C4-IDQA molecules can adjust themselves to realize commensurate epitaxy growth on the inducing layers and exhibited good lattice matching in the thin film phase. The crystalline phase is also observed in thicker C4-IDQA films. The growth behavior of C4-IDQA on the inducing layer is further investigated, including the strong dependence of film morphologies on substrate temperatures and deposition rates due to the poor diffusion ability of C4-IDQA molecules. Moreover, highly crystalline films and high electron field-effect mobility are also obtained for the small molecule N,N'-dioctyl-3,4:9,10-perylene tetracarboxylic diimide (C8-PTCDI), which demonstrate that the weak epitaxy growth method could be an effective way to fabricate highly crystalline films of organic small molecules with flexible side chains. PMID:27116036

  16. Properties of alumina films by atmospheric pressure metal-organic chemical vapour deposition

    NARCIS (Netherlands)

    Haanappel, V.A.C.; Corbach, van H.D.; Fransen, T.; Gellings, P.J.

    1994-01-01

    Thin alumina films were deposited at low temperatures (290–420°C) on stainless steel, type AISI 304. The deposition process was carried out in nitrogen by metal-organic chemical vapour deposition using aluminum tri-sec-butoxide. The film properties including the protection of the underlying substrat

  17. The mechanical properties of thin alumina film deposited by metal-organic chemical vapour deposition

    NARCIS (Netherlands)

    Haanappel, V.A.C.; Gellings, P.J.; Vendel, van de D.; Metselaar, H.S.C.; Corbach, van H.D.; Fransen, T.

    1995-01-01

    Amorphous alumina films were deposited by metal-organic chemical vapour deposition (MOCVD) on stainless steel, type AISI 304. The MOCVD experiments were performed in nitrogen at low and atmospheric pressures. The effects of deposition temperature, growth rate and film thickness on the mechanical pro

  18. Magneto-Photoinduced Absorption in Organic Polymer Films

    Science.gov (United States)

    Gautam, Bhoj; Nguyen, Tho; Ehrenfreund, Eitan; Vardeny, Z. Valy

    2012-02-01

    In order to elucidate the underlying mechanism of magneto-conductivity (MC) in OLEDs we studied magneto-photoinduced absorption (MPA) response in polymer films. The films were based on the MEH-PPV polymer in three different forms, namely: pristine film; film exposed to prolonged UV illumination; and MEH-PPV/PCBM blend having weight ratio 1:1. In pristine film we show that the MPA at low excitation intensity is due to sublevel spin mixing of triplet excitons; whereas at high excitation intensity the MPA is dominated by the triplet-triplet annihilation process. In UV illuminated MEH-PPV films that support photogenerated polarons we show that the MPA is due to sublevel spin-mixing of polaron-pairs via the hyperfine interaction with the closest hydrogen atoms to the chain. This mechanism also explains the MC response of OLED based on MEH-PPV, since its response is similar to that of MPA. Finally we found that the MPA in MEH-PPV/PCBM blend films is dominated by spin mixing of polaron-pair on the polymer and fullerene molecules, via the δg mechanism. Supported by the NSF DMR-1104495, the NSF MRSEC at the UoU, and the BSF program.

  19. Organization of copper nanoclusters in Langmuir–Blodgett films

    Indian Academy of Sciences (India)

    G Hemakanthi; Aruna Dhathathreyan; T Ramasami

    2002-02-01

    Stable nanoclusters of Cu were synthesized using Langmuir–Blodgett films of octadecylsuccinic acid (ODSA) as template. The Langmuir–Blodgett films of ODSA formed from subphase containing copper ions were first subjected to sulphidation (S) using sodium sulphide and then hydrogenated (H) using hydrogen gas. Diffuse reflectance UV-visible spectroscopy (DIR-UV-vis), X-ray photoelectron spectroscopy (XPS) and transmission electron microscopy (TEM) used to characterize these films indicated the formation of Cu(0) metallic clusters ranging in size from 3 ∼ 10 nm.

  20. Computational Redox Potential Predictions: Applications to Inorganic and Organic Aqueous Complexes, and Complexes Adsorbed to Mineral Surfaces

    Directory of Open Access Journals (Sweden)

    Krishnamoorthy Arumugam

    2014-04-01

    Full Text Available Applications of redox processes range over a number of scientific fields. This review article summarizes the theory behind the calculation of redox potentials in solution for species such as organic compounds, inorganic complexes, actinides, battery materials, and mineral surface-bound-species. Different computational approaches to predict and determine redox potentials of electron transitions are discussed along with their respective pros and cons for the prediction of redox potentials. Subsequently, recommendations are made for certain necessary computational settings required for accurate calculation of redox potentials. This article reviews the importance of computational parameters, such as basis sets, density functional theory (DFT functionals, and relativistic approaches and the role that physicochemical processes play on the shift of redox potentials, such as hydration or spin orbit coupling, and will aid in finding suitable combinations of approaches for different chemical and geochemical applications. Identifying cost-effective and credible computational approaches is essential to benchmark redox potential calculations against experiments. Once a good theoretical approach is found to model the chemistry and thermodynamics of the redox and electron transfer process, this knowledge can be incorporated into models of more complex reaction mechanisms that include diffusion in the solute, surface diffusion, and dehydration, to name a few. This knowledge is important to fully understand the nature of redox processes be it a geochemical process that dictates natural redox reactions or one that is being used for the optimization of a chemical process in industry. In addition, it will help identify materials that will be useful to design catalytic redox agents, to come up with materials to be used for batteries and photovoltaic processes, and to identify new and improved remediation strategies in environmental engineering, for example the

  1. Dramatic effect of pore size reduction on the dynamics of hydrogen adsorbed in metal–organic materials

    KAUST Repository

    Nugent, Patrick

    2014-07-21

    The effects of pore size reduction on the dynamics of hydrogen sorption in metal-organic materials (MOMs) were elucidated by studying SIFSIX-2-Cu and its doubly interpenetrated polymorph SIFSIX-2-Cu-i by means of sorption, inelastic neutron scattering (INS), and computational modeling. SIFSIX-2-Cu-i exhibits much smaller pore sizes, which possess high H2 sorption affinity at low loadings. Experimental H2 sorption measurements revealed that the isosteric heat of adsorption (Qst) for H2 in SIFSIX-2-Cu-i is nearly two times higher than that for SIFSIX-2-Cu (8.6 vs. 4.6 kJ mol-1). The INS spectrum for H2 in SIFSIX-2-Cu-i is rather unique for a porous material, as only one broad peak appears at low energies near 6 meV, which simply increases in intensity with loading until the pores are filled. The value for this rotational transition is lower than that in most neutral metal-organic frameworks (MOFs), including those with open Cu sites (8-9 meV), which is indicative of a higher barrier to rotation and stronger interaction in the channels of SIFSIX-2-Cu-i than the open Cu sites in MOFs. Simulations of H2 sorption in SIFSIX-2-Cu-i revealed two hydrogen sorption sites in the MOM: direct interaction with the equatorial fluorine atom (site 1) and between two equatorial fluorine atoms on opposite walls (site 2). The calculated rotational energy levels and rotational barriers for the two sites in SIFSIX-2-Cu-i are in good agreement with INS data. Furthermore, the rotational barriers and binding energies for site 2 are slightly higher than that for site 1, which is consistent with INS results. The lowest calculated transition for the primary site in SIFSIX-2-Cu is also in good agreement with INS data. In addition, this transition in the non-interpenetrating material is higher than any of the sites in SIFSIX-2-Cu-i, which indicates a significantly weaker interaction with the host as a result of the larger pore size. This journal is © the Partner Organisations 2014.

  2. Organic thin-film transistor arrays for active-matrix organic light emitting diode

    Science.gov (United States)

    Lee, Sangyun; Moon, Hyunsik; Kim, Do H.; Koo, Bon-Won; Jeong, Eun-Jeong; Lee, Bang-Lin; Kim, Joo-Young; Lee, Eunkyung; Hahn, Kook-Min; Han, Jeong-Seok; Park, Jung-Il; Seon, Jong-Baek; Kim, Jung-Woo; Chun, Young-Tea; Kim, Sangyeol; Kang, Sung K.

    2007-09-01

    We developed an active matrix organic light-emitting diodes (AMOLEDs) on a glass using two organic thin-film transistors (OTFTs) and a capacitor in a pixel. OTFTs switching-arrays with 64 scan lines and 64 (RGB) data lines were designed and fabricated to drive OLED arrays. In this study, OTFT devices have bottom contact structures with an ink-jet printed polymer semiconductor and an organic insulator as a gate dielectric. The width and length of the switching OTFT is 500μm and 10μm, respectively and the driving OTFT has 900μm channel width with the same channel length. The characteristics of the OTFTs were examined using test cells around display area. On/off ratio, mobility, on-current of switching OTFT and on-current of driving OTFT were 10 6, 0.1 cm2/V-sec, order of 8μA and over 70 μA respectively. These properties were enough to drive the AMOLEDs over 60 Hz frame rate. AMOLEDs composed of the OTFT switching arrays and OLEDs made by deposition of small molecule materials were fabricated and driven to make moving images, successfully.

  3. Adhesive flexible barrier film, method of forming same, and organic electronic device including same

    Science.gov (United States)

    Blizzard, John Donald; Weidner, William Kenneth

    2013-02-05

    An adhesive flexible barrier film comprises a substrate and a barrier layer disposed on the substrate. The barrier layer is formed from a barrier composition comprising an organosilicon compound. The adhesive flexible barrier film also comprises an adhesive layer disposed on the barrier layer and formed from an adhesive composition. A method of forming the adhesive flexible barrier film comprises the steps of disposing the barrier composition on the substrate to form the barrier layer, disposing the adhesive composition on the barrier layer to form the adhesive layer, and curing the barrier layer and the adhesive layer. The adhesive flexible barrier film may be utilized in organic electronic devices.

  4. Influence of organic films on the evaporation and condensation of water in aerosol

    OpenAIRE

    Davies, James F.; Miles, Rachael E H; Haddrell, Allen E; Reid, Jonathan P.

    2013-01-01

    Uncertainties in quantifying the kinetics of evaporation and condensation of water fromatmospheric aerosol are a significant contributor to the uncertainty in predicting cloud droplet number and the indirect effect of aerosols on climate. The influence of aerosol particle surface composition, particularly the impact of surface active organic films, on the condensation and evaporation coefficients remains ambiguous. Here, we report measurements of the influence of organic films on the evaporat...

  5. Combinatorial Techniques to Efficiently Investigate and Optimize Organic Thin Film Processing and Properties

    OpenAIRE

    Hans-Werner Schmidt; Ober, Christopher K.; Christian Neuber; Tristan Kolb; Florian Wieberger

    2013-01-01

    In this article we present several developed and improved combinatorial techniques to optimize processing conditions and material properties of organic thin films. The combinatorial approach allows investigations of multi-variable dependencies and is the perfect tool to investigate organic thin films regarding their high performance purposes. In this context we develop and establish the reliable preparation of gradients of material composition, temperature, exposure, and immersion time. Furth...

  6. Adaptive hydrophobic and hydrophilic interactions of mussel foot proteins with organic thin films

    OpenAIRE

    Yu, J; Kan, Y.; M. Rapp; Danner, E; Wei, W.; Das, S.; Miller, DR; Chen, Y.; Waite, JH; Israelachvili, JN

    2013-01-01

    The adhesion of mussel foot proteins (Mfps) to a variety of specially engineered mineral and metal oxide surfaces has previously been investigated extensively, but the relevance of these studies to adhesion in biological environments remains unknown. Most solid surfaces exposed to seawater or physiological fluids become fouled by organic conditioning films and biofilms within minutes. Understanding the binding mechanisms of Mfps to organic films with known chemical and physical properties the...

  7. Single crystals of fullerene (C60 makes organic thick film solar cells and self supporting organic solar cells possible.

    Directory of Open Access Journals (Sweden)

    M. Umeno

    2008-06-01

    Full Text Available Single crystals of Fullerene (SC-C60 were synthesized by simple liquid/liquid interface precipitation method. Organic thick film solar cell (with an active layer thickness of approximately 20 microns thick is demonstrated by combining SC-C60 with poly(3-octylthiophene. Our preliminary results indicate that organic thick film solar cells are possible; which were considered to be impossible due to low mobility and small exciton diffusion lengths in most of the organic materials including small organic molecules and conjugated conducting polymers. Further, SC-C60 seems to be promising materials for organic photovoltaics. Self supporting organic solar cell is also demonstrated using SC-C60.

  8. Magnetic porous carbon derived from a Zn/Co bimetallic metal-organic framework as an adsorbent for the extraction of chlorophenols from water and honey tea samples.

    Science.gov (United States)

    Li, Menghua; Wang, Junmin; Jiao, Caina; Wang, Chun; Wu, Qiuhua; Wang, Zhi

    2016-05-01

    A novel magnetic porous carbon derived from a bimetallic metal-organic framework, Zn/Co-MPC, was prepared by introducing cobalt into ZIF-8. Magnetic porous carbon that possesses magnetic properties and a large specific surface area was firstly fabricated by the direct carbonization of Zn/Co-ZIF-8. The prepared magnetic porous carbon material was characterized by scanning electron microscopy, transmission electron microscopy, powder X-ray diffraction, N2 adsorption, and vibrating sample magnetometry. The prepared magnetic porous carbon was used as a magnetic solid-phase extraction adsorbent for the enrichment of chlorophenols from water and honey tea samples before high-performance liquid chromatography analysis. Several experimental parameters that could influence the extraction efficiency were investigated and optimized. Under the optimum conditions, good linearities (r > 0.9957) for all calibration curves were obtained with low limits of detection, which are in the range of 0.1-0.2 ng mL(-1) for all the analytes. The results showed that the prepared magnetic porous carbon had an excellent adsorption capability toward the target analytes. PMID:26991637

  9. Adsorptive removal of hydrophobic organic compounds by carbonaceous adsorbents: A comparative study of waste-polymer-based,coal-based activated carbon, and carbon nanotubes

    Institute of Scientific and Technical Information of China (English)

    Fei Lian; Chun Chang; Yang Du; Lingyan Zhu; Baoshan Xing; Chang Liu

    2012-01-01

    Adsorption of the hydrophobic organic compounds (HOCs) trichloroethylene (TCE),1,3-dichlorobenzene (DCB),1,3-dinitrobenzene (DNB) and γ-hexachlorocyclohexane (HCH) on five different carbonaceous materials was compared.The adsorbents included three polymer-based activated carbons,one coal-based activated carbon (F400) and multiwalled carbon nanotubes (MWNT).The polymerbased activated carbons were prepared using KOH activation from waste polymers:polyvinyl chloride (PVC),polyethyleneterephthalate (PET) and tire rubber (TR).Compared with F400 and MWNT,activated carbons derived from PVC and PET exhibited fast adsorption kinetics and high adsorption capacity toward the HOCs,attributed to their extremely large hydrophobic surface area (2700 m2/g) and highly mesoporous structures.Adsorption of small-sized TCE was stronger on the tire-rubber-based carbon and F400 resulting from the pore-filling effect.In contrast,due to the molecular sieving effect,their adsorption on HCH was lower.MWNT exhibited the lowest adsorption capacity toward HOCs because of its low surface area and characteristic of aggregating in aqueous solution.

  10. Organic ferroelectric gate field-effect transistor memory using high-mobility rubrene thin film

    Science.gov (United States)

    Kanashima, Takeshi; Katsura, Yuu; Okuyama, Masanori

    2014-01-01

    An organic ferroelectric gate field-effect transistor (FET) memory has been fabricated using an organic semiconductor of rubrene thin film with a high mobility and a gate insulating layer of poly(vinylidene fluoride-tetrafluoroethylene) [P(VDF-TeFE)] thin film. A rubrene thin-film sheet was grown by physical vapor transport (PVT), and placed onto a spin-coated P(VDF-TeFE) thin-film layer, and Au source and drain electrodes were formed on this rubrene thin film. A hysteresis loop of the drain current-gate voltage (ID-VG) characteristic has been clearly observed in the ferroelectric gate FET, and is caused by the ferroelectricity. The maximum drain current is 1.5 × 10-6 A, which is about two orders of magnitude larger than that of the P(VDF-TeFE) gate FET using a pentacene thin film. Moreover, the mobility of this organic ferroelectric gate FET using rubrene thin film is 0.71 cm2 V-1 s-1, which is 35 times larger than that of the FET with pentacene thin film.

  11. Characterisation of molecular thin films grown by organic molecular beam deposition

    CERN Document Server

    Bayliss, S M

    2000-01-01

    This work concerns the growth and characterisation of molecular thin films in an ultra high vacuum regime by organic molecular beam deposition (OMBD). Films of three different molecular materials are grown, namely free base phthalocyanine (H sub 2 Pc), perylene 3,4,9,10-tetracarboxylic dianhydride (PTCDA) and aluminium tris-8-hydroxyquinoline (Alq sub 3). The relationship between the growth parameters such as film thickness, growth rate, and substrate temperature during and after growth, and the structural, optical and morphological properties of the film are investigated. These investigations are carried out using various ex-situ techniques. X-ray diffraction, Raman spectroscopy and electronic absorption spectroscopy are used to probe the bulk film characteristics, whilst Nomarski microscopy and atomic force microscopy are used to study the surface morphology. Three different levels of influence of the growth parameters on the film properties are observed. In the case of H sub 2 Pc, two crystal phases are fo...

  12. Exciton-polaron quenching in organic thin-film transistors studied by fluorescence lifetime imaging microscopy

    DEFF Research Database (Denmark)

    Jensen, Per Baunegaard With; Leißner, Till; Osadnik, Andreas;

    Organic semiconductors show great potential in electronic and optical applications. However, a major challenge is the degradation of the semiconductor materials that cause a reduction in device performance. Here, we present our investigations of Organic Thin Film Transistors (OTFT) based on the m......Organic semiconductors show great potential in electronic and optical applications. However, a major challenge is the degradation of the semiconductor materials that cause a reduction in device performance. Here, we present our investigations of Organic Thin Film Transistors (OTFT) based...

  13. In-Line Sputtered Gallium and Aluminum Codoped Zinc Oxide Films for Organic Solar Cells

    Directory of Open Access Journals (Sweden)

    Shang-Chou Chang

    2014-01-01

    Full Text Available Gallium and aluminum codoped zinc oxide (GAZO films were deposited at different temperatures by in-line sputtering. Aluminum is thermally unstable compared to other elements in GAZO films. The grains of GAZO films increase with deposition temperature. Coalescence between grains was observed for GAZO films deposited at 250°C. The deposition temperature exhibits positive influence on crystallinity, and electrical and optical properties of GAZO films. The carrier concentration and mobility of GAZO films increase, while the electrical resistivity of GAZO films decreases with deposition temperature. The average optical transmittance of GAZO films rises with deposition temperature. In-line sputtering demonstrates a potential method with simplicity, mass production, and large-area deposition to produce GAZO films with good electrical and optical quality. The electrical resistivity of 4.3 × 10−4 Ω cm and the average optical transmittance in the visible range from 400 to 800 nm of 92% can be obtained for GAZO films deposited at 250°C. The hybrid organic solar cells (OSC were fabricated on GAZO-coated glass substrates. Blended poly(3-hexylthiophene (P3HT and [6,6]-phenyl C61 butyric acid methyl ester (PCBM were the photoactive materials in OSC. The power conversion efficiency of OSC is 0.65% for the OSC with the 250°C deposited GAZO electrode.

  14. Adsorbate-modified growth of ultrathin rare-earth oxide films on silicon and complementary studies of cerium oxide on ruthenium; Adsorbat-modifiziertes Wachstum ultraduenner Seltenerdoxid-Filme auf Silizium und komplementaere Studien von Ceroxid auf Ruthenium

    Energy Technology Data Exchange (ETDEWEB)

    Kaemena, Bjoern

    2013-11-27

    Rare-earth oxides (REOx) are extensively investigated due to their extraordinary physical and chemical properties, which essentially arise from the unfilled 4f electron shell, in order to reveal the nature of these exceptional properties and ultimately to utilize them for multiple technological applications. To maintain the exponential increase in integration density in CMOS technology, which is also known as Moore s law, there is a strong desire for ultrathin, well-ordered, epitaxial REOx layers with a precisely engineered interface, which is essential for reliable, ultrahigh-performance devices. So far this has been considerably impeded by RE-promoted silicon oxidation, leading to amorphous silicon oxide and RE silicon formation. By using complementary synchrotron radiation methods such as X-ray standing waves (XSW), X-ray photoelectron spectroscopy (XPS) and X-ray diffraction (XRD), structural and spectroscopic information are inferred simultaneously from ultrathin ceria and lanthana films grown on chlorine, silver and gallium passivated silicon(111). In general, it is revealed that the chemical and structural composition of the interface and the crystallinity of ultrathin REOx layers on silicon can be precisely controlled by adsorbate-mediated growth. This might represent a crucial step towards a perfectly engineered interface, eventually allowing for the integration of REOx as high-k gate oxides in microelectronics. In catalysis inverse model catalysts are studied with the aim of getting an in-depth understanding of the basic principles of catalysis. These model systems are employed to study, e. g., the nature of active sites and the reaction pathways in complex catalytic converters. However, a lot remains unknown about the chemical activity and selectivity as a function of the growth mechanism, structure and morphology of these model systems. The powerful spectroscopic photoemission and low-energy electron microscope, which is able to reveal the surface

  15. Processing and performance of organic insulators as a gate layer in organic thin film transistors fabricated on polyethylene terephthalate substrate

    Indian Academy of Sciences (India)

    Saumen Mandal; Monica Katiyar

    2013-08-01

    Fabrication of organic thin film transistor (OTFT) on flexible substrates is a challenge, because of its low softening temperature, high roughness and flexible nature. Although several organic dielectrics have been used as gate insulator, it is difficult to choose one in absence of a comparative study covering processing of dielectric layer on polyethylene terephthalate (PET), characterization of dielectric property, pentacene film morphology and OTFT characterization. Here, we present the processing and performance of three organic dielectrics, poly(4-vinylphenol) (PVPh), polyvinyl alcohol (PVA) and poly(methylmethacrylate) (PMMA), as a gate layer in pentacene-based organic thin film transistor on PET substrate. We have used thermogravimetric analysis of organic dielectric solution to determine annealing temperature for spin-coated films of these dielectrics. Comparison of the leakage currents for the three dielectrics shows PVA exhibiting lowest leakage (in the voltage range of −30 to +30 V). This is partly because solvent is completely eliminated in the case of PVA as observed by differential thermogravimetric analysis (DTGA). We propose that DTGA can be a useful tool to optimize processing of dielectric layers. From organic thin film transistor point of view, crystal structure, morphology and surface roughness of pentacene film on all the dielectric layers were studied using X-ray diffraction (XRD), atomic force microscopy (AFM) and scanning electron microscopy (SEM).We observe pyramidal pentacene on PVPh whereas commonly observed dendritic pentacene on PMMA and PVA surface. Pentacene morphology development is discussed in terms of surface roughness, surface energy and molecular nature of the dielectric layer.

  16. Fabrication of organic-inorganic perovskite thin films for planar solar cells via pulsed laser deposition

    Energy Technology Data Exchange (ETDEWEB)

    Liang, Yangang; Zhang, Xiaohang; Gong, Yunhui; Shin, Jongmoon; Wachsman, Eric D.; Takeuchi, Ichiro, E-mail: takeuchi@umd.edu [Department of Materials Science and Engineering, University of Maryland, College Park, Maryland 20740 (United States); Yao, Yangyi; Hsu, Wei-Lun; Dagenais, Mario [Department of Electrical and Computer Engineering, University of Maryland, College Park, Maryland 20740 (United States)

    2016-01-15

    We report on fabrication of organic-inorganic perovskite thin films using a hybrid method consisting of pulsed laser deposition (PLD) of lead iodide and spin-coating of methylammonium iodide. Smooth and highly crystalline CH{sub 3}NH{sub 3}PbI{sub 3} thin films have been fabricated on silicon and glass coated substrates with fluorine doped tin oxide using this PLD-based hybrid method. Planar perovskite solar cells with an inverted structure have been successfully fabricated using the perovskite films. Because of its versatility, the PLD-based hybrid fabrication method not only provides an easy and precise control of the thickness of the perovskite thin films, but also offers a straightforward platform for studying the potential feasibility in using other metal halides and organic salts for formation of the organic-inorganic perovskite structure.

  17. Fabrication of organic-inorganic perovskite thin films for planar solar cells via pulsed laser deposition

    International Nuclear Information System (INIS)

    We report on fabrication of organic-inorganic perovskite thin films using a hybrid method consisting of pulsed laser deposition (PLD) of lead iodide and spin-coating of methylammonium iodide. Smooth and highly crystalline CH3NH3PbI3 thin films have been fabricated on silicon and glass coated substrates with fluorine doped tin oxide using this PLD-based hybrid method. Planar perovskite solar cells with an inverted structure have been successfully fabricated using the perovskite films. Because of its versatility, the PLD-based hybrid fabrication method not only provides an easy and precise control of the thickness of the perovskite thin films, but also offers a straightforward platform for studying the potential feasibility in using other metal halides and organic salts for formation of the organic-inorganic perovskite structure

  18. Tracing the 4000 year history of organic thin films: From monolayers on liquids to multilayers on solidsa)

    Science.gov (United States)

    Greene, J. E.

    2015-03-01

    The recorded history of organic monolayer and multilayer thin films spans approximately 4000 years. Fatty-acid-based monolayers were deposited on water by the ancients for applications ranging from fortune telling in King Hammurabi's time (˜1800 BC, Mesopotamia) to stilling choppy waters for sailors and divers as reported by the Roman philosopher Pliny the Elder in ˜78 AD, and then much later (1774) by the peripatetic American statesman and natural philosopher Benjamin Franklin, to Japanese "floating-ink" art (suminagashi) developed ˜1000 years ago. The modern science of organic monolayers began in the late-1800s/early-1900s with experiments by Lord Rayleigh and the important development by Agnes Pockels, followed two decades later by Irving Langmuir, of the tools and technology to measure the surface tension of liquids, the surface pressure of organic monolayers deposited on water, interfacial properties, molecular conformation of the organic layers, and phase transitions which occur upon compressing the monolayers. In 1935, Katherine Blodgett published a landmark paper showing that multilayers can be synthesized on solid substrates, with controlled thickness and composition, using an apparatus now known as the Langmuir-Blodgett (L-B) trough. A disadvantage of LB films for some applications is that they form weak physisorbed bonds to the substrate. In 1946, Bigelow, Pickett, and Zisman demonstrated, in another seminal paper, the growth of organic self-assembled monolayers (SAMs) via spontaneous adsorption from solution, rather than from the water/air interface, onto SiO2 and metal substrates. SAMs are close-packed two-dimensional organic crystals which exhibit strong covalent bonding to the substrate. The first multicomponent adsorbed monolayers and multilayer SAMs were produced in the early 1980s. Langmuir monolayers, L-B multilayers, and self-assembled mono- and multilayers have found an extraordinarily broad range of applications including controlled wetting

  19. Tracing the 4000 year history of organic thin films: From monolayers on liquids to multilayers on solids

    Energy Technology Data Exchange (ETDEWEB)

    Greene, J. E. [University of Illinois, Urbana, Illinois 61801 (United States); Linköping University, 581 83 Linköping (Sweden); National Taiwan University of Science and Technology, Taipei 10607, Taiwan (China)

    2015-03-15

    The recorded history of organic monolayer and multilayer thin films spans approximately 4000 years. Fatty-acid-based monolayers were deposited on water by the ancients for applications ranging from fortune telling in King Hammurabi's time (∼1800 BC, Mesopotamia) to stilling choppy waters for sailors and divers as reported by the Roman philosopher Pliny the Elder in ∼78 AD, and then much later (1774) by the peripatetic American statesman and natural philosopher Benjamin Franklin, to Japanese “floating-ink” art (suminagashi) developed ∼1000 years ago. The modern science of organic monolayers began in the late-1800s/early-1900s with experiments by Lord Rayleigh and the important development by Agnes Pockels, followed two decades later by Irving Langmuir, of the tools and technology to measure the surface tension of liquids, the surface pressure of organic monolayers deposited on water, interfacial properties, molecular conformation of the organic layers, and phase transitions which occur upon compressing the monolayers. In 1935, Katherine Blodgett published a landmark paper showing that multilayers can be synthesized on solid substrates, with controlled thickness and composition, using an apparatus now known as the Langmuir-Blodgett (L-B) trough. A disadvantage of LB films for some applications is that they form weak physisorbed bonds to the substrate. In 1946, Bigelow, Pickett, and Zisman demonstrated, in another seminal paper, the growth of organic self-assembled monolayers (SAMs) via spontaneous adsorption from solution, rather than from the water/air interface, onto SiO{sub 2} and metal substrates. SAMs are close-packed two-dimensional organic crystals which exhibit strong covalent bonding to the substrate. The first multicomponent adsorbed monolayers and multilayer SAMs were produced in the early 1980s. Langmuir monolayers, L-B multilayers, and self-assembled mono- and multilayers have found an extraordinarily broad range of applications including

  20. Tracing the 4000 year history of organic thin films: From monolayers on liquids to multilayers on solids

    International Nuclear Information System (INIS)

    The recorded history of organic monolayer and multilayer thin films spans approximately 4000 years. Fatty-acid-based monolayers were deposited on water by the ancients for applications ranging from fortune telling in King Hammurabi's time (∼1800 BC, Mesopotamia) to stilling choppy waters for sailors and divers as reported by the Roman philosopher Pliny the Elder in ∼78 AD, and then much later (1774) by the peripatetic American statesman and natural philosopher Benjamin Franklin, to Japanese “floating-ink” art (suminagashi) developed ∼1000 years ago. The modern science of organic monolayers began in the late-1800s/early-1900s with experiments by Lord Rayleigh and the important development by Agnes Pockels, followed two decades later by Irving Langmuir, of the tools and technology to measure the surface tension of liquids, the surface pressure of organic monolayers deposited on water, interfacial properties, molecular conformation of the organic layers, and phase transitions which occur upon compressing the monolayers. In 1935, Katherine Blodgett published a landmark paper showing that multilayers can be synthesized on solid substrates, with controlled thickness and composition, using an apparatus now known as the Langmuir-Blodgett (L-B) trough. A disadvantage of LB films for some applications is that they form weak physisorbed bonds to the substrate. In 1946, Bigelow, Pickett, and Zisman demonstrated, in another seminal paper, the growth of organic self-assembled monolayers (SAMs) via spontaneous adsorption from solution, rather than from the water/air interface, onto SiO2 and metal substrates. SAMs are close-packed two-dimensional organic crystals which exhibit strong covalent bonding to the substrate. The first multicomponent adsorbed monolayers and multilayer SAMs were produced in the early 1980s. Langmuir monolayers, L-B multilayers, and self-assembled mono- and multilayers have found an extraordinarily broad range of applications including

  1. A flexible organic active matrix circuit fabricated using novel organic thin film transistors and organic light-emitting diodes

    KAUST Repository

    Gutiérrez-Heredia, Gerardo

    2010-10-04

    We present an active matrix circuit fabricated on plastic (polyethylene naphthalene, PEN) and glass substrates using organic thin film transistors and organic capacitors to control organic light-emitting diodes (OLEDs). The basic circuit is fabricated using two pentacene-based transistors and a capacitor using a novel aluminum oxide/parylene stack (Al2O3/ parylene) as the dielectric for both the transistor and the capacitor. We report that our circuit can deliver up to 15 μA to each OLED pixel. To achieve 200 cd m-2 of brightness a 10 μA current is needed; therefore, our approach can initially deliver 1.5× the required current to drive a single pixel. In contrast to parylene-only devices, the Al2O 3/parylene stack does not fail after stressing at a field of 1.7 MV cm-1 for >10 000 s, whereas \\'parylene only\\' devices show breakdown at approximately 1000 s. Details of the integration scheme are presented. © 2010 IOP Publishing Ltd.

  2. A flexible organic active matrix circuit fabricated using novel organic thin film transistors and organic light-emitting diodes

    Science.gov (United States)

    Gutiérrez-Heredia, G.; González, L. A.; Alshareef, H. N.; Gnade, B. E.; Quevedo-López, M.

    2010-11-01

    We present an active matrix circuit fabricated on plastic (polyethylene naphthalene, PEN) and glass substrates using organic thin film transistors and organic capacitors to control organic light-emitting diodes (OLEDs). The basic circuit is fabricated using two pentacene-based transistors and a capacitor using a novel aluminum oxide/parylene stack (Al2O3/parylene) as the dielectric for both the transistor and the capacitor. We report that our circuit can deliver up to 15 µA to each OLED pixel. To achieve 200 cd m-2 of brightness a 10 µA current is needed; therefore, our approach can initially deliver 1.5× the required current to drive a single pixel. In contrast to parylene-only devices, the Al2O3/parylene stack does not fail after stressing at a field of 1.7 MV cm-1 for >10 000 s, whereas 'parylene only' devices show breakdown at approximately 1000 s. Details of the integration scheme are presented.

  3. Ordered organic thin films self-assembled from the vapor phase

    Science.gov (United States)

    Debe, M. K.

    1993-01-01

    Organic films self-assembled from a liquid phase, as in Langmuir-Blodgett or adsorption from solution, have received much attention in the past decade as techniques to achieve highly oriented-ordered polymeric thin films. Many organic compounds including some of the same fatty acids have been vapor deposited as well. However, organic pigments and dyes comprise a major class of important materials which have very low solubilities yet excellent thermal stabilities, making them ideally suited for film deposition from the vapor phase. Surprisingly, such molecular systems exhibit a significant propensity to self order, a high sensitivity to deposition parameters, and a range of microstructural forms that cannot be duplicated by the less energetic mechanisms associated with solution adsorption processes. Molecular solids such as heterocyclic polynuclear aromatics are excellent candidates for film formation by vacuum deposition means. Over the past decade, our work and that of others investigating a wide variety of perylene and phthalocyanine derivatives identified five deposition parameters that can significantly affect film morphology, physical microstructure, and type and extent of ordering developed in vacuum and vapor transport grown films. These parameters are substrate temperature, deposition rate, substrate chemistry and epitaxy, ambient gas convective flows, and post deposition annealing. Examples of how each of these conditions manifest themselves in the film structure and ordering, most frequently revealed by scanning electron microscopy, reflection absorption infrared spectroscopy (RAIR), and grazing incidence x-ray diffraction (GIX), are presented.

  4. Study of intermolecular interactions in hetero-organic thin films

    OpenAIRE

    Stadtmüller, Benjamin

    2013-01-01

    The interest in organic semiconductors is based on their great potential to serve as active materials in electronic devices such as organic light-emitting diodes or organic photovoltaic cells. The performance of these molecular assemblies does not only depend on the properties of the organic bulk materials but also on the interfaces formed by the contact between different materials. Therefore, the physical properties of interfaces between metal contacts and organic materials have been studied...

  5. Analysis of surface films on lithium in various organic electrolytes

    Energy Technology Data Exchange (ETDEWEB)

    Kominato, A.; Yasukawa, E.; Sato, N.; Ijuuin, T.; Asahina, H.; Mori, S. [Mitsubishi Chemical Corp., Ibaraki (Japan). Tsukuba Research Center

    1997-10-01

    The surface films formed on lithium metal in ethylene carbonate (EC)+dimethyl carbonate (DMC) containing LiPF{sub 6}, LiClO{sub 4} and LiN(SO{sub 2}CF{sub 3}){sub 2} electrolytes were analysed by using Auger electron spectroscopy (AES), temperature-programmed decomposition mass spectrography (TPD-MS), FT-IR, ion chromatography (IC) and atomic adsorption spectroscopy (AAS). The morphology of the film was observed by using scanning electron microscopy (SEM). The film formed in the LiPF{sub 6} solution exhibited spherical morphology and was found to contain LiF, lithium oxide compounds (most of which seems to be inorganic), (CH{sub 2}OCO{sub 2}Li){sub 2} and CH{sub 3}OCO{sub 2}Li. The films in LiClO{sub 4} and LiN(SO{sub 2}CF{sub 3}){sub 2} were dendritic and contained the lithium oxide compounds, (CH{sub 2}OCO{sub 2}Li){sub 2} and CH{sub 3}OCO{sub 2}Li. (orig.)

  6. Poly(methyl methacrylate) films for organic vapour sensing

    CERN Document Server

    Capan, R; Hassan, A K; Tanrisever, T

    2003-01-01

    Optical constants and fabrication parameters are investigated using surface plasmon resonance (SPR) studies on spun films of poly(methyl methacrylate) (PMMA) derivatives in contact with two different dielectric media. A value of 1.503 for the refractive index of PMMA films produced from a solution having concentration of 1 mg ml sup - sup 1 at the speed of 3000 rpm is in close agreement with the data obtained from ellipsometric measurements. The film thickness shows a power-law dependence on the spin speed but the thickness increases almost linearly with the concentration of the spreading solution. These results are in good agreement with the hydrodynamic theory for a low-viscosity and highly volatile liquid. On the basis of SPR measurements under dynamic conditions, room temperature response of PMMA films to benzene vapours is found to be fast, highly sensitive and reversible. The sensitivity of detection of toluene, ethyl benzene and m-xylene is much smaller than that of benzene.

  7. Nucleation and strain-stabilization during organic semiconductor thin film deposition.

    Science.gov (United States)

    Li, Yang; Wan, Jing; Smilgies, Detlef-M; Bouffard, Nicole; Sun, Richard; Headrick, Randall L

    2016-01-01

    The nucleation mechanisms during solution deposition of organic semiconductor thin films determine the grain morphology and may influence the crystalline packing in some cases. Here, in-situ optical spectromicroscopy in reflection mode is used to study the growth mechanisms and thermal stability of 6,13-bis(trisopropylsilylethynyl)-pentacene thin films. The results show that the films form in a supersaturated state before transforming to a solid film. Molecular aggregates corresponding to subcritical nuclei in the crystallization process are inferred from optical spectroscopy measurements of the supersaturated region. Strain-free solid films exhibit a temperature-dependent blue shift of optical absorption peaks due to a continuous thermally driven change of the crystalline packing. As crystalline films are cooled to ambient temperature they become strained although cracking of thicker films is observed, which allows the strain to partially relax. Below a critical thickness, cracking is not observed and grazing incidence X-ray diffraction measurements confirm that the thinnest films are constrained to the lattice constants corresponding to the temperature at which they were deposited. Optical spectroscopy results show that the transition temperature between Form I (room temperature phase) and Form II (high temperature phase) depends on the film thickness, and that Form I can also be strain-stabilized up to 135 °C. PMID:27600905

  8. Thin films of metal-organic compounds and metal nanoparticle-embedded polymers for nonlinear optical applications

    Indian Academy of Sciences (India)

    S Philip Anthony; Shatabdi Porel; D Narayana Rao; T P Radhakrishnan

    2005-11-01

    Thin films based on two very different metal-organic systems are developed and some nonlinear optical applications are explored. A family of zinc complexes which form perfectly polar assemblies in their crystalline state are found to organize as uniaxially oriented crystallites in vapor deposited thin films on glass substrate. Optical second harmonic generation from these films is investigated. A simple protocol is developed for the in-situ fabrication of highly monodisperse silver nanoparticles in a polymer film matrix. The methodology can be used to produce free-standing films. Optical limiting capability of the nanoparticle-embedded polymer film is demonstrated.

  9. Comparison of physicomechanical properties of films prepared from organic solutions and aqueous dispersion of Eudragit RL

    Directory of Open Access Journals (Sweden)

    H Afrasiabi Garekani

    2011-05-01

    Full Text Available Background and the purpose of the study: Mechanical properties of films prepared from aqueous dispersion and organic solutions of Eudragit RL were assessed and the effects of plasticizer type, concentration and curing were examined. Methods: Films were prepared from aqueous dispersion and solutions of Eudragit RL (isopropyl alcohol-water 9:1 containing 0, 10 or 20% (based on polymer weight of PEG 400 or Triethyl Citrate (TEC as plasticizer using casting method. Samples of films were stored in oven at 60ºC for 24 hrs (Cured. The stress-strain curve was obtained for each film using material testing machine and tensile strength, elastic modulus, %elongation and work of failure were calculated. Results and major conclusion: The films with no plasticizer showed different mechanical properties depending on the vehicle used. Addition of 10% or 20% of plasticizer decreased the tensile strength and elastic modulus and increased %elongation and work of failure for all films. The effect of PEG400 on mechanical properties of Eudragit RL films was more pronounced. The differences in mechanical properties of the films due to vehicle decreased by addition of plasticizer and increase in its concentration. Curing process weakened the mechanical properties of the films with no plasticizer and for films with 10% plasticizer no considerable difference in mechanical properties was observed before and after curing. For those with 20% plasticizer only films prepared from aqueous dispersion showed remarkable difference in mechanical properties before and after curing. Results of this study suggest that the mechanical properties of the Eudragit RL films were affected by the vehicle, type of plasticizer and its concentration in the coating liquid.

  10. Indium-Doped Zinc Oxide Thin Films as Effective Anodes of Organic Photovoltaic Devices

    Directory of Open Access Journals (Sweden)

    Ziyang Hu

    2011-01-01

    Full Text Available Indium-doped zinc oxide (IZO thin films were prepared by low-cost ultrasonic spray pyrolysis (USP. Both a low resistivity (3.13×10−3 Ω cm and an average direct transmittance (400∼1500 nm about 80% of the IZO films were achieved. The IZO films were investigated as anodes in bulk-heterojunction organic photovoltaic (OPV devices based on poly(3-hexylthiophene and [6,6]-phenyl C61-butyric acid methyl ester. The device fabricated on IZO film-coated glass substrate showed an open circuit voltage of 0.56 V, a short circuit current of 8.49 mA cm-2, a fill factor of 0.40, and a power conversion efficiency of 1.91%, demonstrating that the IZO films prepared by USP technique are promising low In content and transparent electrode candidates of low-cost OPV devices.

  11. Fabrication of a molecular-level multilayer film on organic polymer surfaces via chemical bonding assembly.

    Science.gov (United States)

    Zhao, Hongchi; Yang, Peng; Deng, Jianping; Liu, Lianying; Zhu, Jianwu; Sui, Yuan; Lu, Jiaoming; Yang, Wantai

    2007-02-13

    A fresh multilayer film was fabricated on a molecular level and successfully tethered to the surface of a hydroxylated organic substrate via chemical bonding assembly (CBA). Sulfate anion groups (SO4-) were preintroduced onto the surface of biaxially oriented polypropylene (BOPP) films via a reference method. Upon hydrolysis of the SO4- groups, hydroxyl groups (--OH) were formed that subsequently acted as initial reagents for a series of alternate reactions with terephthalyl chloride (TPC) and bisphenol A (BPA). A stable and well-defined multilayer film was thus fabricated via the CBA method. As a result of the nanoscale multilayer fresh film being abundant with reactive groups, it is believed that the film and its fabrication method should provide a fundamental platform for further surface functionalization and direct the design of advanced materials with desired properties.

  12. Flexible barrier film, method of forming same, and organic electronic device including same

    Science.gov (United States)

    Blizzard, John; Tonge, James Steven; Weidner, William Kenneth

    2013-03-26

    A flexible barrier film has a thickness of from greater than zero to less than 5,000 nanometers and a water vapor transmission rate of no more than 1.times.10.sup.-2 g/m.sup.2/day at 22.degree. C. and 47% relative humidity. The flexible barrier film is formed from a composition, which comprises a multi-functional acrylate. The composition further comprises the reaction product of an alkoxy-functional organometallic compound and an alkoxy-functional organosilicon compound. A method of forming the flexible barrier film includes the steps of disposing the composition on a substrate and curing the composition to form the flexible barrier film. The flexible barrier film may be utilized in organic electronic devices.

  13. Organic thin film transistor integration a hybrid approach

    CERN Document Server

    Li, Flora; Wu, Yiliang; Ong, Beng S

    2013-01-01

    Research on organic electronics (or plastic electronics) is driven by the need to create systems that are lightweight, unbreakable, and mechanically flexible. With the remarkable improvement in the performance of organic semiconductor materials during the past few decades, organic electronics appeal to innovative, practical, and broad-impact applications requiring large-area coverage, mechanical flexibility, low-temperature processing, and low cost. Thus, organic electronics appeal to a broad range of electronic devices and products including transistors, diodes, sensors, solar cells, lighting

  14. Organic-​organic interfaces and unoccupied electronic states of thin films of perylene and naphthalene derivatives

    DEFF Research Database (Denmark)

    Kamounah, Fadhil S.; Komolov, A.S; Juul Møller, Preben;

    2005-01-01

    ,4,5,8-naphthalenetetracarboxylic dianhydride (NTCDA, Fig. 1c) film surfaces, respectively, in order to form organic–organic interfaces so that molecules constituting the interfacing layers differ by the substituent group. The surface potential and the density of unoccupied electron states (DOUS) located 5–25 eV above the Fermi...

  15. Fine structures of organic photovoltaic thin films probed by frequency-shift electrostatic force microscopy

    Science.gov (United States)

    Araki, Kento; Ie, Yutaka; Aso, Yoshio; Matsumoto, Takuya

    2016-07-01

    The localized charge and electrostatic properties of organic photovoltaic thin films are predominating factors for controlling energy conversion efficiency. The surface potential and electrostatic structures of organic photovoltaic thin films were investigated by frequency shift mode Kelvin force microscopy (KFM) and electrostatic force microscopy (EFM). The KFM images of a poly[2-methoxy-5-(3‧,7‧-dimethyloctyloxy)-1,4-phenylene vinylene]/phenyl-C61-butyric-acid-methyl ester (PCBM) blend thin film reveals that the PCBM domains precipitate as the topmost layer on the thin films. We find fine structures that were not observed in the topography and KFM images. The bias dependence of the EFM images suggests that the EFM contrast reflects the field-induced polarization, indicating the presence of charge trapping sites.

  16. The Dynamics and Structures of Adsorbed Surfaces

    DEFF Research Database (Denmark)

    Nielsen, M; Ellenson, W. D.; McTague, J. P.

    1978-01-01

    Reviews neutron scattering work performed on films of simple gas atoms and molecules adsorbed primarily on graphite surfaces. Exfoliated graphite substrates such as Grafoil were first used in this kind of measurements about five years ago and new results have been reported at an increasing pace. ...

  17. Corrosion protection by sonoelectrodeposited organic films on zinc coated steel.

    Science.gov (United States)

    Et Taouil, Abdeslam; Mahmoud, Mahmoud Mourad; Lallemand, Fabrice; Lallemand, Séverine; Gigandet, Marie-Pierre; Hihn, Jean-Yves

    2012-11-01

    A variety of coatings based on electrosynthesized polypyrrole were deposited on zinc coated steel in presence or absence of ultrasound, and studied in terms of corrosion protection. Cr III and Cr VI commercial passivation were used as references. Depth profiling showed a homogeneous deposit for Cr III, while SEM imaging revealed good surface homogeneity for Cr VI layers. These chromium-based passivations ensured good protection against corrosion. Polypyrrole (PPy) was also electrochemically deposited on zinc coated steel with and without high frequency ultrasound irradiation in aqueous sodium tartrate-molybdate solution. Such PPy coatings act as a physical barrier against corrosive species. PPy electrosynthesized in silent conditions exhibits similar properties to Cr VI passivation with respect to corrosion protection. Ultrasound leads to more compact and more homogeneous surface structures for PPy, as well as to more homogeneous distribution of doping molybdate anions within the film. Far better corrosion protection is exhibited for such sonicated films. PMID:22516111

  18. A Naphthalenediimide-Based Metal-Organic Framework and Thin Film Exhibiting Photochromic and Electrochromic Properties.

    Science.gov (United States)

    Xie, Yi-Xin; Zhao, Wen-Na; Li, Guo-Chang; Liu, Peng-Fei; Han, Lei

    2016-01-19

    A multifunctional metal-organic framework, NBU-3, has been explored as a 2D three-connected network based on a naphthalenediimide-based ligand. The NBU-3 crystals display photochromic properties, and NBU-3 thin films on FTO substrates exhibit electrochromic properties. NBU-3 is the first example of MOF materials containing both photochromic and electrochromic properties, which can be desirable for thin film devices. PMID:26713454

  19. Simulation of heterojunction organic thin film devices and exciton diffusion analysis in stacked-hetero device

    Science.gov (United States)

    Kamohara, Itaru; Townsend, Mark; Cottle, Bob

    2005-01-01

    A two-dimensional device simulation methodology for organic heterojunction thin film devices has been developed. Multilayer organic light emitting diodes, organic thin film heterojunction field effect transistors, and stacked heterojunction organic complementary devices were simulated. Heterojunction organic layer devices have been analyzed using a two-dimensional simulator with heterointerface models and organic material specific models. The stacked heterojunction organic double carrier device exhibits both horizontal and vertical carrier flow in the organic thin film. This unique dual-directional carrier flow shows efficient electron-hole recombination resulting in exciton generation in the organic heterojunction layers. Furthermore, the enhanced behavior of the generated excitons has been analyzed using a self-consistent exciton diffusion model. The vertical (thickness) diffusion of the excitons and the lateral (along heterointerface) diffusion (accompanied by exciton hopping) were simulated. The exciton diffusion model is applicable to electroluminescent characteristics in organic devices. This feature is one of the essential differences between the present model for high-injected polymer devices and conventional drift-diffusion transport in nonpolymer semiconductor devices.

  20. Plasmon-enhanced charge carrier generation in organic photovoltaic films using silver nanoprisms.

    Science.gov (United States)

    Kulkarni, Abhishek P; Noone, Kevin M; Munechika, Keiko; Guyer, Samuel R; Ginger, David S

    2010-04-14

    We use photoinduced absorption spectroscopy to measure long-lived photogenerated charge carriers in optically thin donor/acceptor conjugated polymer blend films near plasmon-resonant silver nanoprisms. We measure up to 3 times more charge generation, as judged by the magnitude of the polaron absorption signal, in 35 nm thin blend films of poly(3-hexylthiophene)/phenyl-C(61)-butyric acid methyl ester on top of films of silver nanoprisms (approximately 40-100 nm edge length). We find that the polaron yields increase linearly with the total sample extinction. These excitation enhancements could in principle be used to increase photocurrents in thin organic solar cells.

  1. Nanostructuring on zinc phthalocyanine thin films for single-junction organic solar cells

    Science.gov (United States)

    Chaudhary, Dhirendra K.; Kumar, Lokendra

    2016-05-01

    Vertically aligned and random oriented crystalline molecular nanorods of organic semiconducting Zinc Phthalocyanine (ZnPc) have been grown on ITO coated glass substrate using solvent volatilization method. Interesting changes in surface morphology were observed under different solvent treatment. Vertically aligned nanorods of ZnPc thin film were observed in the films treated with acetone, where as the random oriented nanorods were observed in the films treated with chloroform. The X-ray diffraction (XRD), scanning electron microscopy (SEM), atomic force microscopy (AFM) have been used for characterization of nanostructures. The optical properties of the nanorods have been investigated by UV-Vis. absorption spectroscopy.

  2. Removal of formaldehyde by hydroxyapatite layer biomimetically deposited on polyamide film.

    Science.gov (United States)

    Kawai, Takahiro; Ohtsuki, Chikara; Kamitakahara, Masanobu; Tanihara, Masao; Miyazaki, Toshiki; Sakaguchi, Yoshimitsu; Konagaya, Shigeji

    2006-07-01

    Some harmful volatile organic compounds (VOCs), such as formaldehyde, are regulated atmospheric pollutants. Therefore, development of a material to remove these VOCs is required. We focused on hydroxyapatite, which had been biomimetically coated on a polyamide film, as an adsorbent and found that formaldehyde was successfully removed by this adsorbent. The amount of formaldehyde adsorbed increased with the area of the polyamide film occupied by hydroxyapatite. The amount of adsorbed formaldehyde and its rate of adsorption were larger for hydroxyapatite deposited on polyamide film than for the commercially available calcined hydroxyapatite powder. This high adsorption ability is achieved by the use of nanosized particles of hydroxyapatite with low crystallinity and containing a large number of active surface sites. Therefore, hydroxyapatite biomimetically coated on organic substrates can become a candidate material for removing harmful VOCs such as formaldehyde.

  3. An experimental investigation of polymolecular solvate (adsorbed) films as applied to the development of a mathematical theory of the stability of colloids

    Science.gov (United States)

    Derjaguin, B.; Kussakov, M.

    1992-05-01

    After a critical discussion of the current concepts of solvation of surfaces and colloid particles, as well as of the methods of studying solvation, a new quantitative definition of solvation is advanced. This definition connects solvation with the disjoining action of thin layers of liquids, discovered and studied in earlier experiments described in the preceding papers of this series. The present paper describes a new, more convenient method of measuring both the thickness and disjoining action of thin layers for cases when they separate gas bubbles from solids (wetting films). Observations of non-equilibrium states of such wetting films are described. Experimental data are quoted, which are used in establishing an equation of state of a solvate layer. This equation expresses the equilibrium pressure (disjoining action) of a solvate layer for aqueous and non-aqueous media as a function of the thickness of the layer. The effect of electrolytes on the thickness of aqueous solvate films. as well as the influence of surface-active substances upon vaseline-oil films on steel surfaces, has been investigated. A theory of interaction of micelles, taking into account the disjoining action of thin layers of dispersion medium between the micelle surfaces, is advanced. In conclusion, the computations used in the latter theory are employed to elaborate a theory of slow coagulation and stability of colloids and disperse systems.

  4. Wrinkling of YBa2Cu3O7-x film prepared by trifluoroacetate metal organic deposition

    Science.gov (United States)

    Jin, L. H.; Li, C. S.; Yu, Z. M.; Feng, J. Q.; Zhang, S. N.; Sulpice, A.; Wang, Y.; Zhang, P. X.

    2015-11-01

    YBa2Cu3O7-x (YBCO) films with wrinkles have been fabricated on LaAlO3(1 0 0) substrates by trifluoroacetate metal organic deposition (TFA-MOD). The decomposition behavior of YBCO-TFA gel and the formation mechanism of wrinkles were analyzed by thermal analysis, Fourier transform infrared spectroscopy, and atomic force microscopy. The effects of wrinkles on the texture, microstructure and critical current density of the final crystallized film were also investigated by X-ray diffraction and scanning electron microscopy. The heating rate in the decomposition process was a crucial parameter to control the wavelength and wave amplitude of wrinkles on the surface of YBCO precursor film. Furthermore, the wrinkles of precursor films were transformed into the ridges of crystallized films during the crystallization process. Large ridges resulted in the degradation of texture of YBCO crystallized films. The decrease of critical current density (Jc) of YBCO crystallized films could be ascribed to the formation of ridges, the segregated phases and the degradation of texture. It suggested that the smooth morphology of YBCO precursor films would be beneficial to the enhancement of Jc value.

  5. Water Pollution and Treatments Part I: Evaluation of Organic, Inorganic and Marine Products as Adsorbents For Petroleum Pollutants Present In Aqueous Wastes

    International Nuclear Information System (INIS)

    The main objective of the present work is to perform a comparative laboratory study using an adsorption technique for oil removal from the waste water drained to sea from refineries, offshore and/or onshore petroleum installations. Different crushed adsorbent materials, namely, cotton fibers, charcoal, petroleum coke, agriculture wastes (such as, rice straws, wheat stems, milled dry leaves and lignin), inorganic adsorbents (such as sand, and bricks) and a marine Product (such as sponge) are included in this study. They were tested for oil recovery from laboratory prepared oily salt water samples. Two different Egyptian crude oils varying in their properties and several refined products (gasoline, kerosene, gas oil, diesel oil, fuel oil, lubricating oil) and skimmed oil were employed. Their adsorptive efficiencies were tested. Good results were obtained with sponge and cotton fibers. The used agricultural wastes show better adsorption compared with coke and inorganic adsorbents.

  6. Growth-related properties and postgrowth phenomena in organic molecular thin films

    Science.gov (United States)

    Campione, M.; Borghesi, A.; Laicini, M.; Sassella, A.; Goletti, C.; Bussetti, G.; Chiaradia, P.

    2007-12-01

    The problem of monitoring the structural and morphological evolutions of thin films of organic molecular materials during their growth by organic molecular beam epitaxy and in the postgrowth stage is addressed here by a combination of in situ optical reflectance anisotropy measurements, ex situ optical and morphological investigations, and theoretical simulation of the material optical response. For α-quaterthiophene, a representative material in the class of organic molecular semiconductors, the results show that molecules crystallize in the first stage of growth in metastable structures, even when deposition is carried out at room temperature. In the postdeposition stage, the film structure evolves within a few days to the known equilibrium structure of the low temperature polymorph. When deposition is carried out at low substrate temperatures, an evolution of the film morphology is also demonstrated.

  7. Singlet Exciton Lifetimes in Conjugated Polymer Films for Organic Solar Cells

    KAUST Repository

    Dimitrov, Stoichko

    2016-01-13

    The lifetime of singlet excitons in conjugated polymer films is a key factor taken into account during organic solar cell device optimization. It determines the singlet exciton diffusion lengths in polymer films and has a direct impact on the photocurrent generation by organic solar cell devices. However, very little is known about the material properties controlling the lifetimes of singlet excitons, with most of our knowledge originating from studies of small organic molecules. Herein, we provide a brief summary of the nature of the excited states in conjugated polymer films and then present an analysis of the singlet exciton lifetimes of 16 semiconducting polymers. The exciton lifetimes of seven of the studied polymers were measured using ultrafast transient absorption spectroscopy and compared to the lifetimes of seven of the most common photoactive polymers found in the literature. A plot of the logarithm of the rate of exciton decay vs. the polymer optical bandgap reveals a medium correlation between lifetime and bandgap, thus suggesting that the Energy Gap Law may be valid for these systems. This therefore suggests that small bandgap polymers can suffer from short exciton lifetimes, which may limit their performance in organic solar cell devices. In addition, the impact of film crystallinity on the exciton lifetime was assessed for a small bandgap diketopyrrolopyrrole co-polymer. It is observed that the increase of polymer film crystallinity leads to reduction in exciton lifetime and optical bandgap again in agreement with the Energy Gap Law.

  8. Singlet Exciton Lifetimes in Conjugated Polymer Films for Organic Solar Cells

    Directory of Open Access Journals (Sweden)

    Stoichko D. Dimitrov

    2016-01-01

    Full Text Available The lifetime of singlet excitons in conjugated polymer films is a key factor taken into account during organic solar cell device optimization. It determines the singlet exciton diffusion lengths in polymer films and has a direct impact on the photocurrent generation by organic solar cell devices. However, very little is known about the material properties controlling the lifetimes of singlet excitons, with most of our knowledge originating from studies of small organic molecules. Herein, we provide a brief summary of the nature of the excited states in conjugated polymer films and then present an analysis of the singlet exciton lifetimes of 16 semiconducting polymers. The exciton lifetimes of seven of the studied polymers were measured using ultrafast transient absorption spectroscopy and compared to the lifetimes of seven of the most common photoactive polymers found in the literature. A plot of the logarithm of the rate of exciton decay vs. the polymer optical bandgap reveals a medium correlation between lifetime and bandgap, thus suggesting that the Energy Gap Law may be valid for these systems. This therefore suggests that small bandgap polymers can suffer from short exciton lifetimes, which may limit their performance in organic solar cell devices. In addition, the impact of film crystallinity on the exciton lifetime was assessed for a small bandgap diketopyrrolopyrrole co-polymer. It is observed that the increase of polymer film crystallinity leads to reduction in exciton lifetime and optical bandgap again in agreement with the Energy Gap Law.

  9. Latent organizations in the film industry: contracts, rewards and resources

    NARCIS (Netherlands)

    J.J. Ebbers; N.M. Wijnberg

    2009-01-01

    The main aim of this article is to study the extent to which the project-based organization (PBO) and the latent organization determine the actual behavior of actors in a project-based industry and how this is mediated by the types of contracts and rewarding practices these organizational forms allo

  10. Ethanol-mediated metal transfer printing on organic films.

    Science.gov (United States)

    Aldakov, Dmitry; Tondelier, Denis; Palacin, Serge; Bonnassieux, Yvan

    2011-03-01

    Ethanol-mediated metal transfer printing (mTP) is a soft method, which allows to efficiently deposit metals onto various organic surfaces for applications in organic electronics. This simple approach in based on the stronger adhesion of the metals to the organic materials in the presence of thin ethanol layer between the metallized PDMS and the substrate due to the capillary action. Patterns with a resolution of at least 20 μm have been obtained on organic polymeric materials and photoresists without heating or applied pressure. Compared to other methods ethanol mediated mTP is considerably faster and has smaller limitations on the stamp depth. Residual silicone layer detected on the metal surface after the transfer by XPS studies has been mostly removed by UV/ozone treatment. Organic field-effect transistors (OTFTs) based on the metal electrodes deposited by mTP have been successfully fabricated and tested.

  11. Solution-Processed Organic Thin-Film Transistor Array for Active-Matrix Organic Light-Emitting Diode

    Science.gov (United States)

    Harada, Chihiro; Hata, Takuya; Chuman, Takashi; Ishizuka, Shinichi; Yoshizawa, Atsushi

    2013-05-01

    We developed a 3-in. organic thin-film transistor (OTFT) array with an ink-jetted organic semiconductor. All layers except electrodes were fabricated by solution processes. The OTFT performed well without hysteresis, and the field-effect mobility in the saturation region was 0.45 cm2 V-1 s-1, the threshold voltage was 3.3 V, and the on/off current ratio was more than 106. We demonstrated a 3-in. active-matrix organic light-emitting diode (AMOLED) display driven by the OTFT array. The display could provide clear moving images. The peak luminance of the display was 170 cd/m2.

  12. High mobility organic thin-film transistors based on p-p heterojunction buffer layer

    Science.gov (United States)

    Qian, Xianrui; Wang, Tong; Yan, Donghang

    2013-10-01

    The p-p heterojunction of 5, 6, 11, 12-tetraphenylnaphthacene/vanadyl phthalocyanine, which has been used as the buffer layer, is demonstrated. The highest field-effect mobility is 5.1 cm2/Vs, which is one of the highest reported for polycrystalline rubrene thin film transistors. Current versus voltage characteristics of heterojunction diodes are utilized to investigate the charge injection mechanism, revealing the factors that bring about the improvement of carrier injection and the reduction of contact resistance. These results suggest that our approach is very promising to fabricate high performance organic thin-film transistors for practical applications in organic electronics.

  13. Transmission through Ag/Organic Multilayers Using Continuous and Island Metal Films

    Institute of Scientific and Technical Information of China (English)

    LI Heng; ZHENG Ning

    2011-01-01

    @@ We present the results of transmission spectrum measurements of Ag/tetraphenyldiphenyldiamine periodic mul- tilayers, as well as Ag/SiO in the visible and near IR spectral range.Using continuous silver films, these one-dimensional multilayers transmit visible light in controllable bands and stop IR light.Using island metal films, surface plasmon modes are excited, which exhibits broad absorption features covering the entire visible spectral range.This work successfully extends the discussion of metal-dielectric one-dimensional photonic crys- tals to metal-organic cases and exhibits the linear optical properties of surface plasmon modes at the island metal/organic interface.

  14. Metal-Organic Coordination Network Thin Film by Surface-Induced Assembly.

    Science.gov (United States)

    Laokroekkiat, Salinthip; Hara, Mitsuo; Nagano, Shusaku; Nagao, Yuki

    2016-07-01

    The growth of metal-organic coordination network thin films on surfaces has been pursued extensively and intensively to manipulate the molecular arrangement. For this study, the oriented multilayer thin films based on porphyrinic nanoarchitecture were synthesized toward metal-organic coordination networks using surface-induced assembly (SIA). Nanoscale molecular thin films were prepared at room temperature using cobalt(II) ion and porphyrin building blocks as precursors. Stepwise growth with a highly uniform layer was characterized using UV-vis, AFM, IR, and XPS studies. The grazing incidence small-angle X-ray scattering and X-ray reflectivity results remarkably suggested a periodic structure in in-plane direction with constant and high mass density (ca. 1.5 g/cm(3)) throughout the multilayer formation. We propose that orientation of the porphyrin macrocycle plane with a hexagonal packed model by single anchoring mode was tilted approximately 60° with respect to the surface substrate. It is noteworthy that the well-organized structure of porphyrin-based macrocyclic framework on the amine-terminated surface substrate can be achieved efficiently using a simple SIA approach under mild synthetic conditions. The synthesized thin film provides a different structure from that obtained using bulk synthesis. This result suggests that the SIA technique can control not only the film thickness but also the structural arrangement on the surface. This report of our research provides insight into the ordered porphyrin-based metal-organic coordination network thin films, which opens up opportunities for exploration of unique thin film materials for diverse applications.

  15. Molecular Dynamics Study of Ionic Liquid Film Based on [emim][Tf2N] and [emim][TfO] Adsorbed on Highly Oriented Pyrolytic Graphite

    Institute of Scientific and Technical Information of China (English)

    XUE Xiang-gui; ZHAO Li; L(U) Zhong-yuan; QIAN Hu-iun

    2013-01-01

    Molecular dynamics simulation was used to study the ionic liquid(IL) crystalline film based on 1-ethyl-3-methylimidazolium bis[trifluoromethylsulfonyl]imide([emim][Tf2N]) and 1-ethyl-3-methylimidazolium trifluoromethanesulfonate([emim][TfO]) on the graphite surface.Our results show that the cations are parallelly dis-tributed to the surface in the l/2 monolayer(ML) crystalline film.The [Tf2N] anions are parallel to the surface with the oxygen atoms at the bottom,whereas the [TfO] anions are perpendicularly distributed to the surface also with the oxygen atoms at the bottom in the 1/2 ML crystalline film.It has been found that the IL-vapor interface strongly influences the arrangement of ions at the interface.The anions in the top layer with the oxygen atoms outmost turn over to make themselves with the F atoms outmost so as to form C-H...O hydrogen bonds with the cations.The calculated orientational ordering shows that in the outmost layer at the IL-vapor interface,the cation rings present either parallel or perpendicular to the surface at 350 K.

  16. VERUCLAY – a new type of photo-adsorbent active in the visible light range: modification of montmorillonite surface with organic surfactant

    Science.gov (United States)

    Montmorillonite K10 was treated with VeruSOL-3, a biodegradable and food-grade surfactant mixture of coconut oil, castor oil and citrus extracts, to manufacture a benign catalytic adsorbent that is active in the visible light. Veruclay was characterized by SEM, XRD, TGA, UVDRS, a...

  17. Batch Scale Removal of an Organic Pollutant Amaranth Dye from Aqueous Solution using Pisum sativum Peels and Arachis hypogaea Shells as Adsorbents

    International Nuclear Information System (INIS)

    The goal of this study was to utilize low cost and environmentally friendly adsorbents for batch scale removal of Amaranth dye from aqueous medium. Peels of Pisum sativum (Pea) and Arachis hypogaea (Peanut) were utilized to investigate their dye removing capacity. The optimized adsorption conditions for Pisum sativum (P.S.P) and Arachis hypogaea (A.H.S) were: adsorbent dose; 0.6 and 0.4 g, contact time; 45 and 10 minutes, pH; 2.0 for both, agitation speed; 150 and 100 rpm and temperature; 60 and 50 degree C for P.S.P and A.H.S respectively. The adsorption data well suited to Langmuir isotherm. Maximum adsorption capacities were found to be 144.93 and 10.53 mg/g for P.S.P and A.H.S respectively. Feasibility of the process was indicated by negative values of thermodynamic parameters delta G/sup 0/ for both adsorbents. Kinetic studies indicated that adsorption of Amaranth dye from aqueous medium by Pisum sativum peels and Arachis hypogaea shells followed pseudo-seconder order kinetics. It was concluded that Pisum sativum peels are more effective adsorbent for removal of Amaranth from aqueous solution as compared to Arachis hypogaea shells. (author)

  18. Optical properties of organic semiconductor thin films. Static spectra and real-time growth studies

    Energy Technology Data Exchange (ETDEWEB)

    Heinemeyer, Ute

    2009-07-20

    The aim of this work was to establish the anisotropic dielectric function of organic thin films on silicon covered with native oxide and to study their optical properties during film growth. While the work focuses mainly on the optical properties of Diindenoperylene (DIP) films, also the optical response of Pentacene (PEN) films during growth is studied for comparison. Spectroscopic ellipsometry and differential reflectance spectroscopy are used to determine the dielectric function of the films ex-situ and in-situ, i.e. in air and in ultrahigh vacuum. Additionally, Raman- and fluorescence spectroscopy is utilized to characterize the DIP films serving also as a basis for spatially resolved optical measurements beyond the diffraction limit. Furthermore, X-ray reflectometry and atomic force microscopy are used to determine important structural and morphological film properties. The absorption spectrum of DIP in solution serves as a monomer reference. The observed vibronic progression of the HOMO-LUMO transition allows the determination of the Huang-Rhys parameter experimentally, which is a measure of the electronic vibrational coupling. The corresponding breathing modes are measured by Raman spectroscopy. The optical properties of DIP films on native oxide show significant differences compared to the monomer spectrum due to intermolecular interactions. First of all, the thin film spectra are highly anisotropic due to the structural order of the films. Furthermore the Frenkel exciton transfer is studied and the energy difference between Frenkel and charge transfer excitons is determined. Real-time measurements reveal optical differences between interfacial or surface molecules and bulk molecules that play an important role for device applications. They are not only performed for DIP films but also for PEN films. While for DIP films on glass the appearance of a new mode is visible, the spectra of PEN show a pronounced energy red-shift during growth. It is shown how the

  19. Organic-inorganic Hybrids Towards the Preparation of Nanoporous Composite Thin Films for Microelectronic Application

    Institute of Scientific and Technical Information of China (English)

    2002-01-01

    Silicon containing materials have traditionally been used in microelectronic fabrication. Semiconductor devices often have one or more arrays of patterned interconnect levels that serve to electrically couple the individual circuit elements forming an integrated circuit. These interconnect levels are typically separated by an insulating or dielectric film. Previously, a silicon oxide film was the most commonly used material for such dielectric films having dielectric constants(k) near 4. 0. However, as the feature size is continuously scaling down, the relatively high k of such silicon oxide films became inadequate to provide efficient electrical insulation. As such, there has been an increasing market demand for materials with even lower dielectric constant for Interlayer Dielectric (ILD) applications, yet retaining thermal and mechanical integrity. We wish to report here our investigations on the preparation of ultra-low k ILD materials using a sacrificial approach whereby organic groups are burnt out to generate low k porous ORMOSIL films. We have been able to prepare a variety of organically modified silicone resins leading to highly microporous thin films, exhibiting ultra-low k from 1.80 to 2.87, and good to high modulus, 1.5 to 5.5 Gpa. Structure property influences on porosity, dielectric constant and modulus will be discussed.

  20. Controlled Microstructure and Photochromism of Inorganic-organic Thin Films by Ultrasound

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    A series of inorganic-organic thin films based on uniformly dispersed nanoparticles of polyoxometalates (POM)entrapped in polyacrylamide (PAM) matrix were prepared by ultrasonic method with different irradiation time.The microstructure, photochromic behavior and mechanism of the films were studied by transmission electron microscopy (TEM), ultraviolet-visible spectra (UV-VIS) and Fourier transform-infrared spectroscopy (FT-IR).The microstructure and photochromic properties of the hybrid thin films could be controlled by ultrasound.TEM image revealed that the average size of phosphotungstic acid (PWA) nanoparticles decreased from 20 to 10 nm with the ultrasound irradiation time from 30 to 60 min. After irradiated with ultraviolet light,the transparent films changed from colorless to blue and showed reversible photochromism. The hybrid film, with ultrasound irradiation for 60 min had higher photochromic efficiency and faster bleaching reaction than the one with ultrasound irradiation for 30 min. FT-IR spectra showed that the Keggin geometry of heteropolyoxometalate was still preserved inside the composites, and the interactions between polyanions and polymer matrix increased as the ultrasound time prolonged. It is suggested that the mechanism of the different photochromic properties for the inorganic-organic thin films is the variation of the microstructure and interfacial interactions induced by ultrasound.

  1. Biological activities of organic compounds adsorbed onto ambient air particles: comparison between the cities of Teplice and Prague during the summer and winter seasons 2000-2001

    Energy Technology Data Exchange (ETDEWEB)

    Binkova, Blanka; Cerna, Milena; Pastorkova, Anna; Jelinek, Richard; Benes, Ivan; Novak, Jiri; Sram, Radim J

    2003-04-09

    The capital of the Czech Republic, Prague, appears today to be one of the most polluted residential areas in the country, whereas air pollution in the Northern Bohemia region (the former 'Black Triangle Region') has substantially decreased during the last decade, especially with respect to the gaseous pollutant SO{sub 2}. This study evaluated the biological activities of complex mixtures of organic compounds adsorbed onto ambient air particles (PM10) collected during the summer and winter seasons of 2000-2001 at three monitoring sites - Teplice (TP), Prague-Smichov (PRG-SM) (city centre) and Prague-Libus (PRG-LB) (suburban area). The following short-term in vitro assays with strikingly different endpoints were used: a bacterial mutagenicity test using the Salmonella typhimurium tester strain TA98 and YG1041, an acellular assay (CT DNA) combined with {sup 32}P-postlabelling to evaluate DNA adduct-forming potency and the chick embryotoxicity screening test (CHEST). The results of the mutagenicity test with the YG1041 strain, the acellular genotoxicity (DNA adducts) and the embryotoxicity tests responded to the amount of eight carcinogenic polycyclic aromatic hydrocarbons (PAHs) analysed in the EOM (dichloromethane extractable organic matter) samples tested. Nevertheless, the biological effects of the EOM did not differ between locations. The highest biological activity of the ambient air in terms of organic compounds associated with particles (per unit volume of air) was seen in the Prague city centre during both summer and winter seasons. At this location, B[a]P concentration ranged from 0.1 to 8.9 ng/m{sup 3} (mean 0.3 and 3.6 ng/m{sup 3} for summer and winter seasons, respectively), 13 PAHs ranged from 11 to 343 ng/m{sup 3} (mean 52 and 160 ng/m{sup 3} for summer and winter seasons, respectively). Generally, using in vitro tests, higher ambient air activity was found in the winter season as compared with the summer season at all three monitoring sites

  2. XANES analysis of tribochemical and thermal films generating from some organic polysulfides

    Institute of Scientific and Technical Information of China (English)

    YI Hongling; ZENG Xiangqiong; CAO Yan; REN Tianhui; M. Kasrai; G. M. Bancroft

    2006-01-01

    X-ray absorption near edge structure (XANES) spectroscopy has been firstly used to characterize the chemical nature of tribochemical and thermal films generated from alkyl, benzyl and acylcontaining organic polysulfides. It has been found that the thermal films generated from these polysulfides are mainly composed of FeSO4, and alkyl disulfides also exist in the subsurface and bulk of thermal films generated from acyl-containing polysulfides. Under tribochemical conditions, the composition of film is dependent on the molecular structure of the additives.Namely, the tribochemical film generated from alkyl polysulfide is composed of alkyl disulfide in the out surface, a mixture of FeSO4, FeS2 and sulfoxide in the subsurface, and FeSO4 in the bulk; the composition of the tribochemical film for benzyl polysulfide consists of FeSO4 in the out surface, while the composition in subsurface and bulk is the same as the alkyl polysulfide. For acyl-containing polysulfides, the tribochemical films consist of alkyl disulfide in the out surface, and FeS2 in the subsurface and bulk.

  3. Rapidly Thermal Annealed Si-Doped In2O3 Films for Organic Photovoltaics.

    Science.gov (United States)

    Lee, Hye-Min; Kim, Han-Ki

    2015-10-01

    We report the electrical, optical, and structural properties of Si-doped In2O3 (ISO) films prepared using co-sputtering system with multi cathode guns for use in organic photovoltaics (OPVs). We investigated the effect of Si doping power on the electrical, optical, and structural properties of ISO film that was rapidly thermally annealed at a temperature of 400 °C. Due to the high Lewis acid strength (8.096) of the Si dopant, the ISO films showed high mobility and low resistivity despite the low Si doping concentration. Low resistivity of the annealed ISO films indicated that Si(4+) acts as an effective dopant of an In2O3 matrix by substitution with the In(3+) site. At a Si doping power of 50 W, ISO film showed a sheet resistance of 19.7 Ohm/square and optical transparency of 76.7%, which are acceptable values for fabrication of OPVs. Successful operation of OPV cells fabricated on transparent ISO film indicates that ISO is a promising high mobility transparent electrode material and alternative to conventional ITO films.

  4. Nanomechanical investigation of thin-film electroceramic/metal-organic framework multilayers

    International Nuclear Information System (INIS)

    Thin-film multilayer stacks of mechanically hard magnetron sputtered indium tin oxide (ITO) and mechanically soft highly porous surface anchored metal-organic framework (SURMOF) HKUST-1 were studied using nanoindentation. Crystalline, continuous, and monolithic surface anchored MOF thin films were fabricated using a liquid-phase epitaxial growth method. Control over respective fabrication processes allowed for tuning of the thickness of the thin film systems with a high degree of precision. It was found that the mechanical indentation of such thin films is significantly affected by the substrate properties; however, elastic parameters were able to be decoupled for constituent thin-film materials (EITO ≈ 96.7 GPa, EHKUST−1 ≈ 22.0 GPa). For indentation of multilayer stacks, it was found that as the layer thicknesses were increased, while holding the relative thickness of ITO and HKUST-1 constant, the resistance to deformation was significantly altered. Such an observation is likely due to small, albeit significant, changes in film texture, interfacial roughness, size effects, and controlling deformation mechanism as a result of increasing material deposition during processing. Such effects may have consequences regarding the rational mechanical design and utilization of MOF-based hybrid thin-film devices

  5. Nanomechanical investigation of thin-film electroceramic/metal-organic framework multilayers

    Energy Technology Data Exchange (ETDEWEB)

    Best, James P., E-mail: james.best@empa.ch, E-mail: engelbert.redel@kit.edu, E-mail: christof.woell@kit.edu; Michler, Johann; Maeder, Xavier [Empa, Swiss Federal Laboratories for Materials Science and Technology, Laboratory for Mechanics of Materials and Nanostructures, Feuerwerkerstrasse 39, CH-3602 Thun (Switzerland); Liu, Jianxi; Wang, Zhengbang; Tsotsalas, Manuel; Liu, Jinxuan; Gliemann, Hartmut; Weidler, Peter G.; Redel, Engelbert, E-mail: james.best@empa.ch, E-mail: engelbert.redel@kit.edu, E-mail: christof.woell@kit.edu; Wöll, Christof, E-mail: james.best@empa.ch, E-mail: engelbert.redel@kit.edu, E-mail: christof.woell@kit.edu [Institute of Functional Interfaces (IFG), Karlsruhe Institute of Technology (KIT), Hermann-von-Helmholtz-Platz 1, 76344 Eggenstein-Leopoldshafen (Germany); Röse, Silvana [Preparative Macromolecular Chemistry, Institute for Chemical Technology and Polymer Chemistry (ICTP), Karlsruhe Institute of Technology (KIT), Engesserstrasse 18, 76128 Karlsruhe (Germany); Institute for Biological Interfaces (IBG), Karlsruhe Institute of Technology (KIT), Herrmann-von-Helmholtz-Platz 1, 76344 Eggenstein-Leopoldshafen (Germany); Oberst, Vanessa [Institute of Applied Materials (IAM), Karlsruhe Institute of Technology (KIT), Hermann-von-Helmholtz-Platz 1, 76344 Eggenstein-Leopoldshafen (Germany); Walheim, Stefan [Institute of Nanotechnology (INT), Karlsruhe Institute of Technology (KIT), Hermann-von-Helmholtz-Platz 1, 76344 Eggenstein-Leopoldshafen (Germany)

    2015-09-07

    Thin-film multilayer stacks of mechanically hard magnetron sputtered indium tin oxide (ITO) and mechanically soft highly porous surface anchored metal-organic framework (SURMOF) HKUST-1 were studied using nanoindentation. Crystalline, continuous, and monolithic surface anchored MOF thin films were fabricated using a liquid-phase epitaxial growth method. Control over respective fabrication processes allowed for tuning of the thickness of the thin film systems with a high degree of precision. It was found that the mechanical indentation of such thin films is significantly affected by the substrate properties; however, elastic parameters were able to be decoupled for constituent thin-film materials (E{sub ITO} ≈ 96.7 GPa, E{sub HKUST−1} ≈ 22.0 GPa). For indentation of multilayer stacks, it was found that as the layer thicknesses were increased, while holding the relative thickness of ITO and HKUST-1 constant, the resistance to deformation was significantly altered. Such an observation is likely due to small, albeit significant, changes in film texture, interfacial roughness, size effects, and controlling deformation mechanism as a result of increasing material deposition during processing. Such effects may have consequences regarding the rational mechanical design and utilization of MOF-based hybrid thin-film devices.

  6. Ordered nanocolumn-array organic semiconductor thin films with controllable molecular orientation

    Science.gov (United States)

    Yang, Bingchu; Duan, Haichao; Zhou, Conghua; Gao, Yongli; Yang, Junliang

    2013-12-01

    Ordered nanocolumn-array phthalocynine semiconductor thin films with controllable molecular orientation were fabricated by combining molecular template growth (MTG) and glancing angle deposition (GLAD) techniques. The pre-deposited planar perylene-3,4,9,10-tetracarboxylic-3,4,9,10-dianhydride (PTCDA) molecular template layer induces phthalocynine molecules arrange with a lying-down molecular orientation, in which the π-π stacking is vertical to the substrate improving the charge transport along the vertical direction; While the GLAD technique supports the formation of nanocolumn-array thin films, supplying a much larger exposed surface area than the conventional compact thin films. The ordered nanocolumn-array thin films with controllable molecular orientation fabricated by combining MTG and GLAD techniques show the potentials to fabricate ordered bulk heterojunction for improving the performance in organic photovoltaics.

  7. Tunable electrical conductivity in oriented thin films of tetrathiafulvalene-based covalent organic framework

    Energy Technology Data Exchange (ETDEWEB)

    Cai, SL; Zhang, YB; Pun, AB; He, B; Yang, JH; Toma, FM; Sharp, ID; Yaghi, OM; Fan, J; Zheng, SR; Zhang, WG; Liu, Y

    2014-09-16

    Despite the high charge-carrier mobility in covalent organic frameworks (COFs), the low intrinsic conductivity and poor solution processability still impose a great challenge for their applications in flexible electronics. We report the growth of oriented thin films of a tetrathiafulvalene-based COF (TTF-COF) and its tunable doping. The porous structure of the crystalline TTF-COF thin film allows the diffusion of dopants such as I-2 and tetracyanoquinodimethane (TCNQ) for redox reactions, while the closely packed 2D grid sheets facilitate the cross-layer delocalization of thus-formed TTF radical cations to generate more conductive mixed-valence TTF species, as is verified by UV-vis-NIR and electron paramagnetic resonance spectra. Conductivity as high as 0.28 S m(-1) is observed for the doped COF thin films, which is three orders of magnitude higher than that of the pristine film and is among the highest for COF materials.

  8. Preparation of porous titanium oxide films onto indium tin oxide for application in organic photovoltaic devices

    Energy Technology Data Exchange (ETDEWEB)

    Macedo, Andreia G. [Laboratorio de Dispositivos Nanoestruturados, Departamento de Fisica, Universidade Federal do Parana, Curitiba, Parana (Brazil); Mattos, Luana L.; Spada, Edna R.; Serpa, Rafael B.; Campos, Cristiani S. [Laboratorio de Sistemas Nanoestruturados, Departamento de Fisica, Universidade Federal de Santa Catarina, Florianopolis, Santa Catarina (Brazil); Grova, Isabel R.; Ackcelrud, Leni [Laboratorio de Polimeros Paulo Scarpa, Departamento de Quimica, Universidade Federal do Parana, Curitiba, Parana (Brazil); Reis, Francoise T.; Sartorelli, Maria L. [Laboratorio de Sistemas Nanoestruturados, Departamento de Fisica, Universidade Federal de Santa Catarina, Florianopolis, Santa Catarina (Brazil); Roman, Lucimara S., E-mail: lsroman@fisica.ufpr.br [Laboratorio de Dispositivos Nanoestruturados, Departamento de Fisica, Universidade Federal do Parana, Curitiba, Parana (Brazil)

    2012-05-01

    In this work, porous ordered TiO{sub 2} films were prepared through sol gel route by using a monolayer of polystyrene spheres as template on indium-tin oxide/glass substrate. These films were characterized by SEM, AFM, Raman spectroscopy, UV-vis absorbance and XRD. The UV-vis absorbance spectrum show a pseudo band gap (PBG) with maxima at 460 nm arising from the light scattering and partial or total suppression of the photon density of states, this PBG can be controlled by the size of the pore. We also propose the use of this porous film as electron acceptor electrode in organic photovoltaic cells; we show that devices prepared with porous titania displayed higher efficiencies than devices using compact titania films as electrode. Such behaviour was observed in both bilayer and bulk heterojunction devices.

  9. Mapping chemical concentration in binary thin organic films via multi-wavelength scanning absorption microscopy (MWSAM)

    Science.gov (United States)

    Berriman, Garth; Routley, Ben; Holdsworth, John; Zhou, Xiaojing; Belcher, Warwick; Dastoor, Paul

    2014-09-01

    The composition and thickness of binary thin organic films is determined by measuring the optical absorption at multiple wavelengths across the film surface and performing a component analysis fit to absorption standards for the materials. The multiple laser wavelengths are focused onto the surface using microscope objectives and raster scanned across the film surface using a piezo-electric actuator X-Y stage. All of the wavelengths are scanned simultaneously with a frequency division multiplexing system used to separate the individual wavelength response. The composition values are in good quantitative agreement with measurements obtained by scanning transmission x-ray microscopy (STXM). This new characterization technique extends quantitative compositional mapping of thin films to thickness regimes beyond that accessible by STXM.

  10. Thin aligned organic polymer films for liquid crystal devices

    CERN Document Server

    Foster, K E

    1997-01-01

    This project was designed to investigate the possibility of producing alignment layers for liquid crystal devices by cross-linking thin films containing anisotropic polymer bound chromophores via irradiation with polarised ultraviolet light. Photocross-linkable polymers find use in microelectronics, liquid crystal displays, printing and UV curable lacquers and inks; so there is an increasing incentive for the development of new varieties of photopolymers in general. The synthesis and characterisation of two new photopolymers that are suitable as potential alignment layers for liquid crystal devices are reported in this thesis. The first polymer contains the anthracene chromophore attached via a spacer unit to a methacrylate backbone and the second used a similarly attached aryl azide group. Copolymers of the new monomers with methyl methacrylate were investigated to establish reactivity ratios in order to understand composition drift during polymerisation.

  11. Thin aligned organic polymer films for liquid crystal devices

    International Nuclear Information System (INIS)

    This project was designed to investigate the possibility of producing alignment layers for liquid crystal devices by cross-linking thin films containing anisotropic polymer bound chromophores via irradiation with polarised ultraviolet light. Photocross-linkable polymers find use in microelectronics, liquid crystal displays, printing and UV curable lacquers and inks; so there is an increasing incentive for the development of new varieties of photopolymers in general. The synthesis and characterisation of two new photopolymers that are suitable as potential alignment layers for liquid crystal devices are reported in this thesis. The first polymer contains the anthracene chromophore attached via a spacer unit to a methacrylate backbone and the second used a similarly attached aryl azide group. Copolymers of the new monomers with methyl methacrylate were investigated to establish reactivity ratios in order to understand composition drift during polymerisation. (author)

  12. Characteristic energy losses of electrons in organic NTCDA-films

    CERN Document Server

    Komolov, S A; Sidorenko, A G; Alyaev, Y G; Novolodskij, V A

    2001-01-01

    The studies on the characteristic energy losses of slow electrons in the NTCDA thin film on the ZnO (0001) surface are presented. It is shown, that the spectrum of the energy losses (E sub p =4.0; 5.6; 12.5 and 14.5 eV) in the area of low energies (< 60 eV) reflects the structure of transitions between the valency zone and the conductivity zone. The energy losses on the plasma oscillations excitation the excitation of pi-plasmon with the energy of 6.5 eV and excitation of the pi-sigma plasmon with the energy of 25 eV become prevailing with the growth of the initial electrons energy

  13. Layer-by-layer deposited organic/inorganic hybrid multilayer films containing noncentrosymmetrically orientated azobenzene chromophores.

    Science.gov (United States)

    Kang, En-Hua; Bu, Tianjia; Jin, Pengcheng; Sun, Junqi; Yang, Yanqiang; Shen, Jiacong

    2007-07-01

    Organic/inorganic hybrid multilayer films with noncentrosymmetrically orientated azobenzene chromophores were fabricated by the sequential deposition of ZrO2 layers by a surface sol-gel process and subsequent layer-by-layer (LbL) adsorption of the nonlinear optical (NLO)-active azobenzene-containing polyanion PAC-azoBNS and poly(diallyldimethylammonium chloride) (PDDA). Noncentrosymmetric orientation of the NLO-active azobenzene chromophores was achieved because of the strong repulsion between the negatively charged ZrO(2) and the sulfonate groups of the azobenzene chromophore in PAC-azoBNS. Regular deposition of ZrO(2)/PAC-azoBNS/PDDA multilayer films was verified by UV-vis absorption spectroscopy and quartz crystal microbalance measurements. Both UV-vis absorption spectroscopy and transmission second harmonic generation (SHG) measurements confirmed the noncentrosymmetric orientation of the azobenzene chromophores in the as-prepared ZrO2/PAC-azoBNS/PDDA multilayer films. The square root of the SHG signal (I(2omega)(1/2)) increases with the increase of the azobenzene graft ratio in PAC-azoBNS as the number of deposition cycles of the ZrO(2)/PAC-azoBNS/PDDA films remains the same, while the second-order susceptibility chi(zzz)(2) of the film decreases with the increase of the azobenzene graft ratio. Furthermore, the present method was successfully extended to realize the noncentrosymmetric orientation of azobenzene chromophores in multilayer films when small organic azobenzene compounds with carboxylic acid and/or hydroxyl groups at one end and sulfonate groups at the other end were used. The present method was characterized by its simplicity and flexibility in film preparation, and it is anticipated to be a facile way to fabricate second-order nonlinear optical film materials. PMID:17555337

  14. V2O5 thin film deposition for application in organic solar cells

    Science.gov (United States)

    Arbab, Elhadi A. A.; Mola, Genene Tessema

    2016-04-01

    Vanadium pentoxide V2O5 films were fabricated by way of electrochemical deposition technique for application as hole transport buffer layer in organic solar cell. A thin and uniform V2O5 films were successfully deposited on indium tin oxide-coated glass substrate. The characterization of surface morphology and optical properties of the deposition suggest that the films are suitable for photovoltaic application. Organic solar cell fabricated using V2O5 as hole transport buffer layer showed better devices performance and environmental stability than those devices fabricated with PEDOT:PSS. In an ambient device preparation condition, the power conversion efficiency increases by nearly 80 % compared with PEDOT:PSS-based devices. The devices lifetime using V2O5 buffer layer has improved by a factor of 10 over those devices with PEDOT:PSS.

  15. Film-coupled nanoparticles by atomic layer deposition: Comparison with organic spacing layers

    Energy Technology Data Exchange (ETDEWEB)

    Ciracì, Cristian, E-mail: cristian.ciraci@duke.edu; Mock, Jack J.; McGuire, Felicia; Liu, Xiaojun; Smith, David R. [Center for Metamaterials and Integrated Plasmonics and Department of Electrical and Computer Engineering, Duke University, Durham, North Carolina 27708 (United States); Chen, Xiaoshu; Oh, Sang-Hyun [Department of Electrical and Computer Engineering, University of Minnesota, Minneapolis, Minnesota 55455 (United States)

    2014-01-13

    Film-coupled nanoparticle systems have proven a reliable platform for exploring the field enhancement associated with sub-nanometer sized gaps between plasmonic nanostructures. In this Letter, we present a side-by-side comparison of the spectral properties of film-coupled plasmon-resonant, gold nanoparticles, with dielectric spacer layers fabricated either using atomic layer deposition or using organic layers (polyelectrolytes or self-assembled monolayers of molecules). In either case, large area, uniform spacer layers with sub-nanometer thicknesses can be accurately deposited, allowing extreme coupling regimes to be probed. The observed spectral shifts of the nanoparticles as a function of spacer layer thickness are similar for the organic and inorganic films and are consistent with numerical calculations taking into account the nonlocal response of the metal.

  16. Hard X-rays for processing hybrid organic-inorganic thick films.

    Science.gov (United States)

    Jiang, Yu; Carboni, Davide; Pinna, Alessandra; Marmiroli, Benedetta; Malfatti, Luca; Innocenzi, Plinio

    2016-01-01

    Hard X-rays, deriving from a synchrotron light source, have been used as an effective tool for processing hybrid organic-inorganic films and thick coatings up to several micrometres. These coatings could be directly modified, in terms of composition and properties, by controlled exposure to X-rays. The physico-chemical properties of the coatings, such as hardness, refractive index and fluorescence, can be properly tuned using the interaction of hard X-rays with the sol-gel hybrid films. The changes in the microstructure have been correlated especially with the modification of the optical and the mechanical properties. A relationship between the degradation rate of the organic groups and the rise of fluorescence from the hybrid material has been observed; nanoindentation analysis of the coatings as a function of the X-ray doses has shown a not linear dependence between thickness and film hardness.

  17. Maximum probing depth of low-energy photoelectrons in an amorphous organic semiconductor film

    Energy Technology Data Exchange (ETDEWEB)

    Ozawa, Yusuke [Graduate School of Advanced Integration Science, Chiba University, 1-33 Yayoi-cho, Inage-ku, Chiba 263-8522 (Japan); Nakayama, Yasuo, E-mail: nkym@restaff.chiba-u.jp [Graduate School of Advanced Integration Science, Chiba University, 1-33 Yayoi-cho, Inage-ku, Chiba 263-8522 (Japan); Machida, Shin’ichi; Kinjo, Hiroumi [Graduate School of Advanced Integration Science, Chiba University, 1-33 Yayoi-cho, Inage-ku, Chiba 263-8522 (Japan); Ishii, Hisao [Graduate School of Advanced Integration Science, Chiba University, 1-33 Yayoi-cho, Inage-ku, Chiba 263-8522 (Japan); Center for Frontier Science, Chiba University, 1-33 Yayoi-cho, Inage-ku, Chiba 263-8522 (Japan)

    2014-12-15

    Highlights: • Photoelectron attenuation lengths (AL) through amorphous organic films were examined. • In the energy range below 9 eV, AL fluctuates unlike a prediction by universal curve. • AL of photoelectron yield spectroscopy (PYS) measurements was found to be ∼3.6 nm. • PYS signals still survived through an 18 nm-thick film despite such a moderate AL. • This indicates buried interfaces in practical organic devices can be accessed by PYS. - Abstract: The attenuation length (AL) of low energy photoelectrons inside a thin film of a π-conjugated organic semiconductor material, 2,2′,2″-(1,3,5-benzinetriyl)-tris(1-phenyl-1-H-benzimidazole), was investigated using ultraviolet photoelectron spectroscopy (UPS) and photoelectron yield spectroscopy (PYS) to discuss their probing depth in amorphous organic thin films. The present UPS results indicated that the AL is 2–3 nm in the electron energy range of 6.3–8.3 eV with respect to the Fermi level, while the PYS measurements which collected the excited electrons in a range of 4.5–6 eV exhibited a longer AL of 3.6 nm. Despite this still short AL in comparison to a typical thickness range of electronic devices that are a few tens of nm-thick, the photoemission signal penetrating through further thicker (18 nm) organic film was successfully detected by PYS. This fact suggests that the electronic structures of “buried interfaces” inside practical organic devices are accessible using this rather simple measurement technique.

  18. Thermal stability and partial dewetting of crystalline organic thin films: 3,4,9,10-perylenetetracarboxylic dianhydride on Ag(111)

    OpenAIRE

    Krause, B.; Dürr, A. C.; Schreiber, F.; Dosch, H.; Seeck, O

    2003-01-01

    The thermal stability and dewetting effects of crystalline organic thin films on inorganic substrates have been investigated for a model system for organic epitaxy, 3,4,9,10-perylenetetracarboxylic dianhydride (PTCDA) on Ag(111). The thin films deposited under a variety of growth conditions have been annealed stepwise and studied by in situ x-ray diffraction and noncontact atomic force microscopy. It has been found that comparatively smooth films deposited at temperatures T(g)less than or sim...

  19. Solvent Vapor Treatment Effects on Poly(3-hexylthiophene Thin Films and its Application for Interpenetrating Heterojunction Organic Solar Cells

    Directory of Open Access Journals (Sweden)

    Masanori Ozaki

    2010-11-01

    Full Text Available The solvent vapor treatment (SVT for poly(3-hexylthiophene (PAT6 films and its application to interpenetrating heterojunction organic solar cells have been studied. It was found that SVT could improve the crystallinity and electrical characteristics of the PAT6 films. We fabricated organic solar cells with an interpenetrating structure of PAT6 and fullerenes utilizing the SVT process, and discuss the improved performance of the solar cells by taking the film crystallinity, optical properties, and morphology into consideration.

  20. Influence of source gas flow ratio on the proteins adsorbability of F-DLC film%源气体流量比对氟化类金刚石薄膜蛋白吸附能力的影响

    Institute of Scientific and Technical Information of China (English)

    戴永丰; 江美福; 杨亦赏; 周杨

    2011-01-01

    用316L不锈钢(SU316L)作基片,以高纯石墨作靶、CHF3和Ar作源气体,采用反应磁控溅射法在不同流量比R(CHF3/Ar)下制备了氟化类金刚石(F-DLC)薄膜.利用双蒸水液滴法、BCA(二喹啉甲酸)法和傅里叶红外光谱(FTIR)探讨了影响薄膜蛋白吸附能力的因素.结果表明,镀有F-DLC薄膜的SU316L表面的血小板黏附量明显减少,血小板的变形程度显著减轻,相应的白蛋白与纤维蛋白原的吸附比普遍高于未镀膜的SU316L表面的相应值,说明镀上F-DLC薄膜可以改善样品的血液相容性.流量比为2:1左右时制备出的F-DLC薄膜,其白蛋白与纤维蛋白原的吸附比值达到最大,相应的血液相容性最佳.对薄膜的接触角和表面能以及FTIR光谱分析研究表明,SU316L表面的F-DLC薄膜的白蛋白与纤维蛋白原的吸附比及血液相容性与薄膜的中的—CFx键的含量(F/C比)和表面能(疏水性)直接相关,控制源气体流量比可以实现对薄膜的血液相容性的调制.%The fluorinated diamond-like carbon (F-DLC) films are prepared by reactive magnetron sputtering under different gas flow radios with trifluoromethane (CHF3) and argon (Ar) used as source gases and pure graphite as a target on the surface of 316L stainless steel (SU316L).Factors which influence the protein adsorbability are discussed by double-stilled water,BCA and FTIR spectra.The results show that the surface of SU316L coated with F-DLC film could obviously reduce the number of adherent platelets and dramatically relieves the deformation of platelets,leading to a ratio of higher albumin to fibrinogen adsorption higher than that with using the SU316L substrates,which indicates that the SU316L coated with F-DLC film can improve the blood compatibility.The film has the highest ratio of albumin to fibrinogen adsorption and the best hemocompatibility when the ratio of gas flow is 2∶1.Furthermore,the measurements of

  1. Organic donor-acceptor thin film systems. Towards optimized growth conditions

    Energy Technology Data Exchange (ETDEWEB)

    Keller, Kerstin Andrea

    2009-06-30

    In this work the preparation of organic donor-acceptor thin films was studied. A chamber for organic molecular beam deposition was designed and integrated into an existing deposition system for metallic thin films. Furthermore, the deposition system was extended by a load-lock with integrated bake-out function, a chamber for the deposition of metallic contacts via stencil mask technique and a sputtering chamber. For the sublimation of the organic compounds several effusion cells were designed. The evaporation characteristic and the temperature profile within the cells was studied. Additionally, a simulation program was developed, which calculates the evaporation characteristics of different cell types. The following processes were integrated: evaporation of particles, migration on the cell walls and collisions in the gas phase. It is also possible to consider a temperature gradient within the cell. All processes can be studied separately and their relative strength can be varied. To verify the simulation results several evaporation experiments with different cell types were employed. The thickness profile of the prepared thin films was measured position-dependently. The results are in good agreement with the simulation. Furthermore, the simulation program was extended to the field of electron beam induced deposition (EBID). The second part of this work deals with the preparation and characterization of organic thin films. The focus hereby lies on the charge transfer salt (BEDT-TTF)(TCNQ), which has three known structure variants. Thin films were prepared by different methods of co-evaporation and were studied with optical microscopy, X-ray diffraction and energy dispersive X-ray spectroscopy (EDX).The formation of the monoclinic phase of (BEDT-TTF)(TCNQ) could be shown. As a last part tunnel structures were prepared as first thin film devices and measured in a He{sub 4} cryostat. (orig.)

  2. Antifouling polymeric films against marine organisms. Kaiyo seibutsu fuchaku boshi to kobunshi

    Energy Technology Data Exchange (ETDEWEB)

    Yamamori, N. (Nippon Paint Co. Ltd., Tokyo (Japan))

    1991-07-15

    An introduction is made on prevention of marine organisms from depositing on bridges and vessels, and on anti-fouling function of highly anti-fouling silicone resin and hydrolytic resins. First, in the case of silicone rubber, its surface is hydrophobic making it more difficult for sticking constituent (glycoprotein) in a depositing organism to deposit, in addition to its resilience, which sheds off easily the deposited organisms by its impact resilience. On the one hand, organism deposition can be prevented by means of micro-domain structure. Further, a description is given on the hydrolytic resins as to their anti-fouling agent releasing mechanism in hydrolytic paint film, and capability of prolonging the anti-fouling life by means of making the film thicker because the anti-fouling life is proportional to film thickness. In addition, explanations are given on elusion mechanism of hydrolytic resins, their behaviors in anti-fouling agent dispersion, the importance of controlling the elusion since the film elusion amount is an important factor to determine the release amount of the dispersed anti-fouling agent and the anti-fouling life, and the improvement of anti-fouling performance of the resins by means of adding monobasic acid into copper-acrylic resin. 9 refs., 13 figs., 8 tabs.

  3. Organic thin film transistors with polymer brush gate dielectrics synthesized by atom transfer radical polymerization

    DEFF Research Database (Denmark)

    Pinto, J.C.; Whiting, G.L.; Khodabakhsh, S.;

    2008-01-01

    Low operating voltage is an important requirement that must be met for industrial adoption of organic field-effect transistors (OFETs). We report here solution fabricated polymer brush gate insulators with good uniformity, low surface roughness and high capacitance. These ultra thin polymer films...

  4. Strongly Dichroic Organic Films via Controlled Assembly of Modular Aromatic Charge-Transfer Liquid Crystals.

    Science.gov (United States)

    Bé, Ariana Gray; Tran, Cheryl; Sechrist, Riley; Reczek, Joseph J

    2015-10-01

    The formation of highly anisotropic organic thin films based on the designed self-assembly of mixed-stack liquid crystals is reported. A series of alkoxyanthracene donors is combined in a modular fashion with a naphthalenediimide acceptor to generate new charge-transfer columnar liquid crystals. Materials characterization and molecular modeling provides insight into structure-function relationships in these organic materials that lead to the striking bulk dichroic properties of certain molecular assemblies. PMID:26375256

  5. Low-Temperature Solution-Processed Gate Dielectrics for High-Performance Organic Thin Film Transistors

    Directory of Open Access Journals (Sweden)

    Jaekyun Kim

    2015-10-01

    Full Text Available A low-temperature solution-processed high-k gate dielectric layer for use in a high-performance solution-processed semiconducting polymer organic thin-film transistor (OTFT was demonstrated. Photochemical activation of sol-gel-derived AlOx films under 150 °C permitted the formation of a dense film with low leakage and relatively high dielectric-permittivity characteristics, which are almost comparable to the results yielded by the conventionally used vacuum deposition and high temperature annealing method. Octadecylphosphonic acid (ODPA self-assembled monolayer (SAM treatment of the AlOx was employed in order to realize high-performance (>0.4 cm2/Vs saturation mobility and low-operation-voltage (<5 V diketopyrrolopyrrole (DPP-based OTFTs on an ultra-thin polyimide film (3-μm thick. Thus, low-temperature photochemically-annealed solution-processed AlOx film with SAM layer is an attractive candidate as a dielectric-layer for use in high-performance organic TFTs operated at low voltages.

  6. Optical performance of mesostructured composite silica film loaded with organic dye.

    Science.gov (United States)

    Guli, Mina; Chen, Shijian; Zhang, Dingke; Li, Xiaotian; Yao, Jianxi; Chen, Lei; Xiao, Li

    2014-01-10

    A mesoporous composite silica film loaded with organic dye has been successfully synthesized by a solgel reaction process and a simple postgrafting method at room temperature. The composite film was characterized by x-ray diffraction, transmission electron microscopy, UV-Vis, photoluminescence (PL) spectra, and laser performance, and the results confirmed the existence of dyes in the channels of the silica film. A blue-shift and fluorescence property in the PL spectrum was observed from the composite film compared with that of dye molecules in C₂H₅OH solution. The spectrum narrowing phenomena has been observed when the composite film is pumped at λp=355  nm by a Nd:YAG pulsed laser. A narrower, higher peak was observed in emission spectra from the mesostructured composite silica film compared with the PL spectrum of dye in C₂H₅OH solution. There is a substantial reduction in the full width at half-maximum of the emitting light, which results in peaks with linewidths of 26 nm or more. This collapse of the emission spectrum is one of the signatures of the presence of amplified spontaneous emission. PMID:24514063

  7. Lithography-Free Broadband Ultrathin-Film Absorbers with Gap-Plasmon Resonance for Organic Photovoltaics.

    Science.gov (United States)

    Choi, Minjung; Kang, Gumin; Shin, Dongheok; Barange, Nilesh; Lee, Chang-Won; Ko, Doo-Hyun; Kim, Kyoungsik

    2016-05-25

    Strategies to confine electromagnetic field within ultrathin film emerge as essential technologies for applications from thin-film solar cells to imaging and sensing devices. We demonstrate a lithography-free, low-cost, large-scale method to realize broadband ultrathi-film metal-dielectric-metal (MDM) absorbers, by exploiting gap-plasmon resonances for strongly confined electromagnetic field. A two-steps method, first organizing Au nanoparticles via thermal dewetting and then transferring the nanoparticles to a spacer-reflector substrate, is used to achieve broader absorption bandwidth by manipulating geometric shapes of the top metallic layer into hemiellipsoids. A fast-deposited nominal Au film, instead of a conventional slow one, is employed in the Ostwald ripening process to attain hemiellipsoidal nanoparticles. A polymer supported transferring step allows a wider range of dewetting temperature to manipulate the nanoparticles' shape. By incorporating circularity with ImageJ software, the geometries of hemiellipsoidal nanoparticles are quantitatively characterized. Controlling the top geometry of MDM structure from hemisphere to hemiellipsoid increases the average absorption at 500-900 nm from 23.1% to 43.5% in the ultrathin film and full width at half-maximum of 132-324 nm, which is consistently explained by finite-difference time-domain simulation. The structural advantages of our scheme are easily applicable to thin-film photovoltaic devices because metal electrodes can act as metal reflectors and semiconductor layers as dielectric spacers. PMID:27160410

  8. Lithography-Free Broadband Ultrathin-Film Absorbers with Gap-Plasmon Resonance for Organic Photovoltaics.

    Science.gov (United States)

    Choi, Minjung; Kang, Gumin; Shin, Dongheok; Barange, Nilesh; Lee, Chang-Won; Ko, Doo-Hyun; Kim, Kyoungsik

    2016-05-25

    Strategies to confine electromagnetic field within ultrathin film emerge as essential technologies for applications from thin-film solar cells to imaging and sensing devices. We demonstrate a lithography-free, low-cost, large-scale method to realize broadband ultrathi-film metal-dielectric-metal (MDM) absorbers, by exploiting gap-plasmon resonances for strongly confined electromagnetic field. A two-steps method, first organizing Au nanoparticles via thermal dewetting and then transferring the nanoparticles to a spacer-reflector substrate, is used to achieve broader absorption bandwidth by manipulating geometric shapes of the top metallic layer into hemiellipsoids. A fast-deposited nominal Au film, instead of a conventional slow one, is employed in the Ostwald ripening process to attain hemiellipsoidal nanoparticles. A polymer supported transferring step allows a wider range of dewetting temperature to manipulate the nanoparticles' shape. By incorporating circularity with ImageJ software, the geometries of hemiellipsoidal nanoparticles are quantitatively characterized. Controlling the top geometry of MDM structure from hemisphere to hemiellipsoid increases the average absorption at 500-900 nm from 23.1% to 43.5% in the ultrathin film and full width at half-maximum of 132-324 nm, which is consistently explained by finite-difference time-domain simulation. The structural advantages of our scheme are easily applicable to thin-film photovoltaic devices because metal electrodes can act as metal reflectors and semiconductor layers as dielectric spacers.

  9. Do organic surface films on sea salt aerosols influence atmospheric chemistry? ─ a model study

    Directory of Open Access Journals (Sweden)

    R. von Glasow

    2007-11-01

    Full Text Available Organic material from the ocean's surface can be incorporated into sea salt aerosol particles often producing a surface film on the aerosol. Such an organic coating can reduce the mass transfer between the gas phase and the aerosol phase influencing sea salt chemistry in the marine atmosphere. To investigate these effects and their importance for the marine boundary layer (MBL we used the one-dimensional numerical model MISTRA. We considered the uncertainties regarding the magnitude of uptake reduction, the concentrations of organic compounds in sea salt aerosols and the oxidation rate of the organics to analyse the possible influence of organic surfactants on gas and liquid phase chemistry with a special focus on halogen chemistry. By assuming destruction rates for the organic coating based on laboratory measurements we get a rapid destruction of the organic monolayer within the first meters of the MBL. Larger organic initial concentrations lead to a longer lifetime of the coating but lead also to an unrealistically strong decrease of O3 concentrations as the organic film is destroyed by reaction with O3. The lifetime of the film is increased by assuming smaller reactive uptake coefficients for O3 or by assuming that a part of the organic surfactants react with OH. With regard to tropospheric chemistry we found that gas phase concentrations for chlorine and bromine species decreased due to the decreased mass transfer between gas phase and aerosol phase. Aqueous phase chlorine concentrations also decreased but aqueous phase bromine concentrations increased. Differences for gas phase concentrations are in general smaller than for liquid phase concentrations. The effect on gas phase NO2 or NO is very small (reduction less than 5% whereas liquid phase NO2 concentrations increased in some cases by nearly 100%. We list suggestions for further laboratory studies which are needed for improved model studies.

  10. Molecular Adsorber Coating

    Science.gov (United States)

    Straka, Sharon; Peters, Wanda; Hasegawa, Mark; Hedgeland, Randy; Petro, John; Novo-Gradac, Kevin; Wong, Alfred; Triolo, Jack; Miller, Cory

    2011-01-01

    A document discusses a zeolite-based sprayable molecular adsorber coating that has been developed to alleviate the size and weight issues of current ceramic puck-based technology, while providing a configuration that more projects can use to protect against degradation from outgassed materials within a spacecraft, particularly contamination-sensitive instruments. This coating system demonstrates five times the adsorption capacity of previously developed adsorber coating slurries. The molecular adsorber formulation was developed and refined, and a procedure for spray application was developed. Samples were spray-coated and tested for capacity, thermal optical/radiative properties, coating adhesion, and thermal cycling. Work performed during this study indicates that the molecular adsorber formulation can be applied to aluminum, stainless steel, or other metal substrates that can accept silicate-based coatings. The coating can also function as a thermal- control coating. This adsorber will dramatically reduce the mass and volume restrictions, and is less expensive than the currently used molecular adsorber puck design.

  11. How long may a breath sample be stored for at  -80 °C? A study of the stability of volatile organic compounds trapped onto a mixed Tenax:Carbograph trap adsorbent bed from exhaled breath.

    Science.gov (United States)

    Kang, S; Paul Thomas, C L

    2016-01-01

    Thermal desorption is used extensively in exhaled breath volatile organic compound (VOC) analysis, and it is often necessary to store the adsorbent tube samples before analysis. The possible introduction of storage artefacts is an important potential confounding factor in the development of standard methodologies for breath sampling and analysis. The stability of VOCs trapped from breath samples onto a dual bed Tenax(®) TA:Carbograph adsorbent tube and stored  -80°C was studied over 12.5 month. 25 samples were collected from a single male participant over 3 h and then stored at  -80 °C. Randomly selected adsorbent tubes were subsequent analysed by thermal desorption-gas chromatography-mass spectrometry at 5 times points throughout the 12.5 month of the study. Toluene-d8, decane-d22 and hexadecane-d34 internal standards were used to manage the instrument variability throughout the duration of the study. A breath-matrix consisting of 161 endogenous and 423 exogenous VOC was created. Iterative orthogonal partial least squared discriminant analysis (OPLS-DA) and principal components analysis (PCA) indicated that it was not possible to detect storage artefacts at 1.5 month storage. By 6 month storage artefacts were discernible with significant changes observed for 27% of the recovered VOC. Endogenous VOC were observed to be more susceptible to storage. A paired two-tailed t-test on the endogenous compounds indicated that the maximum storage duration under these conditions was 1.5 month with 94% of the VOCs stable. This study indicates that a prudent approach is best adopted for the storage of adsorbent samples; storage times should be minimised, and storage time examined as a possible discriminatory factor in multivariate analysis. PMID:27272219

  12. Combinatorial Techniques to Efficiently Investigate and Optimize Organic Thin Film Processing and Properties

    Directory of Open Access Journals (Sweden)

    Hans-Werner Schmidt

    2013-04-01

    Full Text Available In this article we present several developed and improved combinatorial techniques to optimize processing conditions and material properties of organic thin films. The combinatorial approach allows investigations of multi-variable dependencies and is the perfect tool to investigate organic thin films regarding their high performance purposes. In this context we develop and establish the reliable preparation of gradients of material composition, temperature, exposure, and immersion time. Furthermore we demonstrate the smart application of combinations of composition and processing gradients to create combinatorial libraries. First a binary combinatorial library is created by applying two gradients perpendicular to each other. A third gradient is carried out in very small areas and arranged matrix-like over the entire binary combinatorial library resulting in a ternary combinatorial library. Ternary combinatorial libraries allow identifying precise trends for the optimization of multi-variable dependent processes which is demonstrated on the lithographic patterning process. Here we verify conclusively the strong interaction and thus the interdependency of variables in the preparation and properties of complex organic thin film systems. The established gradient preparation techniques are not limited to lithographic patterning. It is possible to utilize and transfer the reported combinatorial techniques to other multi-variable dependent processes and to investigate and optimize thin film layers and devices for optical, electro-optical, and electronic applications.

  13. Research on the electronic and optical properties of polymer and other organic molecular thin films

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    1997-02-01

    The main goal of the work is to find materials and methods of optimization of organic layered electroluminescent cells and to study such properties of polymers and other organic materials that can be used in various opto-electronic devices. The summary of results obtained during the first year of work is presented. They are: (1) the possibility to produce electroluminescent cells using a vacuum deposition photoresist technology for commercial photoresists has been demonstrated; (2) the idea to replace the polyaryl polymers by other polymers with weaker hole conductivity for optimization of electroluminescent cells with ITO-Al electrodes has been suggested. The goal is to obtain amorphous processable thin films of radiative recombination layers in electroluminescent devices; (3) procedures of preparation of high-quality vacuum-deposited poly (p-phenylene) (PPP) films on various substrates have been developed; (4) it was found for the first time that the fluorescence intensity of PPP films depends on the degree of polymerization; (5) the role of interfaces between organic compounds, on one side, and metals or semiconductors, on the other side, has been studied and quenching of the fluorescence caused by semiconductor layer in thin sandwiches has been observed; (6) studies of the dynamics of photoexcitations revealed the exciton self-trapping in quasi-one-dimensional aggregates; and (7) conditions for preparation of highly crystalline fullerene C{sub 60} films by vacuum deposition have been found. Composites of C{sub 60} with conjugated polymers have been prepared.

  14. Solution coating of large-area organic semiconductor thin films with aligned single-crystalline domains

    KAUST Repository

    Diao, Ying

    2013-06-02

    Solution coating of organic semiconductors offers great potential for achieving low-cost manufacturing of large-area and flexible electronics. However, the rapid coating speed needed for industrial-scale production poses challenges to the control of thin-film morphology. Here, we report an approach - termed fluid-enhanced crystal engineering (FLUENCE) - that allows for a high degree of morphological control of solution-printed thin films. We designed a micropillar-patterned printing blade to induce recirculation in the ink for enhancing crystal growth, and engineered the curvature of the ink meniscus to control crystal nucleation. Using FLUENCE, we demonstrate the fast coating and patterning of millimetre-wide, centimetre-long, highly aligned single-crystalline organic semiconductor thin films. In particular, we fabricated thin films of 6,13-bis(triisopropylsilylethynyl) pentacene having non-equilibrium single-crystalline domains and an unprecedented average and maximum mobilities of 8.1±1.2 cm2 V-1 s -1 and 11 cm2 V-1 s-1. FLUENCE of organic semiconductors with non-equilibrium single-crystalline domains may find use in the fabrication of high-performance, large-area printed electronics. © 2013 Macmillan Publishers Limited. All rights reserved.

  15. Electric dipolar interaction assisted growth of single crystalline organic thin films

    Energy Technology Data Exchange (ETDEWEB)

    Jin-ming, Cai [Material Science and Technology Division, Oak Ridge National Laboratory; Yu-Yang, Zhang [Institute of Physics, Chinese Academy of Sciences, Beijing 100190, China; Hao, Hu [Institute of Physics, Chinese Academy of Sciences, Beijing 100190, China; Li-Hong, Bao [Institute of Physics, Chinese Academy of Sciences, Beijing 100190, China; Li-Da, Pan [Institute of Physics, Chinese Academy of Sciences, Beijing 100190, China; Wei, Tang [Institute of Physics, Chinese Academy of Sciences, Beijing 100190, China; Guo, Li [Institute of Physics, Chinese Academy of Sciences, Beijing 100190, China; Shi-Xuan, Du [Institute of Physics, Chinese Academy of Sciences, Beijing 100190, China; Jian, Shen [Material Science and Technology Division, Oak Ridge National Laboratory; Hong-Jun, Gao [Institute of Physics, Chinese Academy of Sciences, Beijing 100190, China

    2010-01-01

    We report on a forest-like-to-desert-like pattern evolution in the growth of an organic thin film observed by using an atomic force microscope. We use a modified diffusion limited aggregation model to simulate the growth process and are able to reproduce the experimental patterns. The energy of electric dipole interaction is calculated and determined to be the driving force for the pattern formation and evolution. Based on these results, single crystalline films are obtained by enhancing the electric dipole interaction while limiting effects of other growth parameters.

  16. Nanoscale aluminum concaves for light-trapping in organic thin-films

    Science.gov (United States)

    Goszczak, Arkadiusz Jarosław; Adam, Jost; Cielecki, Paweł Piotr; Fiutowski, Jacek; Rubahn, Horst-Günter; Madsen, Morten

    2016-07-01

    Anodic aluminum oxide (AAO) templates, fabricated from oxalic acid and phosphoric acid, lead to non-periodic nanoscale concave structures in their underlying aluminum layer, which are investigated for their field-enhancement properties by applying a thin-film polymer coating based laser ablation technique. Local ablation spots, corresponding to field enhancement on the ridge edges of the aluminum concave nanostructures, are observed in surface-covering polymer films, and confirmed with FDTD studies. The field enhancement leads to improved light absorption in the applied polymer layers, which may be used as an efficient method for enhancing the power conversion efficiency of organic solar cells.

  17. Recent Progress in Evaluation Techniques and Device Applications of Organic and Composite Thin Films

    Science.gov (United States)

    Kato, Keizo; Shinbo, Kazunari; Okamoto, Tetsushi; Aoki, Yusuke; Iechi, Hiroyuki

    Evaluation techniques and the device applications of organic and composite thin films are described. One of the evaluation techniques is the surface plasmon resonance (SPR) spectroscopy. It has become a widely accepted method for the characterization and study of ultrathin films, interfaces and kinetic processes at surfaces, and it has been investigated in the applications of SPR sensors and plasmonic novel devices. Properties, functionalization and various applications of hybrid materials, nanocomposites, and nanoparticles are also introduced, and the application to industry is mentioned. Moreover, electronic device application of monolithic organic logic circuit using a stacked structure of two organic static induction transistors is explained. The advantages of this novel device structure are the controllability of the operational characteristics and simple device fabrication process.

  18. Metal-Organic Framework Thin Films as Platforms for Atomic Layer Deposition of Cobalt Ions To Enable Electrocatalytic Water Oxidation.

    Science.gov (United States)

    Kung, Chung-Wei; Mondloch, Joseph E; Wang, Timothy C; Bury, Wojciech; Hoffeditz, William; Klahr, Benjamin M; Klet, Rachel C; Pellin, Michael J; Farha, Omar K; Hupp, Joseph T

    2015-12-30

    Thin films of the metal-organic framework (MOF) NU-1000 were grown on conducting glass substrates. The films uniformly cover the conducting glass substrates and are composed of free-standing sub-micrometer rods. Subsequently, atomic layer deposition (ALD) was utilized to deposit Co(2+) ions throughout the entire MOF film via self-limiting surface-mediated reaction chemistry. The Co ions bind at aqua and hydroxo sites lining the channels of NU-1000, resulting in three-dimensional arrays of separated Co ions in the MOF thin film. The Co-modified MOF thin films demonstrate promising electrocatalytic activity for water oxidation.

  19. Comparison of Structural and Electrochemical Properties of V2O5 Thin Films Prepared by Organic/Inorganic Precursors

    International Nuclear Information System (INIS)

    Vanadium pentoxide thin films were produced from organic and inorganic precursors by sol gel dip-coating method. Fourier transform infrared spectroscopy and UV Vis spectroscopy were made to figure out structural properties of the films. Electrochemical properties were investigated by cyclic voltammetry. The shape of the curves was in agreement with a typical diffusion controlled cyclic voltammograms of amorphous V2O5 films for a reversible lithium ion intercalation/deintercalation process showing yellow–green–blue multi-electrochromism. V2O5 films, synthesized from organic precursor, indicated lower band gap energy, higher charge capacity as well as homogeneous and low granule size compared to inorganic route

  20. Preparation and characterization of LaNiO3 films grown by metal–organic deposition

    Indian Academy of Sciences (India)

    Yao Wang; Guofang Zhang; Chengshan Li; Guo Yan; Yafeng Lu

    2011-12-01

    We have investigated the synthesis and characterization of LaNiO3 (LNO) layers deposited on YSZ (100) substrate by metal–organic deposition (MOD). Texture, morphology and electrical properties of the LaNiO3 films were characterized by X-ray diffraction (XRD), atomic force microscopy (AFM), scanning electron microscopy (SEM) and electrical resistivity measurement. It has been found that the formation of (ℎ00) orientation depends on pyrolysis temperature, annealing temperature and thickness of LaNiO3 layers. The LaNiO3 films prepared under optimal condition indicate highly (ℎ00) orientation and a rather smooth surface. The LaNiO3 films show a metallic behaviour in the measured temperature range.

  1. Substrate mediated growth of organic semiconducting thin films; Templateffekte bei der Strukturierung organischer Halbleiterfilme

    Energy Technology Data Exchange (ETDEWEB)

    Goetzen, Jan

    2010-09-17

    Since electronic properties of molecular materials are closely related to their structural order a precise control of the molecular packing and crystalline orientation of thin films is of vital interest for an optimization of organic electronic devices. Of particular interest in this respect is the initial stage of film formation which is largely governed by the interplay of intermolecular and molecule-substrate interactions. One approach to control the molecular film structure is based on substrate mediated growth. In this respect we have studied structural properties of thin films of pentacene, pentacene- 5,7,12,14-tetrone and perfluoro-pentacene which were grown onto various substrates including metals, metal oxides and graphite. On metal surfaces the molecules initially form a chemisorbed monolayer where molecules even can be uniformly aligned when using appropriate substrates with twofold symmetry. Further deposition, however, is accompanied by a pronounced dewetting and formation of disjoined islands which results from a large structural mismatch between the molecular arrangement in the monolayer and the crystalline phase. In some cases it is possible to orient such islands by utilizing step mediated nucleation and decoration of step bunches which allows the preparation of azimuthally well oriented elongated islands. On single crystalline oxides the growth parallels the situation found before for SiO{sub 2} where islands of upright oriented molecules are formed. The growth on graphite is somewhat particular since the lattice provides a natural template for acenes yielding epitaxially ordered monolayer films with planar adsorption geometry like in case of metals. Interestingly, however, no dewetting occurs upon further growth and instead rather smooth films are formed. The detailed analysis for the case of pentacene showed that the substrate-molecule interaction actually is weaker than the intermolecular interaction so that multilayer films can lift the

  2. Recent progress on thin-film encapsulation technologies for organic electronic devices

    Science.gov (United States)

    Yu, Duan; Yang, Yong-Qiang; Chen, Zheng; Tao, Ye; Liu, Yun-Fei

    2016-03-01

    Among the advanced electronic devices, flexible organic electronic devices with rapid development are the most promising technologies to customers and industries. Organic thin films accommodate low-cost fabrication and can exploit diverse molecules in inexpensive plastic light emitting diodes, plastic solar cells, and even plastic lasers. These properties may ultimately enable organic materials for practical applications in industry. However, the stability of organic electronic devices still remains a big challenge, because of the difficulty in fabricating commercial products with flexibility. These organic materials can be protected using substrates and barriers such as glass and metal; however, this results in a rigid device and does not satisfy the applications demanding flexible devices. Plastic substrates and transparent flexible encapsulation barriers are other possible alternatives; however, these offer little protection to oxygen and water, thus rapidly degrading the devices. Thin-film encapsulation (TFE) technology is most effective in preventing water vapor and oxygen permeation into the flexible devices. Because of these (and other) reasons, there has been an intense interest in developing transparent barrier materials with much lower permeabilities, and their market is expected to reach over 550 million by 2025. In this study, the degradation mechanism of organic electronic devices is reviewed. To increase the stability of devices in air, several TFE technologies were applied to provide efficient barrier performance. In this review, the degradation mechanism of organic electronic devices, permeation rate measurement, traditional encapsulation technologies, and TFE technologies are presented.

  3. Polymer assisted solution processing of Ti-doped indium oxide transparent conducting thin films for organic solar cells

    International Nuclear Information System (INIS)

    Highlights: • Polymer assisted solution process. • Ti-doped indium oxide (TIO) transparent conducting films. • Replacement of sputtered ITO with polymer-assisted-solution-coated TIO films. • High mobility transparent conducting films. • Application of polymer-assisted-solution-coated TIO films to organic solar cells. - Abstract: We report the preparation and evaluation of Ti-doped indium oxide (TIO) transparent conducting films by a polymer-assisted solution (PAS) process, as well as the evaluation of this type of film as a transparent cathode in an inverted organic solar cell (IOCS). Both Ti- and In-PASs have been synthesized by coordinating Ti- and In-anionic complexes with polyethyleneimine. The final TIO–PAS was formed by mixing Ti-PAS into In-PAS with a Ti concentration between 1 at.% and 7 at.%. The TIO–PAS was spin-coated onto glass substrates to form uniform thin films of Ti-doped indium oxide, which were then annealed at high temperature. The optimum Ti concentration to achieve the best electrical and optical properties of PAS–TIO films was found to be 3 at.%. With the film thickness of 650 nm, PAS–TIO films had a sheet resistance of 65 Ω/sq and an optical transmittance greater than 85%. The feasibility of PAS-coated TIO thin film as a transparent electrode was evaluated by applying it to the fabrication of IOSCs, which showed the energy conversion efficiency of 4.60%

  4. Self-assembly of ferromagnetic organic-inorganic perovskite-like films.

    Science.gov (United States)

    Akhtar, Naureen; Polyakov, Alexey O; Aqeel, Aisha; Gordiichuk, Pavlo; Blake, Graeme R; Baas, Jacob; Amenitsch, Heinz; Herrmann, Andreas; Rudolf, Petra; Palstra, Thomas T M

    2014-12-10

    Perovskite-based organic-inorganic hybrids hold great potential as active layers in electronics or optoelectronics or as components of biosensors. However, many of these applications require thin films grown with good control over structure and thickness--a major challenge that needs to be addressed. The work presented here is an effort towards this goal and concerns the layer-by-layer deposition at ambient conditions of ferromagnetic organic-inorganic hybrids consisting of alternating CuCl4-octahedra and organic layers. The Langmuir-Blodgett technique used to assemble these structures provides intrinsic control over the molecular organization and film thickness down to the molecular level. Magnetic characterization reveals that the coercive field for these thin films is larger than that for solution-grown layered bulk crystals. The strategy presented here suggests a promising cost effective route to facilitate the excellently controlled growth of sophisticated materials on a wide variety of substrates that have properties relevant for the high density storage media and spintronic devices. PMID:25059565

  5. [Effects of white organic light-emitting devices using color conversion films on electroluminescence spectra].

    Science.gov (United States)

    Hou, Qing-Chuan; Wu, Xiao-Ming; Hua, Yu-Lin; Qi, Qing-Jin; Li, Lan; Yin, Shou-Gen

    2010-06-01

    The authors report a novel white organic light-emitting device (WOLED), which uses a strategy of exciting organic/ inorganic color conversion film with a blue organic light-emitting diode (OLED). The luminescent layer of the blue OLED was prepared by use of CBP host blended with a blue highly fluorescent dye N-BDAVBi. The organic/inorganic color conversion film was prepared by dispersing a mixture of red pigment VQ-D25 and YAG : Ce3+ phosphor in PMMA. The authors have achieved a novel WOLED with the high color stability by optimizing the thickness and fluorescent pigment concentration of the color conversion film. When the driving voltage varied between 6 and 14 V, the color coordinates (CIE) varied slightly from (0.354, 0.304) to (0.357, 0.312) and the maximum current efficiency is about 5.8 cd x A(-1) (4.35 mA x cm(-2)), the maximum brightness is 16 800 cd x m(-2) at the operating voltage of 14 V. PMID:20707129

  6. Fabrication of organic semiconducting materials and high-performance organic thin-film transistors based on electron-irradiated polystyrene

    Energy Technology Data Exchange (ETDEWEB)

    Lee, Hyeok Moo

    2011-02-15

    It was discovered that non-luminescent polystyrene (PS) can be converted to luminescent materials whose color can be changed in a wide visible range by electron irradiation. After the analyses of electron-irradiated PS, it was found that polycyclic aromatic hydrocarbons are produced by the irradiation and these PAHs are the origin of the luminescence from the electron-irradiated polymer. Based on the finding, a straightforward approach to produce desired light-emitting nanoarchitectures and nanopatterns only by irradiating an electron beam to the polymer was presented. In particular, the top-down irradiation approach provides a powerful tool to fabricate a variety of interesting nanoarchitectures when combined with bottom-up approaches; PS nanostructures prepared by self-assembling techniques can be directly transformed to luminescent nanostructures by electron irradiation while keeping their pristine morphologies. Light-emitting materials are widely used for optical, photonic, chemical and biomedical devices and a rapid progress in the devices requires well-defined luminescent nanoarchitectures. The approach presented here will be useful for a wide range of research fields including optics, photonics, chemistry, and biologics. On the other hand, a very simple but effective approach to produce high-performance rubrene organic thin-film transistors (OTFTs) with characteristics better than amorphous silicon TFTs was presented. Only by an abrupt heating process, high-quality crystalline rubrene semiconductor thin films that have almost ideal structures for OTFTs are created. The produced crystalline thin films consist of highly ordered, uniaxially oriented single-crystalline grains with large average sizes and the grains are interconnected with one another to form continuous films over the whole dielectric surfaces. Such high-quality crystalline rubrene thin films are remarkably rapidly produced in just 30 sec through this approach. Moreover, the increase of carrier

  7. Improvement of the outcoupling efficiency of an organic light-emitting device by attaching microstructured films

    Science.gov (United States)

    Lin, Hoang-Yan; Lee, Jiun-Haw; Wei, Mao-Kuo; Dai, Ching-Liang; Wu, Chia-Fang; Ho, Yu-Hsuan; Lin, Hung-Yi; Wu, Tung-Chuan

    2007-07-01

    In this paper, we present and analyse the optical characteristics, such as spectral shift, CIE coordinates, viewing angle dependence, luminous current efficiency and luminous power efficiency, of an organic light-emitting device (OLED) with a commercial diffuser film or a brightness-enhancement film (BEF) attached. Compared to a planar green OLED, the luminous current efficiencies of the OLED with an attached diffuser film or BEF increase by 29% and 23%, respectively. The overall luminous power efficiencies are enhanced by 28% and 7%. Compared to the planar green device, we observe blue shifts at different viewing angles when microstructured films are attached, which is the evidence that the waveguiding modes are being extracted. In our planar OLED, the peak wavelength blue shifts and the full width at the half maximum (FWHM) decrease with increasing viewing angles due to the microcavity effect. When the diffuser is attached, the spectral peak has a constant blue shift (6 nm) compared to that of the planar OLED. On the other hand, in the BEF case, the spectral shift depends on the viewing angle (2-12 nm blue shifts from 0 to 80°). This is due to the different operating principles (scattering and redirected light) of the diffuser and BEF. Since the transmittance spectra of both the diffuser film and the BEF are flat over the visible range, it is suitable for lighting applications by using white OLED. When attaching the films on a commercial white OLED, the luminous current efficiencies of the OLED with an attached diffuser film or BEF increase by 34% and 31%, respectively. The overall luminous power efficiencies are enhanced by 42% and 8%.

  8. DESORPTION OF VOCs FROM POLYMERIC ADSORBENTS UNDER MICROWAVE FIELD

    Institute of Scientific and Technical Information of China (English)

    2001-01-01

    Desorption of volatile organic compounds (VOCs)from polymeric adsorbents by microwave was investigated experimentally. Two kinds of organic compounds, benzene and toluene,were separately used as adsorbates in this work. Results showed that the application of microwave to regenerate the polymeric adsorbents not only can get higher regeneration efficiency in comparison with the use of heat regeneration, but also make the temperatures of the fixed beds much lower than that when using the heat regeneratton The weaker the polarity of a polymeric adsorbent, the easier its regeneration was.

  9. Molecular organization in the thin films of chloroaluminium hexadecafluorophthalocyanine revealed by polarized Raman spectroscopy

    International Nuclear Information System (INIS)

    The molecular arrangement in the thin films of chloroaluminium hexadecafluorophthalocyanine (AlClPcF16) grown by physical vapor deposition has been studied using atomic force microscopy and optical spectroscopy techniques. It was shown that AlClPcF16 films, 20 nm thick, prepared on the quartz substrate at 60 °C are well organized and characterized by a predominantly co-facial parallel arrangement of molecules vertical to the surface. According to the polarized Raman spectroscopy measurements, the mean tilt angle between the AlClPcF16 species and the substrate surface was found to be 75 ± 5°. All intense bands in the experimental Infrared and Raman spectra of AlClPcF16 were assigned using density functional theory calculations. The theoretically predicted geometry and wavenumbers are in a good agreement with the experimental values. Apart from this, the temperature dependence of vapor pressure and sublimation enthalpy of AlClPcF16 were determined by the Knudsen effusion method. - Highlights: • Aluminium hexadecafluorophthalocyanine films were grown by physical vapor deposition. • Orientation of molecules in the films was studied using polarized Raman spectroscopy. • Films have a co-facial parallel arrangement of molecules vertical to the surface. • Temperature dependence of vapor pressure was determined by Knudsen effusion method

  10. Synthesis of metal-organic framework films by pore diffusion method

    Science.gov (United States)

    Murayama, Naohiro; Nishimura, Yuki; Kajiro, Hiroshi; Kishida, Satoru; Kinoshita, Kentaro; Tottori Univ Team; Nippon Steel; Sumitomo Metal Co. Collaboration; Tottori Integrated Frontier Resaerch Center (Tifrec) Collaboration; Tottori University Electronic Display Resaerch Center (Tedrec) Collaboration

    Metal-organic frameworks (MOFs) presents high controllability in designing the nano-scale pore, and this enable molecular storages, catalysts, gas sensors, gas separation membranes, and electronic devices for next-generation. Therefore, a simple method for film synthesis of MOFs compared with conventional methods [1] is strongly required. In this paper, we provide pore diffusion method, in which a substrate containing constituent metals of MOF is inserted in solution that includes only linker molecules of MOF. As a result, 2D growth of MOF was effectively enhanced, and the formation of flat and dense MOF films was attained. The growth time, t, dependence of film thickness, d, can be expressed by the relation of d = Aln(t + 1) + B, where A and B are constants. It means that ionized coppers diffuse through the pores of MOFs and the synthesis reaction proceeds at the MOF/solvent interface. We demonstrated the fabrication of a HKUST-1/Cu-TPA hetero structure by synthesizing a Cu-TPA film continuously after the growth of a HKUST-1 film on the CuOx substrate.

  11. An anode with aluminum doped on zinc oxide thin films for organic light emitting devices

    International Nuclear Information System (INIS)

    Doped zinc oxides are attractive alternative materials as transparent conducting electrode because they are nontoxic and inexpensive compared with indium tin oxide (ITO). Transparent conducting aluminum-doped zinc oxide (AZO) thin films have been deposited on glass substrates by DC reactive magnetron sputtering method. Films were deposited at a substrate temperature of 150-bar oC in 0.03 Pa of oxygen pressure. The electrical and optical properties of the film with the Al-doping amount of 2 wt% in the target were investigated. For the 300-nm thick AZO film deposited using a ZnO target with an Al content of 2 wt%, the lowest electrical resistivity was 4x10-4Ωcm and the average transmission in the visible range 400-700 nm was more than 90%. The AZO film was used as an anode contact to fabricate organic light-emitting diodes. The device performance was measured and the current efficiency of 2.9 cd/A was measured at a current density of 100 mA/cm2

  12. PEDOT as a Flexible Organic Electrode for a Thin Film Acoustic Energy Harvester.

    Science.gov (United States)

    Kim, Younghoon; Na, Jongbeom; Park, Chihyun; Shin, Haijin; Kim, Eunkyoung

    2015-08-01

    An efficient thin film acoustic energy harvester was explored using flexible poly(3,4-ethylene dioxythiophene) (PEDOT) films as electrodes in an all-organic triboelectric generator (AO-TEG). A thin film AO-TEG structured as PEDOT/Kapton//PET/PEDOT was prepared by the solution casting polymerization(SCP) on the dielectric polymer films. As-prepared AO-TEG showed high flexibility and durability due to the strong adhesion between the electrodes and the dielectric polymer. The short-circuit current density (Jsc), open-circuit voltage (Voc), and maximum power density (Pw) reached 50 mA/m(2), 700 V, and 12.9 W/m(2) respectively. The output current density decreased with the increase in the electrode resistance (Re), but the energy loss in the organic electrodes was negligible. The AO-TEG could light up 180 LEDs instantaneously upon touching of the AO-TEG with a palm (∼120 N). With the flexible structure, the AO-TEG was worn as clothes and generated electricity to light LEDs upon regular human movement. Furthermore, the AO-TEG was applicable as a thin film acoustic energy harvester, which used music to generate electricity enough for powering of 5 LEDs. An AO-TEG with a PEDOT electrode (Re = 200 Ω) showed instantaneous peak-to-peak voltage generation of 11 V under a sound pressure level (SPL) of 90-100 dB. The harvested acoustic energy through the AO-TEG was 350 μJ from the 4 min playing of the same single song. This is the first demonstration of a flexible triboelectric generator (TEG) using an organic electrode for harvesting acoustic energy from ambient environment.

  13. PEDOT as a Flexible Organic Electrode for a Thin Film Acoustic Energy Harvester.

    Science.gov (United States)

    Kim, Younghoon; Na, Jongbeom; Park, Chihyun; Shin, Haijin; Kim, Eunkyoung

    2015-08-01

    An efficient thin film acoustic energy harvester was explored using flexible poly(3,4-ethylene dioxythiophene) (PEDOT) films as electrodes in an all-organic triboelectric generator (AO-TEG). A thin film AO-TEG structured as PEDOT/Kapton//PET/PEDOT was prepared by the solution casting polymerization(SCP) on the dielectric polymer films. As-prepared AO-TEG showed high flexibility and durability due to the strong adhesion between the electrodes and the dielectric polymer. The short-circuit current density (Jsc), open-circuit voltage (Voc), and maximum power density (Pw) reached 50 mA/m(2), 700 V, and 12.9 W/m(2) respectively. The output current density decreased with the increase in the electrode resistance (Re), but the energy loss in the organic electrodes was negligible. The AO-TEG could light up 180 LEDs instantaneously upon touching of the AO-TEG with a palm (∼120 N). With the flexible structure, the AO-TEG was worn as clothes and generated electricity to light LEDs upon regular human movement. Furthermore, the AO-TEG was applicable as a thin film acoustic energy harvester, which used music to generate electricity enough for powering of 5 LEDs. An AO-TEG with a PEDOT electrode (Re = 200 Ω) showed instantaneous peak-to-peak voltage generation of 11 V under a sound pressure level (SPL) of 90-100 dB. The harvested acoustic energy through the AO-TEG was 350 μJ from the 4 min playing of the same single song. This is the first demonstration of a flexible triboelectric generator (TEG) using an organic electrode for harvesting acoustic energy from ambient environment. PMID:26153798

  14. Continuous, Highly Flexible, and Transparent Graphene Films by Chemical Vapor Deposition for Organic Photovoltaics

    KAUST Repository

    Gomez De Arco, Lewis

    2010-05-25

    We report the implementation of continuous, highly flexible, and transparent graphene films obtained by chemical vapor deposition (CVD) as transparent conductive electrodes (TCE) in organic photovoltaic cells. Graphene films were synthesized by CVD, transferred to transparent substrates, and evaluated in organic solar cell heterojunctions (TCE/poly-3,4- ethylenedioxythiophene:poly styrenesulfonate (PEDOT:PSS)/copper phthalocyanine/fullerene/bathocuproine/aluminum). Key to our success is the continuous nature of the CVD graphene films, which led to minimal surface roughness (∼ 0.9 nm) and offered sheet resistance down to 230 Ω/sq (at 72% transparency), much lower than stacked graphene flakes at similar transparency. In addition, solar cells with CVD graphene and indium tin oxide (ITO) electrodes were fabricated side-by-side on flexible polyethylene terephthalate (PET) substrates and were confirmed to offer comparable performance, with power conversion efficiencies (η) of 1.18 and 1.27%, respectively. Furthermore, CVD graphene solar cells demonstrated outstanding capability to operate under bending conditions up to 138°, whereas the ITO-based devices displayed cracks and irreversible failure under bending of 60°. Our work indicates the great potential of CVD graphene films for flexible photovoltaic applications. © 2010 American Chemical Society.

  15. Dielectric properties of crystalline organic molecular films in the limit of zero overlap

    International Nuclear Information System (INIS)

    We present the calculation of the static dielectric susceptibility tensor and dipole field sums in thin molecular films in the well-defined limit of zero intermolecular overlap. Microelectrostatic and charge redistribution approaches are applied to study the evolution of dielectric properties from one to a few molecular layers in films of different conjugated molecules with organic electronics applications. Because of the conditional convergence of dipolar interactions, dipole fields depend on the shape of the sample and different values are found in the middle layer of a thick film and in the bulk. The shape dependence is eliminated when depolarization is taken into account, and the dielectric tensor of molecular films converges to the bulk limit within a few molecular layers. We quantify the magnitude of surface effects and interpret general trends among different systems in terms of molecular properties, such as shape, polarizability anisotropy, and supramolecular organization. A connection between atomistic models for molecular dielectrics and simpler theories for polarizable atomic lattices is also provided

  16. Dielectric properties of crystalline organic molecular films in the limit of zero overlap.

    Science.gov (United States)

    D'Avino, Gabriele; Vanzo, Davide; Soos, Zoltán G

    2016-01-21

    We present the calculation of the static dielectric susceptibility tensor and dipole field sums in thin molecular films in the well-defined limit of zero intermolecular overlap. Microelectrostatic and charge redistribution approaches are applied to study the evolution of dielectric properties from one to a few molecular layers in films of different conjugated molecules with organic electronics applications. Because of the conditional convergence of dipolar interactions, dipole fields depend on the shape of the sample and different values are found in the middle layer of a thick film and in the bulk. The shape dependence is eliminated when depolarization is taken into account, and the dielectric tensor of molecular films converges to the bulk limit within a few molecular layers. We quantify the magnitude of surface effects and interpret general trends among different systems in terms of molecular properties, such as shape, polarizability anisotropy, and supramolecular organization. A connection between atomistic models for molecular dielectrics and simpler theories for polarizable atomic lattices is also provided. PMID:26801038

  17. Dielectric properties of crystalline organic molecular films in the limit of zero overlap

    Energy Technology Data Exchange (ETDEWEB)

    D’Avino, Gabriele, E-mail: gabriele.davino@gmail.com [Laboratory for Chemistry of Novel Materials, University of Mons, Place du Parc 20, BE-7000 Mons, Belgium and Department of Physics, University of Liège, Allée du 6 Août 17, BE-4000 Liège (Belgium); Vanzo, Davide; Soos, Zoltán G., E-mail: soos@princeton.edu [Department of Chemistry, Princeton University, Princeton, New Jersey 08544 (United States)

    2016-01-21

    We present the calculation of the static dielectric susceptibility tensor and dipole field sums in thin molecular films in the well-defined limit of zero intermolecular overlap. Microelectrostatic and charge redistribution approaches are applied to study the evolution of dielectric properties from one to a few molecular layers in films of different conjugated molecules with organic electronics applications. Because of the conditional convergence of dipolar interactions, dipole fields depend on the shape of the sample and different values are found in the middle layer of a thick film and in the bulk. The shape dependence is eliminated when depolarization is taken into account, and the dielectric tensor of molecular films converges to the bulk limit within a few molecular layers. We quantify the magnitude of surface effects and interpret general trends among different systems in terms of molecular properties, such as shape, polarizability anisotropy, and supramolecular organization. A connection between atomistic models for molecular dielectrics and simpler theories for polarizable atomic lattices is also provided.

  18. Performance improvement in pentacene organic thin film transistors by inserting a C60 ultrathin layer

    Institute of Scientific and Technical Information of China (English)

    Sun Qin-Jun; Xu Zheng; Zhao Su-Ling; Zhang Fu-Jun; Gao Li-Yan

    2011-01-01

    The contact effect on the performances of organic thin film transistors is studied here. A C60 ultrathin layer is inserted between Al source-drain electrode and pentacene to reduce the contact resistance. By a 3 nm C60 modification,the injection harrier is lowered and the contact resistance is reduced. Thus, the field-effect mobility increases from 0.12to 0.52 cm2/(V.s). It means that inserting a C60 ultra thin layer is a good method to improve the organic thin film transistor (OTFT) performance. The output curve is simulated by using a charge drift model. Considering the contact of OTFTs should be carried out.

  19. Effect of Processing Parameters on Performance of Spray-Deposited Organic Thin-Film Transistors

    Directory of Open Access Journals (Sweden)

    Jack W. Owen

    2011-01-01

    Full Text Available The performance of organic thin-film transistors (OTFTs is often strongly dependent on the fabrication procedure. In this study, we fabricate OTFTs of soluble small-molecule organic semiconductors by spray-deposition and explore the effect of processing parameters on film morphology and device mobility. In particular, we report on the effect of the nature of solvent, the pressure of the carrier gas used in deposition, and the spraying distance. We investigate the surface morphology using scanning force microscopy and show that the molecules pack along the π-stacking direction, which is the preferred charge transport direction. Our results demonstrate that we can tune the field-effect mobility of spray-deposited devices two orders of magnitude, from 10−3 cm2/Vs to 10−1 cm2/Vs, by controlling fabrication parameters.

  20. Regenerative adsorbent heat pump

    Science.gov (United States)

    Jones, Jack A. (Inventor)

    1991-01-01

    A regenerative adsorbent heat pump process and system is provided which can regenerate a high percentage of the sensible heat of the system and at least a portion of the heat of adsorption. A series of at least four compressors containing an adsorbent is provided. A large amount of heat is transferred from compressor to compressor so that heat is regenerated. The process and system are useful for air conditioning rooms, providing room heat in the winter or for hot water heating throughout the year, and, in general, for pumping heat from a lower temperature to a higher temperature.

  1. Improved sensor selectivity for chemical vapors using organic thin-film transistors

    OpenAIRE

    Royer, James Edward

    2012-01-01

    Organic thin-film transistors (OTFTs) offer unique methods for chemical vapor detection due to multiple device parameters which are influenced by reactive gases. The simplest conventional readout for OTFT sensors is the drain current; however, the drain current is dependent on changes in fundamental device characteristics such as mobility and/or threshold voltage. The chemical properties of the analyte determine whether the mobility or threshold voltage response is dominant for the OTFT. The ...

  2. Nonlinear Transport in Organic Thin Film Transistors with Soluble Small Molecule Semiconductor.

    Science.gov (United States)

    Kim, Hyeok; Song, Dong-Seok; Kwon, Jin-Hyuk; Jung, Ji-Hoon; Kim, Do-Kyung; Kim, SeonMin; Kang, In Man; Park, Jonghoo; Tae, Heung-Sik; Battaglini, Nicolas; Lang, Philippe; Horowitz, Gilles; Bae, Jin-Hyuk

    2016-03-01

    Nonlinear transport is intensively explained through Poole-Frenkel (PF) transport mechanism in organic thin film transistors with solution-processed small molecules, which is, 6,13-bis(triisopropylsilylethynyl) (TIPS) pentacene. We outline a detailed electrical study that identifies the source to drain field dependent mobility. Devices with diverse channel lengths enable the extensive exhibition of field dependent mobility due to thermal activation of carriers among traps. PMID:27455707

  3. Liquid- and Gas-Phase Diffusion of Ferrocene in Thin Films of Metal-Organic Frameworks

    OpenAIRE

    Wencai Zhou; Christof Wöll; Lars Heinke

    2015-01-01

    The mass transfer of the guest molecules in nanoporous host materials, in particular in metal-organic frameworks (MOFs), is among the crucial features of their applications. By using thin surface-mounted MOF films in combination with a quartz crystal microbalance (QCM), the diffusion of ferrocene vapor and of ethanolic and hexanic ferrocene solution in HKUST-1 was investigated. For the first time, liquid- and gas-phase diffusion in MOFs was compared directly in the identical sample. The diff...

  4. Ultraselective Gas Separation by Nanoporous Metal-Organic Frameworks Embedded in Gas-Barrier Nanocellulose Films.

    Science.gov (United States)

    Matsumoto, Makoto; Kitaoka, Takuya

    2016-03-01

    Metal-organic frameworks (MOFs) are synthesized at carboxy groups on crystalline TEMPO-oxidized cellulose nanofibers (TOCNs). MOF-TOCN films coated on a paper filter have a hierarchical structure from the nano- to macroscale, and demonstrate a high CO2 /CH4 selectivity, over 120 for CO2 at a high gas flux, by the combination of the nanoporous MOFs and the gas-barrier TOCNs, which have strong affinity with each other. PMID:26669724

  5. Photoactive self-assembled monolayers for optically switchable organic thin-film transistors

    OpenAIRE

    Salinas, Michael; Halik, Marcus

    2013-01-01

    We investigate the photoconductive and photovoltaic effects in organic thin-film transistors with thin hybrid dielectrics composed of aluminum oxide and self-assembled monolayers (SAMs). By using SAM molecules with an electro-optical functionality tuning of the photoinduced charge transfer at the interface of semiconductor and SAM upon illumination with laser light can be achieved. Control of the threshold voltage by the SAM composition enables the optical operation of the transistors without...

  6. High index of refraction films for dielectric mirrors prepared by metal-organic chemical vapor deposition

    International Nuclear Information System (INIS)

    A wide variety of metal oxides with high index of refraction can be prepared by Metal-Organic Chemical Vapor Deposition. We present some recent optical and laser damage results on oxide films prepared by MOCVD which could be used in a multilayer structure for highly reflecting (HR) dielectric mirror applications. The method of preparation affects both optical properties and laser damage threshold. 10 refs., 8 figs., 4 tabs

  7. Nonlinear Transport in Organic Thin Film Transistors with Soluble Small Molecule Semiconductor.

    Science.gov (United States)

    Kim, Hyeok; Song, Dong-Seok; Kwon, Jin-Hyuk; Jung, Ji-Hoon; Kim, Do-Kyung; Kim, SeonMin; Kang, In Man; Park, Jonghoo; Tae, Heung-Sik; Battaglini, Nicolas; Lang, Philippe; Horowitz, Gilles; Bae, Jin-Hyuk

    2016-03-01

    Nonlinear transport is intensively explained through Poole-Frenkel (PF) transport mechanism in organic thin film transistors with solution-processed small molecules, which is, 6,13-bis(triisopropylsilylethynyl) (TIPS) pentacene. We outline a detailed electrical study that identifies the source to drain field dependent mobility. Devices with diverse channel lengths enable the extensive exhibition of field dependent mobility due to thermal activation of carriers among traps.

  8. The formation of organic (propolis films)/inorganic (layered crystals) interfaces for optoelectronic applications

    Science.gov (United States)

    Drapak, S. I.; Bakhtinov, A. P.; Gavrylyuk, S. V.; Kovalyuk, Z. D.; Lytvyn, O. S.

    2008-10-01

    Propolis (honeybee glue) organic films were prepared from an alcoholic solution on the surfaces of inorganic layered semiconductors (indium, gallium and bismuth selenides). Atomic force microscopy (AFM) and X-ray diffraction (XRD) are used to characterize structural properties of an organic/inorganic interfaces. It is shown that nanodimensional linear defects and nanodimensional cavities of various shapes are formed on the van der Waals (VDW) surfaces of layered crystals as a result of chemical interaction between the components of propolis (flavonoids, aminoacids and phenolic acids) and the VDW surfaces as well as deformation interaction between the VDW surfaces and propolis films during their polymerization. The nanocavities are formed as a result of the rupture of strong covalent bonds in the upper layers of layered crystals and have the shape of hexagons or triangles in the (0001) plane. The shape, lateral size and distribution of nanodimensional defects on the VDW surfaces depends on the type of crystals, the magnitude and distribution of surface stresses. We have obtained self-organized nanofold structures of propolis/InSe interface. It is established that such heterostructures have photosensitivity in the infrared range hν<1.2 eV (the values of energy gap are 1.2 eV for InSe and 3.07 eV for propolis films at room temperature).

  9. Optical Properties of Hybrid Inorganic/Organic Thin Film Encapsulation Layers for Flexible Top-Emission Organic Light-Emitting Diodes.

    Science.gov (United States)

    An, Jae Seok; Jang, Ha Jun; Park, Cheol Young; Youn, Hongseok; Lee, Jong Ho; Heo, Gi-Seok; Choi, Bum Ho; Lee, Choong Hun

    2015-10-01

    Inorganic/organic hybrid thin film encapsulation layers consist of a thin Al2O3 layer together with polymer material. We have investigated optical properties of thin film encapsulation layers for top-emission flexible organic light-emitting diodes. The transmittance of hybrid thin film encapsulation layers and the electroluminescent spectrum of organic light-emitting diodes that were passivated by hybrid organic/inorganic thin film encapsulation layers were also examined as a function of the thickness of inorganic Al203 and monomer layers. The number of interference peaks, their intensity, and their positions in the visible range can be controlled by varying the thickness of inorganic Al2O3 layer. On the other hand, changing the thickness of monomer layer had a negligible effect on the optical properties. We also verified that there is a trade-off between transparency in the visible range and the permeation of water vapor in hybrid thin film encapsulation layers. As the number of dyads decreased, optical transparency improved while the water vapor permeation barrier was degraded. Our study suggests that, in top-emission organic light-emitting diodes, the thickness of each thin film encapsulation layer, in particular that of the inorganic layer, and the number of dyads should be controlled for highly efficient top-emission flexible organic light-emitting diodes.

  10. High mobility high efficiency organic films based on pure organic materials

    Science.gov (United States)

    Salzman, Rhonda F.; Forrest, Stephen R.

    2009-01-27

    A method of purifying small molecule organic material, performed as a series of operations beginning with a first sample of the organic small molecule material. The first step is to purify the organic small molecule material by thermal gradient sublimation. The second step is to test the purity of at least one sample from the purified organic small molecule material by spectroscopy. The third step is to repeat the first through third steps on the purified small molecule material if the spectroscopic testing reveals any peaks exceeding a threshold percentage of a magnitude of a characteristic peak of a target organic small molecule. The steps are performed at least twice. The threshold percentage is at most 10%. Preferably the threshold percentage is 5% and more preferably 2%. The threshold percentage may be selected based on the spectra of past samples that achieved target performance characteristics in finished devices.

  11. Ta2O5 as gate dielectric material for low-voltage organic thin-film transistors

    NARCIS (Netherlands)

    Bartic, Carmen; Jansen, H.; Campitelli, Andrew; Borghs, Staf

    2002-01-01

    In this paper we report the use of Ta2O5 as gate dielectric material for organic thin-film transistors. Ta2O5 has already attracted a lot of attention as insulating material for VLSI applications. We have deposited Ta2O5 thin-films with different thickness by means of electron-beam evaporation. Bein

  12. An introduction to ultrathin organic films from Langmuir-Blodgett to self-assembly

    CERN Document Server

    Ulman, Abraham

    1991-01-01

    The development of oriented organic monomolecular layers by the Langmuir-Blodgett (LB) and self-assembly (SA) techniques has led researchers toward their goal of assembling individual molecules into highly ordered architectures. Thus the continually growing contribution of LB and SA systems to the chemistry and physics of thin organic films is widely recognized. Equally well-known is the difficulty in keeping up to date with the burgeoning multidisciplinary research in this area. Dr. Ulman provides a massive survey of the available literature. The book begins with a section on analytical tools

  13. INFLUENCE OF FILM STRUCTURE AND LIGHT ON CHARGE TRAPPING AND DISSIPATION DYNAMICS IN SPUN-CAST ORGANIC THIN-FILM TRANSISTORS MEASURED BY SCANNING KELVIN PROBE MICROSCOPY

    Energy Technology Data Exchange (ETDEWEB)

    Teague, L.; Moth, M.; Anthony, J.

    2012-05-03

    Herein, time-dependent scanning Kelvin probe microscopy of solution processed organic thin film transistors (OTFTs) reveals a correlation between film microstructure and OTFT device performance with the location of trapped charge within the device channel. The accumulation of the observed trapped charge is concurrent with the decrease in I{sub SD} during operation (V{sub G}=-40 V, V{sub SD}= -10 V). We discuss the charge trapping and dissipation dynamics as they relate to the film structure and show that application of light quickly dissipates the observed trapped charge.

  14. Humidity effect on organic semiconductor NiPc films deposited at different gravity conditions

    Science.gov (United States)

    Fatima, N.; Ahmed, M. M.; Karimov, Kh. S.; Ahmedov, Kh.

    2016-08-01

    In this study, thin films of Nickel Phthalocyanine (NiPc) were deposited by centrifugation at high gravity (70g), and also at normal gravity (1g) conditions to fabricate humidity sensors. Ceramic alumina sheet, coated with silver electrodes, having interelectrode distance of 0.2l mm were used to assess the electrical properties of the sensors. Room temperature capacitance and impedance variations were measured as a function of relative humidity ranging from 25% ∼⃒ 95% at 1 kHz frequency. It was observed that sensors fabricated at 70g were more sensitive compared to sensors fabricated at 1g. Sensors fabricated at 70g exhibited 1.8 times decrease in their impedance and1.5 times increase in their capacitance at peak ambient humidity. SEM images showed more roughness for the films deposited at 70g compared to films deposited at 1g. It was assumed that surface irregularities might have increased active surface area of 70g sensors hence changed the electrical response. Impedance-humidity and capacitance-humidity relationships were modeled and a good agreement was observed between experimental and modeled data. Experimental data showed that NiPc films could be useful for instrumentation industry to fabricate organic humidity sensors.

  15. Deposition of highly (111)-oriented PZT thin films by using metal organic chemical deposition

    CERN Document Server

    Bu, K H; Choi, D K; Seong, W K; Kim, J D

    1999-01-01

    Lead zirconate titanate (PZT) thin films have been grown on Pt/Ta/SiNx/Si substrates by using metal organic chemical vapor deposition with Pb(C sub 2 H sub 5) sub 4 , Zr(O-t-C sub 4 H sub 9) sub 4 , and Ti(O-i-C sub 3 H sub 7) sub 4 as source materials and O sub 2 as an oxidizing gas. The Zr fraction in the thin films was controlled by varying the flow rate of the Zr source material. The crystal structure and the electrical properties were investigated as functions of the composition. X-ray diffraction analysis showed that at a certain range of Zr fraction, highly (111)-oriented PZT thin films with no pyrochlore phases were deposited. On the other hand, at low Zr fractions, there were peaks from Pb-oxide phases. At high Zr fractions, peaks from pyrochlore phase were seen. The films also showed good electrical properties, such as a high dielectric constant of more than 1200 and a low coercive voltage of 1.35 V.

  16. Spin coated graphene films as the transparent electrode in organic photovoltaic devices

    International Nuclear Information System (INIS)

    Many research efforts have been devoted to the replacement of the traditional indium–tin-oxide (ITO) electrode in organic photovoltaics. Solution-based graphene has been identified as a potential replacement, since it has less than two percent absorption per layer, relative high carrier mobility, and it offers the possibility of deposition on large area and flexible substrates, compatible with roll to roll manufacturing methods. In this work, soluble reduced graphene films with high electrical conductivity and transparency were fabricated and incorporated in poly(3-hexylthiophene) [6,6]-phenyl-C61-butyric acid methyl ester photovoltaic devices, as the transparent electrode. The graphene films were spin coated on glass from an aqueous dispersion of functionalized graphene, followed by a reduction process combining hydrazine vapor and annealing under argon, in order to reduce the sheet resistance. The photovoltaic devices obtained from the graphene films showed lower performance than the reference devices with ITO, due to the higher sheet resistance (2 kΩ/sq) and the poor hydrophilicity of the spin coated graphene films.

  17. Charge Transfer-Induced Molecular Hole Doping into Thin Film of Metal-Organic Frameworks.

    Science.gov (United States)

    Lee, Deok Yeon; Kim, Eun-Kyung; Shrestha, Nabeen K; Boukhvalov, Danil W; Lee, Joong Kee; Han, Sung-Hwan

    2015-08-26

    Despite the highly porous nature with significantly large surface area, metal-organic frameworks (MOFs) can be hardly used in electronic and optoelectronic devices due to their extremely poor electrical conductivity. Therefore, the study of MOF thin films that require electron transport or conductivity in combination with the everlasting porosity is highly desirable. In the present work, thin films of Co3(NDC)3DMF4 MOFs with improved electronic conductivity are synthesized using layer-by-layer and doctor blade coating techniques followed by iodine doping. The as-prepared and doped films are characterized using FE-SEM, EDX, UV/visible spectroscopy, XPS, current-voltage measurement, photoluminescence spectroscopy, cyclic voltammetry, and incident photon to current efficiency measurements. In addition, the electronic and semiconductor properties of the MOF films are characterized using Hall Effect measurement, which reveals that, in contrast to the insulator behavior of the as-prepared MOFs, the iodine doped MOFs behave as a p-type semiconductor. This is caused by charge transfer-induced hole doping into the frameworks. The observed charge transfer-induced hole doping phenomenon is also confirmed by calculating the densities of states of the as-prepared and iodine doped MOFs based on density functional theory. Photoluminescence spectroscopy demonstrates an efficient interfacial charge transfer between TiO2 and iodine doped MOFs, which can be applied to harvest solar radiations. PMID:26226050

  18. Theoretical Insight of Physical Adsorption for a Single Component Adsorbent + Adsorbate System: II. The Henry Region

    KAUST Repository

    Chakraborty, Anutosh

    2009-07-07

    The Henry coefficients of a single component adsorbent + adsorbate system are calculated from experimentally measured adsorption isotherm data, from which the heat of adsorption at zero coverage is evaluated. The first part of the papers relates to the development of thermodynamic property surfaces for a single-component adsorbent + adsorbate system1 (Chakraborty, A.; Saha, B. B.; Ng, K. C.; Koyama, S.; Srinivasan, K. Langmuir 2009, 25, 2204). A thermodynamic framework is presented to capture the relationship between the specific surface area (Ai) and the energy factor, and the surface structural and the surface energy heterogeneity distribution factors are analyzed. Using the outlined approach, the maximum possible amount of adsorbate uptake has been evaluated and compared with experimental data. It is found that the adsorbents with higher specific surface areas tend to possess lower heat of adsorption (ΔH°) at the Henry regime. In this paper, we have established the definitive relation between Ai and ΔH° for (i) carbonaceous materials, metal organic frameworks (MOFs), carbon nanotubes, zeolites + hydrogen, and (ii) activated carbons + methane systems. The proposed theoretical framework of At and AH0 provides valuable guides for researchers in developing advanced porous adsorbents for methane and hydrogen uptake. © 2009 American Chemical Society.

  19. Hemolysis effect and calcium-phosphate precipitation of heat-organic-film treated magnesium

    Institute of Scientific and Technical Information of China (English)

    GAO Jia-cheng; QIAO Li-ying; LI Long-chuan; WANG Yong

    2006-01-01

    A heat-organic-films process was employed to induce calcium-phosphate apatites formation on magnesium, consequently the corrosion resistance and hemolysis properties of magnesium were improved for biomedical applications. Firstly, magnesium samples were heat-treated at 773 K for 10 h; secondly, stearic acid films were coated on the surface of the heat-treated magnesium.Then the surface modified magnesium was soaked in simulated body fluid (SBF) to test its corrosion resistance. The results show that the heat treatment process allows magnesium to form a dense oxide layer with a thickness of around 20 μm, thereby the surface modified magnesium has higher corrosion resistance. After 24 h in SBF island apatite was deposited on magnesium. The unevenly precipitates were characterized by XRD and FTIR as the mixture of hydroxyapatite(HA) and octacalcium phosphate(OCP). The preliminary hemolysis experiment indicates that untreated magnesium has hemolytic effect (about 60%); whereas the heat-organic film treated samples has no hemolytic effect. The mechanism of fast nucleation and growth of calcium-phosphate apatites on surface modified magnesium in SBF was also discussed.

  20. Polysilsesquioxanes for Gate-Insulating Materials of Organic Thin-Film Transistors

    Directory of Open Access Journals (Sweden)

    Kimihiro Matsukawa

    2012-01-01

    Full Text Available Printable organic thin-film transistor (O-TFT is one of the most recognized technical issues nowadays. Our recent progress on the formation of organic-inorganic hybrid thin films consists of polymethylsilsesquioxane (PMSQ, and its applications for the gate-insulating layer of O-TFTs are introduced in this paper. PMSQ synthesized in toluene solution with formic acid catalyst exhibited the electric resistivity of higher than 1014 Ω cm after thermal treatment at 150°C, and the very low concentration of residual silanol groups in PMSQ was confirmed. The PMSQ film contains no mobile ionic impurities, and this is also important property for the practical use for the gate-insulating materials. In the case of top-contact type TFT using poly(3-hexylthiophene (P3HT with PMSQ gate-insulating layer, the device properties were comparable with the TFTs having thermally grown SiO2 gate-insulating layer. The feasibility of PMSQ as a gate-insulating material for O-TFTs, which was fabricated on a flexible plastic substrate, has been demonstrated. Moreover, by the modification of PMSQ, further functionalities, such as surface hydrophobicity, high permittivity that allows low driving voltage, and photocurability that allows photolithography, could be appended to the PMSQ gate-insulating layers.

  1. Organosilicon Ion-Exchange and Complexing Adsorbents

    Institute of Scientific and Technical Information of China (English)

    M. Voronkov; N. Vlasova; Yu. Pozhidaev; L. Belousova

    2005-01-01

    @@ 1Introduction Modification of mineral synthetic or natural substrates by organosilicon G-functionally substituted monomers, copolycondensation of the latter with organic and organosilicon compounds, and hydrolytic polycondensation of these monomers are the most widely used methods of synthesis of organosilicon adsorbents.

  2. Organic solar cells based on liquid crystalline and polycrystalline thin films

    Science.gov (United States)

    Yoo, Seunghyup

    This dissertation describes the study of organic thin-film solar cells in pursuit of affordable, renewable, and environmentally-friendly energy sources. Particular emphasis is given to the molecular ordering found in liquid crystalline or polycrystalline films as a way to leverage the efficiencies of these types of cells. Maximum efficiencies estimated based on excitonic character of organic solar cells show power conversion efficiencies larger than 10% are possible in principle. However, their performance is often limited due to small exciton diffusion lengths and poor transport properties which may be attributed to the amorphous nature of most organic semiconductors. Discotic liquid crystal (DLC) copper phthalocyanine was investigated as an easily processible building block for solar cells in which ordered molecular arrangements are enabled by a self-organization in its mesophases. An increase in photocurrent and a reduction in series resistance have been observed in a cell which underwent an annealing process. X-ray diffraction (XRD) and atomic force microscopy (AFM) measurements suggest that structural and morphological changes induced after the annealing process are related to these improvements. In an alternative approach, p-type pentacene thin films prepared by physical vapor deposition were incorporated into heterojunction solar cells with C60 as n-type layers. Power conversion efficiencies of 2.7% under broadband illumination (350--900 nm) with a peak external quantum efficiency of 58% have been achieved with the broad spectral coverage across the visible spectrum. Analysis using an exciton diffusion model shows this efficient carrier generation is mainly due to the large exciton diffusion length of pentacene films. Joint XRD and AFM studies reveal that the highly crystalline nature of pentacene films can account for the observed large exciton diffusion length. In addition, the electrical characteristics are studied as a function of light intensity using

  3. Interface Engineering of Organic Thin Film Transistors with Self-assembled Organophosphonic Acids

    Science.gov (United States)

    Liu, Danqing

    Organic thin film transistors (OTFTs) are interface devices with their performance highly dependent on the interface between organic semiconductors and gate dielectrics no matter whether the organic semiconductors are processed by vacuum deposition or solution-based methods. Detailed in this thesis are studies of interface engineering for OTFTs with self-assembled organophosphonic acids, which play important roles in tuning the properties of the dielectric surface for high-performance OTFTs. The poor crystallinity of rubrene in conventional vacuum deposited films is a well-known obstacle limiting practical applications of rubrene in thin film transistors. As described in Chapter 2, a template layer of diazapentacene (DAP) is introduced to induce crystallization of rubrene in thin film transistors. This study demonstrates that DAP is a suitable template molecule with negligible contribution to the conduction channel leading to polycrystalline thin films of rubrene with field effect mobility as high as 0.68 cm2 V --1 s--1. This induced-crystallization strategy highly depends on a unique octadecylphosphonic acid (ODPA) bilayer-step surface, which plays important roles in controlling the growth of both DAP and rubrene. In solution-processed OTFTs, one key factor that affects the nucleation and growth of semiconductor molecules during solution-based processing is the wetting behavior of the semiconductor solution on the dielectric surface. Reported in Chapter 3 is a new strategy for preparing solution-processed OTFTs based on enhancing the surface energy of self-assembled monolayers (SAMs) by inserting polar oxygen atoms into the long alkyl chain of phosphonic acids. SAMs of these phosphonic acids on a high-k metal oxide layer of AlOy /TiOx lead to solution-processed n-channel OTFTs with high field effect mobility of up to 2.5 cm2 V--1 s--1 and low operational voltage. Chapter 4 puts forth a new design of SAMs for interface engineering of high-performance OTFTs. This

  4. Organic Semiconductors and Nanodielectrics for Flexible, Low Voltage Thin-Film Transistors

    Science.gov (United States)

    Marks, Tobin

    2006-03-01

    Molecular materials scientists are skilled at designing and constructing individual molecules with the goal of imbuing them with predetermined chemical and physical properties. However, the subsequent task of rationally assembling them into organized, functional supramolecular architectures with precise, nanometer-level control of bulk opt-electronic properties presents another level of challenge. In this lecture, synthetic and computational approaches to addressing such problems are described in which the ultimate goal is the fabrication of flexible electronic circuits employing unconventional materials classes and unconventional fabrication techniques. The issues here concern not only the rational design, realization, and understanding of high-mobility p- and n-type organic semiconductors, but also robust enabling nanoscopic gate dielectrics having ultra-high capacitance, low leakage, and high breakdown fields. In the former area, routes to and properties of, new high-mobility heterocyclic materials are described. These materials are then used to fabricate high-performance organic thin film transistors and CMOS circuits. In the latter topic, the design, synthesis, and characterization of new high-k nanoscopic gate dielectrics are described. It is then shown how these dielectrics can be employed to significantly enhance the performance of thin-film transistors and other devices fabricated from a wide variety of both organic as well as inorganic semiconductors.

  5. Persistent photocurrent (PPC) in solution-processed organic thin film transistors: Mechanisms of gate voltage control

    Science.gov (United States)

    Singh, Subhash; Mohapatra, Y. N.

    2016-07-01

    There is a growing need to understand mechanisms of photoresponse in devices based on organic semiconductor thin films and interfaces. The phenomenon of persistent photocurrent (PPC) has been systematically investigated in solution processed TIPS-Pentacene based organic thin film transistors (OTFTs) as an important example of an organic semiconductor material system. With increasing light intensity from dark to 385 mW/cm2, there is a significant shift in threshold voltage (VTh) while the filed-effect mobility remains unchanged. The OTFT shows large photoresponse under white light illumination due to exponential tail states with characteristic energy parameter of 86 meV. The photo-induced current is observed to persist even for several hours after turning the light off. To investigate the origin of PPC, its quenching mechanism is investigated by a variety of methods involving a combination of gate bias, illumination and temperature. We show that a coherent model of trap-charge induced carrier concentration is able to account for the quenching behavior. Analysis of isothermal transients using time-analyzed transient spectroscopy shows that the emission rates are activated and are also field enhanced due to Poole-Frankel effect. The results shed light on the nature, origin, and energetic distribution of the traps controlling PPC in solution processed organic semiconductors and their interfaces.

  6. Characterization of amorphous organic thin films, determination of precise model for spectroscopic ellipsometry measurements

    International Nuclear Information System (INIS)

    The optical properties of tris(8-hydroxyquinoline) aluminum (Alq3), N,N'-diphenyl-N,N'-bis(1-naphthyl)-1-1'biphenyl-4,4''diamine (α-NPD) and other amorphous organic materials for OLEDs application, e.g. 4,4-bis(2,2-diphenyl vinyl)-1,1-biphenyl (DPVBI) and Spiro-DPVBI have been studied by multi-angle spectroscopic ellipsometry (SE). The thin films of these materials have been deposited by organic vapor phase deposition (OVPD). The structural characterization has been performed using atomic force microscopy (AFM) and X-ray reflectometry (XRR). Comparison of the measurements using these different independent techniques enables the precise determination of the optical model for dielectric function of these thin films. The detail analyses on Alq3 and α-NPD show that the Kim model with Gaussian broadening provides a significantly better fit to the ellipsometry data than the frequently used harmonic oscillator model. This conclusion is further proved by performing similar measurements on other amorphous organic samples for OLEDs application, e.g. DPVBI and Spiro-DPVBI. This result can be explained by the characteristic features of electronic states in organic molecules.

  7. Electrical and physicochemical properties of Poly(3,4-ethylenedioxythiophene)-based organic-inorganic hybrid conductive thin films

    International Nuclear Information System (INIS)

    Conductive polymer coating precursors were prepared using poly (3, 4-ehtylenedioxythiophene) (PEDOT) and three kinds of silane precursors (Q type, T type, and bridged T type) through an in-situ organic/inorganic hybrid sol-gel process. The spin-coated precursor films on Poly(ethyleneterephthalate) substrate exhibited fairly good surface resistance (∼ 104 Ω/□), transparency (∼ 80%) and pencil hardness (2 - 4 H). The solvent resistance of the film using 2, 5-bis (triethoxysilyl)-3, 4-ethylenedioxythiophene (BTES-EDOT) was excellent as compared with the films that used silane precursors due to a high degree of BTES-EDOT crosslinking in the hybrid film. Moreover, EDOT moiety in the BTES-EDOT molecule may contribute to homogeneous dispersion of the PEDOT in the organic-inorganic hybrid film.

  8. Metal–organic framework thin films with well-controlled growth directions confirmed by x-ray study

    Directory of Open Access Journals (Sweden)

    Kazuya Otsubo

    2014-12-01

    Full Text Available Metal–organic frameworks (MOFs have attracted the attention of a variety of researchers because of their structural diversity and designability, and their varied physical properties based on their uniform microporosity. While MOFs are interesting as bulk materials, future applications in functional nanomaterials will require the use of MOFs as thin films, and to achieve this, several thin-film fabrication techniques have been developed. These techniques have provided rational design of a variety of MOF thin films; however, oriented crystal growth of a MOF thin film, which is mainly confirmed by X-ray diffraction, remains a challenge that should be addressed. In this article, we review thin-film fabrications and characterizations, and structural features of MOF thin films with perfect crystalline orientation.

  9. Co-sputtered oxide thin film encapsulated organic electronic devices with prolonged lifetime

    Energy Technology Data Exchange (ETDEWEB)

    Wong, F.L.; Fung, M.K.; Ng, C.Y.; Ng, A.; Bello, I.; Lee, S.T.; Lee, C.S., E-mail: apcslee@cityu.edu.hk

    2011-11-30

    Effective top-side thin film encapsulation for organic light-emitting devices (OLEDs) was achieved by deposition of a multi-layer water diffusion barrier stack to protect the device against moisture permeation. The barrier stack was formed by alternative depositions of co-oxide and fluorocarbon (CF{sub x}) films. The co-oxide layer was fabricated by magnetron co-sputtering of silicon dioxide (SiO{sub 2}) and aluminum oxide (Al{sub 2}O{sub 3}). While the CF{sub x} layer was formed by plasma enhanced chemical vapor deposition. The water vapor transmission rate of the optimized diffusion barrier stack can be down to 10{sup -6} g/m{sup 2}/day. The OLEDs encapsulated with the multilayer stack have been shown to have operation lifetime of over 18,000 h which is nearly the same as devices with conventional glass-cover encapsulation.

  10. Improved Performance by a Double-Insulator Layer in Organic Thin-Film Transistors

    Institute of Scientific and Technical Information of China (English)

    WANG Wei; SHI Jia-Wei; GUO Shu-Xu; ZHANG Hong-Mei; QUAN Bao-Fu; MA Dong-Ge

    2006-01-01

    @@ Organic thin film transistors based on pentacene are fabricated by the method of full evaporation. The thickness of insulator film can be controlled accurately, which influences the device operation voltage markedly. Compared to the devices with a single-insulator layer, the electric performance of devices by using a double-insulator as the gate dielectric has good improvement. It is found that the gate leakage current can be reduced over one order of magnitude, and the on-state current can be enhanced over one order of magnitude. The devices with double-insulator layer exhibit field-effect mobility as large as 0.14 cm2/Vs and near the zero threshold voltage.The results demonstrate that using a proper double insulator as the gate dielectrics is an effective method to fabricate OTFTs with high electrical performance.

  11. Charge Transport in Thin Organic Semiconducting Films: Seebeck and Field Effect Studies

    Science.gov (United States)

    Böhm, W.; Fritz, T.; Leo, K.

    1997-03-01

    We have investigated the charge transport properties of vapor-deposited thin organic films, using the Seebeck effect for determining conduction type and Fermi energy and the field effect to measure mobility and total charge carrier density. We show that the combination of both techniques gives a complete picture of the electrical properties of the films. Wir untersuchen den Ladungsträgertransport in aufgedampften dünnen organischen Schichten, wobei der Seebeck-Effekt zur Bestimmung des Leitfähigkeitstyps und der Lage des Ferminiveaus und der Feldeffekt zur Bestimmung der Leitfähigkeit und der gesamten Ladungsträgerdichte benutzt wird. Es wird gezeigt, daß durch die Kombination beider Methoden ein geschlossenes Bild der elektrischen Eigenschaften erhalten wird.

  12. High efficiency THz-wave modulators based on conjugated polymer-based organic films

    International Nuclear Information System (INIS)

    A study of the modulation mechanisms of conjugated polymer-based organic films and high-efficiency, broadband and all-optically controlled terahertz modulators based on these films is presented in this paper. Under very low-level external laser excitation, modulation efficiency of more than 99% is achieved using MEH-PPV/Si, PFO/Si and F8BT/Si bilayers. By analyzing the changes in the photo-excited carrier density and photoconductivity with changes in the external laser intensity, we introduce a nonlinear photo-induced absorption process to explain the strong attenuation mechanism for the transmitted terahertz waves. Finally, a simple THz communication test is carried out to demonstrate the potential future applications of the high-efficiency all-optically controlled terahertz modulator. (paper)

  13. High efficiency THz-wave modulators based on conjugated polymer-based organic films

    Science.gov (United States)

    He, Ting; Zhang, Bo; Wang, Guo-cui; Zang, Meng-di; Hou, Yan-bing; Shen, Jing-ling

    2016-02-01

    A study of the modulation mechanisms of conjugated polymer-based organic films and high-efficiency, broadband and all-optically controlled terahertz modulators based on these films is presented in this paper. Under very low-level external laser excitation, modulation efficiency of more than 99% is achieved using MEH-PPV/Si, PFO/Si and F8BT/Si bilayers. By analyzing the changes in the photo-excited carrier density and photoconductivity with changes in the external laser intensity, we introduce a nonlinear photo-induced absorption process to explain the strong attenuation mechanism for the transmitted terahertz waves. Finally, a simple THz communication test is carried out to demonstrate the potential future applications of the high-efficiency all-optically controlled terahertz modulator.

  14. FABRICATION AND CHARACTERIZATION OF ORGANIC THIN FILMS WITH NANO—STRUCTURE

    Institute of Scientific and Technical Information of China (English)

    TakashiH,Noritaka; ChenGuorong; 等

    2002-01-01

    A novel method of thin film formation of organic materials with nano-strucure has been successfully developed by using vacuum technique is proposed. The diarylethene(C18H18N2S2)was selected as a model compound for the evaluation of this method.Polymer,we found that the tendency of dye dispersion into the polymer is as follows:PC>PBzMA>PMMA>PHPMA,where no dispersion is observed for PHPMA under the condition of 115℃ for 24 hours ,Thin film of polymer alloy composed of PMMA and polystylene(PS) was loaded into a glass ample with diarylethene,and treated for three days at 100℃,Dispersed state of the dye was evaluated by transmission electron microscope,and concluded that the dye is distributed only in PS domains selectively.Photochromic properties of the PS domain will be evaluated by using a scanning nearfield optical microscope.

  15. Solution-processed hybrid organic-inorganic complementary thin-film transistor inverter

    Science.gov (United States)

    Cheong, Heajeong; Kuribara, Kazunori; Ogura, Shintaro; Fukuda, Nobuko; Yoshida, Manabu; Ushijima, Hirobumi; Uemura, Sei

    2016-04-01

    We investigated hybrid organic-inorganic complementary inverters with a solution-processed indium-gallium-zinc-oxide (IGZO) n-channel thin-film transistor (TFT) and p-channel TFTs using the high-uniformity polymer poly[2,5-bis(alkyl)pyrrolo[3,4-c]pyrrolo-1,4(2H,5H)-dione-alt-5,5-di(thiophene-2-yl)-2,2-(E)-2-(2-(thiophen-2-yl)vinyl)thiophene] (PDVT-10). The IGZO TFT was fabricated at 150 °C for 1 min. It showed a high field-effect mobility of 0.9 cm2·V-1·s-1 and a high on/off current ratio of 107. A hybrid complementary inverter was fabricated by combining IGZO with a PDVT-10 thin-film transistor and its operation was confirmed.

  16. Ultra-thin films of polysilsesquioxanes possessing 3-methacryloxypropyl groups as gate insulator for organic field-effect transistors

    International Nuclear Information System (INIS)

    Polysilsesquioxanes (PSQs) possessing 3-methacryloxypropyl groups as an organic moiety of the side chain were synthesized by sol–gel condensation copolymerization of the corresponding trialkoxysilanes. The ultra-thin PSQ film with a radical initiator and a cross-linking agent was prepared by a spin-coating method, and the film was cured integrally at low temperatures of less than 120 °C through two different kinds of polymeric reactions, which were radical polymerization of vinyl groups and sol–gel condensation polymerization of terminated silanol and alkoxy groups. The obtained PSQ film showed the almost perfect solubilization resistance to acetone, which is a good solvent of PSQ before polymerization. It became clear by atomic force microscopy observation that the surface of the PSQ film was very smooth at a nano-meter level. Furthermore, pentacene-based organic field-effect transistor (OFET) with the PSQ film as a gate insulator showed typical p-channel enhancement mode operation characteristics and therefore the ultra-thin PSQ film has the potential to be applicable for solution-processed OFET systems. - Highlights: ► Polysilsesquioxanes (PSQs) possessing 3-methacryloxypropyl groups were synthesized. ► The ultra-thin PSQ film could be cured at low temperatures of less than 120 °C. ► The PSQ film showed the almost perfect solubilization resistance to organic solvent. ► The surface of the PSQ film was very smooth at a nano-meter level. ► Pentacene-based organic field-effect transistor with the PSQ film was fabricated.

  17. Effects of Alloying on the Optical Properties of Organic-Inorganic Lead Halide Perovskite Thin Films

    Energy Technology Data Exchange (ETDEWEB)

    Ndione, Paul F.; Li, Zhen; Zhu, Kai

    2016-09-07

    Complex refractive index and dielectric function spectra of organic-inorganic lead halide perovskite alloy thin films are presented, together with the critical-point parameter analysis (energy and broadening) of the respective composition. Thin films of methylammonium lead halide alloys (MAPbI3, MAPbBr3, MAPbBr2I, and MAPbBrI2), formamidinium lead halide alloys (FAPbI3, FAPbBr3, and FAPbBr2I), and formamidinium cesium lead halide alloys [FA0.85Cs0.15PbI3, FA0.85Cs0.15PbBrI2, and FA0.85Cs0.15Pb(Br0.4I0.6)3] were studied. The complex refractive index and dielectric functions were determined by spectroscopic ellipsometry (SE) in the photon energy range of 0.7-6.5 eV. Critical point energies and optical transitions were obtained by lineshape fitting to the second-derivative of the complex dielectric function data of these thin films as a function of alloy composition. Absorption onset in the vicinity of the bandgap, as well as critical point energies and optical band transition shift toward higher energies as the concentration of Br in the films increases. Cation alloying (Cs+) has less effect on the optical properties of the thin films compared to halide mixed alloys. The reported optical properties can help to understand the fundamental properties of the perovskite materials and also be used for optimizing or designing new devices.

  18. In-situ study of pn-heterojunction interface states in organic thin film transistors

    International Nuclear Information System (INIS)

    In this paper, we have investigated the density of pn-heterojunction interface states by evaluating the threshold voltage shift with in-situ measurement of electrical characteristics of a sandwich fluorinated copper phthalocyanine/pentacene thin film transistor with various thicknesses of pentacene thin films. A threshold voltage (VT) undergoes a significant shift from + 20.6 to + 0.53 V with increasing the thickness of pentacene. When the thickness of pentacene is more than a critical thickness of 15 nm, VT undergoes hardly any shift. On the other hand, the value of mobility is lightly decreased with increasing the thickness of pentacene due to the effect of the bulk current. Thus the VT shift is attributed to the increase of drain current in the sandwich device. In order to explain the VT shift, a model was assumed in the linear region of thin film transistor operation and the VT shift agrees with a tan−1 function of film thickness. The total charge density (Q0) of 1.53 × 10−7 C/cm2 (9.56 × 1011 electrons or holes/cm2) was obtained. Furthermore, the VT shift and Q0 could be adjusted by selecting a p-type semiconductor. - Highlights: • A threshold voltage was in-situ measured in an organic sandwich thin film transistor. • Density of pn-heterojunction interface states by evaluating the threshold voltage shift. • The threshold voltage shift attributes to the increase of drain current. • In order to explain the threshold voltage shift, a model was assumed

  19. Additive fabrication of microstructures using self-assembled organic thin-film templates

    Science.gov (United States)

    Jeon, Noo Li

    .5-100 mum) and the selective filling of trenches and vias. To demonstrate the viability of patterning thin oxide layers for applications in integrated microelectronics and optoelectronics, patterned PZT (a capacitor material) and LiNbOsb3 (a waveguide material) thin films were deposited on TiN and sapphire substrates, respectively. Strip waveguides of heteroepitaxial LiNbOsb3 with 4 mum widths were fabricated on sapphire. A simple multilayered device, a ferroelectric capacitor with platinum/PZT/platinum layers, was fabricated using the patterning methods developed in this thesis. This achievement demonstrates the possibility of developing a photolithography-free method for fabricating micron-scale metal-oxide-silicon devices based on printed organic thin films of self-assembled monolayers. With further development, the patterning of metal and ceramic thin films directed by SAMs appears to have a great potential in fabricating the three-dimensional thin film structures needed for advanced device technologies.

  20. Determination of the transport levels in thin films of organic semiconductors

    Energy Technology Data Exchange (ETDEWEB)

    Krause, Stefan

    2009-07-27

    The approach of using the combination of Ultraviolet (UPS) and Inverse Photoemission (IPS) to determine the transport levels in thin films of organic semiconductors is the scope of this work. For this matter all influences on the peak position and width in Photoelectron Spectroscopy are discussed with a special focus on organic semiconductors. Many of these influences are shown with experimental results of the investigation of diindenoperylene on Ag(111). These findings are applied to inorganic semiconductors silicon in order to establish the use of UPS and IPS on a well-understood system. Finally, the method is used to determine the transport level of several organic semiconductors (PTCDA, Alq3, CuPc, DIP, PBI-H4) and the corresponding exciton binding energies are calculated by comparison to optical absorption data. (orig.)

  1. Zeolite thin film-coated spherical end-face fiber sensors for detection of trace organic vapors

    Science.gov (United States)

    Ning, Xiangping; Zhao, Chun Liu; Yang, Jingyi; Chan, Chi Chiu

    2016-04-01

    A novel zeolite thin film-coated spherical end face fiber sensor for detection of trace organic vapors was experimentally demonstrated. The spherical end-face was fabricated by electrical arc discharge on the end face of a standard single-mode fiber. The proposed sensor comprise of the fiber's spherical end-face covered with a layer of zeolite thin film. The zeolite film and spherical end face constituted an arc-shaped inline Fabry-Perot (F-P) cavity, which improves the interference performance. The trace chemical vapor concentration was measured by monitoring the shift of F-P interference wavelength which induced by the organic vapor molecular adsorption of the zeolite film. The proposed trace organic vapors sensor performed with the enhanced sensitivity 0.91 nm/ppm with the range from 0 to 70 ppm.

  2. NEXAF/XPS study of organic molecules adsorbed on rutile TiO2(110) and Al2O3/ Ni3Al(111) substrates

    OpenAIRE

    Naboka, Michael

    2014-01-01

    The spectroscopic studies of metal oxide surface interaction with different organic molecules have been performed for the needs of organic electronics, heterogeneous catalysis and surface chemistry. Three different systems: terephthalic acid (TPA) on rutile TiO2(110), azobenzene on rutile-TiO2(110), and tetracene on Al2O3/Ni3Al (111) were investigated.

  3. Effect of fractal silver electrodes on charge collection and light distribution in semiconducting organic polymer films

    Energy Technology Data Exchange (ETDEWEB)

    Chamousis, RL; Chang, LL; Watterson, WJ; Montgomery, RD; Taylor, RP; Moule, AJ; Shaheen, SE; Ilan, B; van de Lagemaat, J; Osterloh, FE

    2014-08-21

    Living organisms use fractal structures to optimize material and energy transport across regions of differing size scales. Here we test the effect of fractal silver electrodes on light distribution and charge collection in organic semiconducting polymer films made of P3HT and PCBM. The semiconducting polymers were deposited onto electrochemically grown fractal silver structures (5000 nm x 500 nm; fractal dimension of 1.71) with PEDOT:PSS as hole-selective interlayer. The fractal silver electrodes appear black due to increased horizontal light scattering, which is shown to improve light absorption in the polymer. According to surface photovoltage spectroscopy, fractal silver electrodes outperform the flat electrodes when the BHJ film thickness is large (>400 nm, 0.4 V photovoltage). Photocurrents of up to 200 microamperes cm(-2) are generated from the bulk heterojunction (BHJ) photoelectrodes under 435 nm LED (10-20 mW cm(-2)) illumination in acetonitrile solution containing 0.005 M ferrocenium hexafluorophosphate as the electron acceptor. The low IPCE values (0.3-0.7%) are due to slow electron transfer to ferrocenium ion and due to shunting along the large metal-polymer interface. Overall, this work provides an initial assessment of the potential of fractal electrodes for organic photovoltaic cells.

  4. Organic and organic-inorganic hybrid polymer thin films deposited by PECVD using TEOS and cyclohexene for ULSI interlayer-dielectric application

    Science.gov (United States)

    Seo, Hyeon Jin; Nam, Sang-Hun; Kim, Sungsoo; Boo, Jin-Hyo

    2015-11-01

    Organic and organic-inorganic hybrid polymer thin films were deposited on Si(1 0 0) substrates at various ratios of TEOS (tetraethoxysilane) to cyclohexene by the plasma enhanced chemical vapor deposition (PECVD) method. The as-grown polymerized thin films were first analyzed by FT-IR and XPS. The results of FT-IR showed that the hybrid polymer thin films were polymerized with each fragmented precursor. The XPS results showed the chemical species and binding energies of each species. The Si 2p core-level spectra from the hybrid polymer thin film showed the status of the Si oxidation number. Impedance analysis was utilized for the measurement of the capacitance values and I-V curves, and an ultra low-k value and leakage current density of 1.75 and 10-9 A/cm2 at 1 MV/cm were obtained, respectively.

  5. The interaction of organic adsorbate vibrations with substrate lattice waves in methyl-Si(111)-(1 × 1)

    International Nuclear Information System (INIS)

    A combined helium atom scattering and density functional perturbation theory study has been performed to elucidate the surface phonon dispersion relations for both the CH3-Si(111)-(1 × 1) and CD3-Si(111)-(1 × 1) surfaces. The combination of experimental and theoretical methods has allowed characterization of the interactions between the low energy vibrations of the adsorbate and the lattice waves of the underlying substrate, as well as characterization of the interactions between neighboring methyl groups, across the entire wavevector resolved vibrational energy spectrum of each system. The Rayleigh wave was found to hybridize with the surface rocking libration near the surface Brillouin zone edge at both the M¯-point and K¯-point. The calculations indicated that the range of possible energies for the potential barrier to the methyl rotation about the Si-C axis is sufficient to prevent the free rotation of the methyl groups at a room temperature interface. The density functional perturbation theory calculations revealed several other surface phonons that experienced mode-splitting arising from the mutual interaction of adjacent methyl groups. The theory identified a Lucas pair that exists just below the silicon optical bands. For both the CH3- and CD3-terminated Si(111) surfaces, the deformations of the methyl groups were examined and compared to previous experimental and theoretical work on the nature of the surface vibrations. The calculations indicated a splitting of the asymmetric deformation of the methyl group near the zone edges due to steric interactions of adjacent methyl groups. The observed shifts in vibrational energies of the -CD3 groups were consistent with the expected effect of isotopic substitution in this system

  6. Detection of saliva-range glucose concentrations using organic thin-film transistors

    Energy Technology Data Exchange (ETDEWEB)

    Elkington, D.; Belcher, W. J.; Dastoor, P. C.; Zhou, X. J. [Centre for Organic Electronics, University of Newcastle, Callaghan, New South Wales 2308 (Australia)

    2014-07-28

    We describe the development of a glucose sensor through direct incorporation of an enzyme (glucose oxidase) into the gate of an organic thin film transistor (OTFT). We show that glucose diffusion is the key determinant of the device response time and present a mechanism of glucose sensing in these devices that involves protonic doping of the transistor channel via enzymatic oxidation of glucose. The integrated OTFT sensor is sensitive across 4 decades of glucose concentration; a range that encompasses both the blood and salivary glucose concentration levels. As such, this work acts as a proof-of-concept for low-cost printed biosensors for salivary glucose.

  7. All solution processed organic thin film transistor-backplane with printing technology for electrophoretic display

    Science.gov (United States)

    Lee, Myung W.; Song, C.K.

    2012-01-01

    In this study, solution processes were developed for backplane using an organic thin film transistor (OTFT) as a driving device for an electrophoretic display (EPD) panel. The processes covered not only the key device of OTFTs but also interlayer and pixel electrodes. The various materials and printing processes were adopted to achieve the requirements of devices and functioning layers. The performance of OTFT of the backplane was sufficient to drive EPD sheet by producing a mobility of 0.12 cm2/v x sec and on/off current ratio of 10(5).

  8. Detection of saliva-range glucose concentrations using organic thin-film transistors

    Science.gov (United States)

    Elkington, D.; Belcher, W. J.; Dastoor, P. C.; Zhou, X. J.

    2014-07-01

    We describe the development of a glucose sensor through direct incorporation of an enzyme (glucose oxidase) into the gate of an organic thin film transistor (OTFT). We show that glucose diffusion is the key determinant of the device response time and present a mechanism of glucose sensing in these devices that involves protonic doping of the transistor channel via enzymatic oxidation of glucose. The integrated OTFT sensor is sensitive across 4 decades of glucose concentration; a range that encompasses both the blood and salivary glucose concentration levels. As such, this work acts as a proof-of-concept for low-cost printed biosensors for salivary glucose.

  9. Nanostructured thin films for organic photovoltaic cells and organic light-emitting diodes

    Science.gov (United States)

    Zheng, Ying

    2009-12-01

    Achieving efficient organic optoelectronic devices, such as organic photovoltaic (OPV) cells and organic light-emitting diodes (OLEDs), relies on the understanding of the formation of various organic nanostructures as well as the fundamental of physical processes in device operation. The research presented in this thesis systematically investigates the controlled growth of organic nanostructure through different approaches and their relationship to OPV cell performance. Moreover, new materials and device structure are explored to achieve efficient OLEDs, which also provide further insight of the physical processes governing the performance of these devices. We first investigated the phase separation process in a molecular mixed donor-acceptor (D -- A) bulk heterojunction (BHJ) composed of pentacene and C60 suing a combination of experimental and computational approaches. Both experiment characterization and the MD simulation reveals that strong aggregation of pentacene exists in the pentacene:C60 mixtures due to the strong pi -- pi interaction among pentacene molecules. By controlling the processing conditions to suppress the pentacene aggregation to nanoscale leads to higher device efficiency as the more photogenerated excitons are able to reach the D -- A interface and contribute to the photocurrent. To circumvent the limits on phase separated D -- A mixed heterojunction, an interdigitated D -- A BHJ is synthesized through the oblique angle deposition (OAD) of copper phthalocyanine (CuPc). The morphology of CuPc nanorod arrays grown under the OAD process can be controlled by careful selection of the processing conditions, and we have achieved a high density, vertically aligned, polycrystalline CuPc nanorod array with nanorod size as small as 20-30 nm. Successful infiltration of [6,6]-phenyl-C61-butyric acid methyl ester (PCBM) into the optimized CuPc nanorod arrays has resulted in doubling of the power conversion efficiency of the OPV cell over planar

  10. Structural Characterization of Sputtered Silicon Thin Films after Rapid Thermal Annealing for Active-Matrix Organic Light Emitting Diode

    Science.gov (United States)

    Mugiraneza, Jean de Dieu; Miyahira, Tomoyuki; Sakamoto, Akinori; Chen, Yi; Okada, Tatsuya; Noguchi, Takashi; Itoh, Taketsugu

    2010-12-01

    The microcrystalline phase obtained by adopting a two-step rapid thermal annealing (RTA) process for rf-sputtered silicon films deposited on thermally durable glass was characterized. The optical properties, surface morphology, and internal stress of the annealed Si films are investigated. As the thermally durable glass substrate allows heating of the deposited films at high temperatures, micro-polycrystalline silicon (micro-poly-Si) films of uniform grain size with a smooth surface and a low internal stress could be obtained after annealing at 750 °C. The thermal stress in the Si films was 100 times lower than that found in the films deposited on conventional glass. Uniform grains with an average grain size of 30 nm were observed by transmission electron microscopy (TEM) in the films annealed at 800 °C. These micro-poly-Si films have potential application for fabrication of uniform and reliable thin film transistors (TFTs) for large scale active-matrix organic light emitting diode (AMOLED) displays.

  11. Metal-organic chemical vapour deposition of lithium manganese oxide thin films via single solid source precursor

    Directory of Open Access Journals (Sweden)

    Oyedotun K.O.

    2015-12-01

    Full Text Available Lithium manganese oxide thin films were deposited on sodalime glass substrates by metal organic chemical vapour deposition (MOCVD technique. The films were prepared by pyrolysis of lithium manganese acetylacetonate precursor at a temperature of 420 °C with a flow rate of 2.5 dm3/min for two-hour deposition period. Rutherford backscattering spectroscopy (RBS, UV-Vis spectrophotometry, X-ray diffraction (XRD spectroscopy, atomic force microscopy (AFM and van der Pauw four point probe method were used for characterizations of the film samples. RBS studies of the films revealed fair thickness of 1112.311 (1015 atoms/cm2 and effective stoichiometric relationship of Li0.47Mn0.27O0.26. The films exhibited relatively high transmission (50 % T in the visible and NIR range, with the bandgap energy of 2.55 eV. Broad and diffused X-ray diffraction patterns obtained showed that the film was amorphous in nature, while microstructural studies indicated dense and uniformly distributed layer across the substrate. Resistivity value of 4.9 Ω·cm was obtained for the thin film. Compared with Mn0.2O0.8 thin film, a significant lattice absorption edge shift was observed in the Li0.47Mn0.27O0.26 film.

  12. Tandem organic light-emitting diode with a molybdenum tri-oxide thin film interconnector layer

    Institute of Scientific and Technical Information of China (English)

    Lu Fei-Ping; Wang Qian; Zhou Xiang

    2013-01-01

    A 10-nm-thick molybdenum tri-oxide (MoO3) thin film was used as the interconnector layer in tandem organic lightemitting devices (OLEDs).The tandem OLEDs with two identical emissive units consisting of N,N'-bis(naphthalen-1-yl)-N,N'-bis(phenyl)-benzidine (NPB) / tris(8-hydroxyquinoline) aluminum (Alq3) exhibited current efficiency-current density characteristics superior to the conventional single-unit devices.At 20 mA/cm2,the current efficiency of the tandem OLEDs using the interconnector layers of MoO3 thin film was about 4.0 cd/A,which is about twice that of the corresponding conventional single-unit device (1.8 cd/A).The tandem OLED showed a higher power efficiency than the conventional single-unit device for luminance over 1200 cd/m2.The experimental results demonstrated that a MoO3 thin film with a proper thickness can be used as an effective interconnector layer in tandem OLEDs.Such an interconnector layer can be easily fabricated by simple thermal evaporation,greatly simplifying the device processing and fabrication processes required by previously reported interconnector layers.A possible explanation was proposed for the carrier generation of the MoO3 interconnector layer.

  13. Natural organic matter interactions with polyamide and polysulfone membranes: Formation of conditioning film

    KAUST Repository

    Gutierrez, Leonardo

    2015-03-31

    A conditioning film changes the physicochemical properties of the membrane surface and strongly affects subsequent fouling behavior. Results from this Atomic Force Microscopy study indicate that Natural Organic Matter (NOM) characteristics, membrane surface properties, and solution chemistry are fundamental during conditioning film formation. Repulsive forces were observed between HUM (humic-NOM) and Polyamide (PA) or Polysulfone (PS) membranes during approach in Na+ and Ca2+ solutions. However, repulsive and attractive forces were randomly recorded during BIOP (biopolymer-NOM) approach to both membranes, possibly caused by low electrostatic repulsion, hydrogen bonding, and presence of chemically/physically heterogeneous regions on membrane surfaces. During retracting, Ca2+ ions increased HUM adhesion to PA and PS membrane, indicating cation bridging/complexation as dominant interacting mechanism for this isolate. BIOP adsorption on PS and PA membrane was stronger than HUM under similar solution conditions, where hydrogen bonding would play an important role. Additionally, irrespective of solution conditions, higher adhesion energy was recorded on PS than on PA membrane for both NOM isolates, indicating membrane hydrophobicity as an important interacting factor. Results from this research will advance our understanding of conditioning film formation for NOM isolates and membranes of different physicochemical characteristics.

  14. Semiconducting organic thin films as monitoring devices for NO2 air pollution

    Science.gov (United States)

    Heilmann, A.; Lantto, V.

    The chemisorption of NO2 on lead phthalocyanine (PbPc) thin films changes the electrical conductivity of this semiconducting organic material and so the detection of NO2 concentration in the ppb range is possible. Some mesurements concerning the NO2 concentration in city air (Oulu, Finland) were carried out using this kind of device (PbPc thin film on metal slit electrodes). In the first part of the study, the sensor devices were heated in a test chamber up to 170 C and air from outside the laboratory was pumped into the test chamber using a conventional pump. In the second part of the study, a PbPc sensor with internal heating and measuring amplifier was installed directly at the city air pollution monitoring station where a commercial equipment based on chemiluminescnece was also used for continuous monitoring of the NO2 concentration in the city air. Good correlation between the sensor response and the chemiluminescence values was obtained under these circumstances. The measurements show that NO2 sensors based on PbPc thin films are suited to monitor NO2 as an air pollutant in city air.

  15. Leakage radiation spectroscopy of organic nanofibers on metal films: evidence for exciton-surface plasmon polariton interaction

    DEFF Research Database (Denmark)

    Jozefowski, Leszek; Fiutowski, Jacek; Bordo, Vladimir;

    2012-01-01

    Leakage radiation spectroscopy of organic nanofibers composed of self-assembled organic molecules (para-Hexaphenylene, p-6P) deposited on a thin (40-60 nm) Ag film has been performed in the spectral range 420-675 nm which overlaps with the nanofiber photoluminescence band. Using a soft transfer t...

  16. Apple, carrot, and hibiscus edible films containing plant antimicrobials inactivate Salmonella Newport in packaged organic leafy greens

    Science.gov (United States)

    The increased demand for organic leafy green may raise the risk of foodborne illness outbreaks due to consumption of contaminated produce. Edible films incorporated with natural antimicrobials have the potential to be used as ingredients into organic bagged salads to control contamination from path...

  17. Transparent conductive PVP/AgNWs films for flexible organic light emitting diodes by spraying method

    Science.gov (United States)

    Hu, Jun-tao; Mei, Wen-juan; Ye, Kang-li; Wei, Qing-qing; Hu, Sheng

    2016-05-01

    In this study, a simple spraying method is used to prepare the transparent conductive films (TCFs) based on Ag nanowires (AgNWs). Polyvinylpyrrolidone (PVP) is introduced to modify the interface of substrate. The transmittance and bending performance are improved by optimizing the number of spraying times and the solution concentration and controlling the annealing time. The spraying times of 20, the concentration of 2 mg/mL and the annealing time of 10 min are chosen to fabricate the PVP/AgNWs films. The transmittance of PVP/AgNWs films is 53.4%—67.9% at 380—780 nm, and the sheet resistance is 30 Ω/□ which is equivalent to that of commercial indium tin oxide (ITO). During cyclic bending tests to 500 cycles with bending radius of 5 mm, the changes of resistivity are negligible. The performance of PVP/AgNW transparent electrodes has little change after being exposed to the normal environment for 1 000 h. The adhesion to polymeric substrate and the ability to endure bending stress in AgNWs network films are both significantly improved by introducing PVP. Spraying method makes AgNWs form a stratified structure on large-area polymer substrates, and the vacuum annealing method is used to weld the AgNWs together at junctions and substrates, which can improve the electrical conductivity. The experimental results indicate that PVP/AgNW transparent electrodes can be used as transparent conductive electrodes in flexible organic light emitting diodes (OLEDs).

  18. Structural measurements of polymer-fullerene blend films for organic photovoltaics

    Science.gov (United States)

    Delongchamp, Dean

    2011-03-01

    Organic photovoltaic (OPV) technology has the potential to greatly lower the cost of solar cell fabrication by enabling ink-based deposition of active layers. In bulk heterojunction (BHJ) OPV devices, the power conversion efficiency critically depends on the distribution of the polymer absorber and the fullerene electron acceptor (e.g., the blend morphology). I will describe measurement methods to probe the structure of OPV devices, with a focus on the morphology of the BHJ layer. For example, the vertical distribution of absorber and electron acceptor in BHJ films follows segregation behavior similar to that of miscible polymer blends. The top (air) interface becomes rich in the polymer absorber, whereas the bottom interface composition depends on the substrate surface energy. Thin film transistors fabricated from BHJs can therefore exhibit ambipolar or hole-only transport depending on the dielectric, because of different interfacial segregation. We extend these results to practical photovoltaic devices by comparing BHJs cast upon hole transport layers that have similar work functions but different surface energies. This study includes the application of variable angle spectroscopic ellipsometry (VASE) to BHJ films, and emphasizes the importance of absorber anisotropy and vertical heterogeneity in the optical model. Additional results will describe the nanometer-scale structure in the BHJ interior. The application of solid-state nuclear magnetic resonance (SS-NMR) can reveal details about the segregation of absorber and acceptor in a BHJ film. Nanoscale BHJ morphology information can also be collected using tomographic transmission electron microscopy (TEM). Together these measurements allow us to reveal a detailed picture of BHJ morphology, explain how the morphology originates from materials and processing choices, and relate the morphology to device performance and stability.

  19. Development of a model to describe organic films on aerosol particles and cloud droplets. Final report; Entwicklung eines Modells zur Beschreibung organischer Filme auf Aerosolteilchen und Wolkentropfen. Abschlussbericht

    Energy Technology Data Exchange (ETDEWEB)

    Forkel, R. (ed.); Seidl, W.

    2000-12-01

    Organic substances with polar groups are enriched on water surfaces and can form monomolecular surface films which can reduce the surface tension. A new model to describe surface films is presented, which describes in detail the film forming properties of fatty acids with up to 22 carbon atoms. The model is applied to measured concentrations of fatty acids (from the literature) in rain water and on aerosol particles and cloud droplets. An investigation of the sources of fatty acids has shown, that abrasion of the wax layer on leaves and needles is the main sources for surface film material in the western USA. Anthropogenic sources in urban areas are meat preparation and cigarette smoke. The agreement between model results and measurements when the model was applied to rain water confirms the original assumption that fatty acids are a main compound of surface films in rain water. For humid aerosol particles the application of the model on measured concentrations of fatty acids only showed strongly diluted films. Only for remote forest areas in western USA concentrated films were found, with the surface tension reduced by 20 to 30%. On cloud droplets the surface films is still more diluted than on aerosol particles. For all investigated cases the films was too much diluted to have an effect on the activation process of cloud droplets. (orig.) [German] Organische Substanzen mit polaren Gruppen reichern sich an der Wasseroberflaeche an und koennen monomolekulare Oberflaechenfilme bilden, die zu einer Verringerung der Oberflaechenspannung fuehren. Es wird ein neues Modell zur Beschreibung eines Oberflaechenfilms beschrieben, das detailliert die filmbildenden Eigenschaften der Fettsaeuren mit bis zu 22 Kohlenstoffatomen erfasst. Dieses Modell ist auf gemessene Konzentrationen von Fettsaeuren (Literaturdaten) in Regenwasser und auf atmosphaerischen Aerosolteilchen und Wolkentropfen angewandt worden. Eine Betrachtung der Quellen der Fettsaeuren zeigte, dass der Abrieb der

  20. Optical and Morphological Studies of Thermally Evaporated PTCDI-C8 Thin Films for Organic Solar Cell Applications

    Directory of Open Access Journals (Sweden)

    Ronak Rahimi

    2013-01-01

    Full Text Available PTCDI-C8 due to its relatively high photosensitivity and high electron mobility has attracted much attention in organic semiconductor devices. In this work, thin films of PTCDI-C8 with different thicknesses were deposited on silicon substrates with native silicon dioxide using a vacuum thermal evaporator. Several material characterization techniques have been utilized to evaluate the structure, morphology, and optical properties of these films. Their optical constants (refractive index and extinction coefficient have been extracted from the spectroscopic ellipsometry (SE. X-ray reflectivity (XRR and atomic force microscopy (AFM were employed to determine the morphology and structure as well as the thickness and roughness of the PTCDI-C8 thin films. These films revealed a high degree of structural ordering within the layers. All the experimental measurements were performed under ambient conditions. PTCDI-C8 films have shown to endure ambient condition which allows pots-deposition characterization.

  1. Fabrication of organically modified oxygen sensing film based on fluorescent quenching

    Institute of Scientific and Technical Information of China (English)

    XIN LingLing; XIAO LaiLong; ZHAO Li; CHEN Xi; WANG XiaoRu

    2007-01-01

    An organically modified silicate (ORMOSIL) as a matrix for oxygen-sensitive sensor, in which dimethyldimethoxysilane was selected as an organic modifier in the precursor, is described. The sensing film with tris-(4,7-diphenyl-1,10-phenanthroline) ruthenium(II) as an indicator developed in this paper was characterized by efficient quenching by oxygen. Blue light-emitting diodes ((max = 475 nm) were employed as light excitation source. The linear range of the dissolved oxygen was from 0.5 to 16 (g/mL. The measured RSD was 2%, the response time (t95) was 60 s, and the determination limit was 0.2 (g/mL. A portable and inexpensive luminescence-based sensor was established and applied to the determination of dissolved oxygen in the surface water.

  2. Low loss spin wave resonances in organic-based ferrimagnet vanadium tetracyanoethylene thin films

    Science.gov (United States)

    Zhu, Na; Zhang, Xufeng; Froning, I. H.; Flatté, Michael E.; Johnston-Halperin, E.; Tang, Hong X.

    2016-08-01

    We experimentally demonstrate high quality factor spin wave resonances in an encapsulated thin film of the organic-based ferrimagnet vanadium tetracyanoethylene ( V [TC N E ] x ˜2 ) coated on an a-plane sapphire substrate by low temperature chemical vapor deposition. The thickness standing wave modes are observed in a broad frequency range (1 GHz-5 GHz) with high quality factor exceeding 3200 in ambient air at room temperature, rivaling those of inorganic magnetic materials. The exchange constant of V [TC N E ] x ˜2 , a crucial material parameter for future study and device design of the V [TC N E ] x ˜2 , is extracted from the measurement with a value of (4.61 ±0.35 ) ×10-16 m2 . Our result establishes the feasibility of using organic-based materials for building hybrid magnonic devices and circuits.

  3. Percolation of Carbon Nanoparticles in Poly(3-Hexylthiophene Enhancing Carrier Mobility in Organic Thin Film Transistors

    Directory of Open Access Journals (Sweden)

    Chang-Hung Lee

    2014-01-01

    Full Text Available To improve the field-effect mobility of all-inkjet-printed organic thin film transistors (OTFTs, a composite material consisted of carbon nanoparticles (CNPs and poly(3-hexylthiophene (P3HT was reported by using homemade inkjet-printing system. These all-inkjet-printed composite OTFTs represented superior characteristics compared to the all-inkjet-printed pristine P3HT OTFTs. To investigate the enhancement mechanism of the blended materials, the percolation model was established and experimentally verified to illustrate the enhancement of the electrical properties with different blending concentrations. In addition, experimental results of OTFT contact resistances showed that both contact resistance and channel resistance were halved. At the same time, X-ray diffraction measurements, Fourier transform infrared spectra, ultraviolet-visible light, and photoluminescence spectra were also accomplished to clarify the material blending effects. Therefore, this study demonstrates the potential and guideline of carbon-based nanocomposite materials in all-inkjet-printed organic electronics.

  4. MOLECULAR DYNAMICS SIMULATION OF SELF-ORGANIZED STRUCTURE IN MICRO-PHASE SEPARATION OF NANO-SCALE FILM

    Institute of Scientific and Technical Information of China (English)

    Dexiang Tang; Wei Ge; Jinghai Li

    2004-01-01

    Self-organization in thin micro-films has shown potential for the production of microelements with specific structures and functions; however, little is known about its mechanism of formation. A 2-D molecular dynamics (MD)simulation on this process is carried out in this paper for films between two parallel walls (substrates) under different initial conditions. The films consist of two immiscible components (A and B). The simulation results in alternative columns perpendicular to the walls, which are rich either in A or in B molecules, respectively, apparently owing to their different interactions with the walls. The characteristic breadths of the columns depend on the distance between the two walls. By providing microscopic details of the self-organization processes and the resulted structures, MD simulation proves itself as a unique way for analyzing the dynamics of thin films.

  5. Preparation and characterization of BiFeO3 thin films by the LPD on OH-functionalized organic SAMs

    Institute of Scientific and Technical Information of China (English)

    2010-01-01

    BiFeO3 (BFO) thin films were grown on OH-functionalized organic self-assembled monolayers (SAMs) via liquid-phase deposition (LPD) method at a temperature below 100°C. The BiFeO3 thin films were induced to synthesize on the OH-functionalized organic OTS monolayers prepared on hydroxylated glass substrate by self-assembling technique. The hydrophilic characteristic of the as-prepared OTS-SAMs was measured by contact angle tester. The crystal phase composition, microstructure and topography of the as-synthesized BFO thin films were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), energy disperse spectroscopy (EDS) and atomic force microscope (AFM), respectively. Results show that compact and homogeneous BFO thin films can be formed on the OH-functionalized SAMs at low temperature.

  6. Diffusion of metal atoms on organic thin films studied by PEEM

    International Nuclear Information System (INIS)

    Full text: Recently there has been much interest in organic devices. The stability of metal microstructure deposited on organic films is crucial for these devices of higher integration. In this study, we measured photoelectron emission microscopy (PEEM) images of metals (In, Au, Al) microstructure, deposited onto perylene-3,4,9,10-tetracarboxylic acid-dianhydride (PTCDA) thin films prepared on MoS2 substrate through a mesh (10μm x 10μm square opening, 25μm periodicity). In PEEM experiments, a D2 lamp (hv 2, the PEEM images showed a periodic triangle pattern, although the deposited shape of the In microstructure was square. The triangular shape area was larger than the mesh opening, indicating that In atoms diffuse to three lateral directions. The three directions of diffusion were found to correspond with surface crystal axes of MoS2. Such three directional diffusion was not observed for Au/PTCDA/MoS2, Al/PTCDA/MoS2, In(1 Angstroms)/PTCDA(submonolayer)/MoS2 and In/MoS2. These results suggest that the diffusion originates from (1) strong chemical interaction between PTCDA and In, and (2) the molecular packing structure of PTCDA which depends on substrate surfaces

  7. The Integration and Applications of Organic Thin Film Transistors and Ferroelectric Polymers

    Science.gov (United States)

    Hsu, Yu-Jen

    Organic thin film transistors and ferroelectric polymer (polyvinylidene difluoride) sheet material are integrated to form various sensors for stress/strain, acoustic wave, and Infrared (heat) sensing applications. Different from silicon-based transistors, organic thin film transistors can be fabricated and processed in room-temperature and integrated with a variety of substrates. On the other hand, polyvinylidene difluoride (PVDF) exhibits ferroelectric properties that are highly useful for sensor applications. The wide frequency bandwidth (0.001 Hz to 10 GHz), vast dynamic range (100n to 10M psi), and high elastic compliance (up to 3 percent) make PVDF a more suitable candidate over ceramic piezoelectric materials for thin and flexible sensor applications. However, the low Curie temperature may have impeded its integration with silicon technology. Organic thin film transistors, however, do not have the limitation of processing temperature, hence can serve as transimpedance amplifiers to convert the charge signal generated by PVDF into current signal that are more measurable and less affected by any downstream parasitics. Piezoelectric sensors are useful for a range of applications, but passive arrays suffer from crosstalk and signal attenuation which have complicated the development of array-based PVDF sensors. We have used organic field effect transistors, which are compatible with the low Curie temperature of a flexible piezoelectric polymer,PVDF, to monolithically fabricate transimpedance amplifiers directly on the sensor surface and convert the piezoelectric charge signal into a current signal which can be detected even in the presence of parasitic capacitances. The device couples the voltage generated by the PVDF film under strain into the gate of the organic thin film transistors (OFET) using an arrangement that allows the full piezoelectric voltage to couple to the channel, while also increasing the charge retention time. A bipolar detector is created by

  8. The response of quartz crystals coated with thin fatty acid film to organic gases

    CERN Document Server

    Jin, C N; Kim, K H; Kwon, Y S

    1999-01-01

    We tried to apply a quartz crystal as a sensor by using the resonant frequency and the resistance properties of quartz crystals. Four kinds of fatty acids that have the same head groups were coated on the surfaces of the quartz crystals, and the shift of the resonant frequency and the resistance were observed based on the lengths of the tail groups. Myristic acid (C sub 1 sub 4), palmitic acid (C sub 1 sub 6), stearic acid (C sub 1 sub 8), and arachidic acid (C sub 2 sub 0) were deposited on the surfaces of quartz crystals by using the Langmuir-Blodgett (LB) method. As a result, the resonant frequency change was more sensitive to high molecular-weight fatty acids than to low molecular-weight ones. We also observed the effect of temperature on stearic acid LB films, and the response properties of quartz crystals coated with stearic-acid LB films to organic gases were investigated. As a result, the sensitivity of quartz crystals to organic gases was higher for higher molecular-weight gas, and we found that quar...

  9. In situ preparation of biomimetic thin films and their surface-shielding effect for organisms in high vacuum.

    Directory of Open Access Journals (Sweden)

    Hiroshi Suzuki

    Full Text Available Self-standing biocompatible films have yet to be prepared by physical or chemical vapor deposition assisted by plasma polymerization because gaseous monomers have thus far been used to create only polymer membranes. Using a nongaseous monomer, we previously found a simple fabrication method for a free-standing thin film prepared from solution by plasma polymerization, and a nano-suit made by polyoxyethylene (20 sorbitan monolaurate can render multicellular organisms highly tolerant to high vacuum. Here we report thin films prepared by plasma polymerization from various monomer solutions. The films had a flat surface at the irradiated site and were similar to films produced by vapor deposition of gaseous monomers. However, they also exhibited unique characteristics, such as a pinhole-free surface, transparency, solvent stability, flexibility, and a unique out-of-plane molecular density gradient from the irradiated to the unirradiated surface of the film. Additionally, covering mosquito larvae with the films protected the shape of the organism and kept them alive under the high vacuum conditions in a field emission-scanning electron microscope. Our method will be useful for numerous applications, particularly in the biological sciences.

  10. Molecular beam deposition and polymerization of parylene-N ultrathin films: Effective buffers in organic light emitting diodes

    International Nuclear Information System (INIS)

    Highlights: • Parylene-N (PPXN) films prepared by using a home-made Knudsen Cell were identified and characterized. • 1 nm PPXN thin films were inserted at different locations in the hole transport layers of organic light emitting diodes. • For an optimized PPXN inserted organic light emitting diodes, current efficiency improvement of 11% was achieved. • The device current efficiency improvement and the current density variation under operation were discussed. - Abstract: Ultrathin Parylene-N (PPXN) films were prepared by using a home-made Knudsen Cell (KC). The PPXN films were identified by infrared (IR) spectra. The morphology and insulativity of PPXN films were measured by atomic force microscope (AFM) and current density versus voltage (j–V) characteristics. Well controlled 1-nm-thick PPXN thin films were inserted at different locations in the N′-bis(naphthalene-1-yl)-N, N′-bis(phenyl) benzidine (NPB) layers of organic light emitting diodes (OLEDs) with the structure of ITO/NPB/tris (8-hydroxyquinolato) aluminum (Alq3)/LiF/Al. For an optimized PPXN inserted structure, current efficiency of 6.27 cd/A was achieved, 11% higher than the 5.64 cd/A of the control one with 1-nm-thick PPXN buffer inserted at the anode interface. The device current efficiency improvement is due to the electron blocking of PPXN buffers, and the current density variation of devices under operation was explained by tunneling barrier reduction

  11. Nanostructured films of inorganic-organic hybrid materials for application in photovoltaics; Nanostrukturierte Filme aus anorganisch-organischen Hybridmaterialien fuer die Photovoltaik

    Energy Technology Data Exchange (ETDEWEB)

    Perlich, Jan

    2009-06-25

    Nanostructured thin films of crystalline TiO{sub 2} for applications in photovoltaics were studied. The fabrication of the thin films is based on a hybrid approach. The anorganic metal oxide prepared via a sol-gel synthesis is structurated by the template properties of the applied organic block-copolymer. Via the film epitaxy by means of centrifugal coating first hybrid films (polymer-nanocomposite films) were fabricated, which were changed by calcination into crystalline TiO{sub 2} films with taylored morphology. The successful development of novel preparation approaches to the adaption to consisting conditions in the application field of photovoltaics contains a route to the fine-tuning of the morphology as well as the fabrication of hierarchical morphologies in different configurations. The structural study of the single nanostructurated TiO{sub 2} films up to the functional multilayer arrangement as photovoltaic demonstration cell was performed with conventionally imaging methods, as for instance scanning force microscopy and electron microscopy as well as the special small-angle X-ray scattering method under rigid incident angle (GISAXS). [German] Es wurden nanostrukturierte duenne Filme aus kristallinem TiO{sub 2} fuer Anwendungen in der Photovoltaik untersucht. Die Herstellung der duennen Filme basiert auf einem Hybridansatz. Das ueber eine Sol-Gel-Synthese bereitgestellte anorganische Metalloxid wird durch die Template-Eigenschaften des eingesetzten organischen Block-Copolymers strukturiert. Ueber die Filmaufbringung mittels Schleuderbeschichtung wurden zunaechst Hybridfilme (Polymer-Nanokompositfilme) hergestellt, die durch Kalzinierung in kristalline TiO{sub 2}-Filme mit massgeschneiderter Morphologie umgewandelt werden. Die erfolgreiche Entwicklung von neuartigen Praeparationsansaetzen zur Adaption an bestehende Gegebenheiten im Anwendungsgebiet der Photovoltaik beinhaltet eine Route zur Feineinstellung der Morphologie sowie die Herstellung von

  12. In situ intercalation dynamics in inorganic-organic layered perovskite thin films.

    Science.gov (United States)

    Ahmad, Shahab; Kanaujia, Pawan K; Niu, Wendy; Baumberg, Jeremy J; Vijaya Prakash, G

    2014-07-01

    The properties of layered inorganic semiconductors can be manipulated by the insertion of foreign molecular species via a process known as intercalation. In the present study, we investigate the phenomenon of organic moiety (R-NH3I) intercalation in layered metal-halide (PbI2)-based inorganic semiconductors, leading to the formation of inorganic-organic (IO) perovskites [(R-NH3)2PbI4]. During this intercalation strong resonant exciton optical transitions are created, enabling study of the dynamics of this process. Simultaneous in situ photoluminescence (PL) and transmission measurements are used to track the structural and exciton evolution. On the basis of the experimental observations, a model is proposed which explains the process of IO perovskite formation during intercalation of the organic moiety through the inorganic semiconductor layers. The interplay between precursor film thickness and organic solution concentration/solvent highlights the role of van der Waals interactions between the layers, as well as the need for maintaining stoichiometry during intercalation. Nucleation and growth occurring during intercalation matches a Johnson-Mehl-Avrami-Kolmogorov model, with results fitting both ideal and nonideal cases. PMID:24905435

  13. In Situ Intercalation Dynamics in Inorganic–Organic Layered Perovskite Thin Films

    Science.gov (United States)

    2014-01-01

    The properties of layered inorganic semiconductors can be manipulated by the insertion of foreign molecular species via a process known as intercalation. In the present study, we investigate the phenomenon of organic moiety (R-NH3I) intercalation in layered metal-halide (PbI2)-based inorganic semiconductors, leading to the formation of inorganic–organic (IO) perovskites [(R-NH3)2PbI4]. During this intercalation strong resonant exciton optical transitions are created, enabling study of the dynamics of this process. Simultaneous in situ photoluminescence (PL) and transmission measurements are used to track the structural and exciton evolution. On the basis of the experimental observations, a model is proposed which explains the process of IO perovskite formation during intercalation of the organic moiety through the inorganic semiconductor layers. The interplay between precursor film thickness and organic solution concentration/solvent highlights the role of van der Waals interactions between the layers, as well as the need for maintaining stoichiometry during intercalation. Nucleation and growth occurring during intercalation matches a Johnson–Mehl–Avrami–Kolmogorov model, with results fitting both ideal and nonideal cases. PMID:24905435

  14. Elaboration of transparent conductive oxide films for flexible organic electroluminescent devices

    Science.gov (United States)

    Lucas, Bruno; Rammal, Wassim; El Amrani, Aumeur; Moliton, André; Séguy, Isabelle

    2006-04-01

    In this study, we presented high-performance flexible organic light-emitting diodes (FOLEDs); to do so, we prepared indium-tin oxide (ITO) thin layers by ion beam sputtering (IBS) on polyethylene terephtalate (PET) substrates in soft low temperature conditions. The IBS technology seems well adapted to us to adjust the conduction level of the interface films to the one of the various organic materials making up the fabrication processes of the organic optoelectronic components; moreover this technique does not require a high substrate temperature or an annealing after ITO deposition to crystallize the obtained layers. Because of the great number of deposition parameters (oxygen flow, substrate temperature, deposition rate...) playing interdependent roles and strongly influencing the electrical, optical and structural properties of the layers, we optimized the effects of these different parameters separately by using electrical and optical characterizations as well as X-ray diffraction analyses. The performances of FOLEDs on PET substrate with different ITO thicknesses were investigated and compared to the ones of a conventional organic light-emitting diode realized on glass substrate and according to the same device configuration.

  15. Filter-adsorber aging assessment

    International Nuclear Information System (INIS)

    An aging assessment of high-efficiency particulate (HEPA) air filters and activated carbon gas adsorption units was performed by the Pacific Northwest Laboratory as part of the U.S. Nuclear Regulatory Commission's (USNRC) Nuclear Plant Aging Research (NPAR) Program. This evaluation of the general process in which characteristics of these two components gradually change with time or use included the compilation of information concerning failure experience, stressors, aging mechanisms and effects, and inspection, surveillance, and monitoring methods (ISMM). Stressors, the agents or stimuli that can produce aging degradation, include heat, radiation, volatile contaminants, and even normal concentrations of aerosol particles and gasses. In an experimental evaluation of degradation in terms of the tensile breaking strength of aged filter media specimens, over forty percent of the samples did not meet specifications for new material. Chemical and physical reactions can gradually embrittle sealants and gaskets as well as filter media. Mechanisms that can lead to impaired adsorber performance are associated with the loss of potentially available active sites as a result of the exposure of the carbon to airborne moisture or volatile organic compounds. Inspection, surveillance, and monitoring methods have been established to observe filter pressure drop buildup, check HEPA filters and adsorbers for bypass, and determine the retention effectiveness of aged carbon. These evaluations of installed filters do not reveal degradation in terms of reduced media strength but that under normal conditions aged media can continue to effectively retain particles. However, this degradation may be important when considering the likelihood of moisture, steam, and higher particle loadings during severe accidents and the fact it is probable that the filters have been in use for an extended period

  16. High performance Mo adsorbent PZC

    Energy Technology Data Exchange (ETDEWEB)

    Anon.

    1998-10-01

    We have developed Mo adsorbents for natural Mo(n, {gamma}){sup 99}Mo-{sup 99m}Tc generator. Among them, we called the highest performance adsorbent PZC that could adsorb about 250 mg-Mo/g. In this report, we will show the structure, adsorption mechanism of Mo, and the other useful properties of PZC when you carry out the examination of Mo adsorption and elution of {sup 99m}Tc. (author)

  17. Sub-micron phase coexistence in small-molecule organic thin films revealed by infrared nano-imaging

    Science.gov (United States)

    Westermeier, Christian; Cernescu, Adrian; Amarie, Sergiu; Liewald, Clemens; Keilmann, Fritz; Nickel, Bert

    2014-06-01

    Controlling the domain size and degree of crystallization in organic films is highly important for electronic applications such as organic photovoltaics, but suitable nanoscale mapping is very difficult. Here we apply infrared-spectroscopic nano-imaging to directly determine the local crystallinity of organic thin films with 20-nm resolution. We find that state-of-the-art pentacene films (grown on SiO2 at elevated temperature) are structurally not homogeneous but exhibit two interpenetrating phases at sub-micrometre scale, documented by a shifted vibrational resonance. We observe bulk-phase nucleation of distinct ellipsoidal shape within the dominant pentacene thin-film phase and also further growth during storage. A faint topographical contrast as well as X-ray analysis corroborates our interpretation. As bulk-phase nucleation obstructs carrier percolation paths within the thin-film phase, hitherto uncontrolled structural inhomogeneity might have caused conflicting reports about pentacene carrier mobility. Infrared-spectroscopic nano-imaging of nanoscale polymorphism should have many applications ranging from organic nanocomposites to geologic minerals.

  18. Mercury adsorption properties of sulfur-impregnated adsorbents

    Science.gov (United States)

    Hsi, N.-C.; Rood, M.J.; Rostam-Abadi, M.; Chen, S.; Chang, R.

    2002-01-01

    Carbonaceous and noncarbonaceous adsorbents were impregnated with elemental sulfur to evaluate the chemical and physical properties of the adsorbents and their equilibrium mercury adsorption capacities. Simulated coal combustion flue gas conditions were used to determine the equilibrium adsorption capacities for Hg0 and HgCl2 gases to better understand how to remove mercury from gas streams generated by coal-fired utility power plants. Sulfur was deposited onto the adsorbents by monolayer surface deposition or volume pore filling. Sulfur impregnation increased the total sulfur content and decreased the total and micropore surface areas and pore volumes for all of the adsorbents tested. Adsorbents with sufficient amounts of active adsorption sites and sufficient microporous structure had mercury adsorption capacities up to 4,509 ??g Hg/g adsorbent. Elemental sulfur, organic sulfur, and sulfate were formed on the adsorbents during sulfur impregnation. Correlations were established with R2>0.92 between the equilibrium Hg0/HgCl2 adsorption capacities and the mass concentrations of elemental and organic sulfur. This result indicates that elemental and organic sulfur are important active adsorption sites for Hg0 and HgCl2.

  19. Preparation of Composited Graphene/PEDOT:PSS Film for Its Possible Application in Graphene-based Organic Solar Cells

    Institute of Scientific and Technical Information of China (English)

    YU Yue; LI Meicheng; CHU Lihua; YU Hakki; Wodtke A M; ZHAO Yan; ZHANG Zhongmo

    2015-01-01

    The interface between graphene and organic layers is a key factor responsible for the performance of gra-phene-based organic solar cells (OSCs). In this paper, we focus on coating PEDOT:PSS onto the surface of graphene. We demonstrate two approaches, applying UV/Ozone treatment on graphene and modifying PEDOT:PSS with Zonyl, to get a PEDOT:PSS well-coated graphene film . Our results prove that both methods can be effective to solve the interface issue between graphene and PEDOT: PSS. Thereby it shows a positive application of the composited gra-phene/PEDOT:PSS film on graphene-based OSCs.

  20. Microchip electrophoresis with background electrolyte containing polyacrylic acid and high content organic solvent in cyclic olefin copolymer microchips for easily adsorbed dyes.

    Science.gov (United States)

    Wei, Xuan; Sun, Ping; Yang, Shenghong; Zhao, Lei; Wu, Jing; Li, Fengyun; Pu, Qiaosheng

    2016-07-29

    Plastic microchips can significantly reduce the fabrication cost but the adsorption of some analytes limits their application. In this work, background electrolyte containing ionic polymer and high content of organic solvent was adopted to eliminate the analyte adsorption and achieve highly efficient separation in microchip electrophoresis. Two dyes, rhodamine 6G (Rh6G) and rhodamine B (RhB) were used as the model analytes. By using methanol as the organic solvent and polyacrylic acid (PAA) as a multifunctional additive, successful separation of the two dyes within 75μm id. microchannels was realized. The role of PAA is multiple, including viscosity regulator, selectivity modifier and active additive for counteracting analyte adsorption on the microchannel surface. The number of theoretical plate of 7.0×10(5)/m was attained within an effective separation distance of 2cm using background electrolyte consisting 80% methanol, 0.36% PAA and 30mmol/L phosphate at pH 5.0. Under optimized conditions, relative standard deviations of Rh6G and RhB detection (n=5) were no more than 1.5% for migration time and 2.0% for peak area, respectively. The limit of detection (S/N=3) was 0.1nmol/L for Rh6G. The proposed technique was applied in the determination of both Rh6G and RhB in chilli powder and lipstick samples with satisfactory recoveries of 81.3-103.7%.

  1. Microchip electrophoresis with background electrolyte containing polyacrylic acid and high content organic solvent in cyclic olefin copolymer microchips for easily adsorbed dyes.

    Science.gov (United States)

    Wei, Xuan; Sun, Ping; Yang, Shenghong; Zhao, Lei; Wu, Jing; Li, Fengyun; Pu, Qiaosheng

    2016-07-29

    Plastic microchips can significantly reduce the fabrication cost but the adsorption of some analytes limits their application. In this work, background electrolyte containing ionic polymer and high content of organic solvent was adopted to eliminate the analyte adsorption and achieve highly efficient separation in microchip electrophoresis. Two dyes, rhodamine 6G (Rh6G) and rhodamine B (RhB) were used as the model analytes. By using methanol as the organic solvent and polyacrylic acid (PAA) as a multifunctional additive, successful separation of the two dyes within 75μm id. microchannels was realized. The role of PAA is multiple, including viscosity regulator, selectivity modifier and active additive for counteracting analyte adsorption on the microchannel surface. The number of theoretical plate of 7.0×10(5)/m was attained within an effective separation distance of 2cm using background electrolyte consisting 80% methanol, 0.36% PAA and 30mmol/L phosphate at pH 5.0. Under optimized conditions, relative standard deviations of Rh6G and RhB detection (n=5) were no more than 1.5% for migration time and 2.0% for peak area, respectively. The limit of detection (S/N=3) was 0.1nmol/L for Rh6G. The proposed technique was applied in the determination of both Rh6G and RhB in chilli powder and lipstick samples with satisfactory recoveries of 81.3-103.7%. PMID:27371017

  2. Effects of neutral particle beam on nano-crystalline silicon thin films, with application to thin film transistor backplane for flexible active matrix organic light emitting diodes

    Energy Technology Data Exchange (ETDEWEB)

    Jang, Jin Nyoung; Song, Byoung Chul; Lee, Dong Hyeok [Dept. of Display and Semiconductor Physics, Korea University, Chungnam (Korea, Republic of); Yoo, Suk Jae; Lee, Bonju [National Fusion Research Institute, 52, Yuseong-Gu, Deajeon, 305-333 (Korea, Republic of); Hong, MunPyo, E-mail: goodmoon@korea.ac.kr [Dept. of Display and Semiconductor Physics, Korea University, Chungnam (Korea, Republic of)

    2011-08-01

    A novel deposition process for nano-crystalline silicon (nc-Si) thin films was developed using neutral beam assisted chemical vapor deposition (NBaCVD) technology for the application of the thin film transistor (TFT) backplane of flexible active matrix organic light emitting diode (AMOLED). During the formation of a nc-Si thin film, the energetic particles enhance nano-sized crystalline rather microcrystalline Si in thin films. Neutral Particle Beam (NPB) affects the crystallinity in two ways: (1) NPB energy enhances nano-crystallinity through kinetic energy transfer and chemical annealing, and (2) heavier NPB (such as Ar) induces damage and amorphization through energetic particle impinging. Nc-Si thin film properties effectively can be changed by the reflector bias. As increase of NPB energy limits growing the crystalline, the performance of TFT supports this NPB behavior. The results of nc-Si TFT by NBaCVD demonstrate the technical potentials of neutral beam based processes for achieving high stability and reduced leakage in TFT backplanes for AMOLEDs.

  3. Thermodynamic study of fatty acids adsorption on different adsorbents

    International Nuclear Information System (INIS)

    This work has as objective the study about the adsorption behavior of fatty acids (acetic, propionic, and butyric) on activated carbon and on modified and unmodified montmorillonite clays as a function of temperature and initial concentration of the adsorbate, through adsorption isotherms and their thermodynamic parameters (ΔG, ΔH, and ΔS). The activated carbon presented a higher adsorption capacity due to its relatively large surface area, compared to others adsorbents. The polar characteristic of fatty acids decreased with the increase in the length of non-polar hydrocarbon chain, improving the affinity between the activated carbon (non-polar adsorbent) and the acids. The adsorption capacity of modified montmorillonite (polar adsorbent) was favored due to the presence of the organic cation among its layers, which make the surface more hydrophobic and organophilic when compared to the unmodified montmorillonite surface. The amount of fatty acids adsorbed in the adsorbents surface increased with the concentration, at constant temperature, and decreased with the increase of temperature, at constant concentration. The amount of fatty acids adsorbed in the three adsorbents was related to the surface area and polarity of the adsorbent, concentration and solubility of the adsorbate and temperature of the solution. The negative values of ΔG and ΔH showed that the adsorption on activated carbon and on modified and unmodified montmorillonite clays was a spontaneous and an exothermic process. The decrease in the values of ΔG, with the increase of temperature, demonstrated that the adsorption was benefited by the high temperature and the positive values of ΔS showed that the fatty acids molecules were in a more randomic condition in the adsorbed state than in solution. The experimental results obtained at the temperatures of (298, 303, 313, and 323) K showed that experimental data were well represented by the Langmuir and Freundlich isotherms models

  4. Study of Optical and Electrical Properties of Organic Thin Films for Photovoltaic Applications

    Directory of Open Access Journals (Sweden)

    Jan Pospisil

    2015-09-01

    Full Text Available The paper deals with the study of optical, electrical and dielectric properties of thin film organic materials suitable for the preparation of optoelectronic devices (e.g. photodiodes, phototransistors, photovoltaic cells. As active layers palladium phthalocyanine (PdPc[t-Bu]4, fullerene (acceptor material, PCBM and their mixture (9:5 mass % were used. Thin films were prepared by two methods: by spin coating (Chemat technology Spin Coater and by material inkjet printing (Dimatix Materials Printer DMP-2800. UV-VIS spectroscopy and ellipsometry were used to study the optical properties. The paper also presents results of electrical and dielectric measurements. We found out that the properties of all structures prepared by spin coating depend on the rotational speed of spin coater, on the mode of solution casting (static, dynamic and in the case of material inkjet printing they are too much influenced by the substrate. Samples prepared on the substrate at 60 °C showed a photovoltaic effect with fill factor about 0.25 and the conversion efficiency about 0.2 %.DOI: http://dx.doi.org/10.5755/j01.ms.21.3.7278

  5. Impedimetric and amperometric bifunctional glucose biosensor based on hybrid organic-inorganic thin films.

    Science.gov (United States)

    Wang, Huihui; Ohnuki, Hitoshi; Endo, Hideaki; Izumi, Mitsuru

    2015-02-01

    A novel glucose biosensor with an immobilized mediator was studied using electrochemical impedance spectroscopy (EIS) and amperometry measurements. The biosensor has a characteristic ultrathin form and is composed of a self-assembled monolayer anchoring glucose oxidase (GOx) covered with Langmuir-Blodgett (LB) films of Prussian blue (PB). The immobilized PB in the LB films acts as a mediator and enables the biosensor to work under a low potential (0.0V vs. Ag/AgCl). In the EIS measurements, a dramatic decrease in charge transfer resistance (Rct) was observed with sequential addition of glucose, which can be attributed to enzymatic activity. The linearity of the biosensor response was observed by the variation of the sensor response (1/Rct) as a function of glucose concentration in the range 0 to 25mM. The sensor also showed linear amperometric response below 130mM glucose. The organic-inorganic system of GOx and PB nanoclusters demonstrated bifunctional sensing action, both amperometry and EIS modes, as well as long sensing stability for 4 days. PMID:25014167

  6. An optimization algorithm for designing robust and simple antireflection films for organic photovoltaic cells

    Science.gov (United States)

    Kubota, S.; Kanomata, K.; Momiyama, K.; Suzuki, T.; Hirose, F.

    2013-10-01

    We propose an optimization algorithm to design multilayer antireflection (AR) structure, which has robustness against variations in layer thicknesses, for organic photovoltaic cells. When a set of available materials are given, the proposed method searches for the material and thickness of each AR layer to maximize the short-circuit current density (Jsc). This algorithm allows for obtaining a set of solutions, including optimal and quasi-optimal solutions, at the same time, so that we can clearly make comparison between them. In addition, the effects of deviations in the thicknesses of the AR layers are examined for the (quasi-)optimal solutions obtained. The expectation of the decrease in the AR performance is estimated by calculating the changes in Jsc when the thicknesses of all AR layers are varied independently. We show that some of quasi-optimal solutions may have simpler layer configuration and can be more robust against the deviations in film thicknesses, than the optimal solution. This method indicates the importance of actively searching valuable, nonoptimal solutions for practical design of AR films. We also discuss the optical conditions that lead to light absorption in the back metal contact and the effects of changing active layer thicknesses.

  7. Photo-induced halide redistribution in organic-inorganic perovskite films

    Science.gov (United States)

    Dequilettes, Dane W.; Zhang, Wei; Burlakov, Victor M.; Graham, Daniel J.; Leijtens, Tomas; Osherov, Anna; Bulović, Vladimir; Snaith, Henry J.; Ginger, David S.; Stranks, Samuel D.

    2016-05-01

    Organic-inorganic perovskites such as CH3NH3PbI3 are promising materials for a variety of optoelectronic applications, with certified power conversion efficiencies in solar cells already exceeding 21%. Nevertheless, state-of-the-art films still contain performance-limiting non-radiative recombination sites and exhibit a range of complex dynamic phenomena under illumination that remain poorly understood. Here we use a unique combination of confocal photoluminescence (PL) microscopy and chemical imaging to correlate the local changes in photophysics with composition in CH3NH3PbI3 films under illumination. We demonstrate that the photo-induced `brightening' of the perovskite PL can be attributed to an order-of-magnitude reduction in trap state density. By imaging the same regions with time-of-flight secondary-ion-mass spectrometry, we correlate this photobrightening with a net migration of iodine. Our work provides visual evidence for photo-induced halide migration in triiodide perovskites and reveals the complex interplay between charge carrier populations, electronic traps and mobile halides that collectively impact optoelectronic performance.

  8. In situ vibrational spectroscopy of thin organic films confined at the solid-solid interface

    CERN Document Server

    Haydock, S A

    2002-01-01

    Raman scattering was used to study thin films, of hexadecane, octamethyltetrasiloxane (OMCTS), 1-undecanol and Langmuir-Blodgett (LB) monolayers consisting of zinc stearate, zinc arachidate and zinc behenate, all at the solid-solid interface. This thesis contains the first unenhanced Raman spectrum of an organic monolayer confined in the contact between two solid surfaces. The LB monolayers were also investigated with sum-frequency spectroscopy in order that comparisons could be made between results from the two techniques. Thin films were confined between an optical prism and an optical lens at pressures ranging from 30 MPa to 200 MPa. I have shown that the deposited LB monolayers were conformationally ordered and that this high degree of order was retained at applied pressures of up to 200 MPa. However, the application of pressure caused the hydrocarbon chains to tilt from the surface normal. The changes observed in the overall intensity of the Raman spectra on formation of the solid-solid contact can be ex...

  9. Poly(3-hexylthiophene) films by electrospray deposition for crystalline silicon/organic hybrid junction solar cells

    Energy Technology Data Exchange (ETDEWEB)

    Hiate, Taiga; Miyauchi, Naoto; Tang, Zeguo; Ishikawa, Ryo; Ueno, Keiji; Shirai, Hajime [Graduate School of Science and Engineering, Saitama University, 255 Shimo-Okubo, Sakura, Saitama 858-3676 (Japan)

    2012-10-15

    The electrospray deposition (ESD) of poly(3-hexylthiophene) (P3HT) and conductive poly(3,4-ethylenedioxythiophene):poly(styrene sulfonate) (PEDOT:PSS) on P3HT for use in crystalline silicon/organic hybrid heterojunction solar cells on CZ crystalline silicon (c-Si) (100) wafer was investigated using real-time characterization by spectroscopic ellipsometry (SE). In contrast to the nonuniform deposition of products frequently obtained by conventional spin-coating, a uniform deposition of P3HT and PEDOT:PSS films were achieved on flat and textured hydrophobic c-Si(100) wafers by adjusting the deposition conditions. The c-Si/P3HT/PEDOT:PSS heterojunction solar cells exhibited efficiencies of 4.1 and 6.3% on flat and textured c-Si(100) wafers, respectively. These findings suggest that ESD is a promising method for the uniform deposition of P3HT and PEDOT:PSS films on flat and textured hydrophobic substrates. (copyright 2012 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim) (orig.)

  10. Light-induced processes on atoms and clusters confined in nanoporous silica and organic films

    Science.gov (United States)

    Moi, L.; Burchianti, A.; Bogi, A.; Marinelli, C.; Maibohm, C.; Mariotti, E.

    2007-03-01

    The study of light induced processes on atoms and nanoparticles confined in organic films or in dielectric structures is motivated both by fundamental interest and applications in optics and photonics. Depending on the light intensity and frequency and the kind of confinement, different processes can be activated. Among them photodesorption processes have a key role. Non thermal light induced atomic desorption has been observed from siloxane and paraffin films previously exposed to alkali vapors. This effect has been extensively investigated and used both to develop photo-atom sources and to load magneto-optical traps. Recently we observed huge photodesorption of alkali atoms embedded in nanoporous silica. In this case the atomic photodesorption causes, by properly tuning the light frequency, either formation or evaporation of clusters inside the silica matrix. Green-blue light desorbs isolated adatoms from the glass surface eventually producing clusters, whereas red-near infrared (NIR) light causes cluster evaporation due to direct excitation of surface plasmon oscillations. Green-blue light induces cluster formation taking advantage of the dense atomic vapor, which diffuses through the glass nano-cavities. Both processes are reversible and even visible to the naked eye. By alternatively illuminating the porous glass sample with blue-green and red-NIR light we demonstrate that the glass remembers the illumination sequences behaving as an effective rereadable and rewritable optical medium.

  11. Inverted organic light-emitting diodes using different transparent conductive oxide films as a cathode

    Science.gov (United States)

    Takada, Makoto; Kobayashi, Takashi; Nagase, Takashi; Naito, Hiroyoshi

    2016-03-01

    We report on poly(dioctylfluorene-alt-benzothiadiazole) (F8BT) based inverted organic light-emitting diodes (iOLEDs) using commercially available transparent conductive oxide (TCO) films as a cathode, indium tin oxide (ITO), Ga doped ZnO (GZO), and Al doped ZnO (AZO). The ITO, GZO, and AZO glasses work as an electron-injecting layer (EIL) and cathode. The device configuration that we prepared is ITO, GZO, or AZO/F8BT/MoO3/Au. The device characteristics of these iOLEDs are almost comparable to those of conventional iOLEDs with ZnO films prepared by spray pyrolysis as an EIL, indicating that the electron injection properties of ITO, GZO, or AZO as a cathode are similar to those of ZnO layer in conventional iOLEDs. These results demonstrate the low-cost fabrication of iOLEDs utilizing commercially available TCO glasses as a cathode without deposition of ZnO layers on ITO glass.

  12. Effects of Plasma Polymer Films and Their Deposition Powers on the Barrier Characteristics of the Multilayer Encapsulation for Organic Devices.

    Science.gov (United States)

    Kim, Hoonbae; Ban, Wonjin; Kwon, Sungruel; Yong, Sanghyun; Chae, Heeyeop; Jung, Donggeun

    2016-05-01

    Organic electronic devices (OEDs) are quite suitable for use in flexible devices due to their ruggedness and flexibility. A number of researchers have studied the use of OEDs on flexible substrates in transparent, flexible devices in the near future. However, water and oxygen can permeate through the flexible substrates and can reduce the longevity of OEDs made from organic materials, which are weak to moisture and oxygen. In order to prevent the degradation of the OEDs, researchers have applied an encapsulation layer to the flexible substrates. In this study, Al2O3/plasma polymer film/Al2O3 multi-layers were deposited on polyethylene-naphthalate substrates through a combination of atomic layer deposition and plasma-enhanced chemical vapor deposition (PECVD). The plasma polymer film, which is located between the Al2O3 films, is deposited via PECVD with the use of a tetrakis(trimethylsilyloxy)silane precursor. The power of the plasma deposition varied from 10 to 50 W. The hydrophobicity of the plasma polymer film surfaces was investigated by measuring the water contact angle. The chemical structures of the plasma polymer films were measured via ex-situ Fourier transform infrared analysis. The permeation curves of the various films were analyzed by performing a calcium (Ca)-test. PMID:27483936

  13. Electrokinetic investigations of solid/organic liquid dispersions: Effects of temperature treatment of the solid and alkyl chain length of adsorbed amines

    Energy Technology Data Exchange (ETDEWEB)

    Jada, A.; Siffert, B.; Eleli-Letsango, J. [Centre de Recherches sur la Physico-Chimie des Surfaces Solides 24, avenue du President Kenedy 68200 MULHOUSE (France)

    1996-01-01

    Zeta potential of two oxides TiO{sub 2} and Al{sub 2}O{sub 3}, dispersed in various organic solvents were measured at room temperature. The inorganic particles were dried at temperatures ranging from 100 to 500{degree}C for several days and were allowed to cool under vacuum just before use. Electrokinetic investigations of TiO{sub 2} particles in n-alkylamine-hexane solutions with various amine chain lengths (C{sub n}H{sub 2n+1}NH{sub 2}, n=1{endash}10) were also done and allowed the determination of the shear plane position in the eventual electric double layer surrounding the solid surface. Furthermore, in order to estimate the thickness {delta} of the electrical double layer surrounding the solid surface, DLVO theory was applied to TiO{sub 2} particles dispersed in n-hexane, in the presence of butylamine. {copyright} {ital 1996 American Institute of Physics.}

  14. I. Fundamental Practicum: Temperature Measurements of Falling Droplets, July, 1989. II. Industrial Practicum: Interaction and Effect of Adsorbed Organics on Reference Clays and Reservoir Rock, April, 1988. III. Apprenticeship Practicum: Studies of Group XIII Metal Inclusion Complexes, March, 1987

    Science.gov (United States)

    Wells, Mark Richard

    The temperature of 225 μm decane droplets falling through a hot, quiescent, oxygen -free environment were measured using laser-induced exciplex fluorescence thermometry. The temperature of the droplets was found to increase approximately 0.42^ circC/^circC increase in the environment temperature as the environment temperature was increased to 250^circ C. Less than 10% evaporation of the droplets was observed at the highest environment temperatures. This represents one of the first successful applications of a remote-sensing technique for the temperature determination of droplets in a dynamic system. Industrial practicum. The industrial practicum report, entitled "Interaction and Effect of Adsorbed Organics on Reference Clays and Reservoir Rock," is a discussion of the measurement of the effect adsorbed organic material, especially from crude petroleum, has on the surface area, cation exchange capacity, and zeta potential of reference clay material and reservoir rock. In addition, the energetics of adsorption of a petroleum extract onto several reference clays and reservoir rock were measured using both flow and batch microcalorimetry. These results are very important in evaluating and understanding the wettability of reservoir rock and its impact on the recovery of crude oil from a petroleum reservoir. Apprenticeship practicum. "Studies of Group XIII Metal Inclusion Complexes" investigates the structure and dynamics of liquid inclusion complexes having the general formula (R_4N) (Al_2 Me_6I) cdot (C_6H_6) _{rm x}. ^1H and ^{13}C spin-lattice relaxation times, nuclear Overhauser enhancements, and molecular correlation times were measured as well as diffusion coefficients of the various species in solution. The dynamics of transfer between "guest" and free solvent molecules were measured using a variety of techniques. The inherent structure of liquid inclusion complexes as an ordered medium for homogeneous catalysis was studied using hydrogenation catalyzed by

  15. New diarylmethanofullerene derivatives and their properties for organic thin-film solar cells

    Directory of Open Access Journals (Sweden)

    Daisuke Sukeguchi

    2009-02-01

    Full Text Available A number of diarylmethanofullerene derivatives were synthesized. The cyclopropane ring of the derivatives has two aryl groups substituted with electron-withdrawing and -donating groups, the latter with long alkyl chains to improve solubility in organic solvents, an important property in processing cells. First reduction potentials of most derivatives were less negative than that of [6,6]-phenyl-C61-butyric acid methyl ester (PCBM, which is possibly ascribed to their electron-withdrawing nature. Organic thin-film photovoltaic cells fabricated with poly(3-hexylthiophene (P3HT as the electron-donor and diarylmethanofullerene derivatives as the electron-acceptor material were examined. The {(methoxycarbonylphenyl[bis(octyloxyphenyl]methano}fullerene showed power conversion efficiency as high as PCBM, but had higher solubility in a variety of organic solvents than PCBM. The Voc value was higher than that of PCBM, which is derived from the electron-donating (octyloxyphenyl group, possibly raising the LUMO level. Photovoltaic effects of the devices fabricated with the derivatives having some electron-withdrawing groups were also examined.

  16. Flexible suspended gate organic thin-film transistors for ultra-sensitive pressure detection

    Science.gov (United States)

    Zang, Yaping; Zhang, Fengjiao; Huang, Dazhen; Gao, Xike; di, Chong-An; Zhu, Daoben

    2015-03-01

    The utilization of organic devices as pressure-sensing elements in artificial intelligence and healthcare applications represents a fascinating opportunity for the next-generation electronic products. To satisfy the critical requirements of these promising applications, the low-cost construction of large-area ultra-sensitive organic pressure devices with outstanding flexibility is highly desired. Here we present flexible suspended gate organic thin-film transistors (SGOTFTs) as a model platform that enables ultra-sensitive pressure detection. More importantly, the unique device geometry of SGOTFTs allows the fine-tuning of their sensitivity by the suspended gate. An unprecedented sensitivity of 192 kPa-1, a low limit-of-detection pressure of <0.5 Pa and a short response time of 10 ms were successfully realized, allowing the real-time detection of acoustic waves. These excellent sensing properties of SGOTFTs, together with their advantages of facile large-area fabrication and versatility in detecting various pressure signals, make SGOTFTs a powerful strategy for spatial pressure mapping in practical applications.

  17. Flexible All-organic, All-solution Processed Thin Film Transistor Array with Ultrashort Channel

    Science.gov (United States)

    Xu, Wei; Hu, Zhanhao; Liu, Huimin; Lan, Linfeng; Peng, Junbiao; Wang, Jian; Cao, Yong

    2016-07-01

    Shrinking the device dimension has long been the pursuit of the semiconductor industry to increase the device density and operation speed. In the application of thin film transistors (TFTs), all-organic TFT arrays made by all-solution process are desired for low cost and flexible electronics. One of the greatest challenges is how to achieve ultrashort channel through a cost-effective method. In our study, ultrashort-channel devices are demonstrated by direct inkjet printing conducting polymer as source/drain and gate electrodes without any complicated substrate’s pre-patterning process. By modifying the substrate’s wettability, the conducting polymer’s contact line is pinned during drying process which makes the channel length well-controlled. An organic TFT array of 200 devices with 2 μm channel length is fabricated on flexible substrate through all-solution process. The simple and scalable process to fabricate high resolution organic transistor array offers a low cost approach in the development of flexible and wearable electronics.

  18. Flexible All-organic, All-solution Processed Thin Film Transistor Array with Ultrashort Channel.

    Science.gov (United States)

    Xu, Wei; Hu, Zhanhao; Liu, Huimin; Lan, Linfeng; Peng, Junbiao; Wang, Jian; Cao, Yong

    2016-01-01

    Shrinking the device dimension has long been the pursuit of the semiconductor industry to increase the device density and operation speed. In the application of thin film transistors (TFTs), all-organic TFT arrays made by all-solution process are desired for low cost and flexible electronics. One of the greatest challenges is how to achieve ultrashort channel through a cost-effective method. In our study, ultrashort-channel devices are demonstrated by direct inkjet printing conducting polymer as source/drain and gate electrodes without any complicated substrate's pre-patterning process. By modifying the substrate's wettability, the conducting polymer's contact line is pinned during drying process which makes the channel length well-controlled. An organic TFT array of 200 devices with 2 μm channel length is fabricated on flexible substrate through all-solution process. The simple and scalable process to fabricate high resolution organic transistor array offers a low cost approach in the development of flexible and wearable electronics. PMID:27378163

  19. Ordered conducting polymer multilayer films and its application for hole injection layers in organic light-emitting devices

    International Nuclear Information System (INIS)

    We reported a controlled architecture growth of layer-ordered multilayer film of poly(3,4-ethylene dioxythiophene) (PEDOT) via a modified Langmuir-Blodgett (LB) method. An in situ polymerization of 3,4-ethylene dioxythiophene (EDOT) monomer in multilayer LB film occurred for the formation of ordered conducting polymer embedded multilayer film. The well-distribution of conducting polymer particles was characterized by secondary-ion mass spectrometry (SIMS). The conducting film consisting of ordered PEDOT ultrathin layers was investigated as a hole injection layer for organic light-emitting diodes (OLEDs). The results showed that, compared to conventional spin-coating PEDOT film and electrostatic self-assembly (ESA) film, the improved performance of OLEDs was obtained after using ordered PEDOT LB film as hole injection layer. It also indicated that well-ordered structure of hole injection layer was attributed to the improvement of OLED performance, leading to the increase of charged carrier mobility in hole injection layer and the recombination rate of electrons and holes in the electroluminescent layer.

  20. Ordered conducting polymer multilayer films and its application for hole injection layers in organic light-emitting devices

    Science.gov (United States)

    Xu, Jianhua; Yang, Yajie; Yu, Junsheng; Jiang, Yadong

    2009-01-01

    We reported a controlled architecture growth of layer-ordered multilayer film of poly(3,4-ethylene dioxythiophene) (PEDOT) via a modified Langmuir-Blodgett (LB) method. An in situ polymerization of 3,4-ethylene dioxythiophene (EDOT) monomer in multilayer LB film occurred for the formation of ordered conducting polymer embedded multilayer film. The well-distribution of conducting polymer particles was characterized by secondary-ion mass spectrometry (SIMS). The conducting film consisting of ordered PEDOT ultrathin layers was investigated as a hole injection layer for organic light-emitting diodes (OLEDs). The results showed that, compared to conventional spin-coating PEDOT film and electrostatic self-assembly (ESA) film, the improved performance of OLEDs was obtained after using ordered PEDOT LB film as hole injection layer. It also indicated that well-ordered structure of hole injection layer was attributed to the improvement of OLED performance, leading to the increase of charged carrier mobility in hole injection layer and the recombination rate of electrons and holes in the electroluminescent layer.

  1. Organic Film Photovoltaic Cells with Gadolinium Complex as an Electron Acceptor

    Institute of Scientific and Technical Information of China (English)

    范镝; 初蓓; 李文连; 洪自若

    2004-01-01

    A series of organic photovoltaic (PV) cells in which the electron acceptor and donor are gadolinium (dibenzoylmethanato)3(bathophenanthroline) [Gd(DBM)3bath] and N,N′-diphenyl-N,N′bis(3-methylphenyl)-1,1′-diphenyl-4,4′-diamine [TPD], respectively, were fabricated. Although TPD acts as an active layer in the bilayered cells, insertion of a Gd-complex film between TPD and the alloy cathode is necessary for efficient carrier photogeneration. Open-circuit voltage of 3.2 V was obtained due to efficient exciton dissociation near the interface between Gd(DBM)3bath and TPD. By incorporating an ultrathin mixed layer of Gd-complex and TPD, external quantum efficiency is improved significantly. Photovoltaic performance of the devices has a common origin, exciplex formation, which results in broadband emission during both photoluminescent and the electroluminescent processes.

  2. Preparation and characteristics of flexible all-organic thin-film field-effect transistor

    Institute of Scientific and Technical Information of China (English)

    QIU Yong; HU Yuanchuan; Dong Guifang; WANG Liduo; Xie Junfeng; MA Yaning

    2003-01-01

    All-organic thin-film field-effect transistor was prepared on flexible poly(ethylene-terephthalate) (PET) substrate. Poly(methyl-methacrylate) (PMMA) and pentacene are used as a dielectric layer and a semiconductor layer, respectively. The hole mobility of the transistor can reach 2.10×10-2 cm2/Vs, and the on/off current ratio was larger than 105. The performances of the transistor, when the substrate is cured under different radius, were also measured. It was found that the device performance did not change when the curly direction was vertical to the channel length direction and when the curly direction was parallel to the channel length direction with 3.67 cm curvature radius, the mobility of the device increased by more than 20% and the on/off ratio decreased more than one order.

  3. Transient phases during fast crystallization of organic thin films from solution

    Directory of Open Access Journals (Sweden)

    Jing Wan

    2016-01-01

    Full Text Available We report an in situ microbeam grazing incidence X-ray scattering study of 2,7-dioctyl[1]benzothieno[3,2-b][1]benzothiophene (C8-BTBT organic semiconductor thin film deposition by hollow pen writing. Multiple transient phases are observed during the crystallization for substrate temperatures up to ≈93 °C. The layered smectic liquid-crystalline phase of C8-BTBT initially forms and preceedes inter-layer ordering, followed by a transient crystalline phase for temperature >60 °C, and ultimately the stable phase. Based on these results, we demonstrate a method to produce extremely large grain size and high carrier mobility during high-speed processing. For high writing speed (25 mm/s, mobility up to 3.0 cm2/V-s has been observed.

  4. Metal-Organic Framework Thin Films as Stationary Phases in Microfabricated Gas-Chromatography Columns.

    Energy Technology Data Exchange (ETDEWEB)

    Read, Douglas [Sandia National Lab. (SNL-NM), Albuquerque, NM (United States); Sillerud, Colin Halliday [Sandia National Lab. (SNL-NM), Albuquerque, NM (United States)

    2016-01-01

    The overarching goal of this project is to integrate Sandia's microfabricated gas-chromatography ( GC) columns with a stationary phase material that is capable of retaining high-volatility chemicals and permanent gases. The successful integration of such a material with GCs would dramatically expand the repertoire of detectable compounds for Sandia's various microanalysis systems. One such promising class of candidate materials is metal-organic frameworks (MOFs). In this report we detail our methods for controlled deposition of HKUST-1 MOF stationary phases within GC columns. We demonstrate: the chromatographic separation of natural gas; a method for determining MOF film thickness from chromatography alone; and the first-reported GC x GC separation of natural gas -- in general -- let alone for two disparate MOF stationary phases. In addition we determine the fundamental thermodynamic constant for mass sorption, the partition coefficient, for HKUST-1 and several light hydrocarbons and select toxic industrial chemicals.

  5. Liquid- and Gas-Phase Diffusion of Ferrocene in Thin Films of Metal-Organic Frameworks

    Directory of Open Access Journals (Sweden)

    Wencai Zhou

    2015-06-01

    Full Text Available The mass transfer of the guest molecules in nanoporous host materials, in particular in metal-organic frameworks (MOFs, is among the crucial features of their applications. By using thin surface-mounted MOF films in combination with a quartz crystal microbalance (QCM, the diffusion of ferrocene vapor and of ethanolic and hexanic ferrocene solution in HKUST-1 was investigated. For the first time, liquid- and gas-phase diffusion in MOFs was compared directly in the identical sample. The diffusion coefficients are in the same order of magnitude (~10−16 m2·s−1, whereas the diffusion coefficient of ferrocene in the empty framework is roughly 3-times smaller than in the MOF which is filled with ethanol or n-hexane.

  6. Selective sorption of perfluorooctane sulfonate on molecularly imprinted polymer adsorbents

    Institute of Scientific and Technical Information of China (English)

    Shubo DENG; Danmeng SHUAI; Qiang YU; Jun HUANG; Gang YU

    2009-01-01

    Perfluorooctane sulfonate (PFOS), as a potential persistent organic pollutant, has been widely detected in water environments, and has become a great concern in recent years. PFOS is very stable and difficult to decompose using conventional techniques. Sorption may be an attractive method to remove it from water. In this study, the molecularly imprinted polymer (MIP) adsorbents were prepared through the polymerization of 4-vinylpyridine under different preparation conditions in order to remove perfluorooctane sulfonate (PFOS) from water. The MIP adsorbents using perfluorooctanoic acid (PFOA) as the template had good imprinting effects and could selectively remove PFOS from aqueous solution. The sorption behaviors including sorption kinetics,isotherms, and effect of pH, salt, and competitive anions were investigated. Experimental results showed that the sorption of PFOS On the MIP adsorbents was very fast, pH-dependent, and highly selective. The achieved fast sorption equilibrium within 1 h was attributed to the surface sorption on the fine adsorbents. The sorption isotherms showed that the sorption selectivity of PFOS on the MIP adsorbents decreased at high PFOS concentrations, which may be due to the double-layer sorption and the formation of PFOS micelles on the sorbent surface. The sorption of PFOS on the MIP adsorbents was mainly dominated by the electrostatic interaction between the protonated vinylpyridine on the adsorbent surface and the anionic PFOS. The prepared MIP adsorbents can potentially be applied in water and wastewater treatment for selective removal of PFOS.

  7. The effect of pH and DNA concentration on organic thin-film transistor biosensors

    KAUST Repository

    Khan, Hadayat Ullah

    2012-03-01

    Organic electronics are beginning to attract more interest for biosensor technology as they provide an amenable interface between biology and electronics. Stable biosensor based on electronic detection platform would represent a significant advancement in technology as costs and analysis time would decrease immensely. Organic materials provide a route toward that goal due to their compatibility with electronic applications and biological molecules. In this report, we detail the effects of experimental parameters, such as pH and concentration, toward the selective detection of DNA via surface-bound peptide nucleic acid (PNA) sequences on organic transistor biosensors. The OTFT biosensors are fabricated with thin-films of the organic semiconductor, 5,5′-bis-(7-dodecyl-9H-fluoren-2-yl)-2,2′-bithiophene (DDFTTF), in which they exhibit a stable mobility of 0.2 cm 2 V -1 s -1 in buffer solutions (phosphate-buffer saline, pH 7.4 or sodium acetate, pH 7). Device performance were optimized to minimize the deleterious effects of pH on gate-bias stress such that the sensitivity toward DNA detection can be improved. In titration experiments, the surface-bound PNA probes were saturated with 50 nM of complementary target DNA, which required a 10-fold increase in concentration of single-base mismatched target DNA to achieve a similar surface saturation. The binding constant of DNA on the surface-bound PNA probes was determined from the concentration-dependent response (titration measurements) of our organic transistor biosensors. © 2011 Elsevier B.V. All rights reserved.

  8. Adaptive hydrophobic and hydrophilic interactions of mussel foot proteins with organic thin films.

    Science.gov (United States)

    Yu, Jing; Kan, Yajing; Rapp, Michael; Danner, Eric; Wei, Wei; Das, Saurabh; Miller, Dusty R; Chen, Yunfei; Waite, J Herbert; Israelachvili, Jacob N

    2013-09-24

    The adhesion of mussel foot proteins (Mfps) to a variety of specially engineered mineral and metal oxide surfaces has previously been investigated extensively, but the relevance of these studies to adhesion in biological environments remains unknown. Most solid surfaces exposed to seawater or physiological fluids become fouled by organic conditioning films and biofilms within minutes. Understanding the binding mechanisms of Mfps to organic films with known chemical and physical properties therefore is of considerable theoretical and practical interest. Using self-assembled monolayers (SAMs) on atomically smooth gold substrates and the surface forces apparatus, we explored the force-distance profiles and adhesion energies of three different Mfps, Mfp-1, Mfp-3, and Mfp-5, on (i) hydrophobic methyl (CH3)- and (ii) hydrophilic alcohol (OH)-terminated SAM surfaces between pH 3 and pH 7.5. At acidic pH, all three Mfps adhered strongly to the CH3-terminated SAM surfaces via hydrophobic interactions (range of adhesive interaction energy = -4 to -9 mJ/m(2)) but only weakly to the OH-terminated SAM surfaces through H- bonding (adhesive interaction energy ≤ -0.5 mJ/m(2)). 3, 4-Dihydroxyphenylalanine (Dopa) residues in Mfps mediate binding to both SAM surface types but do so through different interactions: typical bidentate H-bonding by Dopa is frustrated by the longer spacing of OH-SAMs; in contrast, on CH3-SAMs, Dopa in synergy with other nonpolar residues partitions to the hydrophobic surface. Asymmetry in the distribution of hydrophobic residues in intrinsically unstructured proteins, the distortion of bond geometry between H-bonding surfaces, and the manipulation of physisorbed binding lifetimes represent important concepts for the design of adhesive and nonfouling surfaces.

  9. The influence of sediment particle size on the properties of adsorbed dissolved organic matter in the Yangtze Estuary and its interactions with As/Sb.

    Science.gov (United States)

    Wang, Ying; Zhang, Manman; Zhang, Di; Shen, Zhenyao

    2016-04-15

    The characteristics of dissolved organic matter (DOM) extracted from sediments with four particle sizes (200μm) in the Yangtze Estuary were compared. The differences in their binding capacities for individual fluorescent components with As/Sb were studied using fluorescence-quenching titrations combined with excitation-emission matrix (EEM) spectra. The results indicated that the particle size influenced the quality and quantity of extracted DOM. With increasing particle size, the extracted DOM content, value of UV280 and acidic functional group content of the DOM decreased. Three protein-like components (C2, C3 and C4) and one humic-like component (C1) were identified using the parallel factor analysis (PARAFAC) model. Wherein, protein-like material dominated in DOM on different particle-size fractions and possessed a stronger complex capacity with As/Sb. A significant positive correlation between the complexation capacity of extracted DOM from samples, as well as with the acidic functional group content, was observed. PMID:26965093

  10. Synthesis, characterization, antimicrobial activity and applications of polyanilineTi(IV)arsenophosphate adsorbent for the analysis of organic and inorganic pollutants.

    Science.gov (United States)

    Bushra, Rani; Shahadat, Mohammad; Ahmad, Anees; Nabi, S A; Umar, Khalid; Oves, M; Raeissi, A S; Muneer, M

    2014-01-15

    A novel polyaniline based composite cation exchange material has been synthesized by simple chemical route and characterized on the basis of sophisticated techniques. XRD and SEM analyses reveal the amorphous morphology of the material. The partition coefficient studies of different metal ions on the material were performed in DMW and diverse concentrations of HClO4 solutions. On the basis of high Kd values some significant separations of heavy toxic metal ions were achieved from synthetic mixtures as well as tap water samples by using columns of this exchanger. For the optimum adsorption of dye on the material, the effect of various parameters along with Langmuir and Freundlich adsorption isotherm were examined. The observed result of conducting measurement indicates that the material covers semiconductor range. The photochemical degradation of industrial dyes and antimicrobial activity were also investigated which show significant results than some of the known antibiotics. On the basis of good ion exchange capacity along with photochemical degradation and microbial activity, polyanilineTi(IV)arsenophosphate can be considered as an excellent conducting material for the treatment metal ions and degradation of organic pollutants.

  11. Structural features of resorcinol-formaldehyde resin chars and interfacial behavior of water co-adsorbed with low-molecular weight organics

    Science.gov (United States)

    Gun'ko, Vladimir M.; Bogatyrov, Viktor M.; Turov, Vladimir V.; Leboda, Roman; Skubiszewska-Zięba, Jadwiga; Urubkov, Iliya V.

    2013-10-01

    Products of resorcinol-formaldehyde resin carbonization (chars) are characterized by different morphology (particle shape and sizes) and texture (specific surface area, pore volume and pore size distribution) depending on water content during resin polymerization. At a low amount of water (Cw = 37.8 wt.%) during synthesis resulting in strongly cross-linked polymers, carbonization gives nonporous particles. An increase in the water content to 62.7 wt.% results in a nano/mesoporous char, but if Cw = 73.3 wt.%, a char is purely nanoporous. Despite these textural differences, the Raman spectra of all the chars are similar because of the similarity in the structure of their carbon sheets with a significant contribution of sp3 C atoms. However, the difference in the spatial organization of the carbon sheet stacks in the particles results in the significant differences in the textural and morphological characteristics and in the adsorption properties of chars with respect to water, methane, benzene, hydrogen, methylene chloride, and dimethylsulfoxide.

  12. Structural features of resorcinol–formaldehyde resin chars and interfacial behavior of water co-adsorbed with low-molecular weight organics

    Energy Technology Data Exchange (ETDEWEB)

    Gun’ko, Vladimir M., E-mail: vlad_gunko@ukr.net [Chuiko Institute of Surface Chemistry, 17 General Naumov Street, 03164 Kyiv (Ukraine); Bogatyrov, Viktor M.; Turov, Vladimir V. [Chuiko Institute of Surface Chemistry, 17 General Naumov Street, 03164 Kyiv (Ukraine); Leboda, Roman; Skubiszewska-Zięba, Jadwiga [Faculty of Chemistry, Maria Curie-Skłodowska University, 20031 Lublin (Poland); Urubkov, Iliya V. [Kurdyumov Institute of Metal Physics, 36 Vernadsky Boulevard, 03142 Kyiv (Ukraine)

    2013-10-15

    Products of resorcinol–formaldehyde resin carbonization (chars) are characterized by different morphology (particle shape and sizes) and texture (specific surface area, pore volume and pore size distribution) depending on water content during resin polymerization. At a low amount of water (C{sub w} = 37.8 wt.%) during synthesis resulting in strongly cross-linked polymers, carbonization gives nonporous particles. An increase in the water content to 62.7 wt.% results in a nano/mesoporous char, but if C{sub w} = 73.3 wt.%, a char is purely nanoporous. Despite these textural differences, the Raman spectra of all the chars are similar because of the similarity in the structure of their carbon sheets with a significant contribution of sp{sup 3} C atoms. However, the difference in the spatial organization of the carbon sheet stacks in the particles results in the significant differences in the textural and morphological characteristics and in the adsorption properties of chars with respect to water, methane, benzene, hydrogen, methylene chloride, and dimethylsulfoxide.

  13. V{sub 2}O{sub 5} thin film deposition for application in organic solar cells

    Energy Technology Data Exchange (ETDEWEB)

    Arbab, Elhadi A.A.; Mola, Genene Tessema [University of KwaZulu-Natal, School of Chemistry and Physics, Pietermaritzburg Campus, Private Bag X01, Scottsville (South Africa)

    2016-04-15

    Vanadium pentoxide V{sub 2}O{sub 5} films were fabricated by way of electrochemical deposition technique for application as hole transport buffer layer in organic solar cell. A thin and uniform V{sub 2}O{sub 5} films were successfully deposited on indium tin oxide-coated glass substrate. The characterization of surface morphology and optical properties of the deposition suggest that the films are suitable for photovoltaic application. Organic solar cell fabricated using V{sub 2}O{sub 5} as hole transport buffer layer showed better devices performance and environmental stability than those devices fabricated with PEDOT:PSS. In an ambient device preparation condition, the power conversion efficiency increases by nearly 80 % compared with PEDOT:PSS-based devices. The devices lifetime using V{sub 2}O{sub 5} buffer layer has improved by a factor of 10 over those devices with PEDOT:PSS. (orig.)

  14. Characterizations of arsenic-doped zinc oxide films produced by atmospheric metal-organic chemical vapor deposition

    International Nuclear Information System (INIS)

    p-type ZnO films were prepared by atmospheric metal-organic chemical vapor deposition technique using arsine (AsH3) as the doping source. The electrical and optical properties of arsenic-doped ZnO (ZnO:As) films fabricated at 450–600 °C with various AsH3 flow rates ranging from 8 to 21.34 μmol/min were analyzed and compared. Hall measurements indicate that stable p-type ZnO films with hole concentrations varying from 7.2 × 1015 to 5.8 × 1018 cm−3 could be obtained. Besides, low temperature (17 K) photoluminescence spectra of all ZnO:As films also demonstrate the dominance of the line related to the neutral acceptor-bound exciton. Moreover, the elemental identity and chemical bonding information for ZnO:As films were examined by X-ray photoelectron spectroscopy. Based on the results obtained, the effects of doping conditions on the mechanism responsible for the p-type conduction were studied. Conclusively, a simple technique to fabricate good-quality p-type ZnO films has been recognized in this work. Depositing the film at 550 °C with an AsH3 flow rate of 13.72 μmol/min is appropriate for producing hole concentrations on the order of 1017 cm−3 for it. Ultimately, by increasing the AsH3 flow rate to 21.34 μmol/min for doping and depositing the film at 600 °C, ZnO:As films with a hole concentration over 5 × 1018 cm−3 together with a mobility of 1.93 cm2V−1 s−1 and a resistivity of 0.494 ohm-cm can be achieved.

  15. A computational chemical study of penetration and displacement of water films near mineral surfaces

    Directory of Open Access Journals (Sweden)

    Larter Steve R

    2001-08-01

    Full Text Available A series of molecular dynamics simulations have been performed on organic–water mixtures near mineral surfaces. These simulations show that, in contrast to apolar compounds, small polar organic compounds such as phenols can penetrate through thin water films to adsorb on these mineral surfaces. Furthermore, additional simulations involving demixing of an organic–water mixture near a surfactant-covered mineral surface demonstrate that even low concentrations of adsorbed polar compounds can induce major changes in mineral surface wettability, allowing sorption of apolar molecules. This strongly supports a two-stage adsorption mechanism for organic solutes, involving initial migration of small polar organic molecules to the mineral surface followed by water film displacement due to co-adsorption of the more apolar organic compounds, thus converting an initial water-wet mineral system to an organic-covered surface. This has profound implications for studies of petroleum reservoir diagenesis and wettability changes.

  16. The effect of dissolved organic carbon on bacterial adhesion to conditioning films adsorbed on glass from natural seawater collected during different seasons

    NARCIS (Netherlands)

    Bakker, D.P.; Klijnstra, J.W.; Busscher, H.J.; Mei, H.C. van der

    2003-01-01

    Adhesion of three marine bacterial strains, i.e. Marinobacter hydrocarbonoclasticus, Psychrobacter sp. and Halomonas pacifica with different cell surface hydrophobicities was measured on glass in a stagnation point flow chamber. Prior to bacterial adhesion, the glass surface was conditioned for 1 h

  17. The effect of dissolved organic carbon on bacterial adhesion to conditioning films adsorbed on glass from natural seawater collected during different seasons

    NARCIS (Netherlands)

    Bakker, DP; Klijnstra, JW; Busscher, HJ; van der Mei, HC

    2003-01-01

    Adhesion of three marine bacterial strains, i.e. Marinobacter hydrocarbonoclasticus , Psychrobacter sp. and Halomonas pacifica with different cell surface hydrophobicities was measured on glass in a stagnation point flow chamber. Prior to bacterial adhesion, the glass surface was conditioned for 1 h

  18. 有机薄膜太阳能电池%Organic Thin Film Solar Cells

    Institute of Scientific and Technical Information of China (English)

    郭军; 李博; 胡来归

    2011-01-01

    有机太阳能电池作为一种新兴的有着巨大潜力的光电转换器件,吸引了越来越多的关注.综述了有机薄膜太阳能电池主要的两种器件结构的研究进展,即基于无机异质结发展出来的双异质结型有机太阳能电池和基于扩展双层异质结活性层受限的接触面积而提出的体异质结型太阳能电池;阐述了这两种器件结构的工作原理、影响有机太阳能电池光电转换效率的因素以及两种结构的不足之处,并展望了有机太阳能电池发展的广阔前景.%Organic solar cells, as a kind of new optoelectronic devices with high potential, have attracted much attention. Two common device structures of organic thin film solar cells, double heterojunction and bulk heterojunc tion are reviewed. The double heterojunction structure is developed based on inorganic heterojunction solar cell, while the bulk heterojunction is based on the expanding the contact area of p-n junctions in the double heterojunction struc ture. In addition, the working principles of these two kinds of structures are also introduced, as well as various effects on the optoelectronic conversion efficiency of organic solar cells and the shortcoming of these structures. Broad pros pects of organic solar cell are finally given.

  19. Monolithically integrated, flexible display of polymer-dispersed liquid crystal driven by rubber-stamped organic thin-film transistors

    International Nuclear Information System (INIS)

    This letter describes the monolithic integration of rubber-stamped thin-film organic transistors with polymer-dispersed liquid crystals (PDLCs) to create a multipixel, flexible display with plastic substrates. We report the electro-optic switching behavior of the PDLCs as driven by the organic transistors, and we show that our displays operate robustly under flexing and have a contrast comparable to that of newsprint. [copyright] 2001 American Institute of Physics

  20. Thiol anchoring and catalysis of gold nanoparticles at the liquid interface of thin-organic film-modified electrodes

    OpenAIRE

    Mirceski, Valentin; Aleksovska, Angela; Pejova, Biljana; Ivanovski, Vladimir; Mitrova, Biljana; Mitreska, Nikolina; Gulaboski, Rubin

    2014-01-01

    The deposition of in-situ formed gold nanoparticles at the liquid/liquid (L/L) interface is studied by means of thin-organic-film-modified electrodes (TFE). The degree of ordering and aggregation of gold nanoparticles can be tuned by adding a lipophilic and hydrophilic thiol in the organic and aqueous phase, respectively. The ordered thiol-anchored gold nanoparticles exhibit pronounced catalytic effect toward electron-transfer reactions across the L/L interface.

  1. Studying the ion transfer across liquid interface of thin organic-film-modified electrodes in the presence of glucose oxidase

    OpenAIRE

    Mirceski, Valentin; Mitrova, Biljana; Ivanovski, Vladimir; Mitreska, Nikolina; Aleksovska, Angela; Gulaboski, Rubin

    2015-01-01

    A coupled electron-ion transfer reaction at thin organic-film-modified electrodes (TFE) is studied in the presence of glucose oxidase (GOx) under voltammetric conditions. TFE consists of a graphite electrode modified with a nitrobenzene solution of decamethylferrocene (DMFC) as a redox mediator and tetrabuthylammonium perchlorate as an organic-supporting electrolyte, in contact with aqueous buffer solutions containing percholarte ions and GOx. The redox turnover of DMFC coupled with perchl...

  2. Substrate-adsorbate coupling in CO-adsorbed copper

    CERN Document Server

    Lewis, S P; Lewis, Steven P.; Rappe, Andrew M.

    1996-01-01

    The vibrational properties of carbon monoxide adsorbed to the copper (100) surface are explored within density functional theory. Atoms of the substrate and adsorbate are treated on an equal footing in order to examine the effect of substrate--adsorbate coupling. This coupling is found to have a significant effect on the vibrational modes, particularly the in-plane frustrated translation, which mixes strongly with substrate phonons and broadens into a resonance. The predicted lifetime due to this harmonic decay mechanism is in excellent quantitative agreement with experiment.

  3. Organic photovoltaic cells based on ZnO thin film electrodes.

    Science.gov (United States)

    Ghica, C; Ion, L; Epurescu, G; Nistor, L; Antohe, S; Dinescu, M

    2010-02-01

    Due to its wide band-gap (ca. 3.4 eV), ZnO is a possible candidate material to be used as transparent electrode for a new class of photovoltaic (PV) cells. Also, an increased interest for the photovoltaic properties of several organic monomers and polymers (merocyanines, phthalocyanines and porphyrins) was noticed, because of their high optical absorption in the visible region of the spectrum allowing them to be used as potential inexpensive materials for solar cells. Preparation and properties of CuPc (copper phthalocyanine) based photovoltaic cells using ZnO thin films as transparent conductor electrodes are presented in this paper. ZnO layers are grown by pulsed laser deposition, while the organic layers are obtained by thermal evaporation. Structural characterization is performed by electron microscopy. Optical and transport properties of the mutilayered structures are obtained by electrical and spectro-photometric measurements. The influence of the ZnO-polymer interface on the external quantum efficiency (EQE) of the photovoltaic cell is clearly evidenced by our measurements.

  4. Natural evolution inspired design of light trapping structure in thin film organic solar cells

    Science.gov (United States)

    Wang, Chen; Yu, Shuangcheng; Chen, Wei; Sun, Cheng

    2013-09-01

    Light trapping has been developed to effectively enhance the efficiency of the thin film solar cell by extending the pathlength for light interacting with the active materials. Searching for optimal light trapping design requires a delicate balance among all the competing physical processes, including light refraction, reflection, and absorption. The existing design methods mainly depend on engineers' intuition to predefine the topology of the light-trapping structure. However, these methods are not capable of handling the topological variation in reaching the optimal design. In this work, a systematic approach based on Genetic Algorithm is introduced to design the scattering pattern for effective light trapping. Inspired by natural evolution, this method can gradually improve the performance of light trapping structure through iterative procedures, producing the most favorable structure with minimized reflection and substantial enhancement in light absorption. Both slot waveguide based solar cell and a more realistic organic solar with a scattering layer consisting of nano-scale patterned front layer is optimized to maximize absorption by strongly coupling incident sun light into the localized photonic modes supported by the multilayer system. Rigorous coupled wave analysis (RCWA) is implemented to evaluate the absorbance. The optimized slot waveguide cell achieves a broadband absorption efficiency of 48.1% and more than 3-fold increase over the Yablonovitch limit and the optimized realistic organic cell exhibits nearly 50% average absorbance over the solar spectrum with short circuit current density five times larger than the control case using planar ITO layer.

  5. Plasma-polymerized films providing selective affinity to the polarity of vaporized organic solvents

    International Nuclear Information System (INIS)

    Plasma-polymerized films (PPFs) were fabricated as recognition membranes for a vapor-sensing device, and their affinity to vaporized organic solvents was evaluated with surface plasmon resonance. The affinity we intended to create is the selective sorption of the vaporized organic solvents depending on their polarity. For this purpose, acetonitrile, ethylenediamine (EDA), styrene, hexamethyldisiloxane (HMDSO), and hexamethyldisilazane were used to fabricate PPFs. Vaporized methanol, ethanol, and 1-propanol were used as high-polar solvents to be analyzed. Hexane, toluene, and p-xylene were used as low-polar solvents. As a result, the HMDSO-PPF with 97.3o of contact angle was found to provide affinity to the low-polar solvents. In contrast, the EDA-PPF with 7.1o of contact angle provided affinity to the high-polar solvents. Observations of the surface morphology of the HMDSO- and EDA-PPFs with a scanning electron microscope revealed that they are composed of nano-scale islands.

  6. THE USE OF LOW COST ADSORBENTS FOR PURIFICATION WASTEWATER

    OpenAIRE

    Višekruna, Antonija; Štrkalj, Anita; Marinić Pajc, Ljiljana

    2011-01-01

    Adsorption is one of the effective methods of advanced wastewater treatment, which industries employ to reduce hazardous organic and inorganic wastes in effluents. The use of low cost adsorbent has been investigated as a replacement for current costly methods of removing toxic substances from wastewater. In this article, the use of low cost adsorbents for the removal of toxic substances from wastewater has been reviewed.

  7. The Production of Organic-Inorganic Compound Film-Coated Urea and the Characteristics of Its Nutrient Release

    Institute of Scientific and Technical Information of China (English)

    ZOU Hong-tao; WANG Yao-sheng; SONG Hao-wen; HAN Yan-yu; YU Na; ZHANG Yu-ling; DANG Xiu-li; HUANG Yi; ZHANG Yu-long

    2009-01-01

    The effect of different concentrations of natural macromolecular compound on the characteristics of nutrient release in the membrane materials of organic-inorganic compound film-coated urea was discussed,and the optimal concentrations for better nutrient release was proposed.The characteristics of nutrient release of film-coated urea were evaluated by soil column leaching experiment.Organic-inorganic compound film-coated urea showed good characteristics of nutrient release,which could be well simulated by Logistic curve.The two parameters in this curve,a and r,can be used to present nutrient release of film-coated urea,and followed the order of B > C > A and C < B < A,respectively,indicating that the release was stronger with the increasing concentration of natural maeromolecular compound in the membrane,which implied better controllability of nutrient release.The concentration of 5% of natural macromolecular compound showed better characteristic of nutrient release and can be utilized as a membrane material combined with inorganic mineral powders to develop film-coated slow-release fertilizer.

  8. Electrochemical behavior of high performance on-chip porous carbon films for micro-supercapacitors applications in organic electrolytes

    Science.gov (United States)

    Brousse, K.; Huang, P.; Pinaud, S.; Respaud, M.; Daffos, B.; Chaudret, B.; Lethien, C.; Taberna, P. L.; Simon, P.

    2016-10-01

    Carbide derived carbons (CDCs) are promising materials for preparing integrated micro-supercapacitors, as on-chip CDC films are prepared via a process fully compatible with current silicon-based device technology. These films show good adherence on the substrate and high capacitance thanks to their unique nanoporous structure which can be fine-tuned by adjusting the synthesis parameters during chlorination of the metallic carbide precursor. The carbon porosity is mostly related to the synthesis temperature whereas the thickness of the films depends on the chlorination duration. Increasing the pore size allows the adsorption of large solvated ions from organic electrolytes and leads to higher energy densities. Here, we investigated the electrochemical behavior and performance of on-chip TiC-CDC in ionic liquid solvent mixtures of 1-ethyl-3-methylimidazolium tetrafluoroborate (EMIBF4) diluted in either acetonitrile or propylene carbonate via cyclic voltammetry and electrochemical impedance spectroscopy. Thin CDC films exhibited typical capacitive signature and achieved 169 F cm-3 in both electrolytes; 65% of the capacitance was still delivered at 1 V s-1. While increasing the thickness of the films, EMI+ transport limitation was observed in more viscous PC-based electrolyte. Nevertheless, the energy density reached 90 μW h cm-2 in 2M EMIBF4/ACN, confirming the interest of these CDC films for micro-supercapacitors applications.

  9. Characterization of MgZnO films grown by plasma enhanced metal-organic chemical vapor deposition

    Energy Technology Data Exchange (ETDEWEB)

    Asahara, Hirokazu, E-mail: hirokazu.asahara@dsn.rohm.co.j [New Industry Creation Hatchery Center, Tohoku University, 6-6-10 Aza Aoba, Aramaki, Aoba-ku, Sendai, 980-8579 (Japan); Graduate School of Engineering, Tohoku University, 6-6-05 Aza Aoba, Aramaki, Aoba-ku, Sendai, 980-8579 (Japan); ROHM Co., Ltd., 21 Saiin Mizosaki-cho, Ukyo-ku, Kyoto, 615-8585 (Japan); Takamizu, Daiju [ROHM Co., Ltd., 21 Saiin Mizosaki-cho, Ukyo-ku, Kyoto, 615-8585 (Japan); Inokuchi, Atsutoshi [New Industry Creation Hatchery Center, Tohoku University, 6-6-10 Aza Aoba, Aramaki, Aoba-ku, Sendai, 980-8579 (Japan); Tokyo Electron, Ltd., 650 Mitsusawa, Hosaka, Nirasaki, Yamanashi, 407-0192 (Japan); Hirayama, Masaki; Teramoto, Akinobu [New Industry Creation Hatchery Center, Tohoku University, 6-6-10 Aza Aoba, Aramaki, Aoba-ku, Sendai, 980-8579 (Japan); Saito, Shin; Takahashi, Migaku [Graduate School of Engineering, Tohoku University, 6-6-05 Aza Aoba, Aramaki, Aoba-ku, Sendai, 980-8579 (Japan); Ohmi, Tadahiro [New Industry Creation Hatchery Center, Tohoku University, 6-6-10 Aza Aoba, Aramaki, Aoba-ku, Sendai, 980-8579 (Japan); WPI Research Center, Tohoku University, 6-6-10 Aza Aoba, Aramaki, Aoba-ku, Sendai, 980-8579 (Japan)

    2010-03-31

    MgZnO (magnesium-zinc-oxide) films were grown on (11-20) sapphire substrates and Zn-polar ZnO substrates by plasma enhanced metal-organic chemical vapor deposition (PE-MOCVD) employing microwave-excited plasma. Structural, electrical and optical properties were investigated by X-ray diffraction, atomic force microscope, Hall, transmittance and photoluminescence measurement. The c-axis lattice constant decreases proportionally to an increase in the Mg content of Mg{sub x}Zn{sub 1-x}O films. Therefore, this indicates that Mg atoms can be substituted in the Zn sites. Mg contents in films on ZnO substrates increase up to 0.11. In addition, Ga doped ZnO films were grown on (11-20) sapphire substrates. The resistivity of the films on (11-20) sapphire is controlled between 1.2 x 10{sup -3} {Omega} cm to 1 {Omega} cm by changing the process conditions. The overall results indicate the promising potential of this PE-MOCVD method for related (Zn, Mg)O films formation because of the reactivity of the radicals, such as oxygen radicals (O*).

  10. Preparation of TiO2 thin film by the LPD method on functionalized organic self-assembled monolayers

    Institute of Scientific and Technical Information of China (English)

    2009-01-01

    In this paper, uniform titania (TiO2) films have been formed at 50℃ on silanol SAMs by the liquid-phase deposition (LPD) method at a temperature below 100℃. OTS (Octadecyltrichloro-Silane) selfassembled monolayers (SAMs) on glass wafers were used as substrates for the deposition of titanium dioxide thin films. This functionalized organic surface has shown to be effective for promoting the growth of films from titanic aqueous solutions by the LPD method at a low temperature below 100℃. The crystal phase composition, microstructure and topography of the as-prepared films were characterized by various techniques, including X-ray diffraction (XRD), scanning electron microscopy (SEM), and atomic force microscopy (AFM). The results indicate that the as-prepared thin films are purely crystallized anatase TiO2 constituted by nanorods after being annealed at 500℃. The pH values, concentration of reactants, and deposition temperatures play important roles in the growth of TiO2 thin films.

  11. Preparation of TiO2 thin film by the LPD method on functionalized organic self-assembled monolayers

    Institute of Scientific and Technical Information of China (English)

    HE ZhongLiang; YU ZhiWei; MIAO HongYan; TAN GuoQiang; LIU Yan

    2009-01-01

    In this paper, uniform titania (TiO2) films have been formed at 50℃ on silanol SAMs by the liquid-phase deposition (LPD) method at a temperature below 100℃. OTS (Octadecyltrichloro-Silane) self-assembled monolayers (SAMs) on glass wafers were used as substrates for the deposition of titanium dioxide thin films. This functionalized organic surface has shown to be effective for promoting the growth of films from titanic aqueous solutions by the LPD method at a low temperature below 10012. The crystal phase composition, microstructure and topography of the as-prepared films were characterized by various techniques, including X-ray diffraction (XRD), scanning electron microscopy (SEM), and atomic force microscopy (AFM). The results indicate that the as-prepared thin films are purely crystallized anatase TiO2 constituted by nanorods after being annealed at 500℃. The pH values, concentration of reactants, and deposition temperatures play important roles in the growth of TiO2 thin films.

  12. Method for Aluminum Oxide Thin Films Prepared through Low Temperature Atomic Layer Deposition for Encapsulating Organic Electroluminescent Devices

    Directory of Open Access Journals (Sweden)

    Hui-Ying Li

    2015-02-01

    Full Text Available Preparation of dense alumina (Al2O3 thin film through atomic layer deposition (ALD provides a pathway to achieve the encapsulation of organic light emitting devices (OLED. Unlike traditional ALD which is usually executed at higher reaction n temperatures that may affect the performance of OLED, this application discusses the development on preparation of ALD thin film at a low temperature. One concern of ALD is the suppressing effect of ambient temperature on uniformity of thin film. To mitigate this issue, the pumping time in each reaction cycle was increased during the preparation process, which removed reaction byproducts and inhibited the formation of vacancies. As a result, the obtained thin film had both high uniformity and density properties, which provided an excellent encapsulation performance. The results from microstructure morphology analysis, water vapor transmission rate, and lifetime test showed that the difference in uniformity between thin films prepared at low temperatures, with increased pumping time, and high temperatures was small and there was no obvious influence of increased pumping time on light emitting performance. Meanwhile, the permeability for water vapor of the thin film prepared at a low temperature was found to reach as low as 1.5 × 10−4 g/(m2·day under ambient conditions of 25 °C and 60% relative humidity, indicating a potential extension in the lifetime for the OLED.

  13. Hydrophilic property of SiO2/TiO2 double layer films

    International Nuclear Information System (INIS)

    The hydrophilicity of the SiO2(top)/TiO2(under) double layer films prepared by vacuum evaporation was investigated. The as-deposited SiO2/TiO2 double layer films showed very good hydrophilicity (water contact angle: ∼0o). Their hydrophilicity, however, is deteriorated by the organic contamination adsorbed on the film but the hydrophilicity can be recovered by UV light irradiation. TOF-SIMS (time-of-flight secondary-ion-mass-spectrometry) measurements revealed that the amount of organic compounds adsorbed on the films decreased with the UV light irradiation. Secondarily, the amount of both Si-OH and Ti-OH groups changed little by the UV light irradiation. Thus, it can be concluded that the hydrophilicity of the SiO2/TiO2 double layer films is due to the stable Si-OH groups and the photo-catalytic TiO2 underlayer maintains the hydrophilicity of the double layer films by decomposing organic contaminants on the film surface. This SiO2/TiO2 double layer film has been in practical use for the automobiles' exterior rear view mirrors

  14. Zeolites as alcohol adsorbents from aqueous solutions

    Directory of Open Access Journals (Sweden)

    Cekova Blagica

    2006-01-01

    Full Text Available The potential usage of zeolites as adsorbents for the removal of organic molecules from water was investigated in a series of experiments with aqueous solutions of lower alcohols. This could represent a simple solution to the problem of cleaning up industrial wastewater as well as recovering valuable chemicals at relatively low costs. Adsorption isotherms of the Langmuir type were applied, and calculations showed that the amount of propanol adsorbed on silicalite corresponded to approximately 70% of the pore volume. The adsorption process is simple, and recovery of the more concentrated products is easily done by heat treatment and/or at lowered pressures. Adsorption experiments with aqueous acetone showed that silicalite had approximately the same adsorption capacity for acetone as for n-propanol. Heats of adsorption were determined calorimetrically.

  15. Effect of Polymer Binders on UV-Responsive Organic Thin-Film Phototransistors with Benzothienobenzothiophene Semiconductor.

    Science.gov (United States)

    Ljubic, Darko; Smithson, Chad S; Wu, Yiliang; Zhu, Shiping

    2016-02-17

    The influence of polymer binders on the UV response of organic thin-film phototransistors (OTF-PTs) is reported. The active channel of the OTF-PTs was fabricated by blending a UV responsive 2,7-dipenty-[1]benzothieno[2,3-b][1]benzothiophene (C5-BTBT) as small molecule semiconductor and a branched unsaturated polyester (B-upe) as dielectric binder (ratio 1:1). To understand the influence of the polymer composition on the photoelectrical properties and UV response of C5-BTBT, control blends were prepared using common dielectric polymers, namely, poly(vinyl acetate) (PVAc), polycarbonate (PC), and polystyrene (PS), for comparison. Thin-film morphology and nanostructure of the C5-BTBT/polymer blends were investigated by means of optical and atomic force microscopy, and powder X-ray diffraction, respectively. Electrical and photoelectrical characteristics of the studied OTF-PTs were evaluated in the dark and under UV illumination with a constant light intensity (P = 3 mW cm(-2), λ = 365 nm), respectively, using two- and three-terminal I-V measurements. Results revealed that the purposely chosen B-upe polymer binder strongly affected the UV response of OTF-PTs. A photocurrent increase of more than 5 orders of magnitude in the subthreshold region was observed with a responsivity as high as 9.7 AW(-1), at VG = 0 V. The photocurrent increase and dramatic shift of VTh,average (∼86 V) were justified by the high number of photogenerated charge carriers upon the high trap density in bulk 8.0 × 10(12) cm(-2) eV(-1) generated by highly dispersed C5-BTBT in B-upe binder. Compared with other devices, the B-upe OTF-PTs had the fastest UV response times (τr1/τr2 = 0.5/6.0) reaching the highest saturated photocurrent (>10(6)), at VG = -5 V and VSD = -60 V. The enhanced UV sensing properties of B-upe based OTF-PTs were attributed to a self-induced thin-film morphology. The enlarged interface facilitated the electron withdrawing/donating functional groups in the polymer chains in

  16. Evaluation of the Process of Solvent Vapor Annealing on Organic Thin Films

    KAUST Repository

    Ren, Yi

    2011-07-01

    Solvent vapor annealing has recently emerged as an intriguing, room-temperature, and highly versatile alternative to thermal annealing. The chemically selective interaction between solvents and organic semiconductors opens new opportunities to selectively anneal certain components of the device, while leaving others intact. On the downside, these interactions are complex and rather unpredictable, requiring further investigation. We propose a novel methodology to investigate solvent-film interactions, based on use of an in situ quartz crystal microbalance with dissipation (QCM-D) capability and in situ grazing incidence wide angle X-ray scattering (GIWAXS). These methods make it possible to investigate both qualitatively and quantitatively the solvent vapor uptake, the resulting softening and changes (reversible and/or irreversible) in crystallinity. Using this strategy, we have investigated the solvent vapor annealing of traditional donor and acceptor materials, namely poly(3-hexylthiophene-2,5-diyl) (P3HT) and [6,6]-Phenyl-C61-butyric acid methyl ester (PCBM). We find these materials retain their rigid structure during toluene vapor annealing and do not dewet. We also investigated the toluene vapor annealing of several newly proposed acceptor molecules (pentacene-based) modified with various silyl groups and electron withdrawing groups to tune the packing structure of the acceptor domains and energy levels at the donor-acceptor interface. We found a dramatic effect of the electron-withdrawing group on vapor uptake and whether the film remains rigid, softens, or dissolves completely. In the case of trifluoromethyl electron-withdrawing group, we found the film dissolves, resulting in complete and irreversible loss of long range order. By contrast, the cyano group prevented loss of long range order, instead promoting crystallization in some cases. The silyl groups had a secondary effect in comparison to these. In the last part of the thesis, we investigated the

  17. A Boltzmann-weighted hopping model of charge transport in organic semicrystalline films

    KAUST Repository

    Kwiatkowski, Joe J.

    2011-01-01

    We present a model of charge transport in polycrystalline electronic films, which considers details of the microscopic scale while simultaneously allowing realistically sized films to be simulated. We discuss the approximations and assumptions made by the model, and rationalize its application to thin films of directionally crystallized poly(3-hexylthiophene). In conjunction with experimental data, we use the model to characterize the effects of defects in these films. Our findings support the hypothesis that it is the directional crystallization of these films, rather than their defects, which causes anisotropic mobilities. © 2011 American Institute of Physics.

  18. Fabrication of water-stable organic transistors using crystalline rubrene thin-film and polymer-treated dielectric (Presentation Recording)

    Science.gov (United States)

    Kim, Jaejoon; Lee, Hyoek Moo; Cho, Sung Oh

    2015-10-01

    For the real application of organic electronics, stable operation of electronic devices in humid or aqueous condition is essential and desirable. However, most of organic semiconductors were very weak to the oxygen or water and especially, cannot be operated well in aqueous condition without an encapsulation. Here, we present water-stable organic thin-film transistors with highly crystallized rubrene and polymer-treated dielectrics. These high water-stability could be achieved by two factors. First, rubrene, a well-known p-type semiconducting material, showed high air and water stability after the crystallization of `abrupt heating'. By the fabrication and aqueous operation of rubrene thin film transistor, we could show the water stability of crystallized thin-film rubrene. Such high environmental stability is attributed to the fact that rubrene has comparatively low HOMO level of -5.4 eV and large bandgap energy of 3.2 eV and that the rubrene thin-film is composed of well-interconnected orthorhombic rubrene crystals. Second, the polymer-treatment of dielectrics can enhance long-term water stability of fabricated rubrene thin-film transistor. By the complete immersion test of transistors, we could characterize the increase of water-stability after the treatment of dielectrics with cross-linked polymer. For this purpose, polystyrene is cross-linked by electron irradiation and the water penetration into semiconductor/dielectric interface was decreased due to the decreased surface energy of polymer dielectric compared to the SiO₂. The fabricated rubrene thin-film transistors showed a field-effect mobility of ~0.5 cm2V-1s-1 and long-term stability under ambient and aqueous conditions. Also, we investigated their potential applications in chemical or bio sensors.

  19. Research Update: Hybrid organic-inorganic perovskite (HOIP) thin films and solar cells by vapor phase reaction

    Science.gov (United States)

    Shen, Po-Shen; Chiang, Yu-Hsien; Li, Ming-Hsien; Guo, Tzung-Fang; Chen, Peter

    2016-09-01

    With the rapid progress in deposition techniques for hybrid organic-inorganic perovskite (HOIP) thin films, this new class of photovoltaic (PV) technology has achieved material quality and power conversion efficiency comparable to those established technologies. Among the various techniques for HOIP thin films preparation, vapor based deposition technique is considered as a promising alternative process to substitute solution spin-coating method for large-area or scale-up preparation. This technique provides some unique benefits for high-quality perovskite crystallization, which are discussed in this research update.

  20. Research Update: Hybrid organic-inorganic perovskite (HOIP thin films and solar cells by vapor phase reaction

    Directory of Open Access Journals (Sweden)

    Po-Shen Shen

    2016-09-01

    Full Text Available With the rapid progress in deposition techniques for hybrid organic-inorganic perovskite (HOIP thin films, this new class of photovoltaic (PV technology has achieved material quality and power conversion efficiency comparable to those established technologies. Among the various techniques for HOIP thin films preparation, vapor based deposition technique is considered as a promising alternative process to substitute solution spin-coating method for large-area or scale-up preparation. This technique provides some unique benefits for high-quality perovskite crystallization, which are discussed in this research update.

  1. Effect of titanium oxide-polystyrene nanocomposite dielectrics on morphology and thin film transistor performance for organic and polymeric semiconductors

    Energy Technology Data Exchange (ETDEWEB)

    Della Pelle, Andrea M. [LGS Innovations, 15 Vreeland Rd., Florham Park, NJ 07932 (United States); Department of Chemistry, University of Massachusetts Amherst, 710 N. Pleasant St. Amherst, MA 01003 (United States); Maliakal, Ashok, E-mail: maliakal@lgsinnovations.com [LGS Innovations, 15 Vreeland Rd., Florham Park, NJ 07932 (United States); Sidorenko, Alexander [Department of Chemistry and Biochemistry, University of the Sciences, 600 South 43rd St., Philadelphia, PA 191034 (United States); Thayumanavan, S. [Department of Chemistry, University of Massachusetts Amherst, 710 N. Pleasant St. Amherst, MA 01003 (United States)

    2012-07-31

    Previous studies have shown that organic thin film transistors with pentacene deposited on gate dielectrics composed of a blend of high K titanium oxide-polystyrene core-shell nanocomposite (TiO{sub 2}-PS) with polystyrene (PS) perform with an order of magnitude increase in saturation mobility for TiO{sub 2}-PS (K = 8) as compared to PS devices (K = 2.5). The current study finds that this performance enhancement can be translated to alternative small single crystal organics such as {alpha}-sexithiophene ({alpha}-6T) (enhancement factor for field effect mobility ranging from 30-100 Multiplication-Sign higher on TiO{sub 2}-PS/PS blended dielectrics as compared to homogenous PS dielectrics). Interestingly however, in the case of semicrystalline polymers such as (poly-3-hexylthiophene) P3HT, this dramatic enhancement is not observed, possibly due to the difference in processing conditions used to fabricate these devices (film transfer as opposed to thermal evaporation). The morphology for {alpha}-sexithiophene ({alpha}-6T) grown by thermal evaporation on TiO{sub 2}-PS/PS blended dielectrics parallels that observed in pentacene devices. Smaller grain size is observed for films grown on dielectrics with higher TiO{sub 2}-PS content. In the case of poly(3-hexylthiophene) (P3HT) devices, constructed via film transfer, morphological differences exist for the P3HT on different substrates, as discerned by atomic force microscopy studies. However, these devices only exhibit a modest (2 Multiplication-Sign ) increase in mobility with increasing TiO{sub 2}-PS content in the films. After annealing of the transferred P3HT thin film transistor (TFT) devices, no appreciable enhancement in mobility is observed across the different blended dielectrics. Overall the results support the hypothesis that nucleation rate is responsible for changes in film morphology and device performance in thermally evaporated small molecule crystalline organic semiconductor TFTs. The increased nucleation

  2. Effect of titanium oxide–polystyrene nanocomposite dielectrics on morphology and thin film transistor performance for organic and polymeric semiconductors

    International Nuclear Information System (INIS)

    Previous studies have shown that organic thin film transistors with pentacene deposited on gate dielectrics composed of a blend of high K titanium oxide–polystyrene core–shell nanocomposite (TiO2–PS) with polystyrene (PS) perform with an order of magnitude increase in saturation mobility for TiO2–PS (K = 8) as compared to PS devices (K = 2.5). The current study finds that this performance enhancement can be translated to alternative small single crystal organics such as α-sexithiophene (α-6T) (enhancement factor for field effect mobility ranging from 30-100× higher on TiO2–PS/PS blended dielectrics as compared to homogenous PS dielectrics). Interestingly however, in the case of semicrystalline polymers such as (poly-3-hexylthiophene) P3HT, this dramatic enhancement is not observed, possibly due to the difference in processing conditions used to fabricate these devices (film transfer as opposed to thermal evaporation). The morphology for α-sexithiophene (α-6T) grown by thermal evaporation on TiO2–PS/PS blended dielectrics parallels that observed in pentacene devices. Smaller grain size is observed for films grown on dielectrics with higher TiO2–PS content. In the case of poly(3-hexylthiophene) (P3HT) devices, constructed via film transfer, morphological differences exist for the P3HT on different substrates, as discerned by atomic force microscopy studies. However, these devices only exhibit a modest (2×) increase in mobility with increasing TiO2–PS content in the films. After annealing of the transferred P3HT thin film transistor (TFT) devices, no appreciable enhancement in mobility is observed across the different blended dielectrics. Overall the results support the hypothesis that nucleation rate is responsible for changes in film morphology and device performance in thermally evaporated small molecule crystalline organic semiconductor TFTs. The increased nucleation rate produces organic polycrystalline films with small grain size which are

  3. Controlled growth of epitaxial CeO2 thin films with self-organized nanostructure by chemical solution method

    DEFF Research Database (Denmark)

    Yue, Zhao; Grivel, Jean-Claude

    2013-01-01

    Chemical solution deposition is a versatile technique to grow oxide thin films with self-organized nanostructures. Morphology and crystallographic orientation control of CeO2 thin films grown on technical NiW substrates by a chemical solution deposition method are achieved in this work. Based...... a fluorite structure but exhibits an alternative in-plane texture with eight fold symmetry on the surface. According to phase and texture stability studies, these off-stoichiometric phases gradually transform back to fully oxidized CeO2 with a 45° rotated cube texture during storage in ambient air. Moreover...

  4. Methyl blue dyed polyethylene oxide films: Optical and electrochemical characterization and application as a single layer organic device

    Science.gov (United States)

    Kamath, Archana; Raghu, S.; Devendrappa, H.

    2016-01-01

    A single layer organic device employing methyl blue (MB) dyed polyethylene oxide (PEO) film has been fabricated and studied. The cyclic voltammetry was used to estimate the redox potential and energy band diagram of the device. The polymer film with highest concentration of the dye in PEO (PMB2%) possessing highest conductivity exhibited energy band gap of 2.62 eV with HOMO and LUMO values of 5.34 and 2.72 eV respectively. Based on cyclic voltammetry data, the electron affinity, ionization potential and energy band diagram of the device are discussed.

  5. Preparation of Titanium Oxide-containing Organic Film by Dipping Ti(OR)4 and Cold Plasma oxidizing on PET

    International Nuclear Information System (INIS)

    Low temperature process to prepare titanium oxide film on the surface of PET was investigated in this study. The substrates were pre-treated by oxygen plasma activated procedure, and then spin coating of Ti(OR)4 precursor solution was carried out to prepare Ti-containing organic films. Finally, O2 plasma was employed to decompose organic compounds and oxidize Ti to form oxides. Oxygen plasma post treatment can oxidize the organic compounds to form titanium oxide carbon subsequently. From the IR and ESCA analysis could be observed that -CH bond decreases and Ti-O, C-O bonds increase after O2 plasma treatment. Their surface hydrophilicity was enhanced by UV-irradiation, the degree of water contact angle decreased from 60 deg. to 10 deg.

  6. Enabling Lambertian-Like Warm White Organic Light-Emitting Diodes with a Yellow Phosphor Embedded Flexible Film

    Directory of Open Access Journals (Sweden)

    Cheng-Chang Chen

    2014-01-01

    Full Text Available We demonstrate in this report a new constructive method of fabricating white organic light-emitting devices (OLEDs with a flexible plastic film embedded with yellow phosphor. The flexible film is composed of polydimethylsiloxane (PDMS and fabricated by using spin coating followed by peeling technology. From the results, the resultant electroluminescent spectrum shows the white OLED to have chromatic coordinates of 0.38 and 0.54 and correlated color temperature of 4200 K. The warm white OLED exhibits the yield of 10.3 cd/A and the luminous power efficiency of 5.4 lm/W at a luminance of 1000 cd/m2. A desirable Lambertian-like far-field pattern is detected from the white OLEDs with the yellow phosphor containing PDMS film. This method is simple, reproducible, and cost-effective, proving to be a highly feasible approach to realize white OLED.

  7. Enhanced electrical properties of pentacene-based organic thin-film transistors by modifying the gate insulator surface

    Science.gov (United States)

    Tang, J. X.; Lee, C. S.; Chan, M. Y.; Lee, S. T.

    2008-09-01

    A reliable surface treatment for the pentacene/gate dielectric interface was developed to enhance the electrical transport properties of organic thin-film transistors (OTFTs). Plasma-polymerized fluorocarbon (CFx) film was deposited onto the SiO 2 gate dielectric prior to pentacene deposition, resulting in a dramatic increase of the field-effect mobility from 0.015 cm 2/(V s) to 0.22 cm 2/(V s), and a threshold voltage reduction from -14.0 V to -9.9 V. The observed carrier mobility increase by a factor of 10 in the resulting OTFTs is associated with various growth behaviors of polycrystalline pentacene thin films on different substrates, where a pronounced morphological change occurs in the first few molecular layers but the similar morphologies in the upper layers. The accompanying threshold voltage variation suggests that hole accumulation in the conduction channel-induced weak charge transfer between pentacene and CFx.

  8. The multiscale simulation of metal organic chemical vapor deposition growth dynamics of GaInP thin film

    Institute of Scientific and Technical Information of China (English)

    2010-01-01

    As a Group III–V compound, GaInP is a high-efficiency luminous material. Metal organic chemical vapor deposition (MOCVD) technology is a very efficient way to uniformly grow multi-chip, multilayer and large-area thin film. By combining the computational fluid dynamics (CFD) and the kinetic Monte Carlo (KMC) methods with virtual reality (VR) technology, this paper presents a multiscale simulation of fluid dynamics, thermodynamics, and molecular dynamics to study the growth process of GaInP thin film in a vertical MOCVD reactor. The results of visualization truly and intuitively not only display the distributional properties of the gas’ thermal and flow fields in a MOCVD reactor but also display the process of GaInP thin film growth in a MOCVD reactor. The simulation thus provides us with a fundamental guideline for optimizing GaInP MOCVD growth.

  9. Interfacial diffusion in a MOCVD grown barium titanate film[Metal Organic Chemical Vapor Deposition

    Energy Technology Data Exchange (ETDEWEB)

    Datta, A.; Chattopadhyay, S.; Richter, A.G.; Kmetko, J.; Lee, C.B.

    2000-07-01

    A combination of two nondestructive techniques, Grazing Incidence X-ray Reflectivity and High Resolution X-ray Diffraction, is used to study (at around 10{angstrom} resolution) the composition profile across a 500{angstrom} thick film of BaTiO{sub 3} grown epitaxially on (100) MgO by MOCVD. Results form both studies indicate diffusion of Mg to about 250{angstrom} into the film at film-substrate interface, consistent with the diffuse ferroelectric phase transition observed in this film. The lattice parameter a shows a progressive decrease as the authors move into the film from the interface, and an anomalously low value in the Mg-free portion of the film.

  10. Growth of epitaxial sodium-bismuth-titanate films by metal-organic chemical vapor phase deposition

    Energy Technology Data Exchange (ETDEWEB)

    Schwarzkopf, J., E-mail: schwarzkopf@ikz-berlin.de [Leibniz Institute for Crystal Growth, Max-Born-Strasse 2, 12489 Berlin (Germany); Schmidbauer, M.; Duk, A.; Kwasniewski, A. [Leibniz Institute for Crystal Growth, Max-Born-Strasse 2, 12489 Berlin (Germany); Anooz, S. Bin [Leibniz Institute for Crystal Growth, Max-Born-Strasse 2, 12489 Berlin (Germany); Physics Department, Faculty of Science, Hadhramout University of Science and Technology, Mukalla 50511, Republic of Yemen (Yemen); Wagner, G. [Leibniz Institute for Crystal Growth, Max-Born-Strasse 2, 12489 Berlin (Germany); Devi, A. [Inorganic Materials Chemistry, Ruhr-University Bochum, Universitaetsstr. 150, 44801 Bochum (Germany); Fornari, R. [Leibniz Institute for Crystal Growth, Max-Born-Strasse 2, 12489 Berlin (Germany)

    2011-10-31

    The liquid-delivery spin metal-organic chemical vapor phase deposition method was used to grow epitaxial sodium-bismuth-titanate films of the system Bi{sub 4}Ti{sub 3}O{sub 12} + xNa{sub 0.5}Bi{sub 0.5}TiO{sub 3} on SrTiO{sub 3}(001) substrates. Na(thd), Ti(O{sup i}Pr){sub 2}(thd){sub 2} and Bi(thd){sub 3}, solved in toluene, were applied as source materials. Depending on the substrate temperature and the Na/Bi ratio in the gas phase several structural phases of sodium-bismuth-titanate were detected. With increasing temperature and/or Na/Bi ratio, phase transitions from an Aurivillius phase with m = 3 to m = 4 via an interleaved state with m = 3.5, and, finally, to Na{sub 0.5}Bi{sub 0.5}TiO{sub 3} with perovskite structure (m = {infinity}) were established. These phase transitions proceed at remarkably lower temperatures than in ceramics or bulk crystals for which they had been exclusively observed so far.

  11. Universal diffusion-limited injection and the hook effect in organic thin-film transistors.

    Science.gov (United States)

    Liu, Chuan; Huseynova, Gunel; Xu, Yong; Long, Dang Xuan; Park, Won-Tae; Liu, Xuying; Minari, Takeo; Noh, Yong-Young

    2016-01-01

    The general form of interfacial contact resistance was derived for organic thin-film transistors (OTFTs) covering various injection mechanisms. Devices with a broad range of materials for contacts, semiconductors, and dielectrics were investigated and the charge injections in staggered OTFTs was found to universally follow the proposed form in the diffusion-limited case, which is signified by the mobility-dependent injection at the metal-semiconductor interfaces. Hence, real ohmic contact can hardly ever be achieved in OTFTs with low carrier concentrations and mobility, and the injection mechanisms include thermionic emission, diffusion, and surface recombination. The non-ohmic injection in OTFTs is manifested by the generally observed hook shape of the output conductance as a function of the drain field. The combined theoretical and experimental results show that interfacial contact resistance generally decreases with carrier mobility, and the injection current is probably determined by the surface recombination rate, which can be promoted by bulk-doping, contact modifications with charge injection layers and dopant layers, and dielectric engineering with high-k dielectric materials. PMID:27440253

  12. Poly(3-Methylthiophene) Thin Films Deposited Electrochemically on QCMs for the Sensing of Volatile Organic Compounds

    Science.gov (United States)

    Öztürk, Sadullah; Kösemen, Arif; Şen, Zafer; Kılınç, Necmettin; Harbeck, Mika

    2016-01-01

    Poly(3-methylthiophene) (PMeT) thin films were electrochemically deposited on quartz crystal microbalance QCM transducers to investigate their volatile organic compound (VOC) sensing properties depending on ambient conditions. Twelve different VOCs including alcohols, ketones, chlorinated compounds, amines, and the organosphosphate dimethyl methylphosphonate (DMMP) were used as analytes. The responses of the chemical sensors against DMMP were the highest among the tested analytes; thus, fabricated chemical sensors based on PMeT can be evaluated as potential candidates for selectively detecting DMMP. Generally, detection limits in the low ppm range could be achieved. The gas sensing measurements were recorded at various humid air conditions to investigate the effects of the humidity on the gas sensing properties. The sensing performance of the chemical sensors was slightly reduced in the presence of humidity in ambient conditions. While a decrease in sensitivity was observed for humidity levels up to 50% r.h., the sensitivity was nearly unaffected for higher humidity levels and a reliable detection of the VOCs and DMMP was possible with detection limits in the low ppm range. PMID:27023539

  13. A hybrid mask mould lithography scheme and its application in nanoscale organic thin film transistors

    Science.gov (United States)

    Cheng, Xing; Li, Dawen; Guo, L. Jay

    2006-02-01

    Nanoimprint lithography (NIL) has stimulated great interest in both academic research and industrial development due to its high resolution, high throughput and low cost advantages. Though NIL has been demonstrated to be very successful in replicating nanoscale features, it also has its limitations as a general lithography technique. Its fundamental moulding characteristics (i.e. physically displacing polymer materials) frequently lead to pattern defects when replicating arbitrary patterns, especially patterns with broad size distribution. To solve this problem, we have developed a combined nanoimprint and photolithography technique that uses a hybrid mould to achieve good pattern definitions. In this work, we applied this technique to fabricate finger-shaped nanoelectrodes, and demonstrated nanoscale pentacene organic thin film transistors (OTFTs). Methods of the hybrid mask-mould (HMM) fabrication and results on the device electrical characteristics are provided. With combined advantages of both photolithography and NIL, and the applicability to general nanoscale device and system fabrication, this method can become a valuable choice for low cost mass production of micro- and nanoscale structures, devices and systems.

  14. Preparation of inorganic-organic hybrid titania sol-gel nanocomposite films, and their dielectric properties

    Science.gov (United States)

    Kim, Hoon; Pramanik, Nimai Chand; Yeop Ahn, Bok; Seok, Sang Il

    2006-06-01

    Hybrid titania materials were prepared by a process involving the phase separation of TiO2 by hydrolysis and polycondensation from hybrids between titanium tetraisopropoxide (TTIP) and 3-(methacryloyloxy)propyl trimethoxysilane (MPTS) with excess acidic water at an elevated temperature (80 °C). The formation of TiO2 nanoparticles within the hybrid materials was studied as a function of the ageing time as well as the Ti/Si molar ratio. The crystalline phases of the TiO2 nanoparticles formed in situ within the inorganic-organic hybrid matrix were characterized by X-ray diffraction and Fourier transform infrared studies. The microstructures and the morphologies of thick films of the hybrid materials were studied using scanning and transmission electron microscopy, which showed the existence of nanocrystalline TiO2 within the crack-free hybrid matrix. The dielectric constants of the composites were found to be in the range 5.0-7.1, depending on the measuring frequency and the composite composition.

  15. Ultrasensitive organic phototransistors with multispectral response based on thin-film/single-crystal bilayer structures

    Science.gov (United States)

    Pinto, R. M.; Gouveia, W.; Neves, A. I. S.; Alves, H.

    2015-11-01

    We report on highly efficient organic phototransistors (OPTs) based on thin-film/single-crystal planar bilayer junctions between 5,6,11,12-tetraphenyltetracene (rubrene) and [6,6]-phenyl-C61-butyric acid methyl ester (PC61BM). The OPTs show good field-effect characteristics in the dark, with high hole-mobility (4-5 cm2 V-1 s-1), low-contact resistance (20 kΩ cm), and low-operating voltage (≤5 V). Excellent sensing capabilities allow for light detection in the 400-750 nm range, with photocurrent/dark current ratio as high as 4 × 104, responsivity on the order of 20 AW-1 at 27 μW cm-2, and an external quantum efficiency of 52 000%. Photocurrent generation is attributed to enhanced electron and hole transfer at the interface between rubrene and PC61BM, and fast response times are observed as a consequence of the high-mobility of the interfaces. The optoelectronic properties exhibited in these OPTs outperform those typically provided by a-Si based devices, enabling future applications where multifunctionality in a single-device is sought.

  16. Ultrasensitive organic phototransistors with multispectral response based on thin-film/single-crystal bilayer structures

    Energy Technology Data Exchange (ETDEWEB)

    Pinto, R. M., E-mail: rpinto@inesc-mn.pt [INESC MN and IN, Rua Alves Redol 9, 1000-029 Lisboa (Portugal); CQFM, Instituto Superior Técnico, Av. Rovisco Pais, 1049-001 Lisboa (Portugal); Gouveia, W. [INESC MN and IN, Rua Alves Redol 9, 1000-029 Lisboa (Portugal); Neves, A. I. S. [INESC MN and IN, Rua Alves Redol 9, 1000-029 Lisboa (Portugal); College of Engineering, Mathematics and Physical Sciences, University of Exeter, EX4 4QL Exeter (United Kingdom); Alves, H. [INESC MN and IN, Rua Alves Redol 9, 1000-029 Lisboa (Portugal); CICECO, Physics Department, Universidade de Aveiro, 3810-193 Aveiro (Portugal)

    2015-11-30

    We report on highly efficient organic phototransistors (OPTs) based on thin-film/single-crystal planar bilayer junctions between 5,6,11,12-tetraphenyltetracene (rubrene) and [6,6]-phenyl-C{sub 61}-butyric acid methyl ester (PC{sub 61}BM). The OPTs show good field-effect characteristics in the dark, with high hole-mobility (4–5 cm{sup 2} V{sup −1} s{sup −1}), low-contact resistance (20 kΩ cm), and low-operating voltage (≤5 V). Excellent sensing capabilities allow for light detection in the 400–750 nm range, with photocurrent/dark current ratio as high as 4 × 10{sup 4}, responsivity on the order of 20 AW{sup −1} at 27 μW cm{sup −2}, and an external quantum efficiency of 52 000%. Photocurrent generation is attributed to enhanced electron and hole transfer at the interface between rubrene and PC{sub 61}BM, and fast response times are observed as a consequence of the high-mobility of the interfaces. The optoelectronic properties exhibited in these OPTs outperform those typically provided by a-Si based devices, enabling future applications where multifunctionality in a single-device is sought.

  17. Titania nanotubes from weak organic acid electrolyte: fabrication, characterization and oxide film properties.

    Science.gov (United States)

    Munirathinam, Balakrishnan; Neelakantan, Lakshman

    2015-04-01

    In this study, TiO2 nanotubes were fabricated using anodic oxidation in fluoride containing weak organic acid for different durations (0.5h, 1h, 2h and 3h). Scanning electron microscope (SEM) micrographs reveal that the morphology of titanium oxide varies with anodization time. Raman spectroscopy and X-ray diffraction (XRD) results indicate that the as-formed oxide nanotubes were amorphous in nature, yet transform into crystalline phases (anatase and rutile) upon annealing at 600°C. Wettability measurements show that both as-formed and annealed nanotubes exhibited hydrophilic behavior. The electrochemical behavior was ascertained by DC polarization and AC electrochemical impedance spectroscopy (EIS) measurements in 0.9% NaCl solution. The results suggest that the annealed nanotubes showed higher impedance (10(5)-10(6)Ωcm(2)) and lower passive current density (10(-7)Acm(-2)) than the as-formed nanotubes. In addition, we investigated the influence of post heat treatment on the semiconducting properties of the oxides by capacitance measurements. In vitro bioactivity test in simulated body fluid (SBF) showed that precipitation of Ca/P is easier in crystallized nanotubes than the amorphous structure. Our study uses a simple strategy to prepare nano-structured titania films and hints the feasibility of tailoring the oxide properties by thermal treatment, producing surfaces with better bioactivity. PMID:25686985

  18. Analysis of a gas-liquid film plasma reactor for organic compound oxidation.

    Science.gov (United States)

    Hsieh, Kevin; Wang, Huijuan; Locke, Bruce R

    2016-11-01

    A pulsed electrical discharge plasma formed in a tubular reactor with flowing argon carrier gas and a liquid water film was analyzed using methylene blue as a liquid phase hydroxyl radical scavenger and simultaneous measurements of hydrogen peroxide formation. The effects of liquid flow rate, liquid conductivity, concentration of dye, and the addition of ferrous ion on dye decoloration and degradation were determined. Higher liquid flow rates and concentrations of dye resulted in less decoloration percentages and hydrogen peroxide formation due to initial liquid conductivity effects and lower residence times in the reactor. The highest decoloration energy yield of dye found in these studies was 5.2g/kWh when using the higher liquid flow rate and adding the catalyst. The non-homogeneous nature of the plasma discharge favors the production of hydrogen peroxide in the plasma-liquid interface over the chemical oxidation of the organic in the bulk liquid phase and post-plasma reactions with the Fenton catalyst lead to complete utilization of the plasma-formed hydrogen peroxide. PMID:27267693

  19. Effects of diamond-like carbon thin film in organic light emitting devices

    Energy Technology Data Exchange (ETDEWEB)

    Yap, Seong-Shan; Yong, Thian-Khok [Faculty of Engineering, Multimedia University, Cyberjaya, 63100 Selangor (Malaysia); Tou, Teck-Yong, E-mail: tytou@mmu.edu.m [Faculty of Engineering, Multimedia University, Cyberjaya, 63100 Selangor (Malaysia)

    2009-07-01

    Ultrathin diamond-like carbon (DLC) was deposited by pulsed Nd:YAG laserablation of graphite target on the indium tin oxide (ITO) surface that functioned as the buffered anode for single-layer organic light emitting devices (OLEDs). Deposited by 355 nm Nd:YAG laser, DLC films were characterized by the Raman spectroscopy and the bulk resistivity measurement. Insertion of DLC in the hole-transport ITO/DLC/TPD/Al device slightly increased the injection current density and reduced the turn-on voltage. But DLC insertion in the electron-transport ITO/DLC/Alq{sub 3}/Al device greatly decreased the injection current density and increased the turn-on voltage. For the ITO/DLC/(TPD + Alq{sub 3} + PVK)/Al device, that was doped with Alq{sub 3} and TPD, improved performance with a higher current density and brightness were consistently obtained. Possible mechanisms for the DLC effect in these single-layer devices were discussed.

  20. Universal diffusion-limited injection and the hook effect in organic thin-film transistors

    Science.gov (United States)

    Liu, Chuan; Huseynova, Gunel; Xu, Yong; Long, Dang Xuan; Park, Won-Tae; Liu, Xuying; Minari, Takeo; Noh, Yong-Young

    2016-07-01

    The general form of interfacial contact resistance was derived for organic thin-film transistors (OTFTs) covering various injection mechanisms. Devices with a broad range of materials for contacts, semiconductors, and dielectrics were investigated and the charge injections in staggered OTFTs was found to universally follow the proposed form in the diffusion-limited case, which is signified by the mobility-dependent injection at the metal-semiconductor interfaces. Hence, real ohmic contact can hardly ever be achieved in OTFTs with low carrier concentrations and mobility, and the injection mechanisms include thermionic emission, diffusion, and surface recombination. The non-ohmic injection in OTFTs is manifested by the generally observed hook shape of the output conductance as a function of the drain field. The combined theoretical and experimental results show that interfacial contact resistance generally decreases with carrier mobility, and the injection current is probably determined by the surface recombination rate, which can be promoted by bulk-doping, contact modifications with charge injection layers and dopant layers, and dielectric engineering with high-k dielectric materials.