Relevant bibliographies by topics / Molecular self-Assembly of insulating

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers
  6. Reports

Academic literature on the topic 'Molecular self-Assembly of insulating'

Author: Grafiati
Published: 4 June 2021
Last updated: 25 May 2024

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Journal articles on the topic "Molecular self-Assembly of insulating"

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Onoda, Mitsuyoshi, Kazuya Tada, and Hiroshi Nakayama. "Conducting Polymer/Insulating Polymer Composite Films Prepared by the Molecular Self-Assembly Process." Japanese Journal of Applied Physics 38, Part 1, No. 6A (June 15, 1999): 3736–41. http://dx.doi.org/10.1143/jjap.38.3736.

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Onoda, Mitsuyoshi, Kazuya Tada, and Hiroshi Nakayama. "Preparation of conducting polymer/insulating polymer composite films using molecular self-assembly process." Synthetic Metals 102, no. 1-3 (June 1999): 1253. http://dx.doi.org/10.1016/s0379-6779(98)01454-4.

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Kittelmann, Markus, Philipp Rahe, and Angelika Kühnle. "Molecular self-assembly on an insulating surface: interplay between substrate templating and intermolecular interactions." Journal of Physics: Condensed Matter 24, no. 35 (August 16, 2012): 354007. http://dx.doi.org/10.1088/0953-8984/24/35/354007.

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Onoda, Mitsuyoshi, Daisuke Fujita, Kenichiro Isaki, and Hiroshi Nakayama. "Preparation and functions of conductive polymer/insulating polymer composite films using molecular self-assembly." Electrical Engineering in Japan 128, no. 1 (July 15, 1999): 1–8. http://dx.doi.org/10.1002/(sici)1520-6416(19990715)128:1<1::aid-eej1>3.0.co;2-j.

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Rahe, Philipp, Markus Nimmrich, and Angelika Kühnle. "Substrate Templating upon Self-Assembly of Hydrogen-Bonded Molecular Networks on an Insulating Surface." Small 8, no. 19 (July 6, 2012): 2969–77. http://dx.doi.org/10.1002/smll.201200681.

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Onoda, Mitsuyoshi, Daisuke Fujita, Kenichiro Isaki, and Hiroshi Nakayama. "Preparation of Conducting Polymer/Insulating Polymer Composite Films Using Molecular Self-Assembly Process and Its Function." IEEJ Transactions on Fundamentals and Materials 117, no. 12 (1997): 1227–32. http://dx.doi.org/10.1541/ieejfms1990.117.12_1227.

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Rahe, Philipp, Markus Nimmrich, and Angelika Kühnle. "Templating: Substrate Templating upon Self-Assembly of Hydrogen-Bonded Molecular Networks on an Insulating Surface (Small 19/2012)." Small 8, no. 19 (October 2, 2012): 2968. http://dx.doi.org/10.1002/smll.201290103.

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Hauke, Christopher M., Ralf Bechstein, Markus Kittelmann, Christof Storz, Andreas F. M. Kilbinger, Philipp Rahe, and Angelika Kühnle. "Controlling Molecular Self-Assembly on an Insulating Surface by Rationally Designing an Efficient Anchor Functionality That Maintains Structural Flexibility." ACS Nano 7, no. 6 (May 15, 2013): 5491–98. http://dx.doi.org/10.1021/nn401589u.

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Wang, Youyuan, Yudong Li, Zhanxi Zhang, Haisen Zhao, and Yanfang Zhang. "Repair Performance of Self-Healing Microcapsule/Epoxy Resin Insulating Composite to Physical Damage." Applied Sciences 9, no. 19 (October 1, 2019): 4098. http://dx.doi.org/10.3390/app9194098.

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Minor physical damage can reduce the insulation performance of epoxy resin, which seriously threatens the reliability of electrical equipment. In this paper, the epoxy resin insulating composite was prepared by a microcapsule system to achieve its self-healing goal. The repair performance to physical damage was analyzed by the tests of scratch, cross-section damage, electric tree, and breakdown strength. The results show that compared with pure epoxy resin, the composite has the obvious self-healing performance. For mechanical damage, the maximum repair rate of physical structure is 100%, and the breakdown strength can be restored to 83% of the original state. For electrical damage, microcapsule can not only attract the electrical tree and inhibit its propagation process, but also repair the tubules of electrical tree effectively. Moreover, the repair rate is fast, which meets the application requirements of epoxy resin insulating material. In addition, the repair behavior is dominated by capillarity and molecular diffusion on the defect surface. Furthermore, the electrical properties of repaired part are greatly affected by the characteristics of damage interface and repair product. In a word, the composite shows better repair performance to physical damage, which is conducive to improving the reliability of electrical insulating materials.
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Baker, MV, and J. Landau. "Self Assembled Alkanethiolate Monolayers as Thin Insulating Films." Australian Journal of Chemistry 48, no. 6 (1995): 1201. http://dx.doi.org/10.1071/ch9951201.

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Simple devices that contain alkanethiolate monolayers sandwiched between conducting films were prepared by fixing a gold film to the surface of an alkanethiolate monolayer (on a gold substrate) with silver paint. These devices, and similar devices that did not contain alkanethiolate monolayers, were tested as resistors in d.c . circuits. The devices that contained octadecanethiolate monolayers had resistances of approximately 1012 Ω, 10 orders of magnitude higher than the resistance of devices that contained no monolayers. Sulfur- terminated alkanethiolate monolayers were prepared by treatment of carboxylic acid-terminated monolayers with vapours of thionyl chloride followed by vapours of hexane-1,6-dithiol. Attempts to use the sulfur-containing groups at the surface of this monolayer as 'molecular glue' to attach a flexible gold film to the surface of the monolayer were unsuccessful.
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Dissertations / Theses on the topic "Molecular self-Assembly of insulating"

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Amrous, Ania. "Etude d'auto-assemblages moléculaires sur surfaces isolantes par microscopie à force atomique en mode non-contact sous ultravide à température ambiante." Thesis, Aix-Marseille, 2016. http://www.theses.fr/2016AIXM4368.

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Dans ce rapport de thèse, nous présentons les résultats obtenus avec la croissance d'assemblages supramoléculaires hautement cristallins et stables à température ambiante sur des surfaces isolantes d'halogénures d'alcalins. L'objectif de cette étude est de caractériser structurellement ces réseaux auto-assemblés et de mettre en évidence l'ensemble des forces d'interaction mises en œuvre dans les processus de croissance et de diffusion, en combinant la microscopie à force atomique en mode non contact (nc-AFM) sous ultravide et des calculs théoriques basés sur la théorie de la fonctionnelle de la densité (DFT) et la dynamique moléculaire. Nous montrons comment des paramètres bien définis concernant le choix de la molécule d'une part tels que sa taille, sa forme, sa symétrie, sa flexibilité et sa fonctionnalité, et le choix du substrat d'autre part, influent sur la morphologie de croissance et permettent de contrôler les propriétés de diffusion des molécules en surface et donc la structure supramoléculaire résultante
In this thesis, we report the results obtained with the growth of highly crystalline and stable supramolecular assemblies at room temperature on insulating surfaces of bulk alkali halides single crystals. The objective of this study is to structurally characterize these self-assembled networks and understand all the interaction forces involved in the growth and diffusion processes. This is performed by joint non-contact atomic force microscopy (nc-AFM) experiments in ultrahigh vacuum and theoretical calculations based on density functional theory (DFT) and molecular dynamics. We show how well-defined parameters for the choice of the molecule on the one hand such as size, shape, symmetry, flexibility and functionality, and the choice of the substrate on the other hand, influence the morphology growth and serve to steer the structure and diffusion properties of such systems
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Amrous, Ania. "Etude d'auto-assemblages moléculaires sur surfaces isolantes par microscopie à force atomique en mode non-contact sous ultravide à température ambiante." Electronic Thesis or Diss., Aix-Marseille, 2016. http://www.theses.fr/2016AIXM4368.

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Dans ce rapport de thèse, nous présentons les résultats obtenus avec la croissance d'assemblages supramoléculaires hautement cristallins et stables à température ambiante sur des surfaces isolantes d'halogénures d'alcalins. L'objectif de cette étude est de caractériser structurellement ces réseaux auto-assemblés et de mettre en évidence l'ensemble des forces d'interaction mises en œuvre dans les processus de croissance et de diffusion, en combinant la microscopie à force atomique en mode non contact (nc-AFM) sous ultravide et des calculs théoriques basés sur la théorie de la fonctionnelle de la densité (DFT) et la dynamique moléculaire. Nous montrons comment des paramètres bien définis concernant le choix de la molécule d'une part tels que sa taille, sa forme, sa symétrie, sa flexibilité et sa fonctionnalité, et le choix du substrat d'autre part, influent sur la morphologie de croissance et permettent de contrôler les propriétés de diffusion des molécules en surface et donc la structure supramoléculaire résultante
In this thesis, we report the results obtained with the growth of highly crystalline and stable supramolecular assemblies at room temperature on insulating surfaces of bulk alkali halides single crystals. The objective of this study is to structurally characterize these self-assembled networks and understand all the interaction forces involved in the growth and diffusion processes. This is performed by joint non-contact atomic force microscopy (nc-AFM) experiments in ultrahigh vacuum and theoretical calculations based on density functional theory (DFT) and molecular dynamics. We show how well-defined parameters for the choice of the molecule on the one hand such as size, shape, symmetry, flexibility and functionality, and the choice of the substrate on the other hand, influence the morphology growth and serve to steer the structure and diffusion properties of such systems
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Gutzler, Rico. "Surface-Confined Molecular Self-Assembly." Diss., lmu, 2010. http://nbn-resolving.de/urn:nbn:de:bvb:19-127201.

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Theobald, James Andrew. "Self-assembly of hydrogen-bonded molecular traps." Thesis, University of Nottingham, 2004. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.416730.

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Puntambekar, Smita. "Molecular self assembly in fluorocarbon surfactant/water systems." Thesis, University of Central Lancashire, 2000. http://clok.uclan.ac.uk/20906/.

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The work presented is a continuation of the study of a homologous series of tetrabutylammonium perfluoroalkylcarboxylate surfactants in water. These systems showed phase behaviour uncharacteristic of ionic perfluorocarbon surfactant systems in that they exhibit a clouding phenomenon with increasing temperature. This behaviour was ascribed to the tight association of the large, hydrophobic counterions with the poiar head group region. In this study a series of perfluorocarbon surfactants have been synthesised in which the hycirophobicity of the counterion is varied. The counterion is W (CH2CH2CH2CH3)(CH3) 41 whilst the surfactant ion remains unchanged throughout the series as periluorodecanoate. The number of butyl chains. 'n' controls the hydrophobicity of the counterion and, in these experiments, n = 4, 2, 1 and 0. The phase diagrams and the detailed phase structures have been investigated using optical polarising microscopy, 2H NMR spectroscopy and small angle x-ray scattering. As n decreases, the phase diagrams change, recovering the "generic" phase behaviour more usual for a perfluorocarbon surfactant - water system. X-ray measurements show that in the n = 4 (tetrabutylammonium perfluorodecanoate) system, all the phases (both liquid crystalline and non-liquid crystalline) have uniform mean interfacial curvature. The phases observed are L 1 (vesicles), L. and L 2. With decreasing counterion hydrophobicity, the population of counterions associated with the interface decreases, introducing greater curvature into the system. The mean curvature of the phase structures also becomes nonuniform. For n = 0 (tetramethylammonium perfluorodecarioate) no classical mesophases are observed. Much of the liquid crystalline region is taken up with a random mesh intermediate phase, Mh 1 (0) and an extensive rhombohedral mesh intermediate phase, Mh1 (R3 m). Phase behaviour intermediate between the two extremes is observed at n = 1 (butyltrimethylammonium perfluorodecanoate). In this system, the clouding phenomenon is not observed but there is a two phase region of L 1 + L. at low concentration and high temperatures. The phase structures also possess uniform mean curvature. In keeping with the less hydrophobic systems, the L. phase is less temperature sensitive at high concentrations. This work has shown that the but'l groups of the counterion are, in part, responsible for the unusual phase behaviour observed in the TBA surfactants. The hydrophobic nature of the counterion has a major impact on the structures formed even at high dilution. This nature probably drives the counterion to the interface which affects the type of mesophase formed at higher concentrations and also determines its stability with respect to temperature and concentration.
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Keeling, David Leslie. "Molecular manipulation and self assembly on semiconductor surfaces." Thesis, Nottingham Trent University, 2003. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.275909.

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Marx, Eike. "Self-assembly of CdSe nanocrystals for molecular electronics." Thesis, University of Cambridge, 2004. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.616244.

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Bellaiche, Mathias Moussine Jacques. "Molecular mechanisms of protein self-assembly and aggregation." Thesis, University of Cambridge, 2018. https://www.repository.cam.ac.uk/handle/1810/277621.

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In this thesis, we investigate the mechanisms driving the self-assembly of peptides and proteins using computational and theoretical tools, always validating our results with experimental measures when possible. In the first part, Chapters 2-5, we focus on the Aβ system, a peptide whose aggregation is intimately linked with the development of Alzheimer's Disease. We begin by simulating the major alloforms of the peptide, Aβ_40 and Aβ_42, demonstrating that the two populate similar disordered ensembles and matching experimental data. Next we investigate how disordered Aβ_42 monomers interact with each other, finding that oligomerisation into amorphous aggregates is driven largely by hydrophobic, non-specific forces. We then move on to probing the aggregation of Aβ_42 into amyloid structures using a native-centric coarse-grained model, and explain the results with a novel Markov state analysis from which we are able to extract structural, kinetic and thermodynamic information on elongation reactions. Finally, we probe the interactions of Aβ_42 monomers with Aβ_42 fibrillar surfaces using a specially designed enhanced sampling scheme, which allows us to obtain enthalpy-driven binding thermodynamics consistent with experiments and to propose major polar binding modes. In the second part of the thesis, Chapters 6 and 7, we model the aggregation of two other self-assembling systems, viruses and a truncated form of the molecular chaperone Hsp70. We first develop a data analysis platform to extract information on the microscopic mechanisms of viral capsid self-assembly from experimental data, synthesising the results from several different systems to draw general evolutionary conclusions about the assembly mechanism. Finally, we model the oligomerisation of Hsp70 thermodynamically and kinetically, showing that its self-assembly is a highly cooperative reaction that is under strong structural constraints.
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Zhou, Yangbin. "Molecular Design, Precise Synthesis and Solution Self-assembly of Molecular Patchy Particles." University of Akron / OhioLINK, 2016. http://rave.ohiolink.edu/etdc/view?acc_num=akron1460324862.

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Szymonik, Michal Piotr. "Fabrication of molecular devices based on DNA self-assembly." Thesis, University of Leeds, 2012. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.590280.

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Advances in molecular engineering have enabled the formation of increasingly sophisticated molecular systems. Use of DNA and other biomolecules has proven a particularly powerful tool for nanotechnology, with their unique chemistry allowing the synthesis of self-assembling nanoscale devices with complex structures and functionalities. The ability to integrate such constructs with solid state electronic devices would be of great value for the development of these technologies into practical devices. In this project, a method was developed allowing the specific targeted alignment and binding of single molecules to sites on nano-patterned metal electrodes, relying on the highly specific molecular recognition capabilities of DNA. The patterning method utilised self-assembled monolayers of I-mercapto11- undecanol as a molecular resist, which could be removed via reductive electrochemical desorption of the gold-thiol bond. This allowed the patterning of thiolated DNA probes on selected electrodes in an array. A DNA strand with sticky ends complementary to the surface probes can then specifically bind to the surface, bridging between sites where this enables the simultaneous hybridisation of both its single stranded regions. The surface binding and hybridisation of thiolated DNA oligonucleotides was tested using a colorimetric surface staining technique and the quality of monolayers was investigated using several methods. These trials informed the development of DNA-coated surfaces resistant to non-specific binding. The electrochemical desorption of SAMs was then investigated as a means for the high-resolution patterning of surfaces. Employing these techniques, the specific bridging of gold electrodes separated. by 70nm with 330 basepair DNA strands was demonstrated. Additionally, the selective thermal melt ing of different DNA probes and the ligation of surface-bound DNA constructs were examined as further methods of controlling the specificity of the assembly reaction.
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Books on the topic "Molecular self-Assembly of insulating"

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R, Nagarajan. Amphiphiles: Molecular assembly and applications. Washington, DC: American Chemical Society, 2011.

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Fuiita, Makoto, ed. Molecular Self-Assembly Organic Versus Inorganic Approaches. Berlin, Heidelberg: Springer Berlin Heidelberg, 2000. http://dx.doi.org/10.1007/3-540-46591-x.

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service), ScienceDirect (Online, ed. Systems self-assembly: Multidisciplinary snapshots. Amsterdam: Elsevier Science, 2008.

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Frederic, Fages, and Araki K, eds. Low molecular mass gelators: Design, self-assembly, function. Berlin: Springer, 2005.

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Frédéric, Fages, and Araki K, eds. Low molecular mass gelators: Design, self-assembly, function. Berlin: Springer, 2005.

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Comrie, James P., and James P. Comrie. Molecular self-assembly: Advances in chemistry, biology, and nanotechnology. Hauppauge, N.Y: Nova Science Publishers, 2010.

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Comrie, James P. Molecular self-assembly: Advances in chemistry, biology, and nanotechnology. Hauppauge, N.Y: Nova Science Publishers, 2010.

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Pierandrea, Lo Nostro, ed. Molecular forces and self assembly: In colloid, nano sciences and biology. Cambridge: Cambridge University Press, 2010.

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Claessens, Christian Georges. Self-assembly and self-organisation of molecular compounds containing complementary [pi]-[pi] interacting units. Birmingham: University of Birmingham, 1997.

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M, Rotello Vincent, and Thayumanavan Sankaran, eds. Molecular recognition and polymers: Control of polymer structure and self-assembly. Hoboken, N.J: Wiley, 2008.

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Book chapters on the topic "Molecular self-Assembly of insulating"

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Kling, Felix, Ralf Bechstein, Philipp Rahe, and Angelika Kühnle. "Self-assembly of Organic Molecules on Insulating Surfaces." In Noncontact Atomic Force Microscopy, 147–71. Cham: Springer International Publishing, 2015. http://dx.doi.org/10.1007/978-3-319-15588-3_9.

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Heckl, Wolfgang M. "Molecular Self-Assembly." In Laser Physics at the Limits, 505–17. Berlin, Heidelberg: Springer Berlin Heidelberg, 2002. http://dx.doi.org/10.1007/978-3-662-04897-9_46.

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Dong, Xue-Hui, Yiwen Li, Zhiwei Lin, Xinfei Yu, Kan Yue, Hao Liu, Mingjun Huang, Wen-Bin Zhang, and Stephen Z. D. Cheng. "Solution Self-Assembly of Giant Surfactants: An Exploration on Molecular Architectures." In Self-Assembly, 309–29. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2018. http://dx.doi.org/10.1002/9781119001379.ch10.

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Stoddart, J. Fraser. "Molecular Self-Assembly Processes." In Novartis Foundation Symposia, 5–22. Chichester, UK: John Wiley & Sons, Ltd., 2007. http://dx.doi.org/10.1002/9780470514085.ch2.

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Spector, Mark S., Jonathan V. Selinger, and Joel M. Schnur. "Chiral Molecular Self-Assembly." In Materials-Chirality, 281–372. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2004. http://dx.doi.org/10.1002/0471471895.ch5.

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Méndez-Ardoy, Alejandro, Ignacio Insua, Juan R. Granja, and Javier Montenegro. "Cyclization and Self-Assembly of." In Methods in Molecular Biology, 449–66. New York, NY: Springer US, 2021. http://dx.doi.org/10.1007/978-1-0716-1689-5_24.

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Abbott, N. L., H. A. Biebuyck, S. Buchholz, J. P. Folkers, M. Y. Han, A. Kumar, G. P. Lopez, C. S. Weisbecker, and G. M. Whitesides. "Molecular Self-Assembly and Micromachining." In Atomic and Nanometer-Scale Modification of Materials: Fundamentals and Applications, 293–301. Dordrecht: Springer Netherlands, 1993. http://dx.doi.org/10.1007/978-94-011-2024-1_26.

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Stupp, S. I., K. E. Huggins, L. S. Li, L. H. Radzilowski, M. Keser, V. Lebonheur, and S. Son. "Self Assembly of Molecular Materials." In Modular Chemistry, 219–40. Dordrecht: Springer Netherlands, 1997. http://dx.doi.org/10.1007/978-94-011-5582-3_20.

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Ueno, Takafumi. "Coordination Chemistry in Self-Assembly Proteins." In SpringerBriefs in Molecular Science, 61–68. Tokyo: Springer Japan, 2013. http://dx.doi.org/10.1007/978-4-431-54370-1_7.

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Carbone, Alessandra, and Nadrian C. Seeman. "Molecular Tiling and DNA Self-assembly." In Aspects of Molecular Computing, 61–83. Berlin, Heidelberg: Springer Berlin Heidelberg, 2003. http://dx.doi.org/10.1007/978-3-540-24635-0_5.

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Conference papers on the topic "Molecular self-Assembly of insulating"

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Corrales, L. René. "Molecular dynamics simulations of defects and excitons in glasses." In Bragg Gratings, Photosensitivity, and Poling in Glass Fibers and Waveguides. Washington, D.C.: Optica Publishing Group, 1997. http://dx.doi.org/10.1364/bgppf.1997.jma.9.

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The interaction of excited electrons and holes with defects in network semiconducting and insulating glasses is examined. Of particular interest is the diffusion of vacancy sites in oxide materials that can aggregate to form voids and eventually lead to the formation of nanoscale bubbles. This is a process that is known to occur in nuclear waste materials, but the mechanisms remain unclear. A radioactive decay event can release energy in the keV to MeV range that is dispersed amongst the emission of alpha-particles, beta-particles, and gamma rays (depending upon the radionuclide), and into the momentum of the remaining ion. The particle emission lead primarily to electronic excitation energies and self-trapped excitons, whereas the momentum on the ion leads to a recoil cascade. These processes lead to an abundance of bond breaking and topological rearrangement. During the lifetimes of these events, defects such as vacancies, peroxides and E’ centers are formed, and also leads to the etching and formation of molecular oxygen. The underlying physics and chemistry of these processes are studied using a semi-empirical methodology specifically designed to examine amorphous networked materials. The method can be implemented in parallel to study large system sizes as required in the simulation of recoil cascades, and contains enough electronic information to model excited states that lead to the formation of excitons. An overview of the model approach and its application for determining the diffusion barriers of defects in the presence of excitons will be discussed.
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Liu, Yanjing, Aprillya Rosidian, Wei Zhao, Tingying Zeng, Ki D. Oh, and Richard O. Claus. "Ultracapacitors formed by molecular self-assembly." In 1999 Symposium on Smart Structures and Materials, edited by Manfred R. Wuttig. SPIE, 1999. http://dx.doi.org/10.1117/12.352785.

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Szu, Harold, Ann Tate, David Cullin, Marianne Walch, David Demske, Joseph Garcia, Sonlinh Phuvan, and Nicholas Caviris. "Self Assembly SLM for Molecular Computing." In Spatial Light Modulators and Applications. Washington, D.C.: Optica Publishing Group, 1993. http://dx.doi.org/10.1364/slma.1993.swd.1.

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Spatial Light Modulator (SLM) useful Molecular Computing is made on a bacteriorhodopsin (BR) molecule film suspended in a viscous liquid medium, similar to a wet photograph but having adaptive and finer pixels. The natural synergism between the thermal diffusion of BR molecule (induced externally by a write-laser) and its photochromism (generated internally by electronic transitions) is demonstrated in an edge-enhanced laser-image application.
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Mo, Gary C. H., and Daniel Y. Kwok. "Self-Breakup of Microdroplets by Molecular Self-Assembly." In ASME 3rd International Conference on Microchannels and Minichannels. ASMEDC, 2005. http://dx.doi.org/10.1115/icmm2005-75179.

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We report a method of producing minute micro-droplets through nanoscale molecular self-assembly from a given liquid volume without external input. By the branching of hydrophobic restrictions, the drop is forced to separate while translating on a flat surface. Symmetry in the drop front wetted perimeter conduces to equal division of the drop. We show that at least 3 divisions can be performed sequentially on a 1.5 microliter drop to give minute droplets of approximately equal volumes. A division of carrier liquid volume by 1/23 enables multiple analyses on many separate stations in one microfluidic application.
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den Dulk, Remco. "Self-Assembly Experiments with PNA-Derivatized Carbon Nanotubes." In DNA-BASED MOLECULAR ELECTRONICS: International Symposium on DNA-Based Molecular Electronics. AIP, 2004. http://dx.doi.org/10.1063/1.1805375.

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D'Silva, Claudius. "Molecular recognition: A route to the self-assembly of molecular circuitry." In 1992 14th Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE, 1992. http://dx.doi.org/10.1109/iembs.1992.5760921.

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D'Silva. "Molecular Recognition: A Route To The self-assembly of molecular Circuitry." In Proceedings of the Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE, 1992. http://dx.doi.org/10.1109/iembs.1992.589618.

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Ahmed, Mohammad Nasar, Kimia Karimian, and Carla Purdy. "Agent-based modeling of molecular self-assembly mechanisms." In 2011 IEEE 54th International Midwest Symposium on Circuits and Systems (MWSCAS). IEEE, 2011. http://dx.doi.org/10.1109/mwscas.2011.6026446.

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Meng, Ya, and Navin Kashyap. "Controlling errors in the process of molecular self-assembly." In 2009 47th Annual Allerton Conference on Communication, Control, and Computing (Allerton). IEEE, 2009. http://dx.doi.org/10.1109/allerton.2009.5394927.

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Zeng, Tingying, Richard O. Claus, Yanjing Liu, Fajian Zhang, W. Wei, and Kristi L. Cooper. "Synthesis of piezoelectric thin films by molecular self-assembly." In SPIE's 7th Annual International Symposium on Smart Structures and Materials, edited by Yoseph Bar-Cohen. SPIE, 2000. http://dx.doi.org/10.1117/12.387775.

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Reports on the topic "Molecular self-Assembly of insulating"

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CURRO, JOHN G., JOHN DWANE MCCOY, AMALIE L. FRISCHKNECHT, and KUI YU. Molecular Self-Assembly. Office of Scientific and Technical Information (OSTI), November 2001. http://dx.doi.org/10.2172/789581.

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Zhang, Pengpeng. Utilizing Molecular Self-Assembly to Tailor Electrical Properties of Si Nanomembranes. Office of Scientific and Technical Information (OSTI), October 2017. http://dx.doi.org/10.2172/1404698.

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Knowowski, Christopher. Dynamics and statics of polymer nanocomposite self-assembly via molecular dynamics. Office of Scientific and Technical Information (OSTI), May 2015. http://dx.doi.org/10.2172/1417987.

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Iancu, Violeta. Single Molecule Switches and Molecular Self-Assembly: Low Temperature STM Investigations and Manipulations. Office of Scientific and Technical Information (OSTI), August 2006. http://dx.doi.org/10.2172/955626.

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Jen, Alex K. Molecular Self-Assembly and Interfacial Engineering for Highly Efficient Organic Field Effect Transistors and Solar Cells. Fort Belvoir, VA: Defense Technical Information Center, September 2012. http://dx.doi.org/10.21236/ada581366.

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Abbott, Nicholas L., John P. Folkers, and George M. Whitesides. Manipulation of the Wettability of Surfaces on the 0.1 to 1 Micrometer Scale Through Micromachining and Molecular Self-Assembly. Fort Belvoir, VA: Defense Technical Information Center, July 1992. http://dx.doi.org/10.21236/ada254887.

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