Relevant bibliographies by topics / Molecular self-assembly on silicon

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 on silicon'

Author: Grafiati
Published: 4 June 2021
Last updated: 1 February 2022

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Journal articles on the topic "Molecular self-assembly on silicon"

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Lenfant, Stéphane, Christophe Krzeminski, Christophe Delerue, Guy Allan, and Dominique Vuillaume. "Molecular Rectifying Diodes from Self-Assembly on Silicon." Nano Letters 3, no. 6 (June 2003): 741–46. http://dx.doi.org/10.1021/nl034162f.

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Chang, Chia-Ching, Kien Wen Sun, Lou-Sing Kan, and Chieh-Hsiung Kuan. "Guided three-dimensional molecular self-assembly on silicon substrates." Applied Physics Letters 88, no. 26 (June 26, 2006): 263104. http://dx.doi.org/10.1063/1.2216881.

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Ma, Wen Shi, Fang Yang, Bang Jun Deng, Hai Yan Sun, and Xiao Dan Lin. "Studies on Self-Assembly of Methoxy Polyethylene Oxide Propyl Trimethoxysilane on Silicon Substrate." Advanced Materials Research 557-559 (July 2012): 1916–20. http://dx.doi.org/10.4028/www.scientific.net/amr.557-559.1916.

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A novel hydrophilic and self-assemble functional methoxy polyethylene oxide propyl trimethoxysilane was synthesized by hydrosilylation reaction using methoxy polyethylene oxide monoallyl ether and trimethoxysilane. The self-assembled layer of methoxy polyethylene oxide propyl trimethoxysilane was prepared by immersing hydroxylate silicon substrate in silane solution. The structure, morphology and hydrophilicity of self-assembled layer were characterized by means of X-ray photoelectron spectroscopy (XPS), atomic force microscopy (AFM), and water contact angle method. The results show that methoxy polyethylene oxide propyl trimethoxysilane can self-assemble on the surface of hydroxylate silicon substrate. At concentration of 0.80 g/100 mL and the self-assembling time of 60 minutes, the self-assembled layer of methoxy polyethylene oxide propyl trimethoxysilane of average molecular weight of 682 shows a brush-like structure with each brush column size of 10~15 nm in diameter and 5~8 nm in height. The correspondence of the columns height with the average length of the silane molecules suggests that the layer obtained is monolayer and the brush columns are constituted by extended PEO molecular chain units in the silane. The distribution of columns is uniform and the root-mean-square（RMS） roughness of self-assembled monolayer is 0.98 nm. Water contact angle of the monolayer is 7.4°. A super-hydrophilic surface is obtained.
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Abate, Antonio, Raphael Dehmel, Alessandro Sepe, Ngoc Linh Nguyen, Bart Roose, Nicola Marzari, Jun Ki Hong, James M. Hook, Ullrich Steiner, and Chiara Neto. "Halogen-bond driven self-assembly of perfluorocarbon monolayers on silicon nitride." Journal of Materials Chemistry A 7, no. 42 (2019): 24445–53. http://dx.doi.org/10.1039/c9ta04620h.

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Yam, Chi Ming, Adam Dickie, Aramice Malkhasian, Ashok K. Kakkar, and M. A. Whitehead. "Article." Canadian Journal of Chemistry 76, no. 11 (November 1, 1998): 1766–78. http://dx.doi.org/10.1139/v98-151.

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The hydrolysis of surface-bound basic tin-amide moieties with acidic protons of alkynyl chromophores leads to molecular self-assembly of a variety of rigid-rod alkynes on inorganic oxide surfaces such as glass, quartz, and single crystal silicon. Characterization of these newly developed thin films was achieved by contact-angle goniometry, FTIR-ATR, ellipsometry, and X-ray photoelectron spectroscopy, which indicate that these thin films are densely packed. Comparative molecular mechanics modeling studies on unbound and chemisorbed -Sn-Ctriple bondC-H monomer, dimer, trimer, and a 12 × 12 (144 molecule) model substrate, suggest that surface anchoring of Sn-alkynyl units is essential for highly ordered thin-film structures that can effect topochemical polymerization. Preliminary MO calculations on a 4 × 4 model show conjugated molecular orbitals through the system.Key words: molecular self-assembly, rigid-rod alkynes, acid-base hydrolysis, tin-alkynyl thin films, molecular mechanics modeling studies, topochemical polymerization, molecular orbitals.
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Chen, Song, Yong Run Yang, and Jin Dai Wang. "Effect of Silicon Sources on Self-Assembly in Acidic Environment and Impact on Morphology and Grain Size of Mesoporous Material." Solid State Phenomena 121-123 (March 2007): 465–68. http://dx.doi.org/10.4028/www.scientific.net/ssp.121-123.465.

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Alkaline hydrothermal process with using cetyl-trimenthylammonium bromide as template is typical method to prepare MCM-41 mesoporous material. Synthesis in acid media was seldom researched deeply. With cheap inorganic water glass, effect of different silicon sources on self-assembly in acid media was investigated. Not like typical MCM-41 mesoporous materials, it is found that results of analysis are a little different and morphology of mesoporous materials synthesized in acid media does not rely on silicon sources, regardless of organic or inorganic silicon source. It is also noticed that nanometer granule of mesoporous material can be directly made by simply adjusting water dosage, which open up a new way for preparing nanometer material by self-assembly.
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Cisternas, Marcelo A., Francisca Palacios-Coddou, Sebastian Molina, Maria Jose Retamal, Nancy Gomez-Vierling, Nicolas Moraga, Hugo Zelada, Marco A. Soto-Arriaza, Tomas P. Corrales, and Ulrich G. Volkmann. "Dry Two-Step Self-Assembly of Stable Supported Lipid Bilayers on Silicon Substrates." International Journal of Molecular Sciences 21, no. 18 (September 17, 2020): 6819. http://dx.doi.org/10.3390/ijms21186819.

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Artificial membranes are models for biological systems and are important for applications. We introduce a dry two-step self-assembly method consisting of the high-vacuum evaporation of phospholipid molecules over silicon, followed by a subsequent annealing step in air. We evaporate dipalmitoylphosphatidylcholine (DPPC) molecules over bare silicon without the use of polymer cushions or solvents. High-resolution ellipsometry and AFM temperature-dependent measurements are performed in air to detect the characteristic phase transitions of DPPC bilayers. Complementary AFM force-spectroscopy breakthrough events are induced to detect single- and multi-bilayer formation. These combined experimental methods confirm the formation of stable non-hydrated supported lipid bilayers with phase transitions gel to ripple at 311.5 ± 0.9 K, ripple to liquid crystalline at 323.8 ± 2.5 K and liquid crystalline to fluid disordered at 330.4 ± 0.9 K, consistent with such structures reported in wet environments. We find that the AFM tip induces a restructuring or intercalation of the bilayer that is strongly related to the applied tip-force. These dry supported lipid bilayers show long-term stability. These findings are relevant for the development of functional biointerfaces, specifically for fabrication of biosensors and membrane protein platforms. The observed stability is relevant in the context of lifetimes of systems protected by bilayers in dry environments.
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Fairushin, I. I., A. Yu Shemakhin, and A. A. Khabir’yanova. "Molecular Dynamics Simulation of Copper Nanofilm Self-Assembly on Silicon Substrate under Gas-Discharge Plasma Conditions." High Energy Chemistry 55, no. 5 (September 2021): 399–401. http://dx.doi.org/10.1134/s0018143921050039.

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Wan, Congshan, Joe L. Gonzalez, Tianren Fan, Ali Adibi, Thomas K. Gaylord, and Muhannad S. Bakir. "Fiber-Interconnect Silicon Chiplet Technology for Self-Aligned Fiber-to-Chip Assembly." IEEE Photonics Technology Letters 31, no. 16 (August 15, 2019): 1311–14. http://dx.doi.org/10.1109/lpt.2019.2923206.

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Cushing, Kevin W., Timothy L. Vail, Jani C. Ingram, and Ingrid St Omer. "Micropatterned avidin arrays on silicon substrates via photolithography, self-assembly and bioconjugation." Biotechnology and Applied Biochemistry 43, no. 2 (March 1, 2006): 85. http://dx.doi.org/10.1042/ba20050085.

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Dissertations / Theses on the topic "Molecular self-assembly on silicon"

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Dhungana, Daya Sagar. "Growth of InAs and Bi1-xSBx nanowires on silicon for nanoelectronics and topological qubits by molecular beam epitaxy." Thesis, Toulouse 3, 2018. http://www.theses.fr/2018TOU30150/document.

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Grâce à leur propriétés uniques, les nanofils d'InAs et de Bi1-xSbx sont important pour les domaines de la nanoélectronique et de l'informatique quantique. Alors que la mobilité électronique de l'InAs est intéressante pour les nanoélectroniques; l'aspect isolant topologique du Bi1-xSbx peut être utilisé pour la réalisation de Qubits basés sur les fermions de Majorana. Dans les deux cas, l'amélioration de la qualité du matériau est obligatoire et ceci est l'objectif principal cette thèse ou` nous étudions l'intégration des nanofils InAs sur silicium (compatibles CMOS) et où nous développons un nouvel isolant topologique nanométrique: le Bi1-xSbx. Pour une compatibilité CMOS complète, la croissance d'InAs sur Silicium nécessite d'être auto- catalysée, entièrement verticale et uniforme sans dépasser la limite thermique de 450 ° C. Ces normes CMOS, combineés à la différence de paramètre de maille entre l'InAs et le silicium, ont empêché l'intégration de nanofils InAs pour les dispositifs nanoélectroniques. Dans cette thèse, deux nouvelles préparations de surface du Si ont été étudiées impliquant des traitements Hydrogène in situ et conduisant à la croissance verticale et auto-catalysée de nanofils InAs compatible avec les limitations CMOS. Les différents mécanismes de croissance résultant de ces préparations de surface sont discutés en détail et un passage du mécanisme Vapor-Solid (VS) au mécanisme Vapor- Liquid-Solid (VLS) est rapporté. Les rapports d'aspect très élevé des nanofils d'InAs sont obtenus en condition VLS: jusqu'à 50 nm de diamètre et 3 microns de longueur. D'autre part, le Bi1-xSbx est le premier isolant topologique 3D confirmé expérimentalement. Dans ces nouveaux matériaux, la présence d'états surfacique conducteurs, entourant le coeur isolant, peut héberger les fermions de Majorana utilisés comme Qubits. Cependant, la composition du Bi1-xSbx doit être comprise entre 0,08 et 0,24 pour que le matériau se comporte comme un isolant topologique. Nous rapportons pour la première fois la croissance de nanofils Bi1-xSbx sans défaut et à composition contrôlée sur Si. Différentes morphologies sont obtenues, y compris des nanofils, des nanorubans et des nanoflakes. Leur diamètre peut être de 20 nm pour plus de 10 microns de long, ce qui en fait des candidats idéaux pour des dispositifs quantiques. Le rôle clé du flux Bi, du flux de Sb et de la température de croissance sur la densité, la composition et la géométrie des structures à l'échelle nanométrique est étudié et discuté en détail
InAs and Bi1-xSbx nanowires with their distinct material properites hold promises for nanoelec- tronics and quantum computing. While the high electron mobility of InAs is interesting for na- noelectronics applications, the 3D topological insulator behaviour of Bi1-xSbx can be used for the realization of Majorana Fermions based qubit devices. In both the cases improving the quality of the nanoscale material is mandatory and is the primary goal of the thesis, where we study CMOS compatible InAs nanowire integration on Silicon and where we develop a new nanoscale topological insulator. For a full CMOS compatiblity, the growth of InAs on Silicon requires to be self-catalyzed, fully vertical and uniform without crossing the thermal budge of 450 °C. These CMOS standards, combined with the high lattice mismatch of InAs with Silicon, prevented the integration of InAs nanowires for nanoelectronics devices. In this thesis, two new surface preparations of the Silicon were studied involving in-situ Hydrogen gas and in-situ Hydrogen plasma treatments and leading to the growth of fully vertical and self-catalyzed InAs nanowires compatible with the CMOS limitations. The different growth mechanisms resulting from these surface preparations are discussed in detail and a switch from Vapor-Solid (VS) to Vapor- Liquid-Solid (VLS) mechanism is reported. Very high aspect ratio InAs nanowires are obtained in VLS condition: upto 50 nm in diameter and 3 microns in length. On the other hand, Bi1-xSbx is the first experimentally confirmed 3D topololgical insulator. In this new material, the presence of robust 2D conducting states, surrounding the 3D insulating bulk can be engineered to host Majorana fermions used as Qubits. However, the compostion of Bi1-xSbx should be in the range of 0.08 to 0.24 for the material to behave as a topological insula- tor. We report growth of defect free and composition controlled Bi1-xSbx nanowires on Si for the first time. Different nanoscale morphologies are obtained including nanowires, nanoribbons and nanoflakes. Their diameter can be 20 nm thick for more than 10 microns in length, making them ideal candidates for quantum devices. The key role of the Bi flux, the Sb flux and the growth tem- perature on the density, the composition and the geometry of nanoscale structures is investigated and discussed in detail
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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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Brown, Samuel Lynn. "Silicon Nanocrystals| Optical Properties and Self-assembly." Thesis, North Dakota State University, 2018. http://pqdtopen.proquest.com/#viewpdf?dispub=10790537.

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Silicon nanocrystal’s (SiNCs) size dependent optical properties and nontoxic nature portend potential applications across a broad range of industries. With any of these applications, a thorough understanding of SiNC photophysics is desirable to tune their optical properties while optimizing quantum yield. However, a detailed understanding of the photoluminescence (PL) from SiNCs is convoluted by the complexity of the decay mechanisms, including a stretched-exponential relaxation and the presence of both nanosecond and microsecond decays.

In this dissertation, a brief history of semiconductor nanocrystals is given, leading up to the first discovery of room temperature PL in SiNCs. This is then followed by an introduction to the various nanocrystal synthetic schemes and a discussion of quantum dot photophysics in general. Three different studies on the PL from SiNCs are then presented. In the first study, the stretched nature of the time dependent PL is analyzed via chromatically-resolved and full-spectrum PL decay measurements. The second study analyzes the size dependence of the bimodal PL decay, where the amplitude of the nanosecond and microsecond decay are related to nanocrystal size, while the third project analyzes the temperature and microstructure dependencies of the PL from SiNC solids.

After an indepth look at the PL from SiNCs, this report examines preliminary results of SiNC and silver nanocrystal self-assembly. When compared to metal and metal chalcogenide nanoparticles, there is a dearth of literature on the self-assembly of SiNCs. To understand these phenomena, we analyze the size dependent ability of SiNCs to form a ‘superlattice’ and compare this with silver nanocrystals. Although the results on self-assembly are still somewhat preliminary, it appears that factors such as SiNC concentration and size dispersity play a key role in SiNC self-assembly, while suggesting intrinsic differences between the self-assembly of SiNCs and silver nanocrystals.

Finally, at the end of this dissertation, a corollary project is presented on the computational analysis of fluorescent silver nanoclusters (AgNCs). Due to their small size and non-toxic nature, AgNCs are an ideal fluorophore for biological systems, yet there is a limited understanding of their photophysics, which is the focus of this part of the dissertation.

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Brown, Samuel. "Silicon Nanocrystals: Optical Properties and Self Assembly." Diss., North Dakota State University, 2018. https://hdl.handle.net/10365/27926.

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Silicon nanocrystal?s (SiNCs) size dependent optical properties and nontoxic nature portend potential applications across a broad range of industries. With any of these applications, a thorough understanding of SiNC photophysics is desirable to tune their optical properties while optimizing quantum yield. However, a detailed understanding of the photoluminescence (PL) from SiNCs is convoluted by the complexity of the decay mechanisms, including a stretched-exponential relaxation and the presence of both nanosecond and microsecond decays. In this dissertation, a brief history of semiconductor nanocrystals is given, leading up to the first discovery of room temperature PL in SiNCs. This is then followed by an introduction to the various nanocrystal synthetic schemes and a discussion of quantum dot photophysics in general. Three different studies on the PL from SiNCs are then presented. In the first study, the stretched nature of the time dependent PL is analyzed via chromatically-resolved and full-spectrum PL decay measurements. The second study analyzes the size dependence of the bimodal PL decay, where the amplitude of the nanosecond and microsecond decay are related to nanocrystal size, while the third project analyzes the temperature and microstructure dependencies of the PL from SiNC solids. After an indepth look at the PL from SiNCs, this report examines preliminary results of SiNC and silver nanocrystal self-assembly. When compared to metal and metal chalcogenide nanoparticles, there is a dearth of literature on the self-assembly of SiNCs. To understand these phenomena, we analyze the size dependent ability of SiNCs to form a ?superlattice? and compare this with silver nanocrystals. Although the results on self-assembly are still somewhat preliminary, it appears that factors such as SiNC concentration and size dispersity play a key role in SiNC self-assembly, while suggesting intrinsic differences between the self-assembly of SiNCs and silver nanocrystals. Finally, at the end of this dissertation, a corollary project is presented on the computational analysis of fluorescent silver nanoclusters (AgNCs). Due to their small size and non-toxic nature, AgNCs are an ideal fluorophore for biological systems, yet there is a limited understanding of their photophysics, which is the focus of this part of the dissertation.
NSF CBET-1133135
NSF CBET-1603445
DOE DE-FG36-08G088160
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Delafosse, Gregory. "Auto-assemblage de fullerènes C60 sur surfaces d'oxyde de silicium et d'or fonctionnalisées NH2." Thesis, Aix-Marseille 1, 2011. http://www.theses.fr/2011AIX10221/document.

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Au cours de ce travail nous avons étudié la réalisation de couches moléculaires d’accroche terminées amine. Sur l’oxyde de silicium l’aminopropyletriméthoxysilane (APTMS) a été déposé à partir d’une solution, et via une méthode originale par voie sèche qui nous a permis de mettre en évidence les temps caractéristiques de greffage et d’organisation de la couche d’APTMS. Sur l’or, les monocouches d’aminoéthanethiol (AET) et d’aminothiophénol (ATP) ont été réalisées à partir d’une solution. Nous avons ensuite étudié les aspects structuraux et cinétiques du greffage des fullerènes C60 sur de telles couches d’accroche, constituées de terminaisons amines soit sur toute la surface soit en des zones isolées (couches binaires). Les techniques de spectroscopie UV-Visible, IRTF, Raman, et XPS ont permis d’observer le greffage des C60 sur les couches aminées. La spectroscopie Raman en mode exalté (SERS) a mis en lumière que les molécules d’ATP étaient plus inclinées après le greffage à reflux des C60. Les analyses des diverses couches à l’échelle moléculaire ont été menées par microscopie à sondes locales (AFM, STM), et les mesures électriques réalisées sur or à l’aide de la pointe STM ont montré le caractère isolant de la couche d’accroche seule et un gap proche de celui du C60 après greffage des fullerènes. Elles ont également mis en évidence que le C60 était greffé sélectivement sur les zones terminées amines des couches d’accroche binaires. Enfin, une application potentielle des couches de C60 étant les mémoires moléculaires, les propriétés électriques des diverses couches réalisées ont été mesurées à l’aide de contacts électriques évaporés
In this work we studied the preparation of sticking amine- terminated molecular layers. On silicon dioxide, 3-aminopropyltrimethoxysilane (APTMS) was de- posited from a solution, and using an original dry method that allowed us to determine time constants of APTMS layer grafting and organization. On gold surfaces, monolayers of aminoethanethiol (AET) and aminothiophenol (ATP) molecules were prepared from a solution. Then, we studied structural and kinetic aspects of ullerene C60 grafting on such sticking layers, terminated by amines either all over the surface or on isolated areas (binary layers). UV-visible, FTIR, Raman and XPS spectroscopy techniques enabled to observe that C60 was grafted on the amine-terminated layers. Exalted Raman spec- troscopy (SERS) revealed ATP molecules were more tilted after C60 grafting under reflux. Analyses of all the layers were made at a molecular level by local probe microscopy (AFM, STM), and electrical measurements performed on gold using the STM tip showed the in- sulating nature of the sticking layer whereas a gap close to that of C60 appeared after grafting of fullerenes. They also highlighted that C60 was selectively grafted on amine- terminated zones within binary sticking layers. At last, one of potential applications of C60 layers being molecular memory cells, electrical properties of the various studied layers were measured through evaporated electrical contact pads
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Morris, Christopher J. "Capillary-force driven self-assembly of silicon microstructures /." Thesis, Connect to this title online; UW restricted, 2007. http://hdl.handle.net/1773/5963.

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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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Lee, Sangho S. M. Massachusetts Institute of Technology. "Self-assembly of silicon-containing triblock copolymer and terpolymers." Thesis, Massachusetts Institute of Technology, 2018. https://hdl.handle.net/1721.1/121610.

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Thesis: S.M., Massachusetts Institute of Technology, Department of Materials Science and Engineering, 2019
Cataloged from PDF version of thesis.
Includes bibliographical references.
The block copolymer (BCP) self-assembly has garnered significant interest due to its ability to generate periodic nanostructures with a variety of morphologies. Compared to diblock copolymers that have been extensively studied to form the conventional morphologies such as spheres, cylinders, and lamellae depending on the block volume fraction, more complex polymer architectures are expected to offer additional degrees of freedom and a wider range of structures. Solvent vapor annealing (SVA) using a continuous gas flow system allows a precise control over the annealing condition, which can capture intermediate morphologies including perforated lamellae and gyroids and can create unique nanostructures that have not been observed in diblock copolymers. Combining with self-consistent field theory (SCFT) modeling and in situ grazing-incidence small-angle X-ray scattering (GISAXS) measurement, the phase behavior of advanced polymer architectures can be revealed in details.
Here, the self-assembly behavior of silicon-containing triblock copolymer and terpolymers in multi-layered films under SVA is presented. Using both experimental and SCFT approaches, the phase behavior of poly(stryrene-b-dimethylsiloxane-b-styrene) (PS-b-PDMS-b-PS or SDS32) thin films was investigated as a function of the as-cast film thickness and the ratio of two different solvent vapors, toluene and heptane. In comparison with diblock PS-b-PDMS with same molecular weight, the SDS32 offers a simple route to produce a diversity of well-ordered bilayer structures with smaller feature sizes, including the formation of bilayer perforated lamellae over a large process window. In addition, the morphological evolution of core-shell cylinder-forming triblock terpolymers during SVA was monitored in situ using GISAXS. A reversible order-order phase transformation between spheres and cylinders occurred during the annealing process.
One of the final morphologies consisted of the regions of in-plane cylinders, with the majority of the film comprising vertical core-shell cylinders passing through perforated lamellae of poly 1,1-dimethyl silacyclobutane (PDMSB).
by Sangho Lee.
S.M.
S.M. Massachusetts Institute of Technology, Department of Materials Science and Engineering
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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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Books on the topic "Molecular self-assembly on silicon"

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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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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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Liquid crystals: Materials design and self-assembly. Heidelberg: Springer, 2012.

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Gómez-López, Marcos. The self-assembly of novel molecular compounds and their potential device-like properties. Birmingham: University of Birmingham, 1997.

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Yang, Seung Yun. Reaction dynamics, a molecule at a time: Scanning tunneling microscopy (STM) studies of self-assembly and of induced reaction at silicon surfaces. 2005.

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Book chapters on the topic "Molecular self-assembly on silicon"

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Zenou, Noemi, Alexander Zelichenok, Shlomo Yitzchaik, Rami Cohen, and David Cahen. "Tuning the Electronic Properties of Silicon via Molecular Self-Assembly." In ACS Symposium Series, 57–66. Washington, DC: American Chemical Society, 1998. http://dx.doi.org/10.1021/bk-1998-0695.ch005.

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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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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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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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Holder, Simon J., and Richard G. Jones. "The Synthesis, Self-Assembly and Self-Organisation of Polysilane Block Copolymers." In Silicon Based Polymers, 249–77. Dordrecht: Springer Netherlands, 2008. http://dx.doi.org/10.1007/978-1-4020-8528-4_18.

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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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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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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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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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Conference papers on the topic "Molecular self-assembly on silicon"

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Mortuza, S. M., and Soumik Banerjee. "Controlled Self-Assembly of Functionalized Carbon Nanotubes on Silicon Substrates." In ASME 2013 International Mechanical Engineering Congress and Exposition. American Society of Mechanical Engineers, 2013. http://dx.doi.org/10.1115/imece2013-66579.

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Self-assembly of carbon nanotubes (CNTs) on silicon substrates has myriad applications including nanotube based electrochemical energy conversion and storage devices, such as batteries and super-capacitors. Patterned assembly of CNTs is required in order to control the effective electrical conductivity and mechanical properties of these devices and achieve substantial improvement in their performance. Solution-based self-assembly of CNTs provides a cost-effective means to synthesize uniform vertically or horizontally aligned nanostructures on top of substrates. However, self-assembly of CNTs is a complex dynamical process that involves intermolecular interaction between the CNTs and that between the nanotubes and the substrate as well as solvent molecules. The transport properties of CNTs and solvents also play an important role. The scientific literature lacks detailed study of understanding the mechanism of self-assembly of CNTs on substrates during synthesis process. Often times, nanotubes are functionalized in an effort to make them more soluble and induce partial charges to control the self-assembly. Some of the key factors that govern the transportation and self-assembly of functionalized CNTs are surface charge density on substrate and electrostatic interaction of the functionalized CNTs with the substrate. In an effort to mimic the conditions during the synthesis of carbon nanomaterials on silicon substrate, we have employed molecular dynamics simulations to simulate both pure and functionalized CNTs sandwiched between silicon substrates in presence of commonly used solvent, water. Our simulations indicate that both pure and functionalized CNTs are not significantly soluble in water and form agglomerates. Our results also illustrate that neither pure nor functionalized CNTs tend to deposit on silicon substrates in water. Results presented in this study provide fundamental insight that can help to understand the agglomeration and orientation of CNTs in water.
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Chia-Ching Chang, Kien-Wen Sun, Shang-Fan Lee, Lou-Sing Kan, and Chieh-Hsiung Kuan. "Self-assembled Molecular Magnets on Patterned Silicon Substrates." In 2006 IEEE Conference on Emerging Technologies - Nanoelectronics. IEEE, 2006. http://dx.doi.org/10.1109/nanoel.2006.1609712.

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Dong, Jianchun, Babak A. Parviz, Hong Ma, and Alex K. Jen. "Using self-assembly for the construction of nanoscale lateral-transport molecular electronic devices and microscale silicon-based networks." In Optics East, edited by M. Saif Islam and Achyut K. Dutta. SPIE, 2004. http://dx.doi.org/10.1117/12.570819.

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Wang, Ying, Minglai Yang, Linpei Zhu, and Yafei Zhang. "Silicon Nanostructures Formed by Self-organizing Au Nanoparticle Film." In 2006 1st IEEE International Conference on Nano/Micro Engineered and Molecular Systems. IEEE, 2006. http://dx.doi.org/10.1109/nems.2006.334787.

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Chen, Y. B., G. L. Zhang, H. Y. Wu, and G. Q. Qin. "Molecular Dynamics Simulation on Self-Assembly of Nano-porous Structure of Polymer Cross-linked Silica Aerogels." In The International Workshop on Materials, Chemistry and Engineering. SCITEPRESS - Science and Technology Publications, 2018. http://dx.doi.org/10.5220/0007437602840290.

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Yang, Quan, Kaustubh Chitre, Tolulope O. Salami, Scott R. Oliver, and Junghyun Cho. "Development of Protective Coatings for Silicon Devices." In ASME 2003 International Mechanical Engineering Congress and Exposition. ASMEDC, 2003. http://dx.doi.org/10.1115/imece2003-41700.

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Ceramic coatings can be effectively used as a surface protective layer for silicon-based devices due to their inertness and good mechanical properties. One challenge is to avoid the weaknesses that ceramic coatings inherently possess, i.e., low strain tolerance, brittleness, high temperature required to process the film, and difficulty to produce a uniform, dense layer. Therefore, in an attempt to process strain-tolerant ceramic coatings at low temperatures, we develop an aqueous solution precursor processing route. Nanometer scale organic coatings, fabricated by self-assembly processes on the silicon, are used as a ‘template’ to aid the subsequent deposition of hard ceramic coatings (ZrO2). The ceramic coatings are deposited by spin coating. The organic self-assembled monolayer (SAM) coating provides temporary strain tolerance for the overlying hard coating upon mechanical and thermomechanical stresses before being decomposed at high temperatures. Molecular level understanding of the coating microstructure and micromechanics involved in the coating processes is systematically approached via experimental tools such as AFM and nanoindenter, as well as numerical simulation.
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Yanfeng Jiang, Xiaobo Zhang, and Bing Yang. "Study on self-alignment property of silicon nanowire in temperature gradient." In 2009 4th IEEE International Conference on Nano/Micro Engineered and Molecular Systems. IEEE, 2009. http://dx.doi.org/10.1109/nems.2009.5068726.

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Li, Zhi-Xin, and P. Xiao. "MOLECULAR DYNAMICS SIMULATION AND THEORETICAL STUDY ON IN-PLANE THERMAL CONDUCTIVITY OF SINGLE CRYSTAL SILICON FILM AT NANOSCALE." In Annals of the Assembly for International Heat Transfer Conference 13. Begell House Inc., 2006. http://dx.doi.org/10.1615/ihtc13.p8.100.

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Barriga, J., B. Coto, and B. Ferna´ndez. "Packing Structure of OTS on Silicon Surfaces: A Computational Approach." In World Tribology Congress III. ASMEDC, 2005. http://dx.doi.org/10.1115/wtc2005-63497.

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Optimal packing structure of Octadecyltrichlorosilane (OTS) self-assembled monolayer (SAM) adsorbed on a SiO2 surface with a Si (100) substrate was studied performing molecular dynamics (MD) computational simulations. Molecular substitution, substitution pattern and molecular orientation of the OTS molecules on the SiO2 (100) are the main factors studied in order to determine the optimal packing structure taking into account energetic balance. We have used the optimal packing structure to study other properties usually used to characterize SAMs as molecular and system tilt angles, film thickness and gauche defects. These properties and monolayer stability were studied performing MD simulations in a temperature range from 100 K to 600 K and we found that results obtained agree with those from experimental measurements. We found that OTS films are stable up to 500 K. The optimal structure obtained could be used in further MD simulations studies in order to determine tribological properties of OTS-SiO2 systems.
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Creasy, M. Austin, and Donald J. Leo. "Self-Healing Bilayer Lipid Membranes Formed Over Synthetic Substrates." In ASME 2008 Conference on Smart Materials, Adaptive Structures and Intelligent Systems. ASMEDC, 2008. http://dx.doi.org/10.1115/smasis2008-460.

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Biological systems demonstrate autonomous healing of damage and are an inspiration for developing self-healing materials. Our recent experimental study has demonstrated that a bilayer lipid membrane (BLM), also called a black lipid membrane, has the ability to self-heal after mechanical failure. These molecules have a unique property that they spontaneously self assembly into organized structures in an aqueous medium. The BLM forms an impervious barrier to ions and fluid between two volumes and strength of the barrier is dependent on the pressure and electrical field applied to the membrane. A BLM formed over an aperture on a silicon substrate is shown to self-heal for 5 pressurization failure cycles.
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Reports on the topic "Molecular self-assembly on silicon"

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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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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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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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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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Doyle, Jesse D., Nolan R. Hoffman, and M. Kelvin Taylor. Aircraft Arrestor System Panel Joint Improvement. U.S. Army Engineer Research and Development Center, August 2021. http://dx.doi.org/10.21079/11681/41342.

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Aircraft Arresting Systems (AAS) for military applications utilize sacrificial panels made of Ultra-High Molecular Weight polyethylene (UHMWPE) that are embedded into the pavement beneath the AAS cable to protect the pavement from cable damage. Problems have been observed with the materials and practices used to seal the UHMWPE panel joints from water and debris. Data obtained from laboratory and field studies were used make improvements to current practice for sealing UHMWPE panel joints. The study evaluated four joint-sealant materials, eight alternative surface treatment and preparation techniques to promote adhesion to UHMWPE, and seven joint-edge geometries. Bond-strength testing of joint-sealant specimens was conducted in the laboratory, followed by field evaluation of construction techniques. Field performance of the joint systems was monitored for 24 months after installation. Additionally, a thermal response model was developed to refine the joint design dimensions. Results confirmed that the best material to use was self-leveling silicone joint sealant. It was recommended that a dovetail groove be cut into the edge of UHMW panels to provide positive mechanical interlock and to reduce adhesive failures of the sealant. It was also recommended that the panel-to-panel joint-sealant reservoir be widened to prevent sealant compression damage.
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