Relevant bibliographies by topics / Self-assembled monolayer

Academic literature on the topic 'Self-assembled monolayer'

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Published: 4 June 2021
Last updated: 20 July 2024

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Journal articles on the topic "Self-assembled monolayer"

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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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Schön, J. H., H. Meng, and Z. Bao. "Self-Assembled Monolayer Transistors." Advanced Materials 14, no. 4 (February 19, 2002): 323–26. http://dx.doi.org/10.1002/1521-4095(20020219)14:4<323::aid-adma323>3.0.co;2-5.

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Losic, Dusan, Ken Short, Joe G. Shapter, and Justin J. Gooding. "Atomic Force Microscopy Imaging of Glucose Oxidase using Chemically Modified Tips." Australian Journal of Chemistry 56, no. 10 (2003): 1039. http://dx.doi.org/10.1071/ch03122.

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Atomic force microscopy (AFM) tips have been chemically modified using a variety of approaches mostly based on self-assembled monolayers (SAMs). Tips with both a hydrophobic and hydrophilic nature have been prepared and used to image glucose oxidase covalently attached to a self-assembled monolayer.
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Tao, Feng. "Nanoscale surface chemistry in self- and directed-assembly of organic molecules on solid surfaces and synthesis of nanostructured organic architectures." Pure and Applied Chemistry 80, no. 1 (January 1, 2008): 45–57. http://dx.doi.org/10.1351/pac200880010045.

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This article briefly reviews the interplay of weak noncovalent interactions involved in the formation of self-assembled monolayers of organic molecules and the strong chemical binding in directed-assembly of organic molecules on solid surfaces. For a self-assembled monolayer, each molecule involves at least three categories of weak interactions, including molecule-substrate interactions, molecule-molecule interactions in a lamella, and molecule-molecule interactions between two adjacent lamellae. Basically, molecule-substrate interactions play a major role in determining molecular configuration. Molecule-molecule interactions, particularly the interactions of molecular ending functional groups between two adjacent lamellae, such as hydrogen bonds, play a dominant role in determining the molecular packing pattern in a monolayer. These weak interactions may induce or influence molecular chirality. This understanding at the atomic scale allows us to design 2D nanostructured organic materials via precisely manipulating these weak noncovalent interactions. Compared to the self-assembled monolayer formed via weak noncovalent interactions, the structure of directed-assembled monolayer/multilayers formed through strong chemical bonds is significantly dependent on the geometric arrangement and reactivity of active sites on the solid surface. In contrast to the significant role of weak intermolecular interactions in determining molecular packing in a self-assembled monolayer, strong chemical binding between molecules and reactive sites of a substrate plays a major role in determining the molecular packing pattern in a directed-assembly monolayer. Controllable chemical attachment between organic functional groups and reactive sites of the solid surface is crucial for the formation of a highly oriented organic monolayer and the following multilayer.
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Chandrashekhar, Channapura Halappa. "Photoswitchable Polysiloxane Self-Assembled Monolayer." International Journal for Research in Applied Science and Engineering Technology 7, no. 7 (July 31, 2019): 350–56. http://dx.doi.org/10.22214/ijraset.2019.7053.

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Korolkov, Vladimir V., Stephanie Allen, Clive J. Roberts, and Saul J. B. Tendler. "Subsecond Self-Assembled Monolayer Formation." Journal of Physical Chemistry C 114, no. 45 (October 25, 2010): 19373–77. http://dx.doi.org/10.1021/jp106289p.

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Mellott, James M., and Daniel K. Schwartz. "Supercritical Self-Assembled Monolayer Growth." Journal of the American Chemical Society 126, no. 30 (August 2004): 9369–73. http://dx.doi.org/10.1021/ja0489588.

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Herr, Brian R., and Chad A. Mirkin. "Self-Assembled Monolayers of Ferrocenylazobenzenes: Monolayer Structure vs Response." Journal of the American Chemical Society 116, no. 3 (February 1994): 1157–58. http://dx.doi.org/10.1021/ja00082a058.

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Dickie, Adam J., Ashok K. Kakkar, and Michael A. Whitehead. "Molecular modelling of self-assembled alkynyl monolayer structures — Unnatural symmetry units, surface bonding, and topochemical polymerization1." Canadian Journal of Chemistry 81, no. 11 (November 1, 2003): 1228–40. http://dx.doi.org/10.1139/v03-110.

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Geometric modelling techniques are used to map the potential energies of packing for self-assembled alkyl- and phenyl-backboned monolayers across a range of intermolecular separations. Natural packing distances of 4.2–4.4 Å produce less stable, more isotropic monolayers because of repulsive interchain contacts. Optimizations at unnatural surface densities found thin films of lower energy and higher symmetry existed at increased chain–chain separations. Head-group bonding is therefore identified as a force for controlling monolayer order. Analysis of the natural monolayer structures on a silicon dioxide surface determined the favourable head-group structures, and allowed the topochemical polymerization of p-bis(butadiynyl)benzene monolayers to be rationalized.Key words: self-assembled monolayers, molecular modelling studies, repeating symmetry units, thin-film order, topochemical polymerization.
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Jadhav, Sushilkumar. "Self-assembled monolayers (SAMs) of carboxylic acids: an overview." Open Chemistry 9, no. 3 (June 1, 2011): 369–78. http://dx.doi.org/10.2478/s11532-011-0024-8.

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AbstractThe field of self-assembled monolayers (SAMs) of organic compounds on different substrates is of importance because it provides a suitable and efficient method of surface modification. The formation of robust, stable monolayers from carboxylic acids on two and three dimensional surfaces of different substrates have been reported. Carboxylic acids are promising class of organic compounds for monolayer formations where traditional alkanethiols or alkoxysilanes show limitations.
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Dissertations / Theses on the topic "Self-assembled monolayer"

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Sporakowski, Laura. "Controlled patterning of self-assembled monolayer films." Master's thesis, This resource online, 1993. http://scholar.lib.vt.edu/theses/available/etd-03172010-020130/.

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Lu, Kexin. "Organic semiconductors for self-assembled monolayer field effect transistors." Thesis, University of Manchester, 2012. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.559330.

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Molecular self-assembly has recently attracted significant attention for possible application in organic electronic and optoelectronic devices, such as self-assembled monolayer field-effect transistors (SAMFETs) and functional self-assembled integrated circuits. Self-assembly combines the advantages of low temperature solution processability, regio-selective monolayer adsorption and nano-scale control of film thickness. Much progress has been made in improving device performance using self-assembled monolayers (SAMs). However, most SAMFET devices reported to date showed current modulation only with submicrometre channels, with low device yields and poor reproducibility as a result of limited lateral interconnection of the semiconducting layer.In an attempt to address these issues, this thesis presents an investigation of the synthesis and properties of conjugated SAM molecules for use as the charge transporting layer in SAMFETs. Chapter 1 gives a comprehensive introduction to SAM-based surface systems, organic semiconductors and their use in OFETs and SAMFETs. Chapter 2 discusses attempts to design and synthesise p-type conjugated molecules capable of self-assembly on oxide surfaces based on a phenylene-bithiophene semiconducting core. The optical and electrochemical properties, as well as the thermal behaviour of these molecules are studied in detail. This theme is carried over to Chapter 3, which describes the synthesis, chemical and physical characterisation of two families of n-type SAM molecules. These molecules consist of NTCDI cores with hexyl or cyclohexyl chains as end-capping groups. Incorporation of a selection of materials as the active layer in OFETs or SAMFETs to evaluate the charge transport is demonstrated in Chapter 4. Monolayer films based on p-type monochlorosilane-terminated SAM molecules are made using the solution assembly technique and characterised by contact angle and AFM. OFETs made from DH-PTTP by both thermal evaporation and spin coating show high mobilities comparable to the best values reported in the literature. Top-contact SAMFETs show a hole mobility of 1.1 × 10-3 cm2V-1s-1 in air, consistent with those of solution processed DH-PTTP based OFETs. Finally, an overview of the project and some suggestions for future work are presented in Chapter 5.
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Borthwick, Matthew A. "X-ray techniques for probing self-assembled monolayer structures." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1997. http://www.collectionscanada.ca/obj/s4/f2/dsk2/ftp01/MQ44129.pdf.

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Matemadombo, Fungisai. "Substituted phthalocyanines development and self-assembled monolayer sensor studies." Thesis, Rhodes University, 2006. http://hdl.handle.net/10962/d1005029.

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Zinc, cobalt and iron phenylthio substituted phthalocyanines have been synthesized and characterized. Cyclic and square wave voltammetry in dimethylformamide containing tetrabutylammonium perchlorate revealed five and six redox processes respectively for the cobalt and iron phenylthio substituted phthalocyanines. These complexes are easier to reduce compared to the corresponding unsubstituted MPc and to butylthio substituted derivatives. Spectroelectrochemistry (in dimethylformamide containing tetrabutylammonium perchlorate) was employed to assign the cyclic voltammetry peaks, and gave spectra characteristic of Fe(I)Pc for reduction of iron phenylthio substituted phthalocyanine and Co(I)Pc for the reduction of cobalt phenylthio substituted phthalocyanine. The spectrum of the former is particularly of importance since such species have not received much attention in literature. Cobalt and iron phenylthio substituted phthalocyanines have been deposited on Au electrode surfaces through the self assembled monolayer (SAM) technique. The so formed layers were studied using voltammetric techniques. These SAMs blocked a number of Faradic processes and electrocatalyzed the oxidation of L-cysteine. Amine substituted cobalt phthalocyanine (CoTAPc) was deposited on gold surfaces by using an interconnecting SAM of mercaptopropionic acid or dithiobis(N-succinimidyl propionate) through the creation of an amide. Reductive and oxidative desorption of the SAMs limit the useful potential window. The SAM-CoTAPc layers show electrocatalytic activities towards oxygen reduction through the Co(I) central metal ion. Both SAMs were highly stable and hence will be interesting tools for further research in surface modification and sensor development.
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Jang, Chang-Hyun. "AFM-Assisted Nanofabrication using Self-Assembled Monolayers." Diss., Virginia Tech, 2003. http://hdl.handle.net/10919/11103.

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This study describes the covalent and the electrostatic attachment of molecules, nano-particles, and proteins to patterned self-assembled monolayers. A scanning probe nanografting technique was employed to produce patterns of various sizes, down to 10 nm. Thus, we are able to demonstrate a degree of surface patterning which is an order of magnitude smaller than that used in the semiconductor industry. One efficient strategy for creating chemically specific nanostructures is to use the extraordinary catalytic properties of enzymes. However, as the dimension of a catalyst patch is reduced down to nanometer scale, it is difficult to detect the very low concentration of product. This study resolves the problem by developing a new strategy: the surface trapping of a product generated by a nanometer-scale patch of surface-bound enzyme. An array of proteins finds use when the array contains a number of different proteins. Toward this end, a new and convenient method for immobilizing enzymes is developed, which will allow the preparation of thin films containing several different catalytically-active enzymes on the nanoscale. The disadvantage of scanning probe nanografting technique is that the AFM tip loses resolution through wear during the patterning procedure. This study examines the possibility of developing a new AFM lithographic method to avoid wear: the use of enzymes covalently attached to a tip as a site-specific catalyst.
Ph. D.
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Huang, Fei. "Electrophysiological Studies of a Retinal Prosthetic Prototype." Digital WPI, 2012. https://digitalcommons.wpi.edu/etd-theses/970.

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"Retinal prostheses are becoming a viable therapy for inner retinal degeneration caused by age related macular degeneration (AMD) and retinitis pigmentosa (RP). The majority of ocular and periocular prosthetic devices employ photodiodes and a microelectrode interface to convert light into a nerve impulse within the retina. Problems with this design include the need of an external power source, the lack of biocompatibility of the microelectrode array, and the need for complicated surgical procedures. Self-assembled monolayer (SAM) technology offers an alternative strategy, where neurons can be stimulated by light activation of a single layer of a photovoltaic SAM. We have developed a SAM structure where the photoexcitable dye 2-[2-[4-(dibutylamino)phenyl]ethenyl]-3-caboxymethylbenzothiazolium bromide (NK5962) was covalently immobilized to an indium tin oxide (ITO) and 3-(aminopropyl) trimethoxysilane (APTMS) surface. The NK562 derivatized surface was characterized through contact angle goniometry, electrochemical impedance spectroscopy, grazing angle infrared spectroscopy, and ultraviolet-visible absorption spectrophotometry. NG108-15 neurons were differentiated onto the surface and neural responses from electrical stimulation and photostimulation of the system were measured using whole-cell current and voltage clamp methodologies. We found an average 2.9 mV decrease in NG108-15 threshold potential for every 10 mV increase in ITO surface potential. Following photostimulation, there was a 1.8±0.2 fold increase (p < 0.05) in the sodium channel current amplitude and a 2.00 ± 0.22 fold increase (p < 0.05 ) in voltage amplitude of NG108-15 neurons on the ITO-APTMS-NK5962 surface due to transfer of energy from the excited dye surface to the attached neurons. The degree of photostimulation decreased upon using 344, 430, and 603 nm optical filters to block increasing amounts of the wavelengths of incident light capable of being absorbed by NK5962. The sodium current amplitude slightly increased at 50% transmittance of incident light relative to 100% transmittance, then sharply decreased at 12.5%, 6.25%, 3.13% transmittance. Upon addition of tetrodotoxin (TTX), sodium channel blockage was observed and portrayed by decreased sodium current and voltage response amplitudes, validating the voltage and current clamp results described above. Our findings indicate that the NK5962 photoelectric film shows promise as an implant for restoring light sensitivity to the retina. "
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Svedhem, Sofia. "Biomolecular interactions at model interfaces : a self-assembled monolayer approach /." Linköping : Univ, 2001. http://www.bibl.liu.se/liupubl/disp/disp2001/tek677s.pdf.

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Girot, Christine Stoll. "Infrared characterization of a self-assembled catenane monolayer on gold." Virtual Press, 1996. http://liblink.bsu.edu/uhtbin/catkey/1027114.

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The synthesis of the catenane components, a dithiol and a cyclophane, are described using previously reported methods. 1-3 The preparation techniques used to obtain a self-assembled dithiol monolayer and a self-assembled catenane monolayer from dilute solution onto a gold's surface are also reported. Grazing angle reflectance infrared spectroscopy was used to characterize the selfassembled dithiol and catenane monolayers. The infrared spectra revealed evidence for the existence of the dithiol monolayer and possible evidence for the existence of the catenane monolayer. A catenane transmission film spectrum was obtained to provide evidence for the existence of the catenane itself. When the transmission and the monolayer spectra were compared, shifts in a few of the absorption bands revealed some association between the dithiol and the cyclophane.
Department of Chemistry
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Sheikh, Khizar Hussain. "Surface forces in self-assembled monolayer and lipid bilayer systems." Thesis, University of Leeds, 2005. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.424503.

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Lee, Seok-Won 1970. "Molecular adsorption at solid/liquid interfaces using self-assembled monolayer films." Thesis, Massachusetts Institute of Technology, 1999. http://hdl.handle.net/1721.1/50552.

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Thesis (Ph.D.)--Massachusetts Institute of Technology, Dept. of Chemical Engineering, 1999.
Includes bibliographical references.
Many areas of technology rely on interfacial events that are controlled by nanometer-level interactions present at solid/liquid interfaces. Properties of wetting, corrosion inhibition, and molecular recognition provide convenient examples. To investigate such interactions at the molecular level, self-assembled monolayers (SAMs) have been employed as a model system as they offer the ability to produce well-defined organic surfaces of controlled composition. This thesis addresses the development and characterization of such films for controlling the adsorptive properties of surfaces toward various surfactant-like molecules and for proteins. Adsorption is controlled to facilitate the organized assembly of molecular precursors, retard the non-specific adsorption of proteins, provide a specificity for the adsorption of select proteins, and the use of molecular adsorption to generate local surface energy gradients useful for directing self propelled drop movement. A common theme in these studies is the importance of controlling the energetics and compositions of surfaces at the molecular level to influence microscopic events that translate into macroscopically observable changes in behavior. The first part of this thesis details the formation of monolayer films by the solution-phase adsorption of n-alkyl-chained adsorbates [CH 3(CH2)~ Y] onto the polar surfaces of terminally substituted SAMs [Au/S(CH)mX]. The polar tail groups (X and Y) of the adsorbate and SAM included amine, carboxylic acid, and amide groups, and the formation of the adsorbed monomolecular films on the SAMs relied on non-covalent interactions between X and Y. Highly organized monomolecular adlayers could be produced that were as densely packed as the alkanethiolate SAMs on gold comprising the first layer. This thesis also used this molecular adsorption process to cause liquid drops to move spontaneously on surfaces by creating local changes in surface energy. The drops could be directed to move along specified paths using patterned substrates that contained inner tracks of polar functionality and exterior domains of oleophobic methyl groups. The adsorption process allowed sequential transport of two drops on a common track and also regeneration of the initial high energy surface for reuse. The developed system provides an experimental platform for examining reactive flow and offers a novel "pumpless" method for sequentially delivering multiple drops along surfaces and within microfluidic devices. The second part of this thesis discusses various oligo(ethylene glycol)-terminated alkyltrichlorosilanes [C13Si(CH2)11(OCH2CHnX; X = -OCH 3 or -O 2CCH 3, n= 2- 4] that can form robust films on glass and metal oxide surfaces and control the adsorption of proteins. The adsorption of the methyl-capped trichlorosilanes produces densely packed, oriented monolayer films that are 2-3 nm in thickness. The trichlorosilyl group anchors the molecules to the surface, and the resulting film exposes the ethylene glycol units at its surface, as noted by its moderate hydrophilicity. The films are robust with stabilities similar to those of other alkylsiloxane coatings. These oligo(ethylene glycol)-terminated silane reagents produce films that exhibit resistances against the non-specific adsorption of proteins and that are better than for films prepared from octadecyltrichlorosilane. These oligo(ethylene glycol)-siloxane coatings offer performance advantages and could easily provide a direct and superior replacement for protocols that presently use silane reagents to generate hydrophobic, "inert" surfaces. This thesis also discusses the development of an acetate-capped oligo(ethylene glycol)-terminated silane to produce a HO-terminated oligo(ethylene glycol)-based coating on glass and metal oxide surfaces. The HO-termini of these films provide sites for covalently grafting biomolecules to the parent surface. As a demonstration, biotin and mannose moieties were covalently attached to the HO-surfaces to provide a means to induce the specific adsorption of proteins. For these surfaces, the presence of oligo(ethylene glycol) groups reduces the nonspecific adsorption of other competing proteins. The results indicate that the developed systems could offer a strategy to arrange biomolecules selectively on glass and metal oxide surfaces.
by Seok-Won Lee.
Ph.D.
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Books on the topic "Self-assembled monolayer"

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Lüssem, Björn. Molecular electronic building blocks based on self-assembled monolayers. Jülich: Forschungszentrum Jülich GmbH, Zentralbibliothek, 2006.

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Han, Bo. Interfacial electrochemistry and in situ SEIRAS investigations of self assembled organic monolayers on Au-electrolyte interfaces. Jülich: Forschungszentrum, Zentralbibliothek, 2006.

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Vuillaume, D. Molecular electronics based on self-assembled monolayers. Edited by A. V. Narlikar and Y. Y. Fu. Oxford University Press, 2017. http://dx.doi.org/10.1093/oxfordhb/9780199533060.013.9.

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This article considers molecular electronics based on self-assembled monolayers. It begins with a brief overview of the nanofabrication of molecular devices, followed by a discussion of the electronic properties of several basic devices, from simple molecules such as molecular tunnel junctions and molecular semiconducting wires, to more complex ones such as molecular rectifying diodes. It also describes molecular switches and memories, focusing on three approaches called ‘conformational memory’, ‘charge-based memory’ and ‘RTD-based memory’ (RTD is resonant tunnelling diode). It shows that memory can be implemented from resonant tunnelling diodes following cell architecture already used for semiconductor devices. The article concludes with a review of molecular transistors.
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Ulman, Abraham. Self-Assembled Monolayers of Thiols (Thin Films). Academic Press, 1998.

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McGuiness, C. L., R. K. Smith, M. E. Anderson, P. S. Weiss, and D. L. Allara. Nanolithography using molecular films and processing. Edited by A. V. Narlikar and Y. Y. Fu. Oxford University Press, 2017. http://dx.doi.org/10.1093/oxfordhb/9780199533060.013.23.

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This article focuses on the use of molecular films as building blocks for nanolithography. More specifically, it reviews efforts aimed at utilizing organic molecular assemblies in overcoming the limitations of lithography, including self-patterning and directed patterning. It considers the methods of patterning self-assembled organic monolayer films through soft-lithographic methods such as microcontact printing and nanoimprint lithography, through direct ‘write’ or ‘machine’ processes with a nanometer-sized tip and through exposure to electron or photon beams. It also discusses efforts to pattern the organic assemblies via the physicochemical self-assembling interactions, including patterning via phase separation of chemically different molecules and insertion of guest adsorbates into host matrices. Furthermore, it examines the efforts that have been made to couple patterned molecular assemblies with inorganic thin-film growth methods to form spatially constrained, three-dimensional thin films. Finally, it describes a hybrid self-assembly/conventional lithography (i.e. molecular rulers) approach to forming nanostructures.
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Galbiati, Marta. Molecular Spintronics: From Organic Semiconductors to Self-Assembled Monolayers. Springer, 2015.

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Galbiati, Marta. Molecular Spintronics: From Organic Semiconductors to Self-Assembled Monolayers. Springer, 2016.

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Galbiati, Marta. Molecular Spintronics: From Organic Semiconductors to Self-Assembled Monolayers. Springer, 2015.

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Yang, Jinlong, and Qunxiang Li. Theoretical simulations of scanning tunnelling microscope images and spectra of nanostructures. Edited by A. V. Narlikar and Y. Y. Fu. Oxford University Press, 2017. http://dx.doi.org/10.1093/oxfordhb/9780199533046.013.15.

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This article presents theoretical simulations of scanning tunnelling microscope (STM) images and spectra of nanostructures. It begins with an overview of the theories of STM and scanning tunnelling spectroscopy (STS), focusing on four main approaches: the perturbation or Bardeen approach, the Tersoff–Hamann approach and its extension, the scattering theory or Landauer–Bütticker approach, and the non-equilibrium Green's function or Keldysh approach. It then considers conventional STM and STS experimental investigations of various systems including clean surfaces, ad-atoms, single molecules, self-assembled monolayers, and nanostructures. It also discusses STM activities that go beyond conventional STM images and STS, such as functionalized STM tip, inelastic spectroscopy identification, manipulation, molecular electronics and molecular machines.
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Narlikar, A. V., and Y. Y. Fu, eds. Oxford Handbook of Nanoscience and Technology. Oxford University Press, 2017. http://dx.doi.org/10.1093/oxfordhb/9780199533060.001.0001.

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This volume highlights engineering and related developments in the field of nanoscience and technology, with a focus on frontal application areas like silicon nanotechnologies, spintronics, quantum dots, carbon nanotubes, and protein-based devices as well as various biomolecular, clinical and medical applications. Topics include: the role of computational sciences in Si nanotechnologies and devices; few-electron quantum-dot spintronics; spintronics with metallic nanowires; Si/SiGe heterostructures in nanoelectronics; nanoionics and its device applications; and molecular electronics based on self-assembled monolayers. The volume also explores the self-assembly strategy of nanomanufacturing of hybrid devices; templated carbon nanotubes and the use of their cavities for nanomaterial synthesis; nanocatalysis; bifunctional nanomaterials for the imaging and treatment of cancer; protein-based nanodevices; bioconjugated quantum dots for tumor molecular imaging and profiling; modulation design of plasmonics for diagnostic and drug screening; theory of hydrogen storage in nanoscale materials; nanolithography using molecular films and processing; and laser applications in nanotechnology. The volume concludes with an analysis of the various risks that arise when using nanomaterials.
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Book chapters on the topic "Self-assembled monolayer"

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Kurihara, Kazue. "Self-Assembled Monolayer." In Encyclopedia of Polymeric Nanomaterials, 1–3. Berlin, Heidelberg: Springer Berlin Heidelberg, 2015. http://dx.doi.org/10.1007/978-3-642-36199-9_157-1.

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Weik, Martin H. "self-assembled monolayer." In Computer Science and Communications Dictionary, 1541. Boston, MA: Springer US, 2000. http://dx.doi.org/10.1007/1-4020-0613-6_16892.

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Kurihara, Kazue. "Self-Assembled Monolayer." In Encyclopedia of Polymeric Nanomaterials, 2187–89. Berlin, Heidelberg: Springer Berlin Heidelberg, 2015. http://dx.doi.org/10.1007/978-3-642-29648-2_157.

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Kondo, Toshihiro, Ryo Yamada, and Kohei Uosaki. "Self-Assembled Monolayer (SAM)." In Organized Organic Ultrathin Films, 7–42. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2012. http://dx.doi.org/10.1002/9783527654666.ch2.

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Moore, Nicole M., and Matthew L. Becker. "Bioactive Self-Assembled Monolayer Gradients." In Soft Matter Gradient Surfaces, 329–63. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2012. http://dx.doi.org/10.1002/9781118166086.ch13.

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Peroulis, Dimitrios, Prashant R. Waghmare, Sushanta K. Mitra, Supone Manakasettharn, J. Ashley Taylor, Tom N. Krupenkin, Wenguang Zhu, et al. "Charge Transfer on Self-Assembled Monolayer Molecules." In Encyclopedia of Nanotechnology, 411. Dordrecht: Springer Netherlands, 2012. http://dx.doi.org/10.1007/978-90-481-9751-4_100126.

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Jung, D. R., A. W. Czanderna, and G. C. Herdt. "Bonding at metal/self-assembled organic monolayer interfaces." In Polymer Surfaces and Interfaces: Characterization, Modification and Application, 189–221. London: CRC Press, 2023. http://dx.doi.org/10.1201/9780429070297-16.

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Colorado, Ramon, Michael Graupe, Hyun I. Kim, Mitsuru Takenaga, Olugbenga Oloba, Seunghwan Lee, Scott S. Perry, and T. Randall Lee. "Interfacial Properties of Specifically Fluorinated Self-Assembled Monolayer Films." In ACS Symposium Series, 58–75. Washington, DC: American Chemical Society, 2000. http://dx.doi.org/10.1021/bk-2001-0781.ch004.

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Virkar, Ajay. "Low-Voltage Monolayer Pentacene Transistors Fabricated on Ultrathin Crystalline Self-Assembled Monolayer Based Dielectric." In Investigating the Nucleation, Growth, and Energy Levels of Organic Semiconductors for High Performance Plastic Electronics, 107–14. New York, NY: Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-9704-3_6.

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Jung, D. R., and A. W. Czanderna. "Interactions and reactions at metal/self-assembled organic monolayer interfaces." In First International Congress on Adhesion Science and Technology---invited papers, 717–46. London: CRC Press, 2023. http://dx.doi.org/10.1201/9780429087486-47.

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Conference papers on the topic "Self-assembled monolayer"

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Lu, Wei. "Self-Assembled Nanostructures." In 2008 Second International Conference on Integration and Commercialization of Micro and Nanosystems. ASMEDC, 2008. http://dx.doi.org/10.1115/micronano2008-70067.

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A binary monolayer on an elastic substrate may self-organize into ordered nanoscale phase patterns. Here we report a work of using a substrate strain field to guide the self-assembly process. The study shows that straining a substrate uniformly does not influence the pattern. However, a non-uniform strain field significantly influences the size, shape and distribution of self-assembled features. The study suggests a method of strain field design to make various monolayer patterns.
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Bonner, Richard W. "Dropwise Condensation Life Testing of Self Assembled Monolayers." In 2010 14th International Heat Transfer Conference. ASMEDC, 2010. http://dx.doi.org/10.1115/ihtc14-22936.

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The increasing thermal demand of electronics devices has pushed the limits of current two-phase thermal technologies such as heat pipes and vapor chambers. The most obvious area for thermal improvement is centered around the high heat flux generating chips including improved evaporators, thermal interfaces, etc. However, heat fluxes in the sink/condensing regions have also risen as the size of electronics packages has decreased. One way to reduce the thermal resistance associated with condensation is to promote dropwise condensation. In previous work, the condensation performance improvement using self-assembled monolayer coated surfaces (to promote hydrophobicity) has been shown. However, the question of the life of the self-assembled monolayer coatings needs to be addressed before the technology is adopted, as this has plagued other dropwise condensation coatings in the past. Presented here is a general use of self-assembled monolayer coatings to promote dropwise condensation in electronics device applications, including a summary of recent work regarding dropwise condensation on gradient surfaces. Also presented is experimental data from a life test of self-assembled monolayers on copper and gold plated surfaces. In the life test, the surfaces have been continuously exposed to saturated steam at 60°C. Both surfaces have continued to promote dropwise condensation for over 9 months under conditions representative of heat pipe electronics cooling applications.
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Liu, Yanjing, Anbo Wang, and Richard O. Claus. "Ionic self-assembled monolayer multilayer thin films." In Smart Structures and Materials '97, edited by Richard O. Claus. SPIE, 1997. http://dx.doi.org/10.1117/12.275759.

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Timpe, Shannon J. "Mechanical and Environmental Degradation of Self-Assembled Monolayer Coatings for Microelectromechanical Systems." In ASME/STLE 2007 International Joint Tribology Conference. ASMEDC, 2007. http://dx.doi.org/10.1115/ijtc2007-44292.

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Self-assembled monolayer coatings have shown great promise for dramatically reducing the tribological forces of adhesion and friction in microelectro-mechanical systems (MEMS). However, monolayer coatings often display significant degradation when exposed to extreme environments, dynamic sliding contact, and dynamic impact loading. This degradation is coupled with a corresponding increase in the tribological properties. In this study, the degradation of tridecafluorotri(dimethylamino)silane is examined under the typical operating conditions of MEMS technology using a specialized microdevice designed for characterizing the tribological behavior surface micromachines. Results of friction and adhesion degradation under normal loading and sliding contact are interpreted in relation to the primary degradation mechanisms of self-assembled monolayers.
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Masuko, Masabumi, Hiroya Miyamoto, and Akihito Suzuki. "Shear Strength and Durability of Self Assembled Monolayer." In ASME/STLE 2007 International Joint Tribology Conference. ASMEDC, 2007. http://dx.doi.org/10.1115/ijtc2007-44221.

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A well-defined self-assembled monolayer (SAM) of octadecyltrichlorosilane (OTS) on a very smooth Si wafer or glass disk was prepared and the tribological performance was studied using a glass ball and a steel ball as a counter specimen. Shear strength and durability of OTS-SAM were discussed considering a difference of the surface roughness of specimen couples.
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Naik, Tejas, and V. Ramgopal Rao. "Self assembled monolayer applications for nano-scale CMOS." In 2016 IEEE International Nanoelectronics Conference (INEC). IEEE, 2016. http://dx.doi.org/10.1109/inec.2016.7589436.

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Ringk, Andreas, Xiaoran Li, Fatemeh Gholamrezaie, Edsger C. P. Smits, Alfred Neuhold, Armin Moser, Gerwin H. Gelinck, Roland Resel, Dago M. de Leeuw, and Peter Strohriegl. "N-type self-assembled monolayer field-effect transistors." In SPIE Organic Photonics + Electronics, edited by Zhenan Bao and Iain McCulloch. SPIE, 2012. http://dx.doi.org/10.1117/12.929535.

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Casson, Joanna L., Wenxi Huang, Yongwoo Lee, Jean-Francois Bardeau, Malkiat S. Johal, Wang Rong, Alexander D. Li, et al. "NLO studies of a novel phenothiazine self-assembled monolayer." In SPIE's International Symposium on Optical Science, Engineering, and Instrumentation, edited by Manfred Eich and Mark G. Kuzyk. SPIE, 1999. http://dx.doi.org/10.1117/12.368280.

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Shuvalov, Ivan, Rhys Lawson, Hong Ma, Alex K. Jen, and Larry R. Dalton. "Self-assembled monolayer modifications of organic thin film transistors." In Optics East, edited by Warren Y. Lai, Stanley Pau, and O. Daniel Lopez. SPIE, 2005. http://dx.doi.org/10.1117/12.569304.

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Kawaguchi, Tatsuhiko, Takehiro Okura, Yuusuke Suenaga, Tomonori Hanasaki, and Ichiro Fujieda. "A photo-aligned self-assembled monolayer for polymer transistors." In SPIE OPTO, edited by Christopher Tabor, François Kajzar, Toshikuni Kaino, and Yasuhiro Koike. SPIE, 2012. http://dx.doi.org/10.1117/12.906559.

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Reports on the topic "Self-assembled monolayer"

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Miller, Michael B. Ionic Self-Assembled Monolayer (ISAM) Nonlinear Optical Thin Films and Devices. Fort Belvoir, VA: Defense Technical Information Center, May 1998. http://dx.doi.org/10.21236/ada345555.

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Pope, John, and Daniel A. Buttry. Measurement of Through-Space Dipole-Dipole Coupling from Shifts in Vibrational Frequencies for a Stilbazolium Derivative Embedded in a Self-Assembled Monolayer. Fort Belvoir, VA: Defense Technical Information Center, July 1995. http://dx.doi.org/10.21236/ada301450.

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Zawodzinski, T., G. Bar, S. Rubin, F. Uribe, and J. Ferrais. Multifunctional self-assembled monolayers. Office of Scientific and Technical Information (OSTI), June 1996. http://dx.doi.org/10.2172/254339.

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Srinivasan, U., J. D. Foster, U. Habib, R. T. Howe, R. Maboudian, D. C. Senft, and M. T. Dugger. Lubrication of polysilicon micromechanisms with self-assembled monolayers. Office of Scientific and Technical Information (OSTI), June 1998. http://dx.doi.org/10.2172/671989.

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Wang, Wenyong, Takhee Lee, and Mark A. Reed. Intrinsic Electronic Conduction Mechanisms in Self-Assembled Monolayers. Fort Belvoir, VA: Defense Technical Information Center, January 2005. http://dx.doi.org/10.21236/ada465940.

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Teeters, Dale. Self-Assembled Monolayers at the Lithium Electrode/Polymer Electrolyte Interface. Fort Belvoir, VA: Defense Technical Information Center, June 2002. http://dx.doi.org/10.21236/ada404757.

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DeLong, Hugh C., John J. Donohue, and Daniel A. Buttry. Ionic Interactions in Electroactive Self-Assembled Monolayers of Ferrocene Species. Fort Belvoir, VA: Defense Technical Information Center, April 1991. http://dx.doi.org/10.21236/ada235677.

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Sukenik, Chaim N. Fabrication of Functional Ceramic Composites - Zinc Oxide of Organic Self-Assembled Monolayers. Fort Belvoir, VA: Defense Technical Information Center, October 1997. http://dx.doi.org/10.21236/ada336808.

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Majewski, Peter. Reactions Between Contaminants and Functionalized Organic Self-Assembled Monolayers in Aqueous Solutions. Fort Belvoir, VA: Defense Technical Information Center, May 2006. http://dx.doi.org/10.21236/ada473074.

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Liu, J., G. E. Fryxell, S. V. Mattigod, M. Gong, Z. Nie, X. Feng, and K. N. Raymond. Self-assembled monolayers on mesoporous support (SAMMS) technology for contaminant removal and stabilization. Office of Scientific and Technical Information (OSTI), September 1998. http://dx.doi.org/10.2172/663548.

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