Bibliographies thématiques / Electrostatic Assembly

Littérature scientifique sur le sujet « Electrostatic Assembly »

Auteur : Grafiati
Publié le 7 septembre 2023

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Articles de revues sur le sujet "Electrostatic Assembly"

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Martin, Lisal, Sindelka Karel, Sueha Lucie, Limpouchova Zuzana et Prochazka Karel. « Dissipative Particle Dynamics Simulations of Polyelectrolyte Self-Assemblies. Methods with Explicit Electrostatics1, "Высокомолекулярные соединения. Серия С" ». Высокомолекулярные соединения С, no 1 (2017) : 82–107. http://dx.doi.org/10.7868/s2308114717010101.

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Abstract - This feature article is addressed to a broad community of polymer scientists, both theoreticians and experimentalists. We present several examples of our dissipative particle dynamics (DPD) simulations of self- and co-assembling polyelectrolyte systems to illustrate the power of DPD. In the first part, we briefly outline basic principles of DPD. Special emphasis is placed on the incorporation of explicit electrostatic forces into DPD, on their calibration with respect to the soft repulsion forces and on the use of DPD for studying the self-assembly of electrically charged polymer systems. At present, the method with explicit electrostatics is being used in a number of studies of the behavior of single polyelectrolyte chains, their interaction with other components of the system, etc. However, in DPD studies of self-assembly, which require high numbers of chains, only a few research groups use explicit electrostatics. Most studies of polyelectrolyte self-assembly are based on the “implicit solvent ionic strength” approach, which completely ignores the long-range character of electrostatic interactions, because their evaluation complicates and considerably slows down the DPD simulation runs. We aim at the analysis of the impact of explicit electrostatics on simulation results.
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Xian, Yuejiao, Chitra B. Karki, Sebastian Miki Silva, Lin Li et Chuan Xiao. « The Roles of Electrostatic Interactions in Capsid Assembly Mechanisms of Giant Viruses ». International Journal of Molecular Sciences 20, no 8 (16 avril 2019) : 1876. http://dx.doi.org/10.3390/ijms20081876.

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In the last three decades, many giant DNA viruses have been discovered. Giant viruses present a unique and essential research frontier for studies of self-assembly and regulation of supramolecular assemblies. The question on how these giant DNA viruses assemble thousands of proteins so accurately to form their protein shells, the capsids, remains largely unanswered. Revealing the mechanisms of giant virus assembly will help to discover the mysteries of many self-assembly biology problems. Paramecium bursaria Chlorella virus-1 (PBCV-1) is one of the most intensively studied giant viruses. Here, we implemented a multi-scale approach to investigate the interactions among PBCV-1 capsid building units called capsomers. Three binding modes with different strengths are found between capsomers around the relatively flat area of the virion surface at the icosahedral 2-fold axis. Furthermore, a capsomer structure manipulation package is developed to simulate the capsid assembly process. Using these tools, binding forces among capsomers were investigated and binding funnels were observed that were consistent with the final assembled capsid. In addition, total binding free energies of each binding mode were calculated. The results helped to explain previous experimental observations. Results and tools generated in this work established an initial computational approach to answer current unresolved questions regarding giant virus assembly mechanisms. Results will pave the way for studying more complicated process in other biomolecular structures.
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Zhang, Peng, Fenghuan Wang, Yuxuan Wang, Shuangyang Li et Sai Wen. « Self-Assembling Behavior of pH-Responsive Peptide A6K without End-Capping ». Molecules 25, no 9 (26 avril 2020) : 2017. http://dx.doi.org/10.3390/molecules25092017.

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A short self-assembly peptide A6K (H2N−AAAAAAK−OH) with unmodified N− and C−terminus was designed, and the charge distribution model of this short peptide at different pH was established by computer simulation. The pH of the solution was adjusted according to the model and the corresponding self-assembled structure was observed using a transmission electron microscope (TEM). As the pH changes, the peptide will assemble into blocks or nanoribbons, which indicates that the A6K peptide is a pH-responsive peptide. Circular dichroism (CD) and molecular dynamics (MD) simulation showed that the block structure was formed by random coils, while the increase in β-turn content contributes to the formation of intact nanoribbons. A reasonable explanation of the self-assembling structure was made according to the electrostatic distribution model and the effect of electrostatic interaction on self-assembly was investigated. This study laid the foundation for further design of nanomaterials based on pH-responsive peptides.
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Tien, Joe, Andreas Terfort et George M. Whitesides. « Microfabrication through Electrostatic Self-Assembly ». Langmuir 13, no 20 (octobre 1997) : 5349–55. http://dx.doi.org/10.1021/la970454i.

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Ma, Yujie, Mark A. Hempenius et G. Julius Vancso. « Electrostatic Assembly with Poly(ferrocenylsilanes) ». Journal of Inorganic and Organometallic Polymers and Materials 17, no 1 (16 février 2007) : 3–18. http://dx.doi.org/10.1007/s10904-006-9081-4.

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Kutz, A., G. Mariani, R. Schweins, C. Streb et F. Gröhn. « Self-assembled polyoxometalate–dendrimer structures for selective photocatalysis ». Nanoscale 10, no 3 (2018) : 914–20. http://dx.doi.org/10.1039/c7nr07097g.

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Han, Songling, Huijie An, Hui Tao, Lanlan Li, Yuantong Qi, Yongchang Ma, Xiaohui Li, Ruibing Wang et Jianxiang Zhang. « Advanced emulsions via noncovalent interaction-mediated interfacial self-assembly ». Chemical Communications 54, no 25 (2018) : 3174–77. http://dx.doi.org/10.1039/c8cc00016f.

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The traditional emulsification theory is enriched by a self-assembly approach, in which hydrophilic copolymers with one block exhibiting electrostatic or hydrogen-bonding forces with the oil phase self-assemble at the oil–water interface, thereby reducing interfacial tension and forming emulsions.
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Konopelnyk, O. I. « Electrostatic layer-by-layer assembly of poly-3,4-ethylene dioxythiophene functional nanofilms ». Functional materials 20, no 2 (25 juin 2013) : 248–52. http://dx.doi.org/10.15407/fm20.02.248.

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Svensson, Fredric G., Gulaim A. Seisenbaeva, Nicholas A. Kotov et Vadim G. Kessler. « Self-Assembly of Asymmetrically Functionalized Titania Nanoparticles into Nanoshells ». Materials 13, no 21 (29 octobre 2020) : 4856. http://dx.doi.org/10.3390/ma13214856.

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Titania (anatase) nanoparticles were anisotropically functionalized in water-toluene Pickering emulsions to self-assemble into nanoshells with diameters from 500 nm to 3 μm as candidates for encapsulation of drugs and other compounds. The water-phase contained a hydrophilic ligand, glucose-6-phosphate, while the toluene-phase contained a hydrophobic ligand, n-dodecylphosphonic acid. The addition of a dilute sodium alginate suspension that provided electrostatic charge was essential for the self-limited assembly of the nanoshells. The self-assembled spheres were characterized by scanning electron microscopy, elemental mapping, and atomic force microscopy. Drug release studies using tetracycline suggest a rapid release dominated by surface desorption.
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Oertel, Catherine. « Photodetectors Fabricated Using Electrostatic Self-Assembly ». MRS Bulletin 29, no 3 (mars 2004) : 136–37. http://dx.doi.org/10.1557/mrs2004.43.

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Thèses sur le sujet "Electrostatic Assembly"

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Du, Weiwei. « Electrostatic Self-Assembly of Biocompatible Thin Films ». Thesis, Virginia Tech, 1999. http://hdl.handle.net/10919/10106.

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The design of biocompatible synthetic surfaces is an important issue for medical applications. Surface modification techniques provide good approaches to control the interactions between living systems and implanted materials by modifying the surface characteristics. This thesis work demonstrates the feasibility and effectiveness of the novel and low-cost electrostatic self-assembly (ESA) technique for the manufacturing of biocompatible thin film coatings. The ESA process is based on the alternating adsorption of molecular layers of oppositely charged polymers/nanoparticles, and can be applied in the fabrication of well-organized multilayer thin films possessing various biocompatible properties. ESA multilayer assemblies incorporating various biomaterials including metal oxides and polymers were fabricated, the uniformity, thickness, layer-by-layer linearity, and surface morphology of the films were characterized by UV/vis spectroscopy, ellipsometry, and AFM imaging. Preliminary biocompatibility testing was conducted, concentrating on contact angle surface characterization and the in vitro measurements of protein adsorption. The use of Fourier Transform Infrared Reflection-Absorption Spectroscopy (FT-IRAS) for the investigation of the protein adsorption behavior upon the ESA multilayer films is presented.
Master of Science
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Cant, Nicola Elizabeth. « Electrostatic self assembly of multilayer films incorporating metallic nanoparticles ». Thesis, University of Leeds, 2003. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.275671.

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Luo, Zhaoju. « Linear Optical Thin Films Formed by Electrostatic Self-Assembly ». Thesis, Virginia Tech, 2000. http://hdl.handle.net/10919/10168.

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The Electrostatic Self-Assembly (ESA) technique possesses great advantages over traditional thin film fabrication methods, making it an excellent choice for a number of applications in the fields of linear and nonlinear optics, electronics, sensing and surface coatings. The feasibility of fabricating linear optical interference filters by ESA methods is demonstrated in this thesis work. Basic single-anion/single-cation ESA films are synthesized and their optical parameters -- refractive index and average thickness for individual bilayer -- are investigated to provide a basis for the in-depth design of optical filters. High performance dielectric stack filters and narrowband and wideband antireflection coatings are designed using TFCalc simulation software and are fabricated by ESA. Both bulk film sensitivity and layer sensitivity to manufacturing errors are provided. The significant agreement between simulation and experiment demonstrates the strong capability of ESA to precisely control the refractive index and produce excellent thin film filters. The performance of optical thin film filters is largely enhanced compared to the results of previous methods. The experiment results indicate that the ESA process may be used to fabricate optical filters and other optical structures that require precise index profile control.
Master of Science
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Dhru, Shailini Rajiv. « Process Development For The Fabrication Of Mesoscale Electrostatic Valve Assembly ». Master's thesis, University of Central Florida, 2007. http://digital.library.ucf.edu/cdm/ref/collection/ETD/id/4244.

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This study concentrates on two of the main processes involved in the fabrication of electrostatic valve assembly, thick resist photolithography and wet chemical etching of a polyamide film. The electrostatic valve has different orifice diameters of 25, 50, 75 and 100 μm. These orifice holes are to be etched in the silicon wafer with deep reactive ion etching. The photolithography process is developed to build a mask of 15 μm thick resist pattern on silicon wafer. This photo layer acts as a mask for deep reactive ion etching. Wet chemical etching process is developed to etch kapton polyamide film. This etched film is used as a stand off, gap between two electrodes of the electrostatic valve assembly. The criterion is to develop the processed using standard industry tools. Pre post etch effects, such as, surface roughness, etching pattern, critical dimensions on the samples are measured with Veeco profilometer.
M.S.
Other
Engineering and Computer Science
Electrical Engineering MSEE
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Maskaly, Garry R. (Garry Russell) 1978. « Attractive electrostatic self-assembly of ordered and disordered heterogeneous colloids ». Thesis, Massachusetts Institute of Technology, 2005. http://hdl.handle.net/1721.1/16704.

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Thesis (Ph. D.)--Massachusetts Institute of Technology, Dept. of Materials Science and Engineering, 2005.
Includes bibliographical references (p. 187-193).
This electronic version was submitted by the student author. The certified thesis is available in the Institute Archives and Special Collections.
Ionic colloidal crystals are here defined as multicomponent ordered colloidal structures stabilized by attractive electrostatic interactions. These crystals are colloidal analogues to ionic materials including zincblende, rocksalt, cesium chloride, and fluorite. A thermodynamic study revealed that the screening ratio, charge ratio, and monodispersity are critical parameters in ionic colloidal crystal (ICC) formation. Experimentally, small ordered regions were observed under ideal thermodynamic conditions. However, no larger crystalline regions were found in these samples. The kinetics of ICC formation was studied using a variety of computational techniques, including Brownian dynamics, Monte Carlo, and a Newton's method solver. These techniques have each elucidated properties and processing conditions that are important to crystallization. The Brownian dynamics and Monte Carlo simulations showed that the previous experiments were highly undercooled. Furthermore, a narrow crystallization window was found, demonstrating the need to create particle systems that meet the narrow parameter space where ICCs should be stable. Pair interaction potentials were evaluated for their accuracy using a Poisson-Boltzmann (PB) equation solver. The PB solver was also used to further refine crystalline formation energies so that systems can be more accurately tailored. A surprising result from the PB solver showed that the lowest formation energy occurs when the quantity of surface charges on both particles are equal. Although this result is not predicted by any colloidal pair potentials, it was verified experimentally. This further illustrates that thermal mobility in these systems can be sufficient to maintain a stable solution despite attractive electrostatic interactions. Tailoring particle systems to balance the thermal and electrostatic interactions should allow widespread crystallization. However, these conditions require highly monodisperse particles to be fabricated with controlled surface charge and sizes. Currently these particles are not widely available and further research in this area should aid in the full realization of the ICC concept. In conclusion, all results are integrated to predict which particle systems should be produced to allow the formation of large ordered structures.
by Garry R. Maskaly.
Ph.D.
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Della, Pia Ada. « Using electrostatic interactions to control supramolecular self-assembly at surfaces ». Thesis, University of Warwick, 2014. http://wrap.warwick.ac.uk/60286/.

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This thesis is focused on the links between charge transfer (CT) at metalorganic (MO) interfaces, creation of surface dipoles and two-dimensional supra- molecular assembly. Although several examples can be found in the literature where molecular self-assembly on surfaces was in uenced by the formation of interfacial dipoles, only in a few cases were the results fully rationalised and only a posteriori. The MO interface resulting from the deposition of the molecules used for these studies (chosen for their relevance as building blocks for applications in organic opto-electronic, photovoltaic, or proposed organic spintronics devices) is usually very complex. This is mainly due to the chemical structure of these molecules and to their strong interaction with the substrate. A clear identification of the different fundamental processes (such as CT and formation of interfacial dipoles) is thus highly difficult. The approach followed in this thesis is markedly different: specific molecules were rationally designed and subsequently synthesised in order to obtain model systems where the different parameters could be clearly isolated and identified. The presented work is the result of a close collaboration with other two research groups: the organic synthetic chemistry group of Prof. D. Bonifazi and the theoretical group of Prof. A. De Vita. The study was addressed through a complementary multi-disciplinary theoretical and experimental investigation, including the synthesis of new molecules, the analysis of their self-assembly by scanning tunnelling microscopy and spectroscopy and the use of density functional theory calculations and Monte Carlo simulations for the theoretical modelling of the systems. A balance between omnipresent short-range van der Waals attractive forces and long-range repulsive interactions generated by CT at MO interfaces was found to be responsible for the spontaneous formation of novel classes of supramolecular structures. By selecting different metal substrates and by carefully modifying the molecular species through chemical synthesis, the CT was selectively inhibited or enabled. This strategy represents a new paradigm for predicting and controlling the molecular self-assembly at surfaces. Conversely, the appearance of specific molecular linkage patterns is used to reveal the occurrence of CT and provides a novel means for obtaining crucial information on the electronic properties and the energy level alignment of MO interfaces.
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Porter, Benjamin Francis. « Rapid, electrostatic self-assembly of nanoparticles with Kelvin probe characterisation ». Thesis, University of Oxford, 2015. https://ora.ox.ac.uk/objects/uuid:4bed29e9-3c30-4891-af1b-addc5fd97ac6.

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The pick-and-place of components to build up complex working machines, such as the robotic arms on automotive assembly lines, has been integral to the enormous success and complexity of modern heavy industry. Modern nanomanufacturing stands in stark contrast to this strategy, reliant instead on the two-dimensional patterning of radiation-sensitive resists to build high-density machines of relative simplicity. The driving goal of our research has thus been to develop a new method of manipulation that would allow the pick-and-place of nanoscale components to mirror that of the assembly lines. A manipulator that could reliably perform this process would open the door to a new age of complex nanomachines. After analysing the current state-of-the-art in nano-object manipulation, we decided to utilise a combination of voltage-driven electric fields with chemically functional monolayers to achieve this goal. The mechanism was intended to be highly compatible with a Scanning Probe Microscope-style tip that could act as the manipulator tool on such an assembly line. This led to the design of several devices that were intended to capture single nanoparticles from a colloidal suspension, which had a negative surface charge in solution. We used numerical simulations using the Guoy-Chapman model of ionic solutions to determine what electrical and geometrical parameters would create the best devices single particle selectivity. We then describe the fabrication of devices using nanolithography techniques including electron-beam lithography, thin-film deposition and etching. Scanning electron microscopy of these devices after voltage-driven assembly showed that the mechanism had very limited success with few incidences of nanoparticle funnelling. This led through several different troubleshooting analyses of the mechanism that identified a myriad of issues affecting these devices. Ultimately we successfully created a radical new approach that incorporated hydrophobic monolayers with polar surfaces. This method exploited the hydrophobic interaction to overcome the hydrostatic barrier and resulted in repeatable single-particle assembly onto devices in sub 5-minute timeframes. Another aspect identified in this work was that the electronic state of nano-objects and monolayers on device surfaces is very important, but is difficult to pinpoint even when data sheets are available. We developed an emerging method of open-loop Dual-Harmonic Kelvin Probe Microscopy to identify these materials by their electronic surface potentials, successfully performing measurements in electrolytes where nanomanipulation would take place. This line of research led to novel considerations of how the size of the nanoparticles fundamentally distorts KPM measurements. We identify this as an important and often ignored effect that must be considered when using probes to differentiate between different materials at the nanoscale.
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Cheung, Yeuk Kit. « Hemocompatible polymer thin films fabricated by Electrostatic Self-Assembly (ESA) ». Thesis, Virginia Tech, 2004. http://hdl.handle.net/10919/31357.

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Stent is one of the coronary angioplasty techniques that expands the narrowed coronary arteries due to the accumulation of fat, cholesterol and other substances in the lumen of the arteries. The major complication of stent is restenosis. Current development of drug-eluting stents shows successfully reduce the occurrence of restenosis. Other than using drugs, electrostatic self assembled (ESAd) thin films may be the potential candidates to prevent restenosis.

ESA is a process to fabricate thin films bases on the electrostatic attraction between two oppositely charges. We used this technique to fabricate four PVP films and four PEI films. All films were exanimated by XPS and AFM. XPS data showed our coatings were successfully fabricated on substrates. AFM images revealed PVP coating was uniform, but PEI coatings had different morphologies due to diffusion and pH during the process.

Three preliminary hemocompatibility testes were performed to evaluate the hemocompatibility of the coatings. Platelet adhesion study showed the thin films inhibited platelet adhesion. All thin films were able to inhibit coagulation and were less cytotoxic. The studies suggested the ESA films were potentially hemocompatible.
Master of Science

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Cooper, Kristie Lenahan. « Electrostatic Self-Assembly of Linear and Nonlinear Optical Thin Films ». Diss., Virginia Tech, 1999. http://hdl.handle.net/10919/27141.

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This dissertation demonstrates the feasibility of using novel electrostatic self-assembly (ESA) methods to fabricate linear and nonlinear optical thin films and components. The ESA process involves the layer-by-layer alternate adsorption of anionic and cationic complexes from aqueous solutions. Selection of the molecules in each layer, their orientation at the molecular level, and the order in which the layers are assembled determine the film's bulk optical, electronic, magnetic, thermal, mechanical and other properties. In this work, the capability of nanoscale control over film optical properties allowed the fabrication of complicated refractive index profiles required for linear optical interference filters. The inherent ordered nature of ESA films yielded extremely stable noncentrosymmetric thin films for second-order nonlinear optical applications. The ESA technique offers numerous advantages over conventional thin film fabrication methods and offers great potential in commercial applications such as reflectance and AR filters, EO waveguides and modulators and other optoelectronic devices. The structure of each monolayer in ESA films is dependent on the processing parameters, producing subsequent variations in bulk film properties both intentionally and incidentally. As this method is still in its infancy, variations in ESA processing methods, including process automation, are considered first in this document. These results allowed carefully controlled refractive index experiments and the synthesis of both step and graded index structures, several microns thick. Dielectric stack, Rugate, and antireflection optical interference filters were designed, synthesized and demonstrated. c(2) films of both commercially available polymer dyes and novel polymers designed specifically for the ESA process were demonstrated using second harmonic generation. UV/vis spectroscopy, ellipsometry and atomic force microscopy analysis are presented.
Ph. D.
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Riello, Massimo. « Using electrostatic interactions to control supramolecular self-assembly on metallic surfaces ». Thesis, King's College London (University of London), 2014. https://kclpure.kcl.ac.uk/portal/en/theses/using-electrostatic-interactions-to-control-supramolecular-selfassembly-on-metallic-surfaces(21253b66-5b2c-4aa9-8bf2-36025282a95e).html.

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Supramolecular self-assembly on metallic surfaces is the ideal playground for studying a variety of physical and chemical phenomena. Adsorbed molecules will diffuse and self-organise to form assemblies dictated by their functionalities, while the more or less pronounced metal reactivity will accordingly affect both the supramolecular patterns and the interfacial chemistry. Besides structural aspects, electronic properties are central in determining the energy level alignment at the heterojunction and, thus, the performance of organic-based devices. Notably, charge reorganisation at the metal-organic interface will produce surface dipoles, whose effect is to add electrostatic repulsion to the dispersion-driven supramolecular self-assembly and to change the work function of the surface. Herein, the relation between charge migration (i.e., the creation of surface dipoles) and molecular self-assembly is addressed by studying the behaviour of on-purpose designed molecular units on selected metals. We will show that choosing the substrate on the basis of its work function can selectively allow or inhibit the transfer of charge from the organic material to the electrode. When charge transfer occurs, the growing supramolecular structures exhibit a phase modulation driven by the presence of competing interactions. Moreover, the introduction of reactive moieties in formerly inert tectons will be identified as a suitable strategy for promoting the formation of interfacial dipoles upon surface-mediated chemical reactions. Our work paves the way for a more rational approach to the design of metal-organic systems, as we speculate that charge transfer effects and surface chemistry can be predicted at the stage of molecular design, at variance with the current trial and error approach used in the field of organic electronics. This thesis is based on multiscale theoretical modelling of selected metalmolecule couples and it is the result of a fruitful collaboration with the groups of Prof Davide Bonifazi (Université de Namur) and Prof Giovanni Costantini (University of Warwick).
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Chapitres de livres sur le sujet "Electrostatic Assembly"

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Sastry, Murali. « Electrostatic assembly of nanoparticles ». Dans Nanostructure Science and Technology, 225–50. Boston, MA : Springer US, 2004. http://dx.doi.org/10.1007/978-1-4419-9042-6_9.

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Kricheldorf, Hans. « Polycondensation Via Electrostatic Self-Assembly ». Dans Polycondensation, 203–19. Berlin, Heidelberg : Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-39429-4_13.

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Concellón, Alberto, et Verónica Iguarbe. « Ionic Self-Assembly of Dendrimers ». Dans Supramolecular Assemblies Based on Electrostatic Interactions, 85–118. Cham : Springer International Publishing, 2022. http://dx.doi.org/10.1007/978-3-031-00657-9_4.

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Chakraborti, Soumyananda, Antti Korpi, Jonathan G. Heddle et Mauri A. Kostiainen. « Electrostatic Self-Assembly of Protein Cage Arrays ». Dans Methods in Molecular Biology, 123–33. New York, NY : Springer US, 2020. http://dx.doi.org/10.1007/978-1-0716-0928-6_8.

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Drew, Christopher, Xianyan Wang, Lynne A. Samuelson et Jayant Kumar. « Electrostatic Assembly of Polyelectrolytes on Electrospun Fibers ». Dans ACS Symposium Series, 137–48. Washington, DC : American Chemical Society, 2006. http://dx.doi.org/10.1021/bk-2006-0918.ch010.

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Marullo, Salvatore, Carla Rizzo et Francesca D’Anna. « Organic Salts as Tectons for Self-assembly Processes in Solution ». Dans Supramolecular Assemblies Based on Electrostatic Interactions, 309–39. Cham : Springer International Publishing, 2022. http://dx.doi.org/10.1007/978-3-031-00657-9_10.

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Zika, Alexander, Anja Krieger et Franziska Gröhn. « Nano-Objects by Spontaneous Electrostatic Self-Assembly in Aqueous Solution ». Dans Supramolecular Assemblies Based on Electrostatic Interactions, 119–67. Cham : Springer International Publishing, 2022. http://dx.doi.org/10.1007/978-3-031-00657-9_5.

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Yang, Yuqing, Ehsan Raee, Yifan Zhou et Tianbo Liu. « The Role of Electrostatic Interaction in the Self-assembly of Macroions ». Dans Supramolecular Assemblies Based on Electrostatic Interactions, 55–84. Cham : Springer International Publishing, 2022. http://dx.doi.org/10.1007/978-3-031-00657-9_3.

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Guzmán, Eduardo, Ana Mateos-Maroto, Francisco Ortega et Ramón G. Rubio. « Electrostatic Layer-by-Layer Self-Assembly Method : A Physico-Chemical Perspective ». Dans Supramolecular Assemblies Based on Electrostatic Interactions, 169–202. Cham : Springer International Publishing, 2022. http://dx.doi.org/10.1007/978-3-031-00657-9_6.

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Stucki, Martin, Christoph Schumann et Annika Raatz. « Alignment Process for Glass Substrates Using Electrostatic Self-Assembly ». Dans Lecture Notes in Production Engineering, 448–56. Cham : Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-78424-9_50.

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Actes de conférences sur le sujet "Electrostatic Assembly"

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Faleg, Francesco, Pietro Zanella, Stefano Riva, Paolo Fidanzati, Virginie Inguimbert et Gael Murat. « Electrostatic Discharge Tests for JUICE Photovoltaic Assembly ». Dans 2019 European Space Power Conference (ESPC). IEEE, 2019. http://dx.doi.org/10.1109/espc.2019.8931986.

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Mecham, Jeffrey B., Kristi L. Cooper, Keith Huie et Richard O. Claus. « Electrostatic self-assembly processing of functional nanocomposites ». Dans International Symposium on Optical Science and Technology, sous la direction de Emile J. Knystautas, Wiley P. Kirk et Valerie Browning. SPIE, 2001. http://dx.doi.org/10.1117/12.452554.

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Ardanuc, Serhan, Amit Lal et David Reyes. « Process-Independent, Ultrasound-Enhanced, Electrostatic Batch Assembly ». Dans TRANSDUCERS 2007 - 2007 International Solid-State Sensors, Actuators and Microsystems Conference. IEEE, 2007. http://dx.doi.org/10.1109/sensor.2007.4300154.

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Lakhina, G. S., S. V. Singh, A. P. Kakad et J. S. Pickett. « Soliton model for broadband electrostatic noise ». Dans 2011 XXXth URSI General Assembly and Scientific Symposium. IEEE, 2011. http://dx.doi.org/10.1109/ursigass.2011.6051054.

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Wellander, Niklas. « Homogenization of a nonlocal electrostatic equation ». Dans 2011 XXXth URSI General Assembly and Scientific Symposium. IEEE, 2011. http://dx.doi.org/10.1109/ursigass.2011.6050346.

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Zhou, Wenzhan. « Effect of electrostatic field on photoresist coating uniformity ». Dans International Symposium on Microelectronics and Assembly, sous la direction de Chris A. Mack et XiaoCong Yuan. SPIE, 2000. http://dx.doi.org/10.1117/12.404845.

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Claus, Richard O., Yanjing Liu et Kristi L. Cooper. « Electrostatic self-assembly processing of materials and devices ». Dans International Symposium on Optical Science and Technology, sous la direction de Edward W. Taylor. SPIE, 2000. http://dx.doi.org/10.1117/12.405330.

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Lenahan, Kristie M., Yanjing Liu et Richard O. Claus. « Electrostatic self-assembly processes for multilayer optical filters ». Dans 1999 Symposium on Smart Structures and Materials, sous la direction de Manfred R. Wuttig. SPIE, 1999. http://dx.doi.org/10.1117/12.352815.

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Brown, J. Quincy, Kyle B. Guice, Ryan T. Simpson et Michael J. McShane. « Electrostatic self-assembly of nanocomposite hybrid fluorescent sensors ». Dans Biomedical Optics 2004, sous la direction de Alexander N. Cartwright. SPIE, 2004. http://dx.doi.org/10.1117/12.529793.

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Clausen, C. H., J. Jensen, J. Castillo et W. E. Svendsen. « Electrostatic force microscopy of biological self assembly structures ». Dans Scanning Microscopy 2009. SPIE, 2009. http://dx.doi.org/10.1117/12.821790.

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