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Статті в журналах з теми "Graphene liquid interface"
Chen, Xianjue, and Colin L. Raston. "Liquid interface evolution of polyhedral-like graphene." Chemical Communications 51, no. 78 (2015): 14609–12. http://dx.doi.org/10.1039/c5cc05888k.
Повний текст джерелаPeng, Xiaoyi, Pengfei Jiang, Yulou Ouyang, Shuang Lu, Weijun Ren, and Jie Chen. "Reducing Kapitza resistance between graphene/water interface via interfacial superlattice structure." Nanotechnology 33, no. 3 (October 29, 2021): 035707. http://dx.doi.org/10.1088/1361-6528/ac2f5c.
Повний текст джерелаKam, Kevin, Brianne Tengan, Cody Hayashi, Richard Ordonez, and David Garmire. "Polar Organic Gate Dielectrics for Graphene Field-Effect Transistor-Based Sensor Technology." Sensors 18, no. 9 (August 23, 2018): 2774. http://dx.doi.org/10.3390/s18092774.
Повний текст джерелаShao, Jiao-Jing, Si-Da Wu, Shao-Bo Zhang, Wei Lv, Fang-Yuan Su, and Quan-Hong Yang. "Graphene oxide hydrogel at solid/liquid interface." Chemical Communications 47, no. 20 (2011): 5771. http://dx.doi.org/10.1039/c1cc11166c.
Повний текст джерелаXin, Jing, Beibei Xie, Ya Li, Juanjuan Shang, Yujiao Qiu, Libing Liu, Shaofu Zhao, Lidan Fan, and Renjie Zhang. "Formation of graphene oxide films at the liquid/liquid interface." Composite Interfaces 21, no. 7 (May 19, 2014): 623–30. http://dx.doi.org/10.1080/15685543.2014.918789.
Повний текст джерелаWehrhold, Michel, Tilmann J. Neubert, Anur Yadav, Martin Vondráček, Rodrigo M. Iost, Jan Honolka, and Kannan Balasubramanian. "pH sensitivity of interfacial electron transfer at a supported graphene monolayer." Nanoscale 11, no. 31 (2019): 14742–56. http://dx.doi.org/10.1039/c9nr05049c.
Повний текст джерелаPatil, Sagar H., Bihag Anothumakkool, Shivaram D. Sathaye, and Kashinath R. Patil. "Architecturally designed Pt–MoS2 and Pt–graphene composites for electrocatalytic methanol oxidation." Physical Chemistry Chemical Physics 17, no. 39 (2015): 26101–10. http://dx.doi.org/10.1039/c5cp04141d.
Повний текст джерелаChen, Long, Liangliang Huang, and Jiahua Zhu. "Stitching graphene oxide sheets into a membrane at a liquid/liquid interface." Chem. Commun. 50, no. 100 (October 21, 2014): 15944–47. http://dx.doi.org/10.1039/c4cc07558g.
Повний текст джерелаAllaire, Ryan H., Abhijeet Dhakane, Reece Emery, P. Ganesh, Philip D. Rack, Lou Kondic, Linda Cummings, and Miguel Fuentes-Cabrera. "Surface, Interface, and Temperature Effects on the Phase Separation and Nanoparticle Self Assembly of Bi-Metallic Ni0.5Ag0.5: A Molecular Dynamics Study." Nanomaterials 9, no. 7 (July 21, 2019): 1040. http://dx.doi.org/10.3390/nano9071040.
Повний текст джерелаRodgers, Andrew N. J., and Robert A. W. Dryfe. "Oxygen Reduction at the Liquid-Liquid Interface: Bipolar Electrochemistry through Adsorbed Graphene Layers." ChemElectroChem 3, no. 3 (October 22, 2015): 472–79. http://dx.doi.org/10.1002/celc.201500343.
Повний текст джерелаДисертації з теми "Graphene liquid interface"
Rodgers, Andrew Norman John. "Dispersion, assembly and electrochemistry of graphene at the liquid-liquid interface." Thesis, University of Manchester, 2015. https://www.research.manchester.ac.uk/portal/en/theses/dispersion-assembly-and-electrochemistry-of-graphene-at-the-liquidliquid-interface(c2ffd27a-cf5f-45c2-a471-60dcab788e12).html.
Повний текст джерелаBordes, Emilie. "Graphène dans des liquides ioniques : interactions aux interfaces, exfoliation, stabilisation." Thesis, Université Clermont Auvergne (2017-2020), 2017. http://www.theses.fr/2017CLFAC052.
Повний текст джерелаThe liquid-phase exfoliation of graphite is one of the most promising methods to increase production and commercial availability of graphene. The exfoliation process can be conceptually described in four steps: the contact of the graphite with liquid, the intercalation of the solvent between layers, the dispersion of the two dimensional material, and its stabilization in the liquid-phase. Because ionic liquids can be easily obtained with chosen molecular structures and tunable physicochemical properties, they were used in this study as liquid media for the exfoliation of graphite. Our aim is to optimize the exfoliation of graphite through the understanding of the molecular mechanisms and of the interactions involved in each step of the process.The liquid-graphite interfacial energies from measured surface tensions and contact angles, between ionic liquids and pristine graphite surface, were used to determine the affinity of different liquids at the surface of graphite. In order to investigate this interface, molecular dynamics simulations were conducted to analyse the ordering of ionic liquids at the surface of graphite. The free energies necessary to create cavities inside the bulk ionic liquid have also been studied.Molecular simulations were also used to study the exfoliation of one graphene layer from a stack of graphite and hence provide a microscopic view of the intercalation of solvent molecules. The energies involved in the process have been calculated.Polyaromatic compounds were regarded as models for graphene as they can be easily obtained pure, without structure variability, defects or uncontrolled functional groups. Enthalpies of dissolution of polyaromatic hydrocarbons (naphthalene, anthracene and pyrene) in different ionic liquids were measured by solution calorimetry and related with their solubility. The ordering of the ions around this model compounds were studied by molecular simulation and spectroscopy Infra-Red.After exfoliation, samples of suspended graphene in different ionic liquids have been characterized experimentally in terms of flake size (using transmission electron microscopy and atomic force microscopy), number of layers (atomic force microscopy, spectroscopy Raman), total concentration (UV-visible spectroscopy) and purity of the exfoliated material (X-ray photoelectron spectrometry).Twenty different ionic liquids based on imidazolium, pyrrolidinium and ammonium cations and on bis(trifluoromethylsulfonyl)imide, triflate, dicyanamide, tricyanomethanide, and methyl sulfate have been tested. The molecular interactions have been identified thus allowing the establishment of design rules for ionic liquids capable of exfoliating carbon materials. The pyrrolidinium cation has shown promising results in all the steps of exfoliation process, compared to the imidazolium or ammonium cation. Selecting a large and flexible anion reduced the interfacial energy with graphite, dispersed the nanocarbons by increasing the entropy of the system and stabilized the exfoliated graphite in larger quantity. A small anion such as triflate appears to be favorable for obtaining graphene, whereas the size of the layers and their quantity is reduced. An ionic liquid having an important apolar portion will facilitate the insertion and dispersion of graphene layers. For the stabilization of graphite, the alkyl-π et π -π interactions are decisive
Rakotozafy, Samuel. "Étude de films mixtes formés par physisorption sur les plans de base du graphite de deux adsorbats de propriétés de condensation très différentes : transition de déplacement : solutions bidimensionnelles." Nancy 1, 1993. http://www.theses.fr/1993NAN10226.
Повний текст джерелаBickerstaffe, Anna Kristina. "Crystallisation at the solid/liquid interface : carboxylic acids on graphite and ice crystals in solution." Thesis, University of Cambridge, 2006. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.613988.
Повний текст джерелаPavlov, Aleksey D. "Improvement of Electromagnetic Railgun Barrel Performance and Lifetime by Method of Interfaces and Augmented Projectiles." DigitalCommons@CalPoly, 2013. https://digitalcommons.calpoly.edu/theses/986.
Повний текст джерелаParker, Julia Elizabeth. "Adsorption at the solid/liquid interface : adsorption and mixing behaviour of fluorinated alkyl species on the surface of graphite." Thesis, University of Cambridge, 2009. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.611213.
Повний текст джерелаYang, Jing. "Phosphonium ionic liquids : Versatile nanostructuration and interfacial agents for poly(vinylidene fluoride-chlorotrifluoroethylene)." Thesis, Lyon, 2016. http://www.theses.fr/2016LYSEI072/document.
Повний текст джерелаThis thesis work deals with an understanding of the versatile roles of phosphonium ionic liquids (ILs) as nanostructuration and interfacial agents for the fluorinated polymer matrix, i.e.,poly(vinylidene fluoride-chlorotrifluoroethylene) (P(VDF-CTFE)). In this context, two phosphonium ILs with different functionalities in steric hindrance and extra dipolar groups are firstly incorporated in P(VDF-CTFE) matrix to prepare polymer films. The crystalline phase structure, dispersion morphology and crystallization behavior are finely characterized with the goal of providing a full and deep understanding of the versatile and tunable nanostructuration effect of phosphonium ILs. Subsequently, in order to elucidate the mechanism of interfacial influence of IL, a fluorinated phosphonium IL with a cation structure combining three phenyls and a short fluorinated chain is added on the surface of graphene oxide (GO) and reduced graphene oxide (rGO), making them as functional nanofillers to be incorporated into P(VDF-CTFE) matrix. Thus,P(VDF-CTFE)/graphene composite films with different filler contents are prepared in order to investigate the mechanism of interfacial interaction and its influence on the composite films, such as crystalline phase structure, crystallization behavior, chain segmental relaxation behavior, dispersion morphology and the final dielectric properties
Bonatout, Nathalie. "Etude des films de Langmuir d'oxyde de graphène, de liquides ioniques et des systèmes mixtes." Thesis, Paris 6, 2017. http://www.theses.fr/2017PA066291/document.
Повний текст джерелаGraphene and ionic liquids are intensively studied, respectively as electrolyte and as electrode materials, for the development of supercapacitors. In this framework, the characterization between the two species is essential. We realized such kind of interfaces through the Langmuir film procedure and characterized them at different scales, using isotherm measurements, Brewster Angle and Atomic Force Microscopies, and surface X-ray scattering. We studied films formed by different ionic liquids, by graphene oxide and finally by a mixture of the two species. The study on the pure ionic liquids evidences the role of the cation on the film organization at the air-water interface, for the monolayer as well as for the tridimensional phase. Moreover, we showed that the graphene oxide films are composed of a bilayer of sheets à the interface, even at low surface densities. Finally, regarding the mixed film, we observed a vertical segregation of the species for high enough surface pressures. The film is formed by a first layer in contact with the water surface, mostly composed of graphene oxide sheets parallel to the interface, on which a second layer is superimposed, composed of disorganized ionic liquid domains
Nguyen, Doan Chau Yen. "Role of deposition temperature and concentration on the self-assembly and reaction of organic molecules at the solution-graphite interface." Doctoral thesis, Universitätsbibliothek Chemnitz, 2017. http://nbn-resolving.de/urn:nbn:de:bsz:ch1-qucosa-223658.
Повний текст джерелаThe main aim of this thesis is to study the self-assembly of organic molecules at the liquid-solid interface (LSI). Special emphasis is given to controlling the process of self-assembly via suitable parameters such as: the substrate temperature during the initial deposition, the concentration of dissolved molecules, or the chemical nature of solutes and solvents. The investigations are performed using scanning tunneling microscopy (STM). The first focus of this work is the systematic investigation of the effect of the substrate temperature during the deposition out of the solution on the self-assembly of complex molecular architectures at the LSI. These investigations have been done with the planar molecule trimesic acid (TMA), and the non-planar molecule benzene 1,3,5-triphosphonic acid (BTP). We show that the polymorphism of the adsorbate structures of TMA (also with BTP) can be controlled by the substrate temperature during the deposition of the molecules out of the solution for various solvents of different polarity such as phenyloctane, octanoic acid, and undecanol. By increasing the temperature of the pre-heated graphite substrate, the specific 2D supramolecular structure and the corresponding packing density in the adsorbate layer can be precisely tuned for each kind of the solvents studied. Furthermore, the influence of the concentration on the resulting self-assembly of TMA molecules at the LSI is estimated by another experiment using stirring (from 0 h to 40 h) of the solutions of different kinds of solvents. These results demonstrate that choosing different preparation methods (increasing deposition temperatures or stirring) lead to the same tendency in the change of the self-assembled structures as well as the tuning of the packing density from which it can also be concluded that the increase of the concentration at increased deposition temperatures is also the main reason for the observed changes. The second focus of this work is the investigation of chemical reactions of self-assembling molecules. The esterification of TMA with undecanol was observed. Moreover as a first step to study twin polymerization, the oligomerization of the twin monomer 2,2’-spirobi [4H-1,3,2-benzo-dioxasiline] (SBS) was investigated by STM at the SBS-undecanol solution/graphite interface. Firstly, by ultrasonicating the solution of SBS in undecanol for different times the oligomerization of SBS monomer without any catalyst has been observed at the LSI. Secondly, the oligomerization of SBS monomer can also be initiated by the substrate temperature during the deposition of the molecules out of the solution. By stepwise increasing the temperature of the pre-heated substrate, various periodic assemblies of phenolic dimer, trimer, pentamer resin, and so on were observed. Furthermore, the effect of deposition temperature on the self-assembly of solely solvent molecules from the pure liquid at the LSI is described, which is important because the undecanol solvent molecules are always co-adsorbed with the solutes used in this work (TMA, BTP, SBS) to form linear patterns
Arrigoni, Claire. "Monocouches nanoporeuses auto-assemblées sur graphite : contrôle et modulation des propriétés de tamis moléculaire." Phd thesis, Université Pierre et Marie Curie - Paris VI, 2010. http://tel.archives-ouvertes.fr/tel-00623515.
Повний текст джерелаЧастини книг з теми "Graphene liquid interface"
Mohamed, M., M. N. B. Omar, A. I. M. Shaiful, R. Rahman, M. F. Hamid, P. S. Kataraki, and A. B. M. Azhar. "Thermal Properties of the Graphene Oxide (GO) Reinforced Epoxy Composites (Thermal Adhesive Liquid Type): Application of Thermal Interface Materials." In Lecture Notes in Mechanical Engineering, 933–40. Singapore: Springer Singapore, 2021. http://dx.doi.org/10.1007/978-981-16-0866-7_81.
Повний текст джерелаWeilandt, E., A. Menck, M. Binggeli, and O. Marti. "Friction Force Measurements on Graphite Steps under Potential Control." In Nanoscale Probes of the Solid/Liquid Interface, 307–15. Dordrecht: Springer Netherlands, 1995. http://dx.doi.org/10.1007/978-94-015-8435-7_17.
Повний текст джерелаSohrabi, Beheshteh. "Amphiphiles." In Self-Assembly of Materials and Supramolecular Structures [Working Title]. IntechOpen, 2022. http://dx.doi.org/10.5772/intechopen.107880.
Повний текст джерелаBussetti, Gianlorenzo, Rossella Yivlialin, Franco Ciccacci, Lamberto Duó, and Alessandro Podestá. "Blistering at the solid-liquid interface: the graphite case-study." In Reference Module in Chemistry, Molecular Sciences and Chemical Engineering. Elsevier, 2023. http://dx.doi.org/10.1016/b978-0-323-85669-0.00063-5.
Повний текст джерелаТези доповідей конференцій з теми "Graphene liquid interface"
Lopes, Michele Lima, and Douglas Santos Monteiro. "GRAPHENE OXIDE BEHAVIOUR AT AIR-LIQUID INTERFACE." In V Congresso Online Nacional de Química. Congresse.me, 2023. http://dx.doi.org/10.54265/kosm3582.
Повний текст джерелаOrdonez, Richard C., Noah Acosta, Jordan Melcher, Nackieb Kamin, and David Garmire. "Investigation of Liquid Metal Ohmic Contacts for Graphene Photonic Devices." In ASME 2015 International Technical Conference and Exhibition on Packaging and Integration of Electronic and Photonic Microsystems collocated with the ASME 2015 13th International Conference on Nanochannels, Microchannels, and Minichannels. American Society of Mechanical Engineers, 2015. http://dx.doi.org/10.1115/ipack2015-48567.
Повний текст джерелаBramhaiah, K., and Neena S. John. "Reduced graphene oxide based silver sulfide hybrid films formed at a liquid/liquid interface." In SOLID STATE PHYSICS: Proceedings of the 58th DAE Solid State Physics Symposium 2013. AIP Publishing LLC, 2014. http://dx.doi.org/10.1063/1.4872604.
Повний текст джерелаBabaei, Hasan, Pawel Keblinski, and J. M. Khodadadi. "Molecular Dynamics Study of the Interfacial Thermal Conductance at the Graphene/Paraffin Interface in Solid and Liquid Phases." In ASME 2013 Heat Transfer Summer Conference collocated with the ASME 2013 7th International Conference on Energy Sustainability and the ASME 2013 11th International Conference on Fuel Cell Science, Engineering and Technology. American Society of Mechanical Engineers, 2013. http://dx.doi.org/10.1115/ht2013-17478.
Повний текст джерелаWang, Wei, Sehoon Chang, and Gawain Thomas. "Scale-Up Fabrication and Microfluidic Evaluation of Janus Graphene Nanofluids as Novel EOR Agent." In Middle East Oil, Gas and Geosciences Show. SPE, 2023. http://dx.doi.org/10.2118/213484-ms.
Повний текст джерелаHossain, Mohammad K., Md Mahmudur R. Chowdhury, Mahesh Hosur, Shaik Jeelani, and Nydeia W. Bolden. "Enhanced Properties of Epoxy Composite Reinforced With Amino-Functionalized Graphene Nanoplatelets." In ASME 2015 International Mechanical Engineering Congress and Exposition. American Society of Mechanical Engineers, 2015. http://dx.doi.org/10.1115/imece2015-51483.
Повний текст джерелаMcGonigal, G. C., R. H. Bernhardt, Y. H. Yeo, and D. J. Thomson. "STM Imaging of Physisorbed Molecules at the Liquid/Graphite Interface." In Scanned probe microscopy. AIP, 1991. http://dx.doi.org/10.1063/1.41411.
Повний текст джерелаBarisik, Murat, Ziyuan Shi, and Ali Beskok. "Heat Conduction and Interface Thermal Resistance in Liquid Argon Filled Silver and Graphite Nanochannels." In ASME 2012 Third International Conference on Micro/Nanoscale Heat and Mass Transfer. American Society of Mechanical Engineers, 2012. http://dx.doi.org/10.1115/mnhmt2012-75231.
Повний текст джерелаFranek, Friedrich, Andreas Pauschitz, Vladislav E. Lazarev, Georg Vorlaufer, Thomas Dick, and Robin Jisa. "Complex Micromodel Analysis of Wearing Contact Interfaces." In World Tribology Congress III. ASMEDC, 2005. http://dx.doi.org/10.1115/wtc2005-63540.
Повний текст джерелаBurbelko, Andriy A., Daniel Gurgul, Edward Fras´, and Edward Guzik. "Multiscale Modeling of Ductile Iron Solidification With Continuous Nucleation by a Cellular Automaton." In ASME 2010 International Design Engineering Technical Conferences and Computers and Information in Engineering Conference. ASMEDC, 2010. http://dx.doi.org/10.1115/detc2010-28764.
Повний текст джерела