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Journal articles on the topic 'Interactions de surface'

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Author: Grafiati

Published: 28 June 2022

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1

Turov, V. V., V. M. Gun’ko, T. V. Krupskaya, I. S. Protsak, L. S. Andriyko, A. I. Marinin, A. P. Golovan, N. V. Yelagina, and N. T. Kartel. "Interphase interactions of hydrophobic powders based on methilsilica in the water environment." Surface 12(27) (December 30, 2020): 53–99. http://dx.doi.org/10.15407/surface.2020.12.053.

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Using modern physicochemical research methods and quantum chemical modeling, the surface structure, morphological and adsorption characteristics, phase transitions in heterogeneous systems based on methylsilica and its mixtures with hydrophilic silica were studied. It is established that at certain concentrations of interfacial water, hydrophobic silica or their composites with hydrophilic silica form thermodynamically unstable systems in which energy dissipation can be carried out under the influence of external factors: increasing water concentration, mechanical loads and adsorption of air by hydrophobic component. When comparing the binding energies of water in wet powders of wettind-drying samples A-300 and AM-1, which had close values of bulk density (1 g/cm3) and humidity (1 g/g), close to 8 J/g. However, the hydration process of hydrophobic silica is accompanied by a decrease in entropy and the transition of the adsorbent-water system to a thermodynamically nonequilibrium state, which is easily fixed on the dependences of interfacial energy (S) on the amount of water in the system (h). It turned out that for pure AM-1 the interfacial energy of water increases in proportion to its amount in the interparticle gaps only in the case when h < 1 g/g. With more water, the binding energy decreases abruptly, indicating the transition of the system to a more stable state, which is characterized by the consolidation of clusters of adsorbed water and even the formation of a bulk phase of water. Probably there is a partial "collapse" of the interparticle gaps of hydrophobic particles AM-1 and the release of thermodynamically excess water. For mixtures of hydrophobic and hydrophilic silica, the maximum binding of water is shifted towards greater hydration. At AM1/A-300 = 1/1 the maximum is observed at h = 3g/g, and in the case of AM1/A-300 = 1/2 it is not reached even at h = 4 g/g. The study of the rheological properties of composite systems has shown that under the action of mechanical loads, the viscosity of systems decreases by almost an order of magnitude. However, after withstanding the load and then reducing the load to zero, the viscosity of the system increases again and becomes significantly higher than at the beginning of the study. That is, the obtained materials have high thixotropic properties. Thus, a wet powder that has all the characteristics of a solid after a slight mechanical impact is easily converted into a concentrated suspension with obvious signs of liquid.

2

Hunt, John A., and Molly Shoichet. "Biomaterials: surface interactions." Current Opinion in Solid State and Materials Science 5, no. 2-3 (April 2001): 161–62. http://dx.doi.org/10.1016/s1359-0286(01)00012-2.

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3

Lafleur, Trevor, Julian Schulze, and Zoltan Donkó. "Plasma-surface interactions." Plasma Sources Science and Technology 28, no. 4 (April 16, 2019): 040201. http://dx.doi.org/10.1088/1361-6595/ab1380.

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4

A, J. B. "Molecule surface interactions." Journal of Molecular Structure 249, no. 2-4 (September 1991): 391. http://dx.doi.org/10.1016/0022-2860(91)85082-e.

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5

Goeckner, M. J., C. T. Nelson, S. P. Sant, A. K. Jindal, E. A. Joseph, B. S. Zhou, G. Padron-Wells, B. Jarvis, R. Pierce, and L. J. Overzet. "Plasma-surface interactions." Journal of Physics: Conference Series 133 (October 1, 2008): 012010. http://dx.doi.org/10.1088/1742-6596/133/1/012010.

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6

Erath, Johann, Jiaxi Cui, Jasmin Schmid, Michael Kappl, Aránzazu del Campo, and Andreas Fery. "Phototunable Surface Interactions." Langmuir 29, no. 39 (September 19, 2013): 12138–44. http://dx.doi.org/10.1021/la4021349.

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7

Tuson, Hannah H., and Douglas B. Weibel. "Bacteria–surface interactions." Soft Matter 9, no. 17 (2013): 4368. http://dx.doi.org/10.1039/c3sm27705d.

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8

Annich, G. M., B. Ashton, S. I. Merz, D. O. Brant, and R. H. Bartlett. "PLATELET/SURFACE INTERACTIONS." ASAIO Journal 46, no. 2 (March 2000): 234. http://dx.doi.org/10.1097/00002480-200003000-00332.

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9

Chang, J. P., and J. W. Coburn. "Plasma–surface interactions." Journal of Vacuum Science & Technology A: Vacuum, Surfaces, and Films 21, no. 5 (September 2003): S145—S151. http://dx.doi.org/10.1116/1.1600452.

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10

Winkler, A. "Gas-surface interactions." Vacuum 46, no. 8-10 (August 1995): 1241–42. http://dx.doi.org/10.1016/0042-207x(95)00151-4.

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11

Clinton, William L., and Sipra Pal. "Ion-surface interactions." Surface Science 226, no. 1-2 (February 1990): 89–92. http://dx.doi.org/10.1016/0039-6028(90)90156-3.

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12

Weinberg, W. Henry. "Molecule surface interactions." Journal of Colloid and Interface Science 137, no. 1 (June 1990): 312. http://dx.doi.org/10.1016/0021-9797(90)90071-u.

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13

Ahmadi, Ahmad, Rhodri Wyn Evans, and Gary Attard. "Anion—surface interactions." Journal of Electroanalytical Chemistry 350, no. 1-2 (May 1993): 279–95. http://dx.doi.org/10.1016/0022-0728(93)80211-y.

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14

Ahmadi, Ahmad, Emma Bracey, Rhodri Wyn Evans, and Gary Attard. "Anion-surface interactions." Journal of Electroanalytical Chemistry 350, no. 1-2 (May 1993): 297–316. http://dx.doi.org/10.1016/0022-0728(93)80212-z.

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15

Kazakova, O. O. "Quantum-chemical investigation of interactions in supramolecular systems: cholesterol - bile acids - silica in aqueous solutions." Surface 13(28) (December 30, 2021): 39–46. http://dx.doi.org/10.15407/surface.2021.13.039.

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Hypercholesterolemia significantly increases the risk of myocardial infarction associated with COVID-19. Along with pharmacological treatment, the possibility of the excretion of excess cholesterol from an organism by adsorption is also of great interest. The interaction of cholesterol with the surface of partially hydrophobized silica in aqueous solutions of bile acids was investigated by the PM7 method using the COSMO (COnductor-like Screening MOdel) solvation model. The distribution of electrostatic and hydrophobic potentials of molecules and complexes was calculated. The values of free Gibbs energy adsorption of bile acids on the surface of silica correlate with the distribution coefficients in the n-octanol-water system. The energy of interaction of cholesterol with bile acids affects its adsorption on silica. The stronger the bond of cholesterol with the molecules of bile acids, the less it is released from the primary micelles in solution and adsorbed on the surface.

16

Severn, Kathryn Anne, Paul Richard Fleming, and Neil Dixon. "Science of synthetic turf surfaces: Player–surface interactions." Sports Technology 3, no. 1 (February 2010): 13–25. http://dx.doi.org/10.1080/19346190.2010.504279.

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17

USAMI, Seiji. "Gas-solid surface interactions." SHINKU 30, no. 12 (1987): 946–48. http://dx.doi.org/10.3131/jvsj.30.946.

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18

Claesson, P. M. "Measurements of surface interactions." Colloids and Surfaces A: Physicochemical and Engineering Aspects 123-124 (May 1997): 339–40. http://dx.doi.org/10.1016/s0927-7757(96)03805-8.

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19

Steigmann, D. J., and R. W. Ogden. "Elastic surface—substrate interactions." Proceedings of the Royal Society of London. Series A: Mathematical, Physical and Engineering Sciences 455, no. 1982 (February 8, 1999): 437–74. http://dx.doi.org/10.1098/rspa.1999.0320.

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20

McKeown-Longo, Paula J. "Fibronectin-Cell Surface Interactions." Clinical Infectious Diseases 9, Supplement_4 (July 1, 1987): S322—S334. http://dx.doi.org/10.1093/clinids/9.supplement_4.s322.

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21

Komerska, R., and C. Ware. "Haptic state surface interactions." IEEE Computer Graphics and Applications 24, no. 6 (November 2004): 52–59. http://dx.doi.org/10.1109/mcg.2004.53.

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22

Bandaru, Prabhakar, and Eli Yablonovitch. "Semiconductor Surface-Molecule Interactions." Journal of The Electrochemical Society 149, no. 11 (2002): G599. http://dx.doi.org/10.1149/1.1509461.

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23

Marmur, Abraham. "Tip-surface capillary interactions." Langmuir 9, no. 7 (July 1993): 1922–26. http://dx.doi.org/10.1021/la00031a047.

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24

Claesson, Per M., Evgeni Poptoshev, Eva Blomberg, and Andra Dedinaite. "Polyelectrolyte-mediated surface interactions." Advances in Colloid and Interface Science 114-115 (June 2005): 173–87. http://dx.doi.org/10.1016/j.cis.2004.09.008.

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25

Harshman, Dale R. "Muon/muonium surface interactions." Hyperfine Interactions 32, no. 1-4 (December 1986): 847–63. http://dx.doi.org/10.1007/bf02394994.

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26

Salma, Khanam, and Z. J. Ding. "Surface Boundary Effect in Electron-Solid Interactions." Solid State Phenomena 121-123 (March 2007): 1175–80. http://dx.doi.org/10.4028/www.scientific.net/ssp.121-123.1175.

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Electrons impinging or escaping from a solid surface undergo surface electronic excitations which are competitive in nature to other electron-solid interaction channels. The detailed information about electron inelastic scattering probability for surface excitations at solid surface is also important in reflection electron energy loss spectroscopy. A self energy formalism based on quantum mechanical treatment of interaction of electrons with a semi-infinite medium, which uses the optical dielectric function is considered to study surface boundary effect for planar surfaces of Cu and Ni for various conditions of electron-solid interactions. The total surface excitation probability of an electron while crossing the surface boundary once is numerically computed by integrating surface term of spatial and angular dependent differential inelastic cross sections over energy loss and distance from the surface. It is found that surface effect is prominent for low energy electrons and large oblique angles with respect to surface normal and confined to the close vicinity of surface boundary.

27

Díaz Compañy, A., G. Brizuela, and S. Simonetti. "Study of Materials for Drugs Delivery: cis-[PtCl2(NH3)2] Hydrolysis on Functionalized SiO2(100) Surfaces." Journal of Solid State Physics 2013 (December 22, 2013): 1–10. http://dx.doi.org/10.1155/2013/363209.

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The hydrolysis of the cis-platin drug on a SiO2(100) hydrated surface was investigated by computational modeling. The cisplatin molecule presents weak interactions with the neighbouring OH groups of the hydrated surface. The cisplatin hydrolysis is not favourable on the SiO2(100) surface. Consequently, the adsorption properties of SiO2(100) are improved considering the surface's modification with K, Mg, or NH2 functional species. In general, the system is more stable and the molecule-surface distance is reduced when cisplatin is adsorbed on the promoted surfaces. The hydrolysis is a favourable process on the SiO2(100) functionalized surfaces. The cisplatin hydrolysis is most favoured when the surface is functionalized with the NH2 specie. The electron density exchange plays a main role in the adsorption process. cis-[PtCl2(NH3)2] and cis-[PtCl(NH3)2]+ are adsorbed on the functionalized surface via Cl–N and Cl–Si interactions, while the cis-[Pt(NH3)2]2+ complex is adsorbed through Pt–O, Pt–Si, and Pt–H interactions. After adsorption, the strength of the N–Si, Si–O, and N–H superficial bonds of the functionalized SiO2(100) changes favouring the interaction between the molecule and their complexes with the surface.

28

Gillan, M. J., I. J. Ford, and C. F. Clement. "Molecule - surface interactions: theory in surface science." Journal of Aerosol Science 29 (September 1998): S643—S644. http://dx.doi.org/10.1016/s0021-8502(98)00515-1.

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29

Yuan, Lin, Qian Yu, Dan Li, and Hong Chen. "Surface Modification to Control Protein/Surface Interactions." Macromolecular Bioscience 11, no. 8 (February 17, 2011): 1031–40. http://dx.doi.org/10.1002/mabi.201000464.

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30

Lungu, Claudiu N., Melinda E. Füstös, Ireneusz P. Grudziński, Gabriel Olteanu, and Mihai V. Putz. "Protein Interaction with Dendrimer Monolayers: Energy and Surface Topology." Symmetry 12, no. 4 (April 17, 2020): 641. http://dx.doi.org/10.3390/sym12040641.

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Protein interaction with polymers layers is a keystone in designing bio-nano devices. Polyamidoamines (PAMAMs) are well-known polymers. Zero aromatic core dendrimers (ZAC) are molecules with no proven toxic effect in cultured cells. When coating nanodevices with enzymatic systems, active sites are disturbed by an interaction with the biosystem surface. Computational methods were used in order to simulate, characterize, and quantify protein–polymer interaction. Protein corona, i.e., surface proteins disposed on a viral membrane or nanodevice outer surface, are crucial in interactions with a potential pharmacological target or receptor. Corona symmetry has been observed in the Middle East respiratory syndrome-related coronavirus (MERS-CoV), severe acute respiratory syndrome coronavirus (SARS-CoV), and severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). As a protein alpha 1 antitrypsin’s a crystallographic structure was chosen. Protein–mono dendrimer layer systems were generated using in silico methods in order to simulate their interaction. Interactions were quantified using topological and quantum mechanical strategies. Results showed that PAMAM and ZAC interact differently with alpha 1 antitrypsin. Energy and topological surfaces of protein vary accordingly with the dendrimer monolayer. Topological surfaces have a higher sensibility in describing the interactions.

31

Giussani, Lara, Gloria Tabacchi, Enrica Gianotti, Salvatore Coluccia, and Ettore Fois. "Disentangling protein–silica interactions." Philosophical Transactions of the Royal Society A: Mathematical, Physical and Engineering Sciences 370, no. 1963 (March 28, 2012): 1463–77. http://dx.doi.org/10.1098/rsta.2011.0267.

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We present the results of modelling studies aimed at the understanding of the interaction of a 7 nm sized water droplet containing a negatively charged globular protein with flat silica surfaces. We show how the droplet interaction with the surface depends on the electrostatic surface charge, and that adhesion of the droplet occurs when the surface is negatively charged as well. The key role of water and of the charge-balancing counter ions in mediating the surface-protein adhesion is highlighted. The relevance of the present results with respect to the production of bioinorganic hybrids via encapsulation of proteins inside mesoporous silica materials is discussed.

32

TSONG, TIEN T., and CHONG-LIN CHEN. "IMPURITY ADSORPTION INDUCED SURFACE CHARGE-DENSITY OSCILLATION AND INDIRECT ATOMIC INTERACTIONS." Modern Physics Letters B 04, no. 12 (July 10, 1990): 775–82. http://dx.doi.org/10.1142/s0217984990000957.

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Neon field ion image spots of Ta impurities, deposited on the Ir (100) surface, show a halo-ring structure. This image structure is most probably produced by the impurity adsorption induced oscillatory electronic charge-density distribution at the surface. The oscillatory electronic charge-density modulation is the cause of electronic indirect interactions of atoms in alloys and on metal surfaces. Manifestations of these interactions can be found in the compositional variation in the near surface layers of alloys in surface segregation, and in the pair-interaction of adsorbed atoms.

33

Wang, Meng-Jiao, Siegfried Wolff, and Jean-Baptiste Donnet. "Filler-Elastomer Interactions. Part I: Silica Surface Energies and Interactions with Model Compounds." Rubber Chemistry and Technology 64, no. 4 (September 1, 1991): 559–76. http://dx.doi.org/10.5254/1.3538573.

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Abstract Inverse gas-solid chromatography, operated at infinite dilution, has been used to assess the surface energies of silicas, both fumed and precipitated. The dispersive components of the surface free energies of the silicas were calculated from the free energies of adsorption, corresponding to the —CH2— group, obtained from n-alkane adsorption. The specific components of the surface energies were evaluated separately by comparison of the free energies of adsorption of polar probes with those of n-alkanes, based on the surface areas covered by the probe molecules. The results indicate that while the dispersive components of silica surface energies is somewhat higher for the fumed silicas, the specific components are much higher for precipitated silicas, probably resulting from the higher silanol concentration on their surfaces. Moreover, the interaction able to take place between rubber matrix and the silicas are also estimated chromatographically from the adsorptions of low-molecular-weight analogs of elastomers. The free energies and enthalpies indicate that the interactions of functional groups with the fillers decrease in the order of nitrile, phenyl ring, double bond. The saturated rubber analogs show lower interactions with silicas. The lowest interactions of iso-alkanes imply poor interactions between butyl rubber and the fillers. As expected, the experimental data reflect an attenuation of polymer-silica interactions with decreasing content of functional groups and degree of unsaturation in NR, BR, SBR, and NBR.

34

Taylor, Christopher G. P., Jennifer S. Train, and Michael D. Ward. "Interactions of Small-Molecule Guests with Interior and Exterior Surfaces of a Coordination Cage Host." Chemistry 2, no. 2 (June 2, 2020): 510–24. http://dx.doi.org/10.3390/chemistry2020031.

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Coordination cages are well-known to act as molecular containers that can bind small-molecule guests in their cavity. Such cavity binding is associated with interactions of the guests with the surrounding set of surfaces that define the cavity; a guest that is a good fit for the cavity will have many favourable interactions with the interior surfaces of the host. As cages have exterior as well as interior surfaces, possibilities also exist for ‘guests’ that are not well-bound in the cavity to interact with the exterior surface of the cage where spatial constraints are fewer. In this paper, we report a combined solid-state and solution study using an octanuclear cubic M8L12 coordination cage which illustrates the occurrence of both types of interaction. Firstly, crystallographic studies show that a range of guests bind inside the cavity (either singly or in stacked pairs) and/or interact with the cage exterior surface, depending on their size. Secondly, fluorescence titrations in aqueous solution show how some flexible aromatic disulfides show two separate types of interaction with the cage, having different spectroscopic consequences; we ascribe this to separate interactions with the exterior surface and the interior surface of the host cage with the former having a higher binding constant. Overall, it is clear that the idea of host/guest interactions in molecular containers needs to take more account of external surface interactions as well as the obvious cavity-based binding.

35

Mateos, Helena, Alessandra Valentini, Francesco Lopez, and Gerardo Palazzo. "Surfactant Interactions with Protein-Coated Surfaces: Comparison between Colloidal and Macroscopically Flat Surfaces." Biomimetics 5, no. 3 (July 1, 2020): 31. http://dx.doi.org/10.3390/biomimetics5030031.

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Surface interactions with polymers or proteins are extensively studied in a range of industrial and biomedical applications to control surface modification, cleaning, or biofilm formation. In this study we compare surfactant interactions with protein-coated silica surfaces differing in the degree of curvature (macroscopically flat and colloidal nanometric spheres). The interaction with a flat surface was probed by means of surface plasmon resonance (SPR) while dynamic light scattering (DLS) was used to study the interaction with colloidal SiO2 (radius 15 nm). First, the adsorption of bovine serum albumin (BSA) with both SiO2 surfaces to create a monolayer of coating protein was studied. Subsequently, the interaction of these BSA-coated surfaces with a non-ionic surfactant (a decanol ethoxylated with an average number of eight ethoxy groups) was investigated. A fair comparison between the results obtained by these two techniques on different geometries required the correction of SPR data for bound water and DLS results for particle curvature. Thus, the treated data have excellent quantitative agreement independently of the geometry of the surface suggesting the formation of multilayers of C10PEG over the protein coating. The results also show a marked different affinity of the surfactant towards BSA when the protein is deposited on a flat surface or individually dissolved in solution.

36

Hellwig, Maren, Martin Köppen, Albert Hiller, Hans Koslowski, Andrey Litnovsky, Klaus Schmid, Christian Schwab, and Roger De Souza. "Impact of Surface Roughness on Ion-Surface Interactions Studied with Energetic Carbon Ions 13C+ on Tungsten Surfaces." Condensed Matter 4, no. 1 (March 5, 2019): 29. http://dx.doi.org/10.3390/condmat4010029.

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The effect of surface roughness on angular distributions of reflected and physically sputtered particles is investigated by ultra-high vacuum (UHV) ion-surface interaction experiments. For this purpose, a smooth (R a = 5.9 nm) and a rough (R a = 20.5 nm) tungsten (W) surface were bombarded with carbon ions 13C+ under incidence angles of 30 ∘ and 80 ∘ . Reflected and sputtered particles were collected on foils to measure the resulting angular distribution as a function of surface morphology. For the qualitative and quantitative analysis, secondary ion mass spectrometry (SIMS) and nuclear reaction analysis (NRA) were performed. Simulations of ion-surface interactions were carried out with the SDTrimSP (Static Dynamic Transport of Ions in Matter Sputtering) code. For rough surfaces, a special routine was derived and implemented. Experimental as well as calculated results prove a significant impact of surface roughness on the angular distribution of reflected and sputtered particles. It is demonstrated that the effective sticking of C on W is a function of the angle of incidence and surface morphology. It is found that the predominant ion-surface interaction process changes with fluence.

37

Douglas, Jack F. "How does surface roughness affect polymer-surface interactions?" Macromolecules 22, no. 9 (September 1989): 3707–16. http://dx.doi.org/10.1021/ma00199a035.

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38

Kurnik, Martin, Gabriel Ortega, Philippe Dauphin-Ducharme, Hui Li, Amanda Caceres, and Kevin W. Plaxco. "Quantitative measurements of protein−surface interaction thermodynamics." Proceedings of the National Academy of Sciences 115, no. 33 (July 30, 2018): 8352–57. http://dx.doi.org/10.1073/pnas.1800287115.

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Whereas proteins generally remain stable upon interaction with biological surfaces, they frequently unfold on and adhere to artificial surfaces. Understanding the physicochemical origins of this discrepancy would facilitate development of protein-based sensors and other technologies that require surfaces that do not compromise protein structure and function. To date, however, only a small number of such artificial surfaces have been reported, and the physics of why these surfaces support functional biomolecules while others do not has not been established. Thus motivated, we have developed an electrochemical approach to determining the folding free energy of proteins site-specifically attached to chemically well-defined, macroscopic surfaces. Comparison with the folding free energies seen in bulk solution then provides a quantitative measure of the extent to which surface interactions alter protein stability. As proof-of-principle, we have characterized the FynSH3 domain site-specifically attached to a hydroxyl-coated surface. Upon guanidinium chloride denaturation, the protein unfolds in a reversible, two-state manner with a free energy within 2 kJ/mol of the value seen in bulk solution. Assuming that excluded volume effects stabilize surface-attached proteins, this observation suggests there are countervening destabilizing interactions with the surface that, under these conditions, are similar in magnitude. Our technique constitutes an unprecedented experimental tool with which to answer long-standing questions regarding the molecular-scale origins of protein−surface interactions and to facilitate rational optimization of surface biocompatibility.

39

Jensen, K. O., and A. B. Walker. "Positron Transport and Surface Interactions." Materials Science Forum 105-110 (January 1992): 317–24. http://dx.doi.org/10.4028/www.scientific.net/msf.105-110.317.

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40

Senden, Tim J. "Force microscopy and surface interactions." Current Opinion in Colloid & Interface Science 6, no. 2 (May 2001): 95–101. http://dx.doi.org/10.1016/s1359-0294(01)00067-x.

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41

Bastasz, R., and W. Eckstein. "Plasma–surface interactions on liquids." Journal of Nuclear Materials 290-293 (March 2001): 19–24. http://dx.doi.org/10.1016/s0022-3115(00)00557-2.

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42

D’Ippolito, D. A., and J. R. Myra. "ICRF-edge and surface interactions." Journal of Nuclear Materials 415, no. 1 (August 2011): S1001—S1004. http://dx.doi.org/10.1016/j.jnucmat.2010.08.039.

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43

Heinzmann, U., S. Holloway, A. W. Kleyn, R. E. Palmer, and K. J. Snowdon. "Orientation in molecule - surface interactions." Journal of Physics: Condensed Matter 8, no. 19 (May 6, 1996): 3245–69. http://dx.doi.org/10.1088/0953-8984/8/19/002.

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44

Garnier, Philippe. "Photo Lithography - Surface Preparation Interactions." Solid State Phenomena 219 (September 2014): 177–82. http://dx.doi.org/10.4028/www.scientific.net/ssp.219.177.

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More than one third of process operations consist in surface preparations in the integrated circuits’ manufacturing. Most of them are directly or indirectly linked with photo lithography. This paper deals with these interactions.

45

Vasa, Parinda. "Exciton-surface plasmon polariton interactions." Advances in Physics: X 5, no. 1 (January 1, 2020): 1749884. http://dx.doi.org/10.1080/23746149.2020.1749884.

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46

Kjellander, Roland, and Stjepan Marčelja. "Surface interactions in simple electrolytes." Journal de Physique 49, no. 6 (1988): 1009–15. http://dx.doi.org/10.1051/jphys:019880049060100900.

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47

Curtarolo, Stefano, Wahyu Setyawan, and Renee D. Diehl. "Gas-Surface Interactions on Quasicrystals." Israel Journal of Chemistry 51, no. 11-12 (November 17, 2011): 1304–13. http://dx.doi.org/10.1002/ijch.201100129.

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48

Müller, M. M., M. Deserno, and J. Guven. "Geometry of surface-mediated interactions." Europhysics Letters (EPL) 69, no. 3 (February 2005): 482–88. http://dx.doi.org/10.1209/epl/i2004-10368-1.

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49

Perera, Komitige H., and Preethi L. Chandran. "Interactions of Cell Surface Glycoproteins." Biophysical Journal 108, no. 2 (January 2015): 485a. http://dx.doi.org/10.1016/j.bpj.2014.11.2651.

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50

Meyle, J., H. Wolburg, and A. F. Von Recum. "Surface Micromorphology and Cellular Interactions." Journal of Biomaterials Applications 7, no. 4 (April 1993): 362–74. http://dx.doi.org/10.1177/088532829300700404.

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