Multilayer Thin Films
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Characterization of Zirconium Phosphate/Polycation Thin Films Grown by Sequential Adsorption Reactions
1414 Chem. Mater. 1997, 9, 1414-1421 Characterization of Zirconium Phosphate/Polycation Thin Films Grown by Sequential Adsorption Reactions Hyuk-Nyun Kim, Steven W. Keller,† and Thomas E. Mallouk* Department of Chemistry, Pennsylvania State University, University Park, Pennsylvania 16802 Johannes Schmitt Institut fu¨ r Physikalische Chemie, Johannes Gutenberg-Universita¨t, D-55099 Mainz, Germany Gero Decher Institut Charles Sadron, Universite´ Louis Pasteur, F-67083 Strasbourg Cedex, France Received January 6, 1997. Revised Manuscript Received April 7, 1997X Monolayer and multilayer thin films consisting of anionic R-zirconium phosphate (R-ZrP) sheets and polycations (poly(allylamine hydrochloride) (PAH), cytochrome c) were character- ized by transmission electron microscopy (TEM), ellipsometry, UV-visible absorbance spectroscopy, reflectance FT-IR, XPS, and X-ray diffraction. Titration and powder X-ray diffraction experiments confirm that exfoliation of R-ZrP begins to occur when enough tetra- (n-butylammonium) hydroxide (TBA+OH-) has been added to exceed single-layer packing + + - of TBA ions (x 0.50) in the intercalation compound Zr(HPO4)2-x(TBA PO4 )x‚nH2O. The identical contrast≈ of many sheets in TEM micrographs suggests that the suspension is unilamellar. Alternately dipping cationic substrates into R-ZrP-containing suspensions and aqueous PAH gives a multilayer film that resembles the corresponding bulk intercalation compound. X-ray photoelectron spectra of multilayer films show that they are Zr-rich, relative to R-ZrP, consistent with some corrosion during the exfoliation reaction. The R-ZrP/ PAH layer pair thickness is 13/14.7 Å, as measured by ellipsometry/X-ray diffraction, respectively. A 13-layer pair film is sufficiently well-ordered in the stacking direction to give a Bragg peak in the diffraction pattern. -
Localized Enzyme-Assisted Self-Assembly in the Presence of Hyaluronic Acid for Hybrid Supramolecular Hydrogel Coating
polymers Communication Localized Enzyme-Assisted Self-Assembly in the Presence of Hyaluronic Acid for Hybrid Supramolecular Hydrogel Coating Jennifer Rodon Fores 1 , Alexis Bigo-Simon 1 ,Déborah Wagner 1, Mathilde Payrastre 1, Camille Damestoy 1, Lucille Blandin 1, Fouzia Boulmedais 1, Julien Kelber 1, Marc Schmutz 1 , Morgane Rabineau 2,3, Miryam Criado-Gonzalez 1,2,3,* , Pierre Schaaf 1,2,3,* and Loïc Jierry 1,* 1 Institut Charles Sadron (UPR22), Université de Strasbourg, CNRS, 23 rue du Loess, CEDEX 2, BP 84047, 67034 Strasbourg, France; [email protected] (J.R.F.); [email protected] (A.B.-S.); [email protected] (D.W.); [email protected] (M.P.); [email protected] (C.D.); [email protected] (L.B.); [email protected] (F.B.); [email protected] (J.K.); [email protected] (M.S.) 2 Institut National de la Santé et de la Recherche Médicale, INSERM Unité 1121, CRBS, 1 rue Eugène Boeckel, CEDEX, 67085 Strasbourg, France; [email protected] 3 Faculté de Chirurgie Dentaire, Université de Strasbourg, 8 rue Sainte Elisabeth, 67000 Strasbourg, France * Correspondence: [email protected] (M.C.-G.); [email protected] (P.S.); [email protected] (L.J.); Tel.: +91-25-8-74-97 (M.C.-G.); +33-3-68-85-33-87 (P.S.); +33-3-68-41-41-47(L.J.) Abstract: Hydrogel coating is highly suitable in biomaterial design. It provides biocompatibility and avoids protein adsorption leading to inflammation and rejection of implants. Moreover, hydrogels can be loaded with biologically active compounds. In this field, hyaluronic acid has been largely studied as an additional component since this polysaccharide is naturally present in extracellular matrix. -
Electrostatic Effects in Soft Matter and Biophysics NATO Science Series
Electrostatic Effects in Soft Matter and Biophysics NATO Science Series A Series presenting the results of scientific meetings supported under the NArO Science Programme. The Series is published by 10S Press, Amsterdam, and Kluwer Academic Publishers in conjunction with the NATO Scientific Affairs Division Sub-Series 1. Life and Behavioural Sciences 10S Press II. Mathematics, Physics and Chemistry Kluwer Academic Publishers III. Computer and Systems Science 10S Press IV. Earth and Environmental Sciences Kluwer Academic Publishers The NATO Science Series continues the series of books published formerly as the NATO ASI Series. The NATO Science Programme offers support for collaboration in civil science between scientists of countries of the Euro-Atlantic Partnership Council. The types of scientific meeting generally supported are "Advanced Study Institutes" and "Advanced Research Workshops", and the NATO Science Series collects together the results of these meetings. The meetings are co-organized bij scientists from NATO countries and scientists from NATO's Partner countries - countries of the CIS and Central and Eastern Europe. Advanced Study Institutes are high-Ievel tutorial courses offering in-depth study of latest advances in a field. Advanced Research Workshops are expert meetings aimed at critical assessment of a field, and identification of directions for future aetion. As a consequence of the restrueturing of the NATO Science programme in 1999, the NATO Science Series was re-organized to the four sub-series noted above. Please consult the following web sites for information on previous volumes published in the Series. http://www.nato.intlscience http://www.wkap.nl http://www.iospress.nl http://www.wtv-books.de/nato-pco.htm Series II: Mathematics, Physics and Chemistry - Voi. -
Monolithic Cells for Solar Fuels Chem Soc Rev
Volume 43 Number 23 7 December 2014 Pages 7957–8194 Chem Soc Rev Chemical Society Reviews www.rsc.org/chemsocrev Includes a collection of articles on the theme of CO2 Capture and Chemical Recycling ISSN 0306-0012 TUTORIAL REVIEW Johan A. Martens et al. Monolithic cells for solar fuels Chem Soc Rev View Article Online TUTORIAL REVIEW View Journal | View Issue Monolithic cells for solar fuels† a a b c d Cite this: Chem. Soc. Rev., 2014, Jan Ronge´, Tom Bosserez, David Martel, Carlo Nervi, Luca Boarino, a b c a 43,7963 Francis Taulelle, Gero Decher, Silvia Bordiga and Johan A. Martens* Hybrid energy generation models based on a variety of alternative energy supply technologies are considered the best way to cope with the depletion of fossil energy resources and to limit global warming. One of the currently missing technologies is the mimic of natural photosynthesis to convert carbon dioxide and water into chemical fuel using sunlight. This idea has been around for decades, but artificial photosynthesis of organic molecules is still far away from providing real-world solutions. The scientific challenge is to perform in an efficient way the multi-electron transfer reactions of water oxidation and carbon dioxide reduction using holes and single electrons generated in an illuminated semiconductor. In this tutorial review the design of photoelectrochemical (PEC) cells that combine solar water oxidation and CO2 reduction is discussed. In such PEC cells simultaneous transport and efficient use of light, electrons, protons and molecules has to be managed. It is explained how efficiency can be Creative Commons Attribution-NonCommercial 3.0 Unported Licence. -
AND MICROCARRIER FABRICATION a Thes
A NOVEL μ-FLUIDIC CHANNEL ASSISTED ENCAPSULATION TECHNIQUE FOR LAYER-BY-LAYER POLYMER NANO- AND MICROCARRIER FABRICATION A Thesis Presented to The Graduate Faculty of The University of Akron In Partial Fulfillment of the Requirements for the Degree Master of Science Jingyu Li August, 2015 A NOVEL μ-FLUIDIC CHANNEL ASSISTED ENCAPSULATION TECHNIQUE FOR LAYER-BY-LAYER POLYMER NANO- AND MICROCARRIER FABRICATION Jingyu Li Thesis Approved: Accepted: Advisor Department Chair Dr. Younjin Min Dr. Sadhan C. Jana Committee Member Dean of the College Dr. Mukerrem Cakmak Dr. Eric J. Amis Committee Member Interim Dean of the Graduate School Dr. Hossein Tavana Dr. Rex D. Ramsier Date ii ABSTRACT Layer-by-layer (LbL) assembly is a popular technique for fabricating thin multilayer films on templates by depositing alternating layers of oppositely charged polyelectrolytes with rinsing steps in between. The LbL technique fabricated capsules can be used for biomedical applications such as drug and vaccine delivery, biosensors and bioreactors. LbL assembly enables us to use various types, sizes, and shapes of particles as templates, like silica particles, calcium carbonate particles and metal particles. In addition, a suite of water-soluble polymers with different properties can be applied to LbL assembly to meet researchers` requirements. Due to accurate control on size and shape, LbL technique is capable of fabricating small particles below 200 nm, which is in the optimal size for drug carriers and small enough to avoid clogging blood capillaries. The versatility of nano- and microcapsules has captured the attention of researchers to develop fabrication methods of LbL particles. The traditional LbL assembly method has simple process, but which is inefficient and has limitations due to repeated centrifugation steps. -
Gero Decher, Jean-Claude Voegel La Recherche, No
An Introduction to Polyelectrolyte Multilayers Layer-by-Layer Adsorption (LbL): An Enabling Technology for the Nano- construction of Multifunctional Films on Solvent Accessible Surfaces. G. Decher / Institut Charles Sadron Institut Charles Sadron 1 Differences between chemistry in bulk and at interfaces Some trivia: • Surface functional groups accessible only from the solution side. ( SN1 might be favored over SN2 ; reactivities different from bulk) • Typical monolayer thicknesses of 0.5 nm to 5 nm. • Typical surface areas of 0.20 nm2 per molecule, 5 1014 molecules per cm2. • At a mass of 400 g/mol, 1 cm2 of a densely packed monolayer corresponds to 0.33 µg of material. • 5g (semi-preparative scale), would cover an area of 1500 m2. • Monomolecular layers of polymer may be thinner and less dense and typically consist of 0.1 to 1.5 mg of material per 1 m2. • Less than 0.02 mg for chemical analysis and physical characterization Advantage: We only need tiny amounts from colleagues doing synthesis Institut Charles Sadron 4 Build-to-Order Assembled Films Build-to-Order (BTO) is the capability to quickly build standard or mass-customized products upon receipt of spontaneous orders without forecasts. Layer-by-Layer assembly allows to design functional surfaces and surface-based nano-devices in a "build-to-order" fashion. It exceeds simple self-organization under equilibrium conditions by making it possible to arrange many different materials at will with nanoscale precision. Institut Charles Sadron 5 The multilayer films that can do everything . Pierre Schaaf, Gero Decher, Jean-Claude Voegel La Recherche, No. 389, SEPT. -
Gelation-Driven Component Selection in the Generation of Constitutional Dynamic Hydrogels Based on Guanine-Quartet Formation
Gelation-driven component selection in the generation of constitutional dynamic hydrogels based on guanine-quartet formation Nampally Sreenivasachary and Jean-Marie Lehn* Laboratoire de Chimie Supramole´culaire, Institut de Science et d’Inge´nierie Supramole´culaires (ISIS), Universite´Louis Pasteur, 8 Alle´e Gaspard Monge, BP 70028, 67083 Strasbourg Cedex, France Contributed by Jean-Marie Lehn, March 1, 2005 The guanosine hydrazide 1 yields a stable supramolecular hydrogel Such processes form the basis of the recently developed dynamic based on the formation of a guanine quartet (G-quartet) in pres- combinatorial chemistry (5, 6), in which molecular recognition ence of metal cations. The effect of various parameters (concen- events have been implemented toward the generation of optimal tration, nature of metal ion, and temperature) on the properties of binding agents toward artificial or biological (7) molecular recep- this gel has been studied. Proton NMR spectroscopy is shown to tors through a target-driven shift in the distribution of the library allow a molecular characterization of the gelation process. Hydra- constituents toward the best binder(s). Changes in library constit- zide 1 and its assemblies can be reversibly decorated by acylhy- uents may also be caused by redistribution of components induced drazone formation with various aldehydes, resulting in formation by metal ion binding (8, 9) or environmental factors such as of highly viscous dynamic hydrogels. When a mixture of aldehydes temperature and pH (N. Giuseppone and J.-M.L., unpublished is used, the dynamic system selects the aldehyde that leads to the data). most stable gel. Mixing hydrazides 1, 9 and aldehydes 6, 8 in 1:1:1:1 The amplification of a given constituent of a CDL under the ratio generated a constitutional dynamic library containing the pressure of a self-organization process, such as the formation of an four acylhydrazone derivatives A, B, C, and D. -
ADVISORY NOTE Strasbourg, France, October 8Th 2009
ADVISORY NOTE Strasbourg, France, October 8th 2009 Details on SHIP-In R&D project revealed, a world-class project for French Research supported by the Alsace BioValley Cluster The SHIP-In research-and-development project has a single goal: developing new and innovative cellular systems for the biopharmaceutical industry. It received the label of the Alsace BioValley cluster in Alsace, France, in November 2008 and is co-sponsored by France’s Cancer Bio Santé and Medicen research poles. The pharmaceutical industry’s development of new therapeutic molecules requires the development and utilization of experimental cellular models that are both efficient and reliable. For a long time, the only possibility was to use stem cells extracted from human embryos. Apart from the difficulty of ensuring their availability, the use of such cells is also circumscribed by stringent ethical and regulatory constraints, which considerably hamper and slow the discovery of new medicines. Today, a new scientific approach offers an alternative to the use of embryonic stem cells, which is to start with adult human cells and reprogram them as multi-purpose cells. The SHIP-In project consists in optimizing this new technology to cater for the demands of the biopharmaceutical industry. The aim is to provide pharmaceutical and cosmetics companies with an unlimited supply of human cells which meet quality criteria that are not available today. Eventually, SHIP-In should facilitate the discovery of new molecules and generally speed up the therapeutic innovation process. “SHIP-In presents a unique opportunity for participating in the development of scientific advances that have been unanimously hailed at a world level,” declared Nicolas Carboni, the Director of the Alsace BioValley cluster, a partner in the project. -
A Year at the Cnrs
2017 A YEAR AT THE CNRS in Alsace 2017 A YEAR AT THE CNRS IN ALSACE is a regional addition to the activity report sommaire 6 > 10 11 12 > 13 2017, a year at the CNRS THE LIVING WORLD SOCIÉTÉSSOCIETIES MATIÈREMATTER CNRS délégation Alsace 23 rue du Lœss - BP 20 67037 Strasbourg cedex 03 88 10 63 01 2 > 3 2017 in figures www.alsace.cnrs.fr 3 Editorial Patrice Soullie, Publisher Antoine Petit Regional Delegate Editorial director Patrice Soullie Chief editor Céline Delalex-Bindner Scientific committee Dominique Badariotti Frédéric Leroux 4 > 5 Rémi Barillon Frédéric Masson Highlights Christine Brunel Sylviane Muller Pierre-Alain Duc Jean-Serge Rémy Vincente Fortier Vincent Roucoules 18 > 19 Jean-Luc Galzi Bertrand Séraphin Science without borders Christian Gauthier Coordination, writing and iconography William Rowe-Pirra Layout and realisation Olivier Fély 20 Graphic design Céline Hein List of laboratories > Acknowledgements : , 14 15 Anne Bresson Pascaline Toutois 1614 17 Photo de couverture : Cover page: An artistic interpretation of the SAGA complex emerging from the nucleoplasmic sea while 21 grabbing a chromatin thread. Glossary ENGINEERING AND EARTHTERRE AND ET © Jonathon Broughton THE UNIVERSE Table of contents pictures : © CNRS Photothèque DIGITAL SCIENCES ENVIRONNEMENTENVIRONMENT Download this document online at : www.alsace.cnrs.fr | French version available Legal deposit : september 2018 - ISSN : 2270-4876 ÉCO VALO This pictogram indicates that the CNRS is economically involved. A number of facts published in this report, results of scientific equipment*, came to be thanks to the support of the European Union, the Région Grand Est, the Conseils departmentaux du Bas-Rhin et du Haut-Rhin, the Eurométropole de Strasbourg and the Mulhouse Alsace Agglomeration, Somes words are defined as well as numerous nonprofit partners. -
1 Layer-By-Layer Assembly (Putting Molecules to Work) Gero Decher
j1 1 Layer-by-Layer Assembly (Putting Molecules to Work) Gero Decher 1.1 The Whole is More than the Sum of its Parts The properties of a material arise from the structural arrangement of its constituents and their dynamics. In nature, a hierarchical organization assures that a required property of a material is realized with a minimum of constituents and a minimum of complexity through processes of evolutionary selection. In the living world functional entities exist on any length scale ranging from atoms to whole organisms, complex properties of biological materials such as cellular life emerging at the upper end of the nanoscale (Figure 1.1). Chemistry, Physics and Materials Science are increasingly approaching maturity on the molecular and macroscopic length scales, shifting importance toward new nanoscale materials and nanoorganized systems. New materials properties, a pre- requisite for responding to the emerging problems of the world population, will require materials design at the nanoscale, forcing the development of new multi- material nanocomposites. In complex systems, new properties appear that are not observed for each individual component. While it is trivial that electrons and nuclei form atoms (sub-Angstrom scale), that atoms form molecules (Angstrom scale) or that monomers can be transformed into polymers (early nanometer scale), we are just beginning to explore the potential of supramolecular assemblies of multifunctional objects. Figure 1.1 summarizes how complex materials properties evolve hierarchically over a length scale of several orders of magnitude. 1.2 From Self-Assembly to Directed Assembly Imagine a self-assembly experiment involving several different chemical species and obtaining equilibrium. -
Multiple and Time-Scheduled in Situ DNA Delivery Mediated by ß
Multiple and time-scheduled in situ DNA delivery mediated by -cyclodextrin embedded in a polyelectrolyte multilayer N. Jessel*†, M. Oulad-Abdelghani‡, F. Meyer*, P. Lavalle*, Y. Haıˆkel*, P. Schaaf§, and J.-C. Voegel* *Institut National de la Sante´et de la Recherche Me´dicale (INSERM), Unite´595, Faculte´deMe´ decine, 11 Rue Humann, 67085 Strasbourg Cedex, France and Faculte´de Chirurgie Dentaire de l’Universite´Louis Pasteur (ULP), 67000 Strasbourg Cedex, France; ‡Institut de Ge´ne´ tique et de Biologie Mole´culaire et Cellulaire (IGBMC), Institut Clinique de la Souris (ICS), Centre National de la Recherche Scientifique (CNRS)͞INSERM͞ULP, Colle`ge de France, BP10142, 67404 Strasbourg, France; and §Institut Charles Sadron (CNRS͞ULP), 6 Rue Boussingault, 67083 Strasbourg Cedex, France Edited by Pierre Chambon, Institut de Ge´ne´ tique et de Biologie Mole´culaire et Cellulaire, Strasbourg, France, and approved March 17, 2006 (received for review September 21, 2005) The basic premise of gene therapy is that genes can be used to iting specific properties in terms of control of cell activation produce in situ therapeutic proteins. The controlled delivery of (8–11) and may also play a role in the development of local drug DNA complexes from biomaterials offers the potential to enhance delivery systems (12). Peptides and proteins, chemically bound, gene transfer by maintaining an elevated concentration of DNA adsorbed, or embedded in LBL films, have been shown to retain within the cellular microenvironment. Immobilization of the DNA their biological activities (14–16). Cyclodextrins (CDs) consti- to the substrate to which cells adhere maintains the DNA in the cell tute a group of cyclic oligosaccharides that have been shown to microenvironment for subsequent cellular internalization. -
Southern Brazilian Journal of Chemistry
1 /-, C'J l~N(/'(J SOUTHERN BRAZILIAN JOURNAL OF CHEMISTRY ISSN 0104-5431 \ "- I '\i rt· R '\i \ f IO~ A I. FOR l \ 1 I- 0 R ll H R :\ P II) PI IH I< \ fl O ~ OJ- ORl(,I'\ \I SCIF"ITIFI( \Rl l(LFS DFALI'\(, \\ ITII CIU '\.ll~d R\ \ '°' D R I· L \ ff D I ~ I t RD IS ( I PI I r\i A R \ -\ R f. \ S ~l '.\1BER :\lNFlEF'\ I) f, ( • \ 1HE R 2 0 1 I EDITOR LA VINEL G. IONESCU, SCIENCO, Consultoria Cientifka, Viamao, RS, BRA.SIL ASSISTANT EDITOR LUIS ALCIDES BRANDINI DE BONI, Tchequimica LTDA, Porto Alegre, RS. Brasil. EDITORIAL BOARD F ARUK NOME AGUILERA, Departamento de Quimica, Universidade FederaJ de Santa Catarina, Florian6polis, SC, Brasil D. BALASlJBRAMANIAN, Centre for Cellular and Molecular Biology, Hyderabad, INDIA HECTOR E. BERTORELLO, Departamento de Quimica Organica, Facultad de Ciencias Quimicas, Universidad Nacional de Cordoba, Cordoba, ARGENTINA AECIO P. CHAGAS, Instituto de Quimica, UNICAMP, Campinas, SP, BRASIL JUAN JOSE COSA, Departamento de Quimica y Fisica, Facultad de Ciencias Exactas. Universidad Nacional de Rio Cuarto, Rio Cuarto, ARGENTINA GLENN A. CROSBY, Department of Chemistry, Washington State University, Pullman, WA, USA VITTORIO DEGIORGIO, Dipartimento di Elettronica, Sezione di Fisica Applicata, Universita di Pavia, Pavia IT ALIA JOSE C. TEIXEIRA DIAS, Departamento de Quimica, Universidade de Coimbra, Coimbra, PORTUGAL OMAR A. EL SEOUD, Instituto de Quimica, Universidade de Sao Paulo, Sao Paulo, SP, BRASIL FERNANDO GALEMBECK, Instituto de Quimica, UNICAMP, Campinas, SP, BRASIL NISSIM GARTI, Casali Institute of Applied Science, Hebrew University of Jerusalem, Jerusalem, ISRAEL GASPAR GONZALEZ, Centro de Pesquisa, CENPES-PETROBRAS, Ilha do Fundao, Rio de Janeiro, RJ , BRASIL YOSHITAKA GUSHIKEM, Instituto de Quimica, UNICAMP, Campinas, SP, BRASIL WILLIAM HASE, Department of Chemistry, Texas Tech University, Lubbock, Texas, USA I.