Relevant bibliographies by topics / Langmuir-Blodgett technology

Academic literature on the topic 'Langmuir-Blodgett technology'

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Published: 30 May 2022
Last updated: 31 May 2022

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Journal articles on the topic "Langmuir-Blodgett technology"

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Krull, Ulrich J., Michael Thompson, and Hector E. Wong. "Simple instrumentation for Langmuir-Blodgett technology." Analyst 110, no. 11 (1985): 1299. http://dx.doi.org/10.1039/an9851001299.

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Brown, R. Stephen, and Ulrich J. Krull. "Automation of simple instrumentation for Langmuir-Blodgett technology." Analyst 112, no. 8 (1987): 1165. http://dx.doi.org/10.1039/an9871201165.

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MUKHOPADHYAY, S., and A. K. RAY. "Structural studies of Langmuir-Blodgett films: technology and analysis." International Journal of Electronics 73, no. 5 (November 1992): 1055–58. http://dx.doi.org/10.1080/00207219208925767.

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Fiol, Catherine, Jean-Marc Valleton, Norbert Delpire, Gérard Barbey, André Barraud, and Annie Ruaudel-Teixier. "Elaboration of a glucose biosensor based on Langmuir-Blodgett technology." Thin Solid Films 210-211 (April 1992): 489–91. http://dx.doi.org/10.1016/0040-6090(92)90321-2.

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Shibata, Masaaki, Futao Kaneko, Masatoshi Aketagawa, and Satoshi Kobayashi. "Reversible color-phase transitions of langmuir-blodgett polydiacetylene films." Electrical Engineering in Japan 109, no. 2 (March 1989): 33–41. http://dx.doi.org/10.1002/eej.4391090205.

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Periasamy, Vengadesh, Muhammad Musoddiq Jaafar, Karthikeyan Chandrasekaran, Sara Talebi, Fong Lee Ng, Siew Moi Phang, Georgepeter Gnana kumar, and Mitsumasa Iwamoto. "Langmuir–Blodgett Graphene-Based Films for Algal Biophotovoltaic Fuel Cells." Nanomaterials 12, no. 5 (March 2, 2022): 840. http://dx.doi.org/10.3390/nano12050840.

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The prevalence of photosynthesis, as the major natural solar energy transduction mechanism or biophotovoltaics (BPV), has always intrigued mankind. Over the last decades, we have learned to extract this renewable energy through continuously improving solid-state semiconductive devices, such as the photovoltaic solar cell. Direct utilization of plant-based BPVs has, however, been almost impracticable so far. Nevertheless, the electrochemical platform of fuel cells (FCs) relying on redox potentials of algae suspensions or biofilms on functionalized anode materials has in recent years increasingly been demonstrated to produce clean or carbon-negative electrical power generators. Interestingly, these algal BPVs offer unparalleled advantages, including carbon sequestration, bioremediation and biomass harvesting, while producing electricity. The development of high performance and durable BPVs is dependent on upgraded anode materials with electrochemically dynamic nanostructures. However, the current challenges in the optimization of anode materials remain significant barriers towards the development of commercially viable technology. In this context, two-dimensional (2D) graphene-based carbonaceous material has widely been exploited in such FCs due to its flexible surface functionalization properties. Attempts to economically improve power outputs have, however, been futile owing to molecular scale disorders that limit efficient charge coupling for maximum power generation within the anodic films. Recently, Langmuir–Blodgett (LB) film has been substantiated as an efficacious film-forming technique to tackle the above limitations of algal BPVs; however, the aforesaid technology remains vastly untapped in BPVs. An in-depth electromechanistic view of the fabrication of LB films and their electron transference mechanisms is of huge significance for the scalability of BPVs. However, an inclusive review of LB films applicable to BPVs has yet to be undertaken, prohibiting futuristic applications. Consequently, we report an inclusive description of a contextual outline, functional principles, the LB film-formation mechanism, recent endeavors in developing LB films and acute encounters with prevailing BPV anode materials. Furthermore, the research and scale-up challenges relating to LB film-integrated BPVs are presented along with innovative perceptions of how to improve their practicability in scale-up processes.
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TANG, DONGYAN, QIAN FENG, ENYING JIANG, and BAOZHU HE. "FABRICATION AND OPTOELECTRONIC PROPERTIES OF MgxZn1-xO ULTRATHIN FILMS BY LANGMUIR–BLODGETT TECHNOLOGY." Surface Review and Letters 19, no. 04 (July 26, 2012): 1250044. http://dx.doi.org/10.1142/s0218625x12500448.

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By transferring Mg x Zn 1-x O sol and stearic acid onto a hydrophilic silicon wafer or glass plate, the Langmuir–Blodgett (LB) multilayers of Mg x Zn 1-x O (x:0, 0.2, 0.4) were deposited. After calcinations at 350°C for 0.5 h and at 500°C for 3 h, Mg x Zn 1-x O ultrathin films were fabricated. The optimized parameters for monolayer formation and multilayer deposition were determined by the surface pressure-surface (Π-A) area and the transfer coefficient, respectively. The expended areas of stearic acid with Mg x Zn 1-x O sols under Π-A isotherms inferred the interaction of stearic acid with Mg x Zn 1-x O sols during the formation of monolayer at air–water interface. X-ray diffraction (XRD) was used to determine the crystal structures of Mg x Zn 1-x O nanoparticles and ultrathin films. The surface morphologies of Mg x Zn 1-x O ultrathin films were observed by scanning probe microscopy (AFM). And the optoelectronic properties of Mg x Zn 1-x O were detected and discussed based on photoluminescence (PL) spectra.
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Milekhin, Alexander G., Nikolay A. Yeryukov, Larisa L. Sveshnikova, Tatyana A. Duda, Dmitry Yu Protasov, Anton K. Gutakovskii, Stepan A. Batsanov, et al. "CdZnS quantum dots formed by the Langmuir–Blodgett technique." Journal of Vacuum Science & Technology B, Nanotechnology and Microelectronics: Materials, Processing, Measurement, and Phenomena 31, no. 4 (July 2013): 04D109. http://dx.doi.org/10.1116/1.4810782.

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Bauman, Danuta, Robert Hertmanowski, Kamila Stefańska, and Roland Stolarski. "The synthesis of novel perylene-like dyes and their aggregation properties in Langmuir and Langmuir–Blodgett films." Dyes and Pigments 91, no. 3 (December 2011): 474–80. http://dx.doi.org/10.1016/j.dyepig.2011.03.032.

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Gorbachev, I. A., A. V. Smirnov, E. S. Shamsutdinova, V. V. Kashin, S. G. Yudin, V. I. Anisimkin, V. V. Kolesov, and I. E. Kuznetsova. "Studying the Structural and Piezoelectric Properties of PVDF Films Obtained Using Langmuir‒Blodgett Technology." Bulletin of the Russian Academy of Sciences: Physics 85, no. 6 (June 2021): 603–7. http://dx.doi.org/10.3103/s1062873821060101.

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Dissertations / Theses on the topic "Langmuir-Blodgett technology"

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Ibrayev, N. Kh, E. V. Seliverstova, A. R. Tencurina, А. А. Ischenko, and А. Yu Shargaeva. "Preparation and Properties of Nanofilms Based on Polymethine Dyes by Langmuir-Blodgett Technology." Thesis, Sumy State University, 2013. http://essuir.sumdu.edu.ua/handle/123456789/35155.

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A study of physico-chemical properties of monomolecular layers of amphiphilic cationic polymethine dye - thiacarbocyanine on the surface of the water subphase and the conditions of obtaining of Langmuir- Blodgett (LB) films are presented. The value of area, occupied by one molecule of the dye in different states of monolayer was defined. The spectral-luminescent properties of cationic polymethine dye was studied. An excimer fluorescence in LB films was revealed. It was shown, that in LB films, unlike solutions excimer not forms from monomers, but it forms from dimers of dyes. A possible mechanism of their formation was considered. When you are citing the document, use the following link http://essuir.sumdu.edu.ua/handle/123456789/35155
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Sushko, O. A., О. М. Bilash, and M. M. Rozhitskii. "Nanophotonic method of organic carcinogens detection in water objects." Thesis, Technische Universität Ilmenau, 2012. http://openarchive.nure.ua/handle/document/8867.

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Polycyclic aromatic hydrocarbons (PAHs) are ubiquitous environmental agents commonly believed to contribute significantly to human cancers pathologies. PAHs are formed in the process of incomplete combustion of organic material and are found widely in the environment, for example, in water, food, soil etc. so human exposure to PAHs is unavoidable. Like many other carcinogens, polycyclic aromatic hydrocarbons are metabolized enzymatically to various metabolites, of which some are highly reaction active. One of the most dangerous organic PAHs carcinogens is benzo[a]pyrene (BP). There are known methods for PAHs detection in water objects, such as chromatography, immuno-chemical, biological and chemical ones. However, they have several disadvantages, including high cost, duration and complexity of the analysis procedure, high detection limit, low selectivity and some others. So at present a development of new methods of PAHs detection based on modern technologies and materials such as nanotechologies and nanomaterials is a rather relevant and important task.
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Naszályi, Nagy Lívia. "Preparation and characterization of functional nanostructured thin layers composed of silica, ZnO and core/shell silica/ZnO particles." Montpellier 2, 2008. http://www.theses.fr/2008MON20050.

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Sardone, Laura. "Nanostructured molecular films for functional applications." Université Louis Pasteur (Strasbourg) (1971-2008), 2005. http://www.theses.fr/2005STR13007.

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Cette thèse décrit l'étude de différentes méthodologies qui ont été utilisées pour contrôler l'assemblage de trois systèmes moléculaires sur des surfaces, afin de former des structures supramoléculaire hautement ordonnées à l'échelle nanoscopique et microscopique. Les structures de couches minces ont été préliminairement étudiées par microscopie à force atomique (AFM) à l'interface solide-air. La première partie de la thèse porte sur la technique de préparation de couches minces Langmuir-Blodgett (LB). Cette technique permet d'obtenir une croissance latérale de monocouche orientée sur un substrat de mica et ce, à partir de molécules amphiphiles possédant une queue hydrophobe simple ou double. Des monocouches ordonnées ont été réalisées suivant deux méthodes différentes. La première méthode consiste à exploiter le phénomène d'instabilité lié au transfert de molécules sur des substrats dans le procédé Langmuir-Blodgett (LB), ce qui permet de générer des canaux périodiques de taille nanométrique dans le cas de monocouche de dimyristoyl-phosphatidylcholine (DMPC) transférée sur un substrat de mica. La seconde méthode utilisée consiste à utiliser des molécules amphiphiles possédant de grosses têtes amphiphiles interagissant fortement entre elles. L'utilisation des molécules de palmitate de quercetine (QP) ont permis l'obtention de structures supramoléculaires de type fibre et ceci dans des domaines micrométriques. Les images AFM (mode tapping) de films mixtes montrent que les fibres adoptent une conformation courbée conduisant à de nouveaux types de domaines en forme de spirale. Les résultats obtenus ouvrent de nouvelles perspectives pour l'utilisation de films LB comme outil permettant d'organiser des monocouches a plusieurs composants avec un haut degré de précision. La seconde partie de la thèse est consacrée à l'autoassemblage, sur des surfaces, d'une nouvelle classe de système macromoléculaire, des polyrotaxanes conjugués entoures par des cyclodextrines, dans le but d'optimiser les performances des LEDs basés sur ces architectures complexes. En particulier la morphologie de surface des mélanges de poly(4,4'-diphenylenevinylene) PDV, soluble dans l'eau, et de leur forme " rotaxane " -CD-PDV, avec du poly(ethylene oxyde) PEO, déposés par spin coating a été étudié par AFM en mode tapping. Cette dernière technique a permis de révéler l'existence d'un processus de reconnaissance interfacial. Ce phénomène a été mis en évidence par l'absence de ségrégation de phase ainsi que par l'ordre structural induit par le choix du substrat. Ceci démontre la bonne miscibilité des deux constituants hydrophiles, comme le confirment les mesures de luminescence des films et des dispositifs intégrant ces systèmes. Par ailleurs, des analyses AFM effectuées sur films d' epousseur " submonolayer " de polyrotaxane à base de poly-para-phenylene (-CD-PPP) seul ou mélangé avec du PEO, démontre que l'interaction entre les deux composants a lieu à l'échelle moléculaire. Au contraire, pour les mélanges de PEO avec des polymères conjugués solubles dans des solvants organique, comme le poly(9,9'-dioctylfluorene-alt-benzothiadiazole) F8BT ou des CD-polyrotaxanes à base de polyfluorene alkylé, on observe des structures de surface qui indique des séparations de phases. La dernière partie de la thèse traite de la création de nanojunctions d'hybrides organométalliques, qui sont les composants de base pour de futures applications dans le domaine de la nanoélectronique. Ce qui nécessite à la fois la synthèse de structures moléculaires auto assemblées (approche bottom-up) et la fabrication de nanogaps métalliques par des méthodes de lithographie (top-down). L'auto assemblage d'un gélifiant de faible poids moléculaire, le cyclohexane trisamide, en structure colonnaire via des liaisons hydrogènes a été étudié sur des films préparés par drop casting. Le but de cette étude était d'utiliser un champ électrique (DC) pour orienter les fibres entres deux nanoélectrodes. Le champ électrique a été appliqué entre deux électrodes en or fabriquées sur un wafer de silicone à l'aide d'un faisceau d'ions focalisé (FIB). Bien que les fibres tendent à former des superstructures, une faible proportion de ces architectures s'oriente convenablement lors de l'application du champ électrique. Les résultats décrit dans cette thèse montrent qu'il est important de pouvoir contrôler des interactions intramoléculaires ainsi qu'intermoléculaire, sans oublier les interactions spécifique au surfaces afin de pouvoir piloter l'autoassemblage sur des surfaces solides et ainsi créer des architectures nanométriques pré-programmées ayant des fonctions bien définies. De plus, il a été démontré qu'une approche supramoléculaire représente une voie possible vers la fabrication de prototypes de dispositifs pour l'électronique moléculaire avec des performances améliores
In this thesis different methodologies have been used to drive the assembly at surfaces of three different (macro)molecular systems towards highly ordered supramolecular nanoscopic and microscopic structures. The structures of the thin films have been studied at the solid-air interface making use primarily of Scanning Force Microscopy (SFM). The first part of the thesis was focused on the use of the Langmuir-Blodgett (LB) technique to grow laterally ordered monolayers on mica from amphiphilic molecules having either a double or a single hydrophobic tail. Ordered monolayers were produced using two different strategies. The former exploits instability phenomena connected to the LB transfer and allows the generation of periodic nanometric channels, in dimyristoyl-phosphatidylcholine (DMPC) monolayers transferred to mica. The latter strategy consists of assembling amphiphiles having large and strongly mutually interacting heads. In this case, quercetin palmitate (QP) molecules were used to build up micrometric domains of supramolecular fiber-like structures. In the mixed films, the nanoscopic fibers were observed by tapping mode SFM to adopt a curved conformation and wrap up, leading to novel spiral-like domains. The results obtained open new perspectives to the use of LB as a tool for nanopatterning (multicomponents) monolayers with a high degree of precision. The second part of the thesis was devoted to self-assembly at surfaces of a new class of supramolecular system, based on cyclodextrin-threaded conjugated polyrotaxanes, with the final aim of optimizing the performance of LEDs based on these complex architectures. In particular the surface morphology of blends of water soluble poly(4,4'-diphenylenevinylene), PDV and of the correspondent rotaxinated form -CD-PDV, with poly(ethylene oxide), PEO, grown by spin-coating was explored by non-contact SFM. The SFM analysis revealed the occurrence of an interfacial recognition process, which is evidenced by a structural order induced by the chosen substrate, and the absence of phase segregation. This provides evidence for a good miscibility of the two hydrophilic components, as supported by luminescence data from films and devices constituted by those systems. This was also proved by the SFM analysis on sub-monolayer thick films of poly-para-phenylene based polyrotaxane (-CD-PPP) naked and blended with PEO, highlighting the interaction between the two components at single molecule level. Significant surface structures, indicative of phase separations, were instead observed when blending PEO with organic-solvent soluble conjugated polymers, such as poly(9,9'-dioctylfluorene-alt-benzothiadiazole) F8BT, and alkylated polyfluorene based CD-polyrotaxanes. The third part was addressed to the tailoring of hybrid organic-metallic nanojunctions, which are key components for future applications in the field of nanoelectronics. This required the combination of the self-assembly of molecular structures (bottom-up approach) with micro- and nano-fabrication for the production of metallic nanogaps with lithographic methods (top-down). The self-assembly behavior of a low molecular weight gelators, cyclohexane trisamide which self-associate into columnar structures through hydrogen bonding, was studied on films prepared by drop-casting. The goal was to use a DC electric field to place the well-defined ordered supramolecular arrangement in between two facing Au nanoelectrodes, supported on a silicon wafer, nanofabricated by means of Focused Ion Beam. Although the fibers tend to intercoil into super-structures, a weak propensity of these architectures to orient as a consequence of the applied electric field was found. The results described in this thesis reveal that it is of prime importance to achieve a full control over the interplay of intra-molecular as well as inter-molecular and interfacial interactions in order to drive the nanoconstruction at solid surfaces towards pre-programmed architectures with given properties. Moreover it is demonstrated that the supramolecular approach represents a successful route to fabricate prototype of molecular electronics devices with improved performance
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Rajoua, Khalil. "Capteurs résistifs de dihydrogène H2 à base d’assemblages de nanostructures discontinues organisées." Thesis, Montpellier 2, 2014. http://www.theses.fr/2014MON20150/document.

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Les contextes mondiaux énergétiques, climatiques et économiques actuels évoluent de manières telles que le dihydrogène H2 prend une place de plus en plus importante en tant que combustible et vecteur énergétique. Le dihydrogène est un gaz incolore, inodore et non-toxique donc indécelable par les sens humains, mais il est extrêmement inflammable et explosif. De plus, H2 est caractérisé par un domaine d'explosivité très large, de 4 % à 75 % de H2 dans l'air. L'objet de ce travail de thèse a donc été de préparer des capteurs de sécurité ou de quantification originaux et ayant des performances accrues pour la détection de H2. Les capteurs préparés sont de types résistifs et les métaux sensibles utilisés sont le palladium et le platine. Afin d'améliorer les performances de détection de ces capteurs à dihydrogène, plusieurs morphologies de couches sensibles ont été conçues : des monocouches organisées à 2 dimensions de nanoparticules cœurs-coquilles Pd@Au et Pt@Au formées par la méthode de Langmuir-Blodgett ou immobilisés sur les substrats par un agent de couplage de type silane (mercaptopropyltrimethoxysilane), des dépôts physiques à 2 dimensions et des films de nanoparticules à 3 dimensions. Selon la morphologie de la couche préparée et le type de métal sensible utilisé, divers mécanismes de détection ont été mis en évidence et diverses performances de détection ont été observées (type et amplitude de réponse, gamme de détection, temps de réponse et de retour,...). Les modèles de Fuchs-Sondheimer et Mayadas-Shatzkes d'une part, et un modèle de percolation par la création de chemins de conduction d'autre part, ont permis d'expliquer les variations de résistivité électrique des couches sensibles à base respectivement de platine et de palladium lors de l'exposition à l'hydrogène
Hydrogen takes is foreseen as a generalized fuel and energy carrier. It is a colorless, odorless and non-toxic gas, and therefore it is undetectable by the human senses. Hydrogen has a severe drawback as it is an extremely flammable and explosive gas. Moreover, H2 has a wide explosive range, from 4 to 75 % H2 in air. Therefore, the aim of this PhD work was to develop safety and concentration sensors with enhanced performances. Resistive sensing layers were designed on several morphologies and sensing materials : 2D Langmuir-Blodgett organized monolayers of core-shell Pd@Au or Pt@Au nanoparticles, immobilized Pd@Au monolayer grafted through a self assembled monolayer, evaporated 2D metal films of Pt or Pd, and 3D platinum nanoparticles arrays. According to the sensing layer morphology and sensing metal, numerous sensing mechanisms and performances were demonstrated (response type and amplitude, sensing range, response and recovery times,…). Fuchs-Sondheimer and Mayadas-Shatzkes models on the one hand, and a percolation model on the other, allowed the origin of electrical resistance changes to be pointed out, respectively for platinum and palladium sensing layers
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Rouster, Paul. "Layer-by-Layer modification of nanofiltration membranes : development of a regenerable separation layer." Thesis, Strasbourg, 2015. http://www.theses.fr/2015STRAE011.

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Le manque croissant en eau potable dans le monde est un problème d’envergure pour la population. La filtration par des membranes des eaux usées, insalubres ou la désalination apparaît comme une alternative viable pour le futur. La modification de membranes d’ultrafiltration par l’assemblage couche-par-couche permet d’obtenir des propriétés de nanofiltration en contrôlant avec une précision nanométrique l’épaisseur de la couche active de séparation déposée. Lors de cette thèse, nous avons étudié la construction de la couche de séparation ainsi que sa régénérabilité. Pour ce faire, nous avons développé des surfaces « membrane-like » pour étudier la construction sur des surfaces possédant des fonctions chimiques similaires à l’applicative. Par ailleurs, le temps de déposition a aussi été investigué afin de déterminer si les propriétés de séparation des membranes modifiées dépendaient du nombre de couches déposé ou du temps de dépôt. Les membranes ainsi développées présentent une couche de séparation régénérable et des propriétés de nanofiltration
The increasing lack of drinking water in the world is of major concern for the population. Membrane filtration of brackish water, seawater appears to be a viable alternative for the future. Nanofiltration membranes can be obtained by modifying ultrafiltration membranes by the Layer-by-Layer (LbL) technique. This method also the deposition of an ultra-thin separation layer with a nanoscale precision and with tunable properties. During this PhD thesis, the build-up and the regenerability of the separation layer was investigated. For this purpose, mimicry surfaces were developed in order to study the LbL-assembly on surfaces presenting similar chemical functions as the applicative one. In addition, the deposition time was also investigated in order to determine if the separation properties of the membrane depend on the number of deposited layers or on the coating time. The developed membranes possessed a regenerable separation layer presenting nanofiltration properties
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Toulemon, Delphine. "Stratégies d'assemblage par chimie "click" de nanoparticules magnétiques sur des surfaces fonctionnalisées." Phd thesis, Université de Strasbourg, 2013. http://tel.archives-ouvertes.fr/tel-01064023.

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Cette thèse présente une nouvelle méthode d'assemblage de nanoparticules (NPs) magnétiques par une approche de chimie " click " sur des surfaces fonctionnalisées par des molécules organiques (self-assembled monolayers, SAMs). Le contrôle précis de la nanostructure des assemblages permet d'étudier les propriétés magnétiques collectives des NPs modulées par les interactions dipolaires. Un état de l'art des travaux décrits dans la littérature est présenté sur la synthèse de NPs d'oxydes métalliques, les enjeux et méthodes d'assemblage de NPs magnétiques ainsi que les propriétés magnétiques des NPs. Plusieurs types de NPs d'oxydes de fer présentant différentes tailles, morphologies (sphère, cube, tétrapode) et structures internes (coeur-coquille) sont synthétisés par la méthode de décomposition thermique La méthode développée d'assemblage des NPs consiste en une réaction dite " Copper (I) catalyzed alkyne-azide cycloaddition " (CuAAC), basée sur les interactions spécifiques entre des groupes alcyne et azoture présents à la surface des NPs et des SAMs. La fonctionnalisation des NPs et la préparation des SAMs sont également décrites. En modulant les conditions opératoires lors de la réaction d'assemblage, différentes nanostructures (films denses, NPs spatialement isolées ou chaînes de NPs) sont obtenues dans le but d'étudier les propriétés magnétiques collectives des NPs dans les assemblages. Un effet de la distance interparticule et de la mise en forme des NPs en 2D sur les interactions dipolaires sont mis en évidence. La réaction de click pour l'assemblage de NPs est ensuite perfectionnée, d'une part, la diminution du temps de la réaction d'assemblage en présence de radiations microondes, et d'autre part la préparation de films multicouches de NPs " one-pot " en contrôlant la réaction de click par électrochimie. Enfin des dispositifs magnéto-résistifs sont élaborés en déposant des assemblages denses de nanoparticules entre deux électrodes distantes d'une centaine de nanomètres.
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Lee, Shin, and 李欣. "The study on the immobilization of glucose oxidase using the Langmuir-Blodgett technology." Thesis, 2007. http://ndltd.ncl.edu.tw/handle/78196738320358415953.

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碩士
國立成功大學
化學工程學系碩博士班
95
In this study , the main theme is to examine the relationship between the mix-monolayer of stearic acid (SA) and octadecylamine (ODA), and the glucose oxidase (GOx) in subphase . Because the exist of monolayers , there are two equilibrium stage in the adsorption curve for GOx . If we changed the composition of monolayer , the rate of reaching the equilibrium stage and the equilibrium pressure of the second stage also changed. Isotherm and adsorption curve show that the quantity of adsorbed GOx in the first equilibrium stage is more than that the second equilibrium stage . According to the results of relaxation and hysteresis , the adsorption of GOx does not attain the saturated status at the first equilibrium stage . However , the adsorption behavior of GOx at the second equilibrium stage seems to attain the saturated status . The figure of relaxation also interepted that the exist of a monolayer indeed stabilize GOx molecules on air/water interface . We also use cyclic voltammetry to determine the electrochemical activity of the immobile GOx . The curve of open circular potential versus time reveals the catalytic reaction of enzyme ideed happened . Furthermore the response current is affected by the concerntration of glucose in electrolyte and the number of complex on working electrode .
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Chiou, Lin-Jiun, and 邱麟鈞. "Optical properties of metallic coating layers on ordered polystyrene particle films via Langmuir‐Blodgett technology." Thesis, 2011. http://ndltd.ncl.edu.tw/handle/79014901238649495307.

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碩士
中原大學
應用物理研究所
97
We constructed close-packed monolayer films through　Langmuir-Blodgett technology with different sizes of colloidal　polystyrene (PS) particles. In order to keep away from obtaining split-up polystyrene particle films and acquire large ordered area　of films, particles surfaces were functionalized hydrophobically.Then, the monolayer films were coated with 50 nm silver by thermal evaporation. By taking into account experimental data　from the optical transmittance, we studied the optical behavior.By using xenon light source with different angles of incidence, the relation between the resonance absorption and the differenceparticle sizes was observed. 　　The optical transmittance spectra show the localized surfaceplasmon effect, and the　individual peaks are blue shifted　with the particle size getting smaller. According to the Maxwell’s　dispersion formula, the result did not match as expected.It is a more complicated structures than the subwave-length hole　arrays.
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許郁榮. "A study of the preparation technology of merocyanine organic dyes and fatty acids Langmuir-Blodgett films." Thesis, 1988. http://ndltd.ncl.edu.tw/handle/40753290078723348467.

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Book chapters on the topic "Langmuir-Blodgett technology"

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Barraud, A. "Microlithography with Monolayers and Langmuir-Blodgett Films." In Surface and Colloid Science in Computer Technology, 343–51. Boston, MA: Springer US, 1987. http://dx.doi.org/10.1007/978-1-4613-1905-4_21.

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Pomerantz, Melvin. "Experiments on Langmuir-Blodgett Magnetic Monolayers of Manganese Stearate." In Surface and Colloid Science in Computer Technology, 361–73. Boston, MA: Springer US, 1987. http://dx.doi.org/10.1007/978-1-4613-1905-4_23.

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Krull, U. J., M. Thompson, and H. E. Wong. "Langmuir-Blodgett Technology and Receptor Action in Stabilized Lipid Membranes." In ACS Symposium Series, 351–62. Washington, DC: American Chemical Society, 1986. http://dx.doi.org/10.1021/bk-1986-0309.ch021.

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Grieser, Franz, D. Neil Furlong, Robert S. Urquhart, and David J. Elliot. "The Formation and Properties of Nano-Sized Semiconductor Particles in Langmuir-Blodgett Films." In Fine Particles Science and Technology, 733–44. Dordrecht: Springer Netherlands, 1996. http://dx.doi.org/10.1007/978-94-009-0259-6_50.

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Balogh, Débora T., Marystela Ferreira, and Osvaldo N. Oliveira. "Langmuir-Blodgett-Kuhn Multilayer Assemblies: Past, Present, and Future of the LB Technology." In Functional Polymer Films, 113–49. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2011. http://dx.doi.org/10.1002/9783527638482.ch4.

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Krafft, Marie Pierre. "Chapter 7 Highly Fluorinated Langmuir, Langmuir–Blodgett and Gibbs Monolayers." In Interface Science and Technology, 177–91. Elsevier, 2007. http://dx.doi.org/10.1016/s1573-4285(06)14007-7.

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"Wetting Instabilities in Langmuir–Blodgett Film Deposition." In Surfactant Science and Technology, 222–41. CRC Press, 2014. http://dx.doi.org/10.1201/b16802-12.

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Schwartz, D. K. "Langmuir–Blodgett Films, Formation and Structure of." In Encyclopedia of Materials: Science and Technology, 4392–99. Elsevier, 2001. http://dx.doi.org/10.1016/b0-08-043152-6/00769-5.

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"Monolayers, Langmuir-Blodgett Films, and Hybrid LB Films." In Membrane Science and Technology, 137–78. CRC Press, 1992. http://dx.doi.org/10.1201/9781482277203-6.

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Beltsios, K., E. Soterakou, and N. K. Kanellopoulos. "Composite Ceramic Membranes from Langmuir-Blodgett and Self-Assembly Precursors." In Membrane Science and Technology, 417–34. Elsevier, 2000. http://dx.doi.org/10.1016/s0927-5193(00)80018-2.

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Conference papers on the topic "Langmuir-Blodgett technology"

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Mattoso, L. H. C., S. V. Mello, A. Riul, G. D. Telles, and O. N. Oliveira. "Langmuir and Langmuir-Blodgett films of parent polyaniline doped with functionalized acids." In International Conference on Science and Technology of Synthetic Metals. IEEE, 1994. http://dx.doi.org/10.1109/stsm.1994.835767.

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Nakamura, T., G. Yunome, M. Matsumoto, S. Horiuchi, H. Yamochi, G. Saito, H. Isotalo, and H. Stubb. "Metallic transport properties of conducting Langmuir-Blodgett films." In International Conference on Science and Technology of Synthetic Metals. IEEE, 1994. http://dx.doi.org/10.1109/stsm.1994.835626.

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Li, Shuhong, Shihong Ma, Wencheng Wang, Genshui Wang, Xiangjian Meng, Jinglan Sun, and Junhao Chu. "Phase transition in ferroelectric hemicyanine Langmuir-Blodgett multilayers." In Optical Science and Technology, the SPIE 49th Annual Meeting, edited by Randolph E. Longshore and Sivalingam Sivananthan. SPIE, 2004. http://dx.doi.org/10.1117/12.558981.

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Munn, R. W., and M. M. Shabat. "Calculations of nonlinear optical properties of model Langmuir-Blodgett films." In Molecular electronics—Science and Technology. AIP, 1992. http://dx.doi.org/10.1063/1.42657.

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Mattoso, L. H. C., S. V. Mello, O. N. Oliveira, and R. M. Faria. "Doping effect on the fabrication of Langmuir and Langmuir-Blodgett films of poly(0-ethoxyaniline)." In International Conference on Science and Technology of Synthetic Metals. IEEE, 1994. http://dx.doi.org/10.1109/stsm.1994.835780.

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Ikegami, K., S. Kuroda, T. Nakamura, G. Yunome, M. Matsunloto, S. Horiuchi, H. Yamochi, and G. Saito. "ESR study of the Langmuir-Blodgett films containing metallic domains." In International Conference on Science and Technology of Synthetic Metals. IEEE, 1994. http://dx.doi.org/10.1109/stsm.1994.835627.

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Iwamoto, M., and T. Kubota. "Electrical transport and electrostatic properties of polyimide Langmuir-Blodgett films." In International Conference on Science and Technology of Synthetic Metals. IEEE, 1994. http://dx.doi.org/10.1109/stsm.1994.835628.

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Yuan, C. W., C. R. Wu, and Y. Wei. "Template-synthesized AgTCNQ complexes and polypyrrole in Langmuir-Blodgett films." In International Conference on Science and Technology of Synthetic Metals. IEEE, 1994. http://dx.doi.org/10.1109/stsm.1994.835770.

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Kwon, Y. S., D. Y. Kang, and T. Hino. "Diffusion of electron in Langmuir-Blodgett films of MIM structures." In International Conference on Science and Technology of Synthetic Metals. IEEE, 1994. http://dx.doi.org/10.1109/stsm.1994.835783.

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San-Kug Lee, Min-Jong Song, Dong-Myung Shin, Young-Soo Kwon, D. Y. Kang, and Tae Wan Kim. "Thermal annealing effects of n-docosylquinolium-TCNQ Langmuir-Blodgett films." In International Conference on Science and Technology of Synthetic Metals. IEEE, 1994. http://dx.doi.org/10.1109/stsm.1994.835791.

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