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Relevant bibliographies by topics / Langmuir-Blodgett

Academic literature on the topic 'Langmuir-Blodgett'

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Published: 4 June 2021

Last updated: 20 July 2024

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Journal articles on the topic "Langmuir-Blodgett"

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Weis, Martin, Katarína Gmucová, Daniel Haško, and Jarmila Müllerová. "Structural and electronic properties of pentacene/pentacenequinone thin films prepared by Langmuir–Blodgett technique." Collection of Czechoslovak Chemical Communications 74, no. 4 (2009): 565–79. http://dx.doi.org/10.1135/cccc2008210.

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Structural and electronic properties of pentacene/pentacenequinone thin films prepared on various solid-state substrates by the Langmuir–Blodgett technique are reported. Amorphous structure of the prepared films has been proved by XRD measurements. Oxygen-related defects have been identified in the Langmuir–Blodgett films as a consequence of the exposure of pentacene Langmuir layer to air. Crystallization induced by thermal treatment of the prepared amorphous thin films has been observed. Electronic properties of pentacene/ pentacenequinone Langmuir–Blodgett films have been investigated in the contact-less architecture using electrochemical techniques. The energy band diagram of the amorphous pentacene/pentacenequinone Langmuir–Blodgett film on a metallic surface was constructed from the obtained electrochemical data.

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SUGI, Michio. "Langmuir-Blodgett Films." Nihon Kessho Gakkaishi 33, no. 3 (1991): 188–94. http://dx.doi.org/10.5940/jcrsj.33.188.

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Peterson, I. R. "Langmuir-Blodgett films." Journal of Physics D: Applied Physics 23, no. 4 (April 14, 1990): 379–95. http://dx.doi.org/10.1088/0022-3727/23/4/001.

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Kuroda, Shin-ichi, and Michio Sugi. "Langmuir-blodgett films." Kobunshi 36, no. 4 (1987): 266–69. http://dx.doi.org/10.1295/kobunshi.36.266.

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Zasadzinski, J., R. Viswanathan, L. Madsen, J. Garnaes, and D. Schwartz. "Langmuir-Blodgett films." Science 263, no. 5154 (March 25, 1994): 1726–33. http://dx.doi.org/10.1126/science.8134836.

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Agarwal, Vijendra K. "Langmuir‐Blodgett Films." Physics Today 41, no. 6 (June 1988): 40–46. http://dx.doi.org/10.1063/1.881121.

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Lafuente, Carlos, Helene Soyer, Serge Ravaine, Christophe Mingotaud, and Pierre Delhaes. "Magnetic Langmuir-Blodgett Films." Molecular Crystals and Liquid Crystals Science and Technology. Section A. Molecular Crystals and Liquid Crystals 322, no. 1 (November 1998): 91–98. http://dx.doi.org/10.1080/10587259808030205.

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Palto, S., L. Blinov, A. Bune, E. Dubovik, V. Fridkin, N. Petukhova, K. Verkhovskaya, and S. Yudin. "Ferroelectric Langmuir-Blodgett films." Ferroelectrics Letters Section 19, no. 3-4 (May 1995): 65–68. http://dx.doi.org/10.1080/07315179508204276.

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Kim, Franklin, Serena Kwan, Jennifer Akana, and Peidong Yang. "Langmuir−Blodgett Nanorod Assembly." Journal of the American Chemical Society 123, no. 18 (May 2001): 4360–61. http://dx.doi.org/10.1021/ja0059138.

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Schwartz, Daniel K. "Langmuir-Blodgett film structure." Surface Science Reports 27, no. 7-8 (January 1997): 245–334. http://dx.doi.org/10.1016/s0167-5729(97)00003-4.

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Dissertations / Theses on the topic "Langmuir-Blodgett"

1

Colbrook, Richard. "Pyroelectric Langmuir-Blodgett films." Thesis, University of Oxford, 1990. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.257662.

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Júnior, Antonio Riul. "Filmes de Langmuir e Langmuir-Blodgett de Polianilinas." Universidade de São Paulo, 1998. http://www.teses.usp.br/teses/disponiveis/88/88131/tde-03052010-171319/.

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Explorou-se a caracterização de monocamadas e filmes LB de polianilina (PANi), e um oligômero de polianilina, chamado aqui de 16-mero, com estearato de cádmio (CdSt). A análise dos filmes de Langmuir indicou que possivelmente não há mistura em nível molecular da PANi e do 16-mero com CdSt, ainda que a quantidade adicionada em solução de polímero ou oligômero influencie a estabilidade das monocamadas. Utilizou-se UV-vis, FTIR, difração de raios-X, condutividade elétrica, elipsometria, microscopia óptica e potencial de superficie para caracterização dos filmes LB. Os resultados de UV-vis indicaram uma transferência uniforme e ainda que os filmes recém depositados encontram-se desdopados. A análise de FTIR confirma a presença de CdSt nos filmes LB, e o efeito de desdopagem em subfases neutras, corroborando os resultados de UV-vis. A difração de raios-X indica a presença de domínios separados de PANi (e 16-mero) com CdSt nos filmes LB. Resultados elipsométricos indicaram uma espessura por camada em tomo de 25 Å. A excelente uniformidade obtida nos filmes LB mistos foi comprovada pelos resultados de microscopia óptica e potencial de superficie. Esses filmes mistos apresentaram valores de condutividade elétrica em tomo de 10-4 a 10-5 S.cm-1 (van der Pauw), tanto para a PANi quanto para o 16-mero. Investigou-se também o efeito da exposição dos filmes mistos PANi/CdSt aos raios-X. Nota-se um deslocamento para a região do vermelho, na região do visível, nos espectros de UVvis, similar à observada pela dopagem através de ácidos inorgânicos. Verificou-se que os efeitos de umidade da atmosfera de medida são predominantes nesse processo de dopagem. É feita uma análise dos resultados de condutividade elétrica, comparando-os com os encontrados na literatura.
A study has been made of composite Langmuir and Langmuir-Blodgett (LB) films of polyaniline (PANi), and a polyaniline oligomer (l6-mer polyaniline), with cadmium stearate (CdSt). The monolayers studies pointed to a phase separated system containing the polymer (or the 16-mer) and CdSt, with no mixing at the molecular leveI, although the relative contents of PANi and 16-mer in the solution have a strong influence on the monolayer stability. UV-vis, FTIR, X-ray difIraction (XRD), electrical conductivity, ellipsometry, optical microscopy and surface potential measurements were used in the LB film characterization. UV-vis results have shown a uniform transfer, with the as deposited films in the undoped state. FTIR results confirmed the presence of CdSt and undoped polyaniline (and 16-mer) in the transferred LB films, corroborating the UV-vis results. XRD has shown separated domains of CdSt and PANi (l6-mer also) in the LB films. Ellipsometry data indicated a thickness of 25 Å per deposited layer. The high uniformity in these mixed LB films was confirmed by optical microscopy and surface potential measurements. The electrical conductivity was approximately 10-4 to 10-5 S.cm-1 for both PANi and 16-mer. Mixed PANi/CdSt films were also exposed to X-ray irradiation. After a given dose rate there is a red shift in the UV-vis spectra from the 600 nm region to the 800 nm region, similar to the usual acid doping process observed in polyaniline. Humidity effects have a strong influence on the doping process. A comparison is made of the conductivity measurements made here with those reported in the literature.

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Constantino, Carlos José Leopoldo. "Filmes de Langmuir e Langmuir-Blodgett de ligninas." Universidade de São Paulo, 1995. http://www.teses.usp.br/teses/disponiveis/76/76132/tde-18062008-083333/.

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Filmes de Langmuir e Langmuir-Blodgett (LB) foram fabricados a partir de ligninas de bagaço de cana-de-açúcar e da Pinus caribaea hondurensis, extraídas via processo organossolve. Obteve-se nove tipos de lignina de pinus, sendo que cada uma foi extraída com um sol vente diferente, e seis tipos de lignina de cana, as quais passaram por um fracionamento, diminuindo sua polidispersividade. Os filmes de Langmuir foram fabricados sobre subfases de água ultrapura e caracterizados por medidas de pressão e potencial de superfície. Em todos os casos constatou-se a formação de agregados não monomoleculares quando o filme é comprimido além do ponto de colapso, o que é notado pela grande histerese na isoterma pressãoárea. Para ligninas de baixa massa molecular, estruturas estáveis não monomoleculares são formadas antes do colapso. No caso das ligninas menos polidispersas (cana), a massa molecular aumenta linearmente com a área molecular média da lignina. Monocamadas das ligninas de pinus e cana puderam ser transferidas para substratos de vidro, constituindo-se nos primeiros filmes de Langmuir-Blodgett destes materiais. Através do monitoramento da velocidade de imersão e retirada do substrato da subfase pode-se fabricar diferentes tipos de filmes LB, os quais podem ser do tipo Y com a deposição ocorrendo na imersão e retirada do substrato e também dos tipos X e Z se a deposição ocorre preferencialmente na imersão ou retirada do substrato, respectivamente. Os filmes LB foram caracterizados por medidas do potencial de superfície e elipsometria. O potencial de superfície para os filmes de pinus são positivos, enquanto que para os filmes de cana são negativos. Esta inversão de sinal foi surpreendente, pois para as monocamadas os valores de potencial são sempre positivos, tanto para as ligninas de cana como para as de pinus, embora sejam maiores no caso da pinus. A razão para esta inversão é uma contribuição negativa da interface filme/substrato que suplanta a contribuição positiva dos dipolos do filme de lignina de cana. Os dados elipsométricos revelaram que a lignina apresenta um arranjo tridimensional, com muitos espaços vazios e uma espessura em torno de 60 \'angstrom\' por camada.
Langmuir monolayers and Langmuir-Blodgett (LB) films were fabricated from lignins extracted from Pinus caribaea hondurensis and sugar cane bagasse using the organosolv processo Nine types of pinus lignins were obtained by employing different solvents. The lignins of sugar cane bagasse were extracted using only one solvent but the material was fractioned into six fractions according to the molecular sizes. The resulting lignins were then less polydisperse than the pinus lignins. Langmuir monolayers were spread onto ultrapure water subphases and characterized by surface pressure and surface potential measurements. In all cases, non-monomolecular aggregates are formed when the monolayer is compressed beyond the collapse pressure, which is denoted by large hysteresis in pressurearea isotherms. For the low molecular weight lignins, stable multilayer structures are formed even before collapse. In the less polydisperse bagasse lignins, the average area per molecule increases linearly with the molecular weight. Monolayers from both pinus and bagasse lignins could be transferred onto glass substrates, thus forming the first ever reported Langmuir-Blodgett (LB) films of these materials. By controlling the dipping speed one can build-up different types of LB film which can be y-type with deposition occurring in both upstrokes and downstrokes and also Z or x-type if transfer occurs only in the upstrokes or downstrokes, respectively. The deposited LB films were characterized by surface potential and ellipsometric measurements. The surface potential of pinus films is positive whereas that of bagasse lignins is negative. This sign inversion was surprising since the monolayer surface potentials were always positive for all materials, even though they were higher for the Pinus lignins. The reason for the inversion is the negative contribution of the film/substrate interface which surpass the small, positive contribution from the dipole moments in the bagasse lignins. The ellipsometric data showed that the lignin molecules assume a three-dimensional arrangement, even within a single layer. The LB film appears to be a highly porous structure, with a thickness of 60 Á per layer.

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Evans, S. D. "Langmuir-Blodgett superlattices incorporating porphyrins." Thesis, Lancaster University, 1988. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.235169.

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Jones, Carole A. "Pyroelectricity in Langmuir-Blodgett films." Thesis, Durham University, 1987. http://etheses.dur.ac.uk/6784/.

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The fabrication of pyroelectric devices using the Langmuir-Blodgett (LB) technique is described. Studies of a wide range of materials are reported; however, the thesis concentrates on electrical and structural investigations of two specific alternate layer films: 22-tricosenoic acid/l-docosylamine and 22-tricosenoic acid/4-octadecylaniline. The latter system possesses a pyroelectric coefficient of 0.65 nCcm(^-2)K(^-1), representing the largest reported value, to date, for an LB film. The pyroelectric figure of merit (p/e(^1)(_T)) of such films is approximately 0.22 nCcm(^-2)K(^-1), which is comparable with the values for commercially available materials. The difference in pyroelectric coefficient of the two types of alternate layer film is attributed to differences in inter-layer bonding, as revealed by infrared spectroscopy. The dependence of the pyroelectric coefficients on parameters such as film thickness, substrate thickness and temperature is investigated. Structural studies, performed using electron and X-ray diffraction techniques, are also described. These provide information on the orientation of the molecules relative to the substrate and on the d-spacing of the LB films. It is shown that the substrate has a deleterious effect on the responsivity of LB film devices, and studies of films deposited onto different substrate materials indicate that there is a significant piezoelectric ally induced secondary effect contributing to the overall pyroelectric coefficient. This secondary effect is small at low temperatures, but becomes dominant at around 250 K. The results of thermally stimulated discharge experiments indicate that both free charges and dipolar groups are incorporated in the films during deposition, and become tightly bound within the polar structure.

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Christie, P. "Acentric Langmuir-Blodgett film assemblies." Thesis, Durham University, 1985. http://etheses.dur.ac.uk/7128/.

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In recent years there has been considerable interest In the use of Langmuir-Blodgett (LB) films as the basis of active and passive thin film devices. One such application is in room temperature, pyroelectric thermal imaging systems. As the detectivity of these sensors is approximately inversely proportional to thickness, there may be significant advantage in exploiting the ability of the LB process to produce ultra-thin layers. Here we report the use of the LB technique to fabricate molecular assemblies with precisely defined symmetry properties. This has made possible the construction of ultra-thin organic films possessing the spontaneous polarisation necessary for the observation of the pyroelectric effect. Two distinct approaches are adopted to produce the required molecular packing arrangements. The first uses the ability of a novel alternate layer trough to assemble acentric ABAB structures. Various materials are studied for their suitability for alternate layer deposition. The co-deposition of fatty acids and amines produces alternate layer assemblies with a high degree of structural and electrical integrity. The second approach uses a novel polymeric LB film. Polybutadiene (PBD) is observed to deposit in highly asymmetric X-type layers if the transferred monolayer is exposed to u.v. radiation between each deposition step. The structural and electrical properties are characterised. The presence of the unique polar axis associated with pyroelectric materials is investigated using surface potential measurements. Dynamic and quasi-static detection techniques are employed to detect the pyroelectric activity within the assemblies. For the first time pyroelectric activity is observed in "thin" (11 layer) acid/amine assemblies. The pyroelectric coefficient is found to be thickness dependent, increasing for larger numbers of layers; the coefficient for a 99 layer sample is comparable to that of PVDF, a commercially available pyroelectric polymer. The incorporation of LB films into thin PVDF Metal Insulator Metal (MIM) structures is also investigated. The presence of a stable phthalocyanine LB film is shown to increase the electrical breakdown strength of the device. Finally the incorporation of highly polarisable sulphur substitutions into fatty acid LB films is reported. The permittivity is found to increase in proportion to the number of sulphur atoms introduced into the hydrocarbon chain.

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Amiri, M. A. "Optically nonlinear Langmuir Blodgett films." Thesis, Cranfield University, 2003. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.273468.

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Head, David Ian. "Two dimensional Langmuir-Blodgett magnets." Thesis, University of Southampton, 1988. https://eprints.soton.ac.uk/192469/.

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The susceptibility of quasi-two-dimensional magnets formed by the Langmuir-Blodgett deposition of manganese stearate on aluminium foil has been measured at several points between 20 K and 0.4 K. Large area samples of 101 and 11 layers were detected by a SQUID magnetometer. With the magnetic field parallel to the film we deduced an equivalent volume susceptibility of 6.4x10(-3) at 4.2 K. The signals from the multilayers were paramagnetic in nature and no evidence for a transition was found. Unfortunately the signal from a bilayer and monolayer were masked by contaminants on the substrate. The magnetometer used a cold finger to which the sample was attached. This was then moved into the pick-up coil, which was a second order gradiometer capable of cancelling out the signal from the long (150 mm) substrates. The magnetometer was usefully capable of detecting a sample with a moment down to 5x10(-11) Am(2) but vibration noise restricted the magnetic field to below 10 mT, New equations were developed to describe the magnetic signals from a cylindrical magnetised sample within a superconducting shield. They were developed for use on a micro-computer making it possible to simulate the signal from the sample. The tt-A curves for Manganese stearate were also studied. The uncertainty in the measurement of tx using filter papers was studied and estimated to be 2%. The manganese stearate was observed to transfer by Y and forced-Z type dipping.

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Romualdo, Torres Gemma. "Systèmes hybrides en films de Langmuir et Langmuir-Blodgett." Phd thesis, Université Sciences et Technologies - Bordeaux I, 2002. http://tel.archives-ouvertes.fr/tel-00815388.

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Ce travail porte sur la formation et la caractérisation de nouveaux systèmes organiques-inorganiques par l'utilisation de films de Langmuir et de la technique de Langmuir-Blodgett. Plusieurs voies ont ainsi été explorées afin d'obtenir des films minces hybrides aux propriétés multiples, en particulier magnétiques. L'utilisation de l'interaction entre monocouches cationiques et des anions présents en sous-phase a ainsi permis l'organisation de différents polyanions inorganiques en structure lamellaire. Cette stratégie a ensuite été généralisée au cas de colloïdes de Bleu de Prusse, composés bimétalliques étendus. Une large étude (de la préparation à la caractérisation) a été consacrée à ces matériaux mixtes Bleu de Prusse-dérivé amphiphile de Ru(bpy)3 2+. Il a été également montré que la cristallisation du Bleu de Prusse et de ses analogues est favorisée en-dessous des films de Langmuir. Finalement, la coordination d'ions dissous en sous-phase avec des molécules amphiphiles à l'interface permet d'élaborer de nouveaux systèmes pouvant former des films LB, ce qui est notamment le cas d'agencements à base de cyanures métalliques.

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Constantino, Carlos José Leopoldo. "Filmes de Langmuir e Langmuir-Blodgett (LB) de ligninas." Universidade de São Paulo, 1999. http://www.teses.usp.br/teses/disponiveis/88/88131/tde-18112014-162235/.

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Filmes de Langmuir e Langmuir-Blodgett (LB) de ligninas extraídas do bagaço de cana-de-açúcar, via processo organossolve, foram fabricados. As isotermas de pressão revelaram uma área para a seção média da lignina em torno de 100 Å para a monocamada condensada, enquanto a modelagem a partir dos espectros elipsométricos indicou uma espessura por camada de cerca 60 Å para os filmes LB. Porém a deposição não se mostrou homogênea sobre toda a superfície do substrato como observado pelas medidas de microscopia de força atômica (AFM), de forma que filmes mais homogêneos foram obtidos a partir de uma solução mista de Iignina com estearato de cádmio. A área por molécula, calculada com base no número de moléculas de ácido esteárico sobre a subfase, aumenta com a quantidade de lignina na solução mista, indicando a presença de ambos os componentes também na monocamada. Os espectros de infravermelho com transformada de Fourier (FTIR) mostraram que tanto a lignina quanto o estearato de cádmio são transferidos e os espectros de ultravioleta visível (UV-vis) indicaram que esta deposição é homogênea até a 20ª camada. Os difratogramas de raios-X e as medidas de AFM mostram que a deposição de lignina e estearato de cádmio ocorre em domínios separados. As medidas de AFM revelaram ainda um aumento da rugosidade do filme com o aumento do número de camadas depositadas e com a maior irregularidade do substrato utilizado. Vale destacar que os filmes de lignina pura mostraram-se mais homogêneos que os filmes mistos, apesar da maior estabilidade destes sobre a subfase. A uniformidade macroscópica dos filmes LB foram confirmadas por medidas de potencial de superfície. Um estudo comparativo de filmes de Langmuir de ligninas extraídas por diferentes processos e de diferentes fontes (madeira mole, madeira dura e cana-de- açúcar) foi realizado. Destacou-se a importância dos grupos funcionais nas medidas de pressão e potencial de superfície, sendo que a área molecular média mostrou-se aumentar com a massa molar das ligninas em questão. A observação de uma inversão nos valores do potencial de superfície para filmes LB de lignina de cana e de pinus abriu caminho para uma investigação mais detalhada dos fatores que contribuem para o potencial de superfície dos filmes LB. Além da Iignina, filmes LB de polianilina e estearato de cádmio também foram estudados. Os resultados revelaram que os valores do potencial de superfície para estes filmes podem ser melhor compreendidos levando-se em consideração modelos teóricos que tratam tanto da contribuição dipolar das moléculas que constituem o filme como da contribuição da interface filme/substrato, a qual geralmente é negativa e se dá pela injeção de cargas. No caso dos filmes LB de estearato de cádmio o potencial é positivo para um número ímpar de camadas e negativo para um número par
Langmuir monolayers and Langmuir-Blodgett (LB) films were produced from lignins extracted from sugar cane bagasse, via the organosolv process The surface pressure isotherms revealed an area per molecule of 100 Å for a condensed monolayer, and the modelling of ellipsometric data led to a thickness of 60 Å per layer for the LB films. The latter were not homogeneous, as demonstrated by atomic force microscopy (AFM) studies, and therefore mixed monolayers of Iignin and cadmium stearate were transferred with the aim of achieving more homogeneous films. The area per molecule, based on the number of stearic acid molecules on the airlwater interface, increased with the lignin contents in the mixed monolayers, thus confirming the presence of both components in the Langmuir monolayer. Fourier transform infra-red (FTIR) spectroscopy of LB films indicated that cadmium stearate as well as lignin were transferred onto the substrate. An equal amount of material was transferred in each deposition step, as demonstrated by the linear increase in UV-vis absorbance with the number of deposited layers up to the 20ª layer. Lignin and cadmium stearate are transferred in separate domains, which was indicated in X-ray diffraction measurements and AFM images. The latter also reveal that the roughness increases with the number of layers and may depend upon the substrate. Interestingly, films of pure lignin were more homogeneous than mixed films with cadmium searate, in spite of the higher stability and transterability of the mixed monolayers. Surface potential measurements showed a unitorm profile when the probe was scanned across an LB film, which may be taken as demonstration of uniformity at least at the macroscopic levei, though the film comprises domains and is usually rough for a molecular film. A comparative study was made ot monolayer characteristics for lignins obtained trom different sources and using different extracting procedures. The importance of functional groups was highlighted in these measurements, in which the area per molecule increased with the molecular weight ot the material. The observation that LB films from pinus and sugar cane bagasse exhibit surface potentials ot inverted sign has prompted us to investigate the possible contributions to such surface potentials. In addition to Iignins, in this study cadmium stearate and polyaniline LB films were also used. The overall conclusion was that the surface potential depends on the dipole moment of the monolayer-torming molecules, but is also affected substantially by the contribution from the substrate/film interface. The latter arises from charge injection from the electrode and is generally negative. For simple cadmium stearate LB films, the surface potential is positive for an odd number of layers, but negative for even numbers, since the dipole contribution is cancelled out

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Books on the topic "Langmuir-Blodgett"

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Roberts, Gareth, ed. Langmuir-Blodgett Films. Boston, MA: Springer US, 1990. http://dx.doi.org/10.1007/978-1-4899-3716-2.

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1940-, Roberts G. G., ed. Langmuir-Blodgett films. New York: Plenum Press, 1990.

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Langmuir-Blodgett films: An introduction. Cambridge: Cambridge University Press, 1996.

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Aspin, Ian Paul. Langmuir-Blodgett films from preformed polymers. Manchester: University of Manchester, 1992.

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Green, Christopher A. Covalent immobilisation of Langmuir-Blodgett films. Salford: University of Salford, 1993.

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Diniz, Jorge Manuel Boavida Fernandes. Surface thermodynamics of langmuir films for ionic langmuir-blodgett applications. Leicester: Leicester Polytechnic, 1990.

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Simmons, John M. Langmuir-Blodgett films of some novel phthalocyanines. Norwich: University of East Anglia, 1991.

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Dunne, Damien. Langmuir-Blodgett films for second harmonic generation studies. Manchester: University of Manchester, 1993.

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International Conference on Langmuir-Blodgett Films (3rd 1987 Göttingen, Germany). Langmuir-Blodgett films 3: Proceedings of the 3rd International Conference on Langmuir-Blodgett Films, Göttingen, F.R.G., July 26-31, 1987. Edited by Möbius D. London: Elsevier Applied Science, 1988.

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International Conference on Langmuir-Blodgett Films (5th 1991 Paris, France). Langmuir-Blodgett films 5: Proceedings of the 5th International Conference on Langmuir-Blodgett Films, Paris, France, August 26-30, 1991. Edited by Barraud A and Palacin S. Amsterdam: Elsevier, 1992.

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Book chapters on the topic "Langmuir-Blodgett"

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Giles, C. H., S. D. Forrester, and G. G. Roberts. "Historical Introduction." In Langmuir-Blodgett Films, 1–15. Boston, MA: Springer US, 1990. http://dx.doi.org/10.1007/978-1-4899-3716-2_1.

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Hann, R. A. "Molecular Structure and Monolayer Properties." In Langmuir-Blodgett Films, 17–92. Boston, MA: Springer US, 1990. http://dx.doi.org/10.1007/978-1-4899-3716-2_2.

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Petty, M. C., and W. A. Barlow. "Film Deposition." In Langmuir-Blodgett Films, 93–132. Boston, MA: Springer US, 1990. http://dx.doi.org/10.1007/978-1-4899-3716-2_3.

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Petty, M. C. "Characterization and Properties." In Langmuir-Blodgett Films, 133–221. Boston, MA: Springer US, 1990. http://dx.doi.org/10.1007/978-1-4899-3716-2_4.

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5

Möbius, D. "Spectroscopy of Complex Monolayers." In Langmuir-Blodgett Films, 223–72. Boston, MA: Springer US, 1990. http://dx.doi.org/10.1007/978-1-4899-3716-2_5.

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6

Swart, R. M. "Monolayers and Multilayers of Biomolecules." In Langmuir-Blodgett Films, 273–316. Boston, MA: Springer US, 1990. http://dx.doi.org/10.1007/978-1-4899-3716-2_6.

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7

Roberts, G. G. "Potential Applications of Langmuir-Blodgett Films." In Langmuir-Blodgett Films, 317–411. Boston, MA: Springer US, 1990. http://dx.doi.org/10.1007/978-1-4899-3716-2_7.

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8

Hookes, D. E. "Langmuir—Blodgett Films." In Electronic Materials, 431–48. Boston, MA: Springer US, 1991. http://dx.doi.org/10.1007/978-1-4615-3818-9_29.

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Clint, John H. "Langmuir-Blodgett multilayers." In Surfactant Aggregation, 59–81. Dordrecht: Springer Netherlands, 1992. http://dx.doi.org/10.1007/978-94-011-2272-6_4.

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Hodge, P., and N. B. McKeown. "Langmuir—Blodgett films." In Principles and Applications of Nonlinear Optical Materials, 226–49. Dordrecht: Springer Netherlands, 1993. http://dx.doi.org/10.1007/978-94-011-2158-3_9.

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Conference papers on the topic "Langmuir-Blodgett"

1

Metzger, Robert M. "Three Langmuir-Blodgett Monolayer Rectifiers." In STRUCTURAL AND ELECTRONIC PROPERTIES OF MOLECULAR NANOSTRUCTURES: XVI International Winterschool on Electronic Properties of Novel Materials. AIP, 2002. http://dx.doi.org/10.1063/1.1514177.

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2

Neal, D. B., M. C. Petty, G. G. Roberts, M. H. Ahmad, W. J. Feast, I. R. Girling, N. A. Cade, P. V. Kolinski, and I. R. Peterson. "Langmuir-Blodgett Films for Nonlinear Optics." In Sixth IEEE International Symposium on Applications of Ferroelectrics. IEEE, 1986. http://dx.doi.org/10.1109/isaf.1986.201102.

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3

Lu, Xingze, and Zhi-Ming Zhang. "Langmuir-Blodgett films and nonlinear optics." In 1992 Shanghai International Symposium on Quantum Optics, edited by Yuzhu Wang, Yiqiu Wang, and Zugeng Wang. SPIE, 1992. http://dx.doi.org/10.1117/12.130461.

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4

Loulergue, J. C., M. Dumont, and Y. Levy. "Electrooptic Properties Of Langmuir-Blodgett Multilayers." In 14th Congress of the International Commission for Optics, edited by Henri H. Arsenault. SPIE, 1987. http://dx.doi.org/10.1117/12.967368.

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5

Kurosawa, S. "Light emitting intelligent Langmuir-Blodgett films." In First European Conference on Smart Structures and Materials. SPIE, 1992. http://dx.doi.org/10.1117/12.2298110.

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Allen, S., T. D. McLean, P. F. Gordon, B. D. Bothwell, P. Robin, and I. Ledoux. "Properties Of Polyenic Langmuir Blodgett Films." In 32nd Annual Technical Symposium, edited by Garo Khanarian. SPIE, 1988. http://dx.doi.org/10.1117/12.948234.

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Lu, Xingze, Kui Han, Guangpeng Zhou, Yongsheng Xu, JianHua Xu, and Zhi-Ming Zhang. "Flow dichroism in Langmuir-Blodgett multilayers." In Photonics China '96, edited by Manfred Eich, Bruce H. T. Chai, and Minhua Jiang. SPIE, 1996. http://dx.doi.org/10.1117/12.252932.

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Zanoni, R., C. Naselli, J. Bell, G. Stegeman, and C. Seaton. "Brillouin spectra of Langmuir-Blodgett films." In OSA Annual Meeting. Washington, D.C.: Optica Publishing Group, 1985. http://dx.doi.org/10.1364/oam.1985.thv8.

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Abstract:

The Brillouin spectra of thin films of cadmium arachidate have been measured. These films are multiple layers of ordered monolayers (26.8 Å thick) of the cadmium salt of arachidic acid deposited one monolayer at a time onto aluminum and glass substrates by the Langmuir-Blodgett technique.1 The elastic properties of these films can be determined from these Brillouin scattering spectra. Light from a single-mode argon-ion laser at 0.5145 m was scattered by multiple, high frequency, surface acoustic waves guided by LB films of thickness 100, 35, and 11 monolayers. The scattered light was collected and spectrum analyzed with a 9-pass tandem Fabry-Perot interferometer to obtain the velocities of the surface acoustic waves. The use of the tandem interferometer provided the high contrast needed to detect the weak Brillouin signals in the presence of the intense elastically scattered light. The Brillouin spectra are now being analyzed to determine the elastic properties of the Langmuir-Blodgett films.

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Gaididei, Yu B., and A. S. Trofimov. "Photorefractive Effects in Langmuir-Blodgett Films." In Photorefractive Materials, Effects, and Devices II. Washington, D.C.: Optica Publishing Group, 1993. http://dx.doi.org/10.1364/pmed.1993.frh.9.

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Olsen, Eric, Rajesh Guntupalli, Iryna Sorkulova, Robert Long, William Neely, and Vitaly Vodyanoy. "Phage Langmuir-Blodgett films for biosensing applications." In 2010 Ninth IEEE Sensors Conference (SENSORS 2010). IEEE, 2010. http://dx.doi.org/10.1109/icsens.2010.5690208.

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Reports on the topic "Langmuir-Blodgett"

1

Mirley, C. L., and J. T. Koberstein. Tribology of Langmuir-Blodgett Films. Fort Belvoir, VA: Defense Technical Information Center, March 1992. http://dx.doi.org/10.21236/ada250075.

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Rahman, A. K., L. Samuelson, D. Minehan, S. Clough, S. Tripathy, T. Inagaki, X. O. Yang, T. A. Skotheim, and Y. Okamoto. Ordered Langmuir-Blodgett Films of Polypyrrole and Analogs. Fort Belvoir, VA: Defense Technical Information Center, October 1988. http://dx.doi.org/10.21236/ada200615.

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Duran, R. S., W. Sigmund, T. Bailey, and M. Hara. Langmuir Blodgett and STM Investigations of Conducting Polymer Thin Films. Fort Belvoir, VA: Defense Technical Information Center, December 1993. http://dx.doi.org/10.21236/ada274512.

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Zhou, H. C., and R. S. Duran. The Effect of Surface Pressure on Langmuir-Blodgett Polymerization of 2- Pentadecyl Aniline. Fort Belvoir, VA: Defense Technical Information Center, May 1992. http://dx.doi.org/10.21236/ada250993.

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Vlakhov, Todor, George Ivanov, and George Hadjichristov. Phospholipid Langmuir-Blodgett Films and Impedance Spectroscopy for Detection of Acetone and Methanol Vapours. "Prof. Marin Drinov" Publishing House of Bulgarian Academy of Sciences, June 2021. http://dx.doi.org/10.7546/crabs.2021.06.04.

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Bhushan, Bharat, Ashok V. Kulkarni, and Vilas N. Koinkar. Microtribological Characterization of Self Assembled and Langmuir-Blodgett Monolayers by Atomic and Friction Force Microscopy,. Fort Belvoir, VA: Defense Technical Information Center, November 1994. http://dx.doi.org/10.21236/ada298875.

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Cesarano, J. III. Modeling and characterization of molecular structures in self assembled and Langmuir-Blodgett films for controlled fabrication. Office of Scientific and Technical Information (OSTI), October 1997. http://dx.doi.org/10.2172/548662.

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Dr. J. D. Miller. Atomic force microscopy for the study of specially prepared surfaces including transferred Langmuir-Blodgett layers. Final report. Office of Scientific and Technical Information (OSTI), June 1999. http://dx.doi.org/10.2172/765118.

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