Langmuir-Blodgett films substrate

Films spread at liquid-liquid interfaces or on liquids other than water are discussed followed by the important effects of charged monolayers on water. Finally, the most technologically important application of Langmuir films, the Langmuir-Blodgett film deposited on a solid substrate, is reviewed. 

Tredgold R FI, Jones S D, Evans S D and Williams P I 1986 Aluminium oxide as a substrate for the deposition of Langmuir-Blodgett films J. Mol. Electron. 2 147-9... 

In addition to the preparation of Langmuir and Langmuir-Blodgett films, the use of self-assembly techniques also plays an important role in the formation of particle films. Both physisorption, as, for example, electrostatic adsorption of charged particles from colloidal solution, and chemisorption onto a substrate have been investigated. In Section V.A, electrostatic adsorption will be reviewed chemisorption is the subject of Section V.B. 

The material system is a Langmuir-Blodgett film of the S enantiomer of a chiral polymer deposited on a glass substrate. The polymer is a poly(isocyanide)30 functionalized with a nonlinear optical chromophore (see Figure 9.14). In this particular system the optical nonlinearity and chirality are present on two different levels of the molecular structure. The chirality of the polymer is located in the helical backbone whereas the nonlinearity is present in the attached chromophores. Hence, this opens the possibility to optimize both properties independently. 

Langmuir-Blodgett films were prepared by spreading a 2 x 1(T4 M solution of the enantiomerically pure helicenebisquinone in chloroform onto a water surface. After evaporation of the solvent, the monolayer was compressed to a surface pressure of 20 mN/m. After stabilization for 30 min, the monolayers were transferred by the horizontal dipping method onto glass substrates, treated with octadecyltrichlorosilane to make them hydrophobic. 

When some NC particles are surface treated to make them hydrophobic by, e.g., silylation and floated on the surface of water, a nanoparticle layer can be made on a solid substrate by a method similar to Langmuir-Blodgett film formation. Interparticle separation is well controlled by choosing an appropriate surface pressure prior to making LB film, as discussed next. 

Thin films of materials play an important role in modern electronics. Langmuir-Blodgett films (Mort, 1980) are prepared from surface-active molecules that adsorb at the surface of an aqueous solution. The surface is gently compressed to produce a close-packed monolayer, which can be coated on appropriate substrates by dipping at constant surface pressure. The layers so produced are of a precise thickness, and repeated dipping gives multilayers. For example, diacetylenes and other polymerizable... 

Figure 4.1. Schematic diagram of the formation of a Langmuir-Blodgett film. Each amphiphilic molecule is represented by a circle with a tail, where the circle denotes the hydrophilic end of the molecule. The left hand diagram represents the deposition of a monolayer on a hydrophilic substrate moving upwards. The right hand diagram represents the deposition of a second layer during the downward movement of the substrate.

Bryce and co-workers reported that the crown-annulated TTF derivatives 98 and 99 were used for UV-Vis spectroscopic and electrochemical studies of metal complexation <1996J(P2)1587>. Solution electrochemical studies showed that metal complexation to the crown unit leads to a small anodic shift in the first oxidation potential of the TTF system. Langmuir-Blodgett films of amphiphilic 99 have been assembled on solid substrates by Y-type deposition. Compounds 100-104 were used to prepare self-assembled monolayers on gold and platinum surfaces <1998AM395, 2000JOC8269>. The self-assembled monolayers of 104 were the most stable in this series of TTF-crowns. Electrochemical data for the self-assembled monolayers of 100-104 in MeCN showed two reversible one-electron waves, typical of the TTF system. The self-assembled monolayers of 102-104 exhibited an electrochemical response in aqueous electrolyes, which was observed between 50 and 100 cycles. 

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