Thin films
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Molecular self-assembly is the assembly of molecules without guidance
or management from an outside source. There are two types of self-assembly,
intramolecular self-assembly and intermolecular self-assembly. Most
often the term molecular self-assembly refers to intermolecular
self-assembly, while the intramolecular analog is more commonly
called folding.
Molecular self-assembly is directed through noncovalent interactions,
such as hydrogen bonding, metal coordination, hydrophobic forces,
van der Waals forces, pi-pi interactions, and/or electrostatic effects.
Simple examples include the formation of a micelle or a Langmuir
monolayer by surfactant molecules in solution. More advanced examples
of supramolecular assemblies demonstrate that a variety of different
shapes and sizes can be obtained using molecular self-assembly.
In the speculative vision of molecular nanotechnology, microchips
of the future might be made by molecular self-assembly. Using molecular
self-assembly the final (desired) structure is programmed in the
shape and functional groups of the molecules. Self-assembly is referred
to as a 'bottom-up' manufacturing technique in contrast to a 'top-down'
technique such as lithography where the desired final structure
is etched from a bulk material.
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| (a) Height image of the ultrathin film, HI'RES probe. Scan size
500 nm, height 5 nm. Click to magnify. |
(b) Phase contrast of the same area, HI'RES probe. Z-scale
is 30 °.
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| (c) Height image of the thin film at high magnification (scan size
70 nm), HI'RES-C probe. |
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| (d) Height image of the thick film, HI'RES-C probe. Scan size 250
nm. Height 3 nm. |
(e) Height image of the same thick film, conventional
probe. Scan size 250 nm. Height 3 nm. |
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Fig.1. Images courtesy of Dr. S. Magonov
(Veeco Instruments). Samples courtesy of Stoddart Supramolecular Group,
Department
of Chemistry and Biochemistry, University of California, Los Angeles. |
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Fig. 1 presents AFM images taken by a Nanoscope IIIa MultiMode
AFM and a HI'RES-C probe. The images are of self-assemblies of palindromic
rotaxane molecules formed on HOPG (a, b). Ordered structures were
found in ultrathin films (c), and with an increase in film thickness
the top layer becomes grainy. HI'RES images of the grain structure
show very high resolution. Images (d) and (e) compare routine height
scans of the thick film obtained by HI'RES and conventional silicon
tips.
Generally, organic monolayers on hard substrates have enough mechanical
stiffness to be examined with the regular Si probes having stiffness
of ~ 40 N/m. The use of softer probes might be necessary for samples
with increasing layer thickness if topmost topography is of primary
interest. Thicker layers might be necessary to examine with stiff
probes when one can visualize heterogeneities and to reveal sub-surface
morphology that requires a tip penetration into material.
A Langmuir-Blodgett film is a monolayer
of an organic material, transferred from the surface of a liquid
onto a solid by immersing (or pulling) the solid substrate into
(or from) the liquid. An additional monolayer can be added with
each immersion or emersion step, thus films with very accurate thickness
can be formed. The monolayers are usually composed of polar molecules
with a hydrophilic head and a hydrophobic tail (example: fatty acids).
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| Magnetic iron-containing nanoparticles synthesized in a mixed Langmuir
monolayer. |
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| Fig.2.Image courtesy of Radmir Gaynutdinov
(A.V. Shubnikov's SPM group, Crystallography Institute, RAS). Sample
courtesy of G. B. Khomutov's group, Physical Faculty, MSU. |
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Magnetic iron-containing nanoparticles in Fig.2 are synthesized
in a mixed Langmuir monolayer (stearic acid + Fe(CO)5) at the gas/liquid
interface via ultraviolet decomposition of iron pentacarbonyl.
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