1.10 Learning from Biominerals–Form is Function

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Presentation transcript:

1.10 Learning from Biominerals–Form is Function Figure 1.7 The chiton, left, a primivite marine mollusk. Chiton radula, right, composed of biomineralized iron oxide, are hard enough to scrape algae-covered rocks

The organic functions as a blueprint that carries programmed information for the synthesis of materials with natural form and a biological function Biomineralization centers on the idea that organics control the nucleation, growth and form of inorganics, and it is this process that creates hierarchical composite structures with unique chemical and physical properties. Figure 1.8 Synthetic morphology resembling biomineralized systems

1.11 Two-Dimensional Assemblies Repetitive transfer of LB surfactant monolayers provided a rational approach to known thickness of LB multilayer films. Through judicious selection of the structure of the surfactant and due cognizance of interactions between surfactants, it proved possible to create a wide variety of LB multilayer film architectures with structure and composition designed for a particular function A surfactant is an amphiphile, bearing two chemically distinct termini, and understanding the chemical composition of the substrate permits one to know both how the surfactant will orient with respect to it, as well as which end the surfactant will expose to further bind with a properly chosen counterpart

The method involved initial attachment of a,w-alkanehydroxy-phosphonate to glass or an a,w-alkanethiophosphonate to gold surfaces. This was followed by the sequential assembly of Zr4+ and a,w-bisalkanephosphonates to give well-ordered zirconium organophosphonate multilayer films Figure 1.9 LB films formed through the repetitive transfer of amphiphile monolayers, left. Inorganic LB-like films synthesized from diphosphonates and metal ions, right.

Layer-by-Iayer self-assembly of oppositely charged polyelectrolytes to create an electrostatically bound superlattice The method begins with the anchoring of a primer layer such as 3-aminopropyltrimethoxysilane to hydroxyl groups on the surface of glass or silicon. In aqueous solution, the amine groups are protonated and the primer layer develops an overall positive charge. This facilitates the adsorption from solution of a monolayer of a polyanion, such as poly(styrenesulfonate). The process of polyanion adsorption on the primer layer, and as a consequence the formation of an electrical double layer due to dissociation into the aqueous phase of some fraction of counter cations, serves to create a sufficient excess of surface negative charge to allow the subsequent adsorption of a monolayer of a polycation such as poly(allylaminehydrochloride). This method of depositing single layers of polyelectrolytes of alternating charge can be repeated several times to produce multilayer polymer films that exhibit an impressive degree of regularity in the interlayer repeat distance.

Figure 1.10 Iterative formation of layer-by-layer electrostatic multilayers by alternately dipping in solutions of polycations and polyanions

1.12 SAMs and Soft Lithography Long chain alkanethiolates can self-assemble on gold surfaces to give ordered monolayer films, self-assembled monolayers (SAMs) Soft lithography: use of a patterned elastomer made of PDMS, as a mask, stamp or mold. With this simple process, high quality patterns and structures can be created with lateral dimensions from about 5 to 500 mm, in two- and three-dimensions, that cannot easily be achieved by photolithography. Figure 1.11 Square drops of water through soft lithography

1.13 Clever Clusters Nanocluster nucleation, growth and stabilization is achieved through capping with organic ligands, surfactants and polymers Extraordinary control over cluster size and width of the distribution, often better than a single atomic layer, was feasible by controlling the cluster nucleation and growth using the phosphineoxide as a dual-purpose solvent and capping agent Figure 1.12 Solutions of CdSe nanoparticles of different sizes under UV illumination

A biological rather than an optoelectronic application may emerge from this kind of research. It centers on the selective fluorescent labeling of biological materials with brightly emissive and appropriately end-functionalized capped II-VI semiconductor clusters of different size. Specific sites in biological specimens have been tagged with this new class of "inorganic dyes." They have the benefit of narrower emission, higher luminescent yield and greater photochemical stability than currently used organic dye labels.

1.14 Coercing Colloids These periodic dielectric lattices are 3D photonic crystals, the optical analog of the electronic semiconductor Exciting opportunities are emerging for colloidal and inverted colloidal crystals, which take advantage of their ordered porosity and the "structural colors" that emerge from the interference of light with a microstructure, rather than absorption of light by a chromophore Figure 1.13 "Inverse opal" photonic crystal made of titania, templated by an array of polystyrene spheres

1.15 Mesoscale Self-Assembly Microfabrication based on photolithography is inherently a 2D technology. New architectures envisaged for future microelectronic, optoelectronic, photonic and microelectro-mechanical devices such as photonic band-gap crystals, biomimetic structures and neural-type computers, necessitate 3D microfabrication scheme Figure 1.14 Micron-sized self-assembled geodesic dome assembled onto a drop of water in heptane, the scale bar showing 1 mm

1.16 Materials Self-Assembly of Integrated Systems It has become feasible to organize and connect organic, inorganic and polymeric chemical components with well-defined functions into integrated electronic, photonic, mechanical, analytical and chemical systems for a future nanotechnology Smaller units are assembled into larger ones, which in turn are organized at a higher dimension. This construction process is continued until the highest level of structural complexity in the hierarchy has been attained Figure 1.15 Layer-by-layer self-assembled lithium battery PEO: Poly(ethylene oxide) GO: Graphite oxidized by HNO3 and NaClO3 PDDA: Poly(diallyldimethylammonium chloride)