Molecular mechanistic origin of the toughness of natural adhesives, fibres and composites

Molecular mechanistic origin of the toughness of natural adhesives, fibres and composites

24 June 1999 | Bettie L. Smith, Tilman E. Schäffer, Mario Viani, James B. Thompson, Neil A. Frederick, Johannes Kindt, Angela Belcher, Galen D. Stucky, Daniel E. Morse & Paul K. Hansma
The interfacial dielectric constant between silicon and SiO₂ is likely between their respective values. Ellipsometric measurements assume the oxide has a bulk dielectric constant, which may lead to an underestimate of oxide thickness. Probe localization uses a wavepacket with a large momentum spread, losing electronic momentum information. Evanescent states and extended conduction band states are treated equally, making separation difficult. The decay length of evanescent states, λ(E), depends on the energy difference between the interfacial state and the conduction band edge of SiO₂. A satisfactory tunneling barrier forms when the oxide thickness is 6λ, setting a minimum thickness of 0.7 nm for an ideal SiO₂ gate oxide. Interfacial roughness adds 6σr, making the practical minimum 1.2 nm. Induced gap states also impose constraints on minimum thickness for alternative dielectrics. A reaction between the dielectric and silicon may form a silicon oxide interlayer, which could reduce gate capacitance. Natural materials, like spider dragline silk and abalone shell, are known for their strength and toughness. Abalone shell, a composite of calcium carbonate plates and organic material, is 3,000 times more fracture resistant than pure mineral. The organic component, though small, is crucial for nacre's toughness. Organic adhesives and fibers are more fracture resistant than non-laminated ceramics, but synthetic materials lack nacre's toughness. The key to nacre's fracture resistance is the polymer adhesive, studied using atomic force microscopy. The adhesive fibres elongate in a stepwise manner as folded domains or loops are pulled open. The elongation occurs at forces of a few hundred piconewtons, smaller than the forces needed to break the polymer backbone. This 'modular' elongation mechanism may be general for conveying toughness to natural materials. Analysis of the abalone shell's organic matrix revealed a fibrous core, likely acting as an adhesive. Lustrin A, a protein from this matrix, has a modular structure with alternating cysteine-rich and proline-rich domains. Immunohistochemical analysis showed lustrin A as a component of the adhesive between nacre mineral tablets. Rief et al. demonstrated that the modular structure of a single molecule can be examined by attaching it between a flat surface and an AFM cantilever. By pulling on the protein titin, they measured the force required to break open individual subunits. The force-extension curve showed a sawtooth pattern, with each peak corresponding to a single domain unfolding. The cumulative effect of intermediate-strength hydrophobic bonds in titin's immunoglobulin-like domains contributes to the sawtooth force-distance curves. Studies using optical tweezers corroborated these results. These findings suggest that individual titin subunits unfold one at a time, revealing nature's mechanisms in building modular elastic fibers. The study used AFM toThe interfacial dielectric constant between silicon and SiO₂ is likely between their respective values. Ellipsometric measurements assume the oxide has a bulk dielectric constant, which may lead to an underestimate of oxide thickness. Probe localization uses a wavepacket with a large momentum spread, losing electronic momentum information. Evanescent states and extended conduction band states are treated equally, making separation difficult. The decay length of evanescent states, λ(E), depends on the energy difference between the interfacial state and the conduction band edge of SiO₂. A satisfactory tunneling barrier forms when the oxide thickness is 6λ, setting a minimum thickness of 0.7 nm for an ideal SiO₂ gate oxide. Interfacial roughness adds 6σr, making the practical minimum 1.2 nm. Induced gap states also impose constraints on minimum thickness for alternative dielectrics. A reaction between the dielectric and silicon may form a silicon oxide interlayer, which could reduce gate capacitance. Natural materials, like spider dragline silk and abalone shell, are known for their strength and toughness. Abalone shell, a composite of calcium carbonate plates and organic material, is 3,000 times more fracture resistant than pure mineral. The organic component, though small, is crucial for nacre's toughness. Organic adhesives and fibers are more fracture resistant than non-laminated ceramics, but synthetic materials lack nacre's toughness. The key to nacre's fracture resistance is the polymer adhesive, studied using atomic force microscopy. The adhesive fibres elongate in a stepwise manner as folded domains or loops are pulled open. The elongation occurs at forces of a few hundred piconewtons, smaller than the forces needed to break the polymer backbone. This 'modular' elongation mechanism may be general for conveying toughness to natural materials. Analysis of the abalone shell's organic matrix revealed a fibrous core, likely acting as an adhesive. Lustrin A, a protein from this matrix, has a modular structure with alternating cysteine-rich and proline-rich domains. Immunohistochemical analysis showed lustrin A as a component of the adhesive between nacre mineral tablets. Rief et al. demonstrated that the modular structure of a single molecule can be examined by attaching it between a flat surface and an AFM cantilever. By pulling on the protein titin, they measured the force required to break open individual subunits. The force-extension curve showed a sawtooth pattern, with each peak corresponding to a single domain unfolding. The cumulative effect of intermediate-strength hydrophobic bonds in titin's immunoglobulin-like domains contributes to the sawtooth force-distance curves. Studies using optical tweezers corroborated these results. These findings suggest that individual titin subunits unfold one at a time, revealing nature's mechanisms in building modular elastic fibers. The study used AFM to
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Understanding Molecular mechanistic origin of the toughness of natural adhesives%2C fibres and composites