Letters to Nature
Nature 399, 761-763 (24 June 1999) | doi:10.1038/21607; Received 26 February 1999; Accepted 20 April 1999
Molecular mechanistic origin of the toughness of natural adhesives, fibres and composites
Bettye L. Smith1,6, Tilman E. Schäffer4,6, Mario Viani1, James B. Thompson1, Neil A. Frederick1, Johannes Kindt1, Angela Belcher5, Galen D. Stucky2, Daniel E. Morse3 & Paul K. Hansma1
- Department of Physics,
- Department of Chemistry and Materials, and
- Department of Molecular, Cellular, and Developmental Biology, University of California at Santa Barbara, California 93106, USA
- Department of Molecular Biology, Max-Planck-Institute for Biophysical Chemistry, 37070 Gttingen, Germany
- Department of Chemistry, The University of Texas at Austin, Austin, Texas 78712, USA
- These authors contributed equally to this work
Correspondence to: Bettye L. Smith1,6 Correspondence and requests for materials should be addressed to B.L.S. (e-mail: Email: bettye@physics.ucsb.edu).
Natural materials are renowned for their strength and toughness1,2,3,4,5. Spider dragline silk has a breakage energy per unit weight two orders of magnitude greater than high tensile steel1,6, and is representative of many other strong natural fibres3,7,8. The abalone shell, a composite of calcium carbonate plates sandwiched between organic material, is 3,000 times more fracture resistant than a single crystal of the pure mineral4,5. The organic component, comprising just a few per cent of the composite by weight9, is thought to hold the key to nacre's fracture toughness10,11. Ceramics laminated with organic material are more fracture resistant than non-laminated ceramics11,12, but synthetic materials made of interlocking ceramic tablets bound by a few weight per cent of ordinary adhesives do not have a toughness comparable to nacre13. We believe that the key to nacre's fracture resistance resides in the polymer adhesive, and here we reveal the properties of this adhesive by using the atomic force microscope14 to stretch the organic molecules exposed on the surface of freshly cleaved nacre. The adhesive fibres elongate in a stepwise manner as folded domains or loops are pulled open. The elongation events occur for forces of a few hundred piconewtons, which are smaller than the forces of over a nanonewton required to break the polymer backbone in the threads. We suggest that this 'modular' elongation mechanism might prove to be quite general for conveying toughness to natural fibres and adhesives, and we predict that it might be found also in dragline silk.


