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Letters to Nature

Nature 410, 450-453 (22 March 2001) | doi:10.1038/35068529; Received 14 November 2000; Accepted 10 January 2001

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Evolution of nanoporosity in dealloying

Jonah Erlebacher1,2, Michael J. Aziz1, Alain Karma3, Nikolay Dimitrov4 & Karl Sieradzki4

  1. Division of Engineering and Applied Sciences, Harvard University, 9 Oxford Street, Cambridge, Massachusetts 02138, USA
  2. Department of Physics and Center for Interdisciplinary Research on Complex Systems, Northeastern University, 360 Huntington Avenue, Boston, Massachusetts 02115, USA
  3. Department of Mechanical and Aerospace Engineering and Center for Solid State Sciences, Arizona State University, Tempe, Arizona 85287-6106, USA
  4. Present address: Department of Materials Science and Engineering, Johns Hopkins University, Baltimore, Maryland 21218, USA.

Correspondence to: Jonah Erlebacher1,2 Correspondence and requests for materials should be addressed to J.E (e-mail: Email: Jonah.Erlebacher@jhu.edu).

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Dealloying is a common corrosion process during which an alloy is 'parted' by the selective dissolution of the most electrochemically active of its elements. This process results in the formation of a nanoporous sponge composed almost entirely of the more noble alloy constituents1. Although considerable attention has been devoted to the morphological aspects of the dealloying process, its underlying physical mechanism has remained unclear2. Here we propose a continuum model that is fully consistent with experiments and theoretical simulations of alloy dissolution, and demonstrate that nanoporosity in metals is due to an intrinsic dynamical pattern formation process. That is, pores form because the more noble atoms are chemically driven to aggregate into two-dimensional clusters by a phase separation process (spinodal decomposition) at the solid–electrolyte interface, and the surface area continuously increases owing to etching. Together, these processes evolve porosity with a characteristic length scale predicted by our continuum model. We expect that chemically tailored nanoporous gold made by dealloying Ag-Au should be suitable for sensor applications, particularly in a biomaterials context.

  1. Division of Engineering and Applied Sciences, Harvard University, 9 Oxford Street, Cambridge, Massachusetts 02138, USA
  2. Department of Physics and Center for Interdisciplinary Research on Complex Systems, Northeastern University, 360 Huntington Avenue, Boston, Massachusetts 02115, USA
  3. Department of Mechanical and Aerospace Engineering and Center for Solid State Sciences, Arizona State University, Tempe, Arizona 85287-6106, USA
  4. Present address: Department of Materials Science and Engineering, Johns Hopkins University, Baltimore, Maryland 21218, USA.

Correspondence to: Jonah Erlebacher1,2 Correspondence and requests for materials should be addressed to J.E (e-mail: Email: Jonah.Erlebacher@jhu.edu).