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Pattern formation during electrochemical and liquid metal dealloying

Published online by Cambridge University Press:  10 January 2018

Ian McCue ,
Alain Karma  and
Jonah Erlebacher
Ian McCue
Affiliation:
Texas A&M University, USA; imccue1@tamu.edu
Alain Karma
Affiliation:
Northeastern University, USA; a.karma@neu.edu
Jonah Erlebacher
Affiliation:
Department of Materials Science and Engineering, Johns Hopkins University, USA; jonah.erlebacher@jhu.edu
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Abstract

Dealloying has evolved from a problematic corrosion process to a versatile tool for scalable fabrication of nanostructured metals. While the original, and majority of, work in the area has focused on electrochemical dealloying, a powerful variation of dealloying—liquid metal dealloying—has recently gained popularity. This process relies on a melt to carry out selective dissolution, replacing the traditional electrolyte solution. While electrolytes and molten metals are both suitable dealloying media, they can lead to very different morphologies. In this article, we compare and contrast what is known about the microscale physics and chemistry controlling microstructural evolution in electrochemical and liquid metal dealloying. We conclude that the core phenomenology of porosity evolution—a competition between dissolution and interface diffusion—is similar in both dealloying processes, but that the relative magnitudes of these two processes control interfacial pattern formation.

Keywords

nanostructurediffusionmorphologyself-assembly
Type
Dealloyed Nanoporous Materials with Interface-Controlled Behavior
Information
MRS Bulletin , Volume 43 , Issue 1: Dealloyed Nanoporous Materials with Interface-Controlled Behavior , January 2018 , pp. 27 - 34
Copyright
Copyright © Materials Research Society 2018 

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