Mechanochemical spinodal decomposition: a phenomenological theory of phase transformations in multi-component, crystalline solids
Abstract
Here, we present a phenomenological treatment of diffusion-driven martensitic phase transformations in multi-component crystalline solids that arise from non-convex free energies in mechanical and chemical variables. The treatment describes diffusional phase transformations that are accompanied by symmetry-breaking structural changes of the crystal unit cell and reveals the importance of a mechanochemical spinodal, defined as the region in strain-composition space, where the free-energy density function is non-convex. The approach is relevant to phase transformations wherein the structural order parameters can be expressed as linear combinations of strains relative to a high-symmetry reference crystal. The governing equations describing mechanochemical spinodal decomposition are variationally derived from a free-energy density function that accounts for interfacial energy via gradients of the rapidly varying strain and composition fields. A robust computational framework for treating the coupled, higher-order diffusion and nonlinear strain gradient elasticity problems is presented. Because the local strains in an inhomogeneous, transforming microstructure can be finite, the elasticity problem must account for geometric nonlinearity. An evaluation of available experimental phase diagrams and first-principles free energies suggests that mechanochemical spinodal decomposition should occur in metal hydrides such as ZrH2-2c. The rich physics that ensues is explored in several numerical examples in two and three dimensions,more »
- Authors:
-
- Univ. of Michigan, Ann Arbor, MI (United States). Dept. of Mechanical Engineering
- Univ. of California, Santa Barbara, CA (United States). Dept. of Materials
- Univ. of Michigan, Ann Arbor, MI (United States). Dept. of Mechanical Engineering and Dept. of Mathematics
- Publication Date:
- Research Org.:
- Univ. of Michigan, Ann Arbor, MI (United States)
- Sponsoring Org.:
- USDOE Office of Science (SC), Basic Energy Sciences (BES) (SC-22). Materials Sciences & Engineering Division; National Science Foundation (NSF)
- OSTI Identifier:
- 1438027
- Grant/Contract Number:
- SC0008637; CHE1027729; DMR 1105672
- Resource Type:
- Accepted Manuscript
- Journal Name:
- npj Computational Materials
- Additional Journal Information:
- Journal Volume: 2; Journal Issue: 1; Journal ID: ISSN 2057-3960
- Publisher:
- Nature Publishing Group
- Country of Publication:
- United States
- Language:
- English
- Subject:
- 37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CHEMISTRY; 36 MATERIALS SCIENCE; batteries; computational methods; mechanical properties; metals and alloys
Citation Formats
Rudraraju, Shiva, Van der Ven, Anton, and Garikipati, Krishna. Mechanochemical spinodal decomposition: a phenomenological theory of phase transformations in multi-component, crystalline solids. United States: N. p., 2016.
Web. doi:10.1038/npjcompumats.2016.12.
Rudraraju, Shiva, Van der Ven, Anton, & Garikipati, Krishna. Mechanochemical spinodal decomposition: a phenomenological theory of phase transformations in multi-component, crystalline solids. United States. https://doi.org/10.1038/npjcompumats.2016.12
Rudraraju, Shiva, Van der Ven, Anton, and Garikipati, Krishna. Fri .
"Mechanochemical spinodal decomposition: a phenomenological theory of phase transformations in multi-component, crystalline solids". United States. https://doi.org/10.1038/npjcompumats.2016.12. https://www.osti.gov/servlets/purl/1438027.
@article{osti_1438027,
title = {Mechanochemical spinodal decomposition: a phenomenological theory of phase transformations in multi-component, crystalline solids},
author = {Rudraraju, Shiva and Van der Ven, Anton and Garikipati, Krishna},
abstractNote = {Here, we present a phenomenological treatment of diffusion-driven martensitic phase transformations in multi-component crystalline solids that arise from non-convex free energies in mechanical and chemical variables. The treatment describes diffusional phase transformations that are accompanied by symmetry-breaking structural changes of the crystal unit cell and reveals the importance of a mechanochemical spinodal, defined as the region in strain-composition space, where the free-energy density function is non-convex. The approach is relevant to phase transformations wherein the structural order parameters can be expressed as linear combinations of strains relative to a high-symmetry reference crystal. The governing equations describing mechanochemical spinodal decomposition are variationally derived from a free-energy density function that accounts for interfacial energy via gradients of the rapidly varying strain and composition fields. A robust computational framework for treating the coupled, higher-order diffusion and nonlinear strain gradient elasticity problems is presented. Because the local strains in an inhomogeneous, transforming microstructure can be finite, the elasticity problem must account for geometric nonlinearity. An evaluation of available experimental phase diagrams and first-principles free energies suggests that mechanochemical spinodal decomposition should occur in metal hydrides such as ZrH2-2c. The rich physics that ensues is explored in several numerical examples in two and three dimensions, and the relevance of the mechanism is discussed in the context of important electrode materials for Li-ion batteries and high-temperature ceramics.},
doi = {10.1038/npjcompumats.2016.12},
journal = {npj Computational Materials},
number = 1,
volume = 2,
place = {United States},
year = {Fri Jun 10 00:00:00 EDT 2016},
month = {Fri Jun 10 00:00:00 EDT 2016}
}
Web of Science
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