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Theory of Coherent Nucleation in Phase-Separating Nanoparticles

Author(s)
Cogswell, Daniel A.; Bazant, Martin Z.
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Abstract
The basic physics of nucleation in solid single-crystal nanoparticles is revealed by a phase-field theory that includes surface energy, chemical reactions, and coherency strain. In contrast to binary fluids, which form arbitrary contact angles at surfaces, complete “wetting” by one phase is favored at binary solid surfaces. Nucleation occurs when surface wetting becomes unstable, as the chemical energy gain (scaling with area) overcomes the elastic energy penalty (scaling with volume). The nucleation barrier thus decreases with the area-to-volume ratio and vanishes below a critical size. Thus nanoparticles tend to transform in order of increasing size, leaving the smallest particles homogeneous (in the phase of lowest surface energy). The model is used to simulate phase separation in realistic nanoparticle geometries for Li[subscript X]FePO[subscript 4], a popular cathode material for Li-ion batteries, and collapses disparate experimental data for the nucleation barrier with no adjustable parameters. Beyond energy storage, the theory shows how to tailor the elastic and surface properties of a solid nanostructure to achieve desired phase behavior.
Date issued
2013-05
URI
http://hdl.handle.net/1721.1/91184
Department
Massachusetts Institute of Technology. Department of Chemical Engineering; Massachusetts Institute of Technology. Department of Mathematics
Journal
Nano Letters
Publisher
American Chemical Society (ACS)
Citation
Cogswell, Daniel A., and Martin Z. Bazant. “Theory of Coherent Nucleation in Phase-Separating Nanoparticles.” Nano Lett. 13, no. 7 (July 10, 2013): 3036–3041.
Version: Original manuscript
ISSN
1530-6984
1530-6992

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