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  4. Rate equation for the transfer of interstitials across interfaces between equilibrated crystals
 
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Rate equation for the transfer of interstitials across interfaces between equilibrated crystals

Publikationstyp
Journal Article
Date Issued
2026-02-09
Sprache
English
Author(s)
Weissmüller, Jörg  
Werkstoffphysik und -technologie M-22  
TORE-URI
https://hdl.handle.net/11420/61694
Journal
Physical review letters  
Volume
136
Issue
6
Article Number
066201
Citation
Physical Review Letters 136 (6): 066201 (2026)
Publisher DOI
10.1103/kfpq-9dd1
Scopus ID
2-s2.0-105029926548
Publisher
APS
This Letter inspects the thermally activated transfer of solute particles across the interface between two interstitial solid solution phases that equilibrate internally by fast diffusion on conserved arrays of sites. When each phase is considered as an ergodic ensemble of particles, statistical mechanics predicts the occupancy of the transition states at equilibrium to depend on the barrier energy and on the chemical potentials and vacancy fractions in each of the phases. A rate law for the nonequilibrium interfacial transfer, based on a constant transition probability between activated states, naturally satisfies the principle of detailed balance. Contrary to Butler-Volmer-type laws, values of the particle chemical potentials enter explicitly rather than through their differences. This, along with the dependency on the vacancy fractions, implies here an exchange flux density that depends explicitly on the compositions at equilibrium. The results can explain experimental observations of a drastic slowdown in the charging of metal hydrides near phase transformations or miscibility-gap critical points.
Subjects
Energy materials
Interstitials
Kinetic theory
Nanocrystals
Phase transitions
DDC Class
530: Physics
600: Technology
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