Nonlinear phase-field model for electrode-electrolyte interface evolution
Author(s) -
Linyun Liang,
Yue Qi,
Fei Xue,
Saswata Bhattacharya,
Stephen J. Harris,
LongQing Chen
Publication year - 2012
Publication title -
physical review e
Language(s) - English
Resource type - Journals
eISSN - 1550-2376
pISSN - 1539-3755
DOI - 10.1103/physreve.86.051609
Subject(s) - overpotential , non equilibrium thermodynamics , electrolyte , nonlinear system , phase (matter) , electroplating , field (mathematics) , materials science , electrode , thermodynamics , electrochemistry , chemical physics , physics , chemistry , nanotechnology , mathematics , quantum mechanics , layer (electronics) , pure mathematics
A nonlinear phase-field model is proposed for modeling microstructure evolution during highly nonequilibrium processes. We consider electrochemical reactions at electrode-electrolyte interfaces leading to electroplating and electrode-electrolyte interface evolution. In contrast to all existing phase-field models, the rate of temporal phase-field evolution and thus the interface motion in the current model is considered nonlinear with respect to the thermodynamic driving force. It produces Butler-Volmer-type electrochemical kinetics for the dependence of interfacial velocity on the overpotential at the sharp-interface limit. At the low overpotential it recovers the conventional Allen-Cahn phase-field equation. This model is generally applicable to many other highly nonequilibrium processes where linear kinetics breaks down.
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