Thermodynamic stability of driven open systems and control of phase separation by electro-autocatalysis

被引:100
作者
Bazant, Martin Z. [1 ,2 ]
机构
[1] MIT, Dept Chem Engn, Cambridge, MA 02139 USA
[2] MIT, Dept Math, Cambridge, MA 02139 USA
关键词
NONEQUILIBRIUM STEADY-STATES; RECHARGEABLE LITHIUM BATTERIES; RESISTIVE SWITCHING MEMORIES; CHARGE-TRANSFER KINETICS; IN-SALT ELECTROLYTE; FREE-ENERGY; IONIC LIQUIDS; SPINODAL DECOMPOSITION; NONUNIFORM SYSTEM; IRREVERSIBLE-PROCESSES;
D O I
10.1039/c7fd00037e
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Motivated by the possibility of electrochemical control of phase separation, a variational theory of thermodynamic stability is developed for driven reactive mixtures, based on a nonlinear generalization of the Cahn-Hilliard and Allen-Cahn equations. The Glansdorff-Prigogine stability criterion is extended for driving chemical work, based on variations of nonequilibrium Gibbs free energy. Linear stability is generally determined by the competition of chemical diffusion and driven autocatalysis. Novel features arise for electrochemical systems, related to controlled total current (galvanostatic operation), concentration-dependent exchange current (Butler-Volmer kinetics), and negative differential reaction resistance (Marcus kinetics). The theory shows how spinodal decomposition can be controlled by solo-autocatalytic charge transfer, with only a single faradaic reaction. Experimental evidence is presented for intercalation and electrodeposition in rechargeable batteries, and further applications are discussed in solid state ionics, electrovariable optics, electrochemical precipitation, and biological pattern formation.
引用
收藏
页码:423 / 463
页数:41
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