Electrochemomechanics of lithium dendrite growth

被引:217
作者
Jana, Aniruddha [1 ]
Woo, Sang Inn [1 ]
Vikrant, K. S. N. [1 ]
Garcia, R. Edwin [1 ]
机构
[1] Purdue Univ, Sch Mat Engn, W Lafayette, IN 47907 USA
关键词
IN-SITU; LIQUID ELECTROLYTES; METAL ANODE; MECHANISMS; ELECTRODEPOSITION; DEFORMATION; DIFFUSION; DISSOLUTION; NUCLEATION; MICROSCOPY;
D O I
10.1039/c9ee01864f
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A comprehensive roadmap describing the current density- and size-dependent dendrite growth mechanisms is presented. Based on a thermodynamically consistent theory, the combined effects of chemical diffusion, electrodeposition, and elastic and plastic deformation kinetics are analyzed to rationalize their contributions to experimentally observable morphologies. A critical current density, i* = zi(lim)l(Delta G omega kappa(i)), in the t(sigma) < t < t(Sand) range, results in plastic flow at the tips, dendrite bifurcation, and bent and kinked morphologies. Three dendrite growth mechanisms are observed: (1) electrochemical shielding, where there is practically no electrodeposition/electrodissolution; (2) stress-induced electrodissolution and electrodeposition on those interfaces directly facing each other, generating a self-sustained overpotential that pushes the dendrites towards the counter electrode; and (3) local, lateral plastic extrusion in those side branches experiencing non-hydrostatic stresses. Six regimes of lithium electrodeposit growth are identified: (i) thermodynamic suppression regime, (ii) incubation regime, (iii) base-controlled regime, (iv) tip-controlled regime, (v) mixed regime, and (vi) Sand's regime.
引用
收藏
页码:3595 / 3607
页数:13
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