离子
化学物理
锂(药物)
离子运输机
离子键合
电解质
化学
限制电流
导电体
导线
极化(电化学)
快离子导体
阴极
限制
质子
无机化学
材料科学
电化学
电极
物理化学
物理
复合材料
有机化学
内分泌学
工程类
机械工程
医学
量子力学
作者
Guanchen Li,Charles W. Monroe
标识
DOI:10.1016/j.electacta.2021.138563
摘要
Inorganic-solid lithium electrolytes are typically thought of as single-ion conductors, but the presence of secondary carriers can strongly affect their performance. Conventional descriptions of multi-carrier transport neglect both interactions between mobile species and stress diffusion — phenomena which can markedly impact the electrical response. We apply irreversible thermodynamics to develop a chemomechanical transport model for elastic-solid ionic conductors containing two mobile ions. We simulate lithium-ion conducting Li5La3Nb2O12 (LLNO) garnet oxide, a material within which experiments have shown that mobile protons can be freely substituted for lithium to form Li5(1−y)H5yLa3Nb2O12. When subjected to a current, we find that proton-substituted LLNO exhibits bulk lithium polarization, whose extent is partially controlled by cation/cation interactions. Secondary carriers segregate naturally if their global concentration is low, accumulating in a thin boundary layer near the cathode. We quantify the limiting current and Sand's time, and analyze experimental data to show how competitive proton transport affects LLNO performance.
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