Interplay Between Two Adjacent Electrical Double Layers at Metal | Solid Electrolyte | Liquid Electrolyte Interfaces

被引:1
作者
Qin, Yupeng [1 ,2 ]
Huang, Jun [4 ,5 ]
Zhang, Jie [1 ]
Zhao, Zhiwei [1 ]
Guo, Limin [3 ]
Peng, Zhangquan [1 ]
机构
[1] Chinese Acad Sci, Dalian Inst Chem Phys, Lab Adv Spectro Electrochem & Liion Batteries, Dalian 116023, Peoples R China
[2] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
[3] Dalian Univ, Coll Environm & Chem Engn, Dalian 116622, Peoples R China
[4] Forschungszentrum Julich GmbH, Inst Energy & Climate Res, IEK 13 Theory & Computat Energy Mat, D-52425 Julich, Germany
[5] Rhein Westfal TH Aachen, Fac Georesources & Mat Engn, Theory Electrocatalyt Interfaces, D-52062 Aachen, Germany
基金
中国国家自然科学基金; 国家重点研发计划; 中国博士后科学基金;
关键词
SPACE-CHARGE LAYER; DIELECTRIC-CONSTANT; MIXTURE SOLUTION; TRANSPORT; INTERPHASE; CHEMISTRY;
D O I
10.1021/acs.jpcc.4c03879
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
Electrical double layer (EDL) in modern batteries is radically different from that of the mercury electrode for which the conventional EDL models were initially developed. Particularly, the formation of a solid electrolyte interphase (SEI) divides the electrode-solution interface into two adjacent interfaces, while the interplay between these two EDLs is largely unclear. Herein, considering a metal | solid electrolyte | liquid electrolyte (M|SE|LE) system, we developed continuum models to understand the correlation between the charging states of the two adjacent EDLs. In addition to numerical results, analytical solutions of the differential double layer capacitances for two limiting cases, where the mobile charge countering the metal surface charge exists in either the SE or the LE, are obtained. The critical electrode potential marking the transition between the two limiting cases is analyzed. This work contributes to the understanding of nontraditional electrochemical interfaces in modern batteries.
引用
收藏
页码:14654 / 14662
页数:9
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