Differentiating Contributions to "Ion Transfer" Barrier from Interphasial Resistance and Li+ Desolvation at Electrolyte/Graphite Interface

被引:509
作者
Xu, Kang [1 ]
von Cresce, Arthur [1 ]
Lee, Unchul [2 ]
机构
[1] US Army Res Lab, Power & Energy Div, Electrochem Branch, Adelphi, MD 20783 USA
[2] US Army Res Lab, Infrared Mat Branch, Electroopt & Photon Div, Sensor & Elect Devices Directorate, Adelphi, MD 20783 USA
关键词
IONIZATION-MASS-SPECTROSCOPY; LIBOB-BASED ELECTROLYTES; LITHIUM-ION; GRAPHITE/ELECTROLYTE INTERFACE; NONAQUEOUS ELECTROLYTES; SOLVATION SHEATH; CARBON ANODES; BATTERIES; CHEMISTRY; GRAPHITE;
D O I
10.1021/la1009994
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Efforts were made to differentiate the contributions to the so-called ''ion transfer" barrier at the electrolyte/graphite junction from two distinct processes: (1) desolvation of Li+ before it enters graphene interlayer and (2) the subsequent migration of bare Li+ through the ad hoc interphase. By leveraging a scenario where no substantial interphase was formed on Li+ intercalation hosts, we were able to quantity the distribution of "ion transfer" activation energy between these two interfacial processes and hence identify the desolvation process of Li+ as the major energy-consuming step. The result confirmed the earlier belief that the rate-determining step in the charging of a graphitic anode in Li+ in chemistry relates to the stripping of salvation sheath of Li+, which is closely interwoven with the interphasial resistance to Li+ migration.
引用
收藏
页码:11538 / 11543
页数:6
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