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Probing the reversibility and kinetics of Li(+) during SEI formation and (de)intercalation on edge plane graphite using ion-sensitive scanning electrochemical microscopy

Ions at battery interfaces participate in both the solid-electrolyte interphase (SEI) formation and the subsequent energy storage mechanism. However, few in situ methods can directly track interfacial Li(+) dynamics. Herein, we report on scanning electrochemical microscopy with Li(+) sensitive probe...

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Detalles Bibliográficos
Autores principales: Gossage, Zachary T., Hui, Jingshu, Zeng, Yunxiong, Flores-Zuleta, Heriberto, Rodríguez-López, Joaquín
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Royal Society of Chemistry 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6993605/
https://www.ncbi.nlm.nih.gov/pubmed/32055381
http://dx.doi.org/10.1039/c9sc03569a
Descripción
Sumario:Ions at battery interfaces participate in both the solid-electrolyte interphase (SEI) formation and the subsequent energy storage mechanism. However, few in situ methods can directly track interfacial Li(+) dynamics. Herein, we report on scanning electrochemical microscopy with Li(+) sensitive probes for its in situ, localized tracking during SEI formation and intercalation. We followed the potential-dependent reactivity of edge plane graphite influenced by the interfacial consumption of Li(+) by competing processes. Cycling in the SEI formation region revealed reversible ionic processes ascribed to surface redox, as well as irreversible SEI formation. Cycling at more negative potentials activated reversible (de)intercalation. Modeling the ion-sensitive probe response yielded Li(+) intercalation rate constants between 10(–4) to 10(–5) cm s(–1). Our studies allow decoupling of charge-transfer steps at complex battery interfaces and create opportunities for interrogating reactivity at individual sites.