| Literature DB >> 28766928 |
Koji Takada1, Yuki Yamada1,2, Eriko Watanabe1, Jianhui Wang1, Keitaro Sodeyama2,3,4, Yoshitaka Tateyama2,3, Kazuhisa Hirata5, Takeo Kawase5, Atsuo Yamada1,2.
Abstract
The passivation of negative electrodes is key to achieving prolonged charge-discharge cycling with Na-ion batteries. Here, we report the unusual passivation ability of superconcentrated Na-salt electrolytes. For example, a 50 mol % sodium bis(fluorosulfonyl)amide (NaFSA)/succinonitrile (SN) electrolyte enables highly reversible Na+ insertion into a hard carbon negative electrode without any electrolyte additive, functional binder, or electrode pretreatment. Importantly, an anion-derived passivation film is formed via preferential reduction of the anion upon charging, which can effectively suppress further electrolyte reduction. As a structural characteristic of the electrolyte, most anions are coordinated to multiple Na+ cations at high concentration, which shifts the lowest unoccupied molecular orbitals of the anions downward, resulting in preferential anion reduction. The present work provides a new understanding of the passivation mechanism with respect to the coordination state of the anion.Entities:
Keywords: electrolytes; hard carbon; high concentration; passivation; sodium-ion batteries
Year: 2017 PMID: 28766928 DOI: 10.1021/acsami.7b08414
Source DB: PubMed Journal: ACS Appl Mater Interfaces ISSN: 1944-8244 Impact factor: 9.229