| Literature DB >> 31359550 |
Qifeng Zheng1, Shota Miura1, Kasumi Miyazaki1, Seongjae Ko1, Eriko Watanabe1, Masaki Okoshi2,3, Chien-Pin Chou4, Yoshifumi Nishimura4, Hiromi Nakai2,3,4, Takeshi Kamiya5, Tsunetoshi Honda6, Jun Akikusa7, Yuki Yamada1,3, Atsuo Yamada1,3.
Abstract
Aqueous Na- or K-ion batteries could virtually eliminate the safety and cost concerns raised from Li-ion batteries, but their widespread applications have generally suffered from narrow electrochemical potential window (ca. 1.23 V) of aqueous electrolytes that leads to low energy density. Herein, by exploring optimized eutectic systems of Na and K salts with asymmetric imide anions, we discovered, for the first time, room-temperature hydrate melts for Na and K systems, which are the second and third alkali metal hydrate melts reported since the first discovery of Li hydrate melt by our group in 2016. The newly discovered Na- and K- hydrate melts could significantly extend the potential window up to 2.7 and 2.5 V (at Pt electrode), respectively, owing to the merit that almost all water molecules participate in the Na+ or K+ hydration shells. As a proof-of-concept, a prototype Na3 V2 (PO4 )2 F3 |NaTi2 (PO4 )3 aqueous Na-ion full-cell with the Na-hydrate-melt electrolyte delivers an average discharge voltage of 1.75 V, that is among the highest value ever reported for all aqueous Na-ion batteries.Entities:
Keywords: aqueous batteries; asymmetric imide anion; electrochemistry; hydrates; potential window expansion
Year: 2019 PMID: 31359550 DOI: 10.1002/anie.201908830
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336