| Literature DB >> 30403338 |
Yongwu He1, Panxing Bai1, Shuyan Gao2, Yunhua Xu1,3.
Abstract
Inferior rate performance, insufficient cycle life, and low mass loading have restricted the practical application of hard carbon (HC) anodes in sodium-ion batteries (NIBs). Here, a compatible strategy is developed by matching HC anodes with an ether-based electrolyte. Systematical investigation reveals that good compatibility of the electrode-electrolyte systems forms thinner but a more sustainable solid-electrolyte interphase and delivers a higher ionic conductivity and Na+ ion diffusion coefficient than the commonly used ester-based electrolytes. Therefore, an excellent electrochemical performance is demonstrated with a long cycle life (∼196 mA h/g and 90% capacity retention after 2000 cycles at 1 A/g), a super rate capability (∼51% capacity retention at 10 A/g) at a mass loading of 1.5 mg/cm2, and a high initial Coulombic efficiency of 85.9%. More importantly, a high reversible areal capacity of 4.3 mA h/cm2 can be achieved at an ultrahigh mass loading of 17 mg/cm2, superior to all reported HC anodes. Our findings not only shed light on the design of high-performance battery systems but also promise a commercial transformation from the lab test to mass production of NIBs.Entities:
Keywords: ether-based electrolyte; hard carbon anode; high mass-loading anode; interfacial kinetics; sodium-ion battery; solid-electrolyte interphase
Year: 2018 PMID: 30403338 DOI: 10.1021/acsami.8b15274
Source DB: PubMed Journal: ACS Appl Mater Interfaces ISSN: 1944-8244 Impact factor: 9.229