电解质
材料科学
钠
离子
无机化学
有机化学
电极
冶金
物理化学
化学
作者
Rishivandhiga Jayakumar,Travis P. Pollard,Oleg Borodin,Vadim Shipitsyn,Chanmonirath Chak,Glenn Pastel,Allen Zheng,Michel B. Johnson,Fuead Hasan,Christopher M. Bejger,Marshall A. Schroeder,Steve Greenbaum,Wenhua Zuo,Lin Ma
出处
期刊:Nano Energy
[Elsevier]
日期:2024-07-06
卷期号:128: 109969-109969
标识
DOI:10.1016/j.nanoen.2024.109969
摘要
Ethyl acetate (EA) was identified as a promising electrolyte solvent for sodium-ion batteries (SIBs), exhibiting low viscosity, cost-effectiveness, and low toxicity. Despite a significant portion of aggregation being linked to the weak solvation of Na+/EA as revealed by molecular dynamics (MD) simulations, pulsed-field gradient nuclear magnetic resonance (pfg-NMR) analysis identified a noteworthy Na+ diffusion coefficient of 3.95×10-10 m2 s-1 at 25°C in the presence of 1 m NaPF6 salt. Employing fluoroethylene carbonate (FEC) as a film-forming additive to create electrode-electrolyte interphase, this electrolyte surprisingly made ~210 mAh Na0.97Ca0.03[Mn0.39Fe0.31Ni0.22Zn0.08]O2 (NCMFNZO)/hard carbon (HC) pouch cells achieve a lengthy cycling lifetime of 250 cycles with ~80% capacity retention, cycled up to 4.0 V at 40°C. X-ray photoelectron spectroscopy (XPS) revealed increasing interphasial organic species over cycling, augmenting charge transfer resistance on both cathode and anode, particularly during fast charging or low temperatures (<10°C), promoting Na plating. Gas chromatography-mass spectrometry combined with density functional theory identified CO2 as the major gas generated from charged cathode/electrolyte interactions, exhibiting temperature/voltage dependence.
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