Liu Qi, Mu Daobin, Wu Borong, Wang Lei, Gai Liang, Wu Feng
Beijing Key Laboratory of Environment Science and Engineering, Beijing Institute of Technology, Beijing, 100081, P.R. China.
Collaborative Innovation Center of Electric Vehicles in Beijing, Beijing, 100081, P.R. China.
ChemSusChem. 2017 Feb 22;10(4):786-796. doi: 10.1002/cssc.201601356. Epub 2017 Jan 25.
The solid-electrolyte interface (SEI) film in a sodium-ion battery is closely related to capacity fading and cycling stability of the battery. However, there are few studies on the SEI film of sodium-ion batteries and the mechanism of SEI film formation is unclear. The mechanism for the reduction of ethylene carbonate (EC), propylene carbonate (PC), vinylene carbonate (VC), ethylene sulfite (ES), 1,3-propylene sulfite (PS), and fluorinated ethylene carbonate (FEC) is studied by DFT. The reaction activation energies, Gibbs free energies, enthalpies, and structures of the transition states are calculated. It is indicated that VC, ES, and PS additives in the electrolyte are all easier to form organic components in the anode SEI film by one-electron reduction. The priority of one-electron reduction to produce organic SEI components is in the order of VC>PC>EC; two-electron reduction to produce the inorganic Na CO component is different and follows the order of EC>PC>VC. Two-electron reduction for sulfites ES and PS to form inorganic Na SO is harder than that of carbonate ester reduction. It is also suggested that the one- and two-electron reductive decomposition pathway for FEC is more feasible to produce inorganic NaF components.
钠离子电池中的固体电解质界面(SEI)膜与电池的容量衰减和循环稳定性密切相关。然而,关于钠离子电池SEI膜的研究较少,且SEI膜的形成机制尚不清楚。通过密度泛函理论(DFT)研究了碳酸亚乙酯(EC)、碳酸亚丙酯(PC)、碳酸亚乙烯酯(VC)、亚硫酸乙烯酯(ES)、1,3 - 亚硫酸丙烯酯(PS)和氟代碳酸乙烯酯(FEC)的还原机理。计算了反应活化能、吉布斯自由能、焓以及过渡态结构。结果表明,电解质中的VC、ES和PS添加剂都更容易通过单电子还原在阳极SEI膜中形成有机成分。单电子还原生成有机SEI成分的优先级顺序为VC>PC>EC;双电子还原生成无机Na₂CO₃成分的顺序则不同,为EC>PC>VC。亚硫酸酯ES和PS双电子还原形成无机Na₂SO₄比碳酸酯还原更难。研究还表明,FEC的单电子和双电子还原分解途径生成无机NaF成分更可行。