Okuno Yukihiro, Ushirogata Keisuke, Sodeyama Keitaro, Tateyama Yoshitaka
Research and Development Headquarters, FUJIFILM Corporation, 210 Nakanuma, Minamiashigara, Kanagawa 250-0193, Japan.
International Center for Materials Nanoarchitectonics (MANA), National Institute for Materials Science (NIMS), 1-1 Namiki, Tsukuba, Ibaraki 305-0044, Japan.
Phys Chem Chem Phys. 2016 Mar 28;18(12):8643-53. doi: 10.1039/c5cp07583a.
Additives in the electrolyte solution of lithium-ion batteries (LIBs) have a large impact on the performance of the solid electrolyte interphase (SEI) that forms on the anode and is a key to the stability and durability of LIBs. We theoretically investigated effects of fluoroethylene carbonate (FEC), a representative additive, that has recently attracted considerable attention for the enhancement of cycling stability of silicon electrodes and the improvement of reversibility of sodium-ion batteries. First, we intensively examined the reductive decompositions by ring-opening, hydrogen fluoride (HF) elimination to form a vinylene carbonate (VC) additive and intermolecular chemical reactions of FEC in the ethylene carbonate (EC) electrolyte, by using density functional theory (DFT) based molecular dynamics and the blue-moon ensemble technique for the free energy profile. The results show that the most plausible product of the FEC reductive decomposition is lithium fluoride (LiF), and that the reactivity of FEC to anion radicals is found to be inert compared to the VC additive. We also investigated the effects of the generated LiF on the SEI by using two model systems; (1) LiF molecules distributed in a model aggregate of organic SEI film components (SFCs) and (2) a LiF aggregate interfaced with the SFC aggregate. DFT calculations of the former system show that F atoms form strong bindings with the Li atoms of multiple organic SFC molecules and play as a joint connecting them. In the latter interface system, the LiF aggregate adsorbs the organic SFCs through the F-Li bindings. These results suggest that LiF moieties play the role of glue in the organic SFC within the SEI film. We also examined the interface structure between a LiF aggregate and a lithiated silicon anode, and found that they are strongly bound. This strong binding is likely to be related to the effectiveness of the FEC additive in the electrolyte for the silicon anode.
锂离子电池(LIBs)电解液中的添加剂对在阳极上形成的固体电解质界面(SEI)的性能有很大影响,而SEI是LIBs稳定性和耐久性的关键。我们从理论上研究了氟代碳酸乙烯酯(FEC)的作用,FEC作为一种具有代表性的添加剂,最近在增强硅电极的循环稳定性和改善钠离子电池的可逆性方面引起了相当大的关注。首先,我们通过基于密度泛函理论(DFT)的分子动力学和用于自由能分布的蓝月亮系综技术,深入研究了FEC在碳酸乙烯酯(EC)电解液中的开环还原分解、氟化氢(HF)消除以形成碳酸亚乙烯酯(VC)添加剂以及分子间化学反应。结果表明,FEC还原分解最可能的产物是氟化锂(LiF),并且发现FEC与阴离子自由基的反应性与VC添加剂相比是惰性的。我们还通过两个模型系统研究了生成的LiF对SEI的影响;(1)LiF分子分布在有机SEI膜成分(SFCs)的模型聚集体中,以及(2)与SFC聚集体界面相连的LiF聚集体。对前一个系统的DFT计算表明,F原子与多个有机SFC分子的Li原子形成强键,并起到连接它们的作用。在后一个界面系统中,LiF聚集体通过F-Li键吸附有机SFCs。这些结果表明,LiF部分在SEI膜内的有机SFC中起到胶水的作用。我们还研究了LiF聚集体与锂化硅阳极之间的界面结构,发现它们紧密结合。这种紧密结合可能与电解液中FEC添加剂对硅阳极的有效性有关。