Ezzedine Mariam, Zamfir Mihai-Robert, Jardali Fatme, Leveau Lucie, Caristan Eleonor, Ersen Ovidiu, Cojocaru Costel-Sorin, Florea Ileana
LPICM, CNRS, Ecole polytechnique, IP Paris, Palaiseau 91228 Cedex, France.
National Institute for Laser, Plasma & Radiation Physics (INFLPR), Atomistilor Street, No. 409, Magurele, Ilfov RO-077125, Romania.
ACS Appl Mater Interfaces. 2021 Jun 2;13(21):24734-24746. doi: 10.1021/acsami.1c03302. Epub 2021 May 21.
Silicon-based anode fabrication with nanoscale structuration improves the energy density and life cycle of Li-ion batteries. As-synthesized silicon (Si) nanowires (NWs) or nanoparticles (NPs) directly on the current collector represent a credible alternative to conventional graphite anodes. However, the operating potentials of these electrodes are below the electrochemical stability window of all electrolytes used in commercial Li-ion systems. During the first charging phase of the cell, partial decomposition of the electrolyte takes place, which leads to the formation of a layer at the surface of the electrode, called solid electrolyte interphase (SEI). A stable and continuous SEI layer formation is a critical factor to achieve reliable lifetime stability of the battery. Once formed, the SEI acts as a passivation layer that minimizes further degradation of the electrolyte during cycling, while allowing lithium-ion diffusion with their subsequent insertion into the active material and ensuring reversible operation of the electrode. However, one of the major issues requiring deeper investigation is the assessment of the morphological extension of the SEI layer into the active material, which is one of the main parameters affecting the anode performances. In the present study, we use electron tomography with a low electron dose to retrieve three-dimensional information on the SEI layer formation and its stability around SiNWs and SiNPs. The possible mechanisms of SEI evolution could be inferred from the interpretation and analysis of the reconstructed volumes. Significant volume variations in the SiNW and an inhomogeneous distribution of the SEI layer around the NWs are observed during cycling and provide insights into the potential mechanism leading to the generally reported SiNW anode capacity fading. By contrast, analysis of the reconstructed SiNPs' volume for a sample undergoing one lithiation-delithiation cycle shows that the SEI remains homogeneously distributed around the NPs that retain their spherical morphology and points to the potential benefit of such nanoscale Si anode materials to improve their cycling lifetime.
具有纳米级结构的硅基阳极制造工艺可提高锂离子电池的能量密度和循环寿命。直接在集流体上合成的硅(Si)纳米线(NWs)或纳米颗粒(NPs)是传统石墨阳极的可靠替代品。然而,这些电极的工作电位低于商业锂离子系统中使用的所有电解质的电化学稳定窗口。在电池的首次充电阶段,电解质会发生部分分解,这会导致在电极表面形成一层,称为固体电解质界面(SEI)。形成稳定且连续的SEI层是实现电池可靠寿命稳定性的关键因素。一旦形成,SEI就会作为钝化层,在循环过程中使电解质的进一步降解最小化,同时允许锂离子扩散并随后插入活性材料中,并确保电极的可逆操作。然而,需要更深入研究的主要问题之一是评估SEI层向活性材料中的形态扩展,这是影响阳极性能的主要参数之一。在本研究中,我们使用低电子剂量的电子断层扫描来获取关于SEI层形成及其在SiNWs和SiNPs周围稳定性的三维信息。可以从重建体积的解释和分析中推断出SEI演变的可能机制。在循环过程中观察到SiNW中的显著体积变化以及NWs周围SEI层的不均匀分布,这为导致普遍报道的SiNW阳极容量衰减的潜在机制提供了见解。相比之下,对经历一次锂化 -脱锂循环的样品的重建SiNPs体积分析表明,SEI在保持球形形态的NPs周围保持均匀分布,并指出这种纳米级硅阳极材料在提高其循环寿命方面的潜在益处。