Yang Po-Yu, Pao Chun-Wei
Research Center for Applied Sciences, Academia Sinica, Taipei 11529, Taiwan.
Department of Materials Science and Engineering, National Dong Hwa University, Hualien 974301, Taiwan.
ACS Appl Mater Interfaces. 2021 Feb 3;13(4):5017-5027. doi: 10.1021/acsami.0c18783. Epub 2021 Jan 20.
Lithium (Li) metal is regarded as one of the most promising anode materials for use in next-generation high-energy-density rechargeable batteries because of its high volumetric and gravimetric specific capacity, as well as low reduction potential. Unfortunately, uncontrolled dendritic Li growth during cyclic charging/discharging leads to low columbic efficiency and critical safety issues. Hence, comprehensive understanding of the formation mechanism for Li-dendrite growth, particularly at the onset of dendrite formation, is essential for developing Li-metal anode batteries. In this study, reactive molecular dynamics (MD) simulations in combination with the electrochemical dynamics with implicit degrees of freedom (EChemDID) method were performed to investigate the formation and evolution of solid electrolyte interphase (SEI) films for a Li-metal anode under cyclic charging/discharging processes in two distinct dimensions, namely, electrolyte compositions and initial surface morphologies. Our simulations indicated that regardless of the electrolyte compositions and initial anode morphologies, inhomogeneous Li reduction, namely, the formation of Li-reduction "hotspots" during cyclic charging cycles, took place and could serve as the seed for subsequent dendrite growth. The fluorine-containing electrolyte additives could notably mitigate the Li-anode roughening processes by forming dense-SEI-layer products or suppressing electrolyte decomposition. A series of Li-ion-drifting simulations suggest that Li ions navigate through the SEI layer via pathways composed of low-density atoms and become reduced at these reduction hotspots, promoting inhomogeneous deposition and subsequent dendrite growth. The present study reveals atomistic details of the early stage of dendrite growth during cyclic loadings under different electrolyte compositions and anode morphologies, thereby providing insights for designing artificial SEI layers or electrolytes for long-life, high-capacity Li-ion batteries.
锂(Li)金属因其高体积比容量和高重量比容量以及低还原电位,被视为下一代高能量密度可充电电池中最有前景的负极材料之一。不幸的是,在循环充电/放电过程中不受控制的锂枝晶生长会导致低库仑效率和严重的安全问题。因此,全面了解锂枝晶生长的形成机制,特别是在枝晶形成的起始阶段,对于开发锂金属负极电池至关重要。在本研究中,结合具有隐式自由度的电化学动力学(EChemDID)方法进行了反应分子动力学(MD)模拟,以研究在循环充电/放电过程中,在电解质组成和初始表面形态这两个不同维度下锂金属负极的固体电解质界面(SEI)膜的形成和演变。我们的模拟表明,无论电解质组成和初始负极形态如何,在循环充电过程中都会发生不均匀的锂还原,即形成锂还原“热点”,这可以作为后续枝晶生长的种子。含氟电解质添加剂可以通过形成致密的SEI层产物或抑制电解质分解来显著减轻锂负极的粗糙化过程。一系列锂离子漂移模拟表明,锂离子通过由低密度原子组成的路径穿过SEI层,并在这些还原热点处被还原,从而促进不均匀沉积和随后的枝晶生长。本研究揭示了在不同电解质组成和负极形态下循环加载过程中枝晶生长早期阶段的原子细节,从而为设计用于长寿命、高容量锂离子电池的人工SEI层或电解质提供了见解。