Selis Luis A, Seminario Jorge M
Department of Chemical Engineering, Department of Electrical and Computer Engineering, Department of Materials Science and Engineering, Texas A&M University College Station TX 77843 USA
RSC Adv. 2018 Jan 29;8(10):5255-5267. doi: 10.1039/c7ra12690e.
Rechargeable lithium-ion batteries require a vigorous improvement if we want to use them massively for high energy applications. Silicon and metal lithium anodes are excellent alternatives because of their large theoretical capacity when compared to graphite used in practically all rechargeable Li-ion batteries. However, several problems need to be addressed satisfactorily before a major fabrication effort can be launched; for instance, the growth of lithium dendrites is one of the most important to take care due to safety issues. In this work we attempt to predict the mechanism of dendrite growth by simulating possible behaviors of charge distributions in the anode of an already cracked solid electrolyte interphase of a nanobattery, which is under the application of an external field representing the charging of the battery; thus, elucidating the conditions for dendrite growth. The extremely slow drift velocity of the Li-ions of ∼1 mm per hour in a typical commercial Li-ion battery, makes the growth of a dendrite take a few hours; however, once a Li-ion arrives at an active site of the anode, it takes an extremely short time of ∼1 ps to react. This large difference in time-scales allows us to perform the molecular dynamics simulation of the ions at much larger drift velocities, so we can have valuable results in reasonable computational times. The conditions before the growth are assumed and conditions that do not lead to the growth are ignored. We performed molecular dynamics simulations of a pre-lithiated silicon anode with a Li : Si ratio of 21 : 5, corresponding to a fully charged battery. We simulate the dendrite growth by testing a few charge distributions in a nanosized square representing a crack of the solid electrolyte interphase, which is where the electrolyte solution comes into direct contact with the LiSi alloy anode. Depending on the selected charge distributions for such an anode surface, the dendrites grow during the simulation when an external field is applied. We found that dendrites grow when strong deviations of charge distributions take place on the surface of the crack. Results from this work are important in finding ways to constrain lithium dendrite growth using tailored coatings or pre-coatings covering the LiSi alloy anode.
如果我们想将可充电锂离子电池大规模用于高能量应用,就需要大力改进。硅和金属锂阳极是极佳的替代品,因为与几乎所有可充电锂离子电池中使用的石墨相比,它们具有较大的理论容量。然而,在大规模制造之前,有几个问题需要得到令人满意的解决;例如,由于安全问题,锂枝晶的生长是最需要关注的问题之一。在这项工作中,我们试图通过模拟纳米电池已破裂的固体电解质界面阳极中电荷分布的可能行为来预测枝晶生长的机制,该阳极处于代表电池充电的外部场的作用下;从而阐明枝晶生长的条件。在典型的商用锂离子电池中,锂离子的漂移速度极慢,约为每小时1毫米,这使得枝晶的生长需要几个小时;然而,一旦锂离子到达阳极的活性位点,反应只需极短的时间,约为1皮秒。这种时间尺度上的巨大差异使我们能够以大得多的漂移速度对离子进行分子动力学模拟,这样我们就能在合理的计算时间内得到有价值的结果。假设生长前的条件,忽略不导致生长的条件。我们对锂硅比为21∶5的预锂化硅阳极进行了分子动力学模拟,这对应于一个充满电的电池。我们通过在代表固体电解质界面裂纹的纳米尺寸正方形中测试几种电荷分布来模拟枝晶生长,这里是电解液与锂硅合金阳极直接接触的地方。根据为这种阳极表面选择的电荷分布,在施加外部场时,枝晶在模拟过程中生长。我们发现,当裂纹表面的电荷分布出现强烈偏差时,枝晶就会生长。这项工作的结果对于找到使用定制涂层或预涂层覆盖锂硅合金阳极来抑制锂枝晶生长的方法很重要。