Environmental Molecular Sciences Laboratory, Pacific Northwest National Laboratory, Richland, Washington 99352, USA.
ACS Nano. 2013 Jul 23;7(7):6303-9. doi: 10.1021/nn402349j. Epub 2013 Jun 28.
Silicon has been widely explored as an anode material for lithium ion battery. Upon lithiation, silicon transforms to amorphous LixSi (a-LixSi) via electrochemical-driven solid-state amorphization. With increasing lithium concentration, a-LixSi transforms to crystalline Li15Si4 (c-Li15Si4). The mechanism of this crystallization process is not known. In this paper, we report the fundamental characteristics of the phase transition of a-LixSi to c-Li15Si4 using in situ scanning transmission electron microscopy, electron energy loss spectroscopy, and density function theory (DFT) calculation. We find that when the lithium concentration in a-LixSi reaches a critical value of x = 3.75, the a-Li3.75Si spontaneously and congruently transforms to c-Li15Si4 by a process that is solely controlled by the lithium concentration in the a-LixSi, involving neither large-scale atomic migration nor phase separation. DFT calculations indicate that c-Li15Si4 formation is favored over other possible crystalline phases due to the similarity in electronic structure with a-Li3.75Si.
硅已被广泛探索作为锂离子电池的阳极材料。在锂化过程中,硅通过电化学驱动的固态非晶化转变为非晶态 LixSi(a-LixSi)。随着锂离子浓度的增加,a-LixSi 转变为结晶态 Li15Si4(c-Li15Si4)。这种结晶过程的机制尚不清楚。在本文中,我们使用原位扫描透射电子显微镜、电子能量损失光谱和密度泛函理论(DFT)计算报告了 a-LixSi 向 c-Li15Si4 相变的基本特征。我们发现,当 a-LixSi 中的锂离子浓度达到 x = 3.75 的临界值时,a-Li3.75Si 通过仅由 a-LixSi 中的锂离子控制的过程自发且一致地转变为 c-Li15Si4,既不需要大规模原子迁移也不需要相分离。DFT 计算表明,由于与 a-Li3.75Si 的电子结构相似,c-Li15Si4 的形成优于其他可能的晶相。