Department of Materials Science and Engineering, Stanford University, Stanford, California 94305, United States.
Nano Lett. 2011 Sep 14;11(9):4018-25. doi: 10.1021/nl202630n. Epub 2011 Aug 11.
With its high specific capacity, silicon is a promising anode material for high-energy lithium-ion batteries, but volume expansion and fracture during lithium reaction have prevented implementation. Si nanostructures have shown resistance to fracture during cycling, but the critical effects of nanostructure size and native surface oxide on volume expansion and cycling performance are not understood. Here, we use an ex situ transmission electron microscopy technique to observe the same Si nanowires before and after lithiation and have discovered the impacts of size and surface oxide on volume expansion. For nanowires with native SiO(2), the surface oxide can suppress the volume expansion during lithiation for nanowires with diameters <∼50 nm. Finite element modeling shows that the oxide layer can induce compressive hydrostatic stress that could act to limit the extent of lithiation. The understanding developed herein of how volume expansion and extent of lithiation can depend on nanomaterial structure is important for the improvement of Si-based anodes.
硅具有高比容量,是高能锂离子电池有前途的阳极材料,但在锂反应过程中的体积膨胀和断裂阻止了其实际应用。硅纳米结构在循环过程中显示出抗断裂能力,但纳米结构尺寸和本征表面氧化物对体积膨胀和循环性能的关键影响尚不清楚。在这里,我们使用一种原位透射电子显微镜技术来观察同一硅纳米线在锂化前后的情况,并发现了尺寸和表面氧化物对体积膨胀的影响。对于具有本征 SiO(2)的纳米线,表面氧化物可以抑制直径<∼50nm 的纳米线在锂化过程中的体积膨胀。有限元模拟表明,氧化层可以诱导压缩静水压力,从而限制锂化程度。本文对体积膨胀和锂化程度如何取决于纳米材料结构的理解,对于改善硅基阳极非常重要。