Shen Chenfei, Ge Mingyuan, Luo Langli, Fang Xin, Liu Yihang, Zhang Anyi, Rong Jiepeng, Wang Chongmin, Zhou Chongwu
Mork Family Department of Chemical Engineering and Materials Science, University of Southern California, Los Angeles, California 90089, United States.
National Synchrotron Light Source II, Brookhaven National Laboratory, Upton, New York 11973, United States.
Sci Rep. 2016 Aug 30;6:31334. doi: 10.1038/srep31334.
In this work, we study the lithiation behaviours of both porous silicon (Si) nanoparticles and porous Si nanowires by in situ and ex situ transmission electron microscopy (TEM) and compare them with solid Si nanoparticles and nanowires. The in situ TEM observation reveals that the critical fracture diameter of porous Si particles reaches up to 1.52 μm, which is much larger than the previously reported 150 nm for crystalline Si nanoparticles and 870 nm for amorphous Si nanoparticles. After full lithiation, solid Si nanoparticles and nanowires transform to crystalline Li15Si4 phase while porous Si nanoparticles and nanowires transform to amorphous LixSi phase, which is due to the effect of domain size on the stability of Li15Si4 as revealed by the first-principle molecular dynamic simulation. Ex situ TEM characterization is conducted to further investigate the structural evolution of porous and solid Si nanoparticles during the cycling process, which confirms that the porous Si nanoparticles exhibit better capability to suppress pore evolution than solid Si nanoparticles. The investigation of structural evolution and phase transition of porous Si nanoparticles and nanowires during the lithiation process reveal that they are more desirable as lithium-ion battery anode materials than solid Si nanoparticles and nanowires.
在这项工作中,我们通过原位和非原位透射电子显微镜(TEM)研究了多孔硅(Si)纳米颗粒和多孔硅纳米线的锂化行为,并将它们与固态硅纳米颗粒和纳米线进行了比较。原位TEM观察表明,多孔硅颗粒的临界断裂直径达到1.52μm,这比先前报道的结晶硅纳米颗粒的150nm和非晶硅纳米颗粒的870nm大得多。完全锂化后,固态硅纳米颗粒和纳米线转变为结晶Li15Si4相,而多孔硅纳米颗粒和纳米线转变为非晶LixSi相,这是由于第一性原理分子动力学模拟所揭示的畴尺寸对Li15Si4稳定性的影响。进行非原位TEM表征以进一步研究多孔和固态硅纳米颗粒在循环过程中的结构演变,这证实了多孔硅纳米颗粒比固态硅纳米颗粒表现出更好的抑制孔隙演变的能力。对多孔硅纳米颗粒和纳米线在锂化过程中的结构演变和相变的研究表明,与固态硅纳米颗粒和纳米线相比,它们作为锂离子电池负极材料更具优势。