Lin Terri C, Dawson Andrew, King Sophia C, Yan Yan, Ashby David S, Mazzetti Joseph A, Dunn Bruce S, Weker Johanna Nelson, Tolbert Sarah H
Department of Chemistry and Biochemistry, UCLA, Los Angeles, California 90095, United States.
Department of Materials Science and Engineering, UCLA, Los Angeles, California 90095, United States.
ACS Nano. 2020 Nov 24;14(11):14820-14830. doi: 10.1021/acsnano.0c03756. Epub 2020 Nov 2.
Tin-based alloying anodes are exciting due to their high energy density. Unfortunately, these materials pulverize after repetitive cycling due to the large volume expansion during lithiation and delithiation; both nanostructuring and intermetallic formation can help alleviate this structural damage. Here, these ideas are combined in nanoporous antimony-tin (NP-SbSn) powders, synthesized by a simple and scalable selective-etching method. The NP-SbSn exhibits bimodal porosity that facilitates electrolyte diffusion; those void spaces, combined with the presence of two metals that alloy with lithium at different potentials, further provide a buffer against volume change. This stabilizes the structure to give NP-SbSn good cycle life (595 mAh/g after 100 cycles with 93% capacity retention). transmission X-ray microscopy (TXM) showed that during cycling NP-SbSn expands by only 60% in area and then contracts back nearly to its original size with no physical disintegration. The pores shrink during lithiation as the pore walls expand into the pore space and then relax back to their initial size during delithiation with almost no degradation. Importantly, the pores remained open even in the fully lithiated state, and structures are in good physical condition after the 36th cycle. The results of this work should thus be useful for designing nanoscale structures in alloying anodes.
锡基合金阳极因其高能量密度而备受关注。不幸的是,由于锂化和脱锂过程中体积大幅膨胀,这些材料在反复循环后会发生粉碎;纳米结构化和金属间化合物的形成都有助于减轻这种结构损伤。在此,通过一种简单且可扩展的选择性蚀刻方法合成的纳米多孔锑锡(NP-SbSn)粉末将这些理念结合在一起。NP-SbSn呈现出双峰孔隙率,有利于电解质扩散;这些孔隙空间,再加上两种在不同电位下与锂合金化的金属的存在,进一步提供了抵御体积变化的缓冲。这使结构稳定,赋予NP-SbSn良好的循环寿命(100次循环后为595 mAh/g,容量保持率为93%)。透射X射线显微镜(TXM)显示,在循环过程中,NP-SbSn的面积仅膨胀60%,然后收缩回几乎接近其原始尺寸,且没有物理崩解。锂化过程中孔隙会收缩,因为孔壁向孔隙空间扩展,然后在脱锂过程中松弛回其初始尺寸,几乎没有降解。重要的是,即使在完全锂化状态下孔隙仍保持开放,并且在第36次循环后结构仍处于良好的物理状态。因此,这项工作的结果对于设计合金阳极中的纳米级结构应该是有用的。