Department of Nano-Mechanics, Korea Institute of Machinery & Materials (KIMM), 156, Gajeongbuk-ro, Yuseong-gu, Daejeon, 305-343, Republic of Korea.
School of Advanced Materials Science and Engineering, Sungkyunkwan University, Suwon, 16419, Republic of Korea.
Nanoscale. 2017 Apr 6;9(14):4713-4720. doi: 10.1039/c7nr00965h.
Silicon anodes for lithium ion batteries (LiBs) have been attracting considerable attention due to a theoretical capacity up to about 10 times higher than that of conventional graphite. However, huge volume expansion during the cycle causes cracks in the silicon, resulting in the degradation of cycling performance and eventual failure. Moreover, low electrical conductivity and an unstable solid electrolyte interface (SEI) layer resulting from repeated changes in volume still block the next step forward for the commercialization of the silicon material. Herein we demonstrate the carbon nanotube (CNT) aerogel/Si nanohybrid structure for anode materials of LiBs via freeze casting followed by an RF magnetron sputtering process, exhibiting improved capacity retention compared to Si only samples during 1000 electrochemical cycles. The CNT aerogels as 3D porous scaffold structures could provide buffer volume for the expansion/shrinkage of Si lattices upon cycling and increase electrical conductivity. In addition, the nanospherical and relatively thin SEI layers of the CNT aerogel/Si nanohybrid structure show better lithium ion diffusion characteristics during cycling. For this reason, the Si@CNT aerogel anode still yielded a high specific capacity of 1439 mA h g after 1000 charge/discharge cycles with low capacity fading. Our approach could be applied to other group IV LiB materials that undergo large volume changes, and also has promising potential for high performance energy applications.
硅基锂离子电池(LiBs)的阳极由于其理论容量高达传统石墨的约 10 倍,因此受到了广泛关注。然而,在循环过程中巨大的体积膨胀会导致硅的裂纹,从而降低循环性能并最终导致失效。此外,由于体积反复变化导致的低电导率和不稳定的固体电解质界面(SEI)层仍然阻碍了硅材料的商业化进程。在此,我们通过冷冻铸造和射频磁控溅射工艺展示了用于 LiBs 阳极材料的碳纳米管(CNT)气凝胶/Si 纳米杂化结构,与仅含 Si 的样品相比,在 1000 次电化学循环中表现出更好的容量保持率。CNT 气凝胶作为 3D 多孔支架结构,可以为 Si 晶格在循环过程中的膨胀/收缩提供缓冲体积,并提高电导率。此外,CNT 气凝胶/Si 纳米杂化结构的纳米球形和相对较薄的 SEI 层在循环过程中表现出更好的锂离子扩散特性。因此,Si@CNT 气凝胶阳极在 1000 次充放电循环后仍具有 1439 mA h g 的高比容量和低容量衰减。我们的方法可应用于其他经历大体积变化的 IV 族 LiB 材料,并且在高性能能源应用方面也具有广阔的应用前景。