Department of Materials Science and Engineering , Southern University of Science and Technology , No. 1088 Xueyuan Boulevard , Shenzhen , Guangdong 518055 , China.
Environmental Molecular Science Laboratory , Pacific Northwest National Laboratory , 902 Battelle Boulevard , Richland , Washington 99352 , United States.
ACS Appl Mater Interfaces. 2018 Dec 5;10(48):41458-41464. doi: 10.1021/acsami.8b17387. Epub 2018 Nov 19.
Metal sulfide materials such as CuS, SnS, CoS, and MoS are high-capacity anode materials for Li-ion batteries with high capacity. However, these materials go through a conversion reaction with Li, which is accompanied by inevitably huge volume expansions, thereby causing performance degradation. Here, we report a nanoscale engineering route to efficiently control the overall volume expansion for enhanced performance. We engineered CuS with nanoplate assembly on a nanostring, leading to a nanostructure mimicking the crassula baby necklace (CBN) in the natural plant. Using in situ transmission electron microscopy, we probed the lithiation kinetics and dynamic structural transformations. Due to the linkage of the central nanostring, the CuS CBN exhibited a fast Li diffusion along the axial direction and high mechanical stability during lithiation. The volume expansion was minimal for our CuS CBN due to the pre-engineered gap and pores between these plates. The CuS followed a two-step lithiation process, with CuS and LiS formation as the first step and Cu extrusion in the later stage. Interestingly, during the CuS-to-Cu conversion, we observed an incubation period before the metallic Cu extrusion, which is featured by the formation of an amorphous structure due to the large lattice strain and distortion associated with the displacement of Cu by Li ions. In the final stage, the lithiated amorphous phase recrystallized to a composite of Cu nanocrystals in a polycrystalline LiS matrix. Associated with the nanoscale size, the Cu nanocrystals can reversibly dissolve into the matrix upon delithiation. The present work demonstrates tailoring of desired functionality in electrodes using bionic engineering methods.
金属硫化物材料,如 CuS、SnS、CoS 和 MoS,是具有高容量的锂离子电池的高容量阳极材料。然而,这些材料与 Li 发生转化反应,伴随着不可避免的巨大体积膨胀,从而导致性能下降。在这里,我们报告了一种纳米级工程路线,有效地控制整体体积膨胀,以提高性能。我们通过在纳米线上组装纳米板的方法来设计 CuS,从而构建出一种模仿天然植物马齿苋项链(CBN)的纳米结构。通过原位透射电子显微镜,我们探测了锂化动力学和动态结构转变。由于中央纳米线的连接,CuS CBN 表现出沿轴向快速的 Li 扩散和在锂化过程中的高机械稳定性。由于这些板之间预先设计的间隙和孔隙,我们的 CuS CBN 的体积膨胀最小。CuS 遵循两步锂化过程,首先形成 CuS 和 LiS,然后在后期进行 Cu 挤出。有趣的是,在 CuS 到 Cu 的转化过程中,我们观察到一个金属 Cu 挤出之前的潜伏期,这一阶段的特征是由于 Li 离子的取代导致晶格应变和扭曲很大,形成非晶结构。在最后阶段,锂化的非晶相再结晶为多晶 LiS 基质中的 Cu 纳米晶复合材料。与纳米尺寸相关的是,Cu 纳米晶在脱锂时可以可逆地溶解在基质中。本工作展示了使用仿生工程方法在电极中定制所需功能的能力。