Huang Yalan, Zhu He, Zhu Hekang, Zhang Jian, Ren Yang, Liu Qi
Department of Physics, City University of Hong Kong, Hong Kong 999077, People's Republic of China.
Shenzhen Research Institute, City University of Hong Kong, Shenzhen 518057, People's Republic of China.
Nanotechnology. 2021 Apr 27;32(29). doi: 10.1088/1361-6528/abf2ff.
Layered LiNiCoMnO(NCM) is expected to dominate the future cathode technology of the automotive industry, due to its high energy density and low cost. Despite its excellent prospects, however, the severe capacity decay of NCM cathodes has prevented this promising material from achieving further success. The mechanism underlying this phenomenon is controversial and has been generally understood as arising from the complex structural changes that take place upon Li-(de)intercalation. However, deeper insight has not been available due to unclear structural kinetics, in particular, in cycled NCM cathodes. For this study, we conductedhigh-energy synchrotron x-ray diffraction (XRD) measurements on a typical LiNiCoMnO(NCM523) cathode that had been operated for 90 cycles, then compared the results with those collected from a fresh NCM532 electrode. It was revealed that the H1-H2 phase transition that only occurs at the first cycle is irreversible. Remarkably, the-contraction triggered by the H2-H3 transition, which is expected to be the major cause of intergranular cracks in electrodes, became even more profound after cycling. Combining the above results with electrochemical testing and microscopic imaging, we discuss the interplay between structural dynamics and performance degradation in NCM532 in detail. This study provides key evidence for a mechanically induced capacity decay mechanism, which is expected to be extended to NCM materials with various compositions.
层状LiNiCoMnO(NCM)因其高能量密度和低成本,有望主导未来汽车行业的阴极技术。然而,尽管前景广阔,但NCM阴极严重的容量衰减阻碍了这种有前途的材料取得更大成功。这种现象背后的机制存在争议,一般认为是由锂(脱)嵌入时发生的复杂结构变化引起的。然而,由于结构动力学不明确,尤其是在循环的NCM阴极中,尚未获得更深入的见解。在本研究中,我们对一个已运行90个循环的典型LiNiCoMnO(NCM523)阴极进行了高能同步加速器X射线衍射(XRD)测量,然后将结果与从新鲜的NCM532电极收集的结果进行比较。结果表明,仅在第一个循环中发生的H1-H2相变是不可逆的。值得注意的是,预计是电极中晶间裂纹主要原因的H2-H3转变引发的收缩在循环后变得更加明显。将上述结果与电化学测试和微观成像相结合,我们详细讨论了NCM532中结构动力学与性能退化之间的相互作用。本研究为机械诱导容量衰减机制提供了关键证据,预计该机制将扩展到各种组成的NCM材料。