Key Laboratory of Multifunctional Nanomaterials and Smart Systems, Suzhou Institute of Nano-Tech and Nano-Bionics, Chinese Academy of Sciences, Suzhou, Jiangsu 215123, People's Republic of China.
Department of Materials Science and Engineering, North Carolina State University, Raleigh, North Carolina 27695, United States.
ACS Appl Mater Interfaces. 2023 Jul 12;15(27):32656-32666. doi: 10.1021/acsami.3c03209. Epub 2023 Jun 29.
Stress graphitization is a unique phenomenon at the carbon nanotube (CNT)-matrix interfaces in CNT/carbon matrix (CNT/C) composites. A lack of fundamental atomistic understanding of its evolution mechanisms and a gap between the theoretical and experimental research have hindered the pursuit of utilizing this phenomenon for producing ultrahigh-performance CNT/C composites. Here, we performed reactive molecular dynamics simulations along with an experimental study to explore stress graphitization mechanisms of a CNT/polyacrylonitrile (PAN)-based carbon matrix composite. Different CNT contents in the composite were considered, while the nanotube alignment was controlled in one direction in the simulations. We observe that the system with a higher CNT content exhibits higher localized stress concentration in the periphery of CNTs, causing alignment of the nitrile groups in the PAN matrix along the CNTs, which subsequently results in preferential dehydrogenation and clustering of carbon rings and eventually graphitization of the PAN matrix when carbonized at 1500 K. These simulation results have been validated by experimentally produced CNT/PAN-based carbon matrix composite films, with transmission electron microscopy images showing the formation of additional graphitic layers converted by the PAN matrix around CNTs, where 82 and 144% improvements of the tensile strength and Young's modulus are achieved, respectively. The presented atomistic details of stress graphitization can provide guidance for further optimizing CNT-matrix interfaces in a more predictive and controllable way for the development of novel CNT/C composites with high performance.
应力石墨化是 CNT/碳基质(CNT/C)复合材料中 CNT-基质界面的独特现象。对其演化机制的基本原子理解的缺乏以及理论研究与实验研究之间的差距,阻碍了利用这种现象来生产超高性能 CNT/C 复合材料的研究。在这里,我们通过反应分子动力学模拟和实验研究来探索 CNT/聚丙烯腈(PAN)基碳基质复合材料的应力石墨化机制。考虑了复合材料中不同的 CNT 含量,同时在模拟中控制了纳米管的排列方向。我们观察到,具有较高 CNT 含量的系统在 CNT 外围表现出更高的局部应力集中,导致 PAN 基质中的腈基沿 CNT 排列,随后在 1500K 碳化时导致碳环优先脱氢和聚集,最终使 PAN 基质石墨化。这些模拟结果已经通过实验生产的 CNT/PAN 基碳基质复合材料薄膜得到了验证,透射电子显微镜图像显示了在 CNT 周围由 PAN 基质转化的额外石墨层的形成,其中拉伸强度和杨氏模量分别提高了 82%和 144%。所提出的应力石墨化的原子细节可以为进一步优化 CNT-基质界面提供指导,以更具预测性和可控性的方式开发具有高性能的新型 CNT/C 复合材料。