Issman Liron, Kloza Philipp A, Terrones Portas Jeronimo, Collins Brian, Pendashteh Afshin, Pick Martin, Vilatela Juan J, Elliott James A, Boies Adam
Department of Engineering, University of Cambridge, Cambridge CB2 1PZ, United Kingdom.
Department of Materials Science & Metallurgy, University of Cambridge, Cambridge CB3 0FS, United Kingdom.
ACS Nano. 2022 Jun 28;16(6):9583-9597. doi: 10.1021/acsnano.2c02875. Epub 2022 May 31.
Carbon nanotubes (CNTs) individually exhibit exceptional physical properties, surpassing state-of-the-art bulk materials, but are used commercially primarily as additives rather than as a standalone macroscopic product. This limited use of bulk CNT materials results from the inability to harness the superb nanoscale properties of individual CNTs into macroscopic materials. CNT alignment within a textile has been proven as a critical contributor to narrow this gap. Here, we report the development of an altered direct CNT spinning method based on the floating catalyst chemical vapor deposition process, which directly interacts with the self-assembly of the CNT bundles in the gas phase. The setup is designed to apply an AC electric field to continuously align the CNTs in situ during the formation of CNT bundles and subsequent aerogel. A mesoscale CNT model developed to simulate the alignment process has shed light on the need to employ AC rather than DC fields based on a CNT stiffening effect (z-pinch) induced by a Lorentz force. The AC-aligned synthesis enables a means to control CNT bundle diameters, which broadened from 16 to 25 nm. The resulting bulk CNT textiles demonstrated an increase in the specific electrical and tensile properties (up to 90 and 460%, respectively) without modifying the quantity or quality of the CNTs, as verified by thermogravimetric analysis and Raman spectroscopy, respectively. The enhanced properties were correlated to the degree of CNT alignment within the textile as quantified by small-angle X-ray scattering and scanning electron microscopy image analysis. Clear alignment (orientational order parameter = 0.5) was achieved relative to the pristine material (orientational order parameter = 0.19) at applied field intensities in the range of 0.5-1 kV cm at a frequency of 13.56 MHz.
碳纳米管(CNTs)各自展现出卓越的物理性能,超越了最先进的块状材料,但在商业上主要用作添加剂,而非独立的宏观产品。块状碳纳米管材料的这种有限用途是由于无法将单个碳纳米管的卓越纳米级性能应用于宏观材料。已证明碳纳米管在纺织品中的排列是缩小这一差距的关键因素。在此,我们报告了一种基于浮动催化剂化学气相沉积工艺的改进型直接碳纳米管纺丝方法的开发,该方法直接与气相中碳纳米管束的自组装相互作用。该装置设计用于施加交流电场,以便在碳纳米管束形成及随后的气凝胶形成过程中连续原位排列碳纳米管。为模拟排列过程而开发的中尺度碳纳米管模型揭示了基于洛伦兹力引起的碳纳米管硬化效应(z 箍缩)而采用交流电场而非直流电场的必要性。交流电场排列合成法提供了一种控制碳纳米管束直径的方法,其直径从 16 纳米拓宽至 25 纳米。通过热重分析和拉曼光谱分别验证,所得的块状碳纳米管纺织品在不改变碳纳米管数量或质量的情况下,比电导率和拉伸性能分别提高了高达 90%和 460%。增强的性能与通过小角 X 射线散射和扫描电子显微镜图像分析量化的碳纳米管在纺织品中的排列程度相关。在 13.56 MHz 频率下,施加 0.5 - 1 kV/cm 的场强时,相对于原始材料(取向有序参数 = 0.19)实现了清晰的排列(取向有序参数 = 0.5)。