Balbuena Perla B, Zhao Jin, Huang Shiping, Wang Yixuan, Sakulchaicharoen Nataphan, Resasco Daniel E
Department of Chemical Engineering, Texas A&M University, College Station, TX 77843, USA.
J Nanosci Nanotechnol. 2006 May;6(5):1247-58. doi: 10.1166/jnn.2006.141.
Classical molecular dynamics simulations are carried out to analyze the physical state of the catalyst, and the growth of single-wall carbon nanotubes under typical temperature and pressure conditions of their experimental synthesis, emphasizing the role of the catalyst/substrate interactions. It is found that a strong cluster/substrate interaction increases the cluster melting point, modifying the initial stages of carbon dissolution and precipitation on the cluster surface. Experiments performed on model Co-Mo catalysts clearly illustrate the existence of an initial period where the catalyst is formed and no nanotube growth is observed. To quantify the nature of the Co-Mo2C interaction, quantum density functional theory is applied to characterize structural and energetic features of small Co clusters deposited on a (001) Mo2C surface, revealing a strong attachment of Co-clusters to the Mo2C surface, which may increase the melting point of the cluster and prevent cluster sintering.
进行经典分子动力学模拟以分析催化剂的物理状态,以及在单壁碳纳米管实验合成的典型温度和压力条件下其生长情况,重点强调催化剂/衬底相互作用的作用。研究发现,强团簇/衬底相互作用会提高团簇熔点,改变碳在团簇表面溶解和沉淀的初始阶段。在模型Co-Mo催化剂上进行的实验清楚地表明,存在一个催化剂形成但未观察到纳米管生长的初始阶段。为了量化Co-Mo₂C相互作用的性质,应用量子密度泛函理论来表征沉积在(001)Mo₂C表面的小Co团簇的结构和能量特征,揭示了Co团簇与Mo₂C表面的强附着,这可能会提高团簇的熔点并防止团簇烧结。