材料科学
纳米晶材料
成核
等离子体增强化学气相沉积
氢
无定形碳
化学气相沉积
结晶度
无定形固体
碳纤维
化学工程
薄膜
沉积(地质)
动力学蒙特卡罗方法
纳米技术
化学物理
蒙特卡罗方法
复合数
结晶学
有机化学
复合材料
化学
数学
古生物学
沉积物
工程类
生物
统计
作者
Ju Che,Peiyun Yi,Yujun Deng,Di Zhang,Linfa Peng,Xinmin Lai
标识
DOI:10.1021/acsami.3c10157
摘要
Hydrogen-containing nanocrystalline carbon films (n-C:H) with amorphous-nanocrystalline hydrocarbon composite structures exhibit excellent properties in diverse applications. Plasma-enhanced chemical vapor deposition (PECVD) is commonly employed to prepare n-C:H films due to its ability to create an adjustable deposition environment and control film compositions. However, the atomic-scale growth mechanism of n-C:H remains poorly understood, obstructing the design of the appropriate deposition parameters and film compositions. This paper employs a state-of-the-art hybrid molecular dynamics-time-stamped force-biased Monte Carlo model (MD/tfMC) to simulate the plasma-assisted growth of n-C:H. Our results reveal that optimizing the energy of ion bombardments, deposition temperature, and precursor's H:C ratio is crucial for achieving the nucleation and growth of highly ordered n-C:H films. These findings are further validated through experimental observations and density functional theory calculations, which show that hydrogen atoms can promote the formation of nanocrystalline carbon through chemical catalytic processes. Additionally, we find that the crystallinity reaches its optimum when the H/C ratio is equal to 1. These theoretical insights provide an effective strategy for the controlled preparation of hydrogen-containing nanocrystalline carbon films.
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