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基于分子动力学-蒙特卡罗模拟的等离子体增强化学气相沉积过程中含氢纳米晶碳膜的生长控制策略

Growth Control Strategy of Hydrogen-Containing Nanocrystalline Carbon Films during Plasma-Enhanced Chemical Vapor Deposition based on Molecular Dynamics-Monte Carlo Simulations.

作者信息

Che Ju, Yi Peiyun, Deng Yujun, Zhang Di, Peng Linfa, Lai Xinmin

机构信息

State Key Laboratory of Mechanical System and Vibration, Shanghai Jiao Tong University, Shanghai 200240, P. R. China.

Shanghai Key Laboratory of Digital Manufacture for Thin-Walled Structures, Shanghai Jiao Tong University, Shanghai 200240, P. R. China.

出版信息

ACS Appl Mater Interfaces. 2023 Sep 27;15(38):45475-45484. doi: 10.1021/acsami.3c10157. Epub 2023 Sep 13.

DOI:10.1021/acsami.3c10157
PMID:37703433
Abstract

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.

摘要

具有非晶-纳米晶碳氢复合结构的含氢纳米晶碳膜(n-C:H)在多种应用中表现出优异的性能。由于等离子体增强化学气相沉积(PECVD)能够创建可调节的沉积环境并控制薄膜成分,因此通常用于制备n-C:H薄膜。然而,n-C:H在原子尺度上的生长机制仍知之甚少,这阻碍了合适的沉积参数和薄膜成分的设计。本文采用了一种先进的混合分子动力学-时间戳力偏置蒙特卡罗模型(MD/tfMC)来模拟n-C:H的等离子体辅助生长。我们的结果表明,优化离子轰击能量、沉积温度和前驱体的H:C比对于实现高度有序的n-C:H薄膜的成核和生长至关重要。这些发现通过实验观察和密度泛函理论计算得到了进一步验证,结果表明氢原子可以通过化学催化过程促进纳米晶碳的形成。此外,我们发现当H/C比等于1时,结晶度达到最佳。这些理论见解为含氢纳米晶碳膜的可控制备提供了一种有效的策略。

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