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前驱体对PECVD制备类金刚石涂层的结构与性能的影响OA

Influence of Precursor on Structure and Properties of Diamond-like Carbon Coatings Prepared by PECVD

中文摘要英文摘要

目的 探究不同含氢量的碳氢前驱体对直流脉冲PECVD制备DLC涂层的结构(化学键、sp3含量)和力学性能(硬度、弹性模量)的影响规律.方法 采用直流脉冲PECVD技术,以乙炔、氢稀释乙炔、甲烷、氢稀释甲烷为前驱体,制备4 种类金刚石涂层,即DLC(C2H2)、DLC(C2H2+H2)、DLC(CH4)、DLC(CH4+H2).通过扫描电子显微镜、拉曼光谱、X 射线光电子能谱和纳米压痕技术系统研究不同含氢量前驱体对涂层厚度、化学键结构、sp3含量、力学性能的影响.结果 DLC(C2H2)的沉积速度为 0.83 μm/h,是DLC(CH4)涂层的3 倍,氢稀释轻微影响涂层的沉积速度.随着前驱体含氢量的升高,总体趋势是DLC涂层的ID/IG降低,G峰红移,sp3含量增加,硬度和弹性模量下降.DLC(C2H2)具有最大的ID/IG(3.1)、最高的G峰峰位(1 567 cm-1)和较低的sp3含量(6.1%).同时,DLC(C2H2)表现出最大的硬度和弹性模量,分别为26.9、240 GPa.结论 采用C2H2 制备DLC涂层具有优质、高效的特点,C2H2 是硬质DLC涂层最佳的前驱体.前驱体含氢量提高了DLC涂层中sp3-CHn含量,未提高sp3-CC含量,而sp3-CHn终止CC网络,导致DLC涂层的力学性能下降.氢掺入减小了DLC涂层中sp2团簇尺寸,同时增大了键角无序度.

Diamond-like carbon(DLC)coatings have attracted significant attention in various industrial and scientific applications,including mechanical seals,biomedical implants,and microelectronic devices,owing to their exceptional combination of high hardness,superior wear resistance,and high chemical stability.These properties primarily arise from the unique hybridized carbon bonding structure(sp3/sp2 ratio)and hydrogen content within the coatings.However,the performance of DLC coatings is highly sensitive to deposition parameters,such as plasma power,substrate bias,and precursor gas composition,which influence the chemical bonding structure and microstructure of the coatings. In this study,the effects of hydrocarbon precursor hydrogen content on the structural and mechanical properties of DLC coatings deposited by direct current pulse plasma-enhanced chemical vapor deposition(DC-PECVD)were systematically investigated.Four distinct DLC coatings were synthesized with different precursor gases:pure acetylene(DLC-C2H2),hydrogen-diluted acetylene(DLC-C2H2+H2),pure methane(DLC-CH4),and hydrogen-diluted methane(DLC-CH4+H2).The influence of precursor hydrogen content on coating thickness,chemical bonding configuration(sp3/sp2 ratio),and mechanical properties(hardness and elastic modulus)was comprehensively characterized by scanning electron microscopy(SEM),Raman spectroscopy,X-ray photoelectron spectroscopy(XPS),and nanoindentation techniques. The deposition rate of DLC coatings was found to be strongly dependent on the precursor gas composition.Specifically,the DLC-C2H2 coating exhibited the highest deposition rate(0.83 μm/h),which was approximately three times greater than that of the DLC-CH4 coating(0.28 μm/h).This disparity was attributed to the higher carbon density and more efficient plasma dissociation of C2H2 compared with CH4.Interestingly,hydrogen dilution had a negligible impact(<10%)on the deposition rates of both precursor systems,suggesting that hydrogen primarily influenced the chemical bonding structure rather than the growth kinetics.Raman spectroscopy revealed a clear correlation between precursor hydrogen content and the structural evolution of DLC coatings.As the hydrogen content increased,the intensity ratio of the D peak to the G peak(ID/IG)decreased,accompanied by a redshift in the G peak position.These observations aligned with the Casiraghi model,which described the structural transition from a more graphitic(sp2-rich)to a more diamond-like(sp3-rich)configuration with increasing hydrogen incorporation.XPS analysis demonstrated that the sp3 carbon fraction in DLC coatings exhibited a positive correlation with precursor hydrogen content.The highest sp3 content(14.5%)was achieved in the DLC-CH4+H2 coating,confirming the critical role of hydrogen in stabilizing sp3-hybridized carbon bonds.In contrast,the DLC-C2H2 coating,deposited under low hydrogen conditions,exhibited the lowest sp3 content(6.1%),indicating a predominantly sp2-bonded structure.Nanoindentation measurements revealed that the DLC-C2H2 coating possessed the highest hardness(26.9 GPa)and elastic modulus(240 GPa),despite its relatively low sp3 content.This finding challenged the conventional paradigm that high hardness in DLC coatings was solely governed by a high sp3 fraction.Instead,the results suggested that a cross-linked sp2 network,formed under low hydrogen conditions,contributed significantly to mechanical reinforcement;the cognition that the sp3 fraction determined the hardness of DLC coatings originated from hydrogen-free DLC coat and was not applicable to hydrogenated DLC coatings.Furthermore,hydrogen dilution was found to generally reduce coating hardness,particularly in the CH4-based system,where a notable 18%reduction in hardness was observed. This study reveals how the hydrogen content in precursor gases and the resulting chemical bonds affect the properties of DLC coatings.Key findings show that using C2H2 instead of CH4 speeds up coating growth due to more efficient carbon delivery.While hydrogen helps form more sp3 bonds,high hardness can also come from a dense sp2 network-not just sp3 content.This means the current model linking structure to properties needs updating.Overall,tuning the gas mixture and hydrogen level allows custom-designed DLC coatings with improved mechanical and wear performance for specific applications.

黄志宏

温州职业技术学院 智能制造学院,浙江 温州 325035

矿业与冶金

类金刚石碳PECVD拉曼前驱体sp3硬度弹性模量

diamond-like carbonPECVDRamanprecursorsp3hardnesselastic modulus

《表面技术》 2026 (1)

115-121,7

温州市重大科技创新项目(ZG2023009) Wenzhou Major Science and Technology Innovation Project(ZG2023009)

10.16490/j.cnki.issn.1001-3660.2026.01.010

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