Effect of the RF power on the characteristic properties of high-performance silicon nitride single-layer permeation barriers

材料科学 等离子体增强化学气相沉积 氮化硅 分析化学(期刊) 聚对苯二甲酸乙二醇酯 基质(水族馆) 光电子学 渗透 复合材料 化学 色谱法 生物化学 海洋学 地质学
作者
Jun S. Lee,Bibhuti B. Sahu,Jeon G. Han
出处
期刊:Surface & Coatings Technology [Elsevier BV]
卷期号:364: 63-69 被引量:10
标识
DOI:10.1016/j.surfcoat.2019.02.032
摘要

Permeation barriers for organic devices and packaging on flexible substrates are realized by using a simple single-layered silicon nitride (SiNx) film deposited via radio frequency (RF) plasma-enhanced chemical vapor deposition (PECVD) at a low temperature (~70 °C) with plasma and radical control. Several operation parameters like RF power and treatment time duration were changed to study the impact of plasma parameters (electron excitation temperature, atomic N radical and N+ ions) on the barrier films. Optical emission spectroscopy (OES) diagnostic is used to explore the deposition conditions to improve the quality and the properties of the permeation barriers deposited on a polyethylene terephthalate (PET) substrate. OES measurements revealed that the minimum electron excitation temperature and high intensity of the N+ ion observed by an 870.2 nm emission line were the crucial parameters to achieve the minimum water vapor transmission rate (WVTR) by changing the film microstructure factor with all other operation parameters remained fixed. By incorporating plasma and radical treatment at different RF powers, a minimum WVTR of 1.8 × 10−2 g/m2/day, measured at room temperature was achieved relevant to the condition of the maximum N+ ion emission intensity. The decrease in permeability is attributed to the rearrangement of the atoms at the interfaces when the average transferred ion energy to the substrate exceeds the threshold of displacement energy = electron excitation temperature ~ electron temperature. Also, this work reports on the correlations between the plasma chemistry and the chemical, mechanical, barrier, and optical properties of the deposited films.
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