等离子体处理表面的地形和化学特征在分期时间路径上的演变

I. Arellano, Amor Zapanta
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引用次数: 0

摘要

等离子体处理是一种广泛应用于半导体和电子工业的表面处理工艺,通过去除污染和表面活化,促进界面粘附,从而提高线材的粘合性,减少界面分层的发生。由于表面对周围环境的敏感性,活化后的表面逐渐失去润湿性。因此,正面的等离子体处理效果会随着时间的推移而减弱,这就提出了一个关键问题,即表面的活性持续时间。在装配过程控制的术语中,这个时间被定义为分段时间;从等离子体处理到完成下一个工艺步骤,即线焊或成型的总时间。在这项研究中,我们监测了等离子体处理前、等离子体处理后以及等离子体处理后72小时内表面的地形和化学演变,目的是将接触角(CA)等可测量参数与表面的地形(粗糙度)和化学性质(氧化物厚度和功能)联系起来。利用扫描电子显微镜(SEM)和非接触原子力显微镜(NC-AFM)、固滴接触角计和连续电还原分析(SERA),我们发现等离子体处理过程所带来的润湿性的改善源于表面形貌的稳定性(物理)和Cu2O层的促进(化学)。表面活化的损失可能是由于Cu2O层的减少,导致其转化为CuO。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Evolution of the topographical and chemical signatures of plasma-treated surfaces along the staging time pathway
Plasma treatment is a widely used process in the semiconductor and electronics industries for surface preparation, via contamination removal and surface activation, promoting interfacial adhesion resulting in improved wire bondability and decreased occurrence of delamination at the interface. Due to the sensitivity of the surface to its immediate environment, the activated surface gradually lose its wettability. Thus, the positive plasma treatment effect diminishes over time, prompting the critical question about the duration wherein the surface is active. In the jargon of assembly process control, this duration is defined as the staging time; the total time from plasma treatment to the completion of the next process step, i.e., wirebond or molding. In this study, we monitor the topographical and chemical evolution of the surface prior to plasma treatment, immediately after plasma treatment, and at certain time points up to 72 h after plasma treatment, with the aim of correlating a measurable parameter such as contact angle (CA) to the topography (roughness) and chemical nature (oxide thickness and functionality) of the surface. Using scanning electron microscopy (SEM) and non-contact atomic force microscopy (NC-AFM), sessile drop contact angle meter, and sequential electro-reduction analysis (SERA), we show that the improvement of wettability imparted by the plasma treatment process arises from the stability of the surface topography (physical) and the promotion of the Cu2O layer (chemical). The loss of surface activation is possibly due to the reduction of the Cu2O layer, resulting from its conversion to CuO.
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