Evaluation of Ionic Salt Photodefinable Polyimides As Mcm-D Dielectrics with Copper Metallization

C. N. Lazaridis, D. K. Flattery, W. J. Lautenberger, Y. Yamamoto, K. Imai
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Abstract

The excellent film properties given by BPDA/PPD make it a prime candidate for the dielectric material in MCM-D fabrications, and photodefinable versions offer the additional advantages of reduced labor and material costs. However, less than adequate adhesion to the preferred copper metallurgy coupled with prolonged development times may limit widespread adoption of this chemistry. Modifications to the BPDA/PPD backbone were made in a series of photodefinable polyimides prepared as the ionic salt precursors, and key performance and processing parameters were determined. Significant adhesion of the highly rigid BPDA/PPD backbone to copper metal was only achieved after substantial incorporation of either more flexible co-monomers, especially those containing fluorine substituents, or by incorporation of an assumed surface reactive, hydroxyl-substituted co-monomer. These modifications generally also resulted in reduced development times. Self-adhesion of polyimide to polyimide layers was optimized by using a partial cure process for the bottom polyimide layer, and appropriate cure temperatures were determined for each structure to prevent solvent-induced cracking of the bottom layer upon application of the top layer while retaining self-adhesion. Operable processing windows were found for several candidates which maximized adhesion and minimized cracking.
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离子盐光定聚酰亚胺作为铜金属化Mcm-D介电材料的评价
BPDA/PPD优异的薄膜性能使其成为MCM-D制造中介电材料的首选材料,光定义版本提供了减少劳动力和材料成本的额外优势。然而,对首选铜冶金的附着力不够,再加上开发时间延长,可能会限制这种化学物质的广泛采用。以离子盐为前驱体制备了一系列光可定义聚酰亚胺,对BPDA/PPD骨架进行了改性,确定了关键性能和工艺参数。高度刚性的BPDA/PPD骨架与铜金属的显著粘附只有在大量加入更灵活的共聚单体(特别是含有氟取代基的共聚单体)或加入假设的表面反应性羟基取代共聚单体后才能实现。这些修改通常也会减少开发时间。通过对底层聚酰亚胺层采用局部固化工艺,优化了聚酰亚胺层与聚酰亚胺层的自粘附性,并确定了每种结构的适当固化温度,以防止在应用顶层时底层发生溶剂性开裂,同时保持自粘附性。为几个候选材料找到了可操作的加工窗口,使附着力最大化,开裂最小化。
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