All-Hydrocarbon Low-Dielectric Loss Benzocyclobutene-Encapsulated Photoresist with High Pattern Resolution

IF 3.7 3区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY ACS Omega Pub Date : 2025-04-12 DOI:10.1021/acsomega.4c1094010.1021/acsomega.4c10940
Hanlin Du, Hongyan Xia, Yun Tang, Ke Cao, Jiajun Ma* and Junxiao Yang*, 
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Abstract

UV-curable resins with a low dielectric constant can be processed or patterned to form required shapes, making them highly applicable to special fields. Unlike conventional photoresists limited by the polarization effect due to highly polar bonds, an all-hydrocarbon-type low-dielectric photoresist was designed and synthesized with excellent performance. Based on previous works, the film-forming resin poly 1-(4-vinylphenyl)-2-(4-benzocyclobutenyl)ethylene-styrene (P-DVB-St) was prepared by introducing styrene (St) into the 1-(4-vinylphenyl)-2-(4-benzocyclobutenyl)ethene (DVB) backbone via anionic polymerization, and the photoresist properties were improved by adjusting the cross-linking density of the polymer. The introduction of styrene improved the mechanical properties while maintaining the photolithographic patterning properties of the photoresist. Since the resin has a dual UV/thermal-cured structure, it has better thermal stability (T5% = 401 °C), lower dielectric constant (2.62 at 10 MHz) and dielectric loss (1.7 × 10–3), and better photolithographic patterning (the graphic resolution is 5 μm).

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具有高图案分辨率的全烃低介电损耗苯并环丁烯封装光刻胶
具有低介电常数的紫外线固化树脂可以加工或图案化形成所需的形状,因此非常适用于特殊领域。与传统光刻胶受限于高极性键导致的极化效应不同,本研究设计并合成了一种性能优异的全烃型低介电常数光刻胶。在前人研究的基础上,通过阴离子聚合将苯乙烯(St)引入 1-(4-乙烯基苯基)-2-(4-苯并环丁烯基)乙烯(DVB)骨架,制备了成膜树脂聚 1-(4-乙烯基苯基)-2-(4-苯并环丁烯基)乙烯-苯乙烯(P-DVB-St),并通过调节聚合物的交联密度改善了光刻胶的性能。苯乙烯的引入改善了光刻胶的机械性能,同时保持了光刻胶的光刻图案性能。由于该树脂具有紫外线/热固化双重结构,因此具有更好的热稳定性(T5% = 401 °C)、更低的介电常数(10 MHz 时为 2.62)和介电损耗(1.7 × 10-3)以及更好的光刻图案性能(图形分辨率为 5 μm)。
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来源期刊
ACS Omega
ACS Omega Chemical Engineering-General Chemical Engineering
CiteScore
6.60
自引率
4.90%
发文量
3945
审稿时长
2.4 months
期刊介绍: ACS Omega is an open-access global publication for scientific articles that describe new findings in chemistry and interfacing areas of science, without any perceived evaluation of immediate impact.
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