首页> 外文期刊>Journal of Vacuum Science & Technology B: Microelectronics and Nanometer Structures >Photoresist modifications by plasma vacuum ultraviolet radiation: The role of polymer structure and plasma chemistry
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Photoresist modifications by plasma vacuum ultraviolet radiation: The role of polymer structure and plasma chemistry

机译:等离子体真空紫外线辐射对光致抗蚀剂的改性:聚合物结构和等离子体化学的作用

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While vacuum ultraviolet (VUV) photon irradiation has been shown to significantly contribute to material modifications of polymers during plasma exposures, the impact of radiation-induced material alterations on roughness development during plasma processing has remained unclear. The authors have studied the interaction of the radiation of Ar and C4F8/Ar plasma discharges with 193 and 248 nm advanced photoresists (PRs). Optical filters were used to vary the radiation exposure wavelength range in the ultraviolet (UV) and VUV emission spectra. This enables clarification of the respective roles of plasma photon radiation wavelength and PR polymer structure on the chemical and structural changes produced in the materials. Chemical changes in polymer composition at the film surface and in the material bulk were determined by vacuum transfer x-ray photoelectron spectroscopy and Fourier-transform infrared spectroscopy. Morphological changes, film thickness reduction, and changes in surface and pattern morphology were characterized by ellipsometry, scanning electron microscopy, and atomic force microscopy. The exposure of methacrylate based 193 nm PR to photon radiation in the UV/VUV spectral range (λ=112–143 nm) leads to detachment and removal of oxygen containing polymer pendant groups to a depth of about 200 nm. This causes changes in the polymer structure by chain scission, significant film thickness reduction, and reduced pattern critical dimensions and line edge roughness. Chain-scission reactions and residual detached polymer pendant groups are expected to effectively soften layers of 193 nm PR. In contrast to 193 nm PR, styrene based 248 nm PR was found to be significantly more stable under plasma-produced irradiation due to the low oxygen content, low ester linkage concentration, and absence of lactone. Small thickness reduc-n-ntion, reduced oxygen loss, and cross-linking were observed in the surface region of 248 nm PR. Radiation-induced material modifications of both PR materials decreased with increasing photon wavelength in Ar discharges. Increasing modification of 193 nm PR was observed for increasing photon flux at higher wavelengths (λ=143–300 nm) by the emission characteristic of fluorocarbon containing plasmas. In C4F8/Ar plasma, the authors observed strongly increased loss of oxygen at the film surface and in the COC and CO lactone bonds in the material bulk along with film thickness reduction compared to pure Ar discharges. These modifications are directly relevant to plasma processes used for pattern transfer, which often contain fluorocarbon species.
机译:尽管真空紫外线(VUV)光子辐照已显示出在等离子体暴露过程中显着促进聚合物的材料改性,但仍不清楚在等离子体处理过程中辐射引起的材料变化对粗糙度发展的影响。作者研究了Ar和C4F8 / Ar等离子体放电的辐射与193和248 nm高级光刻胶(PRs)的相互作用。使用滤光片来改变紫外线(V)和VUV发射光谱中的辐射暴露波长范围。这使得能够阐明等离子体光子辐射波长和PR聚合物结构对材料中产生的化学和结构变化的各自作用。通过真空转移X射线光电子能谱和傅里叶变换红外光谱法确定膜表面和材料块中聚合物组成的化学变化。形态学变化,膜厚度减小以及表面和图案形态的变化通过椭圆光度法,扫描电子显微镜和原子力显微镜表征。基于甲基丙烯酸酯的193 nm PR暴露于UV / VUV光谱范围(λ= 112–143 nm)的光子辐射中,导致含氧聚合物侧基的分离和去除深度约为200 nm。这将导致聚合物结构的断链,显着的膜厚减少以及图案临界尺寸和线边缘粗糙度的降低。断链反应和残留的游离聚合物侧基残基有望有效软化193 nm PR的层。与193 nm PR相反,由于低氧含量,低酯键浓度和不存在内酯,基于苯乙烯的248 nm PR在等离子体产生的辐射下明显更稳定。在248 nm PR的表面区域观察到较小的厚度减小,氧损失减少和交联。两种PR材料的辐射诱导材料改性都随着Ar放电中光子波长的增加而降低。通过含碳氟化合物的等离子体的发射特性,观察到对193 nm PR的修饰增加,从而在更高的波长(λ= 143-300 nm)下增加了光子通量。与纯Ar放电相比,在C4F8 / Ar等离子体中,观察到材料表面的薄膜表面以及CbulkOC和CO内酯键中的氧损失大大增加,并且薄膜厚度减小。这些修改与用于图案转移的等离子工艺直接相关,该工艺通常包含碳氟化合物。

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