Yufei You, Ziwei He, Jianwei Zhou, Yuhang Qi, Chong Luo
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引用次数: 0
摘要
随着集成电路特征尺寸的不断缩小,铜互连中的电迁移现象日益严重。由于Ru具有电子平均自由程短、耐电迁移等优异性能,具有成为下一代互连材料的潜力。钌化学机械抛光(CMP)是集成电路制造的关键步骤,氧化是限制钌去除率的步骤,影响半导体制造效率。本研究采用H2O2/PDS/FeIII-NTA体系,在pH = 7时,无磨料CMP对Ru的去除率提高到1202 Å min−1;表面粗糙度仅为0.94 nm,在原子水平上表现出优异的表面质量。该体系具有协同催化机制,生成活性氧化剂HO•、SO4•−和FeIV = o。这些活性氧化剂具有较强的氧化能力,可将Ru氧化为RuO2和RuO3,继而氧化为可溶的RuO4−和RuO42−,从而在Ru表面形成多孔氧化层。氧化和机械作用达到平衡状态,加速了钌的脱除。
Enhanced Ruthenium Removal and Superior Surface Quality via Abrasive-Free Chemical Mechanical Polishing Using Synergistic Catalysis with the H2O2/PDS/FeIII-NTA System
As the feature sizes of integrated circuits continue to shrink, the phenomenon of electrical migration in Cu interconnects becomes more severe. Due to the excellent properties of Ru such as short electron mean free path and good resistance to electrical migration, it has the potential to become the next-generation interconnect material. Ru chemical mechanical polishing (CMP) is a crucial step in the fabrication of integrated circuits, with oxidation being the step limiting the Ru removal rate, which affects the efficiency of semiconductor manufacturing. In this study, using the H2O2/PDS/FeIII-NTA system, the removal rate of Ru is improved to 1202 Å min−1 via abrasive-free CMP at pH = 7; the surface roughness is only 0.94 nm, demonstrating superior surface quality at the atomic level. This system features a synergistic catalytic mechanism, producing the active oxidants HO•, SO4•−, and FeIV = O. These active oxidants have strong oxidation capacity and lead to the oxidation of Ru into RuO2 and RuO3 and their subsequent oxidation into soluble RuO4− and RuO42−, which results in the formation of a porous oxide layer on the surface of Ru. The oxidation and mechanical effects reach an equilibrium state and accelerate the removal of Ru.
期刊介绍:
Small serves as an exceptional platform for both experimental and theoretical studies in fundamental and applied interdisciplinary research at the nano- and microscale. The journal offers a compelling mix of peer-reviewed Research Articles, Reviews, Perspectives, and Comments.
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