Synergistic Plasma Activation-Enabled Low-Temperature Cobalt/SiO2 Hybrid Bonding without Oxide Interfaces

IF 8.2 2区 材料科学 Q1 MATERIALS SCIENCE, MULTIDISCIPLINARY
Xiaoyun Qi, Yufei Bai, Han Yan, Xiaohui Yuan, Yan Ma, Tadatomo Suga and Chenxi Wang*, 
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Abstract

Metal passivation participating in bonding is a promising method for hybrid bonding to fabricate high-density devices and high-computing instruments, by turning Cu/SiO2 bonding into passivation/SiO2 bonding and evading the obstacles of Cu oxidation. However, the performance of the passivated metal bonding interface and the process compatibility for SiO2–SiO2 bonding are crucial for higher speed and lower power consumption but neglected. In this article, we introduce cobalt (Co) as a hybrid bonding metal and demonstrate a facile bonding method for combining Co–Co, Co–SiO2, and SiO2–SiO2. This approach enables cobalt-participated hybrid bonding through synergistic NH3/H2O → Ar plasma treatment. Cobalt (Co) reduction and SiO2 hydrophilization are simultaneously realized by a one-step NH3/H2O plasma activation from vaporized ammonia liquid for ease of metallization and dehydration bonding to be obtained, respectively. Moreover, by introducing the subsequent Ar plasma treatment, the reoxidation from the oxygen-containing process and overadsorption of H2O are evaded without hindering the construction of the interface. Additionally, the roughness of surfaces is significantly smoothed without gas-storage microstructure topography. The well-prepared surfaces enable surface reaction and interface construction without void generation thanks to the effective activation and process tune-up. Remarkably, the atomic interconnection is facilitated for both homo- and heterogeneous bonding at temperatures as low as ∼200 °C. With the increase in yield of the bonding area, the three bonded interfaces can obtain about 1.5 times the promotion with a 25% decrease in Co–Co interfacial resistivity. The Co-passivated hybrid bonding with synergistic activation could be used for high-density integration with efficient communication due to their favorable interfacial performance and feasible process.

Abstract Image

协同等离子体激活低温钴/SiO2杂化键合,无氧化物界面
金属钝化参与键合是将Cu/SiO2键合转变为钝化/SiO2键合,避开Cu氧化障碍的一种很有前途的混合键合方法,可用于制造高密度器件和高计算仪器。然而,钝化金属键合界面的性能和SiO2-SiO2键合的工艺兼容性对于提高速度和降低功耗至关重要,但却被忽视了。在本文中,我们介绍了钴(Co)作为一种杂化键合金属,并演示了一种结合Co - Co、Co - sio2和SiO2-SiO2的简便键合方法。该方法通过协同NH3/H2O→Ar等离子体处理实现钴参与杂化键。通过一步NH3/H2O等离子体活化,可同时实现钴(Co)的还原和SiO2的亲水性,以方便金属化和脱水结合。此外,通过引入后续的Ar等离子体处理,避免了含氧过程中的再氧化和H2O的过度吸附,同时又不妨碍界面的构建。此外,表面粗糙度明显平滑,没有储气组织形貌。由于有效的活化和工艺调整,精心制备的表面可以实现表面反应和界面构建,而不会产生空隙。值得注意的是,在低至~ 200°C的温度下,原子间的连接有利于同质键和异质键的形成。随着键合面积成品率的增加,三个键合界面的提升幅度约为1.5倍,Co-Co界面电阻率降低25%。协同活化的共钝化杂化键具有良好的界面性能和可行的工艺,可用于高密度集成和高效通信。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
ACS Applied Materials & Interfaces
ACS Applied Materials & Interfaces 工程技术-材料科学:综合
CiteScore
16.00
自引率
6.30%
发文量
4978
审稿时长
1.8 months
期刊介绍: ACS Applied Materials & Interfaces is a leading interdisciplinary journal that brings together chemists, engineers, physicists, and biologists to explore the development and utilization of newly-discovered materials and interfacial processes for specific applications. Our journal has experienced remarkable growth since its establishment in 2009, both in terms of the number of articles published and the impact of the research showcased. We are proud to foster a truly global community, with the majority of published articles originating from outside the United States, reflecting the rapid growth of applied research worldwide.
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