Cu/SiO 2 hybrid bonding with planarized dielectric and isolated metal connections can realize ultradense interconnects (e.g., ≤1 μm) by eliminating the microbumps and underfill through the direct bonding of Cu–Cu and SiO 2 –SiO 2 . However, the low-temperature bonding of Cu–Cu (oxide-free surface) and SiO 2 –SiO 2 (hydroxylated surface) is difficult to be compatible in a mechanism. We circumvent this contradiction by constructing a co-hydroxylated functional surface on a Cu/SiO 2 hybrid platform. By combining and optimizing the protocol of Ar/O 2 plasma activation and formic acid solution immersion, an −OH active layer was successfully established on the Cu and SiO 2 surfaces simultaneously, and the increased total surface area provided more adsorption sites for hydroxyl groups. A Cu–Cu interface with sufficient atom diffusion, substantial grain growth, and fewer microvoids was obtained at 200 °C. Notably, the carbon-related interlayer that may degrade the interfacial performance could be effectively inhibited across the optimized SiO 2 –SiO 2 interface even if organic acid was introduced in the protocol. This low-temperature Cu/SiO 2 hybrid bonding via a co-hydroxylated strategy may inspire the development of a memory-centric chip architecture and functional integrated circuits delivering a monolithic-like performance in the future hyperscaling era.
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Kang et al. (2021) studied this question.
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