Hydrophilic direct bonding of (100) diamond and deposited SiO2 substrates
T. Chen (TU Delft - Quantum Circuit Architectures and Technology, TU Delft - Quantum & Computer Engineering)
J. Hermias (TU Delft - Safety and Security Science, TU Delft - Quantum & Computer Engineering)
S. Nur (TU Delft - Quantum Circuit Architectures and Technology, TU Delft - Quantum & Computer Engineering)
R. Ishihara (TU Delft - Quantum & Computer Engineering, TU Delft - Communication QuTech, TU Delft - Quantum Circuit Architectures and Technology, TU Delft - QID/Ishihara Lab)
More Info
expand_more
Other than for strictly personal use, it is not permitted to download, forward or distribute the text or part of it, without the consent of the author(s) and/or copyright holder(s), unless the work is under an open content license such as Creative Commons.
Abstract
Diamond has emerged as a leading material for solid-state spin quantum systems and extreme environment electronics. However, a major limitation is that most diamond devices and structures are fabricated using bulk diamond plates. The absence of a suitable diamond-on-insulator (DOI) substrate hinders the advanced nanofabrication of diamond quantum and electronic devices, posing a significant roadblock to large-scale, on-chip diamond quantum photonics and electronics systems. In this work, we demonstrate the direct bonding of (100) single-crystal diamond plates to PECVD-grown SiO2/Si substrates at low temperatures and atmospheric conditions. The surfaces of the SiO2 and diamond plates are then activated using oxygen plasma and Piranha solution, respectively. Bonding occurs when the substrates are brought into contact with water in between and annealed at 200 °C under atmospheric conditions, resulting in a DOI substrate. We systematically studied the influence of Piranha solution treatment time and diamond surface roughness on the shear strength of the bonded substrate, devising an optimal bonding process that achieves a high yield rate of 90% and a maximum shear strength of 9.6 MPa. X-ray photoelectron spectroscopy was used for quantitative analysis of the surface chemicals at the bonding interface. It appears that the amount of -OH bindings increases with the initial roughness of the diamond, facilitating the strong bonding with SiO2. This direct bonding method will pave the way for scalable manufacturing of diamond nanophotonic devices and enable large-scale integration of diamond quantum and electronic systems.