Hydrophilic direct bonding of (100) diamond and deposited SiO$_2$ substrates

Fuente: arXiv
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Autori principali: Chen, Tianyin, Hermias, Jeffrel, Nur, Salahuddin, Ishihara, Ryoichi
Natura: Preprint
Pubblicazione: 2025
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author Chen, Tianyin
Hermias, Jeffrel
Nur, Salahuddin
Ishihara, Ryoichi
author_facet Chen, Tianyin
Hermias, Jeffrel
Nur, Salahuddin
Ishihara, Ryoichi
contents 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 (SC) diamond plates to PECVD-grown SiO$_2$/Si substrates at low temperatures and atmospheric conditions. The surfaces of the SiO$_2$ 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$^{\circ}$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 (XPS) 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 the SiO$_2$. 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.
format Preprint
id arxiv_https___arxiv_org_abs_2501_12831
institution arXiv
publishDate 2025
record_format arxiv
spellingShingle Hydrophilic direct bonding of (100) diamond and deposited SiO$_2$ substrates
Chen, Tianyin
Hermias, Jeffrel
Nur, Salahuddin
Ishihara, Ryoichi
Materials Science
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 (SC) diamond plates to PECVD-grown SiO$_2$/Si substrates at low temperatures and atmospheric conditions. The surfaces of the SiO$_2$ 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$^{\circ}$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 (XPS) 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 the SiO$_2$. 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.
title Hydrophilic direct bonding of (100) diamond and deposited SiO$_2$ substrates
topic Materials Science
url https://arxiv.org/abs/2501.12831