Mechanistic Study of Low-Temperature Plasma-Activated InP/Al2O3/SOI Direct Wafer Bonding for High Bonding Energy

Abstract Silicon-based photonic integrated circuits (PICs) are the core hardware for advanced optoelectronic integration, yet silicon’s indirect band gap limits the realization of high-performance on-chip light sources. Heterogeneous integration of direct band gap indium phosphide (InP) on Si thus provides a critical pathway to high-performance PIC with monolithically integrated light sources. However, the interfacial chemical mechanisms governing the strength and reliability of plasma-activated InP/silicon-on-insulator (SOI) direct bonding remain poorly understood. In this work, we demonstrate that high-strength and high-reliability InP/SOI bonding is dominated by two key interfacial factors: preservation of surface reactive hydroxyl groups and suppression of oxide-driven interfacial diffusion on InP. We elucidate how these processes determine bonding interface formation and failure via Water Contact Angle (WCA) measurements, molecular dynamics (MD) simulations, in situ X-ray photoelectron spectroscopy (XPS), and transmission electron microscopy (TEM). We find that Al2O3 outperforms SiO2 as the interlayer: stable Al–OH formed after activation inhibits hydroxyl self-condensation and retains higher reactive hydroxyl density for interfacial bonding, while Si–OH self-condensation on activated SiO2 depletes reactive hydroxyls and weakens heterogeneous bonding. We further show that N2 plasma activation forms a passivation layer on InP to suppress surface oxidation and interfacial interdiffusion, enabling smooth, high-quality bonding interfaces. In contrast, O2 plasma activation causes pronounced interfacial diffusion and brittle In2O3 formation, triggering interfacial embrittlement and reduced bonding strength. Guided by these mechanistic insights, we achieved a maximum bonding strength of 12.5 MPa. This work identifies the key interfacial chemical mechanisms of plasma-activated InP/SOI bonding, providing a solid mechanistic foundation and a practical route for high-reliability heterogeneous integration in high-speed, low-power optical interconnects.

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Publication Details

Journal
ACS Omega
Published
2026-08-20
DOI
https://doi.org/10.1021/acsomega.6c05801
Primary Topic
3D IC and TSV technologies
Type
article
Field-Weighted Citation Impact
0.00

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article

Mechanistic Study of Low-Temperature Plasma-Activated InP/Al2O3/SOI Direct Wafer Bonding for High Bonding Energy

E Shao, Yetong Zhang, Qiushi Kang, Haiyun Xue et al.
ACS Omega
3D IC and TSV technologies
article

Mechanistic Study of Low-Temperature Plasma-Activated InP/Al2O3/SOI Direct Wafer Bonding for High Bonding Energy

E Shao, Yetong Zhang, Qiushi Kang, Haiyun Xue, Chenxi Wang, Cheng Peng, Qidong Wang, Yihao Meng, Renxi Jin, Siwei Sun, Liqiang Cao, Wenxuan Ma
article en

Abstract

Abstract Silicon-based photonic integrated circuits (PICs) are the core hardware for advanced optoelectronic integration, yet silicon’s indirect band gap limits the realization of high-performance on-chip light sources. Heterogeneous integration of direct band gap indium phosphide (InP) on Si thus provides a critical pathway to high-performance PIC with monolithically integrated light sources. However, the interfacial chemical mechanisms governing the strength and reliability of plasma-activated InP/silicon-on-insulator (SOI) direct bonding remain poorly understood. In this work, we demonstrate that high-strength and high-reliability InP/SOI bonding is dominated by two key interfacial factors: preservation of surface reactive hydroxyl groups and suppression of oxide-driven interfacial diffusion on InP. We elucidate how these processes determine bonding interface formation and failure via Water Contact Angle (WCA) measurements, molecular dynamics (MD) simulations, in situ X-ray photoelectron spectroscopy (XPS), and transmission electron microscopy (TEM). We find that Al2O3 outperforms SiO2 as the interlayer: stable Al–OH formed after activation inhibits hydroxyl self-condensation and retains higher reactive hydroxyl density for interfacial bonding, while Si–OH self-condensation on activated SiO2 depletes reactive hydroxyls and weakens heterogeneous bonding. We further show that N2 plasma activation forms a passivation layer on InP to suppress surface oxidation and interfacial interdiffusion, enabling smooth, high-quality bonding interfaces. In contrast, O2 plasma activation causes pronounced interfacial diffusion and brittle In2O3 formation, triggering interfacial embrittlement and reduced bonding strength. Guided by these mechanistic insights, we achieved a maximum bonding strength of 12.5 MPa. This work identifies the key interfacial chemical mechanisms of plasma-activated InP/SOI bonding, providing a solid mechanistic foundation and a practical route for high-reliability heterogeneous integration in high-speed, low-power optical interconnects.

ACS Omega
Harbin Institute of Technology (CN), Integrated Device Technology (United States) (US), Institute of Microelectronics (SG), Institute of Microelectronics (CN), University of Chinese Academy of Sciences (CN)
National Natural Science Foundation of China, Youth Innovation Promotion Association of the Chinese Academy of Sciences
Affordable and clean energy
Openalex Percentile: Top 19%
3D IC and TSV technologies
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