Phosphorus-doped silicon oxidation for carbon-free SiO2 formation on silicon carbide: Lowering of interface state density

Z Zhen-Yu Wang (Institute of Wide Bandgap Semiconductors and Future Lighting, Academy for Engineering & Technology, Fudan University 1 , Shanghai 200433,) C Cheng-Xi Ding (Institute of Wide Bandgap Semiconductors and Future Lighting, Academy for Engineering & Technology, Fudan University 1 , Shanghai 200433,) Y Yun-Duo Guo (Institute of Wide Bandgap Semiconductors and Future Lighting, Academy for Engineering & Technology, Fudan University 1 , Shanghai 200433,) Z Zhao-Peng Bai (Institute of Wide Bandgap Semiconductors and Future Lighting, Academy for Engineering & Technology, Fudan University 1 , Shanghai 200433,) Q Qi-Min Huang (Institute of Wide Bandgap Semiconductors and Future Lighting, Academy for Engineering & Technology, Fudan University 1 , Shanghai 200433,) Y Yi Shen (College of Chemistry, Chemical Engineering and Materials Science, and State Key Laboratory of Radiation Medicine and Protection) L Lin Gu A An-Feng Wang (Institute of Wide Bandgap Semiconductors and Future Lighting, Academy for Engineering & Technology, Fudan University 1 , Shanghai 200433,) Q Qing-Chun Zhang (Institute of Wide Bandgap Semiconductors and Future Lighting, Academy for Engineering & Technology, Fudan University 1 , Shanghai 200433,) H Hong-Ping Ma

Abstract

In this study, a novel strategy for the formation of SiC gate oxide layers has been introduced through re-oxidation of a phosphorus-doped (P-doped) n-type silicon layer grown on SiC. This approach allows for the addition of controlled, low-dose P atoms at room temperature, thereby enabling a first-ever investigation into the impact of P-doping on the trap density distribution near the conduction band of SiC in the absence of carbon. The electrical properties of the P-doped oxide were compared with directly oxidized intrinsic silicon. The phosphorus treatment reduced the density of interface states from 4.03 × 1011 to 2.01 × 1010 cm−2 eV−1. Additionally, the findings of the study revealed a suppression of the flatband voltage hysteresis as a result of the P-doping treatment. Furthermore, the underlying mechanisms through which P-doping enhanced the interfacial performance have been explored in detail using atomic force microscopy, x-ray photoelectron spectroscopy, and first-principles calculations. The results indicated that this doping and re-oxidation method substantially optimized the elemental distribution and morphology of the SiC/SiO2 interface, thereby reducing defects near the interface.

Article Details

Volume / Issue Vol. 138, Issue 7
Published August 21, 2025
ISSN 0021-8979
Publisher American Institute of Physics

Journal Info

Journal of Applied Physics

American Institute of Physics

ISSN: 0021-8979 Physical Sciences

Authors (10)

Z

Zhen-Yu Wang

Institute of Wide Bandgap Semiconductors and Future Lighting, Academy for Engineering & Technology, Fudan University 1 , Shanghai 200433,

C

Cheng-Xi Ding

Institute of Wide Bandgap Semiconductors and Future Lighting, Academy for Engineering & Technology, Fudan University 1 , Shanghai 200433,

Y

Yun-Duo Guo

Institute of Wide Bandgap Semiconductors and Future Lighting, Academy for Engineering & Technology, Fudan University 1 , Shanghai 200433,

Z

Zhao-Peng Bai

Institute of Wide Bandgap Semiconductors and Future Lighting, Academy for Engineering & Technology, Fudan University 1 , Shanghai 200433,

Q

Qi-Min Huang

Institute of Wide Bandgap Semiconductors and Future Lighting, Academy for Engineering & Technology, Fudan University 1 , Shanghai 200433,

Y

Yi Shen

College of Chemistry, Chemical Engineering and Materials Science, and State Key Laboratory of Radiation Medicine and Protection

L

Lin Gu

A

An-Feng Wang

Institute of Wide Bandgap Semiconductors and Future Lighting, Academy for Engineering & Technology, Fudan University 1 , Shanghai 200433,

Q

Qing-Chun Zhang

Institute of Wide Bandgap Semiconductors and Future Lighting, Academy for Engineering & Technology, Fudan University 1 , Shanghai 200433,

H

Hong-Ping Ma