<i>In situ</i> nitrogen doping of <b> <i>β</i> </b>-Ga2O3 during MOCVD homoepitaxy: A theoretical and experimental study

Y Yaoping Lu (College of Physics and Information Engineering, Fuzhou University 1 , Fuzhou 350108,) A Ancang Yang (Faculty of Material Science and Engineering, Kunming University of Science and Technology 3 , Kunming 650093,) T Titao Li (College of Physics and Information Engineering, Fuzhou University 1 , Fuzhou 350108,) J Jinxin Zhang L Lemin Jia (College of Physics and Information Engineering, Fuzhou University 1 , Fuzhou 350108,) D Duanyang Chen (Advanced Laser and Optoelectronic Functional Materials Department, Shanghai Institute of Optics and Fine Mechanics, Chinese Academy of Sciences 4 , Shanghai 201800,) H Hongji Qi (Advanced Laser and Optoelectronic Functional Materials Department, Shanghai Institute of Optics and Fine Mechanics, Chinese Academy of Sciences 4 , Shanghai 201800,) H Haizhong Zhang (Zhejiang Key Laboratory of Low‐carbon Control Technology for Industrial Pollution College of Environment Zhejiang University of Technology No. 18 Chaowang Road Hangzhou 310014 China) X Xiaoqiang Lu (College of Physics and Information Engineering, Fuzhou University 1 , Fuzhou 350108,)

Abstract

The precise control of acceptor doping concentrations in epilayers is critical for fabricating key β-Ga2O3-based power electronic structures, including current-blocking layers, p-type epilayers, and drift layers. Unintentional nitrogen (N) compensating dopants introduced by N2O (a common oxygen precursor) during β-Ga2O3 metalorganic chemical vapor deposition growth significantly affects electrical properties. This study demonstrates that N concentration in epilayers is largely determined by growth temperature and surface adsorption efficiency. As the epitaxial temperature increases, the N doping concentration in the epilayer decreases. When the epitaxial temperature exceeds 1000 °C, the efficiency of N adsorption on β-Ga2O3 surfaces is influenced by both epitaxial parameters and substrate orientation. Modifying epitaxial parameters, especially by increasing chamber pressure, enhances the N concentration in β-Ga2O3 epilayers. Stronger N adsorption occurs on the (100)-plane compared to the (001)-plane epilayer; however, the (001)-plane epilayer allows better N concentration tuning through adjustments in parameters. First-principles calculations indicate that such observed differences in adsorption efficiency are attributable to variations in adsorption energies specific to each plane, coupled with competitive interactions between nitrogen (N) and oxygen (O) atoms during surface reactions. This study offers fundamental insights that advance the engineering of β-Ga2O3 homoepilayers for power electronics applications.

Article Details

Volume / Issue Vol. 127, Issue 7
Published August 18, 2025
ISSN 0003-6951
Publisher American Institute of Physics

Journal Info

Applied Physics Letters

American Institute of Physics

ISSN: 0003-6951 Physical Sciences

Authors (9)

Y

Yaoping Lu

College of Physics and Information Engineering, Fuzhou University 1 , Fuzhou 350108,

A

Ancang Yang

Faculty of Material Science and Engineering, Kunming University of Science and Technology 3 , Kunming 650093,

T

Titao Li

College of Physics and Information Engineering, Fuzhou University 1 , Fuzhou 350108,

J

Jinxin Zhang

L

Lemin Jia

College of Physics and Information Engineering, Fuzhou University 1 , Fuzhou 350108,

D

Duanyang Chen

Advanced Laser and Optoelectronic Functional Materials Department, Shanghai Institute of Optics and Fine Mechanics, Chinese Academy of Sciences 4 , Shanghai 201800,

H

Hongji Qi

Advanced Laser and Optoelectronic Functional Materials Department, Shanghai Institute of Optics and Fine Mechanics, Chinese Academy of Sciences 4 , Shanghai 201800,

H

Haizhong Zhang

Zhejiang Key Laboratory of Low‐carbon Control Technology for Industrial Pollution College of Environment Zhejiang University of Technology No. 18 Chaowang Road Hangzhou 310014 China

X

Xiaoqiang Lu

College of Physics and Information Engineering, Fuzhou University 1 , Fuzhou 350108,