Hongcai Yang, Xuelin Yang, Han Yang, Kexin Zhang, Zhenghao Chen, Junkang Wu, Xingyu Fu, Faquan Wu, Xuan Liu, Yuxia Feng, Xing Zhang, Yue Wang, Xiangning Kang, Guangxu Ju, F. Xu, Ning Tang, Xinqiang Wang, Bo Shen
The direct epitaxial growth of GaN on diamond substrates offers a fundamental solution for thermal management in high-power-density GaN electronic devices. However, the amorphous layer and the strong C-C bonds on the diamond (111) surface have persistently hindered high-quality III-nitride nucleation. In this work, we overcome this fundamental challenge through the development of high-temperature physical-vapor-deposited AlN (HT-PVD-AlN) nucleation technology. Our approach utilizes high temperatures to eliminate amorphous layers while employing high-energy plasma species to modify diamond surface bonds, resulting in an AlN nucleation layer with exceptional in-plane and out-of-plane crystallographic alignment. On top of this high-quality PVD-AlN nucleation layer, low-dislocation density GaN layers and high-mobility AlGaN/GaN heterostructures have been fabricated. The full width at half maximum values of the x-ray diffraction rocking curves for the GaN (0002) and (10 1¯ 2) planes are 651 and 788 arcsec, respectively. The AlGaN/GaN heterostructures grown on diamond substrates exhibit a record room-temperature electron mobility of 1640 cm2/(V s). This work demonstrates that GaN directly grown on diamond (111) by employing HT-PVD-AlN nucleation layer is promising for next-generation high-performance GaN electronic devices.