Oxygen annealing induced changes in defects within β-Ga2O3 epitaxial films measured using photoluminescence

In this work, we use photoluminescence spectroscopy (PL) to monitor changes in the UV, blue, and green emission bands from n-type (010) Ga2O3 films grown by metalorganic vapor phase epitaxy induced by annealing at different temperatures under O-2 ambient. Annealing at successively higher temperatures decreases the overall PL yield and UV intensity at nearly the same rates, indicating the increase in the formation of at least one non-radiative defect type. Simultaneously, the PL yield ratios of blue/UV and green/UV increase, suggesting that defects associated with these emissions increase in concentration with O-2 annealing. Utilizing the different absorption coefficients of 240 and 266 nm polarization-dependent excitation, we find activation energy for the generation of non-radiative defects of 1.34 eV in the bulk but 2.53 eV near the surface. We also deduce activation energies for the green emission-related defects of 1.20 eV near the surface and 2.21 eV at low temperatures and 0.74 eV at high temperatures through the films, whereas the blue-related defects have activation energy in the range 0.72-0.77 eV for all depths. Lastly, we observe hillock surface morphologies and Cr diffusion from the substrate into the film for temperatures above 1050 degrees C. These observations are consistent with the formation and diffusion of V-Ga and its complexes as a dominant process during O-2 annealing, but further work will be necessary to determine which defects and complexes provide radiative and non-radiative recombination channels and the detailed kinetic processes occurring at surfaces and in bulk amongst defect populations.

Automated summary

In this study, photoluminescence spectroscopy was used to monitor changes in emission bands of n-type Ga2O3 films under different annealing temperatures in an oxygen environment. The results show an increase in non-radiative defects with higher temperatures and a decrease in UV intensity. Different activation energies were observed for defect generation at different depths, indicating the importance of understanding the formation and propagation of defects in materials.