Probing the peculiar emission behaviors of c-Sapphire wafer and β-Ga2O3/c-Sapphire via hard X-ray nanoprobe
Sunny Saurabh1*, Umeshwar Reddy Nallasani2, Tzu-Chi Huang3,1, Chun-Yen Lin2, Yi-Chen Li1, Yu-Hao Wu4,1, Chien-Yu Lee1, Bo-Yi Chen1, Gung-Chian Yin1, Mau-Tsu Tang1, Wu-Ching Chou2, Bi-Hsuan Lin1
1National Synchrotron Radiation Research Center, Hsinchu, Taiwan
2Department of Electrophysics, National Yang Ming Chiao Tung University, Hsinchu, Taiwan
3Department of Materials Science and Engineering, National Tsing Hua University, Hsinchu, Taiwan
4Department of Materials Science and Engineering, National Yang Ming Chiao Tung University, Hsinchu, Taiwan
* Presenter:Sunny Saurabh, email:saurabh.s@nsrrc.org.tw
We report the intriguing phenomena of evolution of color centers (F and F+) using time-dependent X-ray excited optical luminescence (XEOL) in c-plane Sapphire wafer, β-Ga2O3/c-Sapphire and GaSe/β-Ga2O3/c-Sapphire. The increasing emission intensity of F+ and F-color centers over time indicates the formation of new color centers by continuous exposure to X-ray irradiation. These oxygen vacancy defect states remained even after having layer of epitaxial thin film of β-Ga2O3, and subsequent GaSe of sub µm thickness on top due to high penetration depth of X-ray. Interestingly, defect states of β-Ga2O3 decrease with time suggesting passivation of defect states induced by long term exposure to X-ray radiation. Also, we demonstrated the effect of long term X-ray irradiation using XEOL map, revealing spatial variation in defect state emission intensities. Time-resolved XEOL was used to measure dynamics of luminescence decay of F+ color center and defect state emission of Ga2O3. These results suggest that the enhancement in color center emission after hard X-ray irradiation could be of significant importance in the quest of solid-state single-photon sources.
Keywords: Hard X-ray, XEOL