Abstract
AbstractGa2O3 is a promising semiconductor for deep ultraviolet optoelectronics, because of its ultrawide bandgap of 4.85 eV. Here, the bandgap modulation of (AlxGa1−x)2O3 thin films through varying Al contents is reported –and the achievement of high‐performance photodetectors sensitive to the entire solar‐blind UV bands. It is shown that the bandgaps of (AlxGa1‐x)2O3 can be widely tuned from 4.85 eV to 5.9 eV. Solar‐blind ultraviolet photodetectors based on the (AlxGa1–x)2O3 films show detection cut‐off wavelengths varying from 263 to 236 nm, and response peaks varying from 238 to 209 nm. The photodetectors exhibit high performance with a high specific detectivity (up to 1015 Jones), low dark current (<0.35 nA), large photodark current ratio (≈107), UV–vis rejection ratio (>105), and long‐term device stability. Furthermore, a combination of high‐resolution X‐ray photoemission spectroscopy and density functional theory calculations is used to reveal insights into the evolution of electronic structures of (AlxGa1–x)2O3. The wide variations of the bandgap of (AlxGa1−x)2O3 mainly result from the upshift of the conduction band edges induced by the high energy Al 3s state hybridizing with the Ga 4s‐derived conduction band, while the valence band edge keeps almost the same for different Al content.
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