journal article·2026-01-13

Rutile-Structured GeO 2 Thin Films Grown on Various Planes of α-Al 2 O 3 Substrates with Graded Ge x Sn 1– x O 2 Buffer Layers

Kazuki Shimazoe, Masashi Kato, Hiroyuki Nishinaka

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Abstract

Rutile-structured germanium dioxide (r-GeO 2 ) has gained considerable attention owing to its ultrawide bandgap and ambipolar doping ability. In this study, we investigated the mist chemical vapor deposition of r-GeO 2 on various sapphire (α-Al 2 O 3 ) substrate orientations. X-ray diffraction revealed that graded Ge x Sn 1– x O 2 buffer layers facilitated the epitaxial growth of r-GeO 2 on c-, a-, m-, and r-plane α-Al 2 O 3 substrates. Conversely, GeO 2 films grown directly on bare α-Al 2 O 3 substrates exhibited an amorphous or fine crystal state. Scanning electron microscopy demonstrated that the surface morphology of r-GeO 2 varied based on the crystallographic orientation of the underlying α-Al 2 O 3 . The optical transmittance measurements of the (001)-oriented r-GeO 2 grown on m-plane α-Al 2 O 3 demonstrated a forbidden direct transition at 4.60 eV, which is close to the fundamental bandgap of r-GeO 2 . Furthermore, optical measurements suggested the existence of a defect level with an optical absorption at approximately 4 eV in r-GeO 2 . These findings present crucial insights into the heteroepitaxial growth behavior of r-GeO 2 on α-Al 2 O 3 substrates.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Glass properties and applications · Semiconductor materials and devices · Photonic and Optical Devices

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Department of Electrical and Mechanical Engineering

Nagoya Institute of Technology

Faculty of Electrical Engineering and Electronics

Kyoto Institute of Technology

Funding

Japan Society for the Promotion of Science · Fusion Oriented REsearch for disruptive Science and Technology

References (23)

Show source-provided references
1. 10.1063/5.005667410.1063/5.0056674 ↗
2. 10.1002/pssb.20240032610.1002/pssb.202400326 ↗
3. 10.35848/1347-4065/add2b410.35848/1347-4065/add2b4 ↗
4. 10.35848/1882-0786/adc3e810.35848/1882-0786/adc3e8 ↗
5. 10.1021/acs.jpcc.0c0775710.1021/acs.jpcc.0c07757 ↗
6. 10.1116/6.000201110.1116/6.0002011 ↗
7. 10.1016/j.matlet.2022.13294510.1016/j.matlet.2022.132945 ↗
8. 10.1021/acsanm.5c0113710.1021/acsanm.5c01137 ↗
9. 10.1016/j.jallcom.2025.17859110.1016/j.jallcom.2025.178591 ↗
10. 10.1063/5.007191810.1063/5.0071918 ↗
11. 10.1016/j.jlumin.2023.12035310.1016/j.jlumin.2023.120353 ↗
12. 10.1063/5.006078510.1063/5.0060785 ↗
13. 10.1063/1.508837010.1063/1.5088370 ↗
14. 10.35848/1882-0786/ad838e10.35848/1882-0786/ad838e ↗
15. 10.1063/5.024420610.1063/5.0244206 ↗
16. 10.1021/acs.chemmater.2c0175810.1021/acs.chemmater.2c01758 ↗
17. 10.35848/1882-0786/AD106C10.35848/1882-0786/AD106C ↗
18. 10.1063/5.003328410.1063/5.0033284 ↗
19. 10.1016/j.apsusc.2010.10.01310.1016/j.apsusc.2010.10.013 ↗
20. 10.1557/jmr.1995.151610.1557/jmr.1995.1516 ↗
21. 10.1116/6.000396010.1116/6.0003960 ↗
22. 10.1063/1.511131810.1063/1.5111318 ↗
23. 10.1063/5.023671110.1063/5.0236711 ↗