2022•Applied Surface ScienceOpen access

Thermal oxidation of [0001] GaN in water vapor compared with dry and wet oxidation: Oxide properties and impact on GaN

Łukasz Janicki, R. Korbutowicz, Mariusz Rudziński, Paweł Piotr Michałowski, Sebastian Złotnik, M. Grodzicki, Sandeep Madhukar Gorantla, J. Serafińczuk, D. Hommel, R. Kudrawiec

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Abstract

Conventionally thermal oxidation of GaN is performed in either dry or wet oxygen ambient. In this work thermal oxidation in water vapor ambient, together with the two above mentioned modes, is characterized. All three GaN oxidation modes were comprehensively studied structurally and optically using a wide range of experimental methods. Thermal oxidation of GaN at 950 °C in dry oxygen, in wet oxygen, and in water vapor, was performed for up to 20 min. All oxidation modes resulted in β-phase Ga2O3 growth as confirmed by XRD measurements. A different surface morphology was observed between processes, smooth and featureless for the vapor oxidation, and grainy for dry and wet modes. Similarly, the growth rate varied between modes of oxidation with the slowest observed for the vapor mode and the fastest for the dry mode. An oxygen diffusion into GaN was observed for the dry and wet processes with above background levels of O visible over 150 nm below the oxide/GaN interface. Conversely, only negligible diffusion was observed for the vapor oxidized GaN. Optical studies of the structures electronic properties revealed that only the vapor process did not degrade the material underneath the oxide layer.

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Conventionally thermal oxidation of GaN is performed in either dry or wet oxygen ambient. In this work thermal oxidation in water vapor ambient, together with the two above mentioned modes, is characterized. All three GaN oxidation modes were comprehensively studied structurally and optically using a wide range of experimental methods. Thermal oxidation of GaN at 950 °C in dry oxygen, in wet oxygen, and in water vapor, was performed for up to 20 min. All oxidation modes resulted in β-phase Ga2O3 growth as confirmed by XRD measurements. A different surface morphology was observed between processes, smooth and featureless for the vapor oxidation, and grainy for dry and wet modes. Similarly, the growth rate varied between modes of oxidation with the slowest observed for the vapor mode and the fastest for the dry mode. An oxygen diffusion into GaN was observed for the dry and wet processes with above background levels of O visible over 150 nm below the oxide/GaN interface. Conversely, only negligible diffusion was observed for the vapor oxidized GaN. Optical studies of the structures electronic properties revealed that only the vapor process did not degrade the material underneath the oxide layer.

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Available abstract

Conventionally thermal oxidation of GaN is performed in either dry or wet oxygen ambient. In this work thermal oxidation in water vapor ambient, together with the two above mentioned modes, is characterized. All three GaN oxidation modes were comprehensively studied structurally and optically using a wide range of experimental methods. Thermal oxidation of GaN at 950 °C in dry oxygen, in wet oxygen, and in water vapor, was performed for up to 20 min. All oxidation modes resulted in β-phase Ga2O3 growth as confirmed by XRD measurements. A different surface morphology was observed between processes, smooth and featureless for the vapor oxidation, and grainy for dry and wet modes. Similarly, the growth rate varied between modes of oxidation with the slowest observed for the vapor mode and the fastest for the dry mode. An oxygen diffusion into GaN was observed for the dry and wet processes with above background levels of O visible over 150 nm below the oxide/GaN interface. Conversely, only negligible diffusion was observed for the vapor oxidized GaN. Optical studies of the structures electronic properties revealed that only the vapor process did not degrade the material underneath the oxide layer.

Key concepts: Water vapor, Thermal oxidation, Oxygen, Oxide, Wet oxidation, Diffusion, Materials science, Chemistry

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