Towards controllable Si-doping in oxide molecular beam epitaxy using a solid SiO source: Application to β-Ga2O3
Abstract
The oxidation-related issues in controlling Si doping from the Si source material in oxide molecular beam epitaxy (MBE) is addressed by using solid SiO as an alternative source material in a conventional effusion cell. Line-of-sight quadrupole mass spectrometry of the direct SiO-flux (SiO) from the source at different temperatures (TSiO) confirmed SiO molecules to sublime with an activation energy of 3.3eV. The TSiO-dependent SiO was measured in vacuum before and after subjecting the source material to an O2-background of 10-5 mbar (typical oxide MBE regime). The absence of a significant SiO difference indicates negligible source oxidation in molecular O2. Mounted in an oxygen plasma-assisted MBE, Si-doped β-Ga2O3 layers were grown using this source. The SiO at the substrate was evaluated [from 2.9x109 cm-2s-1 (TSiO=700C) to 5.5x1013 cm-2s-1 (TSiO=1000C)] and Si-concentration in the β-Ga2O3 layers measured by secondary ion mass spectrometry highlighting unprecedented control of continuous Si-doping for oxide MBE, i.e., NSi from 4x1017 cm-3 (TSiO=700C) up to 1.7x1020 cm-3 (TSiO=900C). For a homoepitaxial β-Ga2O3 layer an Hall charge carrier concentration of 3x1019 cm-3 in line with the provided SiO (TSiO=800C) is demonstrated. No SiO-incorporation difference was found between β-Ga2O3(010) layers homoepitaxially grown at 750C and β-Ga2O3(-201) layers heteroepitaxially grown at 550C. The presence of activated oxygen (plasma) resulted in partial source oxidation and related decrease of doping concentration (particularly at TSiO<800C) which has been tentatively explained with a simple model. Degassing the source at 1100C reverted the oxidation.
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