In situ etching of β-Ga2O3 using tert-butyl chloride in an MOCVD system

Cameron A. Gorsak, Henry J. Bowman, Katie R. Gann, Joshua T. Buontempo, Kathleen T. Smith, Pushpanshu Tripathi, Jacob Steele, Debdeep Jena, Darrell G. Schlom, Huili Grace Xing, Michael O. Thompson, Hari P. Nair

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9 Scopus citations

Abstract

In this study, we investigate in situ etching of β-Ga2O3 in a metalorganic chemical vapor deposition system using tert-butyl chloride (TBCl). We report etching of both heteroepitaxial 2 ¯ 01 -oriented and homoepitaxial (010)-oriented β-Ga2O3 films over a wide range of substrate temperatures, TBCl molar flows, and reactor pressures. We infer that the likely etchant is HCl (g), formed by the pyrolysis of TBCl in the hydrodynamic boundary layer above the substrate. The temperature dependence of the etch rate reveals two distinct regimes characterized by markedly different apparent activation energies. The extracted apparent activation energies suggest that at temperatures below ∼800 °C, the etch rate is likely limited by desorption of etch products. The relative etch rates of heteroepitaxial 2 ¯ 01 and homoepitaxial (010) β-Ga2O3 were observed to scale by the ratio of the surface energies, indicating an anisotropic etch. Relatively smooth post-etch surface morphology was achieved by tuning the etching parameters for (010) homoepitaxial films.

Original languageEnglish
Article number242103
JournalApplied Physics Letters
Volume125
Issue number24
DOIs
StatePublished - Dec 9 2024
Externally publishedYes

Funding

We acknowledge support from the AFOSR/AFRL ACCESS Center of Excellence under Award No. FA9550-18-10529. C.A.G. acknowledges support from the National Defense Science and Engineering Graduate (NDSEG) Fellowship. H.J.B. acknowledges support from the National Science Foundation (NSF) [Platform for the Accelerated Realization, Analysis and Discovery of Interface Materials (PARADIM)] under Cooperative Agreement No. DMR-1539918. We also acknowledge support from PARADIM for the use of XRD. Substrate dicing and AFM were performed at the Cornell NanoScale Facility, a member of the National Nanotechnology Coordinated Infrastructure (NNCI), which is supported by the NSF (Grant No. NNCI-2025233).

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