Abstract

ZnSnxGe1−xN2 alloys are chemically miscible semiconductor compounds with potential application as earth-abundant alternatives to InxGa1−xN. Preparation of ZnSnxGe1−xN2 thin-films by reactive RF sputter deposition yield low-mobility, nanocrystalline films. In contrast, the growth of ZnSnxGe1−xN2 films by molecular-beam epitaxy (MBE) on c-plane sapphire and GaN templates is described herein. Epitaxial films exhibited 3D growth on sapphire and 2D single-crystal quality on GaN, exhibiting substantial improvements in epitaxy and crystallinity relative to nanocrystalline sputtered films. Films on sapphire were n-type with electronic mobilities as high as 18 cm2 V−1 s−1, an order of magnitude greater than the 2 cm2 V−1 s−1 average mobility observed in this work for sputtered films. Mobility differences potentially arise from strain or surface effects originating from growth techniques, or from differences in film thicknesses. In general, MBE growth has provided desired improvements in electronic mobility, epitaxy, and crystal quality that provide encouragement for the continued study of ZnSnxGe1−xN2 alloys.

Highlights

  • ZnSnxGe1−xN2 alloys are chemically miscible semiconductor compounds with potential application as earth-abundant alternatives to InxGa1−xN

  • InxGa1−xN alloys are widely used in light-emitting diodes (LEDs) and sensors, because alloying enables tuning of the band-gap energy, Eg, within the range set by the two binary compounds, InN (Eg = 0.69 eV) and GaN (Eg = 3.51 eV)[1]

  • ZnSnxGe1−xN2 alloys made by reactive RF sputtering have band gaps between 1.8–3.1 eV3, which encompasses the visible spectrum, thereby suggesting potential applications as photovoltaic absorber materials, LEDs, or optical sensors

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Summary

Introduction

ZnSnxGe1−xN2 alloys are chemically miscible semiconductor compounds with potential application as earth-abundant alternatives to InxGa1−xN. Sputtered ZnSnxGe1−xN2 films have exhibited low electronic mobilities[6] and trap states from defects[7], hindering the development of high-performance ZnSnxGe1−xN2 devices based on this alloy series. RHEED patterns (Fig. 2a,d) for ZnSnN2 and ZnSnxGe1−xN2 films grown on GaN substrates via MBE provided further evidence of epitaxy, smooth interfaces, and lattice mismatch.

Results
Conclusion

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