Passivated SiC Surfaces for Photonic and Quantum Applications: Balancing Chemical Stability and Surface Luminescence

ABSTRACT Silicon carbide (SiC) has emerged as a promising platform for photonic and quantum technologies, yet the role of surface passivation, particularly at low processing temperatures, remains insufficiently understood with respect to long‐term optical stability. Here, we present a systematic study of low‐temperature surface passivation strategies for 4H‐SiC, including atomic layer deposition of Al 2 O 3 and HfO x , plasma‐enhanced chemical vapor deposition of SiN x and SiO 2 , as well as Ar and CF 4 plasma treatments. Surface morphology, chemistry, wettability, and optical background were investigated using atomic force microscopy, X‐ray photoelectron spectroscopy, contact angle measurements, and spatially resolved photoluminescence (PL) imaging, with particular emphasis on environmental stability under ambient conditions. While CF 4 plasma and ALD‐HfO x yield chemically robust surfaces, they do not significantly suppress photoluminescence. In contrast, Ar plasma and PECVD‐SiN x treatments produce smooth surfaces with strongly reduced and spatially homogeneous PL background, with SiN x exhibiting the best overall performance. Notably, both Ar plasma‐ and SiN x ‐passivated surfaces preserve their low PL background even after 1 year of ambient storage. These results demonstrate that optical surface quality is not directly correlated with chemical robustness and must be optimized independently. This work establishes design guidelines for passivation strategies in SiC‐based photonic and quantum devices.

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Publication Details

Journal
Advanced Materials Interfaces
Published
2026-05-08
DOI
https://doi.org/10.1002/admi.70525
Primary Topic
Silicon Nanostructures and Photoluminescence
Type
article
Field-Weighted Citation Impact
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article

Passivated SiC Surfaces for Photonic and Quantum Applications: Balancing Chemical Stability and Surface Luminescence

Patrick Berwian, Marina Scharin-Mehlmann, Christian Gobert, Sarah Saarmann et al.
Advanced Materials Interfaces
Silicon Nanostructures and Photoluminescence
article

Passivated SiC Surfaces for Photonic and Quantum Applications: Balancing Chemical Stability and Surface Luminescence

Patrick Berwian, Marina Scharin-Mehlmann, Christian Gobert, Sarah Saarmann, Robert Köhler
article en

Abstract

ABSTRACT Silicon carbide (SiC) has emerged as a promising platform for photonic and quantum technologies, yet the role of surface passivation, particularly at low processing temperatures, remains insufficiently understood with respect to long‐term optical stability. Here, we present a systematic study of low‐temperature surface passivation strategies for 4H‐SiC, including atomic layer deposition of Al 2 O 3 and HfO x , plasma‐enhanced chemical vapor deposition of SiN x and SiO 2 , as well as Ar and CF 4 plasma treatments. Surface morphology, chemistry, wettability, and optical background were investigated using atomic force microscopy, X‐ray photoelectron spectroscopy, contact angle measurements, and spatially resolved photoluminescence (PL) imaging, with particular emphasis on environmental stability under ambient conditions. While CF 4 plasma and ALD‐HfO x yield chemically robust surfaces, they do not significantly suppress photoluminescence. In contrast, Ar plasma and PECVD‐SiN x treatments produce smooth surfaces with strongly reduced and spatially homogeneous PL background, with SiN x exhibiting the best overall performance. Notably, both Ar plasma‐ and SiN x ‐passivated surfaces preserve their low PL background even after 1 year of ambient storage. These results demonstrate that optical surface quality is not directly correlated with chemical robustness and must be optimized independently. This work establishes design guidelines for passivation strategies in SiC‐based photonic and quantum devices.

Advanced Materials Interfaces
Fraunhofer Institute for Integrated Systems and Device Technology (DE)
Openalex Percentile: Top 10%
Silicon Nanostructures and Photoluminescence
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