Self-activated epitaxial growth of ScN films from molecular nitrogen at low temperatures

Unlike naturally occurring oxide crystals such as ruby and gemstones, there are no naturally occurring nitride crystals because the triple bond of the nitrogen molecule is one of the strongest bonds in nature. Here, we report that when the transition metal scandium is subjected to molecular nitrogen, it self-catalyzes to break the nitrogen triple bond to form highly crystalline layers of ScN, a semiconductor. This reaction proceeds even at room temperature. Self-activated ScN films have a twin cubic crystal structure, atomic layering, and electronic and optical properties comparable to plasma-based methods. We extend our research to showcase Sc’s scavenging effect and demonstrate self-activated ScN growth under various growth conditions and on technologically significant substrates, such as 6H–SiC, AlN, and GaN. Ab initio calculations elucidate an energetically efficient pathway for the self-activated growth of crystalline ScN films from molecular N2. The findings open a new pathway to ultralow-energy synthesis of crystalline nitride semiconductor layers and beyond.

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Publication Details

Journal
APL Materials
Published
2024-11-01
DOI
https://doi.org/10.1063/5.0222995
Citations
8
Primary Topic
Metal and Thin Film Mechanics
Type
article
Field-Weighted Citation Impact
2.15

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article

Self-activated epitaxial growth of ScN films from molecular nitrogen at low temperatures

Guru Khalsa, Suchismita Sarker, Salva Salmani‐Rezaie, Jacob Ruff et al.
8 citations
APL Materials
Metal and Thin Film Mechanics
2.15
article

Self-activated epitaxial growth of ScN films from molecular nitrogen at low temperatures

Guru Khalsa, Suchismita Sarker, Salva Salmani‐Rezaie, Jacob Ruff, Debdeep Jena, Andrej Singer, David Anthony Muller, Thai‐Son Nguyen, Chandrashekhar Savant, Huili Grace Xing, Joseph Casamento, Yu‐Hsin Chen, Len van Deurzen, Zhiren He, Anita Verma, Benjamin Gregory, Jakob Gollwitzer
article en
8 citations

Abstract

Unlike naturally occurring oxide crystals such as ruby and gemstones, there are no naturally occurring nitride crystals because the triple bond of the nitrogen molecule is one of the strongest bonds in nature. Here, we report that when the transition metal scandium is subjected to molecular nitrogen, it self-catalyzes to break the nitrogen triple bond to form highly crystalline layers of ScN, a semiconductor. This reaction proceeds even at room temperature. Self-activated ScN films have a twin cubic crystal structure, atomic layering, and electronic and optical properties comparable to plasma-based methods. We extend our research to showcase Sc’s scavenging effect and demonstrate self-activated ScN growth under various growth conditions and on technologically significant substrates, such as 6H–SiC, AlN, and GaN. Ab initio calculations elucidate an energetically efficient pathway for the self-activated growth of crystalline ScN films from molecular N2. The findings open a new pathway to ultralow-energy synthesis of crystalline nitride semiconductor layers and beyond.

APL MaterialsVol. 12(11)
University of North Texas (US), Cornell University (US), Massachusetts Institute of Technology (US)
National Science Foundation, Semiconductor Research Corporation, Advanced Research Projects Agency - Energy, Cornell Center for Materials Research, Defense Sciences Office, DARPA
Openalex Percentile: Top 13%
Metal and Thin Film Mechanics
2.15
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