LAUSR.org creates dashboard-style pages of related content for over 1.5 million academic articles. Sign Up to like articles & get recommendations!

A novel two-stage synthesis for 3C–SiC nanowires by carbothermic reduction and their photoluminescence properties

Photo from wikipedia

A large quantity of 3C–SiC nanowires (SiCnws) with high purity were fabricated via carbothermic reduction method combined with a novel two-stage temperature program. At the first temperature stage, the reactants… Click to show full abstract

A large quantity of 3C–SiC nanowires (SiCnws) with high purity were fabricated via carbothermic reduction method combined with a novel two-stage temperature program. At the first temperature stage, the reactants were kept at 1600 °C for 4 h to promote the formation of SiC nucleus and SiO intermediate gas. Then they were cooled to 1350 °C for 2 h at the second stage for the growth of SiCnws with fewer defects. Compared with the conventional single temperature method at 1600 °C for 6 h, the product prepared by this new strategy exhibits large yield and high purity with a narrow diameter range. As for the reaction mechanism, “solid–solid” and “solid–vapor” reactions occurring between SiO2, SiO and C dominate at the first stage. While “vapor–vapor” reaction between SiO and CO plays an important role at the second stage. Furthermore, photoluminescence (PL) properties were measured under the room temperature. A sharp violet light emission peak with a significant blue shift is observed at 401 nm compared to bulk 3C–SiC.

Keywords: novel two; two stage; sic nanowires; carbothermic reduction; stage; photoluminescence properties

Journal Title: Journal of Materials Science
Year Published: 2019

Link to full text (if available)


Share on Social Media:                               Sign Up to like & get
recommendations!

Related content

More Information              News              Social Media              Video              Recommended



                Click one of the above tabs to view related content.