Synthesis and carbothermal nitridation mechanism of ultra-long single crystal α-Si 3 N 4 nanobelts

• Published in: Nanotechnology Vol. 31; no. 19; p. 194001
• Main Authors: Wang, Bo, Huang, Xin, Zhou, Xiao-Nan, Zhi, Qiang, Hao, Liu-Cheng, Li, Zi-Xuan, Zhao, Shan, Hou, Bao-Qiang, Yang, Jian-Feng, Ishizaki, Kozo
• Format: Journal Article
• Language: English
• Published: England 08.05.2020
• ISSN: 0957-4484; 1361-6528
• DOI: 10.1088/1361-6528/ab6fd7

One-dimensional Si N nanostructures are desirable for constructing nanoscale electric and optoelectronic devices due to their peculiar morphologies. Herein, a facile and environmentally friendly catalyst-free method is proposed to synthesize ultra-long single crystal α-Si N nanobelts via carbothermal nitridation of carbon nanotubes at 1750 °C. The obtained α-Si N nanobelts with a flat surface (thickness of ∼150 nm, length of several millimeters) exhibited an extremely high aspect ratio, perfect crystal structure, and high specific surface area of 7.34-10.09 m g . In addition, the width was increased from approximately 80 nm to 8 μm by increasing the holding time from 1 to 3 h. The nanobelt formation was governed by the vapor-solid (VS) reaction between SiO vapor, N and carbon nanotubes, and the vapor-vapor reaction between SiO, CO and N . The former was responsible for the initial nucleation and successive base-growth of α-Si N nanotubes. The latter additionally contributed to the nanorod and subsequent proto-nanobelt formation and to the growth of the nanobelts. During high-temperature annealing at 1750 °C, the original Si N nanotubes gradually transformed into nanorods, and, finally, nanobelts with stable shapes as a result of surface energy minimization.