Issue 38, 2011

Novel coaxial SiC–SiO2–BN nanocable: large-scale synthesis, formation mechanism and photoluminescence property

Abstract

Novel one-dimensional heterostructures composed of single crystalline cubic SiC cores, intermediate amorphous SiO2 layers, and single crystalline hexagonal BN (h-BN) sheaths (i.e. SiCSiO2BN nanocable) have been successfully fabricated in large scale using SiCSiO2 nanocables and ammonia borane as starting materials. The structure and chemical composition of the as-synthesized products are determined by powder X-ray diffraction, field emission scanning electron microscopy, high-resolution transmission electron microscopy, X-ray photoelectron spectroscopy, and energy filtered TEM based on electron energy loss spectroscopy. The nanocables are approximately 100 nm in diameter and up to 1 millimetre in length. The intermediate amorphous SiO2 layers and the outer h-BN sheaths are about 10 nm and 5 nm thick, respectively. Interestingly, an increase in the amount of ammonia borane leads to the transformation of SiCSiO2 nanocables into BN nanotubes. Mass spectrometric analysis shows that the vapors decomposed from ammonia borane play crucial roles both in the growth of the BN sheath on the SiCSiO2 nanocables and in the transformation to the BN nanotubes. The SiCSiO2BN nanocable displays similar photoluminescence (PL) characteristics with respect to the original SiCSiO2 nanocable but with the 488.5-nm emission peak blue shifting. The synthetic route has also been extended to fabricate SiCBN nanocables and has proved effective and universal for the synthesis of core–sheath nanostructures with BN sheaths.

Graphical abstract: Novel coaxial SiC–SiO2–BN nanocable: large-scale synthesis, formation mechanism and photoluminescence property

Article information

Article type
Paper
Submitted
07 May 2011
Accepted
14 Jul 2011
First published
15 Aug 2011

J. Mater. Chem., 2011,21, 14432-14440

Novel coaxial SiCSiO2BN nanocable: large-scale synthesis, formation mechanism and photoluminescence property

B. Zhong, L. Song, X. Huang, X. Zhang, G. Wen and Y. Zhou, J. Mater. Chem., 2011, 21, 14432 DOI: 10.1039/C1JM12008E

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