Issue 19, 2009

Synthesis and characterization of V2O3 nanorods

Abstract

In this work, VO2 nanorods have been initially generated as reactive nanoscale precursors to their subsequent conversion to large quantities of highly crystalline V2O3 with no detectable impurities. Structural changes in VO2, associated with the metallic-to-insulating transition from the monoclinic form to the rutile form, have been investigated and confirmed using X-ray diffraction and synchrotron data, showing that the structural transition is reversible and occurs at around 63 °C. When this VO2 one-dimensional sample was subsequently heated to 800 °C in a reducing atmosphere, it was successfully transformed into V2O3 with effective retention of its nanorod morphology. We have also collected magnetic and transport data on these systems that are comparable to bulk behavior and consistent with trends observed in previous experiments.

Graphical abstract: Synthesis and characterization of V2O3 nanorods

Supplementary files

Article information

Article type
Paper
Submitted
19 Dec 2008
Accepted
16 Feb 2009
First published
12 Mar 2009

Phys. Chem. Chem. Phys., 2009,11, 3718-3726

Synthesis and characterization of V2O3 nanorods

A. C. Santulli, W. Xu, J. B. Parise, L. Wu, M.C. Aronson, F. Zhang, C. Nam, C. T. Black, A. L. Tiano and S. S. Wong, Phys. Chem. Chem. Phys., 2009, 11, 3718 DOI: 10.1039/B822902C

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements