Issue 22, 2012

Facile synthesis of nitrogen self-doped rutile TiO2 nanorods

Abstract

Nitrogen doping is a promising method to enhance the visible light absorption and photo-catalytic activity of TiO2. A new method is reported for the synthesis of nitrogen self-doped rutile TiO2 nanorods, along with the formation study of V-shaped N-doped TiO2 nanorods, using TiN as a precursor and using a hydrothermal method. Our synthesis method gives a facile and easy way to control nitrogen doping in a TiO2 lattice. Two types of the V-shaped nanorods, with a (101) coherent boundary of either 114.4° or 134.9° inner angle, were observed. The N-doped TiO2 nanorods exhibit an enhanced visible light absorption and red-shift in band gap in comparison with pure rutile TiO2 nanopowders. The mechanisms of N doping and the formation of the V-shaped nanorods are analyzed and discussed. The oriented attachment and Ostwald ripening are considered responsible for the formation and growth of the straight and V-shaped N-doped TiO2 nanorods.

Graphical abstract: Facile synthesis of nitrogen self-doped rutile TiO2 nanorods

  • This article is part of the themed collection: Nanocrystals

Supplementary files

Article information

Article type
Paper
Submitted
25 May 2012
Accepted
26 Jun 2012
First published
26 Jun 2012

CrystEngComm, 2012,14, 7672-7679

Facile synthesis of nitrogen self-doped rutile TiO2 nanorods

S. Wang, J. Xu, H. Ding, S. Pan, Y. Zhang and G. Li, CrystEngComm, 2012, 14, 7672 DOI: 10.1039/C2CE25827G

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