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Phys. Rev. Lett. 103, 226401 (2009) [4 pages]

Band Gap Narrowing of Titanium Oxide Semiconductors by Noncompensated Anion-Cation Codoping for Enhanced Visible-Light Photoactivity

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Wenguang Zhu1,2, Xiaofeng Qiu3, Violeta Iancu2, Xing-Qiu Chen1, Hui Pan4, Wei Wang4, Nada M. Dimitrijevic5,6, Tijana Rajh5, Harry M. Meyer, III1, M. Parans Paranthaman3, G. M. Stocks1, Hanno H. Weitering2,1, Baohua Gu4, Gyula Eres1, and Zhenyu Zhang1,2
1Materials Science and Technology Division, Oak Ridge National Laboratory, Oak Ridge, Tennessee 37831, USA
2Department of Physics and Astronomy, University of Tennessee, Knoxville, Tennessee 37996, USA
3Chemical Sciences Division, Oak Ridge National Laboratory, Oak Ridge, Tennessee 37831, USA
4Environmental Sciences Division, Oak Ridge National Laboratory, Oak Ridge, Tennessee 37831, USA
5Center for Nanoscale Materials, Argonne National Laboratory, Argonne, Illinois 60439, USA
6Chemical Sciences and Engineering Division, Argonne National Laboratory, Argonne, Illinois 60439, USA

Received 11 September 2009; published 23 November 2009

“Noncompensated n-p codoping” is established as an enabling concept for enhancing the visible-light photoactivity of TiO2 by narrowing its band gap. The concept embodies two crucial ingredients: The electrostatic attraction within the n-p dopant pair enhances both the thermodynamic and kinetic solubilities, and the noncompensated nature ensures the creation of tunable intermediate bands that effectively narrow the band gap. The concept is demonstrated using first-principles calculations, and is validated by direct measurements of band gap narrowing using scanning tunneling spectroscopy, dramatically redshifted optical absorbance, and enhanced photoactivity manifested by efficient electron-hole separation in the visible-light region. This concept is broadly applicable to the synthesis of other advanced functional materials that demand optimal dopant control.

© 2009 The American Physical Society

URL:
http://link.aps.org/doi/10.1103/PhysRevLett.103.226401
DOI:
10.1103/PhysRevLett.103.226401
PACS:
71.20.Nr, 61.72.S-, 84.60.-h