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Defect‐Related Optical Behavior in Surface Modified TiO 2 Nanostructures
Author(s) -
Prokes S. M.,
Gole J. L.,
Chen X.,
Burda C.,
Carlos W. E.
Publication year - 2005
Publication title -
advanced functional materials
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 6.069
H-Index - 322
eISSN - 1616-3028
pISSN - 1616-301X
DOI - 10.1002/adfm.200305109
Subject(s) - materials science , x ray photoelectron spectroscopy , anatase , titanium , surface modification , chemical engineering , electron paramagnetic resonance , nanostructure , nitriding , metal , analytical chemistry (journal) , nanotechnology , layer (electronics) , photocatalysis , metallurgy , catalysis , nuclear magnetic resonance , organic chemistry , chemistry , physics , engineering
The surface modification of TiO 2 nanostructures to incorporate nitrogen and form visible light absorbing titanium oxynitride centers is studied. Anatase TiO 2 structures in the 5–20 nm range, formed by a wet chemical technique, were surface modified and the nitridation of the highly reactive TiO 2 nanocolloid surface, as determined by X‐ray photoelectron spectroscopy (XPS) studies, is achieved by a quick and simple treatment in alkyl ammonium compounds. The nitriding process was also simultaneously accompanied by metal seeding resulting in a metal coating layer on the TiO 2 structures. The structure of the resultant titanium oxynitride nanostructures remains anatase. These freshly prepared samples exhibited a strong emission near 560 nm (2.21 eV), which red‐shifted to 660 nm (1.88 eV) and dropped in intensity with aging in the atmosphere. This behavior was also evident in some of the combined nitrogen doped and metal seeded TiO 2 nanocolloids. Electron spin resonance (ESR) performed on these samples identified a resonance at g = 2.0035, which increased significantly with nitridation. The resonance is attributed to an oxygen hole center created near the surface of the nanocolloid, which correlates well with the observed optical activity.