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Journal
2015 | 13 | 1 |
Article title

Study of N-doped TiO2 thin films for
photoelectrochemical hydrogen
generation from water

Content
Title variants
Languages of publication
EN
Abstracts
EN
The present work deals with nitrogen-doped
stoichiometric TiO2:N and non-stoichiometric TiO2−x:N thin
films deposited by means of dc-pulsed reactive sputtering
for application as photoanodes for hydrogen generation
from water, using solar energy. Stoichiometric thin films
of TiO2 crystallize as a mixture of anatase and rutile while
rutile phase predominates in TiO2:N at higher nitrogen flow
rates as shown by X-ray diffraction at grazing incidence,
XRD GID. Lack of bulk nitridation of stoichiometric
TiO2:N is indicated by valence-to-core X-ray emission
spectroscopy, XES, analysis. The energy band gap as
well as flat band potential remain almost unaffected by
increasing nitrogen flow rate in this case. In contrast to
that, non-stoichiometric thin films of TiO2‑x:N demonstrate
systematic evolution of the structural, morphological,
optical and photolectrochemical properties upon
increasing level of nitrogen doping. Pronounced changes
in the growth pattern of non-stoichiometric TiO2-x:N upon
varied nitrogen flow rate, demonstrated by scanning
electron microscopy, SEM, can be easily correlated with
the crystallographic properties studied by XRD GID.
Relative positions of Kβ’’ XES lines of the TiO2-x:N thin
films, which depend strongly on the nature of the ligands
and their local coordination, change with the increasing
nitrogen flow. Doping of nonstoichiometric titanium
dioxide with nitrogen shifts the absorption spectrum
towards the visible range and increases considerably the
flat band potential which is beneficial for water photolysis.
EN
Publisher

Journal
Year
Volume
13
Issue
1
Physical description
Dates
accepted
4 - 11 - 2014
received
6 - 11 - 2013
online
8 - 4 - 2015
Contributors
  • AGH University of Science
    and Technology, Academic Centre for Materials and Nanotechnology,
    Al. Mickiewicza 30, 30-059 Krakow, Poland
  • AGH University of
    Science and Technology, Faculty of Physics and Applied Computer
    Science, Al. Mickiewicza 30, 30-059 Krakow, Poland
author
  • AGH University of Science
    and Technology, Academic Centre for Materials and Nanotechnology,
    Al. Mickiewicza 30, 30-059 Krakow, Poland
  • AGH University of
    Science and Technology, Faculty of Physics and Applied Computer
    Science, Al. Mickiewicza 30, 30-059 Krakow, Poland
  • AGH University of
    Science and Technology, Faculty of Physics and Applied Computer
    Science, Al. Mickiewicza 30, 30-059 Krakow, Poland
  • AGH University of Science
    and Technology, Faculty of Materials Science and Ceramics,
    Al. Mickiewicza 30, 30-059 Krakow, Poland
author
  • AGH University of Science
    and Technology, Faculty of Materials Science and Ceramics,
    Al. Mickiewicza 30, 30-059 Krakow, Poland
  • AGH University of Science and Technology,
    Faculty of Computer Science, Electronics and Telecommunications,
    Al. Mickiewicza 30, 30-059 Krakow, Poland
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Document Type
Publication order reference
Identifiers
YADDA identifier
bwmeta1.element.-psjd-doi-10_1515_chem-2015-0089
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