Preparation of fluorine-doped TiO(2) photocatalysts with controlled crystalline structure (Journal article)

Todorova, N./ Giannakopoulou, T./ Romanos, G./ Vaimakis, T./ Yu, J. G./ Trapalis, C.


Nanocrystalline F-doped TiO(2) powders were prepared by sol-gel route. The thermal behavior of the powders was recorded by DTA/ TG technique. The crystalline phase of the fluorinated TiO2 powders was determined by X-ray diffraction technique. It was demonstrated that F-doping using CF(3)COOH favors the formation of rutile along with anatase phase even at low temperature. Moreover, the rutile's phase content increases with the increase of the quantity of the fluorine precursor in the starting solution. The surface area of the powders and the pore size distribution were studied by N(2) adsorption-desorption using BET and BJH methods. X-ray photoelectron spectroscopy ( XPS) revealed that the fluorine is presented in the TiO2 powders mainly as metal fluoride in quantities similar to 16 at %. The F-doped TiO(2) showed a red-shift absorption in UV-vis region which was attributed to the increased content of rutile phase in the powders. The powders exhibited enhanced photocatalytic activity in decomposition of acetone. Copyright (C) 2008.
Institution and School/Department of submitter: Πανεπιστήμιο Ιωαννίνων. Σχολή Θετικών Επιστημών. Τμήμα Χημείας
Keywords: light-driven photocatalysis,visible-light,titanium-dioxide,thin-films,powders,microstructures,sol,nitrogen,anatase
URI: http://olympias.lib.uoi.gr/jspui/handle/123456789/8930
ISSN: 1110-662X
Link: <Go to ISI>://000255686600001
http://downloads.hindawi.com/journals/ijp/2008/534038.pdf
Publisher: Hindawi Publishing Corporation
Appears in Collections:Άρθρα σε επιστημονικά περιοδικά ( Ανοικτά)

Files in This Item:
File Description SizeFormat 
Todorova-2008-Preparation of fluor.pdf1.08 MBAdobe PDFView/Open



 Please use this identifier to cite or link to this item:
http://olympias.lib.uoi.gr/jspui/handle/123456789/8930
  This item is a favorite for 0 people.

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.