TY - JOUR
T1 - Photocatalytic and photoelectrochemical studies on N-doped TiO2 photocatalyst
AU - Zhang, Xintong
AU - Udagawa, Keizo
AU - Liu, Zhaoyue
AU - Nishimoto, Shunsuke
AU - Xu, Changshan
AU - Liu, Yichun
AU - Sakai, Hideki
AU - Abe, Masahiko
AU - Murakami, Taketoshi
AU - Fujishma, Akira
N1 - Funding Information:
This work was supported by the Asia S&T Strategic Cooperation Program and a Grant-in-Aid for Scientific Research on Priority Areas (417) from the Ministry of Education, Culture, Sports, Science and Technology (MEXT) of the Japanese Government, and by the Core Research for Evolutional Science and Technology (CREST) Program of the Japan Science and Technology (JST) Agency.
PY - 2009/2/5
Y1 - 2009/2/5
N2 - One of the commercial N-doped TiO2 powders (Sumitomo Chemicals, TPS 201) was studied as a model material by photocatalytic and photoelectrochemical methods in order to evaluate the photoactivity of N-doped TiO2 materials and the possibility of their applications in solar photocatalysis. The N-doped TiO2 powder (TPS) was able to degrade and mineralize phenol under solar or visible light (VL) irradiation, and the degradation rate was strongly dependent on the suspension concentration. Photoelectrochemical studies showed that the VL-irradiated TPS electrode was able to oxidize water, phenol, as well as maleic acid, an open-ring oxidized product of phenol, consistent with the results of photocatalytic studies. Calcining the TPS powder at/over 773 K was found to lower the absorption in the VL region and the photocatalytic activity under VL irradiation, but improve the photocatalytic activity under solar irradiation, suggesting that the mid-gap states introduced by nitrogen doping also worked as recombination centers. Deposition of Pt (0.2 wt%) on the TPS photocatalyst thus greatly increased the degradation rate of phenol under either solar or VL irradiation due to the suppression of charge recombination, and the degradation rate was found to be higher than a pristine TiO2 photocatalyst (ST-01, anatase) either with or without loading of Pt. The potential application of the N-doped TiO2 in solar photocatalysis was discussed on the basis of above-mentioned studies.
AB - One of the commercial N-doped TiO2 powders (Sumitomo Chemicals, TPS 201) was studied as a model material by photocatalytic and photoelectrochemical methods in order to evaluate the photoactivity of N-doped TiO2 materials and the possibility of their applications in solar photocatalysis. The N-doped TiO2 powder (TPS) was able to degrade and mineralize phenol under solar or visible light (VL) irradiation, and the degradation rate was strongly dependent on the suspension concentration. Photoelectrochemical studies showed that the VL-irradiated TPS electrode was able to oxidize water, phenol, as well as maleic acid, an open-ring oxidized product of phenol, consistent with the results of photocatalytic studies. Calcining the TPS powder at/over 773 K was found to lower the absorption in the VL region and the photocatalytic activity under VL irradiation, but improve the photocatalytic activity under solar irradiation, suggesting that the mid-gap states introduced by nitrogen doping also worked as recombination centers. Deposition of Pt (0.2 wt%) on the TPS photocatalyst thus greatly increased the degradation rate of phenol under either solar or VL irradiation due to the suppression of charge recombination, and the degradation rate was found to be higher than a pristine TiO2 photocatalyst (ST-01, anatase) either with or without loading of Pt. The potential application of the N-doped TiO2 in solar photocatalysis was discussed on the basis of above-mentioned studies.
KW - Nitrogen doping
KW - Photocatalysis
KW - Photoelectrochemistry
KW - TiO
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U2 - 10.1016/j.jphotochem.2008.11.007
DO - 10.1016/j.jphotochem.2008.11.007
M3 - Article
AN - SCOPUS:58249098796
SN - 1010-6030
VL - 202
SP - 39
EP - 47
JO - Journal of Photochemistry and Photobiology A: Chemistry
JF - Journal of Photochemistry and Photobiology A: Chemistry
IS - 1
ER -