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Photocatalytic Degradation of NOx Under Visible Light Irradiation Using Fe-Doped Titanium Dioxide

Photocatalytic Degradation of NO_x Under Visible Light Irradiation Using Fe-Doped Titanium Dioxide
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摘要 In order to utilize visible light in photocatalytic conversion of NOx, Fe atoms were doped in commercially available photocatalytic TiO2 powders by impregnating method. The crystal phase of TiO2 was not changed after calcination process. Analysis by both X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS) indicated that Fe atoms were incorporated in TiO2 as Ti-O-Fe linkages. One significant shift of the absorption edge to a lower energy and a higher absorption in the visible light region were observed. The Fe-doped TiO2 powder exhibited photocatalytic activity for the degradation of NOx under visible light irradiation. The sample mixed with 0.2 at% Fe3+and calcined at 600 ℃ showed the best photocatalytic activity. In order to utilize visible light in photocatalytic conversion of NOx, Fe atoms were doped in commercially available photocatalytic TiO2 powders by impregnating method. The crystal phase of TiO2 was not changed after calcination process. Analysis by both X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS) indicated that Fe atoms were incorporated in TiO2 as Ti-O-Fe linkages. One significant shift of the absorption edge to a lower energy and a higher absorption in the visible light region were observed. The Fe-doped TiO2 powder exhibited photocatalytic activity for the degradation of NOx under visible light irradiation. The sample mixed with 0.2 at% Fe^3+ and calcined at 600 ℃ showed the best photocatalytic activity.
出处 《Transactions of Tianjin University》 EI CAS 2007年第4期270-275,共6页 天津大学学报(英文版)
基金 Supported by National Natural Science Foundation of China (No.20276053) .
关键词 PHOTOCATALYSIS Fe-doped titania visible light induced nitrogen oxides 降解作用 二氧化钛 光催化 氧化氮
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  • 1N. U. Zhanpeisov,W. S. Ju,K. Iino,M. Matsuoka,M. Anpo. Local structure of highly dispersed lead species incorporated within zeolite: experimental and theoretical studies[J] 2003,Research on Chemical Intermediates(4):407~416

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