Role of oxygen vacancy in the plasma-treated TiO2 photocatalyst with visible light activity for NO removal

被引:1168
作者
Nakamura, I [1 ]
Negishi, N
Kutsuna, S
Ihara, T
Sugihara, S
Takeuchi, E
机构
[1] Natl Inst Resources & Environm, Tsukuba, Ibaraki 3058569, Japan
[2] Kinki Univ, Dept Chem & Environm Technol, Hiroshima 7392116, Japan
[3] Ecodevice Co Ltd, Sumida Ku, Tokyo 1300026, Japan
关键词
photocatalysis; titanium dioxide; nitric oxide; visible light activity; oxygen vacancy;
D O I
10.1016/S1381-1169(00)00362-9
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The photocatalytic activity for NO removal under an oxidative atmosphere has been studied over commercial TiO2 and plasma-treated TiO2 powders. By the plasma treatment, the photocatalytic activity for NO removal appeared in the visible light region up to 600 nm without a decrease in the ultraviolet light activity. It was found that the NO was removed as nitrate (NO3-) by photocatalytic oxidation over the TiO2 powders, where NO3- was accumulated. No difference in the crystal structure, the crystallinity, and the specific surface area was observed between the raw TiO2 and the plasma-treated TiO2 photocatalysts. In electron spin resonance (ESR) measurements, a sharp signal at g = 2.004, which was identified as the electrons trapped on oxygen vacancies, was detected only for plasma-treated TiO2 under visible light irradiation. The saturated intensity of the ESR signal at g = 2.004 was proportional to the removal percentage of nitrogen oxides, suggesting that the number of trapped electrons determined the activity for the photocatalytic oxidation of NO to NO3-. The appearance of the visible light activity in the plasma-treated TiO2 photocatalyst was ascribed to the newly formed oxygen vacancy state between the valence and the conduction bands in the TiO2 band structure. (C) 2000 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:205 / 212
页数:8
相关论文
共 40 条
[1]   PHOTOCATALYTIC HYDROGENATION OF CH3CCH WITH H2O ON SMALL-PARTICLE TIO2 - SIZE QUANTIZATION EFFECTS AND REACTION INTERMEDIATES [J].
ANPO, M ;
SHIMA, T ;
KODAMA, S ;
KUBOKAWA, Y .
JOURNAL OF PHYSICAL CHEMISTRY, 1987, 91 (16) :4305-4310
[2]   Design of unique titanium oxide photocatalysts by an advanced metal ion-implantation method and photocatalytic reactions under visible light irradiation [J].
Anpo, M ;
Ichihashi, Y ;
Takeuchi, M ;
Yamashita, H .
RESEARCH ON CHEMICAL INTERMEDIATES, 1998, 24 (02) :143-149
[3]  
Anpo M., 1997, CATAL SURV JPN, V1, P169
[4]   VISIBLE-LIGHT INDUCED WATER CLEAVAGE IN COLLOIDAL SOLUTIONS OF CHROMIUM-DOPED TITANIUM-DIOXIDE PARTICLES [J].
BORGARELLO, E ;
KIWI, J ;
GRATZEL, M ;
PELIZZETTI, E ;
VISCA, M .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1982, 104 (11) :2996-3002
[5]   ELECTRICAL PROPERTIES OF TITANIUM DIOXIDE SEMICONDUCTORS [J].
BRECKENRIDGE, RG ;
HOSLER, WR .
PHYSICAL REVIEW, 1953, 91 (04) :793-802
[6]   SURFACE CO-ORDINATION OF OXYGEN ON OXYGEN-DEFICIENT TIO2 AND MOO3 AS REVEALED BY ESR-MEASUREEMENTS [J].
CORNAZ, PF ;
VANHOOFF, JH ;
PLUIJM, FJ ;
SCHUIT, GCA .
DISCUSSIONS OF THE FARADAY SOCIETY, 1966, (41) :290-&
[7]   INFRARED ABSORPTION OF REDUCED RUTILE TIO2 SINGLE CRYSTALS [J].
CRONEMEYER, DC .
PHYSICAL REVIEW, 1959, 113 (05) :1222-1226
[8]  
Forman M. H., 1979, Conference on Electronic Test and Measuring Instrumentation-Testmex 79, P87
[9]   HETEROGENEOUS PHOTOCATALYSIS [J].
FOX, MA ;
DULAY, MT .
CHEMICAL REVIEWS, 1993, 93 (01) :341-357
[10]   PHOTOELECTROLYSIS OF WATER IN SUNLIGHT WITH SENSITIZED SEMICONDUCTOR ELECTRODES [J].
GHOSH, AK ;
MARUSKA, HP .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1977, 124 (10) :1516-1522