Effects of thermal and evacuating treatments on photo-induced hydrophilic conversion at TiO2 surfaces

被引:9
作者
Minabe, T
Fujishima, A
Nakajima, A
Watanabe, T
Hashimoto, K
机构
[1] Univ Tokyo, Adv Sci & Technol Res Ctr, Meguro Ku, Tokyo 1538904, Japan
[2] Univ Tokyo, Sch Engn, Dept Appl Chem, Bunkyo Ku, Tokyo 1138656, Japan
关键词
hydrophilicity; contact angle; titanium dioxide;
D O I
10.5796/electrochemistry.68.779
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
It is well known that the amount of physisorbed water molecules decreases by thermal and evacuating treatments at anatase TiO2 surfaces. (1- 3)) However, the initial water contact angle of the anatase TiO2 surface coated on the glass was little changed (from 24 degrees +-/ 1 degrees to 23 degrees +/- 1 degrees) and the hydrophilicity did not change by the heating treatment at 150 degreesC for 1 hour. On the other hand, the value of its initial contact angle increased remarkably (from 24 degrees +/- 1 degrees to 67 degrees +/- 1 degrees), and the TiO2 surface was hydrophobicized by the evacuation at similar to 5x10(-6) Pa. These observations may show that not only the amount of physisorbed water molecules but also the structure, i.e., OH groups of TiO2 surfaces are related to the hydrophilicity. The photo-decreasing rate of the water contact angle under the ultra violet (UV) illumination at the anatase TiO2 surface (the photo-induced hydrophilic conversion rate) increased by the heating treatment at 150 degreesC for 1 hour. However, photo-induced hydrophilic conversion rates were little changed by the evacuating treatment at similar to 5x10(-6) Pa. These results suggest that the photo-induced hydrophilic conversion phenomena are not necessarily affected by the initial amount of physisorbed water molecules.
引用
收藏
页码:779 / 782
页数:4
相关论文
共 23 条
[1]   ELECTROCHEMICAL PHOTOLYSIS OF WATER AT A SEMICONDUCTOR ELECTRODE [J].
FUJISHIMA, A ;
HONDA, K .
NATURE, 1972, 238 (5358) :37-+
[2]  
FUKUYAMA S, 1995, 187 M EL SOC REN NEV
[3]   Chemistry and applications of photocatalytic oxidation of thin organic films [J].
Heller, A .
ACCOUNTS OF CHEMICAL RESEARCH, 1995, 28 (12) :503-508
[4]   Time-dependent behavior of active oxygen species formed on photoirradiated TiO2 films in air [J].
Ishibashi, K ;
Nosaka, Y ;
Hashimoto, K ;
Fujishima, A .
JOURNAL OF PHYSICAL CHEMISTRY B, 1998, 102 (12) :2117-2120
[5]   INFRARED STUDIES OF RUTILE SURFACES .3. ADSORPTION OF WATER AND DEHYDROXYLATION OF RUTILE [J].
JONES, P ;
HOCKEY, JA .
JOURNAL OF THE CHEMICAL SOCIETY-FARADAY TRANSACTIONS I, 1972, 68 :907-&
[6]   Photocatalytic bactericidal effect of TiO2 thin films: Dynamic view of the active oxygen species responsible for the effect [J].
Kikuchi, Y ;
Sunada, K ;
Iyoda, T ;
Hashimoto, K ;
Fujishima, A .
JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY A-CHEMISTRY, 1997, 106 (1-3) :51-56
[7]   Photooxidation of long-chain organic compounds on TiO2 thin film [J].
Minabe, T ;
Sawunyama, P ;
Kikuchi, Y ;
Fujishima, A ;
Hashimoto, K .
ELECTROCHEMISTRY, 1999, 67 (12) :1132-1134
[8]   DESORBABILITY OF CHEMISORBED WATER ON METAL OXIDE SURFACES .I. DESORPTION TEMPERATURE OF CHEMISORBED WATER ON HEMATITE RUTILE AND ZINC OXIDE [J].
MORIMOTO, T ;
NAGAO, M ;
TOKUDA, F .
BULLETIN OF THE CHEMICAL SOCIETY OF JAPAN, 1968, 41 (07) :1533-+
[9]   PREPARATION OF TRANSPARENT TIO2 THIN-FILM PHOTOCATALYST AND ITS PHOTOCATALYTIC ACTIVITY [J].
NEGISHI, N ;
IYODA, T ;
HASHIMOTO, K ;
FUJISHIMA, A .
CHEMISTRY LETTERS, 1995, (09) :841-842
[10]  
OKAZAKI S, 1971, J CHEM SOC JPN, V74, P1085