TRAPPED HOLES ON TIO2 COLLOIDS STUDIED BY ELECTRON-PARAMAGNETIC-RESONANCE

被引:320
作者
MICIC, OI [1 ]
ZHANG, YN [1 ]
CROMACK, KR [1 ]
TRIFUNAC, AD [1 ]
THURNAUER, MC [1 ]
机构
[1] ARGONNE NATL LAB, DIV CHEM, ARGONNE, IL 60439 USA
关键词
D O I
10.1021/j100130a026
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
An electron paramagnetic resonance (EPR) study of paramagnetic species formed on band gap irradiation of TiO2 colloids, aqueous suspensions of anatase (Degussa P-25), and rutile (Aldrich) powders is reported. The EPR signals (observed at 6-200 K) of the trapped hole in all of these systems exhibit similar properties. Holes produced by band gap irradiation of a TiO2 colloid move from the oxygen lattice to the surface and are trapped directly on oxygen atoms bound to surface Ti(IV) atoms. The results obtained with TiO2 colloids prepared with oxygen-17 enriched water support the identification of trapped holes as an oxygen surface anion radical covalently bound to titanium atoms, Ti(IV)-0-Ti(IV)-O.. The intensity of the EPR signal from the hole trap is very sensitive to hydration and the total surface area available for chemical reactions. The EPR signal disappears with the addition of hole scavengers that are strongly bound to the surface, such as polyvinyl alcohol and KI. The signal obtained for trapped holes at 6-240 K is not the same as that of surface bound or free OH. radicals, since no change in the EPR line width was observed when D2O was used for preparation of colloids instead of H2O. In addition, spectra obtained at Q-band microwave frequency show that the spectral splittings are not due to hyperfine coupling. The EPR signal remains the same with increasing temperature up to 150 K, indicating that primary radicals do not convert into other radicals at higher temperatures. The EPR signal from trapped holes detected in aqueous suspensions of ZnO particles show a similar pattern to that from the TiO2 systems.
引用
收藏
页码:7277 / 7283
页数:7
相关论文
共 79 条
[1]   KINETIC-STUDIES IN HETEROGENEOUS PHOTOCATALYSIS .1. PHOTOCATALYTIC DEGRADATION OF CHLORINATED PHENOLS IN AERATED AQUEOUS-SOLUTIONS OVER TIO2 SUPPORTED ON A GLASS MATRIX [J].
ALEKABI, H ;
SERPONE, N .
JOURNAL OF PHYSICAL CHEMISTRY, 1988, 92 (20) :5726-5731
[2]   ELECTRON-SPIN-RESONANCE AND PHOTOLUMINESCENCE EVIDENCE FOR THE PHOTOCATALYTIC FORMATION OF HYDROXYL RADICALS ON SMALL TIO2 PARTICLES [J].
ANPO, M ;
SHIMA, T ;
KUBOKAWA, Y .
CHEMISTRY LETTERS, 1985, (12) :1799-1802
[3]   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
[4]   PICOSECOND FLASH SPECTROSCOPY OF TIO2 COLLOIDS WITH ADSORBED DYES [J].
ARBOUR, C ;
SHARMA, DK ;
LANGFORD, CH .
JOURNAL OF PHYSICAL CHEMISTRY, 1990, 94 (01) :331-335
[5]  
Aundaithai M., 1988, MATER RES B, V23, P1675
[6]   DETECTION OF THE INTERMEDIATES OF COLLOIDAL TIO2-CATALYZED PHOTOREACTIONS [J].
BAHNEMANN, D ;
HENGLEIN, A ;
SPANHEL, L .
FARADAY DISCUSSIONS, 1984, 78 :151-163
[7]   FLASH-PHOTOLYSIS OBSERVATION OF THE ABSORPTION-SPECTRA OF TRAPPED POSITIVE HOLES AND ELECTRONS IN COLLOIDAL TIO2 [J].
BAHNEMANN, D ;
HENGLEIN, A ;
LILIE, J ;
SPANHEL, L .
JOURNAL OF PHYSICAL CHEMISTRY, 1984, 88 (04) :709-711
[8]  
BARBENI M, 1984, NOUV J CHIM, V8, P547
[9]   PHOTOCHEMICAL DEGRADATION OF CHLORINATED DIOXINS, BIPHENYLS PHENOLS AND BENZENE ON SEMICONDUCTOR DISPERSION [J].
BARBENI, M ;
PRAMAURO, E ;
PELIZZETTI, E ;
BORGARELLO, E ;
SERPONE, N ;
JAMIESON, MA .
CHEMOSPHERE, 1986, 15 (9-12) :1913-1916
[10]   HIGH-PURITY, MONODISPERSE TIO2 POWDERS BY HYDROLYSIS OF TITANIUM TETRAETHOXIDE .2. AQUEOUS INTERFACIAL ELECTROCHEMISTRY AND DISPERSION STABILITY [J].
BARRINGER, EA ;
BOWEN, HK .
LANGMUIR, 1985, 1 (04) :420-428