15N solid state NMR and EPR characterization of N-doped TiO2 photocatalysts

被引:105
作者
Reyes-Garcia, Enrique A. [1 ]
Sun, Yanping [1 ]
Reyes-Gil, Karla [1 ]
Raftery, Daniel [1 ]
机构
[1] Purdue Univ, Dept Chem, W Lafayette, IN 47907 USA
关键词
D O I
10.1021/jp0652289
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 solid-state nuclear magnetic resonance (SSNMR) analysis and structural characterization of N-doped TiO2 nanoparticle and monolayer materials suitable for visible photocatalysis is reported. The SSNMR analysis of N-15-doped TiO2 synthesized using N-15-urea before calcination indicates formation of various amino functionalities of the type NH, NH2, NH3, and probably NH4+, while the NMR spectrum of the yellow powder that results from high-temperature calcination shows that these nitrogen species oxidize to form nitrate. These and nonisotopically labeled materials were characterized also by X-ray diffraction, UV-vis, and electron paramagnetic resonance spectroscopy. Monitoring the oxidation of 1,2-C-13-trichloroethylene (TCE), photochemical activity was confirmed by monitoring the production Of CO2 by C-13 NMR analysis. The powdered form of N-doped TiO2 proved to be a highly efficient visible light catalyst by oxidizing all of the TCE to chlorinated alkyl and acyl containing molecules along with CO2. The performance of a TiO2-N-TiO2/ porous Vycor 7930 borosilicate glass monolayer catalyst was in turn evaluated by monitoring the photochemical oxidation of ethanol and acetone with UV-vis light, and it was found to perform better than TiO2-only monolayers. Direct nitridation of TiO2 powders and monolayers also was conducted to compare the N-15 SSNMR and to discern if there is a nitridic bond in these materials. The SSNMR results provide more evidence supporting the hypothesis that the nitrogen atom in N-doped TiO2 is present in interstitial sites when N is in a highly oxidized state.
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页码:2738 / 2748
页数:11
相关论文
共 103 条
[1]   Phase-compositional control and visible light photocatalytic activity of nitrogen-doped titania via solvothermal process [J].
Aita, Y ;
Komatsu, M ;
Yin, S ;
Sato, T .
JOURNAL OF SOLID STATE CHEMISTRY, 2004, 177 (09) :3235-3238
[2]   A SOLID-STATE N-15 NMR-STUDY OF THE PHASE-TRANSITIONS IN AMMONIUM-NITRATE [J].
ANDERSONALTMANN, KL ;
GRANT, DM .
JOURNAL OF PHYSICAL CHEMISTRY, 1993, 97 (42) :11096-11102
[3]   Preparation, characterization, and reactivities of highly functional titanium oxide-based photocatalysts able to operate under UV-visible light irradiation: Approaches in realizing high efficiency in the use of visible light [J].
Anpo, M .
BULLETIN OF THE CHEMICAL SOCIETY OF JAPAN, 2004, 77 (08) :1427-1442
[4]   Visible-light photocatalysis in nitrogen-doped titanium oxides [J].
Asahi, R ;
Morikawa, T ;
Ohwaki, T ;
Aoki, K ;
Taga, Y .
SCIENCE, 2001, 293 (5528) :269-271
[5]   An EPR study of thermally and photochemically generated oxygen radicals on hydrated and dehydrated titania surfaces [J].
Attwood, AL ;
Murphy, DM ;
Edwards, JL ;
Egerton, TA ;
Harrison, RW .
RESEARCH ON CHEMICAL INTERMEDIATES, 2003, 29 (05) :449-465
[6]   Preparation, testing and characterization of doped TiO2 active in the peroxidation of biomolecules under visible light [J].
Bacsa, R ;
Kiwi, J ;
Ohno, T ;
Albers, P ;
Nadtochenko, V .
JOURNAL OF PHYSICAL CHEMISTRY B, 2005, 109 (12) :5994-6003
[7]   N-15 NUCLEAR MAGNETIC SHIELDING TENSORS IN NITRITE AND NITRATE ION - EXPERIMENTAL AND THEORETICAL DETERMINATIONS [J].
BARRIE, PJ ;
GROOMBRIDGE, CJ ;
MASON, J ;
MOORE, EA .
CHEMICAL PHYSICS LETTERS, 1994, 219 (5-6) :491-496
[8]   Influence of nitrogen doping on the defect formation and surface properties of TiO2 rutile and anatase -: art. no. 026103 [J].
Batzill, M ;
Morales, EH ;
Diebold, U .
PHYSICAL REVIEW LETTERS, 2006, 96 (02)
[9]   TiO2 photocatalytic degradation of dichloromethane:: An FTIR and solid-state NMR study [J].
Borisch, J ;
Pilkenton, S ;
Miller, ML ;
Raftery, D ;
Francisco, JS .
JOURNAL OF PHYSICAL CHEMISTRY B, 2004, 108 (18) :5640-5646
[10]   15N CP/MAS NMR as an instrument in structure investigations of organosilicon polymers [J].
Brendler, E ;
Ebrecht, E ;
Thomas, B ;
Boden, G ;
Breuning, T .
FRESENIUS JOURNAL OF ANALYTICAL CHEMISTRY, 1999, 363 (02) :185-188