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

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JOURNAL OF PHYSICAL CHEMISTRY C
卷 111, 期 6, 页码 2738-2748

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AMER CHEMICAL SOC
DOI: 10.1021/jp0652289

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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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