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<sup>15</sup>N Solid State NMR and EPR Characterization of N-Doped TiO<sub>2</sub> Photocatalysts

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journal contribution
posted on 2007-02-15, 00:00 authored by Enrique A. Reyes-Garcia, Yanping Sun, Karla Reyes-Gil, Daniel Raftery
The solid-state nuclear magnetic resonance (SSNMR) analysis and structural characterization of N-doped TiO<sub>2</sub> nanoparticle and monolayer materials suitable for visible photocatalysis is reported. The SSNMR analysis of <sup>15</sup>N-doped TiO<sub>2</sub> synthesized using <sup>15</sup>N-urea before calcination indicates formation of various amino functionalities of the type NH, NH<sub>2</sub>, NH<sub>3</sub>, and probably NH<sub>4</sub><sup>+</sup>, 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-<sup>13</sup>C-trichloroethylene (TCE), photochemical activity was confirmed by monitoring the production of CO<sub>2</sub> by <sup>13</sup>C NMR analysis. The powdered form of N-doped TiO<sub>2</sub> proved to be a highly efficient visible light catalyst by oxidizing all of the TCE to chlorinated alkyl and acyl containing molecules along with CO<sub>2</sub>. The performance of a TiO<sub>2</sub>−N−TiO<sub>2</sub>/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 TiO<sub>2</sub>-only monolayers. Direct nitridation of TiO<sub>2</sub> powders and monolayers also was conducted to compare the <sup>15</sup>N 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 TiO<sub>2</sub> is present in interstitial sites when N is in a highly oxidized state.

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