4.8 Article

Different Roles of Water in Photocatalytic DeNOx Mechanisms on TiO2: Basis for Engineering Nitrate Selectivity?

Journal

ACS APPLIED MATERIALS & INTERFACES
Volume 9, Issue 20, Pages 17035-17042

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsami.7b01989

Keywords

supported TiO2; synthesis conditions; adsorbed water; NOx; nitrate selectivity

Funding

  1. UK Engineering and Physical Sciences Research Council [EP/M003299/1]
  2. Natural Science Foundation of China International Joint Research Project (EPSRC-NSFC) [51461135005]
  3. EPSRC [EP/M003299/1] Funding Source: UKRI
  4. Engineering and Physical Sciences Research Council [EP/M003299/1] Funding Source: researchfish

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The nitrate selectivity of TiO2 has important consequences for its efficiency as a NOx depollution photocatalyst. Most emphasis is typically given to photocatalyst activity, a measure of the rate at which NOx concentrations are reduced, but a reduction in NOx concentration (mainly NO + NO2) is not necessarily a reduction in atmospheric NO2 concentration because the catalytic process itself generates NO2 center dot With NO2 being considerably more toxic than NO, more emphasis on nitrate selectivity, a measure of the NOx conversion to nitrate, and how to maximize it, should be given in engineering photocatalytic systems for improved urban air quality. This study, on the importance of adsorbed water in the photocatalytic oxidation of NOx, has identified important correlations which differentiate the role that water plays in the oxidation of NO and NO2. This observation is significant and offers insights into controlling nitrate selectivity on TiO2 and the potential for increased effectiveness in environmental photocatalyst applications.

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