4.7 Article

Visible light-responsive Fe-loaded TiO2 photocatalysts for total oxidation of acetaldehyde: Fundamental studies towards large-scale production and applications

Journal

APPLIED SURFACE SCIENCE
Volume 505, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.apsusc.2019.144160

Keywords

Visible light responsive catalyst; High-performing photocatalyst; Volatile organic compounds (VOCs); Large scale production; Real applications

Funding

  1. Basic Science Research Program through the National Research Foundation of Korea (NRF) - Ministry of Education [2017R1D1A1B03034381, 2018R1D1A1B07040916]
  2. Korea Basic Science Institute [D39613]
  3. Technology development Program - Ministry of SMEs and Startups (MSS, Korea) [S2722029]
  4. Korea Technology & Information Promotion Agency for SMEs (TIPA) [S2722029] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)
  5. National Research Council of Science & Technology (NST), Republic of Korea [D39613] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)
  6. National Research Foundation of Korea [2017R1D1A1B03034381] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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Various Fe loadings were applied onto P25 TiO2 using temperature-controlled vapour deposition and the resulting structures were subsequently annealed at 750 degrees C. As-received TiO2 was nearly photo-catalytically inactive for acetaldehyde decomposition under visible light, but when a very small amount of Fe below the threshold was loaded, the activity became maximized. Control of Fe loading is critical to prepare high-performing Fe-TiO2 photocatalysts since a larger amount of Fe forms larger iron oxide particles, which induces non-radiative recombination of the optically excited electron-hole pairs, thereby reducing the photocatalytic activity. Regarding the reaction mechanism, fast oxidation of acetaldehyde into CO2 and a slower path via acetic acid to CO2 were identified, where almost no evolution of secondary pollutant vapour was identified. A strategy towards large-scale production and stable fixation of photocatalyst powder on surfaces of construction materials for real air purification applications are discussed.

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