TY - JOUR
T1 - Visible light-responsive Fe-loaded TiO2 photocatalysts for total oxidation of acetaldehyde
T2 - Fundamental studies towards large-scale production and applications
AU - Saqlain, Shahid
AU - Cha, Byeong Jun
AU - Kim, Soong Yeon
AU - Ahn, Tae Kyu
AU - Park, Cheolwoo
AU - Oh, Ju Myung
AU - Jeong, Eun Cheol
AU - Seo, Hyun Ook
AU - Kim, Young Dok
N1 - Publisher Copyright:
© 2019 Elsevier B.V.
PY - 2020/3/1
Y1 - 2020/3/1
N2 - Various Fe loadings were applied onto P25 TiO2 using temperature-controlled vapour deposition and the resulting structures were subsequently annealed at 750 °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.
AB - Various Fe loadings were applied onto P25 TiO2 using temperature-controlled vapour deposition and the resulting structures were subsequently annealed at 750 °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.
KW - High-performing photocatalyst
KW - Large scale production
KW - Real applications
KW - Visible light responsive catalyst
KW - Volatile organic compounds (VOCs)
UR - https://www.scopus.com/pages/publications/85078671631
U2 - 10.1016/j.apsusc.2019.144160
DO - 10.1016/j.apsusc.2019.144160
M3 - Article
AN - SCOPUS:85078671631
SN - 0169-4332
VL - 505
JO - Applied Surface Science
JF - Applied Surface Science
M1 - 144160
ER -