TY - JOUR
T1 - Enhanced photocatalytic NOx decomposition of visible-light responsive F-TiO2/(N,C)-TiO2 by charge transfer between F-TiO2 and (N,C)-TiO2 through their doping levels
AU - Komatsuda, Shio
AU - Asakura, Yusuke
AU - Vequizo, Junie Jhon M.
AU - Yamakata, Akira
AU - Yin, Shu
N1 - Funding Information:
This work was supported by the JSPS Grant-in-Aid for Scientific Research on Innovative Areas “Mixed anion” (No. 16H06439 , No. 17H05491 ) and for Young Scientists (B) (No. 17K14542 ), and by the Dynamic Alliance for Open Innovation Bridging Human, Environment and Materials in Network Joint Research Center for Materials and Devices.
Publisher Copyright:
© 2018 Elsevier B.V.
PY - 2018/12/15
Y1 - 2018/12/15
N2 - Composite type photocatalyst F-TiO2/(N,C)-TiO2 consisted of anatase-type TiO2 with fluorine-doping (F-TiO2) and TiO2 with nitrogen and carbon-doping ((N,C)-TiO2) was prepared by simple physical mixing to exhibit higher visible-light responsive photocatalytic nitrogen oxide (NOx) decomposition activity than those of F-TiO2 and (N,C)-TiO2. Transient absorption measurement clarified that the composite possessed longer carrier lifetime compared to that of each material (F-TiO2 or (N,C)-TiO2), resulting in higher photocatalytic activity. In the composite, photoexcited holes and electrons, which are not in impurity level but in valence and conduction band, respectively, should photocatalytically decompose NOx, judging from the redox potential of O2/O2・− and the band positions of F-TiO2 and (N,C)-TiO2. The mechanism for higher visible-light photocatalytic activity, or longer carrier lifetime can be explained by charge transfer between F-TiO2 and (N,C)-TiO2 through their impurity levels. The charge transfer should make photoexcited carries spatially separated to enhance the photocatalytic activity.
AB - Composite type photocatalyst F-TiO2/(N,C)-TiO2 consisted of anatase-type TiO2 with fluorine-doping (F-TiO2) and TiO2 with nitrogen and carbon-doping ((N,C)-TiO2) was prepared by simple physical mixing to exhibit higher visible-light responsive photocatalytic nitrogen oxide (NOx) decomposition activity than those of F-TiO2 and (N,C)-TiO2. Transient absorption measurement clarified that the composite possessed longer carrier lifetime compared to that of each material (F-TiO2 or (N,C)-TiO2), resulting in higher photocatalytic activity. In the composite, photoexcited holes and electrons, which are not in impurity level but in valence and conduction band, respectively, should photocatalytically decompose NOx, judging from the redox potential of O2/O2・− and the band positions of F-TiO2 and (N,C)-TiO2. The mechanism for higher visible-light photocatalytic activity, or longer carrier lifetime can be explained by charge transfer between F-TiO2 and (N,C)-TiO2 through their impurity levels. The charge transfer should make photoexcited carries spatially separated to enhance the photocatalytic activity.
KW - Charge transfer
KW - Composites
KW - Doping level
KW - Photocatalytic deNOx
KW - Transient absorption
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U2 - 10.1016/j.apcatb.2018.07.038
DO - 10.1016/j.apcatb.2018.07.038
M3 - Article
AN - SCOPUS:85050141969
SN - 0926-3373
VL - 238
SP - 358
EP - 364
JO - Applied Catalysis B: Environmental
JF - Applied Catalysis B: Environmental
ER -