In situ IR study of surface hydroxyl species of dehydrated TiO2: towards understanding pivotal surface processes of TiO2 photocatalytic oxidation of toluene

The surface species on P25-TiO 2 were characterized by FTIR after evacuation at 50-550 °C. The functions of OH groups on P25-TiO 2 catalysts have been tested by the adsorption and photooxidation of toluene in an in situ IR cell. FTIR studies show that the hydroxyl species on P25-TiO 2 are clearly te...

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Veröffentlicht in:Physical chemistry chemical physics : PCCP 2012-01, Vol.14 (26), p.9468-9474
Hauptverfasser: Lin, Huaxiang, Long, Jinlin, Gu, Quan, Zhang, Wenxin, Ruan, Rusheng, Li, Zhaohui, Wang, Xuxu
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container_end_page 9474
container_issue 26
container_start_page 9468
container_title Physical chemistry chemical physics : PCCP
container_volume 14
creator Lin, Huaxiang
Long, Jinlin
Gu, Quan
Zhang, Wenxin
Ruan, Rusheng
Li, Zhaohui
Wang, Xuxu
description The surface species on P25-TiO 2 were characterized by FTIR after evacuation at 50-550 °C. The functions of OH groups on P25-TiO 2 catalysts have been tested by the adsorption and photooxidation of toluene in an in situ IR cell. FTIR studies show that the hydroxyl species on P25-TiO 2 are clearly temperature-dependent and P25-TiO 2 has six isolated hydroxyls with bands at 3734, 3715, 3688, 3671, 3658 and 3640 cm −1 . The OH groups on P25 play different roles in the photo-oxidation process: surface hydroxyls with bands at 3688, 3671, 3658 and 3640 cm −1 act as adsorption sites while surface hydroxyls with bands at 3734 and 3715 cm −1 act as sources of the &z.rad;OH radical. The isolated hydroxyls on the P25-TiO 2 surface are selective to the adsorption of toluene. The 3688, 3671 and 3640 cm −1 bands were preferentially removed than the 3735 and 3715 cm −1 bands during the initial adsorption of toluene.
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The 3688, 3671 and 3640 cm −1 bands were preferentially removed than the 3735 and 3715 cm −1 bands during the initial adsorption of toluene.</description><identifier>ISSN: 1463-9076</identifier><identifier>EISSN: 1463-9084</identifier><identifier>DOI: 10.1039/c2cp40893g</identifier><identifier>PMID: 22652962</identifier><language>eng</language><publisher>Cambridge: Royal Society of Chemistry</publisher><subject>Catalysis ; Chemistry ; Exact sciences and technology ; General and physical chemistry ; Photochemistry ; Physical chemistry of induced reactions (with radiations, particles and ultrasonics) ; Surface physical chemistry ; Theory of reactions, general kinetics. Catalysis. 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The 3688, 3671 and 3640 cm −1 bands were preferentially removed than the 3735 and 3715 cm −1 bands during the initial adsorption of toluene.</description><subject>Catalysis</subject><subject>Chemistry</subject><subject>Exact sciences and technology</subject><subject>General and physical chemistry</subject><subject>Photochemistry</subject><subject>Physical chemistry of induced reactions (with radiations, particles and ultrasonics)</subject><subject>Surface physical chemistry</subject><subject>Theory of reactions, general kinetics. Catalysis. 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source Royal Society Of Chemistry Journals 2008-; Alma/SFX Local Collection
subjects Catalysis
Chemistry
Exact sciences and technology
General and physical chemistry
Photochemistry
Physical chemistry of induced reactions (with radiations, particles and ultrasonics)
Surface physical chemistry
Theory of reactions, general kinetics. Catalysis. Nomenclature, chemical documentation, computer chemistry
title In situ IR study of surface hydroxyl species of dehydrated TiO2: towards understanding pivotal surface processes of TiO2 photocatalytic oxidation of toluene
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