Raja, P.Bensimon, M.Klehm, U.Albers, P.Laub, D.Kiwi-Minsker, L.Renken, A.Kiwi, J.2007-10-242007-10-242007-10-24200710.1016/j.jphotochem.2006.10.033https://infoscience.epfl.ch/handle/20.500.14299/13294WOS:00024588290002710483Small nanosized clusters of Co3O4 coated on PTFE (polytetrafluoroethylene) flexible film is reported as a novel supported photocatalyst effective in the fast discoloration of the azo-dye Orange II under simulated solar radiation in the presence of oxone (2KHSO5·KHSO4·K2SO4). The photocatalytic discoloration of Orange II on the PTFE/Co3O4 films proceeds within minutes and the process could be repeated many times without a loss in photocatalyst stability. The photodiscoloration proceeds with a photonic efficiency of ∼1. The PTFE seems to act as a structure forming matrix for the colloidal Co3O4 coated on it surface leading to nanosized clusters of Co3O4. Monitoring the amount of Co2+-ions shows the Co2+-ions from the PTFE/Co3O4 during the photocatalysis enter the solution and at a later are stage re-adsorbed the Co3O4 crystallographic network (∼8 min). By elemental analysis (EA) the loading of Co-loading per cm2 PTFE film was found to vary between 1% and 2%. Transmission electron microscopy (TEM) shows the size of the Co3O4 clusters to vary between 3 and 10 nm. Electron dispersive spectrometry (EDS) confirms the presence of Co on the PTFE. X-ray photoelectron spectroscopy (XPS) of the PTFE/Co3O4 films reveal a partial reduction of the Co3O4 after Orange II discoloration leading to a substantial increase of the amount of Co(II) species in the Co3O4. Physical insight is provided into the catalyst film surface by carrying out Ar-sputtering of the PTFE/Co3O4 surface to remove the catalyst overlayers up to ∼20 nm.PhotocatalystPTFE–Co-oxideXPSAzo-dyetext::journal::journal article::research article