000819968 001__ 819968 000819968 005__ 20250129094232.0 000819968 0247_ $$2doi$$a10.1016/j.jallcom.2016.08.211 000819968 0247_ $$2ISSN$$a0925-8388 000819968 0247_ $$2ISSN$$a1873-4669 000819968 0247_ $$2WOS$$aWOS:000386227900091 000819968 037__ $$aFZJ-2016-05535 000819968 082__ $$a670 000819968 1001_ $$0P:(DE-HGF)0$$aMalengreaux, Charline M.$$b0 000819968 245__ $$aStudy of the photocatalytic activity of Fe$^{3+}$, Cr$^{3+}$, La$^{3+}$ and Eu$^{3+}$ single-doped and co-doped TiO$_{2}$ catalysts produced by aqueous sol-gel processing 000819968 260__ $$aLausanne$$bElsevier$$c2017 000819968 3367_ $$2DRIVER$$aarticle 000819968 3367_ $$2DataCite$$aOutput Types/Journal article 000819968 3367_ $$0PUB:(DE-HGF)16$$2PUB:(DE-HGF)$$aJournal Article$$bjournal$$mjournal$$s1478083791_9979 000819968 3367_ $$2BibTeX$$aARTICLE 000819968 3367_ $$2ORCID$$aJOURNAL_ARTICLE 000819968 3367_ $$00$$2EndNote$$aJournal Article 000819968 520__ $$aAn aqueous sol-gel process, previously developed for producing undoped and Cu2+, Ni2+, Zn2+ or Pb2+ doped TiO2 photocatalysts with remarkably high photocatalytic activity without requiring any calcination step, has been adapted to produce Fe3+, Cr3+, La3+ or Eu3+ single-doped TiO2 photocatalysts as well as La3+-Fe3+ and Eu3+-Fe3+ co-doped TiO2 catalysts. The physicochemical properties of the obtained catalysts have been characterized using a suite of complementary techniques, including ICP-AES, XRD, UV–Vis spectroscopy, nitrogen adsorption-desorption and Fe-57 Mössbauer. The active crystalline phase is obtained without requiring any calcination step and all the different catalysts are composed of nanocrystallites of anatase with a size of 6–7 nm and a high specific surface area varying from 181 to 298 m2 g−1. In this study, the effect of the NO3:Ti(IV) mole ratio used to induce the peptisation reaction during the synthesis has been studied and the results revealed that this ratio can influence significantly the textural properties of the resulting catalyst.A screening of the photocatalytic activity of the undoped and Fe3+, Cr3+, La3+ or Eu3+ single-doped and co-doped photocatalysts has been performed by evaluating the degradation of 4-nitrophenol under UV–Visible light (330 nm < λ < 800 nm). This study suggests that the photocatalytic activity is significantly influenced by the dopant nature and content with an optimal dopant content being observed in the case of Fe3+ or La3+ single-doped as well as in the case of La3+-Fe3+ and Eu3+-Fe3+ co-doped catalysts. In the case of Cr3+ single-doped catalysts, a detrimental effect of the dopant on the photocatalytic degradation of 4-nitrophenol has been observed while no significant influence of the dopant has been detected in the case of Eu3+ single-doped catalysts. The role of the different dopants in modulating the photocatalytic activity is discussed. 000819968 536__ $$0G:(DE-HGF)POF3-144$$a144 - Controlling Collective States (POF3-144)$$cPOF3-144$$fPOF III$$x0 000819968 536__ $$0G:(DE-HGF)POF3-524$$a524 - Controlling Collective States (POF3-524)$$cPOF3-524$$fPOF III$$x1 000819968 536__ $$0G:(DE-HGF)POF3-6212$$a6212 - Quantum Condensed Matter: Magnetism, Superconductivity (POF3-621)$$cPOF3-621$$fPOF III$$x2 000819968 536__ $$0G:(DE-HGF)POF3-6213$$a6213 - Materials and Processes for Energy and Transport Technologies (POF3-621)$$cPOF3-621$$fPOF III$$x3 000819968 536__ $$0G:(DE-HGF)POF3-6G4$$a6G4 - Jülich Centre for Neutron Research (JCNS) (POF3-623)$$cPOF3-623$$fPOF III$$x4 000819968 588__ $$aDataset connected to CrossRef 000819968 7001_ $$0P:(DE-HGF)0$$aPirard, Sophie L.$$b1$$eCorresponding author 000819968 7001_ $$0P:(DE-HGF)0$$aLéonard, Géraldine$$b2 000819968 7001_ $$0P:(DE-HGF)0$$aMahy, Julien G.$$b3 000819968 7001_ $$0P:(DE-Juel1)145213$$aHerlitschke, Marcus$$b4 000819968 7001_ $$0P:(DE-Juel1)144500$$aKlobes, Benedikt$$b5 000819968 7001_ $$0P:(DE-Juel1)130706$$aHermann, Raphaël$$b6 000819968 7001_ $$0P:(DE-HGF)0$$aHeinrichs, Benoît$$b7 000819968 7001_ $$0P:(DE-HGF)0$$aBartlett, John R.$$b8 000819968 773__ $$0PERI:(DE-600)2012675-X$$a10.1016/j.jallcom.2016.08.211$$gVol. 691, p. 726 - 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