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<metadata xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:dc="http://purl.org/dc/elements/1.1/"><dc:title>Variations of electronic properties on the behavior of visible light-triggered TiO[sub]2 +Au photocatalysts</dc:title><dc:creator>Slapničar,	Špela	(Avtor)
	</dc:creator><dc:creator>Žerjav,	Gregor	(Avtor)
	</dc:creator><dc:creator>Roškarič,	Matevž	(Avtor)
	</dc:creator><dc:creator>Zavašnik,	Janez	(Avtor)
	</dc:creator><dc:creator>Pintar,	Albin	(Avtor)
	</dc:creator><dc:description>Au catalysts (1 wt% Au) using anatase TiO2 nanorods (TNR, SBET =106 m2/g) or nanospheres (TNP, SBET =86 m2/g). The majority of Au particles in the prepared TiO2 +Au catalysts were in the range of 20–30 nm, with slight differences observed between the TNR +Au and TNP +Au samples. It is noteworthy that the addition of Au did not significantly change the specific surface area and crystallinity of the TiO2 supports. Evaluation of photocatalytic activity using ABTS•+ cation oxidation, DMPO/DMSO spin trapping and bisphenol A (BPA) degradation under visible-light illumination showed different behaviour of TNR +Au and TNP +Au catalysts. The TNR +Au catalyst produced mainly e-, while the TNP +Au catalyst exhibited efficient O2 •- production, which was confirmed by electron paramagnetic resonance spin trapping analyses. Conversely, due to its high Schottky barrier height (SBH) and the properties of the Au nanoparticles, the TNR +Au catalyst could not facilitate an oxygen reduction reaction but effectively produced e- as it reduced ABTS•+. The results show that the degra dation of BPA in the presence of the TNR +Au photocatalyst occurs through the involvement of e- and a small amount of hydroxyl radicals (OH•). Comprehensive characterization techniques provided insights into the intricate relationships between catalyst structure, composition and catalytic activity.</dc:description><dc:date>2025</dc:date><dc:date>2025-04-03 12:43:59</dc:date><dc:type>Neznano</dc:type><dc:identifier>21817</dc:identifier><dc:identifier>UDK: 546</dc:identifier><dc:identifier>ISSN pri članku: 0169-4332</dc:identifier><dc:identifier>DOI: 10.1016/j.apsusc.2025.162923</dc:identifier><dc:identifier>COBISS_ID: 228881667</dc:identifier><dc:source>Applied Surface Science</dc:source><dc:language>sl</dc:language><dc:rights>© 2025 The Author(s). Published by Elsevier B.V.</dc:rights></metadata>
