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dc.contributor.authorZollo, Alessia
dc.contributor.authorLiao, Yu-Kai
dc.contributor.authorHejazi, S. M. Hossein
dc.contributor.authorShahrezaei, Mahdi
dc.contributor.authorDaka, Mario
dc.contributor.authorSalvadori, Enrico
dc.contributor.authorLivraghi, Stefano
dc.contributor.authorNaldoni, Alberto
dc.contributor.authorChiesa, Mario
dc.date.accessioned2025-01-06T13:02:26Z
dc.date.available2025-01-06T13:02:26Z
dc.date.issued2024
dc.identifier.citationJournal of Physical Chemistry C. 2024, vol. 128, issue 16, p. 6971-6978.cs
dc.identifier.issn1932-7447
dc.identifier.issn1932-7455
dc.identifier.urihttp://hdl.handle.net/10084/155442
dc.description.abstractThe photochemical properties of brookite nanorods are systematically explored using light-induced electron-paramagnetic resonance (EPR) techniques at different wavelengths spanning the UV-vis region of the electromagnetic spectrum (355-650 nm). Under UV irradiation, electron-hole pairs are generated, leading to the stabilization of paramagnetic centers, primarily Ti3+ and O- species at the surface. Visible light irradiation at low temperature results in a unique pair of EPR signals, including electrons trapped at titanium cations and a distinct signal resonating at g = 2.004. The pair of signals disappears after annealing at room temperature, indicating that recombination pathways with trapped electrons are available. The chemical reactivity of the different photogenerated species is tested using electron and holes scavengers. While peculiar light-harvesting capabilities are observed for the brookite nanorods, experiments carried out in the presence of a hole scavenger indicate a limited potential for oxidative processes under visible light.cs
dc.language.isoencs
dc.publisherAmerican Chemical Societycs
dc.relation.ispartofseriesJournal of Physical Chemistry Ccs
dc.relation.urihttps://doi.org/10.1021/acs.jpcc.4c01066cs
dc.rights© 2024 American Chemical Societycs
dc.titleDefect-mediated energy states in brookite nanorods: Implications for photochemical applications under ultraviolet and visible lkightcs
dc.typearticlecs
dc.identifier.doi10.1021/acs.jpcc.4c01066
dc.type.statusPeer-reviewedcs
dc.description.sourceWeb of Sciencecs
dc.description.volume128cs
dc.description.issue16cs
dc.description.lastpage6978cs
dc.description.firstpage6971cs
dc.identifier.wos001203933300001


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