Exploring the properties of Ag5–TiO2 interfaces: stable surface polaron formation, UV-Vis optical response, and CO2 photoactivation

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Using a combination of first-principles modelling, X-ray absorption spectroscopy, and diffuse reflectance spectroscopy measurements, we explore the properties of Ag5-modified TiO2 surfaces. A general electron polarization phenomenon associated with surface polarons on TiO2 has been revealed theoretically and confirmed experimentally. First, the Ag5 cluster donates an electron to TiO2, leading to the formation of polaronic Ti3+ 3d1 states on the rutile TiO2(110) surface. The analysis of polarization effects in the nearby electronic structure accompanying the polaron formation is confirmed with X-ray absorption spectroscopy measurements at the Ti K-edge of TiO2 nanoparticles. Next, the UV-Vis optical absorption spectrum of the polaronic state is also computationally modelled and an enlargement of the polaron wavefunction is predicted. Moreover, we find an overall improvement of the UV-Vis optical response of the material through diffuse reflectance spectroscopy measurements. Finally, we predict that charge-transfer processes at the Ag5–TiO2 interface triggered by solar photons might allow for a photoinduced activation of CO2 by sunlight

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J. Mater. Chem. A, 2020,8, 6842-6853

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This work has been partly supported by the Spanish Agencia Estatal de Investigación (AEI) and the Fondo Europeo de Desarrollo Regional (FEDER, UE) under Grant No. MAT2016-75354-P, FIS2017-83473-C2-1-P, by La Caixa Foundation (LCF/PR/PR12/11070003), Ramon Areces Foundation (Project CIVP18A3940), and European Commission through FEDER and H2020 program (0681InveNNta1E; Bac-To-Fuel 825999); MINECO, Spain (MAT2015-67458-P – cofinanced with FEDER Funds – and CTQ2013-44762-R), Xunta de Galicia, Spain (GRC ED-431C2017/22; AEMAT ED431E2018/08), and by ANPCyT (2017-1220 and 2017-3944) and UNLP (Project 11/X790), Argentina. The CESGA super-computer center (Spain) is acknowledged for having provided the computational resources used in this work. Partial support by Laboratório Nacional de Luz Síncrotron (LNLS, Campinas, Brazil) under proposals 20170352 and 20180490 is also acknowledged. D. B. expresses gratitude for a postdoctoral grant from Xunta de Galicia, Spain (ED481D 2017/021). P. L. C. expresses her gratitude for a contract for graduate students from the “Garantía Juvenil” program from the Comunidad de Madrid

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© The Royal Society of Chemistry 2020. Open Access Article. This article is licensed under a Creative Commons Attribution 3.0 Unported Licence

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