Multi-doped Brookite-Prevalent TiO2 Photocatalyst with Enhanced Activity in the Visible Light

Publication date

2018-08-01

Authors

Cataldo, SebastianoISNI 0000000518010255
Weckhuysen, B.M.ORCID 0000-0001-5245-1426ISNI 0000000110540180
Pettignano, Alberto
Pignataro, Bruno

Editors

Advisors

Supervisors

Document Type

Article
Open Access logo

License

taverne

Abstract

© 2018 Springer Science+Business Media, LLC, part of Springer Nature Abstract: Enabling solar and/or visible light-driven photocatalysis is a crucial step to access innovative applications in environmental science and sustainable energy. Titanium dioxide is the most used photocatalyst because of its low cost and toxicity, however it is also limitedly active under visible light irradiation due to its wide band gap. Among its polymorphs, brookite holds promising optoelectronic properties for visible light photocatalysis, which have to the best of our knowledge been limitedly exploited. Here, a C,S,N-doped brookite-based TiO2has been prepared via a rapid one-pot sol–gel synthesis. Besides substantially extending the visible light absorption via band gap narrowing, its photocatalytic activity has been enhanced further by optimising valence and conductive band position and by minimising electron–hole recombination. These materials showed a 100% boost in visible light absorption along with nearly 50-times enhanced photocatalytic activity per specific surface area than standard TiO2Degussa-P25, giving the best performance among the brookite-based photo-catalytically active materials and resulting among the TiO2top-performers under visible light. Graphical Abstract: [Figure not available: see fulltext.]

Keywords

Brookite, Doping, Heterogeneous catalysis, Titanium dioxide, Visible-light photocatalysis, Taverne

Citation

Cataldo, S, Weckhuysen, B M, Pettignano, A & Pignataro, B 2018, 'Multi-doped Brookite-Prevalent TiO2 Photocatalyst with Enhanced Activity in the Visible Light', Catalysis Letters, vol. 148, pp. 2459-2471. https://doi.org/10.1007/s10562-018-2463-8