journal article·2018-08-22Open access

Copper-Modified TiO2 and ZrTiO4: Cu Oxidation State Evolution during Photocatalytic Hydrogen Production

Valeria Polliotto, Stefano Livraghi, Anna Krukowska, Maria Vittoria Dozzi, Adriana Zaleska-Medynska, Elena Selli, Elio Giamello

ACS Applied Materials & Interfaces· Volume 10· Issue 33

Abstract

In the present work, two H2 evolution photocatalysts were prepared by employing two different oxides, TiO2 and zirconium titanate (ZrTiO4), as the support of various copper phases. For both the supports the same Cu loading (0.5% w/w) was adopted, but two different impregnation procedures have been followed, leading to different forms of Cu in the final composite material that are: (i) Cu(II) species dispersed on the oxide surface and (ii) Cu2O particles dispersed on the oxide surface. The present paper based on the parallel use of photocatalytic test and spectroscopic analysis performed in catalytic conditions illustrates the evolution of photocatalytic systems occurring during the H2 evolution reaction tests, pointing out that the as-prepared materials represent a pre-catalyst and they are modified during irradiation leading to the real working systems different from the starting ones. The herein presented spectroscopic analysis aims to contribute to the living debate on the oxidation state of copper in mixed Cu/oxide materials and on its role in hydrogen evolution under photocatalytic conditions.
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Research context

OpenAlex topics: Advanced Photocatalysis Techniques · Copper-based nanomaterials and applications · TiO2 Photocatalysis and Solar Cells

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Dipartimento di Chimica and NIS, Università di Torino, Via P. Giuria 7, 10125 Torino, Italy

Department of Environmental Technology, Faculty of Chemistry, University of Gdansk, 80-308 Gdansk, Poland

Dipartimento di Chimica, Università degli Studi di Milano, Via Golgi 19, 20133 Milano, Italy

Funding

Ministero dell?Istruzione, dell?Universit? e della Ricerca

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