Sn-Doped Hematite for Photoelectrochemical Water Splitting: The Effect of Sn Concentration

Author:

Zhang Siyuan1,Hajiyani Hamidreza2,Hufnagel Alexander G.3,Kampmann Jonathan3,Breitbach Benjamin1,Bein Thomas3,Fattakhova-Rohlfing Dina45,Pentcheva Rossitza2,Scheu Christina1

Affiliation:

1. Max-Planck-Institut für Eisenforschung GmbH, Max-Planck-Straße 1 , 40237 Düsseldorf , Germany

2. Department of Physics and Center for Nanointegration Duisburg-Essen (CENIDE) , Universität Duisburg-Essen , Lotharstraße 1 , 47057 Duisburg , Germany

3. Department of Chemistry and Center for NanoScience (CeNS) , University of Munich (LMU) , Butenandtstraße 5-13 (E) , 81377 Munich , Germany

4. Institute of Energy and Climate Research (IEK-1), Forschungszentrum Jülich GmbH , Wilhelm-Johnen-Straße , 52425 Jülich , Germany

5. Faculty of Engineering and Center for Nanointegration Duisburg-Essen (CENIDE), Universität Duisburg-Essen , Lotharstraße 1 , 47057 Duisburg , Germany

Abstract

Abstract Hematite-based photoanodes have been intensively studied for photoelectrochemical water oxidation. The n-type dopant Sn has been shown to benefit the activity of hematite anodes. We demonstrate in this study that Sn-doped hematite thin films grown by atomic layer deposition can achieve uniform doping across the film thickness up to at least 32 mol%, far exceeding the equilibrium solubility limit of less than 1 mol%. On the other hand, with the introduction of Sn doping, the hematite crystallite size decreases and many twin boundaries form in the film, which may contribute to the low photocurrent observed in these films. Density functional theory calculations with a Hubbard U term show that Sn doping has multiple effects on the hematite properties. With increasing Sn4+ content, the Fe2+ concentration increases, leading to a reduction of the band gap and finally to a metallic state. This goes hand in hand with an increase of the lattice constant.

Publisher

Walter de Gruyter GmbH

Subject

Physical and Theoretical Chemistry

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