Abstract

Metal-halide perovskites have been widely investigated in the photovoltaic sector due to their promising optoelectronic properties and inexpensive fabrication techniques based on solution processing. Here we report the development of inorganic CsPbBr3-based photoanodes for direct photoelectrochemical oxygen evolution from aqueous electrolytes. We use a commercial thermal graphite sheet and a mesoporous carbon scaffold to encapsulate CsPbBr3 as an inexpensive and efficient protection strategy. We achieve a record stability of 30 h in aqueous electrolyte under constant simulated solar illumination, with currents above 2 mA cm−2 at 1.23 VRHE. We further demonstrate the versatility of our approach by grafting a molecular Ir-based water oxidation catalyst on the electrolyte-facing surface of the sealing graphite sheet, which cathodically shifts the onset potential of the composite photoanode due to accelerated charge transfer. These results suggest an efficient route to develop stable halide perovskite based electrodes for photoelectrochemical solar fuel generation.

Highlights

  • Metal-halide perovskites have been widely investigated in the photovoltaic sector due to their promising optoelectronic properties and inexpensive fabrication techniques based on solution processing

  • We further show the versatility of our photoanode architecture by functionalising the graphite sheet (GS) surface with an Ir-based water oxidation catalyst (WOC)

  • While pristine CsPbBr3 has a bandgap of 2.35 eV with an absorption onset corresponding to 530 nm giving rise to its yellow colour, after immersion in water only a semitransparent white material remains (PbBr2)

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Summary

Introduction

Metal-halide perovskites have been widely investigated in the photovoltaic sector due to their promising optoelectronic properties and inexpensive fabrication techniques based on solution processing. The TiO2|CsPbBr3|m-c|GS electrodes operate in water across a very wide pH range (2–13), exhibiting photocurrents of up to 3.8 mA cm−2 at an applied bias of 1.23 VRHE in acidic solution.

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