4.6 Article

Boosting the performance of Cu2O photocathodes for unassisted solar water splitting devices

Journal

NATURE CATALYSIS
Volume 1, Issue 6, Pages 412-420

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/s41929-018-0077-6

Keywords

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Funding

  1. National Research Programme 'Energy Turnaround' (NRP 70) of the Swiss National Science Foundation
  2. PECHouse3 - Swiss Federal Office of Energy [SI/500090-03]
  3. PECDEMO
  4. Europe's Fuel Cell and Hydrogen Joint Undertaking [621252]
  5. Marie Sklodowska-Curie Fellowship from the European Union's Seventh Framework Programme for research, technological development and demonstration [291771]
  6. Thousand Talents Plan for young professionals
  7. European Union's Horizon 2020 programme, through an FET-Open research and innovation action [687008]

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Although large research efforts have been devoted to photoelectrochemical (PEC) water splitting in the past several decades, the lack of efficient, stable and Earth-abundant photoelectrodes remains a bottleneck for practical application. Here, we report a photocathode with a coaxial nanowire structure implementing a Cu2O/Ga2O3-buried p-n junction that achieves efficient light harvesting across the whole visible region to over 600 nm, reaching an external quantum yield for hydrogen generation close to 80%. With a photocurrent onset over +1V against the reversible hydrogen electrode and a photocurrent density of -10 mA cm(-2) at 0 V versus the reversible hydrogen electrode, our electrode constitutes the best oxide photocathode for catalytic generation of hydrogen from sunlight known today. Conformal coating via atomic-layer deposition of a TiO2 protection layer enables stable operation exceeding 100 h. Using NiMo as the hydrogen evolution catalyst, an all Earth-abundant Cu2O photocathode was achieved with stable operation in a weak alkaline electrolyte. To show the practical impact of this photocathode, we constructed an all-oxide unassisted solar water splitting tandem device using state-of-the-art BiVO4 as the photoanode, achieving -3% solar-to-hydrogen conversion efficiency.

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