4.8 Article

Stabilized Solar Hydrogen Production with CuO/CdS Heterojunction Thin Film Photocathodes

Journal

CHEMISTRY OF MATERIALS
Volume 29, Issue 4, Pages 1735-1743

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.chemmater.6b05248

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Funding

  1. University of Zurich
  2. University Research Priority Program (URPP) LightChEC
  3. Swiss National Science foundation (AP Energy) [PYAPP2 160586]
  4. Center for Microscopy and Image Analysis at the University of Zurich

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Cupric oxide (CuO) is a promising material for large-scale, economic solar energy conversion due to the abundance of copper, suitable band gap, and ease of fabrication. For application as a photocathode for water splitting, the main challenge is prevention of the inherent photocorrosion in aqueous media. Photoelectrochemical measurements of bare CuO thin films prepared by oxidation of electroplated Cu indicated that the vast majority of the photocurrent in 1 M phosphate buffer solution (pH 7) comes from photocorrosion of the CuO into metallic Cu, with a faradaic efficiency for hydrogen evolution of similar to 0.01%. We found that deposition of an n-type CdS buffer layer underneath a protective TiO2 layer yielded a stable and efficient photoelectrode, with the champion electrode giving 1.68 mA cm(-2) at 0 V-RHE and an onset potential of ca. 0.45 V-RHE. We attribute a favorable band alignment of CuO/CdS for the record photovoltage obtained with this material and a high conformality of the TiO2 layer on the sulfide surface for the high stability of hydrogen-producing photocurrents (faradaic efficiency similar to 100%).

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