4.6 Article

Potential-Sensing Electrochemical AFM Shows CoPi as a Hole Collector and Oxygen Evolution Catalyst on BiVO4 Water-Splitting Photoanodes

Journal

ACS ENERGY LETTERS
Volume 3, Issue 9, Pages 2286-2291

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsenergylett.8b01150

Keywords

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Funding

  1. Department of Energy, Basic Energy Sciences [DE-SC0014279]
  2. Sloan foundation
  3. Dreyfus foundation
  4. NSF [1309047]
  5. M. J. Murdock Charitable Trust
  6. W. M. Keck Foundation
  7. ONAMI
  8. NSF
  9. Laboratory Directed Research and Development Program of Lawrence Berkeley National Laboratory under U.S. Department of Energy [DE-AC02-05CH11231]
  10. U.S. Department of Energy (DOE) [DE-SC0014279] Funding Source: U.S. Department of Energy (DOE)

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Oxide/(oxy)hydroxide overlayers such as cobalt (oxy)hydroxide phosphate (CoPi) enhance the performance of BiVO4 water-spitting photoanodes, but the mechanism of this enhancement remains unclear. We show that if the BiVO4 layer is thin and incompletely covers an underlying conductive glass, the performance dramatically decreases as CoPi loading is increased. This is consistent with direct contact between the CoPi and conducting glass that leads to shunt recombination of photogenerated holes accumulated in the CoPi. For thicker BiVO4 layers that completely cover the conducting glass, these shunt pathways are blocked. We then use a nanoelectrode atomic force microscopy probe to measure, in operando, the electrochemical potential of CoPi on thick BiVO4 films under illumination. We find that CoPi is charged to a potential necessary to drive water oxidation at a rate consistent with the measured photocurrent. CoPi acts as a hole collector and is the principal driver of water oxidation on BiVO4.

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