4.8 Article

Multifunctional Coatings from Scalable Single Source Precursor Chemistry in Tandem Photoelectrochemical Water Splitting

Journal

ADVANCED ENERGY MATERIALS
Volume 5, Issue 24, Pages -

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/aenm.201501668

Keywords

nanocomposite materials; photocatalysis; photoelectrochemistry; solar energy; water splitting

Funding

  1. Christian Doppler Research Association (Austrian Federal Ministry of Science, Research and Economy)
  2. Christian Doppler Research Association (National Foundation for Research, Technology and Development)
  3. EPSRC [EP/H00338X/2]
  4. Winston Churchill Foundation of United States
  5. EPSRC [EP/H00338X/2] Funding Source: UKRI
  6. Engineering and Physical Sciences Research Council [EP/H00338X/2] Funding Source: researchfish

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The straightforward and inexpensive fabrication of stabilized and activated photoelectrodes for application to tandem photoelectrochemical (PEC) water splitting is reported. Semiconductors such as Si, WO3, and BiVO4 can be coated with a composite layer formed upon hydrolytic decomposition of heterobimetallic single source precursors (SSPs) based on Ti and Ni, or Ti and Co in a simple single-step process under ambient conditions. The resulting 3d-transition metal oxide composite films are multifunctional, as they protect the semiconductor electrode from corrosion with an amorphous TiO2 coating and act as bifunctional electrocatalysts for H-2 and O-2 evolution based on catalytic Ni or Co species. Thus, this approach enables the use of the same precursors for both photoelectrodes in tandem PEC water splitting, and SSP chemistry is thereby established as a highly versatile low-cost approach to protect and activate photoelectrodes. In an optimized system, SSP coating of a Si photocathode and a BiVO4 photoanode resulted in a benchmark noble metal-free dual-photoelectrode tandem PEC cell for overall solar water splitting with an applied bias solar-to-hydrogen conversion efficiency of 0.59% and a half-life photostability of 5 h.

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