4.6 Article

Visible Photoelectrochemical Water Splitting Based on a Ru(II) Polypyridyl Chromophore and Iridium Oxide Nanoparticle Catalyst

Journal

JOURNAL OF PHYSICAL CHEMISTRY C
Volume 119, Issue 29, Pages 17023-17027

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.jpcc.5b05711

Keywords

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Funding

  1. UNC EFRC: Center for Solar Fuels
  2. Energy Frontier Research Center
  3. U.S. Department of Energy, Office of Science, Office of Basic Energy Sciences [DE-SC0001011]

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Preparation of Ru(II) polypyridyl-iridium oxide nanoparticle (IrOX NP) chromophore-catalyst assemblies on an FTO vertical bar nanoITO vertical bar TiO2 core/shell by a layer-by-layer procedure is described for application in dye-sensitized photoelectrosynthesis cells (DSPEC). Significantly enhanced, bias-dependent photocurrents with Lumencor 455 nm 14.5 mW/cm(2) irradiation are observed for core/shell structures compared to TiO2 after derivatization with [Ru(4,4'-PO(3)H(2)bpy)(2)(bpy)](2+) (RuP2) and uncapped IrOX NPs at pH 5.8 in NaSiF6 buffer with a Pt cathode. Photocurrents arising from photolysis of the resulting photoanodes, FTO vertical bar nanoITO vertical bar TiO2 vertical bar-RuP2,IrO2, are dependent on TiO2 shell thickness and applied bias, reaching 0.2 mA/cm(2) at 0.5 V vs AgCl/Ag with a shell thickness of 6.6 nm. Long-term photolysis in the NaSiF6 buffer results in a marked decrease in photocurrent over time due to surface hydrolysis and loss of the chromophore from the surface. Long-term stability, with sustained photocurrents, has been obtained by atomic layer deposition (ALD) of overlayers of TiO2 to stabilize surface binding of -RuP2 prior to the addition of the IrOX NPs.

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