4.8 Article

A monolithically integrated, intrinsically safe, 10% efficient, solar-driven water-splitting system based on active, stable earth-abundant electrocatalysts in conjunction with tandem III-V light absorbers protected by amorphous TiO2 films

Journal

ENERGY & ENVIRONMENTAL SCIENCE
Volume 8, Issue 11, Pages 3166-3172

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c5ee01786f

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Funding

  1. Office of Science of the U.S. Department of Energy [DE-SC0004993]
  2. Gordon and Betty Moore Foundation [GBMF1225]

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A monolithically integrated device consisting of a tandem-junction GaAs/InGaP photoanode coated by an amorphous TiO2 stabilization layer, in conjunction with Ni-based, earth-abundant active electrocatalysts for the hydrogen-evolution and oxygen-evolution reactions, was used to effect unassisted, solar-driven water splitting in 1.0 M KOH(aq). When connected to a Ni-Mo-coated counter-electrode in a two-electrode cell configuration, the TiO2-protected III-V tandem device exhibited a solar-to-hydrogen conversion efficiency, eta STH, of 10.5% under 1 sun illumination, with stable performance for >40 h of continuous operation at an efficiency of gSTH > 10%. The protected tandem device also formed the basis for a monolithically integrated, intrinsically safe solar-hydrogen prototype system (1 cm(2)) driven by a NiMo/GaAs/InGaP/TiO2/Ni structure. The intrinsically safe system exhibited a hydrogen production rate of 0.81 mu L s(-1) and a solar-to-hydrogen conversion efficiency of 8.6% under 1 sun illumination in 1.0 M KOH(aq), with minimal product gas crossover while allowing for beneficial collection of separate streams of H-2(g) and O-2(g).

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