Publication date: 15th December 2014
Two photoelectrode systems were individually optimized for the process of solar-driven overall water splitting in acidic electrolytes: 1) phase-pure Pt-doped anatase TiO2, prepared by Ion Layer Gas Reaction (ILGAR), was employed as an electrocatalytic protection layer on device-grade p-type Cu(In,Ga)Se2. It will be shown that the gradual increase of the Pt-concentration within the TiO2-layer passes through an efficiency- and stability-maximum of the electrode. At this maximum, Incident Photon-to-Current Efficiencies (IPCE) of 80% could be achieved over the full range of the solar spectrum (AM1.5). Photocurrent densities reached more than 12.5 mAcm-2 at the thermodynamic potential for H2-evolution in 0.5 M H2SO4[1]. Further improvements of the heterojunction, realized by atomic layer deposition (ALD), will be discussed. 2) Nanoparticulate RuO2 was deposited on n-type Si by electrophoretic deposition. During deposition, an ultra-thin SiO2 film was simultaneously formed that acts as protection layer. Oxygen evolution photocurrent densities of up to 18 mAcm-2 could be achieved at 1.23 V vs RHE in 0.5M H2SO4. Both photoelectrodes maintained photocurrent densities of 12 mAcm-2 for more than 25 hours, demonstrating the promising stability offered by these novel Pt-TiO2 and SiO2/RuO2 protection layers. The film and interface properties were investigated with photoelectron spectroscopy, electron microscopy and surface photovoltage measurements, offering new insights in the structure of electronic defects in the Pt-doped TiO2 layer and at the Si/RuO2 interface. Finally, device development in combination with a two-junction tandem solar cell will be discussed.
[1] A. Azarpira et al. Advanced Energy Materials (submitted 11/2014)