Abstract

We report the use of amorphous silicon (a-Si) tandem junctions as part of an integral "hybrid" photoelectrochemical (PEC) cell to produce hydrogen directly from water using sunlight. The device configuration consists of stainless steel (SS)/ni<sub>2</sub>pni<sub>1</sub>p/ZnO/WO<sub>3</sub>. When the device is immersed in an electrolyte and illuminated, O<sub>2</sub> is evolved at the WO<sub>3</sub>/electrolyte interface and H<sub>2</sub> is produced at the counter electrode. A voltage >1.23V is required to split water; typically 1.6-1.8V are needed, taking account of losses in a practical water-splitting system. We use a-Si tandem cells, deposited by plasma-enhanced chemical vapor deposition, to supply this voltage. Current matching in the two a-Si subcells is achieved by altering the thicknesses of the two layers (i<sub>1</sub> and i<sub>2</sub>) while keeping their band gaps at ~1.75eV, which results in a device with an open circuit voltage >1.6V, short circuit current density (J<sub>sc</sub>) >6mA/cm<sup>2</sup> (on SS substrates), and a fill factor >0.6. Deposition on a textured SnO<sub>2</sub> coated glass has resulted in J<sub>sc</sub> >9mA/cm<sup>2</sup>. Photoactive WO<sub>3</sub> films, deposited using the RF sputtering technique, have achieved photocurrents >3mA/cm<sup>2</sup> at 1.6V vs. saturated calomel electrode (SCE). The PEC device operates at the point at which the WO<sub>3</sub> photocurrent IV curve and the a-Si (filtered by WO<sub>3</sub>) light IV curve cross, leading to operating currents of 2.5mA/cm<sup>2</sup> and solar-to-hydrogen (STH) conversion efficiency of >3%.

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