Highly Active Oxide Photocathode for Photoelectrochemical Water Reduction

Tuesday, October 18, 2011: 10:30 AM
208 A (Minneapolis Convention Center)
Elijah Thimsen1, Adriana Paracchino2, Vincent Laporte3, Kevin Sivula2 and Michael Graetzel2, (1)Energy, Environmental and Chemical Engineering, Washington University in St. Louis, St. Louis, MO, (2)Institute of Chemical Sciences and Engineering, Ecole Polytechnique Fédérale de Lausanne, Lausanne (VD), Switzerland, (3)Interdisciplinary Centre for Electron Microscopy, Ecole Polytechnique Fédérale de Lausanne, Lasuanne (VD), Switzerland

A clean and efficient way to overcome the limited supply of fossil fuels and the greenhouse effect is the production of hydrogen fuel from sunlight and water through the semiconductor/water junction of a photoelectrochemical (PEC) cell, where energy collection and water electrolysis are combined into a single semiconductor electrode. We present a highly active photocathode for solar H2 production, consisting of electrodeposited cuprous oxide, which was protected against photocathodic decomposition in water by nanolayers of Al-doped zinc oxide and titanium oxide deposited by atomic layer deposition (ALD) and activated for hydrogen evolution with electrodeposited Pt nanoparticles. The roles of the different surface protection components were investigated, and in the best case electrodes showed photocurrents up to –7.6 mA cm–2 at a potential of 0 V vs. RHE  (Reversible Hydrogen Electrode) at mild pH. The electrodes remained active after 1h of testing, cuprous oxide was found to be stable during the water reduction reaction and the Faradaic efficiency was estimated to be close to 100%.

Extended Abstract: File Not Uploaded