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Updated: May 31, 2026

Preparation and Use of Photocatalytically Active Segmented Ag|ZnO and Coaxial TiO2-Ag Nanowires Made by Templated Electrodeposition
Published on: May 2, 2014
Enhancing the activity of oxygen-evolution and chlorine-evolution electrocatalysts by atomic layer deposition of TiO2
Cody E Finke1,2,3, Stefan T Omelchenko3, Justin T Jasper1,2,3
1The Linde Center for Global Environmental Science, Caltech, Caltech, Pasadena, CA 91125, USA.
Abstract:
We report that TiO2 coatings formed via atomic layer deposition (ALD) may tune the activity of IrO2, RuO2, and FTO for the oxygen-evolution and chlorine-evolution reactions (OER and CER). Electrocatalysts exposed to ~3-30 ALD cycles of TiO2 exhibited overpotentials at 10 mA cm-2 of geometric current density that were several hundred millivolts lower than uncoated catalysts, with correspondingly higher specific activities. For example, the deposition of TiO2 onto IrO2 yielded a 9-fold increase in the OER-specific activity in 1.0 M H2SO4 (0.1 to 0.9 mA cmECSA -2 at 350 mV overpotential). The oxidation state of titanium and the potential of zero charge were also a function of the number of ALD cycles, indicating a correlation between oxidation state, potential of zero charge, and activity of the tuned electrocatalysts.
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