Abstract
Producing hydrogen through solar water splitting requires the coverage of large land areas. Abundant metal-based molecular catalysts offer scalability, but only if they match noble metal activities. We report on a highly active p-GaInP2 photocathode protected through a 35-nm TiO2 layer functionalized by a cobaloxime molecular catalyst (GaInP2-TiO2 -cobaloxime). This photoelectrode mediates H2 production with a current density of ∼9 mA cm-2 at a potential of 0 V versus RHE under 1-sun illumination at pH 13. The calculated turnover number for the catalyst during a 20-h period is 139,000, with an average turnover frequency of 1.9 s-1. Bare GaInP2 shows a rapid current decay, whereas the GaInP2-TiO2 -cobaloxime electrode shows ≤5% loss over 20 min, comparable to a GaInP2-TiO2-Pt catalyst particle-modified interface. The activity and corrosion resistance of the GaInP2-TiO2-cobaloxime photocathode in basic solution is made possible by an atomic layer-deposited TiO2 and an attached cobaloxime catalyst.
Original language | American English |
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Pages (from-to) | 456-460 |
Number of pages | 5 |
Journal | Nature Materials |
Volume | 15 |
Issue number | 4 |
DOIs | |
State | Published - 1 Apr 2016 |
Bibliographical note
Publisher Copyright:© 2016 Macmillan Publishers Limited. All rights reserved.
NREL Publication Number
- NREL/JA-5900-64559
Keywords
- cobaltoxime catalysts
- p-GaInP2 photoelectrode
- photoelectrochemical
- solar-photochemistry
- stabilization
- titanium dioxide
- turnover frequency
- turnover number