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Surface Engineering of Anodic WO3 Layers by In Situ Doping for Light-Assisted Water Splitting
Karolina Syrek1, Sebastian Kotarba1, Marta Zych1
1Faculty of Chemistry, Jagiellonian University, Gronostajowa 2, 30-387 Krakow, Poland.
This study introduces a new method for creating cobalt and fluorine-doped tungsten oxide (Co-F-WO3) layers using electrochemical synthesis. These doped layers show enhanced photoelectrochemical activity for solar water splitting.
Area of Science:
- Materials Science
- Electrochemistry
- Nanotechnology
Background:
- Tungsten oxide (WO3) is a promising material for photocatalysis.
- Improving the photoelectrochemical (PEC) performance of WO3 is crucial for applications like solar water splitting.
- Doping WO3 can enhance its properties, but controlled synthesis methods are needed.
Purpose of the Study:
- To develop a novel single-step electrochemical synthesis for anodic Co-F-WO3 layers.
- To investigate the effect of cobalt and fluorine doping on WO3 properties.
- To evaluate the PEC performance of Co-F-WO3 for solar water splitting and the oxygen evolution reaction (OER).
Main Methods:
- Single-step electrochemical synthesis of anodic Co-F-WO3.
- Characterization using EDS, XRD, Raman, photoluminescence, XPS, and Mott-Schottky analysis.
- Photoelectrochemical measurements to assess PEC activity and stability for OER.
Main Results:
- Successfully synthesized nanoporous Co-F-WO3 layers with in situ doping.
- Confirmed doping and incorporation of cobalt and fluorine using various spectroscopic techniques.
- Observed lower absorption and slight band gap shifts in Co-doped materials.
- Demonstrated significantly enhanced PEC activity (up to 5-fold) for Co-F-WO3 in solar water splitting and OER.
- Showcased reusability of the photoanodes for PEC water-splitting experiments.
Conclusions:
- The single-step electrochemical synthesis is effective for producing Co-F-WO3 photoanodes.
- Co-F doping enhances the PEC activity of WO3 for solar water splitting and OER.
- The developed Co-F-WO3 layers show potential as efficient and reusable photoelectrodes.
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