3.9 Article

Improved Photocatalytic Water Splitting Activity of Highly Porous WO3 Photoanodes by Electrochemical H+ Intercalation

Journal

FRONTIERS IN CHEMICAL ENGINEERING
Volume 3, Issue -, Pages -

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fceng.2021.760700

Keywords

intensity modulated photocurrent spectroscopy; hydrogen intercalation; tungsten oxide thin films; anodization; photoelectrochemical water splitting

Funding

  1. European Union [778357]
  2. Marie Curie Actions (MSCA) [778357] Funding Source: Marie Curie Actions (MSCA)

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In this study, WO3 films were obtained by galvanostatic anodization and modified through cathodic reduction and anodic activation. XPS analysis revealed changes in the film composition and properties, leading to improved photocatalytic activity. The modified films exhibited enhanced photoexcited charge carrier generation/separation, improved conductivity, and potentially suppressed bulk recombination.
WO3 photoanodes are widely used in photoelectrochemical catalysis, but typically the as-synthesized material is annealed before application. It is therefore desirable to explore less energy-intensive treatments. In this study, WO3 films of up to 3.9 mu m thickness were obtained by galvanostatic anodization of tungsten foil in a neutral-pH Na2SO4 and NaF electrolyte, also containing a NaH2PO2 additive (to suppress O-2 accumulation on the pore walls). Additionally, the WO3 photoanodes were modified by applying a cathodic reduction (H+ intercalation) and anodic activation treatment in-situ. XPS spectra revealed that intercalation modifies WO3 films; the amount of W5+-O and O-vacancy bonds was increased. Furthermore, subsequent activation leads to a decrease of the W5+ signal, but the amount of O-vacancy bonds remains elevated. The as-prepared and reduced (intercalated & activated) films were tested as OER photoanodes in acidic 0.1 M Na2SO4 media, under illumination with a 365 nm wavelength LED. It was observed that thinner films generated larger photocurrents. The peculiarities detected by XPS for reduced films correlate well with their improved photocatalytic activity. Photo-electrochemical impedance and intensity modulated photocurrent spectroscopies were combined with steady-state measurements in order to elucidate the effects of H+ intercalation on photoelectrochemical performance. The reduction results in films with enhanced photoexcited charge carrier generation/separation, improved conductivity, and possibly even suppressed bulk recombination. Thus, the intercalation & activation adopted in this study can be reliably used to improve the overall activity of as-synthesized WO3 photoanodes, and particularly of those that are initially poorly photoactive.

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