Abstract

In this paper, the synergistic effect of porosity and gradient of Mo doping in BiVO4 photoanodes for improving charge separation and solar water oxidation performance is reported. A simple solution-based, three-step fabrication route was adopted using a layer-by-layer assembling technique. A water oxidation photocurrent of ∼1.73 mA cm–2 at 1.23 V vs reversible hydrogen electrode in neutral pH was achieved without using any sacrificial agent or electrocatalyst. The gradient Mo doping was found to enhance charge separation efficiency, which was verified through a shift in the water oxidation onset potential cathodically to ∼200 mV. In addition, these results were further confirmed by a higher open-circuit photovoltage and flat band potential investigations. This was attributed to the surface energetics played by gradient Mo doping that served as the driving force in reducing the onset potential for water oxidation. The coupled effect of enhanced light absorption and charge separation was revealed by monitoring the difference in decoupling the water oxidation efficiencies of porous and planar Mo:BiVO4 photoanodes. This study demonstrated an improvement in the catalytic and charge separation efficiency of Mo:BiVO4 photoanodes due to the introduction of porous structured homojunctions in a gradient manner. The simple synthesis approach adopted in the present study can be utilized and scaled up in making efficient photoanodes for competent solar water oxidation cells.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.