Charge separation on surfaces of a visible-light driven BiVO4 photoanode for water splitting
a Carnegie Mellon University, Department of Materials Science and Engineering, Pittsburgh, 0, United States
Proceedings of International Conference on New Advances in Materials Research for Solar Fuels Production (SolarFuel14)
Montréal, Canada, 2014 June 25th - 26th
Organizer: Thomas Hamann
Poster, Ratiporn Munprom, 025
Publication date: 16th April 2014
Publication date: 16th April 2014
For solar-driven applications, such as photocatalysts, a crucial problem in materials is an efficiency limitation due to a poor charge separation. Recently, developments of BiVO4 being used as a photoanode for water splitting reactions have been intensively studied. Not only did previous studies report the high performance of BiVO4 photoanode because of its ability to absorb visible light[1], but also the efficient charge separation of faceted BiVO4 has been reported[2].
Herein, we showed spatially selective photochemical reduction reactivity, evidence for the separation of photogenerated charge carriers on polycrystalline BiVO4 surfaces. The experiments used a polycrystalline monoclinic BiVO4 ceramic synthesized by solid-state reaction. Topographic images obtained from atomic force microscopy (AFM) demonstrated ferroelastic domains on the sample surfaces. The sample was then used to photochemically reduce silver from an aqueous silver nitrate solution. Silver ions were photochemically reduced under blue LED illumination (470 nm wavelength) to silver metal which formed as an insoluble product on the BiVO4 surfaces. Topographic AFM images after reduction revealed that the silver metal forms only in specific areas. Silver deposits were found in patterns correlated to contrast in piezoresponse force microscopy (PFM) images and the presence of ferroelastic domains. This finding shows that bulk BiVO4 has charge separation that can promote the photochemical activity for water splitting reactions. Moreover, this could lead BiVO4 to be a high performance material candidate that could be widely used for solar harvesting technologies.
Reference:
[1] Y. Park, K. J. McDonald and K.-S. Choi, Progress in bismuth vanadate photoanodes for use in solar water oxidation, Chem. Soc. Rev. 42, 2321 (2013)
[2] Li, R. et al., Spatial Separation of Photogenerated Electrons and Holes among {010} and {110} Crystal Facets of BiVO4. Nat. Commun. 4:1432 (2013).
Herein, we showed spatially selective photochemical reduction reactivity, evidence for the separation of photogenerated charge carriers on polycrystalline BiVO4 surfaces. The experiments used a polycrystalline monoclinic BiVO4 ceramic synthesized by solid-state reaction. Topographic images obtained from atomic force microscopy (AFM) demonstrated ferroelastic domains on the sample surfaces. The sample was then used to photochemically reduce silver from an aqueous silver nitrate solution. Silver ions were photochemically reduced under blue LED illumination (470 nm wavelength) to silver metal which formed as an insoluble product on the BiVO4 surfaces. Topographic AFM images after reduction revealed that the silver metal forms only in specific areas. Silver deposits were found in patterns correlated to contrast in piezoresponse force microscopy (PFM) images and the presence of ferroelastic domains. This finding shows that bulk BiVO4 has charge separation that can promote the photochemical activity for water splitting reactions. Moreover, this could lead BiVO4 to be a high performance material candidate that could be widely used for solar harvesting technologies.
Reference:
[1] Y. Park, K. J. McDonald and K.-S. Choi, Progress in bismuth vanadate photoanodes for use in solar water oxidation, Chem. Soc. Rev. 42, 2321 (2013)
[2] Li, R. et al., Spatial Separation of Photogenerated Electrons and Holes among {010} and {110} Crystal Facets of BiVO4. Nat. Commun. 4:1432 (2013).
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