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Metal oxide photoanodes for solar hydrogen production

Metal oxide photoanodes for solar hydrogen production

Alexander, Bruce D., Kulesza, Pawel J., Rutkowska, Iwona, Solarska, Renata and Augustynski, Jan (2008) Metal oxide photoanodes for solar hydrogen production. Journal of Materials Chemistry, 18 (20). pp. 2298-2303. ISSN 0959-9428 (doi:

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The development of sustainable hydrogen production is a key target in the further facilitation of a hydrogen economy. Solar hydrogen generation through the photolytic splitting of water sensitised by semiconductor materials is attractive as it is both renewable and does not lead to problematic by-products, unlike current hydrogen sources such as natural gas. Consequently, the development of these semiconductor materials has undergone considerable research since their discovery over 30 years ago and it would seem prescient to review the more practical results of this research. Among the critical factors influencing the choice of semiconductor material for photoelectrolysis of water are the band-gap energies, flat band potentials and stability towards photocorrosion; the latter of these points directs us to focus on metal oxides. Careful design of thin films of photocatalyst material can eliminate potential routes of losses in performance, i.e., recombination at grain boundaries. Methods to overcome these problems are discussed such as coupling a photoanode for photolysis of water to a photovoltaic cell in a 'tandem cell' device.

Item Type: Article
Additional Information: [1] First published on the web 14 Mar 2008. [2] 0959-9428 (Print), 1364-5501 (Online)
Uncontrolled Keywords: chemically-modified n-tio2, mesoporous wo3 films, visible-light, titanium-dioxide, doped tio2, photoelectrochemical oxidation, water photooxidation, nanotube-arrays, electrodes, photoelectrolysis
Subjects: Q Science > QD Chemistry
Q Science > QC Physics
Faculty / School / Research Centre / Research Group: Faculty of Engineering & Science > School of Science (SCI)
Related URLs:
Last Modified: 11 Feb 2020 12:22

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