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      Metal Doping to Enhance the Photoelectrochemical Behavior of LaFeO3 Photocathodes

      1 , 1
      ChemSusChem
      Wiley

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          Analysis of XPS spectra of Fe2+ and Fe3+ ions in oxide materials

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            Inorganic nanostructures for photoelectrochemical and photocatalytic water splitting.

            The increasing human need for clean and renewable energy has stimulated research in artificial photosynthesis, and in particular water photoelectrolysis as a pathway to hydrogen fuel. Nanostructured devices are widely regarded as an opportunity to improve efficiency and lower costs, but as a detailed analysis shows, they also have considerably disadvantages. This article reviews the current state of research on nanoscale-enhanced photoelectrodes and photocatalysts for the water splitting reaction. The focus is on transition metal oxides with special emphasis of Fe(2)O(3), but nitrides and chalcogenides, and main group element compounds, including carbon nitride and silicon, are also covered. The effects of nanostructuring on carrier generation and collection, multiple exciton generation, and quantum confinement are also discussed, as well as implications of particle size on surface recombination, on the size of space charge layers and on the possibility of controlling nanostructure energetics via potential determining ions. After a summary of electrocatalytic and plasmonic nanostructures, the review concludes with an outlook on the challenges in solar fuel generation with nanoscale inorganic materials.
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              Technical and economic feasibility of centralized facilities for solar hydrogen production via photocatalysis and photoelectrochemistry

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                Author and article information

                Journal
                ChemSusChem
                ChemSusChem
                Wiley
                18645631
                June 09 2017
                June 09 2017
                May 08 2017
                : 10
                : 11
                : 2457-2463
                Affiliations
                [1 ]Departament de Química Física i Institut Universitari d'Electroquímica; Universitat d'Alacant, Apartat 99, E-; 03080 Alicante Spain
                Article
                10.1002/cssc.201700166
                e9eb4e0c-b7ca-43f6-995c-d0fc4c7ff3a0
                © 2017

                http://doi.wiley.com/10.1002/tdm_license_1

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