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<dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:invenio="http://invenio-software.org/elements/1.0" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd"><dc:identifier>doi:10.1016/j.ijhydene.2015.04.063</dc:identifier><dc:language>eng</dc:language><dc:creator>Martín-Ramos, P.</dc:creator><dc:creator>Martín-Gil, J.</dc:creator><dc:creator>Dante, R.C.</dc:creator><dc:creator>Vaquero, F.</dc:creator><dc:creator>Navarro, R.M.</dc:creator><dc:creator>Fierro, J.L.G.</dc:creator><dc:title>A simple approach to synthesize g-C3N4 with high visible light photoactivity for hydrogen production</dc:title><dc:identifier>ART-2015-103357</dc:identifier><dc:description>Se-modified g-C3N4 was synthesized from sonicated aqueous suspensions of melamine cyanurate and SeO2. The different thermal condensation temperatures in the 500–650 °C range were found to influence the photophysical properties and hydrogen evolution rates. H2 evolution increased dramatically by two orders of magnitude when Pt co-catalyst (1 wt.%) was incorporated, reaching an HER of 75 µmol H2/h.</dc:description><dc:date>2015</dc:date><dc:source>http://zaguan.unizar.es/record/69166</dc:source><dc:doi>10.1016/j.ijhydene.2015.04.063</dc:doi><dc:identifier>http://zaguan.unizar.es/record/69166</dc:identifier><dc:identifier>oai:zaguan.unizar.es:69166</dc:identifier><dc:relation>info:eu-repo/grantAgreement/ES/MINECO/CTQ2013-48669-P</dc:relation><dc:identifier.citation>International Journal of Hydrogen Energy 40, 23 (2015), 7273-7281</dc:identifier.citation><dc:rights>by-nc-nd</dc:rights><dc:rights>http://creativecommons.org/licenses/by-nc-nd/3.0/es/</dc:rights><dc:rights>info:eu-repo/semantics/openAccess</dc:rights></dc:dc>

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