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<rdf:RDF xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#" xmlns:dc="http://purl.org/dc/elements/1.1/"><rdf:Description rdf:about="https://dirros.openscience.si/IzpisGradiva.php?id=30621"><dc:title>Dual-metal co-catalyst integrated graphitic carbon nitride for photocatalytic hydrogen evolution reaction</dc:title><dc:creator>Gupta,	Suraj	(Avtor)
	</dc:creator><dc:creator>Batool,	Samar	(Avtor)
	</dc:creator><dc:creator>Maček,	Marjeta	(Avtor)
	</dc:creator><dc:creator>Daneu,	Nina	(Avtor)
	</dc:creator><dc:creator>Johny,	Joyal	(Avtor)
	</dc:creator><dc:creator>Spreitzer,	Matjaž	(Avtor)
	</dc:creator><dc:creator>Cherevan,	Alexey	(Avtor)
	</dc:creator><dc:subject>hydrogen evolution reaction</dc:subject><dc:subject>nanosheets</dc:subject><dc:description>Graphitic carbon nitride (g-C3N4) nanosheets are extensively used in photocatalytic applications but are often decorated with noble-metal co-catalysts to yield relevant efficiencies. Herein, we report a dual-metal co-catalyst system comprising cobalt and molybdenum (CoMo) nanoclusters uniformly integrated into heptazine g-C3N4 nanosheets for enhanced visible-light-driven hydrogen evolution reaction (HER). The intimate contact between metals as well as with gC3N4 layer was verified through X-ray absorption and X-ray photoelectron spectroscopies. Mechanistic insights obtained through a combination of experimental and computational studies suggest that Co acts as primary catalytic center, while Mo plays a preliminary role in facilitating surface hydrogen coverage, collectively accelerating the redox rates and achieving 10 times higher performance compared to bare gC3N4. Post-HER analysis reveals disintegration of co-catalyst into Co single-atoms, which then takes the leading role in sustaining the HER. The role of co-catalyst was mainly limited to the surface, acting as electron trap, reducing charge recombination and as a HER catalytic center. The composite exhibits excellent photostability over 13 h of ON/OFF illumination cycles, highlighting its potential for intermittent operations under practical conditions. This study presents a co-catalyst design strategy leveraging dual-metal synergy as a non-noble, scalable alternative to conventional noble-metal-based HER co-catalysts for solar fuel generation.</dc:description><dc:publisher>Elsevier</dc:publisher><dc:date>2027</dc:date><dc:date>2026-06-30 10:43:31</dc:date><dc:type>Neznano</dc:type><dc:identifier>30621</dc:identifier><dc:source>Nizozemska</dc:source><dc:language>sl</dc:language><dc:rights>© 2026 The Author(s).</dc:rights></rdf:Description></rdf:RDF>
