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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://repozitorij.uni-lj.si/IzpisGradiva.php?id=176557"><dc:title>Engineering Ru@Ir core–shell nanoparticles on titanium oxynitride–graphene support for a highly active and durable pH-universal hydrogen evolution reaction</dc:title><dc:creator>Popović,	Aleksandra S.	(Avtor)
	</dc:creator><dc:creator>Marić,	Ivan	(Avtor)
	</dc:creator><dc:creator>Bele,	Marjan	(Avtor)
	</dc:creator><dc:creator>Rems,	Ervin	(Avtor)
	</dc:creator><dc:creator>Huš,	Matej	(Avtor)
	</dc:creator><dc:creator>Pavko,	Luka	(Avtor)
	</dc:creator><dc:creator>Ruiz-Zepeda,	Francisco	(Avtor)
	</dc:creator><dc:creator>Bijelić,	Lazar	(Avtor)
	</dc:creator><dc:creator>Grgur,	Branimir	(Avtor)
	</dc:creator><dc:creator>Hodnik,	Nejc	(Avtor)
	</dc:creator><dc:creator>Smiljanić,	Milutin	(Avtor)
	</dc:creator><dc:subject>hydrogen evolution reaction</dc:subject><dc:subject>iridium</dc:subject><dc:subject>ruthenium</dc:subject><dc:subject>core−shell structures</dc:subject><dc:subject>TiO$_x$N$_y$</dc:subject><dc:subject>MSI</dc:subject><dc:subject>DFT</dc:subject><dc:subject>catalysts</dc:subject><dc:subject>evolution reactions</dc:subject><dc:subject>nanoparticles</dc:subject><dc:subject>oxides</dc:subject><dc:subject>transition metals</dc:subject><dc:description>The rational design of electrocatalysts with high activity, durability, and low precious metal content is key to advancing hydrogen production via water electrolysis. Here, we present a multifunctional electrocatalyst based on Ru@Ir core−shell nanoparticles anchored on a conductive titanium oxynitride−graphene hybrid support (Ru@Ir/TiO$_x$N$_y$-C), achieving superior performance for the hydrogen evolution reaction (HER) in both acidic and alkaline media. The combination of the core−shell Ru@ Ir architecture and the strong metal−support interaction (MSI) with TiO$_x$N$_y$ optimizes hydrogen and hydroxide adsorption energies, as confirmed by X-ray photoelectron spectroscopy and density functional theory (DFT) calculations. In alkaline media, Ru@Ir/ TiO$_x$N$_y$-C outperforms commercial Pt/C with a remarkably low overpotential of 13 mV at 10 mA cm$^{−2}$ and high mass activity, while in acidic conditions, it rivals Pt/C and surpasses monometallic analogs. The long-term stability of the composite is attributed to the enhanced nanoparticle anchoring and structural integrity provided by the TiO$_x$N$_y$ support. This work shows that combining core−shell nanostructures with engineered conductive supports can effectively replace platinum in HER applications. Such a nanocomposite strategy offers a versatile platform for the development of advanced electrocatalysts across a broad range of energy conversion reactions.</dc:description><dc:date>2025</dc:date><dc:date>2025-12-03 14:40:55</dc:date><dc:type>Članek v reviji</dc:type><dc:identifier>176557</dc:identifier><dc:language>sl</dc:language></rdf:Description></rdf:RDF>
