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<metadata xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:dc="http://purl.org/dc/elements/1.1/"><dc:title>Advancing oxygen evolution catalysis with dual-phase nickel sulfide nanostructures</dc:title><dc:creator>Santhosh,	Neelakandan Marath	(Avtor)
	</dc:creator><dc:creator>Gupta,	Suraj	(Avtor)
	</dc:creator><dc:creator>Shvalya,	Vasyl	(Avtor)
	</dc:creator><dc:creator>Košiček,	Martin	(Avtor)
	</dc:creator><dc:creator>Zavašnik,	Janez	(Avtor)
	</dc:creator><dc:creator>Cvelbar,	Uroš	(Avtor)
	</dc:creator><dc:subject>electrocatalysts</dc:subject><dc:description>The production, conversion and storage of energy based on electrocatalysis, mainly assisted by oxygen evolution reaction (OER), plays a crucial role in alkaline water electrolyzers (AWEs) and fuel cells. Nevertheless, the insufficient availability of highly efficient catalyst materials at a reasonable cost that overcome the sluggish electrochemical kinetics of the OER is one of the significant obstacles. Herein, we report a fast and facile synthesis of vapor phase deposition of dual-phase nickel sulfide (Ni-sulfide) using low-temperature annealing in the presence of H2S and demonstrated as an efficient catalyst for OER to address the issues with sluggish electrochemical kinetics. The dual-phase Ni-sulfide structures consist of densely packed 10–50 μm microcrystals with 40–50 individual dual-phase layers, such as NiS and Ni7S6. As an electrocatalyst, the dual-phase Ni-sulfide exhibits excellent OER activity by achieving a current density of 10 mA/cm2 at an overpotential (η10) of 0.29 V and excellent electrochemical stability over 50 h. Besides, the Ni-sulfide displays considerable electrochemical robustness in alkaline conditions and forms OER-active Ni-oxide/hydroxide species during the process. Using an energy-efficient synthesis method, the fabricated unique crystalline nanodesign of dual-phase Ni-sulfide could open new pathways for the controlled synthesis of a high-efficiency group of electrocatalysts for a long-time stable electrochemical catalytic activity.</dc:description><dc:publisher>ACS Publications</dc:publisher><dc:date>2024</dc:date><dc:date>2025-01-17 14:10:26</dc:date><dc:type>Neznano</dc:type><dc:identifier>21245</dc:identifier><dc:identifier>UDK: 544.5/.6</dc:identifier><dc:identifier>ISSN pri članku: 1520-5029</dc:identifier><dc:identifier>DOI: 10.1021/acs.energyfuels.4c05182</dc:identifier><dc:identifier>COBISS_ID: 221574659</dc:identifier><dc:source>ZDA</dc:source><dc:language>sl</dc:language><dc:rights>© 2025 The Authors.</dc:rights></metadata>
