ACS Catalysis · 2016 · 119 citations · 40 references
Natural SciencesChemical EngineeringMaterials ScienceElectrochemistryNanomaterialsNanotechnologyElectrochemical CellsElectrochemical Energy ConversionElectrode MaterialsElectrolysis ProcessesNanocatalysisNanostructured Energy MaterialsCatalytic NanoparticlesCurrent DensityElectrocatalystsHydrogen Evolution CatalystsIron Oxide NanoparticlesMetal Sulfide ElectrocatalysisProton Exchange Membrane ElectrolysisWater Electrolysis
In the context of increased application of proton exchange membrane electrolyzers, the development of cheap and long-lived transition-metal hydrogen evolution reaction electrocatalysts is required to circumvent nonsustainable platinum-based electrocatalysts. Herein we report the synthesis and characterization of robust iron–sulfide nanoparticles from low-cost precursors (i.e., FeCl 3 and thiourea) using an easily scalable soft synthesis technique, which can achieve electrocatalysis. In the series of nanoparticles studied, we show that pyrite FeS 2 is the most active, in comparison with greigite Fe 3 S 4 and pyrrhotite Fe 9 S 10, in a three-electrode electrochemical cell, the electrocatalysis starting at an overpotential of ∼180 mV. These three materials exhibit a very stable behavior during the catalysis, with no activity decrease for at least 5 days. Fe x S y catalysts have been tested in a PEM electrolysis single cell, and pyrite FeS 2 allows achievement of a current density of 2 A/cm 2 at a voltage of 2.3 V.
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Charles C. L. McCrory, Suho Jung, Ivonne M. Ferrer et al. · Journal of the American Chemical Society · 2015 · 4K citations
Natural Sciences, Chemical Engineering, Materials Science +17