Journal of the American Chemical Society · 2024 · 89 citations · 49 references
Natural SciencesChemical EngineeringMaterials ScienceCatalysisElectrochemistrySurface ScienceCatalyst DesignCatalytic MaterialsCatalytic MechanismsCatalytic Reaction EngineeringFerroelectric MaterialsSupported CatalystsHydrogen EvolutionHydrogen Evolution CatalystsHydrogen Evolution KineticsHydrogen Evolution ReactionHydrogen Evolution Reaction KineticsProton Pump ActivityProton TransportStructured Catalysts
The improvement of hydrogen evolution reaction kinetics can be largely accelerated by introducing a well-designed hydrogen spillover pathway into the catalysts. However, the driving force and mechanism of hydrogen migration on the surface of catalysts are poorly understood and are rarely explored in depth. Here, inspired by the specific ferroelectric property of HfO 2, Mn–O–Ca sites in Mn 4 CaO 5, and Fe–Fe sites in hydrogenases, we constructed a bioinspired HfO 2 coupled with Ir catalysts (Ir/HfO 2 @C) with an alkaline hydrogen reverse spillover effect from HfO 2 to interface and acid hydrogen spillover effect from Ir to interface. Benefiting from the bidirectional hydrogen spillover pathways controlled by pH, Ir/HfO 2 @C displays a narrow overpotential difference between acidic and alkaline electrolytes. Remarkably, Ir/HfO 2 @C shows a remarkable mass current density and turnover frequency value, far exceeding the benchmark Ir/C by 20.6 times. More importantly, this Ir/HfO 2 @C achieves extraordinarily low overpotentials of 146 and 39 mV at 10 mV cm –2 in seawater and alkaline seawater, respectively. The anion-exchange membrane water electrolyzer equipped with Ir/HfO 2 @C as a cathode exhibits excellent and stable H 2 -evolution performance on 2.22 V at 1.0 A cm –2 . We expect that the bioinspired strategy will provide a new concept for designing catalytic materials for efficient and pH-universal electrochemical hydrogen production.
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Sustainable Hydrogen Production
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