Reconstructing the Hydrogen-Bonded Network on an IrNi Sponge for the Alkaline Oxygen Evolution Reaction
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![Protein Film Infrared Electrochemistry Demonstrated for Study of H2 Oxidation by a [NiFe] Hydrogenase](/_next/image?url=https%3A%2F%2Fcloudfront.jove.com%2FCDNSource%2Fteasers%2F55858.jpg&w=3840&q=50)
Protein Film Infrared Electrochemistry Demonstrated for Study of H2 Oxidation by a [NiFe] Hydrogenase
Published on: December 4, 2017
Shengjue Deng1, Ziyue Wang1, Yan Zhang1
1Anhui Provincial Key Laboratory of Advanced Catalysis and Energy Materials, School of Chemistry and Chemical Engineering, Anqing Normal University, Anqing246001, P. R. China.
Abstract:
Precise regulation of the interfacial hydrogen-bonded network is critical for enhancing both electrocatalytic activity and long-term stability in the oxygen evolution reaction (OER). Herein, we successfully construct a flexible, metallic fibrous IrNi sponge that effectively reshapes the hydrogen-bonded network, thereby improving alkaline OER performance. The resulting IrNi sponge achieves a low overpotential of 270 mV at 200 mA cm-2 and maintains this current density for over 100 h in 1.0 M KOH, significantly outperforming the Ni sponge and IrO2/Ni sponge. When integrated as the anode in an anion exchange membrane water electrolyzer, the system achieves 0.5 A cm-2 at 1.65 V and exhibits remarkably stable operation for 500 h. Mechanistic investigations reveal that the in situ-generated Lewis acid sites (Irδ+) within the IrNi sponge reinforce the interfacial hydrogen-bonded network. This strengthened network facilitates OH- diffusion and lowers the energy barrier of the rate-determining step (*O → *OOH), thereby markedly enhancing the OER activity. This work underscores the importance of Lewis acid sites in regulating the hydrogen-bonded network and offers a viable design strategy for achieving high-current-density, durable catalysts for water electrolysis.
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