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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
Electrooxidation-enabled electroactive high-valence ferritic species in NiFe layered double hydroxide arrays as
Yujie Wang1, Xinghe Zhang1, Ling Huang2
1Department of Chemistry, College of Resource and Environment, Baoshan University, Baoshan 678000, PR China.
Abstract:
Currently, engineering non-precious NiFe layered double hydroxide (NiFe-LDH) electrocatalysts with excellent oxygen evolution performances at high current densities is highly critical to promoting electrolytic water splitting producing hydrogen for large-scale commercial applications. Herein, an intrigued oxygen vacancy-rich Fe(Ⅱ)-incorporated NiFe-LDH containing electroactive high-valence ferritic species is successfully grown on Ni foam (Fe2+-NiFe-LDH-EO6 h@NF) through an elaborate two-step route including hydrothermal and electrooxidation, and utilized as a high-efficiency elctrocayalyst of alkaline water oxidation possessing abundant exposed active sites, excellent intrinsic catalytic activity and superior durability. Therefore, the Fe2+-NiFe-LDH-EO6 h@NF electrocatalyst towards oxygen evolution reaction (OER) enables the low overpotentials of 239, 285 and 350 mV for the current densities of 10, 100 and 500 mA cm-2, respectively, a small Tafel slope of 48.3 mV dec-1, the low onset potential of 1.451 V, and retains the catalytic activity for 40 h at the large current density of 500 mA cm-2 as well as owns the high turnover frequency (TOF) value of 0.93 s-1 at the overpotential of 300 mV. This work provides a promising avenue to improve the OER performances of NiFe-LDH electrocatalyst for practical applications.
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