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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
Tunable NiSe-Ni3Se2 Heterojunction for Energy-Efficient Hydrogen Production by Coupling Urea Degradation
Ruilian Yin1, Zhiwei Wang2, Jin Zhang3
1College of Materials Science and Engineering, Zhejiang University of Technology, Hangzhou, 310014, China.
Abstract:
Urea-assisted water splitting is a promising energy-saving hydrogen (H2) production technology. However, its practical application is hindered by the lack of high-performance bifunctional catalysts for urea oxidation reaction (UOR) and hydrogen evolution reaction (HER). Herein, a heterostructured catalyst comprising highly active NiSe and Ni3Se2, along with a conductive graphene-coated nickel foam skeleton (NiSe-Ni3Se2/GNF) is reported. The heterostructured NiSe-Ni3Se2 originates from the in situ selenization of graphene-coated nickel foam, allowing for careful regulation of the NiSe to Ni3Se2 ratio by simply adjusting the calcination temperature. Theoretical calculations of the charge transfer between NiSe and Ni3Se2 components can optimize the reaction pathways and reduce the corresponding energy barriers. Accordingly, the designed catalyst exhibits excellent UOR and HER activity and stability. Furthermore, the NiSe-Ni3Se2/GNF-based UOR-HER electrolyzer requires only 1.54 V to achieve a current density of 50 mA cm-2, which is lower than many recent reports and much lower than 1.83 V of NiSe-Ni3Se2/GNF-based OER-HER electrolyzers. Moreover, the UOR-HER electrolyzer exhibited negligible cell voltage variation during a 28-h stability test, indicating satisfactory stability, which provides a new viable paradigm for energy-saving H2 production.
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