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Preparation and electrocatalytic oxygen evolution of bimetallic phosphates (NiFe) 2 P/NF

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Abstract The energy and environmental crisis pose a great challenge to human development in the 21st century. The design and development of clean and renewable energy and the solution for environmental pollution have become a hotspot in the current research. Based on the preparation of transition metal phosphates, transition metals were used as raw materials, Prussian blue-like NiFe(CN) 6 as a precursor, which was in situ grown on nickel foam (NF) substrate. After low temperature phosphating treatment, a bimetallic phosphide electrocatalyst (NiFe) 2 P/NF was prepared on NF substrate. Using 1 mol·L −1 KOH solution as a basic electrolyte, based on the electrochemical workstation of a three-electrode system, the electrochemical catalytic oxygen evolution performance of the material was tested and evaluated. Experiments show that (NiFe) 2 P/NF catalyst has excellent oxygen evolution performance. In an alkaline medium, the overpotential required to obtain the catalytic current density of 10 mA·cm −2 is only 220 mV, and the Tafel slope is 67 mV·dec −1 . This is largely due to: (1) (NiFe)2p/NF nanocatalysts were well dispersed on NF substrates, which increased the number of active sites exposed; (2) the hollow heterostructure of bimetallic phosphates promotes the electron interaction between (NiFe) 2 P and NF, increased the rate of charge transfer, and the electrical conductivity of the material is improved; and (3) theoretical calculations show that (NiFe) 2 P/NF hollow heterostructure can effectively reduce the dissociation barrier of water, promote the dissociation of water; furthermore, the kinetic reaction rate of electrocatalytic oxygen evolution is accelerated. Meanwhile, the catalyst still has high activity and high stability in 30 wt% concentrated alkali solution. Therefore, the construction of (NiFe) 2 P/NF electrocatalysts enriches the application of non-noble metal nanomaterials in the field of oxygen production from electrolytic water.
Title: Preparation and electrocatalytic oxygen evolution of bimetallic phosphates (NiFe) 2 P/NF
Description:
Abstract The energy and environmental crisis pose a great challenge to human development in the 21st century.
The design and development of clean and renewable energy and the solution for environmental pollution have become a hotspot in the current research.
Based on the preparation of transition metal phosphates, transition metals were used as raw materials, Prussian blue-like NiFe(CN) 6 as a precursor, which was in situ grown on nickel foam (NF) substrate.
After low temperature phosphating treatment, a bimetallic phosphide electrocatalyst (NiFe) 2 P/NF was prepared on NF substrate.
Using 1 mol·L −1 KOH solution as a basic electrolyte, based on the electrochemical workstation of a three-electrode system, the electrochemical catalytic oxygen evolution performance of the material was tested and evaluated.
Experiments show that (NiFe) 2 P/NF catalyst has excellent oxygen evolution performance.
In an alkaline medium, the overpotential required to obtain the catalytic current density of 10 mA·cm −2 is only 220 mV, and the Tafel slope is 67 mV·dec −1 .
This is largely due to: (1) (NiFe)2p/NF nanocatalysts were well dispersed on NF substrates, which increased the number of active sites exposed; (2) the hollow heterostructure of bimetallic phosphates promotes the electron interaction between (NiFe) 2 P and NF, increased the rate of charge transfer, and the electrical conductivity of the material is improved; and (3) theoretical calculations show that (NiFe) 2 P/NF hollow heterostructure can effectively reduce the dissociation barrier of water, promote the dissociation of water; furthermore, the kinetic reaction rate of electrocatalytic oxygen evolution is accelerated.
Meanwhile, the catalyst still has high activity and high stability in 30 wt% concentrated alkali solution.
Therefore, the construction of (NiFe) 2 P/NF electrocatalysts enriches the application of non-noble metal nanomaterials in the field of oxygen production from electrolytic water.

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