Catalytic Materials

Study on collaborative strategy between Fe3+ and Ni-based metal-organic frameworks for boosting electrocatalytic oxygen evolution

  • CHEN Xingliang ,
  • FAN Wenjuan ,
  • CHANG Hui ,
  • HUANG Haiping ,
  • JIANG Zhiqiang
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  • 1.Faculty of Meterials Metallurgy and Chemistry,Jiangxi University of Science and Technology,Ganzhou 341000,China
    2.Vanadium and Titanium Resource Comprehensive Utilization Key Laboratory of Sichuan Province,Panzhihua University,Panzhihua 617000,China

Received date: 2023-05-25

  Online published: 2024-02-06

Abstract

The metal-organic framework materials(phen-Ni) were synthesized by solvothermal method,and then Fe@phen-Ni electrocatalys were prepared by doping heterometallic Fe3+.The morphology,crystal structure and chemical composition of Fe@phen-Ni were characterized by X-ray single crystal diffractometer,scanning electron microscope(SEM),transmission electron microscope(TEM) and X-ray photoelectron spectrometer(XPS).The electrochemical oxygen evolution reaction(OER) activity of Fe@phen-Ni was investigated by linear sweep voltammetry(LSV) and electrochemical impedance spectroscopy(EIS).The results exhibited that Fe@phen-Ni had more excellent electrocatalytic performance with an overpotential of 333 mV at the current density of 10 mA/cm2 when compared with that of phen-Ni.The improvement could be attributed to the two factors.The introduction of Fe3+ increased the active site of the electrocatalyst.The synergistic action of Fe3+ and Ni2+ promoted the electron transfer.This work not only confirmed that doping of Fe3+ was beneficial to improve the electrocatalytic oxygen-evolution activity,but also provided a new idea for the preparation of electrocatalytic OER catalysts based on metal-organic frame materials.

Cite this article

CHEN Xingliang , FAN Wenjuan , CHANG Hui , HUANG Haiping , JIANG Zhiqiang . Study on collaborative strategy between Fe3+ and Ni-based metal-organic frameworks for boosting electrocatalytic oxygen evolution[J]. Inorganic Chemicals Industry, 2024 , 56(2) : 152 -158 . DOI: 10.19964/j.issn.1006-4990.2023-0287

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