Journal of Inorganic Materials ›› 2023, Vol. 38 ›› Issue (7): 823-829.DOI: 10.15541/jim20220688

Special Issue: 【能源环境】氢能材料(202409)

• RESEARCH ARTICLE • Previous Articles     Next Articles

Layered NiFeCo-LDH-Ti6C3.75 Catalyst: Preparation and Performance for Oxygen Evolution Reaction

LI Guanglan(), WANG Tianyu, LIU Yichen, LU Zhongfa   

  1. State Key Laboratory of Fine Chemicals, School of Chemical Engineering, Dalian University of Technology, Panjin 124221, China
  • Received:2022-11-17 Revised:2023-01-19 Published:2023-02-01 Online:2023-02-07
  • About author:LI Guanglan (1985-), female, PhD, associate professor. E-mail: guanglanli@dlut.edu.cn
  • Supported by:
    National Natural Science Foundation of China(21805026)

Abstract:

Oxygen evolution reaction (OER) is the key reaction for water splitting, but its slow kinetics limitsits application. Therefore, rational design and construction of efficient OER catalysts are crucial for water splitting. Here, a Co2+ ion doped NiFe layered double hydroxides coupled Ti6C3.75 (NiFeCo-LDH-Ti6C3.75) catalyst was prepared by a simple one-step hydrothermal method using cobalt nitrate, nickel nitrate, iron nitrate, urea, and Ti6C3.75 as raw materials. NiFeCo-LDH-Ti6C3.75 catalyst showed a lamellar stacking structure, which is facilitating exposing more active sites. Introduction of Co2+ and Ti6C3.75 reduced the electronic density of Ni and Fe sites of NiFeCo-LDH-Ti6C3.75 catalyst. Benefiting from these features, the NiFeCo-LDH-Ti6C3.75 catalyst exhibits excellent OER activity with an overpotential of merely 290 mV at a current density of 20 mA·cm-2 and a Tafel slope of 87.84 mV·dec-1 with faster reaction kinetics. NiFeCo-LDH-Ti6C3.75 catalyst shows a relatively low charge transfer resistance, which means a fast charge transfer efficiency. Furthermore, after 6000 cycles of accelerated aging test at 20 mA·cm-2, the overpotential only increased ~7 mV, indicating excellent cycle stability of NiFeCo-LDH-Ti6C3.75.

Key words: NiFe-LDH, Co doping, Ti6C3.75 doping

CLC Number: