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Catalysis02:50

Catalysis

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Lattice Defects Coupled with Support Modification Enable a BiNi-Co3O4/CP Catalyst for High-Efficiency Acidic Oxygen

Xu Ge1, Ke Xu1, Zhiwen Liu1

  • 1State Key Laboratory of Fine Chemicals, Dalian University of Technology, 116024 Dalian, China.

ACS Applied Materials & Interfaces
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Summary

This study introduces a novel Bi and Ni codoped Co3O4 catalyst synthesized via a molten salt method. This engineered catalyst significantly enhances the acidic oxygen evolution reaction (OER) performance and stability.

Keywords:
Co3O4acidic oxygen evolution reactionlattice defectssupport modificationwater electrolysis

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Area of Science:

  • Materials Science
  • Electrochemistry
  • Catalysis

Background:

  • Lattice defect engineering and support modification are key strategies to improve catalyst activity.
  • Optimizing catalyst electronic structures is crucial for enhancing intrinsic activity.

Purpose of the Study:

  • To develop a highly efficient and stable electrocatalyst for the acidic oxygen evolution reaction (OER).
  • To integrate lattice defect engineering and support modification for synergistic performance enhancement.

Main Methods:

  • In situ synthesis of Bi and Ni codoped Co3O4 on carbon paper (BiNi-Co3O4/CP) using a one-step molten salt method.
  • Characterization using in situ diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS).

Main Results:

  • Bi doping induced lattice defects, optimizing Co active sites and boosting catalytic activity.
  • Synergistic Ni-Bi interaction created a porous carbon support, increasing active site exposure and bubble desorption.
  • BiNi-Co3O4/CP demonstrated ultralow overpotential (275 mV at 10 mA cm-2) and 110 h stability in 0.5 M H2SO4 for OER.
  • Reduced formation of the *OOH intermediate and interfacial water adsorption confirmed by DRIFTS.

Conclusions:

  • The synergistic "lattice defect-support modification" approach is effective for designing efficient acidic OER electrocatalysts.
  • BiNi-Co3O4/CP offers a promising paradigm for high-performance and stable electrocatalysis in acidic media.