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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.
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.
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.
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