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Homonuclear/Heteronuclear Bimetallic Conjugated Coordination Polymers with Customized Oxygen Evolution Pathway.
Yuhao Weng1, Lizhi Sun1, Hao Jia2
1Key Laboratory of Green Chemistry and Technology of Ministry of Education, College of Chemistry, Sichuan University, 29 Wangjiang Road, Chengdu 610064, P. R. China.
This study introduces novel 2D bimetallic coordination polymers for oxygen evolution reaction (OER) catalysis. The heteronuclear CoNi-PI catalyst exhibits a faster mechanism and superior performance compared to homonuclear counterparts.
Area of Science:
- Materials Science
- Electrochemistry
- Catalysis
Background:
- Synergistic effects in bimetallic catalysts for oxygen evolution reaction (OER) are not fully understood due to complex structures.
- Synthesizing catalysts with long-range atomic ordering for OER remains challenging.
Purpose of the Study:
- To investigate structure-property correlations in bimetallic catalysts for OER.
- To develop novel two-dimensional (2D) conjugated bimetallic coordination polymers (c-CPs) with well-defined structures.
Main Methods:
- Synthesis of two-dimensional (2D) conjugated bimetallic coordination polymers (c-CPs) involving Cobalt (Co) and Nickel (Ni).
- Electrocatalytic testing of synthesized catalysts for the oxygen evolution reaction (OER).
- Analysis of catalytic mechanisms using electrochemical techniques.
Main Results:
- The heteronuclear CoNi-PI catalyst unexpectedly shifted OER mechanisms from adsorbate evolution to the faster oxide path mechanism.
- CoNi-PI demonstrated high stability and an ultralow overpotential of 282 mV at 100 mA cm-2.
- A low Tafel slope of approximately 42 mV dec-1 was observed for CoNi-PI, indicating efficient kinetics.
Conclusions:
- This study presents a rare crystalline heteronuclear bimetallic catalyst with exceptional OER catalytic properties.
- The findings offer significant insights into catalyst development for efficient OER.
- Understanding the altered catalytic mechanism in CoNi-PI provides a foundation for designing advanced catalysts.
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