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Grain Boundary Engineering in 3D Porous Silver Electrocatalysts for Enhanced CO2-to-CO Conversion
Xiaoqian Xu1, Song Yang1, Yixiang Wang1
1Jiangsu Key Laboratory of Electrochemical Energy Storage Technologies, College of Materials Science and Technology, Nanjing University of Aeronautics and Astronautics, Nanjing 210016, China.
This study presents a novel coral-like porous silver catalyst (CP-Ag) for efficient electrochemical carbon dioxide (CO2) reduction. The CP-Ag catalyst demonstrates enhanced activity and stability for carbon monoxide (CO) production.
Area of Science:
- Materials Science
- Electrochemistry
- Catalysis
Background:
- Silver is a selective electrocatalyst for CO2 reduction to CO.
- A key challenge is the trade-off between silver's catalytic activity and stability.
- Optimizing silver catalysts requires addressing both morphological and crystallographic features.
Purpose of the Study:
- To develop a novel silver catalyst with improved activity and stability for CO2 electroreduction.
- To investigate the structure-activity relationship of a three-dimensional coral-like porous silver (CP-Ag) catalyst.
- To understand how engineered morphology and grain boundaries influence catalytic performance.
Main Methods:
- Seed-assisted nanoparticle attachment synthesis to create a 3D coral-like porous silver (CP-Ag) architecture.
- Electrochemical characterization including Faradaic efficiency (FE) and current density measurements.
- Long-term stability testing in a flow cell setup.
Main Results:
- CP-Ag exhibited >90% FE for CO over a wide potential range (-0.6 to -1.0 V vs. RHE).
- Achieved a 2-times higher current density compared to normal Ag NPs.
- Demonstrated sustained high FE for CO (~90%) for approximately 40 hours at -50 mA cm-2.
Conclusions:
- The 3D coral-like morphology enhances active sites and charge transfer.
- Stable grain boundaries between Ag NPs contribute to increased reaction activity.
- Optimized binding on Ag (100) facets promotes CO intermediate formation, boosting overall performance.
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