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Spatially Separated Plasmonic Catalysts for Selective CO2 Electrochemical Conversion Using Interband/Intraband Hot
Chen Chi1, Xue-Lu Chen1, Jian Li1
1State Key Laboratory of Analytical Chemistry for Life Science, School of Chemistry and Chemical Engineering, Nanjing University, Nanjing 210023, China.
This study introduces a novel gold-molybdenum disulfide hybrid catalyst for efficient solar-driven carbon dioxide (CO2) conversion. The catalyst enhances selectivity for valuable products like methanol, formic acid, and ethanol through controlled hot electron injection.
Area of Science:
- Materials Science
- Catalysis
- Nanotechnology
Background:
- Plasmonic nanostructures offer potential for solar energy utilization in CO2 conversion.
- Noble metals like gold and silver have limitations in mediating multielectron reduction pathways for value-added products.
Purpose of the Study:
- To design and investigate a spatially separated plasmonic-semiconductor hybrid catalyst for improved electrocatalytic CO2 reduction.
- To understand the role of interband and intraband hot electrons in enhancing CO2RR selectivity and activity.
Main Methods:
- Coupling molybdenum disulfide (MoS2) quantum dots to gold (Au) triangle nanoprisms to create a hybrid catalyst.
- Investigating hot electron generation from interband and intraband transitions in Au and their injection into MoS2.
- Analyzing the correlation between different hot electron energies and CO2RR product selectivity.
Main Results:
- The Au-MoS2 hybrid catalyst effectively utilizes hot electrons from both interband and intraband transitions.
- Interband hot electrons selectively enhanced methanol and formic acid production at different overpotentials.
- Intraband hot electrons significantly increased ethanol selectivity through C-C coupling.
Conclusions:
- Spatially separated catalysts offer unique advantages in plasmon-mediated electrochemical reactions.
- Utilizing both interband and intraband hot electrons provides an effective strategy for efficient and selective CO2 reduction.
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