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Published on: January 30, 2015
Mitigating Cobalt Phthalocyanine Aggregation in Electrocatalyst Films through Codeposition with an Axially
William S Dean1, Taylor L Soucy1, Kevin E Rivera-Cruz1
1Department of Chemistry, University of Michigan, Ann Arbor, Michigan, 48109, USA.
Poly(4-vinylpyridine) (P4VP) prevents cobalt phthalocyanine (CoPc) aggregation during CO2 electroreduction, enhancing catalyst performance. This dispersion strategy improves CO2 conversion activity and selectivity on electrode surfaces.
Area of Science:
- Electrochemistry
- Materials Science
- Catalysis
Background:
- Cobalt phthalocyanine (CoPc) is a potential catalyst for aqueous carbon dioxide (CO2) electroreduction.
- Catalyst aggregation at high loadings limits CoPc's efficiency and stability.
- Dispersing CoPc is crucial for enhancing its catalytic activity and selectivity.
Purpose of the Study:
- To investigate the use of poly(4-vinylpyridine) (P4VP) as a dispersing agent for CoPc.
- To evaluate the impact of P4VP on CoPc aggregation and catalytic performance in CO2 electroreduction.
- To compare P4VP with other polymers like Nafion for CoPc dispersion and catalytic efficiency.
Main Methods:
- Codeposition of CoPc with P4VP onto carbon electrode surfaces.
- Characterization using transmission and diffuse reflectance UV-vis spectroscopy to study dispersion.
- Morphological analysis via Scanning Electron Microscopy (SEM).
- Electrochemical measurements to assess CO2 electroreduction activity and selectivity.
Main Results:
- P4VP effectively disperses CoPc in deposition solutions and prevents reaggregation in films through axial coordination and π-stacking.
- SEM images confirmed reduced aggregation and improved morphology of CoPc when codeposited with P4VP.
- CoPc codeposited with P4VP exhibited significantly higher CO2 electroreduction activity and selectivity compared to CoPc codeposited with Nafion.
Conclusions:
- P4VP is a superior dispersing agent for CoPc in CO2 electroreduction compared to Nafion.
- The enhanced dispersion by P4VP leads to improved catalytic activity and selectivity.
- This strategy offers a promising approach to optimize molecular catalysts for CO2 conversion.
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