Related Experiment Video
Updated: Jul 6, 2025

Tuning the Acidity of Pt/ CNTs Catalysts for Hydrodeoxygenation of Diphenyl Ether
Published on: August 17, 2019
Direct propylene epoxidation via water activation over Pd-Pt electrocatalysts
Minju Chung1, Joseph H Maalouf1, Jason S Adams2
1Department of Chemical Engineering, Massachusetts Institute of Technology, Cambridge, MA 02139, USA.
This study introduces a novel palladium-platinum alloy catalyst (PdPtO/C) for sustainable electrochemical propylene epoxidation using water. The catalyst achieves high efficiency, offering a greener alternative to hazardous chemical routes.
Area of Science:
- Electrochemistry
- Catalysis
- Sustainable Chemistry
Background:
- Traditional propylene epoxidation uses hazardous reagents like chlorine or peroxides.
- Developing sustainable and efficient catalytic methods is crucial for green chemistry.
Purpose of the Study:
- To develop a direct electrochemical method for propylene epoxidation using water-oxidation intermediates.
- To investigate the performance of a novel oxidized palladium-platinum alloy catalyst (PdPtO/C).
Main Methods:
- Electrochemical synthesis and characterization of PdPtO/C catalyst.
- Electrochemical propylene epoxidation experiments at ambient conditions.
- Kinetic analysis to elucidate reaction mechanisms.
Main Results:
- The PdPtO/C catalyst achieved a 66 ± 5% Faradaic efficiency for propylene epoxidation.
- High performance was observed at 50 mA/cm² under ambient temperature and pressure.
- Embedding platinum stabilized oxidized platinum species, enhancing catalyst performance.
Conclusions:
- Direct electrochemical propylene epoxidation using water-oxidation intermediates is a viable sustainable alternative.
- The PdPtO/C catalyst demonstrates effective oxygen-atom transfer from water without mediators.
- This strategy holds promise for various electrochemical oxygenation reactions.
Related Concept Videos
Oxidation of Alkenes: Anti Dihydroxylation with Peroxy Acids
Preparation of Epoxides
Epoxides result from alkene oxidation, which can be achieved by a) air, b) peroxy acids, c) hypochlorous acids, and d) halohydrin cyclization.
Epoxidation with Peroxy Acids
Epoxidation of alkenes via oxidation with peroxy acids involves the conversion of a carbon–carbon double bond to an epoxide using the oxidizing agent meta-chloroperoxybenzoic acid, commonly known as MCPBA. Since the O–O bond of peroxy acids is very weak, the addition of electrophilic oxygen of...
Sharpless Epoxidation
Acid-Catalyzed Ring-Opening of Epoxides
Free-Radical Chain Reaction and Polymerization of Alkenes
Base-Catalyzed Ring-Opening of Epoxides

