Related Experiment Video
Updated: Aug 29, 2025

Synthesis and Performance Characterizations of Transition Metal Single Atom Catalyst for Electrochemical CO2 Reduction
Published on: April 10, 2018
CO2 Conversion via Reverse Water Gas Shift Reaction Using Fully Selective Mo-P Multicomponent Catalysts.
Qi Zhang1, Matthew Bown1, Laura Pastor-Pérez1
1Department of Chemical and Process Engineering, University of Surrey, Guildford, GU2 7XH, United Kingdom.
Molybdenum phosphide (MoP) catalysts effectively convert CO2 into synthesis gas via the reverse water gas shift reaction. These earth-abundant catalysts suppress unwanted methane production and show stable performance for CO2 utilization.
Area of Science:
- Catalysis
- Materials Science
- Chemical Engineering
Background:
- The reverse water gas shift (RWGS) reaction is crucial for CO2 utilization, producing synthesis gas.
- Commercialization requires earth-abundant catalysts that prevent methanation and maintain stability at high temperatures.
Purpose of the Study:
- To identify a nonprecious metal catalyst for efficient and selective RWGS.
- To evaluate molybdenum phosphide (MoP) for CO2 conversion and synthesis gas production.
Main Methods:
- Synthesis and characterization of supported molybdenum phosphide (MoP) catalysts.
- Testing catalyst performance in the RWGS reaction under elevated temperatures.
- Assessing catalyst stability and selectivity, particularly suppression of methanation.
Main Results:
- Supported MoP catalysts completely suppressed the competing methanation reaction.
- MoP catalysts demonstrated stable performance with minimal deactivation at high temperatures.
- High conversions were achieved, producing significant quantities of water.
Conclusions:
- Molybdenum phosphide (MoP) is a promising earth-abundant catalyst for the RWGS reaction.
- MoP catalysts offer a viable pathway for CO2 utilization by producing synthesis gas.
- The suppression of methanation and catalyst stability are key advantages for industrial application.
Related Concept Videos
Reduction of Alkenes: Catalytic Hydrogenation
Metals like palladium, platinum, and nickel are commonly used in their solid forms — fine powder on an inert surface. As these catalysts remain insoluble in the reaction mixture, they are referred to as heterogeneous catalysts.
The hydrogenation process takes place on the...
Preparation of Alcohols via Addition Reactions
The acid-catalyzed addition of water to the double bond of alkenes is a large-scale industrial method used to synthesize low-molecular-weight alcohols. An acidic atmosphere is required to allow the hydrogen in the water molecule to act as an electrophile and attack the double bond in an alkene. The addition of a proton to the double bond creates a carbocation intermediate. The proton preferentially bonds to the less substituted end of the double bond to create a more stable carbocation...
Catalysis
Reduction of Benzene to Cyclohexane: Catalytic Hydrogenation
Hydroboration-Oxidation of Alkenes
Reduction of Alkenes: Asymmetric Catalytic Hydrogenation
The metal catalyst used can be either heterogeneous or homogeneous. When hydrogenation of an alkene generates a chiral center, a pair of enantiomeric products is expected to form. However, an enantiomeric excess of one of the products can be facilitated using an enantioselective reaction or an...

