Mechanistic Insights into CO2 Electroreduction on Ni2P: Understanding Its Selectivity toward Multicarbon Products

Recently, nickel phosphides (Ni x P y ) have been reported to enable selective electrochemical formation of multicarbon products (C3 and C4) via the CO2 reduction reaction (CO2RR); nevertheless, their activities remain low. In order to understand the roots of their high selectivity and low activity...

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Bibliographic Details
Published in:ACS catalysis 2021-09, Vol.11 (18), p.11706-11715
Main Authors: Banerjee, Sayan, Kakekhani, Arvin, Wexler, Robert B, Rappe, Andrew M
Format: Article
Language:English
Subjects:
CO2
electroreduction
MATERIALS SCIENCE
multicarbon products
nickel phosphides
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Summary:Recently, nickel phosphides (Ni x P y ) have been reported to enable selective electrochemical formation of multicarbon products (C3 and C4) via the CO2 reduction reaction (CO2RR); nevertheless, their activities remain low. In order to understand the roots of their high selectivity and low activity and to direct the design of more active Ni x P y -based CO2RR catalysts, we investigate the CO2RR mechanism on Ni2P using density functional theory (DFT) calculations. We reveal that the reaction proceeds through the formate pathway, followed by formaldehyde (H2CO*) formation and self-condensation. Moreover, we demonstrate that surface hydride transfer steps, along with surface-mediated C–C coupling, are essential in order to avoid C1 product formation and boost selectivity toward multicarbon products. In addition, we find that the thermal surface hydride transfer from the surface to the physisorbed CO2 is one of the key rate-limiting steps, and since it is not electroactive, it cannot be accelerated by applying an overpotential. Finally, our results also show that the hydrogen affinity of the surface and the dynamic surface reconstruction via H adsorption facilitate selective CO2 reduction and C–C coupling on Ni2P. These findings provide an impetus for exploring materials design space to identify the physical principles that govern the thermodynamics of rate-limiting thermal steps in electrocatalytic processes.
ISSN:2155-5435
2155-5435
DOI:10.1021/acscatal.1c03639