| Literature DB >> 33823079 |
David M Koshy1,2, Sindhu S Nathan1,2, Arun S Asundi1,2, Ahmed M Abdellah3, Samuel M Dull1, David A Cullen4, Drew Higgins3, Zhenan Bao1,2, Stacey F Bent1,2, Thomas F Jaramillo1,2.
Abstract
Understanding the differences between reactions driven by elevated temperature or electric potential remains challenging, largely due to materials incompatibilities between thermal catalytic and electrocatalytic environments. We show that Ni, N-doped carbon (NiPACN), an electrocatalyst for the reduction of CO2 to CO (CO2 R), can also selectively catalyze thermal CO2 to CO via the reverse water gas shift (RWGS) representing a direct analogy between catalytic phenomena across the two reaction environments. Advanced characterization techniques reveal that NiPACN likely facilitates RWGS on dispersed Ni sites in agreement with CO2 R active site studies. Finally, we construct a generalized reaction driving-force that includes temperature and potential and suggest that NiPACN could facilitate faster kinetics in CO2 R relative to RWGS due to lower intrinsic barriers. This report motivates further studies that quantitatively link catalytic phenomena across disparate reaction environments.Entities:
Keywords: carbon dioxide; catalysis; electrochemistry; nitrogen-doped carbon; reverse water-gas shift
Year: 2021 PMID: 33823079 DOI: 10.1002/anie.202101326
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336