| Literature DB >> 28710839 |
Hemma Mistry1,2, Yong-Wook Choi1, Alexander Bagger3, Fabian Scholten1, Cecile S Bonifacio4, Ilya Sinev1, Nuria J Divins1, Ioannis Zegkinoglou1, Hyo Sang Jeon1, Kim Kisslinger5, Eric A Stach5, Judith C Yang4, Jan Rossmeisl3, Beatriz Roldan Cuenya1,6.
Abstract
Efficient, stable catalysts with high selectivity for a single product are essential if electroreduction of CO2 is to become a viable route to the synthesis of industrial feedstocks and fuels. A plasma oxidation pre-treatment of silver foil enhances the number of low-coordinated catalytically active sites, which dramatically lowers the overpotential and increases the activity of CO2 electroreduction to CO. At -0.6 V versus RHE more than 90 % Faradaic efficiency towards CO was achieved on a pre-oxidized silver foil. While transmission electron microscopy (TEM) and operando X-ray absorption spectroscopy showed that oxygen species can survive in the bulk of the catalyst during the reaction, quasi in situ X-ray photoelectron spectroscopy showed that the surface is metallic under reaction conditions. DFT calculations reveal that the defect-rich surface of the plasma-oxidized silver foils in the presence of local electric fields drastically decrease the overpotential of CO2 electroreduction.Entities:
Keywords: CO2 reduction; electrocatalysis; nanostructures; silver
Year: 2017 PMID: 28710839 DOI: 10.1002/anie.201704613
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336