4.8 Article

Heteroatoms Induce Localization of the Electric Field and Promote a Wide Potential-Window Selectivity Towards CO in the CO2 Electroreduction

期刊

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/anie.202212640

关键词

Ag-Based; Electric Filed; Electrochemical CO2 Reduction; Heteroatoms; Intermediate

资金

  1. International Science and Technology Cooperation Program [2017YFE0127800, 2018YFE0203402]
  2. Natural Science Foundation of China [21872174, U1932148]
  3. China postdoctoral science foundation [2021 M703627]
  4. State Key Laboratory of Powder Metallurgy, Hunan Provincial Science and Technology Program [2017XK2026]
  5. Hunan Provincial Natural Science Foundation of China [2020JJ2041, 2020JJ5691]
  6. science and technology innovation Program of Hunan Province [2020WK2002]
  7. Ministry of Science and Technology, Taiwan [MOST 110-2113-M213-002]
  8. e-conversion cluster of excellence from the (DFG, German Research Foundation) under Germany's Excellence Strategy [EXC 2089/1390776260]
  9. Bavarian program Solar Technologies Go Hybrid (SolTech)
  10. Center for NanoScience (CeNS)
  11. European Commission through the ERC Starting Grant CATALIGHT [802989]
  12. Projekt DEAL

向作者/读者索取更多资源

This study demonstrates that the electric field generated by Sn heteroatoms on the Ag/Sn catalyst enhances the adsorption of *COOH, favoring the production of CO during CO2RR process.
Carbon dioxide electroreduction (CO2RR) is a sustainable way of producing carbon-neutral fuels. Product selectivity in CO2RR is regulated by the adsorption energy of reaction-intermediates. Here, we employ differential phase contrast-scanning transmission electron microscopy (DPC-STEM) to demonstrate that Sn heteroatoms on a Ag catalyst generate very strong and atomically localized electric fields. In situ attenuated total reflection infrared spectroscopy (ATR-IR) results verified that the localized electric field enhances the adsorption of *COOH, thus favoring the production of CO during CO2RR. The Ag/Sn catalyst exhibits an approximately 100 % CO selectivity at a very wide range of potentials (from -0.5 to -1.1 V, versus reversible hydrogen electrode), and with a remarkably high energy efficiency (EE) of 76.1 %.

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