Free Standing Nanoporous Palladium Alloys as CO Poisoning Tolerant Electrocatalysts for the Electrochemical Reduction of CO2 to Formate
CO2 electrochemical reduction to formate has emerged as one of the promising routes for CO2 conversion to useful chemicals and energy storage. Palladium has been shown to make formate with a high selectivity at minimal overpotential. However, production of CO as a minor product quickly deactivates t...
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Published in | ACS catalysis Vol. 9; no. 6; pp. 5290 - 5301 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
American Chemical Society
07.06.2019
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Subjects | |
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Abstract | CO2 electrochemical reduction to formate has emerged as one of the promising routes for CO2 conversion to useful chemicals and energy storage. Palladium has been shown to make formate with a high selectivity at minimal overpotential. However, production of CO as a minor product quickly deactivates the catalyst during extended electrolysis. Here, we present nanoporous Pd alloys (np-PdX) formed by electrochemical dealloying of Pd15X85 alloys (X = Co, Ni, Cu, and Ag) as active free-standing electrocatalysts with high formate selectivity and CO poisoning tolerance. Rate of deactivation under constant potential electrolysis, due to CO passivation, is strongly correlated to the identity of the transition metal alloying component. We purport that this composition dependent behavior is due to the induced electronic changes in the active Pd surface, affecting both the CO adsorption strength and the near surface hydrogen solubility, which can impact the adsorption strength of active/inactive intermediates and reaction selectivity. Free-standing np-PdCo and np-PdNi are found to exhibit high areal formate partial current densities, >20 mA cm–2, with high CO poisoning tolerance and minimal active area loss at cathodic potentials, demonstrating the utility of these materials for selective and stable CO2 electrolysis. |
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AbstractList | CO2 electrochemical reduction to formate has emerged as one of the promising routes for CO2 conversion to useful chemicals and energy storage. Palladium has been shown to make formate with a high selectivity at minimal overpotential. However, production of CO as a minor product quickly deactivates the catalyst during extended electrolysis. Here, we present nanoporous Pd alloys (np-PdX) formed by electrochemical dealloying of Pd15X85 alloys (X = Co, Ni, Cu, and Ag) as active free-standing electrocatalysts with high formate selectivity and CO poisoning tolerance. Rate of deactivation under constant potential electrolysis, due to CO passivation, is strongly correlated to the identity of the transition metal alloying component. We purport that this composition dependent behavior is due to the induced electronic changes in the active Pd surface, affecting both the CO adsorption strength and the near surface hydrogen solubility, which can impact the adsorption strength of active/inactive intermediates and reaction selectivity. Free-standing np-PdCo and np-PdNi are found to exhibit high areal formate partial current densities, >20 mA cm–2, with high CO poisoning tolerance and minimal active area loss at cathodic potentials, demonstrating the utility of these materials for selective and stable CO2 electrolysis. |
Author | Hart, James L Taheri, Mitra L Keith, John Snyder, Joshua D Chatterjee, Swarnendu Griego, Charles Li, Yawei |
AuthorAffiliation | Department of Chemical and Petroleum Engineering Department of Materials Science and Engineering Department of Chemical and Biological Engineering |
AuthorAffiliation_xml | – name: Department of Chemical and Petroleum Engineering – name: Department of Chemical and Biological Engineering – name: Department of Materials Science and Engineering |
Author_xml | – sequence: 1 givenname: Swarnendu surname: Chatterjee fullname: Chatterjee, Swarnendu organization: Department of Chemical and Biological Engineering – sequence: 2 givenname: Charles surname: Griego fullname: Griego, Charles organization: Department of Chemical and Petroleum Engineering – sequence: 3 givenname: James L orcidid: 0000-0002-2960-6925 surname: Hart fullname: Hart, James L organization: Department of Materials Science and Engineering – sequence: 4 givenname: Yawei surname: Li fullname: Li, Yawei organization: Department of Chemical and Biological Engineering – sequence: 5 givenname: Mitra L surname: Taheri fullname: Taheri, Mitra L organization: Department of Materials Science and Engineering – sequence: 6 givenname: John orcidid: 0000-0002-6583-6322 surname: Keith fullname: Keith, John organization: Department of Chemical and Petroleum Engineering – sequence: 7 givenname: Joshua D orcidid: 0000-0003-3162-4126 surname: Snyder fullname: Snyder, Joshua D email: jds43@drexel.edu organization: Department of Chemical and Biological Engineering |
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DOI | 10.1021/acscatal.9b00330 |
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Snippet | CO2 electrochemical reduction to formate has emerged as one of the promising routes for CO2 conversion to useful chemicals and energy storage. Palladium has... |
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Title | Free Standing Nanoporous Palladium Alloys as CO Poisoning Tolerant Electrocatalysts for the Electrochemical Reduction of CO2 to Formate |
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