journal article·2021-07-09

Decreasing the Energy Consumption of the CO2 Electrolysis Process Using a Magnetic Field

Saket S. Bhargava, Daniel Azmoodeh, Xinyi Chen, Emiliana R. Cofell, Anne Marie Esposito, Sumit Verma, Andrew A. Gewirth, Paul J. A. Kenis

ACS Energy Letters· Volume 6· Issue 7
Publisher page

Abstract

The renewable electricity-powered electrolysis of CO2 could be a viable carbon-neutral method for producing carbon-based value-added chemicals like carbon monoxide, formic acid, ethylene, and ethanol. A typical CO2 electrolyzer suffers, however, from the high power requirements, mainly due to the energy-intense anode reaction. In this work, we decrease the anode overpotential and thus reduce the overall cell energy consumption by using a NiFe-based bimetallic catalyst at the anode and applying a magnetic field. For a CO2 electrolysis process producing CO in a gas diffusion electrode-based flow electrolyzer, we demonstrate that power savings in the range from 7% to 64% can be achieved at CO partial current densities exceeding −300 mA/cm2 using a NiFe catalyst at the anode and/or by using a magnetic field at the anode. We achieve a maximum CO partial current density of −565 mA/cm2 at a full cell energy efficiency of 45% with 2 M KOH as the electrolyte.
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Research context

OpenAlex topics: CO2 Reduction Techniques and Catalysts · Advanced battery technologies research · Electrocatalysts for Energy Conversion

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Department of Chemical & Biomolecular Engineering, University of Illinois Urbana−Champaign, Urbana, Illinois 61801, United States

International Institute for Carbon Neutral Energy Research (WPI-I2CNER), Kyushu University, Fukuoka 819-0395, Japan

Department of Chemistry, University of Illinois Urbana−Champaign, Urbana, Illinois 61801, United States

Department of Materials Science & Engineering, University of Illinois Urbana−Champaign, Urbana, Illinois 61801, United States

Funding

Link Foundation · Shell

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