4.6 Review

Recent Advances in the Catalyst Design and Mass Transport Control for the Electrochemical Reduction of Carbon Dioxide to Formate

Journal

CATALYSTS
Volume 10, Issue 8, Pages -

Publisher

MDPI
DOI: 10.3390/catal10080859

Keywords

electrochemical reduction; carbon dioxide; formate production

Funding

  1. National Research Foundation of Korea (NRF) - Korean Government (MSIT) [NRF-2020R1C1C1010963, NRF-2016R1A5A1012966]
  2. National Research Foundation of Korea [2016R1A5A1012966] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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Closing the carbon cycle by the electrochemical reduction of CO(2)to formic acid and other high-value chemicals is a promising strategy to mitigate rapid climate change. The main barriers to commercializing a CO(2)reduction reaction (CO2RR) system for formate production are the chemical inertness, low aqueous solubility, and slow mass transport characteristics of CO2, along with the low selectivity and high overpotential observed in formate production via CO(2)reduction. To address those problems, we first explain the possible reaction mechanisms of CO(2)RRs to formate, and then we present and discuss several strategies to overcome the barriers to commercialization. The electronic structure of the catalyst can be tuned to favor a specific intermediate by adjusting the catalyst composition and tailoring the facets, edges, and corners of the catalyst to better expose the active sites, which has primarily led to increased catalytic activity and selectivity. Controlling the local pH, employing a high-pressure reactor, and using systems with three-phase boundaries can tune the mass transport properties of reactants at the catalyst surface. The reported electrocatalytic performances are summarized afterward to provide insight into which strategies have critical effects on the production of formate.

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