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Coelectrolysis of PET and CO2 Using an Electrochemically Restructured Co-MOF-74 Anode and a Polymeric
Raúl Rojas-Luna1,2, Lewis S Cousins3, Rhiannon Germaney1
1Department of Chemistry, School of Natural Sciences, University of Lincoln, Green Lane, Lincoln LN6 7DL, U.K.
Abstract:
Mitigating carbon emissions and plastic waste is a pressing societal challenge due to the disruptive environmental impact of incremental accumulation. A promising strategy to address both issues is coelectrolysis of CO2 and PET-plastic waste to high-value commodity chemicals. Here, we report electrocatalytic upcycling of polyethylene terephthalate (PET) plastic to formate and terephthalic acid using a cobalt-based metal-organic framework (Co-MOF-74). The electrocatalyst underwent oxidative restructuring to cobalt oxyhydroxide under operating conditions and exhibited near-unity faradaic efficiency (FE) for the ethylene glycol oxidation reaction (EGOR) to formate during short-term electrolysis. Notably, EGOR required 0.23 V lower potential compared to the conventional oxygen evolution reaction (OER) at a current density of 100 mA cm-2. When coupled with a CO2 reducing cathode, a maximum combined FE of 156% was achieved for formate (anode) and syngas (cathode) at a cell voltage (Ecell) of 1.6 V. Upon integration of the EGOR electrode in a CO2-fed flow cell, the coupled system required an Ecell of ∼2.3 V to operate at 75 mA cm-2. This work presents a promising integrated approach that offers a compelling solution for mitigating environmental pollution by enabling the electrochemical reforming of CO2 and plastic waste into valuable chemicals under cost-effective and energy-efficient conditions.
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