# Coelectrolysis of PET and CO2 Using an Electrochemically Restructured Co-MOF-74 Anode and a Polymeric Co-Phthalocyanine Cathode

**Authors:** Raúl Rojas-Luna, Lewis S. Cousins, Rhiannon Germaney, Dolores G. Gil-Gavilán, Miguel Castillo-Rodríguez, Dora-Alicia Garcia Osorio, Thomas Doughty, Dolores Esquivel, Charles E. Creissen, Souvik Roy

PMC · DOI: 10.1021/acsami.5c22269 · ACS Applied Materials & Interfaces · 2026-01-20

## TL;DR

This paper presents an electrochemical method to convert plastic waste and CO2 into valuable chemicals using a cobalt-based catalyst system.

## Contribution

The study introduces a novel electrocatalytic system using a restructured Co-MOF-74 anode and a polymeric co-phthalocyanine cathode for coelectrolysis.

## Key findings

- The Co-MOF-74 anode achieved near-unity faradaic efficiency for ethylene glycol oxidation to formate.
- The system achieved a combined faradaic efficiency of 156% for formate and syngas at 1.6 V cell voltage.
- The integrated system operated at 2.3 V in a CO2-fed flow cell at 75 mA cm–2.

## 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 (E
cell) of 1.6 V. Upon integration of the EGOR electrode in a CO2-fed flow cell, the coupled system required an E
cell 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.

## Linked entities

- **Chemicals:** CO2 (PubChem CID 280), formate (PubChem CID 283), terephthalic acid (PubChem CID 7489), ethylene glycol (PubChem CID 174)

## Full-text entities

- **Chemicals:** CO2 (MESH:D002245), oxygen (MESH:D010100), terephthalic acid (MESH:C011363), carbon (MESH:D002244), Co-MOF-74 (-), PET (MESH:D011093), formate (MESH:C030544), cobalt oxyhydroxide (MESH:C477250), ethylene glycol (MESH:D019855), cobalt (MESH:D003035)

## Full text

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## Figures

8 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12884455/full.md

## References

70 references — full list in the complete paper: https://tomesphere.com/paper/PMC12884455/full.md

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Source: https://tomesphere.com/paper/PMC12884455