Electrocatalytic Polyester Waste Upcycling via Lattice Oxygen Redox Activation

Electrocatalytic upcycling of waste polyester plastics into valuable organic acids offers a dual solution for mitigating plastic pollution and promoting sustainable carbon cycling. However, practical implementation remains limited by the scarcity of cost-effective and high-performance electrocatalysts. In this work, we investigate MCo<sub>2</sub>O<sub>4</sub> (where M═Mn, Fe, Co, Cu, and Ni) as model catalysts and identify lattice oxygen activity as a critical factor governing the electrochemical upgrading of waste polyethylene terephthalate (PET). NiCo<sub>2</sub>O<sub>4</sub> demonstrates the highest oxygen activity, characterized by the greatest density of O 2p ligand holes and the closest proximity of the O 2p band center to the Fermi level. Such unique character facilitates lattice oxygen participation in surface electro-oxidation reactions, leading to exceptional performance of up to 98.3% formate selectivity and 98.9% Faraday efficiency, among the highest values reported for transition metal catalysts in alcohol electro-oxidation. We further demonstrate the direct electrocatalytic upcycling of real waste PET plastics, estimating a $739 profit per ton of recycled PET and confirming its economic viability. These results provide critical insights for refining the design principles of electrocatalytic systems aimed at recycling diverse waste materials and pollutants.

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Publication Details

Journal
Angewandte Chemie International Edition
Published
2025-08-25
DOI
https://doi.org/10.1002/anie.202513447
Citations
4
Primary Topic
Conducting polymers and applications
Type
article
Field-Weighted Citation Impact
2.43

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article

Electrocatalytic Polyester Waste Upcycling via Lattice Oxygen Redox Activation

Chenyu Zhou, Shijun Zhao, Xuepeng Xiang, Chenghao Jia et al.
4 citations
Angewandte Chemie International Edition
Conducting polymers and applications
2.43
article

Electrocatalytic Polyester Waste Upcycling via Lattice Oxygen Redox Activation

Chenyu Zhou, Shijun Zhao, Xuepeng Xiang, Chenghao Jia, Yan Chen, Zhang Lin, Shiying Wu, Nian Zhang
article en
4 citations

Abstract

Electrocatalytic upcycling of waste polyester plastics into valuable organic acids offers a dual solution for mitigating plastic pollution and promoting sustainable carbon cycling. However, practical implementation remains limited by the scarcity of cost-effective and high-performance electrocatalysts. In this work, we investigate MCo<sub>2</sub>O<sub>4</sub> (where M═Mn, Fe, Co, Cu, and Ni) as model catalysts and identify lattice oxygen activity as a critical factor governing the electrochemical upgrading of waste polyethylene terephthalate (PET). NiCo<sub>2</sub>O<sub>4</sub> demonstrates the highest oxygen activity, characterized by the greatest density of O 2p ligand holes and the closest proximity of the O 2p band center to the Fermi level. Such unique character facilitates lattice oxygen participation in surface electro-oxidation reactions, leading to exceptional performance of up to 98.3% formate selectivity and 98.9% Faraday efficiency, among the highest values reported for transition metal catalysts in alcohol electro-oxidation. We further demonstrate the direct electrocatalytic upcycling of real waste PET plastics, estimating a $739 profit per ton of recycled PET and confirming its economic viability. These results provide critical insights for refining the design principles of electrocatalytic systems aimed at recycling diverse waste materials and pollutants.

Angewandte Chemie International EditionVol. 64(42)
Guangdong University of Technology (CN), Central South University (CN), City University of Hong Kong (HK), Shanghai Advanced Research Institute (CN), Zero to Three (US), Shanghai Institute of Applied Physics (CN)
National Natural Science Foundation of China, Foundation for Innovative Research Groups of the National Natural Science Foundation of China, Fundamental Research Funds for the Central Universities
Openalex Percentile: Top 11%
Conducting polymers and applications
2.43
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