Hiring in life sciences? Share your open positions with our professional community. Read more Close

Advertisement

Upcycling Spent Graphite Anodes into Bifunctional Photothermal Catalysts for Efficient PET Chemical Recycling.

Created on 17 Sep 2025

Authors

Yeping Xie, Mingle Qiu, Binglei Jiao, Panpan Xu, Muhan Cao, Qiao Zhang, Jinxing Chen

Published in

Advanced science (Weinheim, Baden-Wurttemberg, Germany). Pages e10772. Sep 17, 2025. Epub Sep 17, 2025.

Abstract

The economic recovery of anodes in lithium-ion batteries remains challenging due to their low value. Here, the study presents a cross-sector battery-plastic co-upcycling strategy that transforms spent graphite anodes into bifunctional photothermal catalysts for efficient Polyethylene terephthalate (PET) depolymerization. Upon reaction with ethylene glycol (EG), lithiated graphite spontaneously enables copper foil detachment, graphite regeneration, and in situ formation of organolithium species (C2H4O2Li2-xHx). The resulting catalyst system achieves 95% PET conversion and 64.6% BHET yield within 15 minutes under 0.71 W/cm2 sunlight. Mechanistically, a synergistic effect between solid electrolyte interphase (SEI)-derived Li2CO3/Li2O and organolithium intermediates significantly accelerates glycolysis. Techno-economic modeling for a 90 000 ton/year facility reveals a minimum selling price of $0.956/kg for BHET and annual energy savings of 5.039 × 1011 kJ. This work highlights a scalable, low-cost approach to integrate battery and plastic waste recycling, offering a new paradigm for sustainable urban mining and circular polymer economy.

PMID:
40959876
Bibliographic data and abstract were imported from PubMed on 17 Sep 2025.

Read full publication at:
Please sign in to see all details.

Advertisement

Stats

  • Community rating n/a 0 votes
  • Reviewers' rating n/a 0 votes
  • Your rating

1-terrible, 9-excellent. How would you rate this publication? Sign in in to submit your rating.

  • Recommendations n/a n/a positive of 0 vote(s)
  • Views 51
  • Comments 0

Recommended by

  • No recommendations yet.

Post a comment

You need to be signed in to post comments. You can sign in here.

Comments

There are no comments yet.

Advertisement